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	Gene Summary
	Translation studies in PubMed
	Exon Skipping Events
	Expression
	Expression Regulation
	Associated Genes
	Protein 3D Structure
	Protein-Protein Interaction
	Mutations
	Prognostic Analysis
	Gender Association
	Age Association
	Related Drugs
	Related Diseases

Translation Factor: SYNCRIP (NCBI Gene ID:10492)

Gene Summary

Gene Summary

Gene Information	Gene Name: SYNCRIP
	Gene ID: 10492
	Gene Symbol	SYNCRIP
	Gene ID	10492
	Gene Name	synaptotagmin binding cytoplasmic RNA interacting protein
	Synonyms	GRY-RBP\|GRYRBP\|HNRNPQ\|HNRPQ1\|NSAP1\|PP68\|hnRNP-Q
	Cytomap	6q14.3
	Type of Gene	protein-coding
	Description	heterogeneous nuclear ribonucleoprotein QNS1-associated protein 1glycine- and tyrosine-rich RNA-binding protein
	Modification date	20200327
	UniProtAcc	O60506

Child GO biological process term(s) under GO:0006412

GO ID	GO term
GO:0017148	Negative regulation of translation
GO:0006417	Regulation of translation
GO:0045727	Positive regulation of translation
GO:0002181	Cytoplasmic translation
GO:0006412	Translation

Gene ontology of translaction factor with evidence of Inferred from Direct Assay (IDA) from Entrez

Partner	Gene	GO ID	GO term	PubMed ID
Hgene	SYNCRIP	GO:0017148	negative regulation of translation	23071094
Hgene	SYNCRIP	GO:0071346	cellular response to interferon-gamma	15479637

Inferred gene age of translation factor.

Gene	Inferred gene age group among (0 - 67.6], (67.6 - 355.7], (355.7 - 733], (733 - 1119.25], >1119.25
SYNCRIP	(733 - 1119.25]

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Translation Studies in PubMed

We searched PubMed using 'SYNCRIP[title] AND translation [title] AND human.'

Gene	Title	PMID
SYNCRIP	SYNCRIP, a component of dendritically localized mRNPs, binds to the translation regulator BC200 RNA	18045242

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Exon Skipping Events

Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure.
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
For more annotations, please visit our ExonSkipDB.

Open reading frame (ORF) analsis of exon skipping events based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.

ENST	Exon skip start (DNA)	Exon Skip end (DNA)	ORF
ENST00000369622	86328985	86329135	In-frame
ENST00000369622	86333694	86333830	Frame-shift
ENST00000369622	86346684	86346861	In-frame
ENST00000369622	86346960	86347074	In-frame
ENST00000369622	86351009	86351169	3UTR-3CDS

Exon skipping position in the amino acid sequence.

ENST	Exon skip start (DNA)	Exon Skip end (DNA)	Len(transcript seq)	Exon skip start (mRNA)	Exon Skip end (mRNA)	Len(amino acid seq)	Exon skip start (AA)	Exon Skip end (AA)
ENST00000369622	86328985	86329135	3040	1510	1659	623	336	386
ENST00000369622	86346684	86346861	3040	991	1167	623	163	222
ENST00000369622	86346960	86347074	3040	877	990	623	125	163

Potentially (partially) lost protein functional features of UniProt.

UniProtAcc

Exon skip start (AA)

Exon Skip end (AA)

Function feature start (AA)

Function feature end (AA)

Functional feature type

Functional feature desc.

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Expression

Gene expression level across TCGA pancancer

Gene expression level across GTEx pantissue

Expression level of gene isoforms across TCGA pancancer

Expression level of gene isoforms across GTEx pantissue

Cancer(tissue) type-specific expression level of Translation factor using z-score distriution

Differential expression between tumor and matched normal (in the cancer types with more than 10 matched samples)

Cancer type	Translation factor	FC	adj.pval
STAD	SYNCRIP	-3.24695040489934	0.00222697434946895
THCA	SYNCRIP	-3.15946429809988	2.46790521879123e-10

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Expression Regulation

Translation factor expression regulation through miRNA binding

Cancer type	Gene	miRNA	TargetScan binding score (Context++ score percentile)	Coefficient	Pvalue
BRCA	SYNCRIP	hsa-miR-196b-5p	88	0.307546251217137	0.00601593831679952

Translation factor expression regulation through methylation in the promoter of Translation factor

Cancer type

Gene

methyl group b

methyl group a

DEG pval

avg methyl in b

avg methyl in a

avg exp in b

avg exp in a

Translation factor expression regulation through methylation in the gene body of Translation factor (positive regulation)

Cancer type

Gene

methyl group b

methyl group a

DEG pval

avg methyl in b

avg methyl in a

avg exp in b

avg exp in a

Translation factor expression regulation through copy number variation of Translation factor

Cancer type	Gene	Coefficient	Pvalue
KIRC	SYNCRIP	0.036176445	0.017847429
LIHC	SYNCRIP	0.07895802	0.037502156
MESO	SYNCRIP	-0.074594402	0.047141413

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Associated Genes

Strongly correlated genes belong to cellular important gene groups with SYNCRIP (coefficient>0.8, pval<0.05, node color based on FC between tumor and matched normal). Significantly associated important genes in the individual cancer types. * Cell metabolism gene: cell metabolism genes from REACTOME (black edge), IUPHAR: drug target genes from IUPHAR (blue edge), Kinase: human kinase genes (brown edge), CGC: cancer gene census genes (orange edge), TSG: tumor suppresor genes (purple edge), Epifactor: epigenetic factors (light blue edge), TF: transcription factors (green)

Cancer type	Gene group	Translation factor	Correlated gene	Coefficient	Pvalue
CHOL	IUPHAR	SYNCRIP	SENP6	0.801124691	3.87E-11
KICH	Cell metabolism gene	SYNCRIP	NUP153	0.82960136	3.02E-24
KICH	CGC	SYNCRIP	CDK12	0.811730097	1.69E-22
KICH	IUPHAR	SYNCRIP	CDK12	0.811730097	1.69E-22
KICH	Kinase	SYNCRIP	CDK12	0.811730097	1.69E-22
PRAD	CGC	SYNCRIP	GOPC	0.819356501	1.60E-134
PRAD	CGC	SYNCRIP	BCLAF1	0.836132497	4.90E-145
PRAD	Epifactor	SYNCRIP	HDAC2	0.801884866	1.13E-124
PRAD	Epifactor	SYNCRIP	MAP3K7	0.837866862	3.43E-146
PRAD	IUPHAR	SYNCRIP	HDAC2	0.801884866	1.13E-124
PRAD	IUPHAR	SYNCRIP	TMEM30A	0.81232519	1.96E-130
PRAD	IUPHAR	SYNCRIP	SENP6	0.812692903	1.21E-130
PRAD	IUPHAR	SYNCRIP	MAP3K7	0.837866862	3.43E-146
PRAD	Kinase	SYNCRIP	MAP3K7	0.837866862	3.43E-146
PRAD	TF	SYNCRIP	CDC5L	0.805857765	7.98E-127
THYM	Cell metabolism gene	SYNCRIP	CCNC	0.804664968	6.09E-29
THYM	Cell metabolism gene	SYNCRIP	AGPS	0.830929879	2.42E-32
THYM	Cell metabolism gene	SYNCRIP	NFYA	0.871615598	5.80E-39
THYM	CGC	SYNCRIP	GOPC	0.800635929	1.82E-28
THYM	CGC	SYNCRIP	CCNC	0.804664968	6.09E-29
THYM	CGC	SYNCRIP	CREB1	0.808550274	2.07E-29
THYM	CGC	SYNCRIP	RAD21	0.80891123	1.87E-29
THYM	CGC	SYNCRIP	SUZ12	0.81453594	3.72E-30
THYM	CGC	SYNCRIP	FANCF	0.818382888	1.19E-30
THYM	CGC	SYNCRIP	FGFR1OP	0.826606521	9.62E-32
THYM	CGC	SYNCRIP	MSH2	0.83909927	1.61E-33
THYM	CGC	SYNCRIP	DEK	0.844971119	2.08E-34
THYM	CGC	SYNCRIP	CBL	0.850651844	2.64E-35
THYM	Epifactor	SYNCRIP	ATAD2B	0.803791912	7.74E-29
THYM	Epifactor	SYNCRIP	SENP1	0.808870336	1.89E-29
THYM	Epifactor	SYNCRIP	RCOR1	0.813002279	5.80E-30
THYM	Epifactor	SYNCRIP	SUZ12	0.81453594	3.72E-30
THYM	Epifactor	SYNCRIP	ZNF711	0.820023056	7.30E-31
THYM	Epifactor	SYNCRIP	ING3	0.830970389	2.39E-32
THYM	Epifactor	SYNCRIP	DR1	0.838771269	1.80E-33
THYM	Epifactor	SYNCRIP	DEK	0.844971119	2.08E-34
THYM	Epifactor	SYNCRIP	MBTD1	0.848525376	5.77E-35
THYM	IUPHAR	SYNCRIP	ATAD2B	0.803791912	7.74E-29
THYM	IUPHAR	SYNCRIP	CRY1	0.804313469	6.71E-29
THYM	IUPHAR	SYNCRIP	SENP1	0.808870336	1.89E-29
THYM	IUPHAR	SYNCRIP	SRPK2	0.81683234	1.89E-30
THYM	IUPHAR	SYNCRIP	OXSR1	0.817663111	1.48E-30
THYM	IUPHAR	SYNCRIP	HIPK1	0.827460218	7.35E-32
THYM	Kinase	SYNCRIP	SRPK2	0.81683234	1.89E-30
THYM	Kinase	SYNCRIP	OXSR1	0.817663111	1.48E-30
THYM	Kinase	SYNCRIP	HIPK1	0.827460218	7.35E-32
THYM	TF	SYNCRIP	ZNF143	0.807744636	2.59E-29
THYM	TF	SYNCRIP	CREB1	0.808550274	2.07E-29
THYM	TF	SYNCRIP	E2F7	0.810732168	1.11E-29
THYM	TF	SYNCRIP	ZNF280D	0.815081693	3.17E-30
THYM	TF	SYNCRIP	ZKSCAN4	0.819619356	8.25E-31
THYM	TF	SYNCRIP	ZNF711	0.820023056	7.30E-31
THYM	TF	SYNCRIP	ZBTB2	0.826784116	9.10E-32
THYM	TF	SYNCRIP	CGGBP1	0.827445801	7.38E-32
THYM	TF	SYNCRIP	ZNF184	0.837293107	2.97E-33
THYM	TF	SYNCRIP	DR1	0.838771269	1.80E-33
THYM	TF	SYNCRIP	ZNF519	0.854027047	7.45E-36
THYM	TF	SYNCRIP	NFYA	0.871615598	5.80E-39
THYM	TF	SYNCRIP	CDC5L	0.874288415	1.78E-39
THYM	TF	SYNCRIP	HSF2	0.876319735	7.15E-40
THYM	TSG	SYNCRIP	CCNC	0.804664968	6.09E-29
THYM	TSG	SYNCRIP	SUZ12	0.81453594	3.72E-30
THYM	TSG	SYNCRIP	ING3	0.830970389	2.39E-32
THYM	TSG	SYNCRIP	MSH2	0.83909927	1.61E-33
THYM	TSG	SYNCRIP	CBL	0.850651844	2.64E-35
THYM	TSG	SYNCRIP	LIN9	0.860736978	5.45E-37
UCS	Cell metabolism gene	SYNCRIP	CCNC	0.804664968	6.09E-29
UCS	Cell metabolism gene	SYNCRIP	AGPS	0.830929879	2.42E-32
UCS	Cell metabolism gene	SYNCRIP	NFYA	0.871615598	5.80E-39
UCS	CGC	SYNCRIP	GOPC	0.800635929	1.82E-28
UCS	CGC	SYNCRIP	CCNC	0.804664968	6.09E-29
UCS	CGC	SYNCRIP	CREB1	0.808550274	2.07E-29
UCS	CGC	SYNCRIP	RAD21	0.80891123	1.87E-29
UCS	CGC	SYNCRIP	SUZ12	0.81453594	3.72E-30
UCS	CGC	SYNCRIP	FANCF	0.818382888	1.19E-30
UCS	CGC	SYNCRIP	FGFR1OP	0.826606521	9.62E-32
UCS	CGC	SYNCRIP	MSH2	0.83909927	1.61E-33
UCS	CGC	SYNCRIP	DEK	0.844971119	2.08E-34
UCS	CGC	SYNCRIP	CBL	0.850651844	2.64E-35
UCS	Epifactor	SYNCRIP	ATAD2B	0.803791912	7.74E-29
UCS	Epifactor	SYNCRIP	SENP1	0.808870336	1.89E-29
UCS	Epifactor	SYNCRIP	RCOR1	0.813002279	5.80E-30
UCS	Epifactor	SYNCRIP	SUZ12	0.81453594	3.72E-30
UCS	Epifactor	SYNCRIP	ZNF711	0.820023056	7.30E-31
UCS	Epifactor	SYNCRIP	ING3	0.830970389	2.39E-32
UCS	Epifactor	SYNCRIP	DR1	0.838771269	1.80E-33
UCS	Epifactor	SYNCRIP	DEK	0.844971119	2.08E-34
UCS	Epifactor	SYNCRIP	MBTD1	0.848525376	5.77E-35
UCS	IUPHAR	SYNCRIP	ATAD2B	0.803791912	7.74E-29
UCS	IUPHAR	SYNCRIP	CRY1	0.804313469	6.71E-29
UCS	IUPHAR	SYNCRIP	SENP1	0.808870336	1.89E-29
UCS	IUPHAR	SYNCRIP	SRPK2	0.81683234	1.89E-30
UCS	IUPHAR	SYNCRIP	OXSR1	0.817663111	1.48E-30
UCS	IUPHAR	SYNCRIP	HIPK1	0.827460218	7.35E-32
UCS	Kinase	SYNCRIP	SRPK2	0.81683234	1.89E-30
UCS	Kinase	SYNCRIP	OXSR1	0.817663111	1.48E-30
UCS	Kinase	SYNCRIP	HIPK1	0.827460218	7.35E-32
UCS	TF	SYNCRIP	ZNF143	0.807744636	2.59E-29
UCS	TF	SYNCRIP	CREB1	0.808550274	2.07E-29
UCS	TF	SYNCRIP	E2F7	0.810732168	1.11E-29
UCS	TF	SYNCRIP	ZNF280D	0.815081693	3.17E-30
UCS	TF	SYNCRIP	ZKSCAN4	0.819619356	8.25E-31
UCS	TF	SYNCRIP	ZNF711	0.820023056	7.30E-31
UCS	TF	SYNCRIP	ZBTB2	0.826784116	9.10E-32
UCS	TF	SYNCRIP	CGGBP1	0.827445801	7.38E-32
UCS	TF	SYNCRIP	ZNF184	0.837293107	2.97E-33
UCS	TF	SYNCRIP	DR1	0.838771269	1.80E-33
UCS	TF	SYNCRIP	ZNF519	0.854027047	7.45E-36
UCS	TF	SYNCRIP	NFYA	0.871615598	5.80E-39
UCS	TF	SYNCRIP	CDC5L	0.874288415	1.78E-39
UCS	TF	SYNCRIP	HSF2	0.876319735	7.15E-40
UCS	TSG	SYNCRIP	CCNC	0.804664968	6.09E-29
UCS	TSG	SYNCRIP	SUZ12	0.81453594	3.72E-30
UCS	TSG	SYNCRIP	ING3	0.830970389	2.39E-32
UCS	TSG	SYNCRIP	MSH2	0.83909927	1.61E-33
UCS	TSG	SYNCRIP	CBL	0.850651844	2.64E-35
UCS	TSG	SYNCRIP	LIN9	0.860736978	5.45E-37
UVM	Cell metabolism gene	SYNCRIP	NUP43	0.822399965	8.52E-21
UVM	Cell metabolism gene	SYNCRIP	AGPAT5	0.830681422	1.56E-21
UVM	Cell metabolism gene	SYNCRIP	MED23	0.843460093	9.47E-23
UVM	Cell metabolism gene	SYNCRIP	PGM3	0.858445073	2.52E-24
UVM	CGC	SYNCRIP	FGFR1OP	0.820149599	1.33E-20
UVM	CGC	SYNCRIP	GOPC	0.82255796	8.25E-21
UVM	CGC	SYNCRIP	BCLAF1	0.823012472	7.54E-21
UVM	Epifactor	SYNCRIP	HDAC2	0.858030695	2.80E-24
UVM	IUPHAR	SYNCRIP	HDAC2	0.858030695	2.80E-24
UVM	TF	SYNCRIP	ZBTB2	0.8114723	7.00E-20
UVM	TF	SYNCRIP	ZUFSP	0.855482449	5.33E-24

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Protein structure

Protein 3D structure
Visit iCn3D.

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Protein-Protein Interaction

Protein-protein interaction networks
* Overlap between up-regulated DEGs (log2FC<-1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P))

Overlap between down-regulated DEGs (log2FC>1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P))

* Edge colors based on TCGA cancer types.

* Overlap between DEGs (log2FC>1 and adj.P<0.05) and STRING PPI network per cancer (center: Translation factor, node: DEGs, node color: log2FC, edges: weighted by -log2(adj.P))

Cancer type	Translation factor	Interacting protein coding gene	FC	adj.pval
KICH	SYNCRIP	HNRNPR	1.52076151408335	0.000102996826171875
COAD	SYNCRIP	HNRNPU	-3.25414367586013	0.000109195709228516
STAD	SYNCRIP	HNRNPR	-4.6225661308416	0.000364991836249828
KICH	SYNCRIP	HNRNPU	1.45270865891102	0.000376403331756592
LUAD	SYNCRIP	HNRNPA1	-1.17680399824906	0.000379797766386831
PRAD	SYNCRIP	HNRNPU	-3.59255010200453	0.00074054058184854
STAD	SYNCRIP	EPRS	-1.48171581324647	0.000789262883452143
THCA	SYNCRIP	RPL13A	1.00055529557489	0.00121938003080576
ESCA	SYNCRIP	HNRNPR	-4.72271799081977	0.0029296875
THCA	SYNCRIP	HNRNPK	-8.73422542563389	0.00797530353045887
CHOL	SYNCRIP	HNRNPR	-1.46566948767376	0.01171875
LUSC	SYNCRIP	CSDE1	-1.33200117661228	0.025379830388344
CHOL	SYNCRIP	GAPDH	-3.07354785261475	0.02734375
UCEC	SYNCRIP	HNRNPK	1.64532744504864	0.03125
KIRC	SYNCRIP	RPL13A	-2.22570045477256	1.02382991067149e-08
BRCA	SYNCRIP	GAPDH	-1.37642902567885	1.15182974050406e-18
HNSC	SYNCRIP	CSDE1	-1.92574762956205	1.42088565553422e-05
THCA	SYNCRIP	CSDE1	-1.00581945790421	1.55171507174296e-05
BRCA	SYNCRIP	CSDE1	-1.23575001565702	1.5698167165288e-21
STAD	SYNCRIP	HNRNPU	-1.26566952320815	2.26888805627823e-05
LIHC	SYNCRIP	EPRS	-7.10731017811505	2.28054594243154e-08
LIHC	SYNCRIP	HNRNPU	-1.06098658215773	2.35319665208461e-06
BRCA	SYNCRIP	YBX1	1.10467241966451	4.8741280959683e-05
KIRC	SYNCRIP	HNRNPR	1.79418191557745	5.98807464268008e-07
KIRC	SYNCRIP	HNRNPA1	-6.80688842701016	6.00852501097204e-09
LUAD	SYNCRIP	CSDE1	-1.92573954016457	6.46801743847803e-05
BRCA	SYNCRIP	IGF2BP1	-1.119264636586	6.55843695441879e-13
LUAD	SYNCRIP	GAPDH	-2.39625242862964	7.0750762948169e-11
KICH	SYNCRIP	YBX1	1.86923259160472	8.16583633422851e-06
LUSC	SYNCRIP	HNRNPA1	-2.597423841764	9.46872220956927e-06
PRAD	SYNCRIP	EPRS	-1.76339127457265	9.52775218277559e-05

Protein-protein interactors with this translation factor (BIOGRID-3.4.160)

PPI interactors with SYNCRIP

PTPN11, PUF60, PRKRA, STK24, CNBP, PRMT1, APOBEC1, A1CF, SYT2, SYT7, SYT8, SYT9, SYT1, SYT3, SYT4, GRB2, PLCG1, INSR, MEPCE, CDK9, HNRNPA1, HNRNPH1, KHDRBS2, DOT1L, H2AFX, UBC, Ybx1, AI837181, EBNA-LP, RAD21, SF3A2, SIRT7, PAIP1, CUL3, CUL4B, CUL5, CUL2, CUL1, COPS5, COPS6, DCUN1D1, CAND1, NEDD8, HNRNPD, APP, PABPC1, HNRNPR, HNRNPA3, SRSF1, HNRNPK, HNRNPM, SRSF3, TARDBP, YBX1, ILF3, ILF2, DHX15, SNRPA1, DDX5, RALY, SRRM2, U2AF1, PPP1CA, U2AF2, SNRNP70, DDX42, DDX3X, EIF4H, IGF2BP1, PHB, PTCD3, RPL10, RBMS2, STT3B, WBSCR16, TIMM50, HNRNPA0, NDUFV2, LSM14A, IKBIP, ICT1, MYL12A, STOML2, PLP2, LETM1, RPUSD4, RPN1, SNAP23, DLAT, GAA, TMEM177, LGALS3BP, TXN, MRPS28, RPS20, ESR1, HABP4, SMURF1, FN1, VCAM1, HNRNPU, TP63, IL7R, UBL4A, ITGA4, PRMT8, CD81, IGSF8, ICAM1, HMGA1, HMGA2, CSF2, FBXO6, PARK2, IQGAP1, C14orf166, NELFB, FKBP3, GNB2L1, IARS, RPSA, MAP1S, PSMD7, RPL23A, RPL24, RPS21, RPS27L, rev, RPA3, RPA2, RPA1, STAU1, SPRTN, FUS, NUPR1, CUL7, OBSL1, CCDC8, EED, RNF2, SIRT6, FBXW11, MAEL, DDX17, MORF4L1, MORF4L2, NHP2L1, CAPN1, HNRNPL, KHDRBS1, KHDRBS3, LSM4, LUC7L, LUC7L2, METTL13, NCBP2, SF3B3, THUMPD1, UBE2S, UPF1, XRN1, ZNF598, NTRK1, SCARNA22, APBB2, BAD, BLMH, SLC25A20, CRY1, DKC1, DYNC1H1, ECHS1, PHC2, EIF2B1, CTTN, MTOR, GOLGA3, HBA1, HEXA, HNRNPAB, MAPT, MAP3K4, MKI67, MYH1, NDUFB5, NHS, NOP2, PDCL, PI4KA, PLCB3, PSMD2, PTMA, RECQL, RET, SCO1, SDC2, SS18, TARBP1, ZEB1, GCFC2, TLN1, TNFRSF1A, USP1, ZBTB14, RBM10, USP13, MTA1, PTTG1, COX5A, MRPL33, GTF2IRD1, ARHGAP32, C2CD5, HMGXB4, CEBPZ, SORBS3, TCIRG1, ABCA7, TUBB3, CDK2, HNRNPH2, PCDH7, SORT1, TSNAX, KIF21B, MRPL50, TXNL4A, EBNA1BP2, TRIOBP, HNRNPUL1, FNDC3A, SETD1B, FAM120A, MED13L, DICER1, MACF1, INTS7, TBC1D10B, WDR91, ANKRD11, RACGAP1, PNPLA8, RRP15, TRMT112, PPIL1, PPIL3, APTX, UHRF1BP1, UACA, CEP55, NAT10, UFSP2, DNAJA4, NOP10, PLXNA3, PRPF40A, BIN3, DDX24, ZNF286A, UVSSA, ICE2, IPO4, ELMO3, SBF2, TLN2, KLF16, USP32, FBXO18, SLC25A25, PTGR2, CENPV, LEMD2, NSMCE2, Junb, Nedd1, Nfyc, MCM2, MCM5, SNW1, WWP2, ZNF746, RBMXL1, ANGEL2, RPS27A, APOBEC3D, SFPQ, YTHDF1, HDLBP, RPL26L1, ZNF169, ELAVL4, DUSP11, ZC3H8, KNOP1, DDX54, CCDC137, DDX21, ZRANB2, GAR1, UTP3, QKI, CCDC59, DDX27, ELAVL2, NKAP, YPEL5, CYLD, TRIM25, G3BP1, UBE2A, BRCA1, HBP1, WDR77, CTNNB1, PPIE, YAP1, BMP4, HDAC4, KRAS, PCBP1, TRIP4, UBE2L6, UBE2M, PRPF8, EFTUD2, AAR2, PIH1D1, TNIP2, CHD3, CHD4, TNF, RIOK1, HEXIM1, LARP7, RUNX1, UBE3A, SNAI1, HRAS, AGR2, RECQL4, GPC1, REST, ZFP36L2, MYC, WDR76, HIST1H4A, HIST1H2BB, HIST1H2AB, METTL3, METTL14, KIAA1429, RC3H1, RC3H2, FAF1, CHEK2, DISC1, USP14, NR2C2, HDAC2, MECOM, NHLRC2, VRK1, OASL, MAB21L2, DUSP14, TAF15, MATR3, ITFG1, BIRC3, NFX1, BRD7, TP53, GRIA4, GRIA1, CMTR1, MYPOP, ARIH2, PLEKHA4, KCTD10, PINK1, TFCP2, FANCD2, MIRLET7A1, MIRLET7A2, MIRLET7A3, MIRLET7B, MIRLET7C, MIRLET7D, MIRLET7E, MIRLET7F1, MIRLET7F2, MIRLET7G, MIRLET7I, MIR98, MIR1-1, MIR1-2, MIR7-1, MIR7-2, MIR7-3, MIR9-1, MIR9-2, MIR9-3, MIR10B, MIR15A, MIR15B, MIR16-1, MIR16-2, MIR17, MIR18A, MIR18B, MIR19A, MIR19B1, MIR19B2, MIR20A, MIR20B, MIR21, MIR25, MIR29A, MIR29B1, MIR29B2, MIR29C, MIR31, MIR34A, MIR34B, MIR34C, MIR92A1, MIR92A2, MIR93, MIR106A, MIR106B, MIR107, MIR122, MIR128-1, MIR128-2, MIR138-1, MIR138-2, MIR140, MIR141, MIR143, MIR145, MIR155, MIR199A1, MIR199A2, MIR200A, MIR200B, MIR200C, MIR205, MIR206, MIR214, MIR221, MIR222, MIR363, MIR429, MIR451A, ZC3H18, DUSP1, TOR1AIP1, PKD1L2, CELF1, CPEB4, DAZL, ELAVL1, FUBP3, GRSF1, IGF2BP2, LARP4B, MKRN2, MOV10, PAIP2, PUM1, RBMS1, AIFM1, ALG13, ATXN2, BYSL, CSDE1, DDX20, EIF4ENIF1, FAM120C, GEMIN4, IGF2BP3, IPO8, OTUD4, PRRC2C, R3HDM1, SMG7, SMN1, SND1, TDRD3, TOP3B, YTHDF2, ZCCHC6, XRN2, ZC3HAV1, ANKRD28, DAP3, G3BP2, LARP4, LTV1, MRPS26, PABPC4, CAPRIN1, FMR1, PRRC2A, PRRC2B, SECISBP2, STAU2, YTHDF3, DHX57, LARP1B, MRPS34, ZC3H7A, NEK4, DUX4, CIT, ANLN, AURKB, CHMP4B, CHMP4C, ECT2, KIF14, KIF20A, KIF23, PRC1, TRIM55, TRIM63, ACAD9, C6orf203, MDH2, METTL15, METTL17, MRRF, MTERF3, MTIF3, TUFM, SUMO2, NDN, BRD4, RBM45, CIC, Apc2, RBM39, FBP1, MKRN1, LGALS9, IFI16, N, FAM20C, DNAJC8, EWSR1, OGT, CD274, UFL1, DDRGK1, NR4A1, KIAA1524, FBL, SERBP1, TRIM37, UBQLN1, FZR1, WDR5, NUDCD2, ZBTB2, PRR3, RBM28, RPS3, DHX36, MRPL30, PURG, HNRNPUL2, YTHDC2, HNRNPC, MRPS24, MALSU1, YBX2, SNRPC, GAPDHS, GNA13, BTF3, FBXW7, ORF8, ORF10, ORF6, ORF7b, S, AGO1, SQSTM1, PER2, CPEB1, RB1CC1,

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Mutations

Clinically associated variants from ClinVar.

Gene	Chr	Position	RefSeq	VarSeq	RefSeeq	VarType	Pathogenic	Disease	VarInfo
SYNCRIP	chr6	86324772	TG	AA	Indel	association	Autism_spectrum_disorder	SO:0001583\|missense_variant	SO:0001583\|missense_variant
SYNCRIP	chr6	86324785	C	T	single_nucleotide_variant	Uncertain_significance	Intellectual_disability	SO:0001583\|missense_variant	SO:0001583\|missense_variant
SYNCRIP	chr6	86328600	CA	C	Deletion	Uncertain_significance	not_provided	SO:0001589\|frameshift_variant	SO:0001589\|frameshift_variant
SYNCRIP	chr6	86332348	CCT	C	Microsatellite	Likely_pathogenic	not_provided	SO:0001589\|frameshift_variant	SO:0001589\|frameshift_variant
SYNCRIP	chr6	86332353	G	GT	Duplication	Uncertain_significance	not_provided	SO:0001589\|frameshift_variant	SO:0001589\|frameshift_variant
SYNCRIP	chr6	86346722	A	G	single_nucleotide_variant	association	Autism_spectrum_disorder	SO:0001583\|missense_variant	SO:0001583\|missense_variant
SYNCRIP	chr6	86346961	C	G	single_nucleotide_variant	Uncertain_significance	not_provided	SO:0001583\|missense_variant,SO:0001627\|intron_variant	SO:0001583\|missense_variant,SO:0001627\|intron_variant
SYNCRIP	chr6	86351111	T	C	single_nucleotide_variant	Uncertain_significance	See_cases	SO:0001583\|missense_variant,SO:0001627\|intron_variant	SO:0001583\|missense_variant,SO:0001627\|intron_variant

nsSNVs with sample frequency (size of circle) from TCGA 33 cancers.

SNVs and Indels

Gene	Cancer type	Chromosome	Start	End	RefSeeq	MutSeq	Mutation type	AAchange	# samples
SYNCRIP	SKCM	chr6	86333812	86333812	G	A	Missense_Mutation	p.R229C	5
SYNCRIP	UCEC	chr6	86332381	86332381	T	C	Missense_Mutation	p.Y276C	3
SYNCRIP	LUSC	chr6	86324913	86324913	C	T	Missense_Mutation	p.R478H	3
SYNCRIP	UCEC	chr6	86350171	86350171	T	C	Missense_Mutation	p.H87R	3
SYNCRIP	GBM	chr6	86329023	86329023	G	T	Missense_Mutation		3
SYNCRIP	BRCA	chr6	86350199	86350199	G	A	Nonsense_Mutation	p.Q78*	3
SYNCRIP	BRCA	chr6	86351074	86351074	C	T	Silent	p.Q28	3
SYNCRIP	KIRP	chr6	86332353	86332354	-	T	Frame_Shift_Ins	p.N285fs	3
SYNCRIP	HNSC	chr6	86328538	86328538	T	C	Silent	p.Q426Q	3
SYNCRIP	SARC	chr6	86329023	86329023	G	A	Missense_Mutation	p.A374V	3
SYNCRIP	ESCA	chr6	86324929	86324929	C	G	Missense_Mutation	p.D473H	3
SYNCRIP	PAAD	chr6	86346734	86346734	G	A	Missense_Mutation	p.A206V	3
SYNCRIP	SKCM	chr6	86324795	86324795	G	A	Silent	p.P419P	2
SYNCRIP	TGCT	chr6	86346826	86346826	C	T	Silent		2
SYNCRIP	ESCA	chr6	86324929	86324929	C	G	Missense_Mutation		2
SYNCRIP	HNSC	chr6	86346765	86346765	C	G	Missense_Mutation	p.D196H	2
SYNCRIP	STAD	chr6	86349994	86349994	T	C	Missense_Mutation	p.K107R	2
SYNCRIP	CHOL	chr6	86351134	86351134	T	C	Silent		2
SYNCRIP	TGCT	chr6	86346826	86346826	C	T	Silent	p.E175E	2
SYNCRIP	BRCA	chr6	86332254	86332254	T	C	Silent	p.G318	2
SYNCRIP	PRAD	chr6	86333756	86333756	C	A	Silent	p.V247V	2
SYNCRIP	CHOL	chr6	86351134	86351134	T	C	Silent	p.G8G	2
SYNCRIP	STAD	chr6	86332354	86332354	T	-	Frame_Shift_Del		2
SYNCRIP	STAD	chr6	86346762	86346762	G	A	Missense_Mutation	p.P197S	2
SYNCRIP	UCEC	chr6	86324967	86324967	T	C	Missense_Mutation	p.Y460C	2
SYNCRIP	STAD	chr6	86324913	86324913	C	T	Missense_Mutation		2
SYNCRIP	STAD	chr6	86332298	86332298	G	A	Missense_Mutation	p.R304C	2
SYNCRIP	UCEC	chr6	86328993	86328993	G	T	Missense_Mutation	p.A384D	2
SYNCRIP	LUAD	chr6	86325015	86325015	C	G	Missense_Mutation	p.R444T	2
SYNCRIP	CESC	chr6	86324782	86324782	C	T	Missense_Mutation		2
SYNCRIP	UCEC	chr6	86329047	86329047	C	T	Missense_Mutation	p.R366Q	2
SYNCRIP	STAD	chr6	86329028	86329028	A	T	Missense_Mutation	p.D372E	2
SYNCRIP	CESC	chr6	86324900	86324900	T	C	Silent		2
SYNCRIP	UCEC	chr6	86329085	86329085	A	C	Missense_Mutation	p.I353M	2
SYNCRIP	CESC	chr6	86324748	86324748	C	G	Missense_Mutation		2
SYNCRIP	SARC	chr6	86333723	86333723	C	G	Missense_Mutation		2
SYNCRIP	UCEC	chr6	86332391	86332391	C	T	Missense_Mutation	p.V273I	2
SYNCRIP	LIHC	chr6	86328565	86328565	T	-	Frame_Shift_Del	p.K417fs	2
SYNCRIP	HNSC	chr6	86328627	86328627	C	T	Missense_Mutation	p.E397K	2
SYNCRIP	UCEC	chr6	86350232	86350232	C	A	Nonsense_Mutation	p.E67*	2
SYNCRIP	LIHC	chr6	86350237	86350237	A	-	Frame_Shift_Del	p.L65fs	2
SYNCRIP	LUAD	chr6	86329003	86329003	G	C	Missense_Mutation	p.R381G	2
SYNCRIP	STAD	chr6	86324613	86324613	C	T	Missense_Mutation	p.R578H	2
SYNCRIP	CESC	chr6	86349998	86349998	C	T	Missense_Mutation		2
SYNCRIP	LIHC	chr6	86332354	86332354	T	-	Frame_Shift_Del	p.N285fs	2
SYNCRIP	LUAD	chr6	86351130	86351130	C	T	Missense_Mutation	p.G10S	2
SYNCRIP	HNSC	chr6	86324547	86324547	T	A	Missense_Mutation	p.H600L	2
SYNCRIP	STAD	chr6	86324688	86324688	G	A	Missense_Mutation	p.A553V	2
SYNCRIP	SARC	chr6	86333723	86333723	C	G	Missense_Mutation	p.Q258H	2
SYNCRIP	ESCA	chr6	86332363	86332363	T	A	Missense_Mutation	p.K282M	2
SYNCRIP	LIHC	chr6	86328542	86328542	T	-	Frame_Shift_Del	p.N425fs	2
SYNCRIP	LUAD	chr6	86346828	86346828	C	T	Missense_Mutation	p.E175K	2
SYNCRIP	STAD	chr6	86324832	86324832	C	-	Frame_Shift_Del	p.G505fs	2
SYNCRIP	THYM	chr6	86324703	86324703	C	A	Missense_Mutation	p.R548L	1
SYNCRIP	CESC	chr6	86349998	86349998	C	T	Missense_Mutation	p.E106K	1
SYNCRIP	LGG	chr6	86324825	86324825	A	G	Silent		1
SYNCRIP	LUAD	chr6	86350039	86350040	-	TT	Frame_Shift_Ins	p.C92fs	1
SYNCRIP	SKCM	chr6	86324551	86324553	CAC	-	In_Frame_Del	p.GD598del	1
SYNCRIP	LIHC	chr6	86333780	86333780	T	C	Silent		1
SYNCRIP	BLCA	chr6	86349960	86349963	TCCT	-	Frame_Shift_Del	p.K117fs	1
SYNCRIP	PAAD	chr6	86324728	86324728	C	A	Missense_Mutation		1
SYNCRIP	LIHC	chr6	86332346	86332346	A	G	Missense_Mutation		1
SYNCRIP	SKCM	chr6	86324884	86324884	A	-	Frame_Shift_Del	p.Y453fs	1
SYNCRIP	SKCM	chr6	86324884	86324884	A	-	Frame_Shift_Del	p.Y488fs	1
SYNCRIP	ESCA	chr6	86324911	86324911	C	A	Missense_Mutation	p.G479C	1
SYNCRIP	LUAD	chr6	86324916	86324916	T	A	Missense_Mutation	p.Y477F	1
SYNCRIP	HNSC	chr6	86324795	86324795	G	A	Silent	p.P517P	1
SYNCRIP	STAD	chr6	86332349	86332350	CT	-	Frame_Shift_Del	p.287_287del	1
SYNCRIP	LIHC	chr6	86351138	86351138	T	C	Missense_Mutation		1
SYNCRIP	SKCM	chr6	86324599	86324599	G	A	Nonsense_Mutation	p.Q583X	1
SYNCRIP	THCA	chr6	86324584	86324584	G	T	Missense_Mutation		1
SYNCRIP	LUSC	chr6	86332363	86332363	T	G	Missense_Mutation	p.K282T	1
SYNCRIP	LUAD	chr6	86350282	86350282	C	A	Splice_Site	p.G50_splice	1
SYNCRIP	KIRC	chr6	86324828	86324828	A	G	Silent	p.A506A	1
SYNCRIP	PRAD	chr6	86324853	86324853	C	A	Missense_Mutation	p.R498M	1
SYNCRIP	COAD	chr6	86324792	86324792	G	A	Silent	p.R420R	1
SYNCRIP	LIHC	chr6	86324522	86324522	A	G	Silent		1
SYNCRIP	SKCM	chr6	86333812	86333812	G	A	Missense_Mutation	p.R131C	1
SYNCRIP	THCA	chr6	86324743	86324743	C	T	Missense_Mutation		1
SYNCRIP	LUSC	chr6	86324793	86324793	C	A	Missense_Mutation	p.R518L	1
SYNCRIP	HNSC	chr6	86324547	86324547	T	A	Missense_Mutation		1
SYNCRIP	LUAD	chr6	86349987	86349987	C	G	Silent	p.G109G	1
SYNCRIP	KIRC	chr6	86324775	86324775	G	C	Nonsense_Mutation	p.S524X	1
SYNCRIP	PRAD	chr6	86329033	86329033	T	A	Nonsense_Mutation	p.K371*	1
SYNCRIP	COAD	chr6	86329126	86329126	G	A	Silent	p.L242L	1
SYNCRIP	LIHC	chr6	86350209	86350209	C	A	Missense_Mutation		1
SYNCRIP	SKCM	chr6	86324800	86324800	G	A	Missense_Mutation	p.P418S	1
SYNCRIP	LUSC	chr6	86329009	86329009	C	G	Missense_Mutation	p.D379H	1
SYNCRIP	STAD	chr6	86329066	86329066	G	A	Nonsense_Mutation	p.Q360X	1
SYNCRIP	HNSC	chr6	86346765	86346765	C	G	Missense_Mutation		1
SYNCRIP	KIRP	chr6	86324737	86324740	CTCG	-	Frame_Shift_Del	p.536_537del	1
SYNCRIP	PRAD	chr6	86324701	86324701	C	A	Missense_Mutation	p.G549W	1
SYNCRIP	STAD	chr6	86328633	86328634	-	T	Frame_Shift_Ins	p.D395fs	1
SYNCRIP	THCA	chr6	86324743	86324743	C	T	Missense_Mutation	p.V437I	1
SYNCRIP	COAD	chr6	86333816	86333816	T	G	Missense_Mutation	p.E129D	1
SYNCRIP	LIHC	chr6	86333797	86333797	T	C	Missense_Mutation	p.I234V	1
SYNCRIP	SKCM	chr6	86324551	86324553	CAC	-	In_Frame_Del	p.563_564del	1
SYNCRIP	HNSC	chr6	86324795	86324795	G	A	Silent		1
SYNCRIP	LUSC	chr6	86324670	86324670	C	T	Missense_Mutation	p.G559E	1
SYNCRIP	READ	chr6	86333742	86333742	T	G	Missense_Mutation	p.K154T	1
SYNCRIP	STAD	chr6	86329066	86329066	G	A	Nonsense_Mutation	p.Q360*	1
SYNCRIP	THCA	chr6	86324743	86324743	C	T	Missense_Mutation	p.V535I	1
SYNCRIP	COAD	chr6	86350030	86350030	A	-	Frame_Shift_Del	p.L95fs	1
SYNCRIP	LIHC	chr6	86350164	86350164	C	T	Silent	p.Q89Q	1
SYNCRIP	LUAD	chr6	86324692	86324692	C	T	Missense_Mutation	p.G552S	1
SYNCRIP	SKCM	chr6	86324704	86324704	G	A	Missense_Mutation	p.R548C	1
SYNCRIP	HNSC	chr6	86333818	86333818	C	T	Missense_Mutation		1
SYNCRIP	OV	chr6	86324940	86324940	T	C	Missense_Mutation	p.Y469C	1
SYNCRIP	STAD	chr6	86350006	86350007	-	TGT	In_Frame_Ins	p.R103delinsNR	1
SYNCRIP	LGG	chr6	86324886	86324886	C	G	Missense_Mutation	p.G487A	1
SYNCRIP	STAD	chr6	86329093	86329093	C	A	Nonsense_Mutation	p.E351*	1
SYNCRIP	THYM	chr6	86346757	86346757	G	T	Silent		1
SYNCRIP	COAD	chr6	86350180	86350180	T	C	Missense_Mutation	p.D84G	1
SYNCRIP	LUAD	chr6	86346742	86346742	T	G	Missense_Mutation	p.R203S	1
SYNCRIP	SKCM	chr6	86324599	86324599	G	A	Nonsense_Mutation	p.Q583*	1
SYNCRIP	ACC	chr6	86324650	86324650	T	C	Missense_Mutation	p.K566E	1
SYNCRIP	OV	chr6	86381336	86381336	G	A	Missense_Mutation	p.R577W	1
SYNCRIP	STAD	chr6	86329093	86329093	C	A	Nonsense_Mutation	p.E351X	1
SYNCRIP	CESC	chr6	86332240	86332240	G	T	Missense_Mutation		1
SYNCRIP	LGG	chr6	86332297	86332297	C	T	Missense_Mutation	p.R304H	1
SYNCRIP	SARC	chr6	86350240	86350240	G	T	Missense_Mutation		1
SYNCRIP	STAD	chr6	86328634	86328635	-	T	Frame_Shift_Ins	p.K394fs	1
SYNCRIP	THYM	chr6	86324703	86324703	C	A	Missense_Mutation		1
SYNCRIP	DLBC	chr6	86332210	86332210	A	C	Missense_Mutation	p.V333G	1
SYNCRIP	SKCM	chr6	86332226	86332226	C	G	Missense_Mutation	p.D328H	1
SYNCRIP	BLCA	chr6	86349960	86349963	TCCT	-	Frame_Shift_Del		1
SYNCRIP	OV	chr6	86324762	86324762	A	C	Silent	p.G528	1
SYNCRIP	LGG	chr6	86332297	86332297	C	T	Missense_Mutation		1
SYNCRIP	STAD	chr6	86350007	86350008	-	TGT	In_Frame_Ins	p.R103T	1
SYNCRIP	THYM	chr6	86346757	86346757	G	T	Silent	p.L198L	1
SYNCRIP	SKCM	chr6	86324800	86324800	G	A	Missense_Mutation	p.P516S	1
SYNCRIP	BLCA	chr6	86325058	86325058	C	T	Missense_Mutation	p.D430N	1
SYNCRIP	CESC	chr6	86324748	86324748	C	G	Missense_Mutation	p.R533T	1
SYNCRIP	LGG	chr6	86324886	86324886	C	G	Missense_Mutation		1
SYNCRIP	STAD	chr6	86329066	86329066	G	A	Nonsense_Mutation		1
SYNCRIP	THYM	chr6	86332212	86332212	C	T	Silent	p.E332E	1
SYNCRIP	BLCA	chr6	86349960	86349963	TCCT	-	Frame_Shift_Del	p.KG117fs	1
SYNCRIP	HNSC	chr6	86333818	86333818	C	T	Missense_Mutation	p.E227K	1
SYNCRIP	PAAD	chr6	86324728	86324728	C	A	Nonsense_Mutation	p.G540*	1

Copy number variation (CNV) of SYNCRIP
* Click on the image to open the original image in a new window.

Fusion gene breakpoints (product of the structural variants (SVs)) across SYNCRIP
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

Fusion genes with this translation factor from FusionGDB2.0.

FusionGDB2 ID	Disease	Sample	Hgene	Hchr	Hbp	Hstrand	Tgene	Tchr	Tbp	Tstrand
101351	N/A	AW274852	ATP13A1	chr19	19756133	+	SYNCRIP	chr6	86352841	+
101351	GBM	TCGA-4W-AA9T-01A	DAAM1	chr14	59758024	+	SYNCRIP	chr6	86329135	-
101351	N/A	BC019360	EIF3M	chr11	32605399	-	SYNCRIP	chr6	86352608	-
101351	Non-Cancer	TCGA-CG-5721-11A	FUCA2	chr6	143818525	-	SYNCRIP	chr6	86333830	-
101351	N/A	AI557045	KLHL4	chrX	86827819	-	SYNCRIP	chr6	86326953	-
101351	N/A	CF134851	MAP4K5	chr14	50938878	-	SYNCRIP	chr6	86323920	+
101351	N/A	BU151397	RAVER1	chr19	10433837	-	SYNCRIP	chr6	86328614	-
101351	HNSC	TCGA-CV-6962	SNX14	chr6	86298581	-	SYNCRIP	chr6	86325065	-
101351	HNSC	TCGA-CV-6962	SNX14	chr6	86303297	-	SYNCRIP	chr6	86325065	-
97964	BRCA	TCGA-E2-A14V	SYNCRIP	chr6	86352514	-	CDK19	chr6	111067404	-
97964	BRCA	TCGA-E2-A14V-01A	SYNCRIP	chr6	86352514	-	CDK19	chr6	111067403	-
97964	BRCA	TCGA-E2-A14V-01A	SYNCRIP	chr6	86352515	-	CDK19	chr6	111067404	-
97964	BRCA	TCGA-E2-A14V-01A	SYNCRIP	chr6	86352515	-	CDK19	chr6	111095140	-
103262	Non-Cancer	ERR315404	SYNCRIP	chr6	86352515	-	EEF1A1	chr6	74229779	-
88398	PRAD	TCGA-VN-A88Q	SYNCRIP	chr6	86333694	-	EPB41L2	chr6	131161738	-
88398	N/A	BI495805	SYNCRIP	chr6	86336985	-	KIF3B	chr20	30922814	-
100295	N/A	BD310766	SYNCRIP	chr6	86346797	-	LPP	chr3	187893846	+
96066	OV	TCGA-13-1497-01A	SYNCRIP	chr6	86346685	-	SEMA3A	chr7	83739905	-
101351	N/A	AA846916	SYNCRIP	chr6	86322014	+	SYNCRIP	chr6	86322014	-
101353	N/A	AW022188	ZMYM2	chr13	20663255	+	SYNCRIP	chr6	86336986	+

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Prognostic Analysis

Kaplan-Meier plots with logrank tests of overall survival (OS)

Cancer type

Translation factor

Coefficent

Hazard ratio

Wald test pval

Likelihool ratio pval

Logrank test pval

# samples

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Translation factor and Gender

Differential gene expression between female and male. (Wilcoxon test, pval<0.05)

Cancer type	Translation factor	pval	adj.p
HNSC	SYNCRIP	0.0075701167117917	0.21
UVM	SYNCRIP	0.0244865197498692	0.66
PAAD	SYNCRIP	0.0392904067701055	1

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Translation factor and Age

Differential gene expression between young and old age groups (Wilcoxon test, pval<0.05)

Cancer type	Translation factor	pval	adj.p
LIHC	SYNCRIP	0.00123333195849154	0.039
LUSC	SYNCRIP	0.0355592350127101	1
THCA	SYNCRIP	0.00040758448727485	0.013
BRCA	SYNCRIP	0.00793029393352127	0.25
PCPG	SYNCRIP	0.0335902420492316	1

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Related Drugs

Drugs targeting genes involved in this translation factor.
(DrugBank Version 5.1.8 2021-05-08)

UniProtAcc

DrugBank ID

Drug name

Drug activity

Drug type

Drug status

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Related Diseases

Diseases associated with this translation factor.
(DisGeNet 4.0)

Disease ID	Disease Name	# PubMeds	Disease source
C0023418	leukemia	1	CTD_human