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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:NCOR1-TTC19 (FusionGDB2 ID:57505)

Fusion Gene Summary for NCOR1-TTC19

check button Fusion gene summary
Fusion gene informationFusion gene name: NCOR1-TTC19
Fusion gene ID: 57505
HgeneTgene
Gene symbol

NCOR1

TTC19

Gene ID

9611

54902

Gene namenuclear receptor corepressor 1tetratricopeptide repeat domain 19
SynonymsN-CoR|N-CoR1|PPP1R109|TRAC1|hN-CoR2010204O13Rik|MC3DN2
Cytomap

17p12-p11.2

17p12

Type of geneprotein-codingprotein-coding
Descriptionnuclear receptor corepressor 1protein phosphatase 1, regulatory subunit 109thyroid hormone- and retinoic acid receptor-associated corepressor 1tetratricopeptide repeat protein 19, mitochondrialTPR repeat protein 19
Modification date2020031320200327
UniProtAcc

O75376

.
Ensembl transtripts involved in fusion geneENST00000268712, ENST00000395851, 
ENST00000395857, ENST00000395848, 
ENST00000583226, 		ENST00000261647, 
ENST00000486880, ENST00000497842, 
Fusion gene scores* DoF score30 X 30 X 13=1170010 X 9 X 5=450
# samples 3310
** MAII scorelog2(33/11700*10)=-5.14789869511231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(10/450*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NCOR1 [Title/Abstract] AND TTC19 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNCOR1(15960827)-TTC19(15928330), # samples:1
TTC19(15930017)-NCOR1(15938260), # samples:1
Anticipated loss of major functional domain due to fusion event.NCOR1-TTC19 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
NCOR1-TTC19 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
NCOR1-TTC19 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
NCOR1-TTC19 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneNCOR1

GO:0046329

negative regulation of JNK cascade

11931768


check buttonFusion gene breakpoints across NCOR1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across TTC19 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-FP-A4BENCOR1chr17

15960827

-TTC19chr17

15928330

+


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Fusion Gene ORF analysis for NCOR1-TTC19

check button Open reading frame (ORF) analsis of fusion genes 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
In-frameENST00000268712ENST00000261647NCOR1chr17

15960827

-TTC19chr17

15928330

+
In-frameENST00000268712ENST00000486880NCOR1chr17

15960827

-TTC19chr17

15928330

+
5CDS-3UTRENST00000268712ENST00000497842NCOR1chr17

15960827

-TTC19chr17

15928330

+
Frame-shiftENST00000395851ENST00000261647NCOR1chr17

15960827

-TTC19chr17

15928330

+
Frame-shiftENST00000395851ENST00000486880NCOR1chr17

15960827

-TTC19chr17

15928330

+
5CDS-3UTRENST00000395851ENST00000497842NCOR1chr17

15960827

-TTC19chr17

15928330

+
Frame-shiftENST00000395857ENST00000261647NCOR1chr17

15960827

-TTC19chr17

15928330

+
Frame-shiftENST00000395857ENST00000486880NCOR1chr17

15960827

-TTC19chr17

15928330

+
5CDS-3UTRENST00000395857ENST00000497842NCOR1chr17

15960827

-TTC19chr17

15928330

+
intron-3CDSENST00000395848ENST00000261647NCOR1chr17

15960827

-TTC19chr17

15928330

+
intron-3CDSENST00000395848ENST00000486880NCOR1chr17

15960827

-TTC19chr17

15928330

+
intron-3UTRENST00000395848ENST00000497842NCOR1chr17

15960827

-TTC19chr17

15928330

+
intron-3CDSENST00000583226ENST00000261647NCOR1chr17

15960827

-TTC19chr17

15928330

+
intron-3CDSENST00000583226ENST00000486880NCOR1chr17

15960827

-TTC19chr17

15928330

+
intron-3UTRENST00000583226ENST00000497842NCOR1chr17

15960827

-TTC19chr17

15928330

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)		BP loci
(transcript)		Predicted start
(transcript)		Predicted stop
(transcript)		Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for NCOR1-TTC19


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
NCOR1chr1715960827-TTC19chr1715928330+3.85E-050.9999615
NCOR1chr1715960827-TTC19chr1715928330+3.85E-050.9999615

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for NCOR1-TTC19


check button Go to

FGviewer for the breakpoints of chr17:15960827-chr17:15928330

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NCOR1

O75376

.
FUNCTION: Mediates transcriptional repression by certain nuclear receptors (PubMed:20812024). Part of a complex which promotes histone deacetylation and the formation of repressive chromatin structures which may impede the access of basal transcription factors. Participates in the transcriptional repressor activity produced by BCL6. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). Mediates the NR1D1-dependent repression and circadian regulation of TSHB expression (By similarity). The NCOR1-HDAC3 complex regulates the circadian expression of the core clock gene ARTNL/BMAL1 and the genes involved in lipid metabolism in the liver (By similarity). {ECO:0000250|UniProtKB:Q60974, ECO:0000269|PubMed:14527417, ECO:0000269|PubMed:20812024}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046174_2162130.66666666666652441.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046299_3282130.66666666666652441.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046501_5572130.66666666666652441.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945174_2162027.66666666666672338.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945299_3282027.66666666666672338.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945501_5572027.66666666666672338.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40461032_10352130.66666666666652441.0Compositional biasNote=Poly-Pro
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40461707_17122130.66666666666652441.0Compositional biasNote=Poly-Ala
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40461952_19632130.66666666666652441.0Compositional biasNote=Poly-Ser
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-404658_642130.66666666666652441.0Compositional biasNote=Poly-Gln
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046593_6032130.66666666666652441.0Compositional biasNote=Poly-Ala
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046607_6172130.66666666666652441.0Compositional biasNote=Pro-rich
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39451032_10352027.66666666666672338.0Compositional biasNote=Poly-Pro
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39451707_17122027.66666666666672338.0Compositional biasNote=Poly-Ala
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39451952_19632027.66666666666672338.0Compositional biasNote=Poly-Ser
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-394558_642027.66666666666672338.0Compositional biasNote=Poly-Gln
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945593_6032027.66666666666672338.0Compositional biasNote=Poly-Ala
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945607_6172027.66666666666672338.0Compositional biasNote=Pro-rich
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046435_4862130.66666666666652441.0DomainSANT 1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046623_6742130.66666666666652441.0DomainSANT 2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945435_4862027.66666666666672338.0DomainSANT 1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945623_6742027.66666666666672338.0DomainSANT 2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40461933_19372130.66666666666652441.0MotifNote=CORNR box 1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40462055_20592130.66666666666652441.0MotifNote=CORNR box 2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39451933_19372027.66666666666672338.0MotifNote=CORNR box 1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40462032_21152130.66666666666652441.0RegionID1
TgeneTTC19chr17:15960827chr17:15928330ENST00000261647610237_270225.33333333333334381.0RepeatNote=TPR 3
TgeneTTC19chr17:15960827chr17:15928330ENST00000261647610279_312225.33333333333334381.0RepeatNote=TPR 4
TgeneTTC19chr17:15960827chr17:15928330ENST00000261647610318_351225.33333333333334381.0RepeatNote=TPR 5

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119174_2160915.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119299_3280915.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119501_5570915.0Coiled coilOntology_term=ECO:0000255
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1191032_10350915.0Compositional biasNote=Poly-Pro
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1191707_17120915.0Compositional biasNote=Poly-Ala
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1191952_19630915.0Compositional biasNote=Poly-Ser
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-11958_640915.0Compositional biasNote=Poly-Gln
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119593_6030915.0Compositional biasNote=Poly-Ala
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119607_6170915.0Compositional biasNote=Pro-rich
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119435_4860915.0DomainSANT 1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119623_6740915.0DomainSANT 2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40462263_22672130.66666666666652441.0MotifNote=CORNR box 3
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1191933_19370915.0MotifNote=CORNR box 1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1192055_20590915.0MotifNote=CORNR box 2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1192263_22670915.0MotifNote=CORNR box 3
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39452055_20592027.66666666666672338.0MotifNote=CORNR box 2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39452263_22672027.66666666666672338.0MotifNote=CORNR box 3
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40462212_22732130.66666666666652441.0RegionID2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1192032_21150915.0RegionID1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1192212_22730915.0RegionID2
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39452032_21152027.66666666666672338.0RegionID1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39452212_22732027.66666666666672338.0RegionID2
TgeneTTC19chr17:15960827chr17:15928330ENST0000026164761073_76225.33333333333334381.0Compositional biasNote=Poly-Glu
TgeneTTC19chr17:15960827chr17:15928330ENST0000048688061073_76346.3333333333333502.0Compositional biasNote=Poly-Glu
TgeneTTC19chr17:15960827chr17:15928330ENST00000261647610136_169225.33333333333334381.0RepeatNote=TPR 1
TgeneTTC19chr17:15960827chr17:15928330ENST00000261647610179_212225.33333333333334381.0RepeatNote=TPR 2
TgeneTTC19chr17:15960827chr17:15928330ENST00000486880610136_169346.3333333333333502.0RepeatNote=TPR 1
TgeneTTC19chr17:15960827chr17:15928330ENST00000486880610179_212346.3333333333333502.0RepeatNote=TPR 2
TgeneTTC19chr17:15960827chr17:15928330ENST00000486880610237_270346.3333333333333502.0RepeatNote=TPR 3
TgeneTTC19chr17:15960827chr17:15928330ENST00000486880610279_312346.3333333333333502.0RepeatNote=TPR 4
TgeneTTC19chr17:15960827chr17:15928330ENST00000486880610318_351346.3333333333333502.0RepeatNote=TPR 5


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Fusion Gene Sequence for NCOR1-TTC19


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for NCOR1-TTC19


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046988_18162130.66666666666652441.0ETO
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945988_18162027.66666666666672338.0ETO
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-4046254_3122130.66666666666652441.0SIN3A/B
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-3945254_3122027.66666666666672338.0SIN3A/B
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40461_3732130.66666666666652441.0ZBTB33 and HEXIM1
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39451_3732027.66666666666672338.0ZBTB33 and HEXIM1


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneNCOR1chr17:15960827chr17:15928330ENST00000268712-40461501_24402130.66666666666652441.0C1D
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1191501_24400915.0C1D
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395851-39451501_24402027.66666666666672338.0C1D
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119988_18160915.0ETO
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-119254_3120915.0SIN3A/B
HgeneNCOR1chr17:15960827chr17:15928330ENST00000395848-1191_3730915.0ZBTB33 and HEXIM1


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for NCOR1-TTC19


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for NCOR1-TTC19


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNCOR1C0005684Malignant neoplasm of urinary bladder1CTD_human
HgeneNCOR1C0005695Bladder Neoplasm1CTD_human
HgeneNCOR1C0006142Malignant neoplasm of breast1CGI;CTD_human
HgeneNCOR1C0007138Carcinoma, Transitional Cell1CTD_human
HgeneNCOR1C0014175Endometriosis1CTD_human
HgeneNCOR1C0017636Glioblastoma1CTD_human
HgeneNCOR1C0023903Liver neoplasms1CTD_human
HgeneNCOR1C0033578Prostatic Neoplasms1CTD_human
HgeneNCOR1C0269102Endometrioma1CTD_human
HgeneNCOR1C0334588Giant Cell Glioblastoma1CTD_human
HgeneNCOR1C0345904Malignant neoplasm of liver1CTD_human
HgeneNCOR1C0376358Malignant neoplasm of prostate1CTD_human
HgeneNCOR1C0678222Breast Carcinoma1CGI;CTD_human
HgeneNCOR1C0857007Hyperbilirubinemia, Neonatal1CTD_human
HgeneNCOR1C1257931Mammary Neoplasms, Human1CTD_human
HgeneNCOR1C1458155Mammary Neoplasms1CTD_human
HgeneNCOR1C1565885Direct Hyperbilirubinemia, Neonatal1CTD_human
HgeneNCOR1C1565886Indirect Hyperbilirubinemia, Neonatal1CTD_human
HgeneNCOR1C1621958Glioblastoma Multiforme1CTD_human
HgeneNCOR1C4704874Mammary Carcinoma, Human1CTD_human
TgeneTTC19C0023264Leigh Disease8CLINGEN
TgeneTTC19C1838951LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY8CLINGEN
TgeneTTC19C1850597Leigh Syndrome Due To Mitochondrial Complex II Deficiency8CLINGEN
TgeneTTC19C1850598Leigh Syndrome due to Mitochondrial Complex III Deficiency8CLINGEN
TgeneTTC19C1850599Leigh Syndrome due to Mitochondrial Complex IV Deficiency8CLINGEN
TgeneTTC19C1850600Leigh Syndrome due to Mitochondrial Complex V Deficiency8CLINGEN
TgeneTTC19C2931891Necrotizing encephalopathy, infantile subacute, of Leigh8CLINGEN
TgeneTTC19C3554605MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 22GENOMICS_ENGLAND
TgeneTTC19C0021359Infertility1CTD_human
TgeneTTC19C0027765nervous system disorder1CTD_human
TgeneTTC19C0231686Gait, Unsteady1CTD_human
TgeneTTC19C0231687Spastic gait1CTD_human
TgeneTTC19C0231688Gait, Shuffling1CTD_human
TgeneTTC19C0231689Gait, Athetotic1CTD_human
TgeneTTC19C0231693Charcot Gait1CTD_human
TgeneTTC19C0231694Gait, Festinating1CTD_human
TgeneTTC19C0231695Cerebellar ataxic gait1CTD_human
TgeneTTC19C0231696Gait, Hemiplegic1CTD_human
TgeneTTC19C0231698Gait, Scissors1CTD_human
TgeneTTC19C0231712Waddling gait1CTD_human
TgeneTTC19C0234996Gait, Rigid1CTD_human
TgeneTTC19C0235000Gait, Broadened1CTD_human
TgeneTTC19C0270715Degenerative Diseases, Central Nervous System1CTD_human
TgeneTTC19C0337210Gait, Stumbling1CTD_human
TgeneTTC19C0427128Rapid Fatigue of Gait1CTD_human
TgeneTTC19C0427149Gait, Drop Foot1CTD_human
TgeneTTC19C0427169Marche a Petit Pas1CTD_human
TgeneTTC19C0427177Gait, Hysterical1CTD_human
TgeneTTC19C0524851Neurodegenerative Disorders1CTD_human
TgeneTTC19C0729353Subfertility1CTD_human
TgeneTTC19C0751651Mitochondrial Diseases1GENOMICS_ENGLAND
TgeneTTC19C0751733Degenerative Diseases, Spinal Cord1CTD_human
TgeneTTC19C0751829Gait Disorder, Sensorimotor1CTD_human
TgeneTTC19C0751830Gait Disorders, Neurologic1CTD_human
TgeneTTC19C0751831Gait, Frontal1CTD_human
TgeneTTC19C0751832Gait, Widebased1CTD_human
TgeneTTC19C4074771Sterility, Reproductive1CTD_human