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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:PRKAR1A-NDFIP2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PRKAR1A-NDFIP2
FusionPDB ID: 68659
FusionGDB2.0 ID: 68659
HgeneTgene
Gene symbol

PRKAR1A

NDFIP2

Gene ID

5573

54602

Gene nameprotein kinase cAMP-dependent type I regulatory subunit alphaNedd4 family interacting protein 2
SynonymsACRDYS1|ADOHR|CAR|CNC|CNC1|PKR1|PPNAD1|PRKAR1|TSE1N4WBP5A
Cytomap

17q24.2

13q31.1

Type of geneprotein-codingprotein-coding
DescriptioncAMP-dependent protein kinase type I-alpha regulatory subunitCarney complex type 1cAMP-dependent protein kinase regulatory subunit RIalphacAMP-dependent protein kinase type I-alpha regulatory chainepididymis secretory sperm binding proteinprotein kinNEDD4 family-interacting protein 2MAPK-activating protein PM04 PM05 PM06 PM07NEDD4 WW domain-binding protein 5ANF-kappa-B-activating protein 413putative MAPK-activating protein PM04/PM05/PM06/PM07putative NF-kappa-B-activating protein 413
Modification date2020032920200313
UniProtAcc

P10644

Q9NV92

Ensembl transtripts involved in fusion geneENST idsENST00000358598, ENST00000392711, 
ENST00000536854, ENST00000586397, 
ENST00000588188, ENST00000589228, 
ENST00000494647, ENST00000218652, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score15 X 15 X 8=18004 X 2 X 4=32
# samples 184
** MAII scorelog2(18/1800*10)=-3.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PRKAR1A [Title/Abstract] AND NDFIP2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PRKAR1A(66511717)-NDFIP2(80094945), # samples:1
Anticipated loss of major functional domain due to fusion event.PRKAR1A-NDFIP2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PRKAR1A-NDFIP2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PRKAR1A-NDFIP2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
PRKAR1A-NDFIP2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgenePRKAR1A

GO:2000480

negative regulation of cAMP-dependent protein kinase activity

21812984


check buttonFusion gene breakpoints across PRKAR1A (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across NDFIP2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-D7-A4Z0-01APRKAR1Achr17

66511717

+NDFIP2chr13

80094945

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000358598PRKAR1Achr1766511717+ENST00000218652NDFIP2chr1380094945+4546294117983288
ENST00000392711PRKAR1Achr1766511717+ENST00000218652NDFIP2chr1380094945+46133611841050288
ENST00000589228PRKAR1Achr1766511717+ENST00000218652NDFIP2chr1380094945+455730556994312
ENST00000536854PRKAR1Achr1766511717+ENST00000218652NDFIP2chr1380094945+46674152051104299
ENST00000586397PRKAR1Achr1766511717+ENST00000218652NDFIP2chr1380094945+50087565281445305
ENST00000588188PRKAR1Achr1766511717+ENST00000218652NDFIP2chr1380094945+44291770866288

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
ENST00000358598ENST00000218652PRKAR1Achr1766511717+NDFIP2chr1380094945+0.0001303780.9998696
ENST00000392711ENST00000218652PRKAR1Achr1766511717+NDFIP2chr1380094945+0.0001333870.9998666
ENST00000589228ENST00000218652PRKAR1Achr1766511717+NDFIP2chr1380094945+0.0001298210.9998702
ENST00000536854ENST00000218652PRKAR1Achr1766511717+NDFIP2chr1380094945+0.0001324370.99986756
ENST00000586397ENST00000218652PRKAR1Achr1766511717+NDFIP2chr1380094945+0.0001211680.99987876
ENST00000588188ENST00000218652PRKAR1Achr1766511717+NDFIP2chr1380094945+0.0001225160.99987745

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>68659_68659_1_PRKAR1A-NDFIP2_PRKAR1A_chr17_66511717_ENST00000358598_NDFIP2_chr13_80094945_ENST00000218652_length(amino acids)=288AA_BP=48
MESGSTAASEEARSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFERLEKLLNEEDNSESSAIEQPPTSNPAPQIVQAASS
APALETDSSPPPYSSITVEVPTTSDTEVYGEFYPVPPPYSVATSLPTYDEAEKAKAAAMAAAAAETSQRIQEEECPPRDDFSDADQLRVG
NDGIFMLAFFMAFIFNWLGFCLSFCITNTIAGRYGAICGFGLSLIKWILIVRFSDYFTGYFNGQYWLWWIFLVLGLLLFFRGFVNYLKVR

--------------------------------------------------------------

>68659_68659_2_PRKAR1A-NDFIP2_PRKAR1A_chr17_66511717_ENST00000392711_NDFIP2_chr13_80094945_ENST00000218652_length(amino acids)=288AA_BP=48
MESGSTAASEEARSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFERLEKLLNEEDNSESSAIEQPPTSNPAPQIVQAASS
APALETDSSPPPYSSITVEVPTTSDTEVYGEFYPVPPPYSVATSLPTYDEAEKAKAAAMAAAAAETSQRIQEEECPPRDDFSDADQLRVG
NDGIFMLAFFMAFIFNWLGFCLSFCITNTIAGRYGAICGFGLSLIKWILIVRFSDYFTGYFNGQYWLWWIFLVLGLLLFFRGFVNYLKVR

--------------------------------------------------------------

>68659_68659_3_PRKAR1A-NDFIP2_PRKAR1A_chr17_66511717_ENST00000536854_NDFIP2_chr13_80094945_ENST00000218652_length(amino acids)=299AA_BP=59
MTSAPVSAERTMESGSTAASEEARSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFERLEKLLNEEDNSESSAIEQPPTSN
PAPQIVQAASSAPALETDSSPPPYSSITVEVPTTSDTEVYGEFYPVPPPYSVATSLPTYDEAEKAKAAAMAAAAAETSQRIQEEECPPRD
DFSDADQLRVGNDGIFMLAFFMAFIFNWLGFCLSFCITNTIAGRYGAICGFGLSLIKWILIVRFSDYFTGYFNGQYWLWWIFLVLGLLLF

--------------------------------------------------------------

>68659_68659_4_PRKAR1A-NDFIP2_PRKAR1A_chr17_66511717_ENST00000586397_NDFIP2_chr13_80094945_ENST00000218652_length(amino acids)=305AA_BP=65
MLYSLYKHVCVFFSQRTMESGSTAASEEARSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFERLEKLLNEEDNSESSAIE
QPPTSNPAPQIVQAASSAPALETDSSPPPYSSITVEVPTTSDTEVYGEFYPVPPPYSVATSLPTYDEAEKAKAAAMAAAAAETSQRIQEE
ECPPRDDFSDADQLRVGNDGIFMLAFFMAFIFNWLGFCLSFCITNTIAGRYGAICGFGLSLIKWILIVRFSDYFTGYFNGQYWLWWIFLV

--------------------------------------------------------------

>68659_68659_5_PRKAR1A-NDFIP2_PRKAR1A_chr17_66511717_ENST00000588188_NDFIP2_chr13_80094945_ENST00000218652_length(amino acids)=288AA_BP=48
MESGSTAASEEARSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFERLEKLLNEEDNSESSAIEQPPTSNPAPQIVQAASS
APALETDSSPPPYSSITVEVPTTSDTEVYGEFYPVPPPYSVATSLPTYDEAEKAKAAAMAAAAAETSQRIQEEECPPRDDFSDADQLRVG
NDGIFMLAFFMAFIFNWLGFCLSFCITNTIAGRYGAICGFGLSLIKWILIVRFSDYFTGYFNGQYWLWWIFLVLGLLLFFRGFVNYLKVR

--------------------------------------------------------------

>68659_68659_6_PRKAR1A-NDFIP2_PRKAR1A_chr17_66511717_ENST00000589228_NDFIP2_chr13_80094945_ENST00000218652_length(amino acids)=312AA_BP=72
MRELGTPPPRTRSLAPAAARPQRTMESGSTAASEEARSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFERLEKLLNEEDN
SESSAIEQPPTSNPAPQIVQAASSAPALETDSSPPPYSSITVEVPTTSDTEVYGEFYPVPPPYSVATSLPTYDEAEKAKAAAMAAAAAET
SQRIQEEECPPRDDFSDADQLRVGNDGIFMLAFFMAFIFNWLGFCLSFCITNTIAGRYGAICGFGLSLIKWILIVRFSDYFTGYFNGQYW

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr17:66511717/chr13:80094945)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PRKAR1A

P10644

NDFIP2

Q9NV92

FUNCTION: Regulatory subunit of the cAMP-dependent protein kinases involved in cAMP signaling in cells. {ECO:0000269|PubMed:16491121, ECO:0000269|PubMed:20215566, ECO:0000269|PubMed:26405036}.FUNCTION: Activates HECT domain-containing E3 ubiquitin-protein ligases, including ITCH, NEDD4, NEDD4L, SMURF2, WWP1 and WWP2, and consequently modulates the stability of their targets. As a result, may control many cellular processes. Recruits ITCH, NEDD4 and SMURF2 to endosomal membranes. Negatively regulates KCNH2 potassium channel activity by decreasing its cell-surface expression and interfering with channel maturation through recruitment of NEDD4L to the Golgi apparatus and multivesicular body where it mediates KCNH2 degradation (PubMed:26363003). May modulate EGFR signaling. Together with NDFIP1, limits the cytokine signaling and expansion of effector Th2 T-cells by promoting degradation of JAK1, probably by ITCH- and NEDD4L-mediated ubiquitination (By similarity). {ECO:0000250|UniProtKB:Q91ZP6, ECO:0000269|PubMed:12761501, ECO:0000269|PubMed:19343052, ECO:0000269|PubMed:20534535, ECO:0000269|PubMed:26363003}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208148_151107.01399.3333333333333MotifNote=PPxY motif 1
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208174_177107.01399.3333333333333MotifNote=PPxY motif 2
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208184_186107.01399.3333333333333MotifNote=PPxY motif 3
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208253_257107.01399.3333333333333Topological domainExtracellular
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208279_287107.01399.3333333333333Topological domainCytoplasmic
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208309_336107.01399.3333333333333Topological domainExtracellular
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208232_252107.01399.3333333333333TransmembraneHelical
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208258_278107.01399.3333333333333TransmembraneHelical
TgeneNDFIP2chr17:66511717chr13:80094945ENST0000021865208288_308107.01399.3333333333333TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000358598+21196_10059.0382.0MotifNote=Pseudophosphorylation motif
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000392711+21196_10059.0382.0MotifNote=Pseudophosphorylation motif
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000536854+31296_10059.0382.0MotifNote=Pseudophosphorylation motif
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000586397+11096_10059.0382.0MotifNote=Pseudophosphorylation motif
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000589228+21196_10059.0382.0MotifNote=Pseudophosphorylation motif
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000358598+211137_25459.0382.0Nucleotide bindingNote=cAMP 1
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000358598+211255_38159.0382.0Nucleotide bindingNote=cAMP 2
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000392711+211137_25459.0382.0Nucleotide bindingNote=cAMP 1
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000392711+211255_38159.0382.0Nucleotide bindingNote=cAMP 2
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000536854+312137_25459.0382.0Nucleotide bindingNote=cAMP 1
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000536854+312255_38159.0382.0Nucleotide bindingNote=cAMP 2
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000586397+110137_25459.0382.0Nucleotide bindingNote=cAMP 1
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000586397+110255_38159.0382.0Nucleotide bindingNote=cAMP 2
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000589228+211137_25459.0382.0Nucleotide bindingNote=cAMP 1
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000589228+211255_38159.0382.0Nucleotide bindingNote=cAMP 2
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000358598+2111_13659.0382.0RegionNote=Dimerization and phosphorylation
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000392711+2111_13659.0382.0RegionNote=Dimerization and phosphorylation
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000536854+3121_13659.0382.0RegionNote=Dimerization and phosphorylation
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000586397+1101_13659.0382.0RegionNote=Dimerization and phosphorylation
HgenePRKAR1Achr17:66511717chr13:80094945ENST00000589228+2111_13659.0382.0RegionNote=Dimerization and phosphorylation
TgeneNDFIP2chr17:66511717chr13:80094945ENST00000218652081_231107.01399.3333333333333Topological domainCytoplasmic


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors
PRKAR1APRKAR1B, AKAP1, MYO7A, AKAP10, C2orf88, PLEKHF2, PYCARD, NPRL2, UBE2M, NUAK1, MCRS1, PRKACA, PRKAR1A, AKAP4, ARFGEF2, ARFGEF1, EGFR, GRB2, PRKX, AKAP11, Rrp1b, GABARAPL1, WNK1, UBC, PJA2, CBS, NELL2, C2orf44, BAHD1, ZBED1, MAPK6, TAB1, ELAVL1, SLC2A4, CUL3, PATZ1, PRKACB, PRPF31, SAFB, HSP90AA4P, MEN1, SLC38A5, Akap7, SMURF1, PRPF40A, SMAD2, CDK2, CCNE1, RFC2, PPP1CA, NPM1, SOX2, HIVEP1, CAPN11, SETD7, SET, DYRK1B, DYRK1A, GSK3B, ARPC3, PFDN5, AGO2, AGO3, CEP250, RAF1, CUL7, CCDC8, ILK, MTOR, BTRC, STOML2, PRKACG, PALM2-AKAP2, AKAP3, GPR161, ANKRD26, FRMD5, IFI16, XPO1, VAPA, Prkacb, Prkar2a, Gsk3b, VAPB, PRKAR2B, IQCB1, YWHAZ, DPB3, TCD1, EGLN3, HRAS, KRAS, NRAS, RECQL4, MCL1, MAPK12, TK1, FGFR3, FABP4, AGPAT1, MAP3K5, SPHK2, CANX, RC3H2, PLK1, BIRC3, NFX1, AKAP7, RSPH3, SPG20, DTX1, C11orf49, AKAP5, FAM153B, FBXW8, OBSL1, ARAF, BAD, MAPK7, AKAP12, HSPA8, HSPB1, JUP, PGAM5, GRWD1, AP3S1, RPL6, HIST1H1C, CORO1B, KHDRBS1, ADRM1, HIGD1A, SLC25A11, ROCK1, MEPCE, HIST1H1E, DOCK4, HIGD1C, GNL3, RPL36A, RPL8, STK39, GTF3C5, BCCIP, PDCD2L, UHRF1, ZFP91, GATAD2B, DDX42, CCDC108, LLGL2, SUZ12, USP10, C1QBP, NAP1L1, PYCR1, S100A7A, S100A7, MCM3, GART, EPB41L2, RBFOX3, RBFOX2, RBFOX1, CAMSAP3, FAT1, KDELR1, CFL1, G6PD, SERPINH1, SNRNP40, MAGEB2, HLA-C, HLA-A, COQ6, NXF1, VPS29, GPX8, MOB2, ACACA, AHSA1, MGEA5, AP1G1, ADAM10, PRKCA, PRKCB, PRKCI, PRKCZ, PTK6, RPS6KA3, SH3GL3, ESR1, MAP1LC3B, CDCA5, TULP3, SREBF2, nsp8ab, PTP4A3, ASXL1, DNAJB6, DNAJC28, OGT, KLHL28, EIF1AX, SBNO1, METTL15, FYN, SH3PXD2B, PLCB3, PAXBP1, NBR1, CALCOCO2, SQSTM1,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
PRKAR1Aall structure
NDFIP2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to PRKAR1A-NDFIP2


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to PRKAR1A-NDFIP2


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePRKAR1AC2607929Carney Complex, Type 110CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT
HgenePRKAR1AC3276228ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE8CTD_human;GENOMICS_ENGLAND;UNIPROT
HgenePRKAR1AC0406810Carney Complex6CLINGEN;CTD_human;GENOMICS_ENGLAND
HgenePRKAR1AC0220659Acrodysostosis4CTD_human;GENOMICS_ENGLAND;ORPHANET
HgenePRKAR1AC0010481Cushing Syndrome2CTD_human
HgenePRKAR1AC1864846PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (disorder)2CTD_human;GENOMICS_ENGLAND
HgenePRKAR1AC0001627Congenital adrenal hyperplasia1CTD_human
HgenePRKAR1AC0002170Alopecia1CTD_human
HgenePRKAR1AC0020456Hyperglycemia1CTD_human
HgenePRKAR1AC0021655Insulin Resistance1CTD_human
HgenePRKAR1AC0023487Acute Promyelocytic Leukemia1CTD_human;ORPHANET
HgenePRKAR1AC0026846Muscular Atrophy1CTD_human
HgenePRKAR1AC0028754Obesity1CTD_human
HgenePRKAR1AC0086873Pseudopelade1CTD_human
HgenePRKAR1AC0162311Androgenetic Alopecia1CTD_human
HgenePRKAR1AC0263477Female pattern alopecia (disorder)1CTD_human
HgenePRKAR1AC0270948Neurogenic Muscular Atrophy1CTD_human
HgenePRKAR1AC0920563Insulin Sensitivity1CTD_human
HgenePRKAR1AC1850635Atrial myxoma, familial1CTD_human;ORPHANET
HgenePRKAR1AC1854540Carney Complex, Type 21CTD_human
HgenePRKAR1AC1855520Hyperglycemia, Postprandial1CTD_human
HgenePRKAR1AC3553250ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE1CTD_human
HgenePRKAR1AC3887949Apparent mineralocorticoid excess1CTD_human
HgenePRKAR1AC4083212Alopecia, Male Pattern1CTD_human
HgenePRKAR1AC4304832Primary pigmented nodular adrenocortical disease1ORPHANET
HgenePRKAR1AC4721502Peripheral dysostosis1CTD_human