Gene table of RP9 : retinitis pigmentosa 9 (autosomal dominant)

Gene-disease associations table

Disease IDDisease nameSource of annotation with RP9OMIM linkNumber of associated genesgenes
PS268000RETINITIS PIGMENTOSAClinVar, OMIM, HUMSAVAR link to OMIM 69PDE6A, MAK, FSCN2, DHDDS, RHO, RP9, CNGA1, CRB1, SLC7A14, BEST1, CERKL, PRPF3, C8orf37, PROM1, TOPORS, PRPH2, PRCD, SNRNP200, IMPG2, PDE6B, IDH3B, RGR, TTC8, GUCA1B, CDHR1, PANK2, RDH12, BBS2, MERTK, RP1L1, NEK2, USH2A, ZNF408, LRAT, C2orf71, MYO7A, KLHL7, IMPDH1, ZNF513, RP1, NR2E3, PDE6G, ROM1, CYGB, ARL6, NRL, RPGR, PRPF4, RP2, IFT172, HGSNAT, TULP1, CNGB1, KIZ, EYS, OFD1, RPE65, PRPF6, FAM161A, RBP3, IFT140, PRPF8, ABCA4, CLRN1, PRPF31, SAG, CA4, CRX, SEMA4A

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Annotation of the gene RP9

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST
Associated KEGG pathways
Associated REACTOME pathways
Associated GO terms for Molecular function
GO termGO IDGO IC
cation bindingGO:00431691.4
nucleic acid bindingGO:00036761.44
organic cyclic compound bindingGO:00971591.05
poly(A) RNA bindingGO:00448222.69
ion bindingGO:00431671.36
bindingGO:00054880.18
protein bindingGO:00055150.46
metal ion bindingGO:00468721.41
heterocyclic compound bindingGO:19013631.06
RNA bindingGO:00037232.36