RPGRIP1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 14[12]
- Cytogenetic location
- 14q11.2[17]
- Expressed in
- left testis, sperm, right testis, gonad, testicle, monocyte, granulocyte, blood, right lobe of liver, Achilles tendon[18][19][20][21][22][23]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Leber congenital amaurosis 6, cone-rod dystrophy 13, cone-rod dystrophy[13][14][15]
- HomoloGene ID
- 10679[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en RPGRIP1d
en CORD13
en LCA6
en retinitis pigmentosa GTPase regulator interacting protein 1
en RGI1
en RGRIP
en RPGR interacting protein 1
en RPGRIP
en RPGRIP1
ar RPGRIP١
🔖 Identifiers · 11
- Image (Wikimedia Commons)
- Human RPGRIP1 C2 domain.png ↗
- Ensembl gene ID
- ENSG00000092200
- Ensembl transcript ID
- ENST00000557771, ENST00000382933, ENST00000400017, ENST00000553500, ENST00000553927, ENST00000554303, ENST00000554750, ENST00000555322, ENST00000555489, ENST00000555587, ENST00000556336, ENST00000557351, ENST00000557606
- Entrez Gene ID
- 57096
- Exact match
- identifiers.org
- Freebase ID
- /m/03gyw2b
- HGNC ID
- 13436
- HGNC gene symbol
- RPGRIP1
- OMIM ID
- 605446
- RefSeq RNA ID
- NM_020366, XM_005267879, XM_005267880, XM_005267881, XM_011536978, XM_011536979, XM_011536981, XM_011536982, XM_017021473, XM_024449663, XM_024449664, XM_024449666, NM_001377523, NM_001377948, NM_001377949, NM_001377950, NM_001377951, XM_047431609
- UMLS CUI
- C1421991
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
RPGRIP1 is a gene[1].