IMPG2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 3[11]
- Cytogenetic location
- 3q12.3[14]
- Encodes
- Interphotoreceptor matrix proteoglycan 2[9]
- Expressed in
- right uterine tube, testicle, pineal gland, retina, retinal pigment epithelium, germinal epithelium, Epithelium of choroid plexus, stromal cell of endometrium, Achilles tendon, muscle tissue[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- retinitis pigmentosa 56[12]
- HomoloGene ID
- 9439[3]
- Strand orientation
- reverse strand[13]
🏷️ Also known as
en IMPG2
en interphotoreceptor matrix proteoglycan 2
en IPM200
en RP56
en SPACRCAN
en VMD5
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000081148
- Ensembl transcript ID
- ENST00000193391
- Entrez Gene ID
- 50939
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11gbldp2hj
- HGNC ID
- 18362
- HGNC gene symbol
- IMPG2
- OMIM ID
- 607056
- RefSeq RNA ID
- NM_016247
- UMLS CUI
- C1425472
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Summary
IMPG2 is a gene[1].