PRCD
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 17[11]
- Cytogenetic location
- 17q25.1[14]
- Expressed in
- right hemisphere of cerebellum, C1 segment, substantia nigra, Brodmann area 9, hypothalamus, right auricle of heart, cardiac muscle tissue of right atrium, canal of the cervix, right frontal lobe, corpus callosum[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- retinitis pigmentosa 36[12]
- HomoloGene ID
- 135617[3]
- Strand orientation
- forward strand[13]
🏷️ Also known as
en photoreceptor disc component
en PRCD
en progressive rod-cone degeneration
en RP36
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000214140
- Ensembl transcript ID
- ENST00000593023, ENST00000397630, ENST00000397633, ENST00000465808, ENST00000586148, ENST00000587063, ENST00000587289, ENST00000587813, ENST00000590555, ENST00000591317, ENST00000592014, ENST00000592340, ENST00000592432
- Entrez Gene ID
- 768206
- Exact match
- identifiers.org
- Freebase ID
- /m/011x43hj
- HGNC ID
- 32528
- HGNC gene symbol
- PRCD
- OMIM ID
- 610598
- RefSeq RNA ID
- NM_001077620, NR_033357, XM_017025013, XM_017025014, XM_017025015, XM_047436657, XM_047436658, XM_047436659
- UMLS CUI
- C1826694
🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Instance of 1
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