SLC7A14
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 3[13]
- Cytogenetic location
- 3q26.2[16]
- Expressed in
- cerebellar vermis, postcentral gyrus, Brodmann area 46, middle temporal gyrus, superior frontal gyrus, pons, superior vestibular nucleus, entorhinal cortex, Brodmann area 23, prefrontal cortex[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- retinitis pigmentosa 68[14]
- HomoloGene ID
- 76320[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en PPP1R142
en SLC7A14
en solute carrier family 7 member 14
ar SLC٧A١٤
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000013293
- Ensembl transcript ID
- ENST00000466168, ENST00000231706
- Entrez Gene ID
- 57709
- Exact match
- identifiers.org
- Freebase ID
- /m/011x3k07
- HGNC ID
- 29326
- HGNC gene symbol
- SLC7A14
- OMIM ID
- 615720
- UMLS CUI
- C1822738
🔗 Connections
Expressed in 8
Chromosome 1
Found in taxon 1
Instance of 1
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