NHS
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human X chromosome
- Cytogenetic location
- Xp22.2-p22.13
- Encodes
- NHS actin remodeling regulator[12]
- Expressed in
- buccal mucosa cell, endothelial cell, pancreatic epithelial cell, palpebral conjunctiva, visceral pleura, germinal epithelium, mucosa of paranasal sinus, Brodmann area 23, caput epididymis, endometrium
- Found in taxon
- Homo sapiens[13]
- Genetic association
- Nance-Horan syndrome, zonular cataract and nystagmus
- HomoloGene ID
- 18866[3]
- Strand orientation
- forward strand
🏷️ Also known as
en CTRCT40
en CXN
en NHS
en NHS actin remodeling regulator
en SCML1
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000188158
- Ensembl transcript ID
- ENST00000617601, ENST00000380060, ENST00000398097, ENST00000485305, ENST00000615422, ENST00000648929, ENST00000676302, ENST00000690213, ENST00000690608
- Entrez Gene ID
- 4810
- Exact match
- identifiers.org
- Freebase ID
- /m/03hgly5
- HGNC ID
- 7820
- HGNC gene symbol
- NHS
- OMIM ID
- 300457
- RefSeq RNA ID
- XM_011545528, NM_001136024, NM_001291867, NM_001291868, NM_198270, XM_047442140
- UMLS CUI
- C1417725
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Summary
NHS is a gene[1].