SCN11A
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 3[12]
- Cytogenetic location
- 3p22.2[17]
- Expressed in
- buccal mucosa cell, spinal ganglia, testicle, trigeminal ganglion, gonad, left testis, right testis, sural nerve, spleen, ventricular zone[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- hereditary sensory and autonomic neuropathy type 7, autosomal dominant hereditary sensory and autonomic neuropathy, familial episodic pain syndrome with predominantly lower limb involvement[13][14][15]
- HomoloGene ID
- 8041[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en FEPS3
en HSAN7
en NaN
en NAV1.9
en PN5
en SCN11A
en SCN12A
en SNS-2
en sodium voltage-gated channel alpha subunit 11
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000168356
- Ensembl transcript ID
- ENST00000456224, ENST00000302328, ENST00000444237, ENST00000665106, ENST00000668754, ENST00000676333, ENST00000675223, ENST00000676176, ENST00000674979, ENST00000675269, ENST00000676045, ENST00000674755, ENST00000675672, ENST00000675892
- Entrez Gene ID
- 11280
- Exact match
- identifiers.org
- Freebase ID
- /m/03bxypj
- HGNC ID
- 10583
- HGNC gene symbol
- SCN11A
- Microsoft Academic ID (discontinued)
- 2777776202
- OMIM ID
- 604385
- RefSeq RNA ID
- NM_001287223, NM_014139, XM_011533321, XM_017005650, XM_017005651, XM_017005653, NM_001349253, NR_164473, XM_047447378
- UMLS CUI
- C1419854
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