NMNAT1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[13]
- Cytogenetic location
- 1p36.22[16]
- Expressed in
- muscle of thigh, mucosa of transverse colon, testicle, gastrocnemius muscle, islet of Langerhans, monocyte, Achilles tendon, stromal cell of endometrium, rectum, apex of heart[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- Leber congenital amaurosis 9[14]
- HomoloGene ID
- 39074[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en LCA9
en nicotinamide nucleotide adenylyltransferase 1
en NMNAT
en NMNAT1
en PNAT1
en SHILCA
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- Protein NMNAT1 PDB 1gzu.png ↗
- Ensembl gene ID
- ENSG00000173614
- Ensembl transcript ID
- ENST00000496751, ENST00000377205, ENST00000403197, ENST00000462686, ENST00000492735
- Entrez Gene ID
- 64802
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxq9w
- HGNC ID
- 17877
- HGNC gene symbol
- NMNAT1
- Microsoft Academic ID (discontinued)
- 10316603
- OMIM ID
- 608700
- RefSeq RNA ID
- XM_011541971, NM_001297778, NM_001297779, NM_022787, XM_017002107, XM_017002108, XM_047428076, XM_047428077, XM_047428080, XM_047428082
- UMLS CUI
- C1425150
🔗 Connections
Expressed in 6
Chromosome 1
Found in taxon 1
Instance of 1
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