ABCD1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human X chromosome[13]
- Cytogenetic location
- Xq28[17]
- Expressed in
- mucosa of ileum, left adrenal cortex, right adrenal gland, right adrenal cortex, monocyte, apex of heart, gastrocnemius muscle, muscle of thigh, stromal cell of endometrium, body of uterus[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- X-linked cerebral adrenoleukodystrophy, X-linked adrenoleukodystrophy[14][15]
- HomoloGene ID
- 55426[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en ABC42
en ABCD1
en Adrenoleukodystrophy protein
en ALD
en ALDP
en AMN
en ATP binding cassette subfamily D member 1
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000101986
- Ensembl transcript ID
- ENST00000443684, ENST00000218104, ENST00000370129
- Entrez Gene ID
- 215
- Exact match
- identifiers.org
- Freebase ID
- /m/02qpbbh
- HGNC ID
- 61
- HGNC gene symbol
- ABCD1
- OMIM ID
- 300371
- RefSeq RNA ID
- NM_000033, XM_047441916, XM_047441917
- UMLS CUI
- C1412084
🔗 Connections
Expressed in 2
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
Press Enter · cited answer in seconds
0 sources
Summary
ABCD1 is a gene[1].