MFSD8
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 4
- Cytogenetic location
- 4q28.2
- Expressed in
- Achilles tendon, body of pancreas, bone marrow cell, epithelium of colon, cerebellar hemisphere, sural nerve, pancreatic epithelial cell, monocyte, right hemisphere of cerebellum, anterior pituitary
- Found in taxon
- Homo sapiens[23]
- Genetic association
- neuronal ceroid lipofuscinosis 7, neuronal ceroid lipofuscinosis
- HomoloGene ID
- 115814[3]
- Ortholog
- Mfsd8, F27D9.2, F52F10.2, Cln7, C25E10.5, W01B6.3, W05E10.1, F57A8.7, T28C12.1, T28C12.2, F14D7.6, W03C9.6, C25E10.4, F58G11.4, mfsd8, ZK550.2, mfsd-8, srsx-34, Mfsd8[8][9][10][11][12][13][14][15][16][17][18][19][20][21]
- Strand orientation
- reverse strand
🏷️ Also known as
en CCMD
en CLN7
en major facilitator superfamily domain containing 8
en MFSD8
ar MFSD٨
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000164073
- Ensembl transcript ID
- ENST00000515130, ENST00000296468, ENST00000503928, ENST00000504126, ENST00000505284, ENST00000508441, ENST00000509826, ENST00000513559, ENST00000641695, ENST00000641447, ENST00000641843, ENST00000641830, ENST00000642042, ENST00000642143, ENST00000641356, ENST00000641178, ENST00000641464, ENST00000641690, ENST00000641509, ENST00000641146, ENST00000641928, ENST00000641003, ENST00000641882, ENST00000641369, ENST00000641332, ENST00000641388, ENST00000641658, ENST00000641869, ENST00000641590, ENST00000641134, ENST00000641949, ENST00000641503, ENST00000641742, ENST00000641743, ENST00000641870, ENST00000641508, ENST00000642012, ENST00000641186, ENST00000641686, ENST00000641140, ENST00000641025, ENST00000641092, ENST00000641133, ENST00000641393, ENST00000641482, ENST00000641558, ENST00000642121, ENST00000641340, ENST00000641776, ENST00000641538, ENST00000641264, ENST00000641243, ENST00000641434, ENST00000641753, ENST00000641748, ENST00000642078, ENST00000641147, ENST00000641774, ENST00000641413, ENST00000641228, ENST00000642034, ENST00000641397
- Entrez Gene ID
- 256471
- Exact match
- identifiers.org
- Freebase ID
- /m/06607yq
- HGNC ID
- 28486
- HGNC gene symbol
- MFSD8
- OMIM ID
- 611124
- RefSeq RNA ID
- NM_152778, XM_005262898, XM_011531832, XM_017007989, XM_024453982, XM_024453983, NM_001363520, NM_001363521, NM_001371590, NM_001371591, NM_001371592, NM_001371593, NM_001371594, NM_001371595, NM_001371596, XM_047449992, XM_047449993, XM_047449994, XM_047449995, XM_047449997, XM_047449998, XM_047449999
- UMLS CUI
- C1970174
🔗 Connections
Expressed in 4
← Genetic association 2
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
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