MFF
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[13]
- Cytogenetic location
- 2q36.3[17]
- Encodes
- Mitochondrial fission factor, Mitochondrial fission factor[11]
- Expressed in
- sperm, left testis, right testis, gonad, ganglionic eminence, C1 segment, body of pancreas, Brodmann area 9, anterior cingulate cortex, prefrontal cortex[18][19][20][21][22][23]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome, lethal encephalopathy due to mitochondrial and peroxisomal fission defect[14][15]
- HomoloGene ID
- 137341[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en C2orf33
en EMPF2
en GL004
en MFF
en mitochondrial fission factor
cs Faktor mitochondriálního dělení
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000168958
- Ensembl transcript ID
- ENST00000534203, ENST00000304593, ENST00000337110, ENST00000349901, ENST00000353339, ENST00000354503, ENST00000392059, ENST00000409565, ENST00000409616, ENST00000418961, ENST00000423098, ENST00000436237, ENST00000436791, ENST00000443428, ENST00000452930, ENST00000456345, ENST00000460756, ENST00000470090, ENST00000476262, ENST00000476924, ENST00000477362, ENST00000489696, ENST00000490857, ENST00000524634, ENST00000525195, ENST00000530359, ENST00000531278
- Entrez Gene ID
- 56947
- Exact match
- identifiers.org
- Freebase ID
- /m/0h55wxl
- HGNC ID
- 24858
- HGNC gene symbol
- MFF
- OMIM ID
- 614785
- RefSeq RNA ID
- NM_001277061, NM_001277062, NM_001277063, NM_001277064, NM_001277065, NM_001277066, NM_001277067, NM_001277068, NM_020194, NR_102266, XM_006712637, XM_011511500, XM_017004512, XM_024453009, XM_047445127, XM_047445128, XM_047445129, XM_047445130, XM_047445131, XM_047445132, XM_047445133
- UMLS CUI
- C1540223
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