MFF gene homepage

General information
Gene symbol MFF
Gene name mitochondrial fission factor
Chromosome 2
Chromosomal band q36
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_001277061.1, NM_001277062.1, NM_001277063.1, NM_001277064.1, NM_001277065.1, NM_001277066.1, NM_001277067.1, NM_001277068.1, NM_020194.5, NR_102266.1, XM_005246681.3, XM_005246682.1, XM_005246683.1, XM_005246684.1, XM_005246685.3, XM_005246686.3, XM_005246687.3, XM_005246688.1, XM_006712637.1, XM_006712638.1, XM_006712639.2, XM_011511500.1, XM_011511501.1, XM_011511502.1
Associated with diseases 617086
Citation reference(s) -
Curators (1) Lishuang Shen
Total number of public variants reported 5
Unique public DNA variants reported 5
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Date created May 13, 2016

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 24858
Entrez Gene 56947
PubMed articles MFF
OMIM - Gene 614785
OMIM - Diseases 617086 (Encephalopathy due to defective mitochondrial and peroxisomal fission 2, 617086 (3))
HGMD MFF
GeneCards MFF
GeneTests MFF


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00003931 2 transcript variant 1 NM_001277061.1 NP_001263990.1 5
00003932 2 transcript variant 10 NR_102266.1 - 5
00003933 2 transcript variant 2 NM_020194.5 NP_064579.3 5
00003934 2 transcript variant 3 NM_001277062.1 NP_001263991.1 5
00003935 2 transcript variant 4 NM_001277063.1 NP_001263992.1 5
00003936 2 transcript variant 5 NM_001277064.1 NP_001263993.1 5
00003937 2 transcript variant 6 NM_001277065.1 NP_001263994.1 5
00003938 2 transcript variant 7 NM_001277066.1 NP_001263995.1 5
00003939 2 transcript variant 8 NM_001277067.1 NP_001263996.1 5
00003940 2 transcript variant 9 NM_001277068.1 NP_001263997.1 5
00003944 2 transcript variant X12 XM_005246688.1 XP_005246745.1 5
00003948 2 transcript variant X3 XM_005246682.1 XP_005246739.1 5
00003949 2 transcript variant X4 XM_005246683.1 XP_005246740.1 5
00003952 2 transcript variant X7 XM_005246684.1 XP_005246741.1 5
00003941 2 transcript variant X1 XM_011511500.1 XP_011509802.1 0
00003942 2 transcript variant X10 XM_005246686.3 XP_005246743.1 0
00003943 2 transcript variant X11 XM_005246687.3 XP_005246744.1 0
00003945 2 transcript variant X13 XM_006712639.2 XP_006712702.1 0
00003946 2 transcript variant X14 XM_011511502.1 XP_011509804.1 0
00003947 2 transcript variant X2 XM_005246681.3 XP_005246738.1 0
00003950 2 transcript variant X5 XM_011511501.1 XP_011509803.1 0
00003951 2 transcript variant X6 XM_006712637.1 XP_006712700.1 0
00003953 2 transcript variant X8 XM_006712638.1 XP_006712701.1 0
00003954 2 transcript variant X9 XM_005246685.3 XP_005246742.1 0


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