KEGG   Homo sapiens (human): 56947
Entry
56947             CDS       T01001                                 
Symbol
MFF, C2orf33, EMPF2, GL004
Name
(RefSeq) mitochondrial fission factor
  KO
K22076  mitochondrial fission factor
Organism
hsa  Homo sapiens (human)
Disease
H01900  Encephalopathy due to defective mitochondrial and peroxisomal fission
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    56947 (MFF)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial quality control factors
  Mitochondrial dynamics
   Fission and Fusion factors
    56947 (MFF)
SSDB
Motif
Pfam: Miff DUF3736
Other DBs
NCBI-GeneID: 56947
NCBI-ProteinID: NP_001263990
OMIM: 614785
HGNC: 24858
Ensembl: ENSG00000168958
UniProt: Q9GZY8
Position
2:227325251..227357836
AA seq 342 aa
MSKGTSSDTSLGRVSRAAFPSPTAAEMAEISRIQYEMEYTEGISQRMRVPEKLKVAPPNA
DLEQGFQEGVPNASVIMQVPERIVVAGNNEDVSFSRPADLDLIQSTPFKPLALKTPPRVL
TLSERPLDFLDLERPPTTPQNEEIRAVGRLKRERSMSENAVRQNGQLVRNDSLWHRSDSA
PRNKISRFQAPISAPEYTVTPSPQQARVCPPHMLPEDGANLSSARGILSLIQSSTRRAYQ
QILDVLDENRRPVLRGGSAAATSNPHHDNVRYGISNIDTTIEGTSDDLTVVDAASLRRQI
IKLNRRLQLLEEENKERAKREMVMYSITVAFWLLNSWLWFRR
NT seq 1029 nt   +upstreamnt  +downstreamnt
atgagtaaaggaacaagcagtgacacatcactaggaagggtgagcagggcagcatttcct
tctcccactgctgctgagatggcagaaattagtcgaattcagtacgaaatggaatatact
gaaggcattagtcagcgaatgagggtcccagaaaagttaaaagtagcaccgccaaacgct
gacctggaacaaggattccaagaaggagttccaaatgctagtgtgataatgcaagttccg
gagaggattgttgtagcaggaaataatgaagatgtttcattttcaagaccagcagatctt
gaccttattcagtcaactccctttaaacccctggcactgaaaacaccacctcgtgtactt
acgctgagtgaaagaccactagattttctggatttagaaagacctcctacaacccctcaa
aatgaagaaatccgagcagttggcagactaaaaagagagcggtctatgagtgaaaatgct
gttcgccaaaatggacagctggtcagaaatgattctctgtggcacagatcagattctgcc
ccaagaaataaaatttcaaggttccaggcaccgatttctgcaccggagtacactgtgaca
ccatcgccacaacaggctcgggtctgtcctccccatatgttacctgaagatggagctaat
ctttcctctgctcgtggcattttgtcgcttatccagtcttctactcgtagggcataccag
cagatcttggatgtgctggatgaaaatcgcagacctgtgttgcgtggtgggtctgctgcc
gccacttctaatcctcatcatgacaacgtcaggtatggcatttcaaatatagatacaacc
attgaaggaacgtcagatgacctgactgttgtagatgcagcttcactaagacgacagata
atcaaactaaatagacgtctacaacttctggaagaggagaacaaagaacgtgctaaaaga
gaaatggtcatgtattcaattactgtagctttctggctgcttaatagctggctctggttt
cgccgctag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (33)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (31)   
DNA sequence (62)   
   RefSeq(nuc) (32)   
   GenBank (15)   
   EMBL (15)   
Protein domain (2)   
   Pfam (2)   
All databases (116)   

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