Homo sapiens (human): 56947
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Miff
DUF3736
Motif
Other DBs
NCBI-GeneID:
56947
NCBI-ProteinID:
NP_001263990
OMIM:
614785
HGNC:
24858
Ensembl:
ENSG00000168958
UniProt:
Q9GZY8
LinkDB
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Position
2:227325251..227357836
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AA seq
342 aa
AA seq
DB search
MSKGTSSDTSLGRVSRAAFPSPTAAEMAEISRIQYEMEYTEGISQRMRVPEKLKVAPPNA
DLEQGFQEGVPNASVIMQVPERIVVAGNNEDVSFSRPADLDLIQSTPFKPLALKTPPRVL
TLSERPLDFLDLERPPTTPQNEEIRAVGRLKRERSMSENAVRQNGQLVRNDSLWHRSDSA
PRNKISRFQAPISAPEYTVTPSPQQARVCPPHMLPEDGANLSSARGILSLIQSSTRRAYQ
QILDVLDENRRPVLRGGSAAATSNPHHDNVRYGISNIDTTIEGTSDDLTVVDAASLRRQI
IKLNRRLQLLEEENKERAKREMVMYSITVAFWLLNSWLWFRR
NT seq
1029 nt
NT seq
+upstream
nt +downstream
nt
atgagtaaaggaacaagcagtgacacatcactaggaagggtgagcagggcagcatttcct
tctcccactgctgctgagatggcagaaattagtcgaattcagtacgaaatggaatatact
gaaggcattagtcagcgaatgagggtcccagaaaagttaaaagtagcaccgccaaacgct
gacctggaacaaggattccaagaaggagttccaaatgctagtgtgataatgcaagttccg
gagaggattgttgtagcaggaaataatgaagatgtttcattttcaagaccagcagatctt
gaccttattcagtcaactccctttaaacccctggcactgaaaacaccacctcgtgtactt
acgctgagtgaaagaccactagattttctggatttagaaagacctcctacaacccctcaa
aatgaagaaatccgagcagttggcagactaaaaagagagcggtctatgagtgaaaatgct
gttcgccaaaatggacagctggtcagaaatgattctctgtggcacagatcagattctgcc
ccaagaaataaaatttcaaggttccaggcaccgatttctgcaccggagtacactgtgaca
ccatcgccacaacaggctcgggtctgtcctccccatatgttacctgaagatggagctaat
ctttcctctgctcgtggcattttgtcgcttatccagtcttctactcgtagggcataccag
cagatcttggatgtgctggatgaaaatcgcagacctgtgttgcgtggtgggtctgctgcc
gccacttctaatcctcatcatgacaacgtcaggtatggcatttcaaatatagatacaacc
attgaaggaacgtcagatgacctgactgttgtagatgcagcttcactaagacgacagata
atcaaactaaatagacgtctacaacttctggaagaggagaacaaagaacgtgctaaaaga
gaaatggtcatgtattcaattactgtagctttctggctgcttaatagctggctctggttt
cgccgctag
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