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FGF12

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Fibroblast growth factor 12 is a protein that in humans is encoded by the FGF12 gene.[5][6][7]

AliasesFGF12, FGF12B, FHF1, fibroblast growth factor 12, EIEE47, DEE47
External IDsOMIM: 601513; MGI: 109183; GeneCards: FGF12
PDBOrtholog search: PDBe RCSB
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FGF12
Identifiers
AliasesFGF12, FGF12B, FHF1, fibroblast growth factor 12, EIEE47, DEE47
External IDsOMIM: 601513; MGI: 109183; GeneCards: FGF12
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004113
NM_021032
NM_001377292
NM_001377293
NM_001377294

NM_001276419
NM_001276420
NM_010199
NM_183064
NM_001357064

RefSeq (protein)

NP_004104
NP_066360
NP_001364221
NP_001364222
NP_001364223

NP_001263348
NP_001263349
NP_034329
NP_898887
NP_001343993

Location (UCSC)Chr 3: 192.14 – 192.77 MbChr 16: 27.98 – 28.57 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. Two alternatively spliced transcript variants encoding distinct isoforms have been reported.[7]

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