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FGF14 information


FGF14
Identifiers
AliasesFGF14, FGF-14, FHF-4, FHF4, SCA27, fibroblast growth factor 14
External IDsOMIM: 601515; MGI: 109189; HomoloGene: 3037; GeneCards: FGF14; OMA:FGF14 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_010201
NM_207667

RefSeq (protein)

NP_034331
NP_997550

Location (UCSC)Chr 13: 101.71 – 102.4 MbChr 14: 124.22 – 124.91 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Fibroblast growth factor 14 is a biologically active protein that in humans is encoded by the FGF14 gene.[5][6][7]

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. A mutation in this gene is associated with autosomal dominant cerebellar ataxia. Alternatively spliced transcript variants have been found for this gene.[7]

FGF14 is mainly expressed in the central nervous system and is associated with neurodegenerative diseases such as spinocerebellar ataxia (SCA27). FGF14 deficiency also impairs the maturation of cells in the hippocampus, which is possibly related to the development of schizophrenia.[8]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000102466 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025551 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Smallwood PM, Munoz-Sanjuan I, Tong P, Macke JP, Hendry SH, Gilbert DJ, Copeland NG, Jenkins NA, Nathans J (Oct 1996). "Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development". Proc Natl Acad Sci U S A. 93 (18): 9850–7. Bibcode:1996PNAS...93.9850S. doi:10.1073/pnas.93.18.9850. PMC 38518. PMID 8790420.
  6. ^ Wozniak DF, Xiao M, Xu L, Yamada KA, Ornitz DM (Mar 2007). "Impaired spatial learning and defective theta burst induced LTP in mice lacking fibroblast growth factor 14". Neurobiol Dis. 26 (1): 14–26. doi:10.1016/j.nbd.2006.11.014. PMC 2267915. PMID 17236779.
  7. ^ a b "Entrez Gene: FGF14 fibroblast growth factor 14".
  8. ^ Wang, Lusheng; Jing, Rongrong; Wang, Xing; Wang, Baohui; Guo, Keke; Zhao, Jungang; Gao, Shuang; Xu, Nuo; Xuan, Xuan (June 2021) [11 June 2021]. "A method for the expression of fibroblast growth factor 14 and assessment of its neuroprotective effect in an Alzheimer's disease model". Annals of Translational Medicine. 9 (12): 994. doi:10.21037/atm-21-2492. ISSN 2305-5839. PMC 8267273. PMID 34277794.

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FGF14

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factor 14 is a biologically active protein that in humans is encoded by the FGF14 gene. The protein encoded by this gene is a member of the fibroblast growth...

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Growth factor

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12(FGF12) Fibroblast growth factor 13(FGF13) Fibroblast growth factor 14(FGF14) Fibroblast growth factor 15(FGF15) Fibroblast growth factor 16(FGF16) Fibroblast...

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Spinocerebellar ataxia

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gastrointestinal pain.   2p SCA27 (FGF14) 15–20 yrs Unknown ataxia with poor cognition, dyskinesias and tremor.   FGF14 13q34 SCA35 40–48 years Unknown gait...

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List of genetic disorders

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ATXN7, ATXN8OS, ATXN10, TTBK2, PPP2R2B, KCNC3, PRKCG, ITPR1, TBP, KCND3, FGF14 dominant, recessive or T Split hand split foot-nystagmus syndrome dominant...

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Fibroblast growth factor

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known as basic fibroblast growth factor. Members FGF11, FGF12, FGF13, and FGF14, also known as FGF homologous factors 1-4 (FHF1-FHF4), have been shown to...

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List of OMIM disorder codes

Last Update:

Spinocerebellar ataxia-2; 183090; ATXN2 Spinocerebellar ataxia-27; 609307; FGF14 Spinocerebellar ataxia-5; 600224; SPTBN2 Spinocerebellar ataxia-6; 183086;...

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