FGF14 (Q17928040)

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protein-coding gene in the species Homo sapiens

FGF-14
FHF-4
FHF4
SCA27
fibroblast growth factor 14

Language	Label	Description	Also known as
English	FGF14	protein-coding gene in the species Homo sapiens	FGF-14 FHF-4 FHF4 SCA27 fibroblast growth factor 14

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000102466

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

Fibroblast growth factor 14

1 reference

6 July 2017

UniProt protein ID

genetic association

gestational hypertension

determination method or standard

genome-wide association study

1 reference

http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=2259

http://www.genome.gov/gwastudies/index.cfm?gene=FGF14

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort

14 March 2017

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10591&ncbiId=2259

http://www.genome.gov/gwastudies/index.cfm?gene=FGF14

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort

25 May 2020

spinocerebellar ataxia type 27

1 reference

UniProt protein ID

13 August 2019

human chromosome 13

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

101710804

human chromosome 13

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

102372134

human chromosome 13

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

102402457

human chromosome 13

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

103054124

human chromosome 13

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

cytogenetic location

13q33.1

1 reference

15 May 2022

3037

1 reference

15 May 2022

2 references

HomoloGene build68

3037

Orthologous MAtrix

https://omabrowser.org/oma/vps/Q92915/

2 references

HomoloGene build68

3037

Orthologous MAtrix

https://omabrowser.org/oma/vps/Q92915/

2 references

HomoloGene build68

3037

Orthologous MAtrix

https://omabrowser.org/oma/vps/Q92915/

secondary oocyte

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

middle temporal gyrus

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

bronchial epithelial cell

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

Brodmann area 23

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

cerebellar vermis

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

endothelial cell

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

postcentral gyrus

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

superior frontal gyrus

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

entorhinal cortex

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

primary visual cortex

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000102466

http://identifiers.org/ncbigene/2259

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000102466

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

Ensembl transcript ID

ENST00000468052

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

ENST00000376131

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

ENST00000376143

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

ENST00000418923

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000102466

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(4 entries)

arwiki FGF14
arzwiki FGF14
enwiki FGF14
ukwiki FGF14

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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