(Q17928632)

English

FOXG1

protein-coding gene in the species Homo sapiens

BF1
BF2
FHKL3
FKH2
FKHL1
FKHL2
FKHL3
FKHL4
FOXG1A
FOXG1B
FOXG1C
HBF-1
HBF-2
HBF-3
HBF-G2
HBF2
HFK1
HFK2
HFK3
KHL2
QIN
forkhead box G1

In more languages

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000176165

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

Forkhead box G1

1 reference

6 July 2017

UniProt protein ID

genetic association

1 reference

FOXG1 is responsible for the congenital variant of Rett syndrome

human chromosome 14

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

29235050

human chromosome 14

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

28766787

human chromosome 14

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

28770277

human chromosome 14

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

29238870

human chromosome 14

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

cytogenetic location

14q12

1 reference

15 May 2022

3843

1 reference

15 May 2022

Gene Atlas image

PBB GE FOXG1B 206018 at fs.png
732 × 530; 9 KB

0 references

PBB GE FOXG1B 207658 s at fs.png
732 × 530; 12 KB

0 references

1 reference

HomoloGene build68

3843

1 reference

HomoloGene build68

3843

1 reference

HomoloGene build68

3843

endothelial cell

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

Brodmann area 23

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

ganglionic eminence

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

Region I of hippocampus proper

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

middle temporal gyrus

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

orbitofrontal cortex

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

entorhinal cortex

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

Brodmann area 46

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

postcentral gyrus

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000176165

http://identifiers.org/ncbigene/2290

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

Ensembl gene ID

ENSG00000176165

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

Ensembl transcript ID

ENST00000313071

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000176165

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

Microsoft Academic ID

0 references

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(5 entries)

arwiki FOXG1
arzwiki FOXG1
enwiki FOXG1
ttwiki FOXG1
ukwiki FOXG1

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q17928632&oldid=1915884579"