FHIT (Q17928393)

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protein-coding gene in the species Homo sapiens

AP3Aase
FRA3B
fragile histidine triad
tríada histidina fràgil
fragile histidine triad diadenosine triphosphatase

Language	Label	Description	Also known as
English	FHIT	protein-coding gene in the species Homo sapiens	AP3Aase FRA3B fragile histidine triad tríada histidina fràgil fragile histidine triad diadenosine triphosphatase

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

protein-coding gene

1 reference

NCBI homo sapiens annotation release 107

2 October 2016

Protein FHIT PDB 1fhi.png
883 × 754; 296 KB

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

Fragile histidine triad diadenosine triphosphatase

1 reference

6 July 2017

UniProt protein ID

genetic association

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=2272

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

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

10 April 2020

cleft lip and cleft palate

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0050567&ncbiId=2272

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

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts

10 April 2020

Asperger syndrome

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0050432&ncbiId=2272

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

Variants in several genomic regions associated with asperger disorder

10 April 2020

attention deficit hyperactivity disorder

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1094&ncbiId=2272

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

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

10 April 2020

human chromosome 3

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

59735036

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

59747277

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

61251459

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

61237133

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

cytogenetic location

3p14.2

1 reference

15 May 2022

21661

1 reference

15 May 2022

Gene Atlas image

PBB GE FHIT gnf1h04116 s at fs.png
732 × 530; 12 KB

0 references

1 reference

HomoloGene build68

21661

Saccharomyces cerevisiae S288c

1 reference

HomoloGene build68

21661

1 reference

HomoloGene build68

21661

1 reference

HomoloGene build68

21661

right adrenal gland

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

body of pancreas

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

cingulate gyrus

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

left lobe of thyroid gland

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

caudate nucleus

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000189283

http://identifiers.org/ncbigene/2272

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

Ensembl gene ID

ENSG00000189283

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

Ensembl transcript ID

ENST00000492590

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000341848

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000465330

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000466788

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000468189

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000476844

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000488467

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

ENST00000490952

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000189283

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

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(5 entries)

cawiki FHIT
cywiki FHIT
enwiki FHIT
ttwiki FHIT
ukwiki FHIT

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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