(Q18032734)

English

IFT88

protein-coding gene in the species Homo sapiens

D13S1056E
DAF19
TG737
TTC10
hTg737
intraflagellar transport 88

In more languages

Statements

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000032742

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

Intraflagellar transport 88

1 reference

6 July 2017

UniProt protein ID

Intraflagellar transport protein 88 homolog

1 reference

UniProt protein ID

21 March 2016

language of work or name

genetic association

bipolar disorder

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_3312&ncbiId=8100

http://www.genome.gov/gwastudies/index.cfm?gene=IFT88

Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5419&ncbiId=8100

http://www.genome.gov/gwastudies/index.cfm?gene=IFT88

Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression

25 May 2020

mental depression

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1596&ncbiId=8100

http://www.genome.gov/gwastudies/index.cfm?gene=IFT88

Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression

25 May 2020

human chromosome 13

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

21140585

human chromosome 13

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

20567138

human chromosome 13

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

21265503

human chromosome 13

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

20691444

human chromosome 13

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

cytogenetic location

13q12.11

1 reference

9 January 2022

4761

1 reference

9 January 2022

Gene Atlas image

PBB GE IFT88 204703 at fs.png
732 × 530; 10 KB

0 references

1 reference

HomoloGene build68

4761

1 reference

HomoloGene build68

4761

Drosophila melanogaster

1 reference

HomoloGene build68

4761

Caenorhabditis elegans

1 reference

HomoloGene build68

4761

1 reference

HomoloGene build68

4761

bronchial epithelial cell

1

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

2

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

right uterine tube

3

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

caput epididymis

4

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

5

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

Achilles tendon

6

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

anterior pituitary

7

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

corpus callosum

8

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

9

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

right lobe of thyroid gland

10

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000032742

http://identifiers.org/ncbigene/8100

1 reference

Identifiers.org

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

Identifiers

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

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9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

Ensembl gene ID

ENSG00000032742

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

Ensembl transcript ID

ENST00000537103

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

ENST00000319980

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

ENST00000351808

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

ENST00000389373

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

ENST00000461115

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

ENST00000470695

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

ENST00000482172

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000032742

0 references

HGNC gene symbol

1 reference

9 January 2022

1 reference

9 January 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(5 entries)

arwiki IFT88
arzwiki IFT88
enwiki IFT88
ttwiki IFT88
ukwiki IFT88

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=Q18032734&oldid=1916101059"