(Q18052338)

English

CFAP418

protein-coding gene in the species Homo sapiens

CORD16
RP64
smalltalk
BBS21
chromosome 8 open reading frame 37
FAP418
MOT25
cilia and flagella associated protein 418
C8orf37

In more languages

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000156172

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

Chromosome 8 open reading frame 37

1 reference

6 July 2017

UniProt protein ID

genetic association

cone-rod dystrophy 16

1 reference

UniProt protein ID

13 August 2019

Bardet-Biedl syndrome 21

1 reference

Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)

cone-rod dystrophy

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000156172/Orphanet_1872

based on heuristic

inferred from an Open Targets association score over 0.7

human chromosome 8

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

96257147

human chromosome 8

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

95244913

human chromosome 8

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

95269201

human chromosome 8

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

96281429

human chromosome 8

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

cytogenetic location

8q22.1

1 reference

15 May 2022

18641

1 reference

15 May 2022

1 reference

HomoloGene build68

18641

1 reference

HomoloGene build68

18641

1 reference

HomoloGene build68

18641

1 reference

HomoloGene build68

18641

secondary oocyte

1

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

bronchial epithelial cell

2

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

germinal epithelium

3

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

retinal pigment epithelium

4

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

caput epididymis

5

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

Achilles tendon

6

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

islet of Langerhans

7

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

ganglionic eminence

8

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

smooth muscle tissue

9

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

corpus epididymis

10

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156172

http://identifiers.org/ncbigene/157657

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

Ensembl gene ID

ENSG00000156172

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

Ensembl transcript ID

ENST00000286688

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156172

Google Knowledge Graph ID

0 references

HGNC gene symbol

1 reference

20 March 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(2 entries)

ttwiki C8orf37
ukwiki C8orf37

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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