(Q18049153)

English

FCRL3

protein-coding gene in the species Homo sapiens

CD307c
FCRH3
IFGP3
IRTA3
SPAP2
Fc receptor like 3

In more languages

default for all languages

No label defined

No description defined

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000160856

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

Fc receptor like 3

1 reference

6 July 2017

UniProt protein ID

genetic association

toxic diffuse goiter

determination method or standard

genome-wide association study

1 reference

http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_12361&geneId=376951

http://www.genome.gov/gwastudies/index.cfm?gene=FCRL3

Phenocarta release 2016-02-04

18 May 2016

multiple sclerosis

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_2377&ncbiId=115352

http://www.genome.gov/gwastudies/index.cfm?gene=FCRL3

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

25 May 2020

type-1 diabetes

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9744&ncbiId=115352

http://www.genome.gov/gwastudies/index.cfm?gene=FCRL3

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

25 May 2020

Graves' disease

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12361&ncbiId=115352

http://www.genome.gov/gwastudies/index.cfm?gene=FCRL3

A genome-wide association study identifies two new risk loci for Graves' disease.

29 February 2020

human chromosome 1

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

157674321

human chromosome 1

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

157644111

human chromosome 1

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

157670647

human chromosome 1

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

157700769

human chromosome 1

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

cytogenetic location

1q23.1

1 reference

15 May 2022

76447

1 reference

15 May 2022

mucosa of ileum

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

epithelium of nasopharynx

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

bone marrow cells

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000160856

http://identifiers.org/ncbigene/115352

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

Ensembl gene ID

ENSG00000160856

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

Ensembl transcript ID

ENST00000496769

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000368184

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000368186

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000457799

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000468507

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000473231

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000477837

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000478179

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000480682

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000485028

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000492769

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

ENST00000494724

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000160856

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(5 entries)

arwiki FCRL3
arzwiki FCRL3
enwiki FCRL3
ttwiki FCRL3
ukwiki FCRL3

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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