BCL11A (Q18040602)

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protein-coding gene in the species Homo sapiens

BCL11A-L
BCL11A-S
BCL11A-XL
BCL11a-M
CTIP1
EVI9
HBFQTL5
ZNF856
B-cell CLL/lymphoma 11A
DILOS
B cell CLL/lymphoma 11A
BCL11A, BAF complex component
BAF chromatin remodeling complex subunit BCL11A
SMARCM1

Language	Label	Description	Also known as
English	BCL11A	protein-coding gene in the species Homo sapiens	BCL11A-L BCL11A-S BCL11A-XL BCL11a-M CTIP1 EVI9 HBFQTL5 ZNF856 B-cell CLL/lymphoma 11A DILOS B cell CLL/lymphoma 11A BCL11A, BAF complex component BAF chromatin remodeling complex subunit BCL11A SMARCM1

Statements

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000119866

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

BAF chromatin remodeling complex subunit BCL11A

1 reference

6 July 2017

UniProt protein ID

genetic association

sickle-cell disease

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10923&ncbiId=53335

http://www.genome.gov/gwastudies/index.cfm?gene=BCL11A

Genetic determinants of haemolysis in sickle cell anaemia

25 May 2020

attention deficit hyperactivity disorder

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1094&ncbiId=53335

http://www.genome.gov/gwastudies/index.cfm?gene=BCL11A

Genome-wide association study in German patients with attention deficit/hyperactivity disorder

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5379&ncbiId=53335

http://www.genome.gov/gwastudies/index.cfm?gene=BCL11A

A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E

25 May 2020

beta thalassemia

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12241&ncbiId=53335

http://www.genome.gov/gwastudies/index.cfm?gene=BCL11A

A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E

25 May 2020

Dias-Logan syndrome

3 references

14 September 2020

https://search.clinicalgenome.org/kb/gene-validity/9630f9a3-3f90-49c6-ae8b-6313c950b1b2--2020-09-13T17:18:07

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_9630f9a3-3f90-49c6-ae8b-6313c950b1b2-2020-09-13T171807.228Z

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000119866/MONDO_0014914

based on heuristic

inferred from an Open Targets association score over 0.7

human chromosome 2

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

60678302

human chromosome 2

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

60450520

human chromosome 2

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

60780702

human chromosome 2

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

60554467

human chromosome 2

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

cytogenetic location

2p16.1

1 reference

9 January 2022

11284

1 reference

9 January 2022

Gene Atlas image

PBB GE BCL11A 219498 s at fs.png
732 × 530; 11 KB

0 references

PBB GE BCL11A 210347 s at fs.png
732 × 530; 11 KB

0 references

PBB GE BCL11A 219497 s at fs.png
732 × 530; 11 KB

0 references

2 references

HomoloGene build68

11284

Orthologous MAtrix

https://omabrowser.org/oma/vps/Q9H165/

1 reference

HomoloGene build68

11284

1 reference

HomoloGene build68

11284

ganglionic eminence

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

primary visual cortex

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

Brodmann area 23

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

middle temporal gyrus

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

postcentral gyrus

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

Region I of hippocampus proper

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

ventricular zone

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

superior frontal gyrus

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000119866

http://identifiers.org/ncbigene/53335

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

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

9 January 2022

Ensembl gene ID

ENSG00000119866

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

Ensembl transcript ID

ENST00000631857

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000335712

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000356842

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000358510

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000359629

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000409351

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000477659

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000479026

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000489183

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000489516

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000492272

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000642384

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000644606

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000643004

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000647472

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000642439

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000642180

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000645224

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000645405

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000643716

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000647038

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000642824

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000645455

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000643459

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000647469

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000643222

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

ENST00000646249

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000119866

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(6 entries)

arwiki BCL11A
arzwiki BCL11A
enwiki BCL11A
frwiki BCL11A
ukwiki BCL11A
viwiki BCL11A

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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