BEST1

GENERAL INFORMATION

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Gene name

BEST1

Gene description

Bestrophin 1

Protein class

Disease related genes
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins
Transporters

Predicted localization

Intracellular,Membrane

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Mixed

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

BEST1 (HGNC Symbol)

Synonyms

BEST, BMD, RP50, VMD2

Description

Bestrophin 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008]

Chromosome

11

Cytoband

q12.3

Chromosome location (bp)

61949821 - 61965515

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000167995 (version 78.38)

Entrez gene

7439

UniProt

O76090 (UniProt - Evidence at protein level)

neXtProt

NX_O76090

Antibodypedia

BEST1 antibodies


PROTEIN BROWSER

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ENST00000378043
 
ENST00000449131
 
ENST00000526988
 
ENST00000534553
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

BEST1-001 ENSP00000367282
ENST00000378043
O76090
Show all »
Show » Show » 585 67.7 No 4
BEST1-002 ENSP00000399709
ENST00000449131
O76090
Show all »
Show » Show » 604 69.1 No 3
BEST1-004 ENSP00000431189
ENST00000534553
E9PMB5
Show all »
Show » 55 6.1 No 0
BEST1-006 ENSP00000433195
ENST00000526988
B7Z1N8
Show all »
Show » 329 37.6 No 2