MAL

GENERAL INFORMATION

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Gene name

MAL

Gene description

Mal, T-cell differentiation protein

Protein class

Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (esophagus)
GTEx:Tissue enhanced (esophagus, vagina)

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:  Tissue enriched (esophagus)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (esophagus, vagina)

Organ

Expression



GENE INFORMATION

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Gene name

MAL

Synonyms

Description

Mal, T-cell differentiation protein (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]

Chromosome

2

Cytoband

q11.1

Chromosome location (bp)

95025677 - 95053996

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000172005 (version 78.38)

Entrez gene

4118

UniProt

P21145 (UniProt - Evidence at protein level)

neXtProt

NX_P21145

Antibodypedia

MAL antibodies


PROTEIN BROWSER

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ENST00000309988
 
ENST00000349807
 
ENST00000353004
 
ENST00000354078
 
 
 
 


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)

MAL-001 ENSP00000310880
ENST00000309988
P21145
Show all »
Show » Show » 153 16.7 No 4
MAL-002 ENSP00000306568
ENST00000353004
P21145
Show all »
Show » Show » 111 12.1 No 3
MAL-003 ENSP00000304924
ENST00000354078
P21145
Show all »
Show » Show » 97 10.6 No 2
MAL-004 ENSP00000322860
ENST00000349807
P21145
Show all »
Show » Show » 55 6 No 1