Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4118
Gene name Gene Name - the full gene name approved by the HGNC.
Mal, T cell differentiation protein (MAL blood group)
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MAL
Synonyms (NCBI Gene) Gene synonyms aliases
HLD28, MVP17, VIP17
Disease Acronyms (UniProt) Disease acronyms from UniProt database
HLD28
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q11.1
Summary Summary of gene provided in NCBI Entrez Gene.
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 trans
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001766 Process Membrane raft polarization TAS 12153479
GO:0005515 Function Protein binding IPI 21988832, 22366891, 25416956, 31515488, 32296183
GO:0005783 Component Endoplasmic reticulum IDA 8132541
GO:0006915 Process Apoptotic process NAS
GO:0007417 Process Central nervous system development TAS 10739088
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
188860 6817 ENSG00000172005
Protein
UniProt ID P21145
Protein name Myelin and lymphocyte protein (T-lymphocyte maturation-associated protein)
Protein function May be involved in vesicular trafficking from the Golgi apparatus to the cell membrane. Plays a role in the maintenance of the myelin sheath, and in axon-glia and glia-glia interactions.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01284 MARVEL 18 145 Membrane-associating domain Domain
Sequence
Sequence length 153
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
View all (309 more)
19208741
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
19208741
Carcinoma Squamous cell carcinoma rs121912654, rs555607708, rs786202962, rs1564055259 19445022
Marfan syndrome Mammary Carcinoma, Human rs137854456, rs137854457, rs267606796, rs137854458, rs137854459, rs137854460, rs137854470, rs137854471, rs267606797, rs137854461, rs137854462, rs137854463, rs869025419, rs137854464, rs137854465
View all (942 more)
19208741
Unknown
Disease term Disease name Evidence References Source
Head and neck cancer Malignant Head and Neck Neoplasm 19445022 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Acute Lung Injury Associate 21118491
Adenocarcinoma Associate 24088706, 26482433
Adenoma Associate 21777459
Alzheimer Disease Associate 26482433
Arthritis Rheumatoid Associate 17255320
Asthma Associate 26751474
Barrett Esophagus Associate 24088706
Breast Neoplasms Associate 19208741, 19228724, 23011155, 24927296, 26452468
Carcinogenesis Associate 18346269, 26552048
Carcinoma Basal Cell Associate 21092172