Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2823
Gene name Gene Name - the full gene name approved by the HGNC.
Glycoprotein M6A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPM6A
Synonyms (NCBI Gene) Gene synonyms aliases
GPM6, M6A
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q34.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020434 hsa-miR-106b-5p Microarray 17242205
MIRT024239 hsa-miR-218-5p Sequencing 20371350
MIRT050918 hsa-miR-17-5p CLASH 23622248
MIRT498419 hsa-miR-548e-5p PAR-CLIP 22291592
MIRT498418 hsa-miR-548az-5p PAR-CLIP 22291592
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001764 Process Neuron migration IDA 19298174
GO:0003407 Process Neural retina development IEA
GO:0003407 Process Neural retina development ISS
GO:0005262 Function Calcium channel activity IEA
GO:0005515 Function Protein binding IPI 17500595, 24705354, 31286866, 32814053
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601275 4460 ENSG00000150625
Protein
UniProt ID P51674
Protein name Neuronal membrane glycoprotein M6-a (M6a)
Protein function Involved in neuronal differentiation, including differentiation and migration of neuronal stem cells. Plays a role in neuronal plasticity and is involved in neurite and filopodia outgrowth, filopodia motility and probably synapse formation. GPM6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01275 Myelin_PLP 14 247 Myelin proteolipid protein (PLP or lipophilin) Family
Sequence
Sequence length 278
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Neuroticism Neuroticism N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Abortion Habitual Associate 31281518
Acute erythroleukemia Stimulate 10936857
Acute Kidney Injury Associate 39287046
Adenocarcinoma Associate 36058934
Adenocarcinoma of Lung Associate 33428597, 34359836, 34558724, 34650549, 35035657, 35860262, 36061307
Adrenocortical Carcinoma Associate 33952721
Alzheimer Disease Associate 32301581, 34705667
Arthritis Rheumatoid Associate 32884942
Atherosclerosis Associate 32633395
Bone Diseases Metabolic Associate 36034449