Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4502
Gene name Gene Name - the full gene name approved by the HGNC.
Metallothionein 2A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MT2A
Synonyms (NCBI Gene) Gene synonyms aliases
MT-2, MT-II, MT2
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q13
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the metallothionein family of genes. Proteins encoded by this gene family are low in molecular weight, are cysteine-rich, lack aromatic residues, and bind divalent heavy metal ions, altering the intracellular concentration of heav
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT053519 hsa-miR-23a-3p Immunofluorescence, Immunohistochemistry, In situ hybridization, Luciferase reporter assay, qRT-PCR, Western blot 23553990
MIRT486125 hsa-miR-548c-3p PAR-CLIP 23592263
MIRT486124 hsa-miR-4668-3p PAR-CLIP 23592263
MIRT486123 hsa-miR-553 PAR-CLIP 23592263
MIRT284325 hsa-miR-296-3p PAR-CLIP 23592263
Transcription factors
Transcription factor Regulation Reference
AHR Unknown 23994556
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 12646258, 12970870, 14550308, 15541360, 32814053
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus ISS
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
156360 7406 ENSG00000125148
Protein
UniProt ID P02795
Protein name Metallothionein-2 (MT-2) (Metallothionein-2A) (Metallothionein-II) (MT-II)
Protein function Metallothioneins have a high content of cysteine residues that bind various heavy metals; these proteins are transcriptionally regulated by both heavy metals and glucocorticoids.
PDB 1MHU , 2MHU
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00131 Metallothio 1 61 Metallothionein Domain
Sequence
Sequence length 61
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Mineral absorption   Metallothioneins bind metals
Interferon gamma signaling
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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
Eosinophilia Eosinophilic esophagitis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acquired Immunodeficiency Syndrome Associate 6333258, 7908672
Adenocarcinoma Associate 31721970
Adenocarcinoma of Lung Associate 33839701
Alzheimer Disease Associate 17213040, 30124448
Amblyopia Associate 10803406
Arthritis Rheumatoid Associate 39321281
Astrocytoma Stimulate 30932010
Autism Spectrum Disorder Associate 36077244
Bloom Syndrome Associate 28228606
Bone Diseases Associate 26036762