Gene Gene information from NCBI Gene database.
Entrez ID 4499
Gene name Metallothionein 1M
Gene symbol MT1M
Synonyms (NCBI Gene)
MT-1MMT-IMMT1MT1K
Chromosome 16
Chromosome location 16q13
Summary This gene encodes a member of the metallothionein superfamily, type 1 family. Metallothioneins have a high content of cysteine residues that bind various heavy metals. These genes are transcriptionally regulated by both heavy metals and glucocorticoids. [
miRNA miRNA information provided by mirtarbase database.
1
miRTarBase ID miRNA Experiments Reference
MIRT028853 hsa-miR-26b-5p Microarray 19088304
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
156357 14296 ENSG00000205364
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N339
Protein name Metallothionein-1M (MT-1M) (Metallothionein-IM) (MT-IM)
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.
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 
  Mineral absorption  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CORONARY STENOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 39188714
★☆☆☆☆
Found in Text Mining only
Atherosclerosis Associate 39188714
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Inhibit 33820882
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 24782625, 27808371, 29461597, 34423049, 37120619, 37259059
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy Hypertrophic Associate 35328083
★☆☆☆☆
Found in Text Mining only
Crohn Disease Associate 36466876
★☆☆☆☆
Found in Text Mining only
Dermatomyositis Associate 37259059
★☆☆☆☆
Found in Text Mining only
Down Syndrome Associate 35741790
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Associate 19472401
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Inhibit 33820882
★☆☆☆☆
Found in Text Mining only