GeneInfo:
GeneAttribute
GeneDescription
GeneSymbol
MT1B
FullNmae
metallothionein 1B
LocusType
gene with protein product
Status
Approved
HGNC_id
HGNC:7394
EnsembleID
ENSG00000169688
Uniprot
P07438
Protein Structure:
Gene Description in Publicaton:
GeneSymbol
CellDeathType
PMID
Description
GeneType
MT1B
cuproptosis
38538696 The 18 RCD signatures collected from previous studies. Supplementary Table of Figures.xlsx (https://github.com/zwxiangya/RCDscore)
retulator signature
MT1B
cuproptosis
35964468 Cuproptosis-related gene sets were obtained from a previous study [9] and combined with the Molecular Signature Database (MsigDB) v7.0 database (http://www.gsea-msigdb.org/gsea/msigdb/, GOBP_CELLULAR_COPPER_ION_HOMEOSTASIS, GOBP_CELLULAR_RESPONSE_TO_COPPER_ION).
Cuproptosis-related gene sets obtained from Molecular Signature Database (MsigDB) v7.9 database.
MT1B
cuproptosis
36211378 Forty-three cuproptosis-related genes were selected from the review of Chang et al. (13)
43 cuproptosis-related genes in the study
Go Annotation:
GeneSymbol
Go id
MT1B
GO:0005515,GO:0005634,GO:0005634,GO:0005737,GO:0005737,GO:0006882,GO:0008270,GO:0010273,GO:0045926,GO:0046872,GO:0071276,GO:0071280,GO:0071294,GO:0071294
KEGG Annotation:
GeneSymbol
GeneID
Pathway
Pathway Name
MT1B
hsa:4490 path:hsa04978 Mineral absorption - Homo sapiens (human)
Protein-Protein Interaction(String):
Signalink 3.0 modificators
Source
Target
Pmid
Interactiontype
Methods
Database
EGR1
MT1B
18971253
trascriptional regulation,stimulation
inferred by curator
TFlink
Visualization
