premature aging Gene Set

Dataset MGI Mouse Phenotype Associations 2023
Category disease or phenotype associations
Type phenotype
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Genes

35 gene mutations causing the premature aging phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Symbol Name
ANP32B acidic (leucine-rich) nuclear phosphoprotein 32 family, member B
ARHGAP1 Rho GTPase activating protein 1
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ATR ATR serine/threonine kinase
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CDC14C cell division cycle 14C
CISD2 CDGSH iron sulfur domain 2
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
FSHR follicle stimulating hormone receptor
HAT1 histone acetyltransferase 1
HELLS helicase, lymphoid-specific
KL klotho
LINC-PINT long intergenic non-protein coding RNA, p53 induced transcript
LINC00657 long intergenic non-protein coding RNA 657
LMNA lamin A/C
NTMT1 N-terminal Xaa-Pro-Lys N-methyltransferase 1
POLG polymerase (DNA directed), gamma
PTHLH parathyroid hormone-like hormone
RASSF9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9
RBM38 RNA binding motif protein 38
RPS9 ribosomal protein S9
SIRT6 sirtuin 6
SIRT7 sirtuin 7
SPRTN SprT-like N-terminal domain
SQSTM1 sequestosome 1
STAG1 stromal antigen 1
TACO1 translational activator of mitochondrially encoded cytochrome c oxidase I
TIMM23B translocase of inner mitochondrial membrane 23 homolog B (yeast)
TP53 tumor protein p53
TP63 tumor protein p63
TPP2 tripeptidyl peptidase II
TUSC2 tumor suppressor candidate 2
ZMPSTE24 zinc metallopeptidase STE24