abnormal inner cell mass apoptosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the cells of the blastocyst that develop into the body of the embryo are undergoing programmed cell death (Mammalian Phenotype Ontology, MP_0010380)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010380
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Genes

27 gene mutations causing the abnormal inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHCTF1 AT hook containing transcription factor 1
CDK7 cyclin-dependent kinase 7
CDX2 caudal type homeobox 2
CHORDC1 cysteine and histidine-rich domain (CHORD) containing 1
COPS5 COP9 signalosome subunit 5
DAB2 Dab, mitogen-responsive phosphoprotein, homolog 2 (Drosophila)
DAD1 defender against cell death 1
DMBT1 deleted in malignant brain tumors 1
GINS1 GINS complex subunit 1 (Psf1 homolog)
GINS4 GINS complex subunit 4 (Sld5 homolog)
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
KAT8 K(lysine) acetyltransferase 8
MAD2L1 MAD2 mitotic arrest deficient-like 1 (yeast)
NANOG Nanog homeobox
NBN nibrin
NCAPG2 non-SMC condensin II complex, subunit G2
NLE1 notchless homolog 1 (Drosophila)
NUSAP1 nucleolar and spindle associated protein 1
ODC1 ornithine decarboxylase 1
PRPF19 pre-mRNA processing factor 19
SMARCA5 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
TAF10 TAF10 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 30kDa
TERF1 telomeric repeat binding factor (NIMA-interacting) 1
UBA3 ubiquitin-like modifier activating enzyme 3
UBE2I ubiquitin-conjugating enzyme E2I
ZPR1 ZPR1 zinc finger