abnormal bone marrow cell physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of any of the cells found in the bone marrow (Mammalian Phenotype Ontology, MP_0009278)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009278
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Genes

27 gene mutations causing the abnormal bone marrow cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
AZI2 5-azacytidine induced 2
BCR breakpoint cluster region
BID BH3 interacting domain death agonist
CCND3 cyclin D3
CD247 CD247 molecule
CXCL12 chemokine (C-X-C motif) ligand 12
DKC1 dyskeratosis congenita 1, dyskerin
DOT1L DOT1-like histone H3K79 methyltransferase
ESR1 estrogen receptor 1
FLT3 fms-related tyrosine kinase 3
FPR2 formyl peptide receptor 2
GPR15 G protein-coupled receptor 15
INPP5D inositol polyphosphate-5-phosphatase, 145kDa
KITLG KIT ligand
LIG1 ligase I, DNA, ATP-dependent
MMP2 matrix metallopeptidase 2
MMP9 matrix metallopeptidase 9
NLRP3 NLR family, pyrin domain containing 3
OPRM1 opioid receptor, mu 1
POLG polymerase (DNA directed), gamma
PTPN6 protein tyrosine phosphatase, non-receptor type 6
RPL27A ribosomal protein L27a
SOCS3 suppressor of cytokine signaling 3
TSC22D1 TSC22 domain family, member 1
ZBTB16 zinc finger and BTB domain containing 16
ZFP36L2 ZFP36 ring finger protein-like 2