abnormal bone marrow morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the soft tissue that fills the cavities of bones (Mammalian Phenotype Ontology, MP_0002397)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002397
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Genes

35 gene mutations causing the abnormal bone marrow morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANK1 ankyrin 1, erythrocytic
ARID4A AT rich interactive domain 4A (RBP1-like)
ATR ATR serine/threonine kinase
BBS12 Bardet-Biedl syndrome 12
C6ORF25 chromosome 6 open reading frame 25
CCNE1 cyclin E1
CEBPE CCAAT/enhancer binding protein (C/EBP), epsilon
CLCN7 chloride channel, voltage-sensitive 7
COL10A1 collagen, type X, alpha 1
CRH corticotropin releasing hormone
CSF1 colony stimulating factor 1 (macrophage)
CSF1R colony stimulating factor 1 receptor
CXCR2 chemokine (C-X-C motif) receptor 2
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
EBF1 early B-cell factor 1
ESR2 estrogen receptor 2 (ER beta)
FGF2 fibroblast growth factor 2 (basic)
FLT3 fms-related tyrosine kinase 3
GATA1 GATA binding protein 1 (globin transcription factor 1)
HSPG2 heparan sulfate proteoglycan 2
ID1 inhibitor of DNA binding 1, dominant negative helix-loop-helix protein
LEP leptin
NCOR2 nuclear receptor corepressor 2
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
PI16 peptidase inhibitor 16
PPARG peroxisome proliferator-activated receptor gamma
SGPL1 sphingosine-1-phosphate lyase 1
SIAH2 siah E3 ubiquitin protein ligase 2
SPI1 Spi-1 proto-oncogene
SPTA1 spectrin, alpha, erythrocytic 1
SRC SRC proto-oncogene, non-receptor tyrosine kinase
STIM1 stromal interaction molecule 1
TNS3 tensin 3
UNC13D unc-13 homolog D (C. elegans)
UNC93B1 unc-93 homolog B1 (C. elegans)