increased hemoglobin content Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the total hemoglobin content in the circulating blood (Mammalian Phenotype Ontology, MP_0005564)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005564
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Genes

33 gene mutations causing the increased hemoglobin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
AGTR1 angiotensin II receptor, type 1
BBS5 Bardet-Biedl syndrome 5
CLEC10A C-type lectin domain family 10, member A
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
DKK3 dickkopf WNT signaling pathway inhibitor 3
DPY19L3 dpy-19-like 3 (C. elegans)
EGLN1 egl-9 family hypoxia-inducible factor 1
EPAS1 endothelial PAS domain protein 1
EPOR erythropoietin receptor
FAHD2B fumarylacetoacetate hydrolase domain containing 2B
FAM63A family with sequence similarity 63, member A
FES FES proto-oncogene, tyrosine kinase
GRHL3 grainyhead-like 3 (Drosophila)
HMGB3 high mobility group box 3
HPSE heparanase
IFT20 intraflagellar transport 20
KDM8 lysine (K)-specific demethylase 8
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MB myoglobin
NAGK N-acetylglucosamine kinase
NPR3 natriuretic peptide receptor 3
NPTN neuroplastin
NR1D2 nuclear receptor subfamily 1, group D, member 2
RPRD1B regulation of nuclear pre-mRNA domain containing 1B
RXFP2 relaxin/insulin-like family peptide receptor 2
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TCF7 transcription factor 7 (T-cell specific, HMG-box)
TET2 tet methylcytosine dioxygenase 2
TFR2 transferrin receptor 2
TTLL1 tubulin tyrosine ligase-like family member 1
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
YIPF1 Yip1 domain family, member 1