hematoma Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008817
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Genes

21 gene mutations causing the hematoma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANP32B acidic (leucine-rich) nuclear phosphoprotein 32 family, member B
BRAF B-Raf proto-oncogene, serine/threonine kinase
COL4A1 collagen, type IV, alpha 1
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
FCER1G Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide
FH fumarate hydratase
INS insulin
KLF3 Kruppel-like factor 3 (basic)
KLKB1 kallikrein B, plasma (Fletcher factor) 1
LUM lumican
NOG noggin
OED Oregon eye disease
PROC protein C (inactivator of coagulation factors Va and VIIIa)
PROS1 protein S (alpha)
RASA3 RAS p21 protein activator 3
RTEL1 regulator of telomere elongation helicase 1
SCG5 secretogranin V
SOX18 SRY (sex determining region Y)-box 18
TBX6 T-box 6
ZIC2 Zic family member 2