spinal hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description bleeding into the spine (Mammalian Phenotype Ontology, MP_0006054)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006054
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13 gene mutations causing the spinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRA2 adhesion G protein-coupled receptor A2
C1GALT1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
C1GALT1C1 C1GALT1-specific chaperone 1
CBFB core-binding factor, beta subunit
CLEC1B C-type lectin domain family 1, member B
COL1A1 collagen, type I, alpha 1
FBLN1 fibulin 1
FLI1 Fli-1 proto-oncogene, ETS transcription factor
PSEN1 presenilin 1
RUNX1 runt-related transcription factor 1
SUCO SUN domain containing ossification factor
SYK spleen tyrosine kinase
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)