transmission ratio distortion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the frequency that an allele or haplotype in the offspring of an organism deviates from expected Mendelian ratios (Mammalian Phenotype Ontology, MP_0004179)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004179
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Genes

23 gene mutations causing the transmission ratio distortion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABL2 ABL proto-oncogene 2, non-receptor tyrosine kinase
CAPN3 calpain 3, (p94)
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CTTN cortactin
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
FANCM Fanconi anemia, complementation group M
FOS FBJ murine osteosarcoma viral oncogene homolog
GEM GTP binding protein overexpressed in skeletal muscle
HSPD1 heat shock 60kDa protein 1 (chaperonin)
KRT19 keratin 19, type I
MAPK1 mitogen-activated protein kinase 1
NAT1 N-acetyltransferase 1 (arylamine N-acetyltransferase)
ODF2 outer dense fiber of sperm tails 2
PCSK1 proprotein convertase subtilisin/kexin type 1
PCSK4 proprotein convertase subtilisin/kexin type 4
PPP1R3B protein phosphatase 1, regulatory subunit 3B
RLIM ring finger protein, LIM domain interacting
SHB Src homology 2 domain containing adaptor protein B
SUPV3L1 suppressor of var1, 3-like 1 (S. cerevisiae)
T T, brachyury homolog (mouse)
VAV1 vav 1 guanine nucleotide exchange factor
XIST X inactive specific transcript (non-protein coding)
ZEB1 zinc finger E-box binding homeobox 1