increased length of allograft survival Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description compared to controls, a greater length of time that transplanted tissue, in which the donor and recipient are genetically similar (same species) but not genetically identical, retains function and/or remains alive (Mammalian Phenotype Ontology, MP_0004751)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004751
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Genes

20 gene mutations causing the increased length of allograft survival phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BTLA B and T lymphocyte associated
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CCL17 chemokine (C-C motif) ligand 17
CCR1 chemokine (C-C motif) receptor 1
CCR4 chemokine (C-C motif) receptor 4
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CXCR3 chemokine (C-X-C motif) receptor 3
FGL2 fibrinogen-like 2
FLT3LG fms-related tyrosine kinase 3 ligand
FOXN1 forkhead box N1
IL13 interleukin 13
IL2 interleukin 2
MAP3K14 mitogen-activated protein kinase kinase kinase 14
NOS2 nitric oxide synthase 2, inducible
PRKDC protein kinase, DNA-activated, catalytic polypeptide
SASH3 SAM and SH3 domain containing 3
SUCNR1 succinate receptor 1
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
TNFSF13B tumor necrosis factor (ligand) superfamily, member 13b
TNFSF14 tumor necrosis factor (ligand) superfamily, member 14