abnormal thymus development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation and/or differentiation of the thymus (Mammalian Phenotype Ontology, MP_0000704)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000704
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Genes

17 gene mutations causing the abnormal thymus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANK1 ankyrin 1, erythrocytic
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CBX4 chromobox homolog 4
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
FGFR2 fibroblast growth factor receptor 2
FOXN1 forkhead box N1
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL13RA1 interleukin 13 receptor, alpha 1
JMJD6 jumonji domain containing 6
KAT6A K(lysine) acetyltransferase 6A
RC3H1 ring finger and CCCH-type domains 1
RIPPLY3 ripply transcriptional repressor 3
RPL22 ribosomal protein L22
TBX1 T-box 1
TWSG1 twisted gastrulation BMP signaling modulator 1
ZEB1 zinc finger E-box binding homeobox 1