abnormal thymus medulla morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the inner area of thymus lobules (Mammalian Phenotype Ontology, MP_0002375)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002375
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Genes

27 gene mutations causing the abnormal thymus medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIRE autoimmune regulator
ATCAY ataxia, cerebellar, Cayman type
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
CACYBP calcyclin binding protein
CCR7 chemokine (C-C motif) receptor 7
CD247 CD247 molecule
CSF1 colony stimulating factor 1 (macrophage)
FAS Fas cell surface death receptor
FOXN1 forkhead box N1
HIVEP2 human immunodeficiency virus type I enhancer binding protein 2
IKZF1 IKAROS family zinc finger 1 (Ikaros)
ITPKB inositol-trisphosphate 3-kinase B
JAG2 jagged 2
JAK3 Janus kinase 3
LTA lymphotoxin alpha
LTBR lymphotoxin beta receptor (TNFR superfamily, member 3)
MAP3K14 mitogen-activated protein kinase kinase kinase 14
PIP prolactin-induced protein
RAG2 recombination activating gene 2
RASSF5 Ras association (RalGDS/AF-6) domain family member 5
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RUNX1 runt-related transcription factor 1
SGPL1 sphingosine-1-phosphate lyase 1
TESPA1 thymocyte expressed, positive selection associated 1
THEMIS thymocyte selection associated
TWIST2 twist family bHLH transcription factor 2
ZFP36 ZFP36 ring finger protein