abnormal t cell receptor v(d)j recombination Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process by which T cell receptor V, D, and J, or V and J gene segments, depending on the specific locus, are recombined within a single locus (Mammalian Phenotype Ontology, MP_0008754)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008754
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12 gene mutations causing the abnormal t cell receptor v(d)j recombination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
CADM1 cell adhesion molecule 1
DCLRE1C DNA cross-link repair 1C
LAT linker for activation of T cells
LIG4 ligase IV, DNA, ATP-dependent
MYC v-myc avian myelocytomatosis viral oncogene homolog
NHEJ1 nonhomologous end-joining factor 1
PRKDC protein kinase, DNA-activated, catalytic polypeptide
PSMB11 proteasome (prosome, macropain) subunit, beta type, 11
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RNF168 ring finger protein 168, E3 ubiquitin protein ligase