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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Trip13
thyroid hormone receptor interactor 13
MGI:1916966
51 phenotypes from 4 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Trip13em1(IMPC)J/Trip13em1(IMPC)J
C57BL/6NJ-Trip13em1(IMPC)J/J 		abnormal sleep behavior J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
female infertility J:211773
male infertility J:211773
Trip13Gt(CH0621)Wtsi/Trip13Gt(CH0621)Wtsi
involves: 129P2/OlaHsd * C57BL/6 		abnormal chiasmata formation J:163309
abnormal chromosomal synapsis J:163309
abnormal female meiosis J:163309
abnormal seminiferous tubule morphology J:163309
abnormal synaptonemal complex J:163309
arrest of male meiosis J:163309
impaired ovarian folliculogenesis J:163309
infertility J:163309
small testis J:163309
Trip13Gt(RRB047)Byg/Trip13Gt(RRB047)Byg
involves: 129P2/OlaHsd * C57BL/6 		abnormal chiasmata formation J:163309
abnormal chromosomal synapsis J:163309
abnormal DNA repair J:123677
abnormal double-strand DNA break repair J:123677, J:163309
abnormal female meiosis J:123677, J:163309
abnormal ovary morphology J:123677
abnormal seminiferous tubule morphology J:163309
abnormal synaptonemal complex J:163309
absent ovarian follicles J:123677
arrest of male meiosis J:123677, J:163309
decreased body size J:123677
decreased oocyte number J:123677
immotile sperm J:123677
impaired ovarian folliculogenesis J:163309
infertility J:123677, J:163309
kinked tail J:123677
postnatal lethality, incomplete penetrance J:123677
short tail J:123677
small gonad J:123677
small ovary J:123677
small testis J:123677, J:163309
Trip13tm1.1(KOMP)Vlcg/Trip13+
C57BL/6N-Trip13tm1.1(KOMP)Vlcg/Ucd 		abnormal retina morphology J:211773
increased anxiety-related response J:211773
increased circulating alkaline phosphatase level J:211773
Trip13tm1.1(KOMP)Vlcg/Trip13tm1.1(KOMP)Vlcg
C57BL/6N-Trip13tm1.1(KOMP)Vlcg/Ucd 		abnormal bone structure J:211773
abnormal coat/ hair morphology J:211773
abnormal coat/hair pigmentation J:211773
abnormal digit morphology J:211773
abnormal iris pigmentation J:211773
abnormal lens morphology J:211773
abnormal tail morphology J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased erythrocyte cell number J:211773
decreased grip strength J:211773
decreased hematocrit J:211773
decreased hemoglobin content J:211773
decreased lean body mass J:211773
female infertility J:211773
hyperactivity J:211773
increased blood urea nitrogen level J:211773
increased circulating cholesterol level J:211773
increased circulating HDL cholesterol level J:211773
increased fasting circulating glucose level J:211773
increased leukocyte cell number J:211773
increased mean corpuscular hemoglobin J:211773
increased total body fat amount J:211773
increased vertical activity J:211773
male infertility J:211773
prolonged RR interval J:211773
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory