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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Ankrd31
ankyrin repeat domain 31
MGI:5006716
36 phenotypes from 8 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ankrd31em1(IMPC)Hmgu/Ankrd31em1(IMPC)Hmgu
C57BL/6NCrl-Ankrd31em1(IMPC)Hmgu/Ieg 		abnormal spleen morphology J:211773
Ankrd31em1Atot/Ankrd31em1Atot
involves: C57BL/6J 		abnormal chromosomal synapsis J:276412
abnormal double-strand DNA break repair J:276412
abnormal female meiosis J:276412
abnormal male meiosis J:276412
abnormal meiosis J:276412
abnormal seminiferous tubule morphology J:276412
abnormal spermatocyte morphology J:276412
abnormal synaptonemal complex J:276412
abnormal X-Y chromosome synapsis during male meiosis J:276412
absent chiasmata formation J:276412
arrest of male meiosis J:276412
decreased oocyte number J:276412
decreased testis weight J:276412
early reproductive senescence J:276412
increased female germ cell apoptosis J:276412
increased male germ cell apoptosis J:276412
male infertility J:276412
reduced female fertility J:276412
Ankrd31em1Flor/Ankrd31em1Flor
C57BL/6JCrl-Ankrd31em1Flor 		abnormal male meiosis J:314966
abnormal seminiferous tubule epithelium morphology J:314966
abnormal sperm head morphology J:314966
abnormal sperm nucleus morphology J:314966
asthenozoospermia J:314966
decreased sperm progressive motility J:314966
decreased testis weight J:314966
male infertility J:314966
oligozoospermia J:314966
normal reproductive system phenotype J:314966
small testis J:314966
Ankrd31em1Sky/Ankrd31em1Sky
involves: C57BL/6J * CBA/J 		abnormal chromosomal synapsis J:276385
abnormal double-strand DNA break repair J:276385
abnormal male meiosis J:276385
abnormal oogenesis J:276385
abnormal seminiferous tubule morphology J:276385
abnormal spermatocyte morphology J:276385
abnormal X-Y chromosome synapsis during male meiosis J:276385
absent chiasmata formation J:276385
absent ovarian follicles J:276385
arrest of male meiosis J:276385
arrest of spermatogenesis J:276385
azoospermia J:276385
decreased oocyte number J:276385
decreased primordial ovarian follicle number J:276385
decreased testis weight J:276385
increased male germ cell apoptosis J:276385
male infertility J:276385
premature ovarian failure J:276385
seminiferous tubule degeneration J:276385
small ovary J:276385
small testis J:276385
Ankrd31em2Atot/Ankrd31em2Atot
involves: C57BL/6J 		male infertility J:276412
reduced female fertility J:276412
Ankrd31em2Flor/Ankrd31em2Flor
C57BL/6JCrl-Ankrd31em2Flor 		abnormal male meiosis J:314966
abnormal seminiferous tubule epithelium morphology J:314966
abnormal sperm head morphology J:314966
abnormal sperm nucleus morphology J:314966
asthenozoospermia J:314966
decreased sperm progressive motility J:314966
decreased testis weight J:314966
male infertility J:314966
oligozoospermia J:314966
reproductive system phenotype J:314966
small testis J:314966
Ankrd31em2Sky/Ankrd31em2Sky
involves: C57BL/6J * CBA/J 		decreased testis weight J:276385
Ankrd31em3Flor/Ankrd31em3Flor
C57BL/6JCrl-Ankrd31em3Flor 		abnormal male meiosis J:314966
abnormal seminiferous tubule epithelium morphology J:314966
abnormal sperm head morphology J:314966
abnormal sperm nucleus morphology J:314966
asthenozoospermia J:314966
decreased sperm progressive motility J:314966
decreased testis weight J:314966
male infertility J:314966
oligozoospermia J:314966
reproductive system phenotype J:314966
small testis J:314966
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