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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Zscan21
zinc finger and SCAN domain containing 21
MGI:99182
26 phenotypes from 5 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Tg(Stra8-icre)1Reb/0
Zscan21tm1.1Jiwa/Zscan21tm1.1Jiwa
involves: FVB/NJ
abnormal double-strand DNA break repair J:237046
abnormal spermatid morphology J:237046
abnormal spermatocyte morphology J:237046
abnormal X-Y chromosome synapsis during male meiosis J:237046
arrest of male meiosis J:237046
decreased testis weight J:237046
male infertility J:237046
Tg(Zfp38)A4Htz/0
involves: C57BL/6 * CBA
alopecia J:56546
progressive hair loss J:56546
Tg(Zfp38)D1Htz/0
involves: C57BL/6 * CBA
abnormal cerebellar granule layer morphology J:56546
abnormal cerebellum fissure morphology J:56546
abnormal dermal layer morphology J:56546
abnormal hair follicle morphology J:56546
abnormal hair shaft morphology J:56546
abnormal skin development J:56546
accelerated formation of intralobular fissures J:56546
alopecia J:56546
enlarged cerebellum J:56546
epithelioid cyst J:56546
increased cerebellar granule cell number J:56546
progressive hair loss J:56546
Zscan21tm1Htz/Zscan21tm1Htz
Not Specified
no abnormal phenotype detected J:56546
Zscan21tm2b(EUCOMM)Wtsi/Zscan21+
C57BL/6N-Zscan21tm2b(EUCOMM)Wtsi/Bay
abnormal skin coloration J:211773
decreased respiratory quotient J:211773
decreased total retina thickness J:211773
Zscan21tm2b(EUCOMM)Wtsi/Zscan21tm2b(EUCOMM)Wtsi
C57BL/6N-Zscan21tm2b(EUCOMM)Wtsi/Bay
abnormal retina inner nuclear layer morphology J:211773
decreased total retina thickness J:211773
female infertility J:211773
male infertility J:211773
preweaning lethality, incomplete penetrance 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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory