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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cwc27
CWC27 spliceosome-associated protein
MGI:1914535
12 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cwc27em1Bay/Cwc27em1Bay
C57BL/6J-Cwc27em1Bay
abnormal retina photoreceptor layer morphology J:240676
decreased a-wave amplitude J:240676
decreased b-wave amplitude J:240676
decreased total retina thickness J:240676
thin retina outer plexiform layer J:240676
Cwc27tm1b(KOMP)Wtsi/Cwc27tm1b(KOMP)Wtsi
B6N(Cg)-Cwc27tm1b(KOMP)Wtsi/J
male infertility J:211773
preweaning lethality, incomplete penetrance J:211773
Cwc27tm1Lex/Cwc27tm1Lex
B6;129S5-Cwc27tm1Lex/Mmucd
abnormal behavior J:171883
abnormal blood homeostasis J:171883
abnormal immune system physiology J:171883
postnatal growth retardation J:171883
prenatal growth retardation J:171883
preweaning lethality, incomplete penetrance J:171883

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
04/30/2024
MGI 6.23
The Jackson Laboratory