Stk36 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Stk36
serine/threonine kinase 36
MGI:1920831

39 phenotypes from 5 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Stk36^em1(IMPC)J/Stk36⁺ C57BL/6NJ-Stk36^em1(IMPC)J/J	abnormal sinus arrhythmia	J:211773
Stk36^em1(IMPC)J/Stk36⁺ C57BL/6NJ-Stk36^em1(IMPC)J/J	increased urine microalbumin level	J:211773
Stk36^tm1.1Ptch/Stk36^tm1.1Ptch involves: 129P2/OlaHsd * C57BL/6 * FVB/N * Swiss Webster	decreased body weight	J:131268
	postnatal growth retardation	J:131268
	postnatal lethality, incomplete penetrance	J:131268
Stk36^tm1Fjs/Stk36^tm1Fjs involves: 129S1/Sv * C57BL/6	abnormal cranium morphology	J:116391
	abnormal kidney development	J:116391
	abnormal lung development	J:116391
	ataxia	J:116391
	decreased body size	J:116391
	domed cranium	J:116391
	male infertility	J:116391
	non-obstructive hydrocephaly	J:116391
	postnatal growth retardation	J:116391
	postnatal lethality, complete penetrance	J:116391
	rhinitis	J:116391
	spleen atrophy	J:116391
	thymus atrophy	J:116391
Stk36^tm1Lex/Stk36^tm1Lex involves: 129S5/SvEvBrd * C57BL/6J	abnormal craniofacial morphology	J:185566
	decreased body length	J:185566
	decreased body weight	J:185566
	female infertility	J:185566
	normal growth/size/body region phenotype	J:185566
	hydrocephaly	J:185566
	increased susceptibility to otitis media	J:185566
	postnatal growth retardation	J:185566
	premature death	J:185566
Stk36^tm1Ptch/Stk36^tm1Ptch Tg(Ddx4-cre)1Ptch/0 involves: 129P2/OlaHsd	abnormal manchette morphology	J:208762
	abnormal sperm axoneme morphology	J:208762
	abnormal sperm fibrous sheath morphology	J:208762
	abnormal sperm flagellum morphology	J:208762
	abnormal sperm head morphology	J:208762
	abnormal sperm nucleus morphology	J:208762
	abnormal sperm principal piece morphology	J:208762
	abnormal spermatid morphology	J:208762
	absent sperm head	J:208762
	decreased activated sperm motility	J:208762
	decreased sperm progressive motility	J:208762
	elongated manchette	J:208762
	male infertility	J:208762
	normal mortality/aging	J:208762
	oligozoospermia	J:208762
	normal reproductive system phenotype	J:208762

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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