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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Dync2h1
dynein cytoplasmic 2 heavy chain 1
MGI:107736
35 phenotypes from 10 alleles in 10 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Dync2h1b2b414Clo/Dync2h1b2b414Clo
C57BL/6J-Dync2h1b2b414Clo 		abnormal autopod morphology J:175213
abnormal coronary vessel morphology J:175213
abnormal craniofacial morphology J:175213
abnormal eye morphology J:175213
abnormal inferior vena cava morphology J:175213
abnormal lung lobe morphology J:175213
abnormal mouth morphology J:175213
abnormal respiratory system morphology J:175213
absent kidney J:175213
aorta pulmonary collateral arteries J:175213
balanced complete atrioventricular canal J:175213
common atrium J:175213
complete atrioventricular septal defect J:175213
coronary fistula J:175213
duplex kidney J:175213
holoprosencephaly J:175213
micrognathia J:175213
ocular hypotelorism J:175213
polydactyly J:175213
syndactyly J:175213
tracheoesophageal fistula J:175213
unbalanced complete atrioventricular canal, left dominant J:175213
Dync2h1em1(IMPC)Rbrc/Dync2h1em1(IMPC)Rbrc
C57BL/6NJcl-Dync2h1em1(IMPC)Rbrc/Rbrc 		preweaning lethality, complete penetrance J:211773
Dync2h1Gt(RRM278)Byg/Dync2h1Gt(RRM278)Byg
involves: 129P2/OlaHsd 		abnormal brain morphology J:100466
abnormal direction of heart looping J:100466
embryonic lethality during organogenesis, complete penetrance J:100466
Dync2h1Gt(RRM278)Byg/Dync2h1lln
involves: 129P2/OlaHsd * C57BL/6J 		abnormal brain morphology J:100466
abnormal direction of heart looping J:100466
embryonic lethality during organogenesis, complete penetrance J:100466
Dync2h1lln/Dync2h1lln
involves: C3HeB/FeJ * C57BL/6J 		abnormal left-right axis patterning J:98216
abnormal spinal cord morphology J:98216
embryonic lethality during organogenesis, complete penetrance J:98216
Dync2h1lln/Dync2h1lln
involves: C57BL/6J 		abnormal direction of heart looping J:100466
normal embryo phenotype J:100466
embryonic lethality during organogenesis, complete penetrance J:100466
exencephaly J:100466
polydactyly J:100466
Dync2h1m152Asp/Dync2h1m152Asp
Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N 		abnormal cerebral cortex morphology J:136795
Dync2h1m407Asp/Dync2h1m407Asp
Tg(Rr291-lacZ)#Mekk/0
involves: C57BL/6J * FVB/N 		abnormal forebrain development J:136795
Dync2h1mmi/Dync2h1mmi
Tg(Hlxb9-GFP)1Tmj/?
involves: C57BL/6J * FVB/N 		abnormal motor neuron morphology J:151965
Dync2h1pol/Dync2h1pol
involves: C3H/HeJ * C57BL/6J 		abnormal direction of heart looping J:309102
abnormal motile primary cilium morphology J:309102
embryonic lethality during organogenesis, complete penetrance J:309102
exencephaly J:309102
polydactyly J:309102
Dync2h1Tg(Tyr)2307AOve/Dync2h1Tg(Tyr)2307AOve
FVB/N-Dync2h1Tg(Tyr)2307AOve 		embryonic lethality during organogenesis, complete penetrance J:175597
Dync2h1ttn/Dync2h1ttn
Not Specified 		abnormal cilium morphology J:138139
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
04/23/2024
MGI 6.23 		The Jackson Laboratory