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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Dync2h1
dynein cytoplasmic 2 heavy chain 1
MGI:107736
32 phenotypes from 9 alleles in 8 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
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
Dync2h1em1(IMPC)Rbrc/Dync2h1em1(IMPC)Rbrc
Not Specified
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(mI56i-lacZ)1Mekk/0
involves: C57BL/6J * FVB/N
abnormal cerebral cortex morphology J:136795
Dync2h1m407Asp/Dync2h1m407Asp
Tg(mI56i-lacZ)1Mekk/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
Dync2h1Tg(Tyr)2307AOve/Dync2h1Tg(Tyr)2307AOve
FVB/N-Dync2h1Tg(Tyr)2307AOve
embryonic lethality during organogenesis, complete penetrance J:175597
Dync2h1ttn/Dync2h1ttn
Not Specified
abnormal cell 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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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory