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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Del(19Cyp26a1-Cyp26c1)1Hmd
deletion, Chr 19, Hiroshi Hamada 1
MGI:6473142
21 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Del(19Cyp26a1-Cyp26c1)1Hmd/Del(19Cyp26a1-Cyp26c1)1Hmd
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal cranial ganglia morphology J:119939
abnormal ectomesenchyme morphology J:119939
abnormal facial morphology J:119939
abnormal geniculate ganglion morphology J:119939
abnormal head morphology J:119939
abnormal hindbrain development J:119939
abnormal nervous system development J:119939
abnormal neural crest cell migration J:119939
abnormal rhombomere morphology J:119939
absent trigeminal ganglion J:119939
cochlear ganglion hypoplasia J:119939
embryonic lethality during organogenesis, complete penetrance J:119939
first pharyngeal arch hypoplasia J:119939
forebrain hypoplasia J:119939
increased hindbrain size J:119939
microcephaly J:119939
midbrain hypoplasia J:119939
normal nervous system phenotype J:119939
open neural tube J:119939
second pharyngeal arch hypoplasia J:119939
truncated tail bud J:119939

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