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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fscn1
fascin actin-bundling protein 1
MGI:1352745
26 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fscn1Gt(OST124903)Lex/Fscn1+
Tg(Dct-lacZ)A12Jkn/0
involves: C57BL/6 * CBA
abnormal melanoblast morphology J:197025
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex
B6.129S5-Fscn1Gt(OST124903)Lex
abnormal anterior commissure pars posterior morphology J:205179
abnormal axon morphology J:205179
abnormal breathing pattern J:205179
abnormal cell cycle J:197025
abnormal dendritic cell chemotaxis J:169408
abnormal dendritic cell physiology J:169408
abnormal fibroblast physiology J:205179
abnormal Langerhans cell physiology J:169408
abnormal melanoblast morphology J:197025
abnormal neurite morphology J:205179
absent gastric milk in neonates J:205179
belly spot J:197025
decreased body size J:205179
decreased digit pigmentation J:197025
decreased melanocyte number J:197025
decreased tail pigmentation J:197025
enlarged lateral ventricles J:205179
neonatal lethality, incomplete penetrance J:205179
nervous J:205179
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex
involves: 129S5/SvEvBrd * C57BL/6
normal mortality/aging J:205179
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex
Tg(Dct-lacZ)A12Jkn/0
involves: C57BL/6 * CBA
abnormal melanoblast migration J:197025
abnormal melanoblast morphology J:197025
belly spot J:197025
Fscn1tm1.1(KOMP)Vlcg/Fscn1+
C57BL/6N-Fscn1tm1.1(KOMP)Vlcg/Ucd
abnormal behavior J:211773
decreased thigmotaxis J:211773
hyperactivity J:211773
Fscn1tm1.1(KOMP)Vlcg/Fscn1tm1.1(KOMP)Vlcg
C57BL/6N-Fscn1tm1.1(KOMP)Vlcg/Ucd
preweaning lethality, complete penetrance J:211773
preweaning lethality, incomplete penetrance J:211773

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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
04/23/2024
MGI 6.23
The Jackson Laboratory