About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Fscn1+
wild type
MGI:2438525
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
 		Fscn1tm1.1(KOMP)Vlcg/Fscn1+ C57BL/6N-Fscn1tm1.1(KOMP)Vlcg/Ucd MGI:5883997
cx2
 		Fscn1Gt(OST124903)Lex/Fscn1+
Tg(Dct-lacZ)A12Jkn/0 		involves: C57BL/6 * CBA MGI:6209603


Genotype
MGI:5883997
ht1
Allelic
Composition		 Fscn1tm1.1(KOMP)Vlcg/Fscn1+
Genetic
Background		 C57BL/6N-Fscn1tm1.1(KOMP)Vlcg/Ucd
Cell Lines 14673A-H4
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fscn1tm1.1(KOMP)Vlcg mutation (1 available); any Fscn1 mutation (40 available)
Data Sources
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
behavior/neurological
hyperactivity ( J:211773 )
IMPC - UCD




Genotype
MGI:6209603
cx2
Allelic
Composition		 Fscn1Gt(OST124903)Lex/Fscn1+
Tg(Dct-lacZ)A12Jkn/0
Genetic
Background		 involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fscn1Gt(OST124903)Lex mutation (1 available); any Fscn1 mutation (40 available)
Tg(Dct-lacZ)A12Jkn mutation (5 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
embryo
abnormal melanoblast morphology ( J:197025 )
• in most cases, an intermediate reduction of melanoblasts is observed in dorsal-ventral regions at E13.5 and E15.5

nervous system
abnormal melanoblast morphology ( J:197025 )
• in most cases, an intermediate reduction of melanoblasts is observed in dorsal-ventral regions at E13.5 and E15.5




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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
03/18/2025
MGI 6.24 		The Jackson Laboratory