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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Kif1b+
wild type
MGI:2387928
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Kif1btm1b(KOMP)Wtsi/Kif1b+ C57BL/6N-Kif1btm1b(KOMP)Wtsi/J MGI:5631239
ht2
Kif1btm1Noh/Kif1b+ involves: 129S4/SvJae * C57BL/6J MGI:2387931


Genotype
MGI:5631239
ht1
Allelic
Composition
Kif1btm1b(KOMP)Wtsi/Kif1b+
Genetic
Background
C57BL/6N-Kif1btm1b(KOMP)Wtsi/J
Cell Lines EPD0624_1_H07
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kif1btm1b(KOMP)Wtsi mutation (1 available); any Kif1b mutation (128 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
IMPC - JAX

hematopoietic system

homeostasis/metabolism




Genotype
MGI:2387931
ht2
Allelic
Composition
Kif1btm1Noh/Kif1b+
Genetic
Background
involves: 129S4/SvJae * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kif1btm1Noh mutation (0 available); any Kif1b mutation (128 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• staggering; onset at approximately one year of age; progressive
• at 12 months of age, impairment was observed in a rotarod test and a balance beam test

muscle
• at 12 months of age, evoked compound action potential amplitudes were significantly reduced; the conduction velocity was unaffected

nervous system
• impaired vesicle transport in peripheral nerves

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Charcot-Marie-Tooth disease type 2A1 DOID:0110154 OMIM:118210
J:69772





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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
03/18/2025
MGI 6.24
The Jackson Laboratory