Stock TFH/H

FESA Number

233

Strain Name

TFH/H

Mutation Strain Type

Mutation Type Mutation Subtype Strain Type
IMSR - Spontaneous mutation IMSR - segregating inbred strain

Attribution

Institution name Depositor / Originator Name
MRC Mammalian Genetics Unit Originator Retained
MRC Mammalian Genetics Unit Depositor Retained

Gene/Allele Information

Allele Name Allele MGI ID Gene Name Gene MGI ID Chromosome
T MGI:1856184 T MGI:98472 17
Itpr3<tf> MGI:1857070 Itpr3 MGI:96624 17

Phenotypic Description

Shorter tail, blunt.

Publications

Displaying 1 - 10 of 67 Stock Publications
Pubmed ID Authors Title Journal
7084665 Babiarz B Genetic analysis of the tw73 haplotype of the mouse using deletion mutations: evidence for a parasitic lethal mutation. Genet Res (1 982) 39:111-20
6722884 Lyon MF Transmission ratio distortion in mouse t-haplotypes is due to multiple distorter genes acting on a responder locus. Cell (1 984) 37:621-8
17954925 Wu JI Tint maps to mouse chromosome 6 and may interact with a notochordal enhancer of Brachyury. Genetics (2 007) 177:1151-61
18417102 MacPherson P Impaired fear memory, altered object memory and modified hippocampal synaptic plasticity in split-brain mice. Brain Res (2 008) 1210:179-88
20345893 Wöhr M Reduced scent marking and ultrasonic vocalizations in the BTBR T+tf/J mouse model of autism. Genes Brain Behav (2 011) 10:35-43
Bennett D The T-locus of the mouse. Cell (1 975) 6:441-454
2318411 Lyon MF Search for differences among t haplotypes in distorter and responder genes. Genet Res (1 990) 55:13-9
10617567 Yamaguchi TP T (Brachyury) is a direct target of Wnt3a during paraxial mesoderm specification. Genes Dev (1 999) 13:3185-90
17559418 McFarlane HG Autism-like behavioral phenotypes in BTBR T+tf/J mice. Genes Brain Behav (2 008) 7:152-63
19419429 Yang M Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability. Eur J Neurosci (2 009) 29:1663-77

Pages

Orphanet Categories

Rare developmental defect during embryogenesis
Rare neurologic disease
Rare endocrine disease

EMMA ID

EM:02207

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