The Branch mutation is an A-to-T transversion at base pair 46,560,651 (v38) on chromosome 18, or base pair 13,978 in the GenBank genomic region NC_000084 encoding TICAM2. The mutation, which is within the third and last exon, corresponds to residue 844 in the mRNA sequence NM_173394 and results in an aspartic acid (D) to valine (V) substitution at amino acid position 123 (D123V) of the protein. (J:215010)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Chemically induced
Single point
Semidominant
1
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Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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