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EN
ENU-induced A to T transversion at base pair 117,873,905 (v38) on chromosome 13, or base pair 271,586 in the GenBank genomic region NC_000079 encoding Hcn1. The mutation corresponds to residue 1,402 in the mRNA sequence NM_010408 within exon 4 of 8 total exons. The mutation results in substitution of lysine 340 for a premature stop codon (K340*) in the HCN1 protein. (J:267552)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
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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References Literature
Title
PMID
Journal
Year
IF
