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Gene: Kcnq1dfk (potassium voltage-gated channel subfamily Q member 1;deafness Kyoto) Rattus norvegicus
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Symbol: Kcnq1dfk
Name: potassium voltage-gated channel subfamily Q member 1;deafness Kyoto
Description: A naturally occurring deletion mutation arising on the genetic background of an inbred WTC strain. It is a 2040-bp deletion that included whole exon 7 and its flanking sequences of the Kcnq1 gene.
ASSOCIATED WITH abnormal cardiovascular system physiology; decreased body weight; impaired balance; ASSOCIATED WITH Achlorhydria; Deafness; hypertension
Type: allele  of Kcnq1  
Also known as: Kcnq1dfk
Is Marker For: Strains:   WTC-Kcnq1dfkKyo  
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position: No map positions available.


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Phenotype Annotations
References - curated

Genomics

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Expression


Sequence

Nucleotide Sequences

Additional Information

 
More on Kcnq1dfk
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Ensembl Gene
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CRRD Object Information
CRRD ID: 12802344
Created: 2017-04-05
Species: Rattus norvegicus
Last Modified: 2017-04-05
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.