|Institutional Source||Beutler Lab|
|Gene Name||potassium voltage-gated channel, shaker-related subfamily, member 7|
|Is this an essential gene?||Probably non essential (E-score: 0.130)|
|Stock #||R1721 (G1)|
|Chromosomal Location||45405653-45409763 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 45406921 bp|
|Amino Acid Change||Valine to Alanine at position 187 (V187A)|
|Ref Sequence||ENSEMBL: ENSMUSP00000103403 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000107774]|
|Predicted Effect||possibly damaging
AA Change: V187A
PolyPhen 2 Score 0.946 (Sensitivity: 0.80; Specificity: 0.95)
AA Change: V187A
|Meta Mutation Damage Score||0.1238|
|Coding Region Coverage||
|Validation Efficiency||99% (87/88)|
|MGI Phenotype||FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. The gene is expressed preferentially in skeletal muscle, heart and kidney. It is a candidate gene for inherited cardiac disorders. [provided by RefSeq, Jul 2008]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Kcna7||
(F):5'- GCTTCGATGCGGTGCTCTACTACTA -3'
(R):5'- CCTTGCCACACCTTCTGACTGG -3'
(F):5'- TCTACTACTACCAGTCGGGCG -3'
(R):5'- GGCCAGGTCTTCCCAGG -3'