|Institutional Source||Beutler Lab|
|Gene Name||potassium voltage-gated channel, subfamily H (eag-related), member 7|
|Synonyms||Kv11.3, 9330137I11Rik, erg3|
|Is this an essential gene?||Probably non essential (E-score: 0.106)|
|Stock #||R5822 (G1)|
|Chromosomal Location||62693414-63184287 bp(-) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||G to A at 62716238 bp|
|Amino Acid Change||Arginine to Tryptophan at position 1000 (R1000W)|
|Ref Sequence||ENSEMBL: ENSMUSP00000074563 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000075052]|
|Predicted Effect||probably benign
AA Change: R1000W
PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
AA Change: R1000W
|Meta Mutation Damage Score||0.0898|
|Coding Region Coverage||
|Validation Efficiency||96% (54/56)|
|MGI Phenotype||FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Voltage-gated potassium (Kv) 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. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. There are at least two alternatively spliced transcript variants derived from this gene and encoding distinct isoforms. [provided by RefSeq, Jul 2008]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Kcnh7||
(F):5'- AAACATAGGTTGCTTGATGGC -3'
(R):5'- AGATTCTGGTACTGATTGGAAATGG -3'
(F):5'- GCTTGATGGCAAAAGTATCCTG -3'
(R):5'- CTGGTACTGATTGGAAATGGAGATTG -3'