|Institutional Source||Beutler Lab|
|Gene Name||potassium voltage-gated channel, subfamily H (eag-related), member 8|
|Synonyms||ELK1, C130090D05Rik, Kv12.1|
|Is this an essential gene?||Possibly non essential (E-score: 0.378)|
|Stock #||R5866 (G1)|
|Chromosomal Location||52602709-52979194 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to C at 52956776 bp|
|Amino Acid Change||Isoleucine to Threonine at position 767 (I767T)|
|Ref Sequence||ENSEMBL: ENSMUSP00000049206 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000039366]|
|Predicted Effect||probably benign
AA Change: I767T
PolyPhen 2 Score 0.049 (Sensitivity: 0.94; Specificity: 0.83)
AA Change: I767T
|Predicted Effect||noncoding transcript
|Meta Mutation Damage Score||0.21|
|Coding Region Coverage||
|Validation Efficiency||91% (51/56)|
|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. [provided by RefSeq, Jul 2008]|
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Kcnh8||
(F):5'- GGGAAGTCTTGGCAACTGTG -3'
(R):5'- CAGAAGTGTGGGCTCTCATTGG -3'
(F):5'- AGAGACTCCCATCCATTGTGG -3'
(R):5'- CTCTCATTGGGGGAGACTGATGC -3'