Incidental Mutation 'R1295:Kcnk12'
ID158099
Institutional Source Beutler Lab
Gene Symbol Kcnk12
Ensembl Gene ENSMUSG00000050138
Gene Namepotassium channel, subfamily K, member 12
Synonymsmntk1
MMRRC Submission 039361-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.074) question?
Stock #R1295 (G1)
Quality Score100
Status Validated
Chromosome17
Chromosomal Location87745837-87797994 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 87746373 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Aspartic acid at position 287 (G287D)
Ref Sequence ENSEMBL: ENSMUSP00000053595 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055221]
Predicted Effect probably damaging
Transcript: ENSMUST00000055221
AA Change: G287D

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000053595
Gene: ENSMUSG00000050138
AA Change: G287D

DomainStartEndE-ValueType
low complexity region 2 30 N/A INTRINSIC
Pfam:Ion_trans_2 94 170 5e-16 PFAM
Pfam:Ion_trans_2 220 304 3.1e-18 PFAM
low complexity region 340 350 N/A INTRINSIC
Meta Mutation Damage Score 0.9363 question?
Coding Region Coverage
  • 1x: 98.7%
  • 3x: 97.4%
  • 10x: 93.1%
  • 20x: 82.0%
Validation Efficiency 98% (81/83)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ackr2 A G 9: 121,908,717 S53G possibly damaging Het
Adgrb1 T A 15: 74,550,039 L886Q probably damaging Het
Adprhl1 G A 8: 13,248,624 T102M probably damaging Het
Akap6 A C 12: 52,887,029 K435Q probably damaging Het
Aldh7a1 T C 18: 56,546,950 probably null Het
Amfr T C 8: 93,974,804 R507G probably benign Het
Ap1m1 T A 8: 72,251,875 probably null Het
Arhgap29 A G 3: 121,992,395 H275R probably benign Het
Arhgef17 C A 7: 100,881,269 E428* probably null Het
Atm A T 9: 53,456,530 V2431E probably damaging Het
Atn1 G T 6: 124,747,787 P161Q unknown Het
Atp13a2 T C 4: 140,993,802 S99P probably damaging Het
Ccar1 C A 10: 62,783,882 probably null Het
Cdk18 T C 1: 132,119,960 probably benign Het
Cep85 A G 4: 134,167,400 W32R probably damaging Het
Col5a3 A G 9: 20,808,418 F215S unknown Het
Decr1 T C 4: 15,919,207 N312S possibly damaging Het
Diaph3 A T 14: 87,007,399 W178R probably damaging Het
Dync2h1 A G 9: 7,075,752 probably benign Het
Ehd3 C A 17: 73,828,186 D352E probably damaging Het
Enpp6 T G 8: 47,065,500 I221S probably benign Het
Fam186a T C 15: 99,939,789 probably benign Het
Gm5435 G T 12: 82,495,784 noncoding transcript Het
Gm6990 T A 19: 56,755,334 noncoding transcript Het
Gpr22 A C 12: 31,709,514 I203S probably benign Het
Gpr61 A G 3: 108,150,481 V288A possibly damaging Het
Grik3 G A 4: 125,704,564 probably benign Het
Gstcd T C 3: 133,005,628 N431D probably damaging Het
Haao T A 17: 83,838,838 Q69L probably benign Het
Hist1h1b T C 13: 21,779,999 S186G probably benign Het
Ift140 G T 17: 25,088,933 probably null Het
Ikbke A G 1: 131,270,226 V381A probably benign Het
Ing1 A C 8: 11,561,501 I38L probably benign Het
Ing1 T A 8: 11,561,502 I38N probably damaging Het
Itga4 A G 2: 79,322,689 M907V possibly damaging Het
Kmt2e A C 5: 23,502,404 H1655P probably damaging Het
Mbtd1 A G 11: 93,910,359 Y122C probably damaging Het
Mslnl T C 17: 25,743,240 L204P probably damaging Het
Muc6 T C 7: 141,651,879 E112G probably benign Het
Nav3 T A 10: 109,692,102 D2240V probably damaging Het
Ndufaf3 T C 9: 108,566,693 T9A probably damaging Het
Numb C A 12: 83,796,161 probably benign Het
Prodh2 T C 7: 30,494,089 V79A probably damaging Het
Psmb2 A G 4: 126,687,032 Y73C probably damaging Het
Rmnd5a G A 6: 71,398,455 L80F probably benign Het
Rnf19a G T 15: 36,244,101 Y604* probably null Het
Ros1 T A 10: 52,087,932 E1744V possibly damaging Het
Rpusd2 T C 2: 119,036,927 F219L probably benign Het
Sall2 T C 14: 52,313,725 N671S probably damaging Het
Sele T A 1: 164,050,810 S239R probably damaging Het
Serpina3b T C 12: 104,130,879 F140L probably damaging Het
Stxbp1 A T 2: 32,794,636 S594T probably benign Het
Sufu G A 19: 46,454,720 probably benign Het
Tbx2 A G 11: 85,834,766 E181G probably damaging Het
Thumpd2 A G 17: 81,055,888 V50A probably damaging Het
Tmem56 A G 3: 121,207,291 V231A probably benign Het
Ttn C A 2: 76,743,245 R17441L probably damaging Het
Usp34 A G 11: 23,384,477 Y1157C probably damaging Het
Vmn1r9 T C 6: 57,071,537 V199A probably damaging Het
Vmn2r6 A G 3: 64,538,273 F677S probably damaging Het
Vmn2r84 C T 10: 130,389,139 A501T probably benign Het
Wapl C T 14: 34,724,769 P605S probably damaging Het
Zfp598 A G 17: 24,679,649 N474S probably benign Het
Zfyve26 A G 12: 79,274,920 L975P probably damaging Het
Zp3r C T 1: 130,591,444 G255D probably damaging Het
Other mutations in Kcnk12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01103:Kcnk12 APN 17 87746767 missense probably damaging 0.99
IGL01611:Kcnk12 APN 17 87797067 missense probably benign 0.08
R1672:Kcnk12 UTSW 17 87746319 missense probably benign 0.16
R1806:Kcnk12 UTSW 17 87746109 missense probably benign 0.34
R1807:Kcnk12 UTSW 17 87746040 missense probably benign 0.04
R1873:Kcnk12 UTSW 17 87746071 missense probably damaging 1.00
R1972:Kcnk12 UTSW 17 87797132 missense possibly damaging 0.50
R4116:Kcnk12 UTSW 17 87746156 frame shift probably null
R5202:Kcnk12 UTSW 17 87746605 nonsense probably null
R5888:Kcnk12 UTSW 17 87746649 missense probably benign 0.00
R6017:Kcnk12 UTSW 17 87746736 missense probably damaging 1.00
R7544:Kcnk12 UTSW 17 87746065 missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GCCGGTTGTTCATGATGCCCAG -3'
(R):5'- GCCATGTACACCAGCGTGGAAG -3'

Sequencing Primer
(F):5'- AGCGACACCTTGTTGGAC -3'
(R):5'- TGGAAGGCTGGGACTACG -3'
Posted On2014-02-18