Incidental Mutation 'IGL00418:Kctd19'
ID6209
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Kctd19
Ensembl Gene ENSMUSG00000051648
Gene Namepotassium channel tetramerisation domain containing 19
Synonyms4922504H04Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.058) question?
Stock #IGL00418
Quality Score
Status
Chromosome8
Chromosomal Location105382807-105413502 bp(-) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to T at 105388463 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130831 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063071] [ENSMUST00000167294] [ENSMUST00000168196]
Predicted Effect probably null
Transcript: ENSMUST00000063071
SMART Domains Protein: ENSMUSP00000050687
Gene: ENSMUSG00000051648

DomainStartEndE-ValueType
Pfam:BTB_2 15 92 1.3e-9 PFAM
internal_repeat_1 173 251 8.34e-9 PROSPERO
internal_repeat_1 429 509 8.34e-9 PROSPERO
Predicted Effect probably null
Transcript: ENSMUST00000167294
SMART Domains Protein: ENSMUSP00000130831
Gene: ENSMUSG00000051648

DomainStartEndE-ValueType
Pfam:BTB_2 15 93 3.9e-10 PFAM
internal_repeat_1 173 251 6.24e-9 PROSPERO
internal_repeat_1 406 486 6.24e-9 PROSPERO
Predicted Effect probably benign
Transcript: ENSMUST00000168196
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700097O09Rik A G 12: 55,048,963 I238T probably damaging Het
Akap4 T C X: 7,076,490 V344A possibly damaging Het
Apex2 T C X: 150,572,052 K430E probably benign Het
Aqp9 C T 9: 71,132,731 A90T probably damaging Het
Asb15 T A 6: 24,558,643 probably benign Het
Barhl2 C T 5: 106,455,499 A265T possibly damaging Het
Bspry G T 4: 62,496,105 D312Y probably benign Het
Cdh16 G A 8: 104,623,413 R5W probably benign Het
Ciz1 C T 2: 32,372,388 R461C probably damaging Het
Cldn14 T A 16: 93,919,301 D219V probably benign Het
Clpb A T 7: 101,787,745 T706S probably benign Het
Cyp2d11 A T 15: 82,392,468 M90K probably benign Het
Cyp2j8 T A 4: 96,444,616 I498F possibly damaging Het
Dnah2 A G 11: 69,495,066 probably benign Het
Dpyd T A 3: 118,944,242 F477L probably damaging Het
Dscaml1 C A 9: 45,670,200 S439* probably null Het
Faxc A G 4: 21,958,490 K216E possibly damaging Het
Fmo1 C T 1: 162,836,246 R238Q probably damaging Het
Gm14399 G A 2: 175,131,522 R147* probably null Het
H2-Ab1 G A 17: 34,267,575 V203M probably damaging Het
Heatr5b T C 17: 78,753,141 E2035G probably damaging Het
Hip1 A G 5: 135,426,346 I786T probably damaging Het
Homer1 T C 13: 93,387,688 probably benign Het
Igkv9-120 A G 6: 68,049,987 D2G possibly damaging Het
Irgm1 A T 11: 48,866,005 Y326* probably null Het
Large1 T C 8: 72,823,841 probably null Het
Mzf1 G A 7: 13,044,616 A287V possibly damaging Het
Nes A T 3: 87,976,254 K607* probably null Het
Pars2 T A 4: 106,654,050 V307E probably damaging Het
Pcsk5 T A 19: 17,511,421 I1012F possibly damaging Het
Pole T C 5: 110,303,565 probably benign Het
Rbm14 T C 19: 4,802,548 probably benign Het
Scn2a A T 2: 65,764,522 Q1905L probably benign Het
Slc26a2 A G 18: 61,198,740 F540L probably benign Het
Slco2a1 T C 9: 103,079,441 probably benign Het
Tas2r106 T C 6: 131,677,959 probably null Het
Tmem175 T A 5: 108,645,866 D287E probably benign Het
Trappc12 T C 12: 28,737,836 K416R probably damaging Het
Trim2 A G 3: 84,208,289 L86P probably damaging Het
Vps13c T A 9: 67,876,262 N240K probably damaging Het
Wdr90 A C 17: 25,849,364 I1330S probably damaging Het
Wfdc6a A G 2: 164,584,994 probably null Het
Zc3h12c C T 9: 52,116,665 V466M probably damaging Het
Zswim8 A G 14: 20,718,475 T1025A probably damaging Het
Other mutations in Kctd19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01546:Kctd19 APN 8 105386962 missense probably benign
IGL01786:Kctd19 APN 8 105390304 missense probably benign 0.03
IGL01964:Kctd19 APN 8 105388525 missense probably damaging 0.99
IGL02275:Kctd19 APN 8 105396374 missense probably damaging 0.99
IGL02479:Kctd19 APN 8 105384768 missense probably damaging 1.00
IGL03124:Kctd19 APN 8 105387070 missense possibly damaging 0.48
R0003:Kctd19 UTSW 8 105395361 missense probably damaging 0.99
R1183:Kctd19 UTSW 8 105382966 missense probably benign
R1388:Kctd19 UTSW 8 105392051 missense probably null 0.93
R1491:Kctd19 UTSW 8 105387062 missense possibly damaging 0.60
R1517:Kctd19 UTSW 8 105395376 missense probably damaging 1.00
R1540:Kctd19 UTSW 8 105387879 missense probably damaging 0.96
R1582:Kctd19 UTSW 8 105395460 missense probably damaging 1.00
R1964:Kctd19 UTSW 8 105388470 missense probably damaging 0.98
R1996:Kctd19 UTSW 8 105395300 missense probably null 1.00
R2129:Kctd19 UTSW 8 105385172 missense probably damaging 0.98
R2281:Kctd19 UTSW 8 105387266 missense probably benign 0.00
R3767:Kctd19 UTSW 8 105396480 missense probably benign 0.04
R3768:Kctd19 UTSW 8 105396480 missense probably benign 0.04
R4285:Kctd19 UTSW 8 105382949 unclassified probably benign
R4621:Kctd19 UTSW 8 105396471 missense probably damaging 1.00
R4701:Kctd19 UTSW 8 105390429 missense possibly damaging 0.76
R4969:Kctd19 UTSW 8 105396327 splice site probably null
R5070:Kctd19 UTSW 8 105391999 missense probably damaging 1.00
R5401:Kctd19 UTSW 8 105382985 missense probably benign 0.00
R5582:Kctd19 UTSW 8 105408443 missense probably damaging 1.00
R5783:Kctd19 UTSW 8 105386980 missense probably benign
R6056:Kctd19 UTSW 8 105396450 missense probably damaging 0.99
R6057:Kctd19 UTSW 8 105396450 missense probably damaging 0.99
R6269:Kctd19 UTSW 8 105395360 missense possibly damaging 0.96
R6273:Kctd19 UTSW 8 105385485 missense probably benign
R6631:Kctd19 UTSW 8 105385328 critical splice donor site probably null
R7298:Kctd19 UTSW 8 105382984 missense probably benign 0.01
R7474:Kctd19 UTSW 8 105392032 missense probably benign 0.25
R7540:Kctd19 UTSW 8 105386935 missense probably benign 0.00
R8059:Kctd19 UTSW 8 105396351 missense probably benign 0.02
Z1088:Kctd19 UTSW 8 105385335 missense probably benign 0.02
Z1176:Kctd19 UTSW 8 105385136 missense probably damaging 1.00
Z1177:Kctd19 UTSW 8 105388517 missense probably damaging 1.00
Posted On2012-04-20