Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
G |
7: 119,953,701 (GRCm39) |
N535S |
probably benign |
Het |
Abcc6 |
A |
T |
7: 45,648,165 (GRCm39) |
L717Q |
probably benign |
Het |
Abraxas2 |
C |
A |
7: 132,484,790 (GRCm39) |
Q278K |
probably benign |
Het |
Acap2 |
A |
T |
16: 30,924,342 (GRCm39) |
D637E |
probably benign |
Het |
AI661453 |
A |
G |
17: 47,777,023 (GRCm39) |
|
probably benign |
Het |
Aoah |
A |
T |
13: 21,024,266 (GRCm39) |
E74V |
probably damaging |
Het |
Aoc1l1 |
A |
T |
6: 48,953,629 (GRCm39) |
D518V |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,671,576 (GRCm39) |
L292S |
possibly damaging |
Het |
Astl |
T |
A |
2: 127,189,109 (GRCm39) |
V166E |
probably damaging |
Het |
Bbs1 |
T |
G |
19: 4,953,735 (GRCm39) |
K143Q |
possibly damaging |
Het |
Bbx |
T |
C |
16: 50,094,907 (GRCm39) |
|
probably benign |
Het |
Birc6 |
A |
T |
17: 74,967,408 (GRCm39) |
Q4103L |
possibly damaging |
Het |
C1qtnf2 |
T |
G |
11: 43,381,811 (GRCm39) |
F178V |
probably damaging |
Het |
Camta2 |
A |
G |
11: 70,562,401 (GRCm39) |
F999L |
probably benign |
Het |
Cfap68 |
T |
C |
9: 50,676,174 (GRCm39) |
Y32C |
probably damaging |
Het |
Clcn7 |
A |
G |
17: 25,363,425 (GRCm39) |
I34V |
probably benign |
Het |
Cntn5 |
G |
T |
9: 9,748,420 (GRCm39) |
P487Q |
probably damaging |
Het |
Ctu2 |
T |
A |
8: 123,205,891 (GRCm39) |
I213K |
probably benign |
Het |
Des |
C |
A |
1: 75,340,108 (GRCm39) |
|
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,098,094 (GRCm39) |
D432E |
probably benign |
Het |
Dlgap5 |
G |
A |
14: 47,633,380 (GRCm39) |
R549* |
probably null |
Het |
Dmac2l |
A |
G |
12: 69,787,828 (GRCm39) |
Q88R |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,323,194 (GRCm39) |
T1397A |
probably damaging |
Het |
Dnmt1 |
T |
A |
9: 20,848,451 (GRCm39) |
|
probably benign |
Het |
Dstyk |
T |
A |
1: 132,391,113 (GRCm39) |
M838K |
probably damaging |
Het |
Dtwd1 |
C |
A |
2: 126,001,904 (GRCm39) |
T208N |
probably damaging |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Dync1i2 |
T |
A |
2: 71,044,907 (GRCm39) |
|
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,499,383 (GRCm39) |
M1251K |
probably benign |
Het |
Fmod |
T |
C |
1: 133,968,256 (GRCm39) |
Y99H |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,645,163 (GRCm39) |
V1552D |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,407,739 (GRCm39) |
S281T |
probably damaging |
Het |
Glb1 |
A |
G |
9: 114,293,233 (GRCm39) |
H536R |
probably benign |
Het |
Glis2 |
T |
A |
16: 4,431,506 (GRCm39) |
S344R |
possibly damaging |
Het |
Gm4847 |
A |
T |
1: 166,462,472 (GRCm39) |
S339R |
probably benign |
Het |
Gpr155 |
A |
G |
2: 73,187,002 (GRCm39) |
S44P |
probably benign |
Het |
Gprin1 |
G |
A |
13: 54,886,445 (GRCm39) |
P610S |
probably damaging |
Het |
Gvin3 |
T |
A |
7: 106,202,215 (GRCm39) |
H343L |
possibly damaging |
Het |
H2-Ob |
A |
T |
17: 34,461,554 (GRCm39) |
M98L |
probably benign |
Het |
H3c6 |
T |
C |
13: 23,746,530 (GRCm39) |
T4A |
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,223,943 (GRCm39) |
|
probably benign |
Het |
Ikbke |
C |
A |
1: 131,201,211 (GRCm39) |
V176L |
probably damaging |
Het |
Il13 |
T |
C |
11: 53,523,351 (GRCm39) |
T85A |
possibly damaging |
Het |
Inpp5k |
A |
T |
11: 75,538,017 (GRCm39) |
|
probably null |
Het |
Irgm2 |
T |
C |
11: 58,111,355 (GRCm39) |
S361P |
possibly damaging |
Het |
Itga11 |
C |
T |
9: 62,639,486 (GRCm39) |
|
probably benign |
Het |
Kalrn |
G |
T |
16: 33,829,632 (GRCm39) |
|
probably benign |
Het |
Kcng1 |
C |
A |
2: 168,110,952 (GRCm39) |
G71C |
probably damaging |
Het |
Klhl7 |
A |
T |
5: 24,305,861 (GRCm39) |
M37L |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lhx6 |
C |
T |
2: 35,977,478 (GRCm39) |
V325I |
probably benign |
Het |
Lipc |
A |
G |
9: 70,841,817 (GRCm39) |
I9T |
possibly damaging |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Mast1 |
C |
A |
8: 85,648,107 (GRCm39) |
G458V |
probably damaging |
Het |
Mga |
T |
C |
2: 119,794,638 (GRCm39) |
V2565A |
possibly damaging |
Het |
Mpzl2 |
C |
G |
9: 44,955,471 (GRCm39) |
D127E |
probably benign |
Het |
Mrtfb |
T |
C |
16: 13,230,450 (GRCm39) |
I1045T |
probably damaging |
Het |
Myh3 |
T |
A |
11: 66,981,882 (GRCm39) |
C793S |
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,715,928 (GRCm39) |
L765P |
probably damaging |
Het |
Nup210 |
A |
G |
6: 91,005,858 (GRCm39) |
I1335T |
possibly damaging |
Het |
Or52b3 |
T |
C |
7: 102,204,267 (GRCm39) |
|
probably null |
Het |
Oxr1 |
T |
A |
15: 41,683,340 (GRCm39) |
S254R |
probably damaging |
Het |
Pan3 |
A |
G |
5: 147,466,908 (GRCm39) |
I592V |
possibly damaging |
Het |
Pask |
C |
T |
1: 93,249,019 (GRCm39) |
A794T |
probably benign |
Het |
Pex2 |
T |
C |
3: 5,626,650 (GRCm39) |
E53G |
probably damaging |
Het |
Pfkfb2 |
T |
C |
1: 130,626,460 (GRCm39) |
T438A |
probably benign |
Het |
Phactr4 |
T |
C |
4: 132,098,095 (GRCm39) |
E391G |
probably damaging |
Het |
Pira2 |
A |
T |
7: 3,847,344 (GRCm39) |
L115Q |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,376,273 (GRCm39) |
|
probably null |
Het |
Pnlip |
A |
G |
19: 58,664,876 (GRCm39) |
S235G |
probably benign |
Het |
Prkd1 |
A |
G |
12: 50,536,694 (GRCm39) |
V130A |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,703,999 (GRCm39) |
T1344A |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,001,419 (GRCm39) |
Y780C |
probably damaging |
Het |
Pxn |
T |
A |
5: 115,690,815 (GRCm39) |
|
probably benign |
Het |
Rap1gap2 |
G |
A |
11: 74,316,802 (GRCm39) |
T245M |
probably damaging |
Het |
Rc3h1 |
G |
T |
1: 160,757,827 (GRCm39) |
K48N |
probably damaging |
Het |
Rfwd3 |
T |
C |
8: 112,009,245 (GRCm39) |
I444V |
probably benign |
Het |
Rictor |
C |
T |
15: 6,794,588 (GRCm39) |
R293C |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,001,412 (GRCm39) |
I1622N |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,306,019 (GRCm39) |
V609A |
probably benign |
Het |
Scgb1b2 |
G |
T |
7: 30,991,188 (GRCm39) |
|
probably benign |
Het |
Serac1 |
A |
T |
17: 6,101,060 (GRCm39) |
I448N |
probably damaging |
Het |
Sh3kbp1 |
C |
A |
X: 158,607,492 (GRCm39) |
T200K |
probably benign |
Het |
Sned1 |
T |
A |
1: 93,199,406 (GRCm39) |
F495L |
probably damaging |
Het |
Socs7 |
T |
C |
11: 97,263,950 (GRCm39) |
F281L |
probably benign |
Het |
Spta1 |
C |
T |
1: 174,040,180 (GRCm39) |
L1214F |
probably benign |
Het |
Ssu72 |
A |
G |
4: 155,789,900 (GRCm39) |
E21G |
probably damaging |
Het |
Syngr4 |
A |
G |
7: 45,536,464 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,305,539 (GRCm39) |
M254I |
possibly damaging |
Het |
Tmem130 |
C |
A |
5: 144,680,595 (GRCm39) |
V270L |
probably benign |
Het |
Trim66 |
A |
T |
7: 109,074,320 (GRCm39) |
I647N |
probably damaging |
Het |
Tspyl2 |
A |
T |
X: 151,121,890 (GRCm39) |
D572E |
probably benign |
Het |
Unc45b |
G |
A |
11: 82,808,580 (GRCm39) |
R222H |
probably benign |
Het |
Uxs1 |
T |
C |
1: 43,866,783 (GRCm39) |
Y29C |
probably damaging |
Het |
Virma |
T |
A |
4: 11,548,726 (GRCm39) |
|
probably benign |
Het |
Vmn1r202 |
C |
T |
13: 22,685,953 (GRCm39) |
G155S |
possibly damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,755,972 (GRCm39) |
F15I |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,594,661 (GRCm39) |
T471A |
probably benign |
Het |
Zfa-ps |
T |
A |
10: 52,419,373 (GRCm39) |
|
noncoding transcript |
Het |
Zfp260 |
A |
G |
7: 29,804,765 (GRCm39) |
K222E |
probably damaging |
Het |
Zfp300 |
A |
G |
X: 20,948,190 (GRCm39) |
S525P |
possibly damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,979 (GRCm39) |
D324G |
probably damaging |
Het |
Zfp934 |
T |
C |
13: 62,665,648 (GRCm39) |
D331G |
probably damaging |
Het |
Zscan29 |
T |
C |
2: 121,000,587 (GRCm39) |
R7G |
probably damaging |
Het |
|
Other mutations in Kcnq5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00864:Kcnq5
|
APN |
1 |
21,575,987 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01603:Kcnq5
|
APN |
1 |
21,575,564 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02326:Kcnq5
|
APN |
1 |
21,472,816 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02624:Kcnq5
|
APN |
1 |
21,472,654 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03151:Kcnq5
|
APN |
1 |
21,605,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03367:Kcnq5
|
APN |
1 |
21,473,289 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Kcnq5
|
UTSW |
1 |
21,605,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R0705:Kcnq5
|
UTSW |
1 |
21,605,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R0798:Kcnq5
|
UTSW |
1 |
22,031,399 (GRCm39) |
splice site |
probably null |
|
R1263:Kcnq5
|
UTSW |
1 |
21,549,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Kcnq5
|
UTSW |
1 |
21,475,248 (GRCm39) |
missense |
probably benign |
0.01 |
R1465:Kcnq5
|
UTSW |
1 |
21,539,692 (GRCm39) |
critical splice donor site |
probably null |
|
R1465:Kcnq5
|
UTSW |
1 |
21,539,692 (GRCm39) |
critical splice donor site |
probably null |
|
R1497:Kcnq5
|
UTSW |
1 |
21,472,610 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1515:Kcnq5
|
UTSW |
1 |
21,472,905 (GRCm39) |
missense |
probably benign |
0.01 |
R1610:Kcnq5
|
UTSW |
1 |
21,527,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Kcnq5
|
UTSW |
1 |
21,536,611 (GRCm39) |
missense |
probably benign |
0.04 |
R1999:Kcnq5
|
UTSW |
1 |
21,472,428 (GRCm39) |
missense |
probably null |
0.18 |
R2060:Kcnq5
|
UTSW |
1 |
21,531,821 (GRCm39) |
missense |
probably benign |
0.06 |
R2314:Kcnq5
|
UTSW |
1 |
21,549,595 (GRCm39) |
splice site |
probably null |
|
R2511:Kcnq5
|
UTSW |
1 |
21,576,006 (GRCm39) |
nonsense |
probably null |
|
R2697:Kcnq5
|
UTSW |
1 |
21,549,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R2886:Kcnq5
|
UTSW |
1 |
21,539,771 (GRCm39) |
nonsense |
probably null |
|
R2889:Kcnq5
|
UTSW |
1 |
21,472,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R4176:Kcnq5
|
UTSW |
1 |
21,605,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R4609:Kcnq5
|
UTSW |
1 |
21,475,292 (GRCm39) |
splice site |
probably null |
|
R4720:Kcnq5
|
UTSW |
1 |
21,473,274 (GRCm39) |
missense |
probably damaging |
0.96 |
R4904:Kcnq5
|
UTSW |
1 |
21,494,324 (GRCm39) |
missense |
probably damaging |
0.98 |
R5184:Kcnq5
|
UTSW |
1 |
21,472,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Kcnq5
|
UTSW |
1 |
21,575,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R5373:Kcnq5
|
UTSW |
1 |
22,031,795 (GRCm39) |
missense |
unknown |
|
R5397:Kcnq5
|
UTSW |
1 |
21,476,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5473:Kcnq5
|
UTSW |
1 |
21,527,626 (GRCm39) |
critical splice donor site |
probably null |
|
R5490:Kcnq5
|
UTSW |
1 |
21,549,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R5946:Kcnq5
|
UTSW |
1 |
21,575,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Kcnq5
|
UTSW |
1 |
21,476,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6962:Kcnq5
|
UTSW |
1 |
21,576,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Kcnq5
|
UTSW |
1 |
21,473,099 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7238:Kcnq5
|
UTSW |
1 |
21,472,526 (GRCm39) |
missense |
probably benign |
0.39 |
R7375:Kcnq5
|
UTSW |
1 |
21,539,710 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7584:Kcnq5
|
UTSW |
1 |
21,472,545 (GRCm39) |
missense |
probably benign |
|
R7780:Kcnq5
|
UTSW |
1 |
22,031,555 (GRCm39) |
missense |
probably benign |
0.43 |
R8043:Kcnq5
|
UTSW |
1 |
21,549,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Kcnq5
|
UTSW |
1 |
21,549,620 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8267:Kcnq5
|
UTSW |
1 |
21,575,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8363:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8370:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8371:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8374:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8414:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8528:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:Kcnq5
|
UTSW |
1 |
21,549,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Kcnq5
|
UTSW |
1 |
21,476,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R8723:Kcnq5
|
UTSW |
1 |
21,575,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R9000:Kcnq5
|
UTSW |
1 |
21,557,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Kcnq5
|
UTSW |
1 |
21,539,463 (GRCm39) |
intron |
probably benign |
|
R9152:Kcnq5
|
UTSW |
1 |
21,539,692 (GRCm39) |
critical splice donor site |
probably null |
|
R9426:Kcnq5
|
UTSW |
1 |
21,473,118 (GRCm39) |
missense |
probably benign |
|
Z1088:Kcnq5
|
UTSW |
1 |
21,527,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|