Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
G |
T |
2: 68,445,099 (GRCm39) |
|
probably null |
Het |
5730522E02Rik |
A |
T |
11: 25,719,014 (GRCm39) |
V44E |
unknown |
Het |
Adcy9 |
A |
G |
16: 4,236,673 (GRCm39) |
L246S |
possibly damaging |
Het |
Adk |
C |
T |
14: 21,284,997 (GRCm39) |
H123Y |
probably damaging |
Het |
Adra1b |
T |
A |
11: 43,726,794 (GRCm39) |
D41V |
probably benign |
Het |
Ankib1 |
T |
G |
5: 3,751,911 (GRCm39) |
K710Q |
probably damaging |
Het |
Aoc2 |
T |
A |
11: 101,219,203 (GRCm39) |
V542D |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,081,194 (GRCm39) |
N1221S |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGT |
CACTGGTTCTGTGGTTACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGT |
3: 95,795,450 (GRCm39) |
|
probably benign |
Het |
Bmal1 |
T |
C |
7: 112,898,631 (GRCm39) |
V353A |
probably benign |
Het |
Cacna1a |
C |
A |
8: 85,285,922 (GRCm39) |
R856S |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,590,304 (GRCm39) |
M1559V |
|
Het |
Cdh10 |
G |
C |
15: 19,013,445 (GRCm39) |
E682Q |
probably damaging |
Het |
Celsr1 |
T |
C |
15: 85,916,719 (GRCm39) |
D418G |
possibly damaging |
Het |
Cfap44 |
T |
C |
16: 44,291,111 (GRCm39) |
L1537P |
probably damaging |
Het |
Clca3a2 |
A |
G |
3: 144,519,340 (GRCm39) |
S279P |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,874,040 (GRCm39) |
V1449I |
not run |
Het |
Cpt2 |
A |
G |
4: 107,764,339 (GRCm39) |
F475S |
probably damaging |
Het |
Cpxm1 |
T |
C |
2: 130,235,487 (GRCm39) |
T502A |
probably benign |
Het |
Creb3l2 |
G |
T |
6: 37,356,794 (GRCm39) |
T91N |
probably benign |
Het |
D630045J12Rik |
A |
T |
6: 38,119,601 (GRCm39) |
S1714T |
possibly damaging |
Het |
Dennd1c |
C |
A |
17: 57,379,379 (GRCm39) |
V246F |
probably damaging |
Het |
Dse |
A |
G |
10: 34,028,561 (GRCm39) |
V843A |
probably benign |
Het |
Ern2 |
C |
A |
7: 121,769,756 (GRCm39) |
W810L |
probably damaging |
Het |
Fer1l6 |
G |
A |
15: 58,472,281 (GRCm39) |
D906N |
probably damaging |
Het |
Fry |
A |
G |
5: 150,389,791 (GRCm39) |
E140G |
|
Het |
Galnt7 |
A |
G |
8: 58,005,552 (GRCm39) |
V227A |
probably damaging |
Het |
Gas2l3 |
A |
G |
10: 89,249,763 (GRCm39) |
S452P |
probably benign |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
Gm826 |
A |
T |
2: 160,153,942 (GRCm39) |
S34T |
unknown |
Het |
Gzmk |
A |
T |
13: 113,308,535 (GRCm39) |
I222N |
probably benign |
Het |
Hivep3 |
A |
T |
4: 119,956,027 (GRCm39) |
T1448S |
probably benign |
Het |
Hk1 |
T |
C |
10: 62,131,524 (GRCm39) |
D278G |
probably damaging |
Het |
Ipo7 |
C |
A |
7: 109,638,401 (GRCm39) |
Q223K |
possibly damaging |
Het |
Itga9 |
T |
A |
9: 118,598,179 (GRCm39) |
I571N |
probably damaging |
Het |
Itgb6 |
T |
C |
2: 60,450,720 (GRCm39) |
Y573C |
probably damaging |
Het |
Kmt2c |
T |
A |
5: 25,489,562 (GRCm39) |
H4459L |
probably damaging |
Het |
Limch1 |
T |
G |
5: 67,211,580 (GRCm39) |
S894R |
probably damaging |
Het |
Lrit2 |
A |
T |
14: 36,790,867 (GRCm39) |
Q182L |
possibly damaging |
Het |
Mlph |
A |
T |
1: 90,867,100 (GRCm39) |
H374L |
possibly damaging |
Het |
Mmrn2 |
A |
G |
14: 34,121,374 (GRCm39) |
H748R |
probably damaging |
Het |
Mrpl58 |
T |
C |
11: 115,301,092 (GRCm39) |
V134A |
possibly damaging |
Het |
Nae1 |
A |
T |
8: 105,244,871 (GRCm39) |
D353E |
probably benign |
Het |
Naip5 |
A |
C |
13: 100,353,579 (GRCm39) |
F1227V |
probably benign |
Het |
Nln |
A |
T |
13: 104,205,831 (GRCm39) |
F108I |
probably damaging |
Het |
Nop16 |
C |
T |
13: 54,736,417 (GRCm39) |
V94I |
probably benign |
Het |
Nt5c1b |
A |
T |
12: 10,424,903 (GRCm39) |
T150S |
probably benign |
Het |
Or10d4b |
T |
G |
9: 39,535,268 (GRCm39) |
I281S |
possibly damaging |
Het |
Pcdha4 |
T |
C |
18: 37,087,689 (GRCm39) |
V624A |
probably damaging |
Het |
Pcdhga8 |
T |
C |
18: 37,860,483 (GRCm39) |
I513T |
probably benign |
Het |
Prc1 |
A |
T |
7: 79,959,239 (GRCm39) |
|
probably null |
Het |
Prpf4 |
T |
A |
4: 62,336,113 (GRCm39) |
F280Y |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,051,392 (GRCm39) |
E43G |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,446,485 (GRCm39) |
D181E |
probably benign |
Het |
Rab7 |
A |
G |
6: 87,990,624 (GRCm39) |
S17P |
probably damaging |
Het |
Rgs1 |
T |
C |
1: 144,121,134 (GRCm39) |
Y179C |
probably damaging |
Het |
Rrm1 |
T |
C |
7: 102,103,764 (GRCm39) |
C238R |
probably damaging |
Het |
Rusc2 |
T |
A |
4: 43,426,528 (GRCm39) |
L1484Q |
probably damaging |
Het |
Sall3 |
C |
T |
18: 81,015,920 (GRCm39) |
M669I |
probably benign |
Het |
Saxo1 |
A |
C |
4: 86,363,644 (GRCm39) |
F280V |
probably benign |
Het |
Scn2a |
T |
C |
2: 65,532,352 (GRCm39) |
S655P |
probably damaging |
Het |
Senp6 |
G |
T |
9: 80,031,010 (GRCm39) |
E571* |
probably null |
Het |
Sin3b |
C |
G |
8: 73,473,069 (GRCm39) |
T463S |
probably damaging |
Het |
Sirt7 |
C |
A |
11: 120,509,837 (GRCm39) |
R349L |
probably benign |
Het |
Skor1 |
T |
C |
9: 63,053,730 (GRCm39) |
T80A |
probably damaging |
Het |
Slc12a9 |
C |
A |
5: 137,321,082 (GRCm39) |
A478S |
probably damaging |
Het |
Slc25a23 |
T |
A |
17: 57,359,822 (GRCm39) |
R310* |
probably null |
Het |
Slit2 |
A |
G |
5: 48,377,336 (GRCm39) |
E455G |
probably benign |
Het |
Smo |
G |
C |
6: 29,736,119 (GRCm39) |
G37A |
probably damaging |
Het |
St6galnac1 |
T |
C |
11: 116,660,010 (GRCm39) |
K101R |
probably benign |
Het |
Stat1 |
C |
A |
1: 52,191,530 (GRCm39) |
N628K |
probably benign |
Het |
Syn2 |
A |
T |
6: 115,231,615 (GRCm39) |
Y302F |
probably benign |
Het |
Tapt1 |
T |
G |
5: 44,345,978 (GRCm39) |
Q324P |
probably damaging |
Het |
Tgoln1 |
C |
T |
6: 72,593,403 (GRCm39) |
A26T |
unknown |
Het |
Timm13 |
T |
A |
10: 80,736,378 (GRCm39) |
T43S |
probably benign |
Het |
Tnfrsf19 |
G |
A |
14: 61,242,654 (GRCm39) |
P77S |
possibly damaging |
Het |
Trem3 |
T |
G |
17: 48,564,969 (GRCm39) |
F157V |
probably benign |
Het |
Trgv3 |
T |
A |
13: 19,427,016 (GRCm39) |
M1K |
probably null |
Het |
Trim33 |
T |
A |
3: 103,233,464 (GRCm39) |
S420T |
probably benign |
Het |
Trip11 |
T |
C |
12: 101,851,694 (GRCm39) |
K790R |
probably damaging |
Het |
Trnt1 |
A |
G |
6: 106,755,865 (GRCm39) |
T307A |
probably benign |
Het |
Tshz1 |
T |
C |
18: 84,033,766 (GRCm39) |
Y214C |
probably damaging |
Het |
Vmn2r105 |
T |
A |
17: 20,448,827 (GRCm39) |
T117S |
probably benign |
Het |
Vmn2r45 |
A |
G |
7: 8,484,342 (GRCm39) |
Y488H |
probably benign |
Het |
Vwa8 |
A |
T |
14: 79,320,254 (GRCm39) |
K1088N |
probably benign |
Het |
Wdr35 |
T |
C |
12: 9,036,000 (GRCm39) |
V257A |
probably benign |
Het |
Zfp189 |
T |
A |
4: 49,521,569 (GRCm39) |
S3T |
probably benign |
Het |
Zscan22 |
G |
A |
7: 12,640,833 (GRCm39) |
C359Y |
probably damaging |
Het |
Zscan4-ps2 |
A |
T |
7: 11,251,812 (GRCm39) |
R283* |
probably null |
Het |
|
Other mutations in Slco6c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00547:Slco6c1
|
APN |
1 |
97,015,674 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00571:Slco6c1
|
APN |
1 |
97,015,676 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01483:Slco6c1
|
APN |
1 |
97,055,832 (GRCm39) |
missense |
probably benign |
|
IGL01543:Slco6c1
|
APN |
1 |
97,053,553 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01860:Slco6c1
|
APN |
1 |
97,003,548 (GRCm39) |
splice site |
probably benign |
|
IGL03106:Slco6c1
|
APN |
1 |
96,993,748 (GRCm39) |
splice site |
probably benign |
|
R0087:Slco6c1
|
UTSW |
1 |
97,046,303 (GRCm39) |
missense |
probably benign |
0.00 |
R0543:Slco6c1
|
UTSW |
1 |
97,055,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R0674:Slco6c1
|
UTSW |
1 |
97,032,498 (GRCm39) |
splice site |
probably benign |
|
R0826:Slco6c1
|
UTSW |
1 |
97,055,826 (GRCm39) |
missense |
probably benign |
0.00 |
R0928:Slco6c1
|
UTSW |
1 |
97,032,573 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0969:Slco6c1
|
UTSW |
1 |
97,047,685 (GRCm39) |
missense |
probably benign |
0.05 |
R1366:Slco6c1
|
UTSW |
1 |
97,055,928 (GRCm39) |
start gained |
probably null |
|
R1559:Slco6c1
|
UTSW |
1 |
97,026,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1594:Slco6c1
|
UTSW |
1 |
96,990,163 (GRCm39) |
missense |
probably benign |
0.36 |
R1901:Slco6c1
|
UTSW |
1 |
97,000,707 (GRCm39) |
missense |
probably damaging |
0.98 |
R2005:Slco6c1
|
UTSW |
1 |
97,009,214 (GRCm39) |
missense |
probably damaging |
0.99 |
R2101:Slco6c1
|
UTSW |
1 |
97,000,595 (GRCm39) |
nonsense |
probably null |
|
R2102:Slco6c1
|
UTSW |
1 |
97,055,656 (GRCm39) |
missense |
probably benign |
0.02 |
R2120:Slco6c1
|
UTSW |
1 |
96,993,808 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2135:Slco6c1
|
UTSW |
1 |
97,032,542 (GRCm39) |
missense |
probably benign |
0.01 |
R2295:Slco6c1
|
UTSW |
1 |
97,053,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R2437:Slco6c1
|
UTSW |
1 |
96,990,201 (GRCm39) |
missense |
probably benign |
0.22 |
R4004:Slco6c1
|
UTSW |
1 |
97,003,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Slco6c1
|
UTSW |
1 |
97,009,218 (GRCm39) |
missense |
probably benign |
0.02 |
R4643:Slco6c1
|
UTSW |
1 |
96,990,149 (GRCm39) |
missense |
probably benign |
0.00 |
R4786:Slco6c1
|
UTSW |
1 |
97,015,720 (GRCm39) |
missense |
probably benign |
0.04 |
R4942:Slco6c1
|
UTSW |
1 |
97,009,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5485:Slco6c1
|
UTSW |
1 |
97,053,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Slco6c1
|
UTSW |
1 |
97,055,656 (GRCm39) |
missense |
probably benign |
0.00 |
R5810:Slco6c1
|
UTSW |
1 |
97,003,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Slco6c1
|
UTSW |
1 |
97,009,041 (GRCm39) |
splice site |
probably null |
|
R6033:Slco6c1
|
UTSW |
1 |
97,009,041 (GRCm39) |
splice site |
probably null |
|
R6191:Slco6c1
|
UTSW |
1 |
96,993,808 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6197:Slco6c1
|
UTSW |
1 |
97,000,518 (GRCm39) |
critical splice donor site |
probably null |
|
R6286:Slco6c1
|
UTSW |
1 |
97,053,445 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6404:Slco6c1
|
UTSW |
1 |
97,046,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6430:Slco6c1
|
UTSW |
1 |
97,003,699 (GRCm39) |
missense |
probably benign |
0.43 |
R6492:Slco6c1
|
UTSW |
1 |
97,053,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R6649:Slco6c1
|
UTSW |
1 |
97,053,436 (GRCm39) |
missense |
probably benign |
0.44 |
R6940:Slco6c1
|
UTSW |
1 |
97,000,626 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7138:Slco6c1
|
UTSW |
1 |
97,047,706 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7213:Slco6c1
|
UTSW |
1 |
97,055,671 (GRCm39) |
missense |
probably benign |
|
R7234:Slco6c1
|
UTSW |
1 |
97,053,466 (GRCm39) |
missense |
probably benign |
0.06 |
R7320:Slco6c1
|
UTSW |
1 |
97,055,887 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7375:Slco6c1
|
UTSW |
1 |
97,009,146 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7383:Slco6c1
|
UTSW |
1 |
97,003,608 (GRCm39) |
nonsense |
probably null |
|
R7422:Slco6c1
|
UTSW |
1 |
97,009,207 (GRCm39) |
missense |
probably benign |
0.17 |
R7561:Slco6c1
|
UTSW |
1 |
97,000,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R7890:Slco6c1
|
UTSW |
1 |
96,990,192 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8115:Slco6c1
|
UTSW |
1 |
97,000,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R8409:Slco6c1
|
UTSW |
1 |
97,003,663 (GRCm39) |
missense |
probably damaging |
0.99 |
R8422:Slco6c1
|
UTSW |
1 |
97,053,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R8824:Slco6c1
|
UTSW |
1 |
97,055,884 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8905:Slco6c1
|
UTSW |
1 |
97,053,391 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9183:Slco6c1
|
UTSW |
1 |
96,996,775 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9300:Slco6c1
|
UTSW |
1 |
96,993,809 (GRCm39) |
missense |
probably benign |
0.37 |
R9359:Slco6c1
|
UTSW |
1 |
96,990,248 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9374:Slco6c1
|
UTSW |
1 |
97,055,827 (GRCm39) |
missense |
probably benign |
0.00 |
R9403:Slco6c1
|
UTSW |
1 |
96,990,248 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9499:Slco6c1
|
UTSW |
1 |
97,055,827 (GRCm39) |
missense |
probably benign |
0.00 |
R9551:Slco6c1
|
UTSW |
1 |
97,055,827 (GRCm39) |
missense |
probably benign |
0.00 |
R9674:Slco6c1
|
UTSW |
1 |
97,047,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|