Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
A |
T |
10: 79,841,995 (GRCm39) |
T1043S |
probably benign |
Het |
Acadvl |
T |
A |
11: 69,902,554 (GRCm39) |
K410* |
probably null |
Het |
Adam8 |
C |
T |
7: 139,567,762 (GRCm39) |
G354D |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,590,175 (GRCm39) |
E1366G |
possibly damaging |
Het |
Bahcc1 |
C |
A |
11: 120,165,415 (GRCm39) |
Q949K |
probably benign |
Het |
Bsn |
G |
A |
9: 107,988,651 (GRCm39) |
A2367V |
probably benign |
Het |
Ccdc141 |
T |
A |
2: 76,889,894 (GRCm39) |
Y466F |
possibly damaging |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Cyp4a30b |
C |
A |
4: 115,314,972 (GRCm39) |
Q185K |
probably benign |
Het |
Dlx2 |
A |
T |
2: 71,375,882 (GRCm39) |
I147K |
possibly damaging |
Het |
Dnaaf6rt |
T |
A |
1: 31,262,349 (GRCm39) |
D110E |
probably damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,612,621 (GRCm39) |
L482S |
probably damaging |
Het |
Dnah8 |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
17: 30,979,841 (GRCm39) |
|
probably null |
Het |
Dock7 |
C |
A |
4: 98,971,266 (GRCm39) |
V100F |
|
Het |
Dspp |
C |
A |
5: 104,325,162 (GRCm39) |
D508E |
unknown |
Het |
Duox2 |
G |
T |
2: 122,128,636 (GRCm39) |
T4K |
probably benign |
Het |
Ear1 |
T |
C |
14: 44,056,704 (GRCm39) |
N55D |
probably damaging |
Het |
Echdc1 |
G |
C |
10: 29,210,242 (GRCm39) |
E179Q |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,046,109 (GRCm39) |
M547V |
possibly damaging |
Het |
Erbb2 |
A |
G |
11: 98,319,798 (GRCm39) |
N630S |
possibly damaging |
Het |
Fam227a |
G |
A |
15: 79,514,271 (GRCm39) |
S363L |
possibly damaging |
Het |
Fam98b |
A |
G |
2: 117,101,381 (GRCm39) |
R398G |
unknown |
Het |
Fsip2 |
G |
A |
2: 82,807,430 (GRCm39) |
D1250N |
probably benign |
Het |
Gdnf |
G |
T |
15: 7,864,134 (GRCm39) |
E182* |
probably null |
Het |
Gys2 |
T |
C |
6: 142,406,921 (GRCm39) |
H145R |
probably benign |
Het |
Hcls1 |
A |
G |
16: 36,767,003 (GRCm39) |
K69R |
probably benign |
Het |
Itih5 |
A |
G |
2: 10,239,869 (GRCm39) |
N332S |
probably benign |
Het |
Kcnb2 |
T |
A |
1: 15,382,934 (GRCm39) |
Y87N |
probably damaging |
Het |
Lrriq3 |
A |
G |
3: 154,893,873 (GRCm39) |
N525D |
probably damaging |
Het |
Lsg1 |
A |
T |
16: 30,380,569 (GRCm39) |
W623R |
probably damaging |
Het |
Myo10 |
A |
G |
15: 25,725,158 (GRCm39) |
Y243C |
probably benign |
Het |
Nans |
T |
C |
4: 46,492,814 (GRCm39) |
Y81H |
probably damaging |
Het |
Nup54 |
T |
G |
5: 92,573,605 (GRCm39) |
N199T |
probably benign |
Het |
Or2h1 |
A |
G |
17: 37,404,664 (GRCm39) |
L34P |
probably damaging |
Het |
Or4c126 |
C |
T |
2: 89,824,348 (GRCm39) |
L204F |
probably benign |
Het |
Or4k15 |
T |
C |
14: 50,364,604 (GRCm39) |
I190T |
probably benign |
Het |
Or5w13 |
A |
T |
2: 87,524,088 (GRCm39) |
I46N |
probably damaging |
Het |
Or7d9 |
T |
A |
9: 20,197,337 (GRCm39) |
L122* |
probably null |
Het |
Pcnt |
G |
A |
10: 76,256,039 (GRCm39) |
R734W |
probably damaging |
Het |
Peg10 |
T |
C |
6: 4,755,462 (GRCm39) |
F13L |
possibly damaging |
Het |
Ppfibp1 |
T |
C |
6: 146,902,448 (GRCm39) |
V285A |
possibly damaging |
Het |
Prpf39 |
T |
C |
12: 65,102,036 (GRCm39) |
V371A |
possibly damaging |
Het |
Psmb11 |
G |
A |
14: 54,863,013 (GRCm39) |
C77Y |
probably damaging |
Het |
Rrbp1 |
A |
G |
2: 143,797,053 (GRCm39) |
L1133P |
probably benign |
Het |
Slc16a1 |
G |
T |
3: 104,560,149 (GRCm39) |
M151I |
probably benign |
Het |
Tarm1 |
G |
T |
7: 3,546,037 (GRCm39) |
Q89K |
possibly damaging |
Het |
Tas2r116 |
T |
C |
6: 132,832,540 (GRCm39) |
I47T |
probably damaging |
Het |
Tmod3 |
T |
C |
9: 75,436,680 (GRCm39) |
D85G |
probably damaging |
Het |
Trbv14 |
T |
C |
6: 41,112,299 (GRCm39) |
L32P |
probably benign |
Het |
Trim16 |
T |
C |
11: 62,741,414 (GRCm39) |
L486P |
probably benign |
Het |
Trmt1l |
T |
G |
1: 151,325,727 (GRCm39) |
S391A |
probably benign |
Het |
Ush2a |
T |
A |
1: 188,582,254 (GRCm39) |
N3772K |
probably damaging |
Het |
Vmn1r230 |
G |
T |
17: 21,066,870 (GRCm39) |
A20S |
probably benign |
Het |
Wdr76 |
A |
G |
2: 121,341,179 (GRCm39) |
N75D |
possibly damaging |
Het |
Zfp977 |
A |
G |
7: 42,230,102 (GRCm39) |
L141S |
probably benign |
Het |
Zfp988 |
A |
G |
4: 147,416,808 (GRCm39) |
D414G |
probably benign |
Het |
|
Other mutations in Plcb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00510:Plcb1
|
APN |
2 |
135,093,676 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01152:Plcb1
|
APN |
2 |
134,655,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01945:Plcb1
|
APN |
2 |
135,062,711 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01999:Plcb1
|
APN |
2 |
135,188,238 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02109:Plcb1
|
APN |
2 |
134,628,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Plcb1
|
APN |
2 |
135,229,773 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02207:Plcb1
|
APN |
2 |
135,229,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02566:Plcb1
|
APN |
2 |
135,314,183 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02590:Plcb1
|
APN |
2 |
135,136,784 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02640:Plcb1
|
APN |
2 |
135,062,779 (GRCm39) |
splice site |
probably benign |
|
IGL02926:Plcb1
|
APN |
2 |
135,206,682 (GRCm39) |
splice site |
probably benign |
|
IGL03071:Plcb1
|
APN |
2 |
135,229,722 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03236:Plcb1
|
APN |
2 |
135,188,226 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03252:Plcb1
|
APN |
2 |
135,212,348 (GRCm39) |
missense |
probably benign |
|
IGL03387:Plcb1
|
APN |
2 |
134,655,606 (GRCm39) |
splice site |
probably benign |
|
BB001:Plcb1
|
UTSW |
2 |
135,201,613 (GRCm39) |
missense |
probably benign |
0.00 |
BB011:Plcb1
|
UTSW |
2 |
135,201,613 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Plcb1
|
UTSW |
2 |
135,204,345 (GRCm39) |
missense |
probably benign |
0.06 |
R0024:Plcb1
|
UTSW |
2 |
135,204,345 (GRCm39) |
missense |
probably benign |
0.06 |
R0053:Plcb1
|
UTSW |
2 |
135,136,835 (GRCm39) |
missense |
probably benign |
0.33 |
R0053:Plcb1
|
UTSW |
2 |
135,136,835 (GRCm39) |
missense |
probably benign |
0.33 |
R0308:Plcb1
|
UTSW |
2 |
134,655,534 (GRCm39) |
missense |
probably benign |
0.01 |
R0415:Plcb1
|
UTSW |
2 |
135,179,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Plcb1
|
UTSW |
2 |
135,136,831 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0898:Plcb1
|
UTSW |
2 |
135,229,063 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1071:Plcb1
|
UTSW |
2 |
135,167,577 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1615:Plcb1
|
UTSW |
2 |
135,204,364 (GRCm39) |
splice site |
probably benign |
|
R1617:Plcb1
|
UTSW |
2 |
135,179,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Plcb1
|
UTSW |
2 |
135,167,587 (GRCm39) |
nonsense |
probably null |
|
R1866:Plcb1
|
UTSW |
2 |
135,186,093 (GRCm39) |
missense |
probably benign |
0.01 |
R1869:Plcb1
|
UTSW |
2 |
135,152,934 (GRCm39) |
missense |
probably benign |
0.02 |
R1902:Plcb1
|
UTSW |
2 |
134,655,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1938:Plcb1
|
UTSW |
2 |
135,228,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Plcb1
|
UTSW |
2 |
135,204,340 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2017:Plcb1
|
UTSW |
2 |
135,204,340 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2131:Plcb1
|
UTSW |
2 |
135,167,587 (GRCm39) |
nonsense |
probably null |
|
R2132:Plcb1
|
UTSW |
2 |
135,167,587 (GRCm39) |
nonsense |
probably null |
|
R2133:Plcb1
|
UTSW |
2 |
135,167,587 (GRCm39) |
nonsense |
probably null |
|
R2164:Plcb1
|
UTSW |
2 |
135,188,250 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2419:Plcb1
|
UTSW |
2 |
135,104,020 (GRCm39) |
splice site |
probably benign |
|
R2429:Plcb1
|
UTSW |
2 |
135,179,362 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Plcb1
|
UTSW |
2 |
135,102,428 (GRCm39) |
missense |
probably benign |
0.27 |
R3161:Plcb1
|
UTSW |
2 |
135,177,402 (GRCm39) |
missense |
probably benign |
0.03 |
R3870:Plcb1
|
UTSW |
2 |
135,167,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R4191:Plcb1
|
UTSW |
2 |
135,187,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:Plcb1
|
UTSW |
2 |
135,186,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R4552:Plcb1
|
UTSW |
2 |
135,177,413 (GRCm39) |
missense |
probably benign |
0.44 |
R4553:Plcb1
|
UTSW |
2 |
135,177,413 (GRCm39) |
missense |
probably benign |
0.44 |
R4720:Plcb1
|
UTSW |
2 |
135,093,667 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4946:Plcb1
|
UTSW |
2 |
135,187,015 (GRCm39) |
missense |
probably benign |
0.01 |
R5012:Plcb1
|
UTSW |
2 |
135,175,320 (GRCm39) |
missense |
probably null |
0.97 |
R5151:Plcb1
|
UTSW |
2 |
135,104,165 (GRCm39) |
missense |
probably benign |
0.28 |
R5320:Plcb1
|
UTSW |
2 |
135,094,696 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5415:Plcb1
|
UTSW |
2 |
135,189,322 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5523:Plcb1
|
UTSW |
2 |
135,102,486 (GRCm39) |
missense |
probably benign |
0.08 |
R5568:Plcb1
|
UTSW |
2 |
135,212,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5688:Plcb1
|
UTSW |
2 |
135,177,400 (GRCm39) |
missense |
probably benign |
0.06 |
R5809:Plcb1
|
UTSW |
2 |
135,104,164 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6237:Plcb1
|
UTSW |
2 |
135,212,486 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6315:Plcb1
|
UTSW |
2 |
135,188,261 (GRCm39) |
missense |
probably benign |
0.00 |
R6478:Plcb1
|
UTSW |
2 |
135,177,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R6531:Plcb1
|
UTSW |
2 |
135,167,722 (GRCm39) |
critical splice donor site |
probably null |
|
R6683:Plcb1
|
UTSW |
2 |
134,628,513 (GRCm39) |
missense |
probably benign |
0.32 |
R6760:Plcb1
|
UTSW |
2 |
135,313,980 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6947:Plcb1
|
UTSW |
2 |
135,228,075 (GRCm39) |
missense |
probably benign |
0.08 |
R6976:Plcb1
|
UTSW |
2 |
135,104,159 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7379:Plcb1
|
UTSW |
2 |
135,212,430 (GRCm39) |
missense |
probably benign |
0.45 |
R7473:Plcb1
|
UTSW |
2 |
135,186,196 (GRCm39) |
missense |
probably damaging |
0.98 |
R7492:Plcb1
|
UTSW |
2 |
135,093,684 (GRCm39) |
nonsense |
probably null |
|
R7498:Plcb1
|
UTSW |
2 |
135,104,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R7498:Plcb1
|
UTSW |
2 |
135,104,153 (GRCm39) |
nonsense |
probably null |
|
R7777:Plcb1
|
UTSW |
2 |
135,062,677 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7924:Plcb1
|
UTSW |
2 |
135,201,613 (GRCm39) |
missense |
probably benign |
0.00 |
R8061:Plcb1
|
UTSW |
2 |
135,188,316 (GRCm39) |
missense |
probably benign |
|
R8099:Plcb1
|
UTSW |
2 |
135,093,654 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8299:Plcb1
|
UTSW |
2 |
135,177,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R8394:Plcb1
|
UTSW |
2 |
135,159,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R8549:Plcb1
|
UTSW |
2 |
135,206,853 (GRCm39) |
missense |
probably benign |
0.00 |
R8693:Plcb1
|
UTSW |
2 |
135,094,696 (GRCm39) |
missense |
probably benign |
0.00 |
R8750:Plcb1
|
UTSW |
2 |
135,177,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Plcb1
|
UTSW |
2 |
135,175,429 (GRCm39) |
intron |
probably benign |
|
R8950:Plcb1
|
UTSW |
2 |
135,179,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R9146:Plcb1
|
UTSW |
2 |
135,182,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Plcb1
|
UTSW |
2 |
135,167,610 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9311:Plcb1
|
UTSW |
2 |
135,189,385 (GRCm39) |
missense |
probably benign |
0.00 |
R9459:Plcb1
|
UTSW |
2 |
135,164,558 (GRCm39) |
missense |
probably benign |
0.03 |
S24628:Plcb1
|
UTSW |
2 |
135,179,419 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Plcb1
|
UTSW |
2 |
135,186,974 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1088:Plcb1
|
UTSW |
2 |
135,062,766 (GRCm39) |
missense |
probably benign |
0.04 |
|