Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4galt |
T |
A |
15: 83,112,529 (GRCm39) |
I85F |
probably damaging |
Het |
Abcc6 |
T |
A |
7: 45,661,947 (GRCm39) |
I435F |
probably benign |
Het |
Adam3 |
T |
C |
8: 25,167,332 (GRCm39) |
|
probably benign |
Het |
Adrb3 |
T |
C |
8: 27,717,450 (GRCm39) |
Y333C |
probably damaging |
Het |
Ago4 |
A |
T |
4: 126,419,847 (GRCm39) |
D43E |
probably benign |
Het |
Agt |
T |
A |
8: 125,283,727 (GRCm39) |
Q464L |
probably benign |
Het |
Amdhd1 |
A |
T |
10: 93,367,463 (GRCm39) |
D230E |
probably damaging |
Het |
Aplf |
A |
G |
6: 87,645,405 (GRCm39) |
I33T |
probably damaging |
Het |
Aplf |
A |
T |
6: 87,623,331 (GRCm39) |
N249K |
probably benign |
Het |
Arap2 |
A |
G |
5: 62,906,821 (GRCm39) |
M66T |
probably benign |
Het |
Atf4 |
T |
C |
15: 80,140,434 (GRCm39) |
|
probably benign |
Het |
Bahcc1 |
A |
C |
11: 120,177,491 (GRCm39) |
H2068P |
probably benign |
Het |
Bcor |
C |
T |
X: 11,906,725 (GRCm39) |
R1551Q |
probably damaging |
Het |
Bltp1 |
A |
C |
3: 36,971,851 (GRCm39) |
H528P |
probably damaging |
Het |
Bltp1 |
G |
A |
3: 36,974,050 (GRCm39) |
S600N |
probably benign |
Het |
Catsper1 |
C |
A |
19: 5,391,466 (GRCm39) |
A616D |
possibly damaging |
Het |
Cdkn3 |
A |
G |
14: 47,007,320 (GRCm39) |
D159G |
possibly damaging |
Het |
Cep162 |
T |
C |
9: 87,108,022 (GRCm39) |
|
probably benign |
Het |
Clca3a1 |
T |
A |
3: 144,721,414 (GRCm39) |
I386L |
probably damaging |
Het |
Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
Cmtm3 |
T |
C |
8: 105,070,460 (GRCm39) |
L73P |
probably damaging |
Het |
Cnksr3 |
A |
C |
10: 7,102,925 (GRCm39) |
L149R |
probably benign |
Het |
Cope |
T |
C |
8: 70,755,584 (GRCm39) |
|
probably null |
Het |
Cpa6 |
T |
A |
1: 10,479,562 (GRCm39) |
M224L |
probably benign |
Het |
Cyp2d41-ps |
T |
C |
15: 82,666,154 (GRCm39) |
|
noncoding transcript |
Het |
Ddx55 |
T |
A |
5: 124,706,779 (GRCm39) |
L592* |
probably null |
Het |
Deup1 |
T |
C |
9: 15,499,323 (GRCm39) |
M333V |
probably benign |
Het |
Eif4a1 |
T |
C |
11: 69,558,640 (GRCm39) |
|
probably benign |
Het |
Eif4g3 |
A |
C |
4: 137,897,876 (GRCm39) |
D1026A |
probably damaging |
Het |
Eif5b |
T |
C |
1: 38,090,280 (GRCm39) |
V1153A |
probably damaging |
Het |
Ercc8 |
G |
T |
13: 108,297,301 (GRCm39) |
|
probably benign |
Het |
Fam227a |
C |
A |
15: 79,524,204 (GRCm39) |
|
probably null |
Het |
Fat1 |
A |
G |
8: 45,489,312 (GRCm39) |
I3505V |
probably benign |
Het |
Fat3 |
T |
G |
9: 16,286,448 (GRCm39) |
E1025A |
probably damaging |
Het |
Fat4 |
C |
T |
3: 39,011,601 (GRCm39) |
R2234W |
probably damaging |
Het |
Fer1l4 |
G |
T |
2: 155,887,009 (GRCm39) |
F634L |
probably damaging |
Het |
Fetub |
G |
A |
16: 22,756,624 (GRCm39) |
V162I |
probably benign |
Het |
Fgd4 |
T |
C |
16: 16,302,402 (GRCm39) |
Q51R |
probably benign |
Het |
Fgfr2 |
T |
C |
7: 129,800,175 (GRCm39) |
H140R |
probably benign |
Het |
Flt3 |
T |
A |
5: 147,293,185 (GRCm39) |
|
probably null |
Het |
Gabrb1 |
A |
G |
5: 72,294,121 (GRCm39) |
N465S |
probably damaging |
Het |
Gapdhs |
T |
C |
7: 30,432,691 (GRCm39) |
I206V |
probably benign |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Glp2r |
T |
C |
11: 67,637,529 (GRCm39) |
|
probably null |
Het |
Gm4956 |
T |
A |
1: 21,368,306 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2a1l |
A |
T |
17: 89,022,350 (GRCm39) |
D447V |
probably damaging |
Het |
Hsd3b5 |
A |
G |
3: 98,526,379 (GRCm39) |
W356R |
probably damaging |
Het |
Idh2 |
A |
T |
7: 79,745,847 (GRCm39) |
V335D |
probably damaging |
Het |
Isyna1 |
T |
C |
8: 71,048,146 (GRCm39) |
I184T |
probably damaging |
Het |
Kcnh2 |
A |
G |
5: 24,536,085 (GRCm39) |
S320P |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Kpna6 |
A |
G |
4: 129,541,825 (GRCm39) |
F524S |
probably damaging |
Het |
Lap3 |
A |
T |
5: 45,663,539 (GRCm39) |
M338L |
probably benign |
Het |
Lins1 |
T |
C |
7: 66,359,198 (GRCm39) |
|
probably benign |
Het |
Llgl1 |
C |
T |
11: 60,600,394 (GRCm39) |
P581L |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,639,126 (GRCm39) |
D385G |
probably benign |
Het |
Maf |
T |
C |
8: 116,433,532 (GRCm39) |
D24G |
unknown |
Het |
Nell1 |
T |
C |
7: 49,712,386 (GRCm39) |
S69P |
probably benign |
Het |
Nkapd1 |
G |
T |
9: 50,518,809 (GRCm39) |
Q268K |
probably benign |
Het |
Or13p4 |
C |
T |
4: 118,547,089 (GRCm39) |
V187I |
possibly damaging |
Het |
Or2h1 |
C |
T |
17: 37,404,484 (GRCm39) |
G94E |
probably damaging |
Het |
Or2j6 |
T |
A |
7: 139,980,792 (GRCm39) |
M56L |
probably benign |
Het |
Or51af1 |
T |
C |
7: 103,141,458 (GRCm39) |
D209G |
probably damaging |
Het |
Or5an10 |
A |
G |
19: 12,276,260 (GRCm39) |
S79P |
possibly damaging |
Het |
Or8g54 |
T |
C |
9: 39,707,160 (GRCm39) |
M163T |
possibly damaging |
Het |
Oxld1 |
T |
C |
11: 120,347,862 (GRCm39) |
T112A |
probably benign |
Het |
Parp14 |
T |
C |
16: 35,666,403 (GRCm39) |
N1210S |
probably benign |
Het |
Pcdhb10 |
C |
A |
18: 37,545,887 (GRCm39) |
T321K |
probably benign |
Het |
Pcdhga1 |
T |
A |
18: 37,795,659 (GRCm39) |
I221K |
probably benign |
Het |
Pcdhga9 |
T |
A |
18: 37,871,185 (GRCm39) |
V338E |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,108,325 (GRCm39) |
S1231P |
probably damaging |
Het |
Pde6c |
A |
T |
19: 38,140,013 (GRCm39) |
L325F |
probably damaging |
Het |
Pnpla7 |
T |
A |
2: 24,887,276 (GRCm39) |
|
probably null |
Het |
Pparg |
T |
A |
6: 115,467,071 (GRCm39) |
V478E |
probably damaging |
Het |
Ppib |
T |
C |
9: 65,967,672 (GRCm39) |
V42A |
probably benign |
Het |
Ppox |
T |
C |
1: 171,105,166 (GRCm39) |
M341V |
probably damaging |
Het |
Proc |
T |
C |
18: 32,258,166 (GRCm39) |
K260E |
possibly damaging |
Het |
Ptpro |
C |
T |
6: 137,369,763 (GRCm39) |
P525L |
probably damaging |
Het |
Rnf14 |
C |
A |
18: 38,441,435 (GRCm39) |
A275E |
probably damaging |
Het |
Scnn1b |
C |
T |
7: 121,511,231 (GRCm39) |
P306L |
probably damaging |
Het |
Sec14l5 |
A |
G |
16: 4,994,364 (GRCm39) |
E386G |
probably damaging |
Het |
Sftpa1 |
T |
A |
14: 40,854,509 (GRCm39) |
I32N |
probably damaging |
Het |
Slc26a5 |
A |
G |
5: 22,025,384 (GRCm39) |
I408T |
probably damaging |
Het |
Slc7a13 |
A |
G |
4: 19,841,467 (GRCm39) |
Y438C |
probably damaging |
Het |
Spire1 |
T |
C |
18: 67,652,384 (GRCm39) |
E231G |
possibly damaging |
Het |
Stab1 |
T |
A |
14: 30,873,528 (GRCm39) |
I1014F |
probably benign |
Het |
Steap2 |
T |
C |
5: 5,727,651 (GRCm39) |
Y228C |
probably damaging |
Het |
Tmem131l |
T |
C |
3: 83,806,546 (GRCm39) |
T1487A |
probably benign |
Het |
Tmem171 |
A |
G |
13: 98,828,803 (GRCm39) |
F116L |
possibly damaging |
Het |
Tmem215 |
T |
C |
4: 40,474,520 (GRCm39) |
V199A |
probably damaging |
Het |
Tmem45a |
T |
C |
16: 56,642,652 (GRCm39) |
N173S |
possibly damaging |
Het |
Uqcrc2 |
C |
T |
7: 120,242,301 (GRCm39) |
R148C |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,620,116 (GRCm39) |
K617E |
probably damaging |
Het |
Xrcc6 |
T |
C |
15: 81,924,013 (GRCm39) |
L229P |
probably damaging |
Het |
Yju2 |
A |
G |
17: 56,271,149 (GRCm39) |
D97G |
possibly damaging |
Het |
Zfp184 |
A |
G |
13: 22,133,891 (GRCm39) |
D46G |
probably damaging |
Het |
Zfp790 |
T |
A |
7: 29,528,916 (GRCm39) |
C534S |
possibly damaging |
Het |
Zfp990 |
A |
T |
4: 145,263,407 (GRCm39) |
N135I |
probably damaging |
Het |
|
Other mutations in Pcdhb8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Pcdhb8
|
APN |
18 |
37,488,526 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00574:Pcdhb8
|
APN |
18 |
37,489,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00960:Pcdhb8
|
APN |
18 |
37,489,026 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01103:Pcdhb8
|
APN |
18 |
37,490,253 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01330:Pcdhb8
|
APN |
18 |
37,490,631 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01413:Pcdhb8
|
APN |
18 |
37,489,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01418:Pcdhb8
|
APN |
18 |
37,489,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Pcdhb8
|
APN |
18 |
37,489,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02212:Pcdhb8
|
APN |
18 |
37,489,465 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02582:Pcdhb8
|
APN |
18 |
37,488,427 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02607:Pcdhb8
|
APN |
18 |
37,490,634 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02882:Pcdhb8
|
APN |
18 |
37,489,276 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03005:Pcdhb8
|
APN |
18 |
37,490,587 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Pcdhb8
|
APN |
18 |
37,490,299 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4468001:Pcdhb8
|
UTSW |
18 |
37,489,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0104:Pcdhb8
|
UTSW |
18 |
37,488,718 (GRCm39) |
missense |
probably benign |
0.01 |
R0490:Pcdhb8
|
UTSW |
18 |
37,489,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Pcdhb8
|
UTSW |
18 |
37,490,100 (GRCm39) |
missense |
probably benign |
0.02 |
R1168:Pcdhb8
|
UTSW |
18 |
37,489,780 (GRCm39) |
missense |
probably benign |
|
R1189:Pcdhb8
|
UTSW |
18 |
37,489,620 (GRCm39) |
nonsense |
probably null |
|
R1232:Pcdhb8
|
UTSW |
18 |
37,488,828 (GRCm39) |
missense |
probably benign |
0.28 |
R1503:Pcdhb8
|
UTSW |
18 |
37,489,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1576:Pcdhb8
|
UTSW |
18 |
37,489,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Pcdhb8
|
UTSW |
18 |
37,488,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Pcdhb8
|
UTSW |
18 |
37,489,015 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1909:Pcdhb8
|
UTSW |
18 |
37,489,015 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2215:Pcdhb8
|
UTSW |
18 |
37,490,127 (GRCm39) |
missense |
probably damaging |
0.98 |
R3080:Pcdhb8
|
UTSW |
18 |
37,489,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Pcdhb8
|
UTSW |
18 |
37,489,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Pcdhb8
|
UTSW |
18 |
37,488,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Pcdhb8
|
UTSW |
18 |
37,489,771 (GRCm39) |
missense |
probably benign |
0.43 |
R4879:Pcdhb8
|
UTSW |
18 |
37,489,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Pcdhb8
|
UTSW |
18 |
37,489,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5416:Pcdhb8
|
UTSW |
18 |
37,490,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R5774:Pcdhb8
|
UTSW |
18 |
37,489,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Pcdhb8
|
UTSW |
18 |
37,490,537 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5935:Pcdhb8
|
UTSW |
18 |
37,489,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Pcdhb8
|
UTSW |
18 |
37,489,279 (GRCm39) |
missense |
probably benign |
|
R6228:Pcdhb8
|
UTSW |
18 |
37,490,037 (GRCm39) |
missense |
probably benign |
0.05 |
R6245:Pcdhb8
|
UTSW |
18 |
37,490,222 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6397:Pcdhb8
|
UTSW |
18 |
37,488,516 (GRCm39) |
nonsense |
probably null |
|
R7469:Pcdhb8
|
UTSW |
18 |
37,489,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R7632:Pcdhb8
|
UTSW |
18 |
37,488,648 (GRCm39) |
missense |
probably benign |
0.00 |
R8323:Pcdhb8
|
UTSW |
18 |
37,488,476 (GRCm39) |
missense |
probably benign |
0.23 |
R8735:Pcdhb8
|
UTSW |
18 |
37,489,975 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8841:Pcdhb8
|
UTSW |
18 |
37,488,699 (GRCm39) |
missense |
probably benign |
0.26 |
R8856:Pcdhb8
|
UTSW |
18 |
37,489,776 (GRCm39) |
missense |
probably benign |
0.01 |
R9020:Pcdhb8
|
UTSW |
18 |
37,489,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R9055:Pcdhb8
|
UTSW |
18 |
37,490,585 (GRCm39) |
nonsense |
probably null |
|
R9077:Pcdhb8
|
UTSW |
18 |
37,489,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R9387:Pcdhb8
|
UTSW |
18 |
37,488,751 (GRCm39) |
missense |
probably benign |
|
|