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 |
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 |
Pcdhb8 |
C |
T |
18: 37,489,059 (GRCm39) |
L246F |
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 Cep162 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Cep162
|
APN |
9 |
87,109,220 (GRCm39) |
missense |
probably benign |
0.24 |
IGL00584:Cep162
|
APN |
9 |
87,103,143 (GRCm39) |
splice site |
probably benign |
|
IGL01387:Cep162
|
APN |
9 |
87,093,864 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01862:Cep162
|
APN |
9 |
87,135,986 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02304:Cep162
|
APN |
9 |
87,109,200 (GRCm39) |
splice site |
probably benign |
|
IGL02558:Cep162
|
APN |
9 |
87,107,779 (GRCm39) |
missense |
probably benign |
|
IGL02558:Cep162
|
APN |
9 |
87,107,786 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02602:Cep162
|
APN |
9 |
87,128,206 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02636:Cep162
|
APN |
9 |
87,130,432 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02680:Cep162
|
APN |
9 |
87,128,797 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03195:Cep162
|
APN |
9 |
87,107,839 (GRCm39) |
missense |
probably benign |
0.00 |
circus
|
UTSW |
9 |
87,088,915 (GRCm39) |
missense |
probably damaging |
1.00 |
moscow
|
UTSW |
9 |
87,075,750 (GRCm39) |
missense |
probably damaging |
1.00 |
smiley
|
UTSW |
9 |
87,099,134 (GRCm39) |
nonsense |
probably null |
|
PIT4378001:Cep162
|
UTSW |
9 |
87,099,198 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4431001:Cep162
|
UTSW |
9 |
87,126,398 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4434001:Cep162
|
UTSW |
9 |
87,075,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cep162
|
UTSW |
9 |
87,119,878 (GRCm39) |
splice site |
probably benign |
|
R0218:Cep162
|
UTSW |
9 |
87,093,862 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0366:Cep162
|
UTSW |
9 |
87,102,537 (GRCm39) |
missense |
probably damaging |
0.96 |
R0468:Cep162
|
UTSW |
9 |
87,075,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0764:Cep162
|
UTSW |
9 |
87,083,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Cep162
|
UTSW |
9 |
87,103,255 (GRCm39) |
missense |
probably benign |
|
R1614:Cep162
|
UTSW |
9 |
87,094,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Cep162
|
UTSW |
9 |
87,085,736 (GRCm39) |
missense |
probably benign |
0.23 |
R1831:Cep162
|
UTSW |
9 |
87,088,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Cep162
|
UTSW |
9 |
87,086,133 (GRCm39) |
missense |
probably benign |
0.06 |
R1941:Cep162
|
UTSW |
9 |
87,082,048 (GRCm39) |
missense |
probably benign |
0.14 |
R2228:Cep162
|
UTSW |
9 |
87,126,384 (GRCm39) |
missense |
probably benign |
0.05 |
R2256:Cep162
|
UTSW |
9 |
87,088,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Cep162
|
UTSW |
9 |
87,088,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R2936:Cep162
|
UTSW |
9 |
87,109,467 (GRCm39) |
missense |
probably benign |
|
R3005:Cep162
|
UTSW |
9 |
87,114,113 (GRCm39) |
missense |
probably benign |
0.00 |
R3508:Cep162
|
UTSW |
9 |
87,114,030 (GRCm39) |
critical splice donor site |
probably null |
|
R3689:Cep162
|
UTSW |
9 |
87,107,747 (GRCm39) |
nonsense |
probably null |
|
R3743:Cep162
|
UTSW |
9 |
87,099,230 (GRCm39) |
splice site |
probably benign |
|
R4118:Cep162
|
UTSW |
9 |
87,086,229 (GRCm39) |
missense |
probably benign |
0.30 |
R4380:Cep162
|
UTSW |
9 |
87,082,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R4450:Cep162
|
UTSW |
9 |
87,107,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R4540:Cep162
|
UTSW |
9 |
87,094,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4598:Cep162
|
UTSW |
9 |
87,085,848 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4700:Cep162
|
UTSW |
9 |
87,088,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Cep162
|
UTSW |
9 |
87,088,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Cep162
|
UTSW |
9 |
87,109,290 (GRCm39) |
missense |
probably benign |
0.00 |
R5579:Cep162
|
UTSW |
9 |
87,085,724 (GRCm39) |
missense |
probably benign |
0.26 |
R5859:Cep162
|
UTSW |
9 |
87,086,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Cep162
|
UTSW |
9 |
87,085,763 (GRCm39) |
missense |
probably benign |
|
R6143:Cep162
|
UTSW |
9 |
87,094,904 (GRCm39) |
critical splice donor site |
probably null |
|
R6422:Cep162
|
UTSW |
9 |
87,114,069 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6517:Cep162
|
UTSW |
9 |
87,104,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R6576:Cep162
|
UTSW |
9 |
87,099,198 (GRCm39) |
missense |
probably benign |
0.01 |
R6782:Cep162
|
UTSW |
9 |
87,093,737 (GRCm39) |
missense |
probably benign |
0.07 |
R6867:Cep162
|
UTSW |
9 |
87,099,134 (GRCm39) |
nonsense |
probably null |
|
R7293:Cep162
|
UTSW |
9 |
87,085,836 (GRCm39) |
missense |
probably benign |
0.01 |
R7355:Cep162
|
UTSW |
9 |
87,136,008 (GRCm39) |
nonsense |
probably null |
|
R7391:Cep162
|
UTSW |
9 |
87,130,547 (GRCm39) |
nonsense |
probably null |
|
R7426:Cep162
|
UTSW |
9 |
87,074,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Cep162
|
UTSW |
9 |
87,086,250 (GRCm39) |
missense |
probably benign |
0.40 |
R7710:Cep162
|
UTSW |
9 |
87,114,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7841:Cep162
|
UTSW |
9 |
87,126,369 (GRCm39) |
missense |
probably benign |
0.00 |
R7949:Cep162
|
UTSW |
9 |
87,088,901 (GRCm39) |
missense |
probably benign |
0.04 |
R8351:Cep162
|
UTSW |
9 |
87,074,903 (GRCm39) |
nonsense |
probably null |
|
R8451:Cep162
|
UTSW |
9 |
87,074,903 (GRCm39) |
nonsense |
probably null |
|
R8552:Cep162
|
UTSW |
9 |
87,126,361 (GRCm39) |
missense |
probably benign |
0.34 |
R8755:Cep162
|
UTSW |
9 |
87,114,064 (GRCm39) |
missense |
probably benign |
0.02 |
R8762:Cep162
|
UTSW |
9 |
87,109,314 (GRCm39) |
missense |
probably benign |
0.00 |
R9640:Cep162
|
UTSW |
9 |
87,126,352 (GRCm39) |
missense |
probably benign |
0.06 |
X0063:Cep162
|
UTSW |
9 |
87,104,095 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Cep162
|
UTSW |
9 |
87,082,033 (GRCm39) |
critical splice donor site |
probably null |
|
|