Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130230L23Rik |
A |
G |
5: 66,145,811 (GRCm39) |
F100S |
unknown |
Het |
Abca3 |
A |
G |
17: 24,596,714 (GRCm39) |
Y389C |
possibly damaging |
Het |
Acrbp |
G |
T |
6: 125,031,773 (GRCm39) |
|
probably null |
Het |
Adam21 |
G |
A |
12: 81,605,983 (GRCm39) |
T593I |
possibly damaging |
Het |
Adipor1 |
T |
A |
1: 134,353,698 (GRCm39) |
M161K |
probably benign |
Het |
Agrp |
A |
T |
8: 106,293,821 (GRCm39) |
N48K |
probably benign |
Het |
Asprv1 |
A |
T |
6: 86,605,900 (GRCm39) |
M249L |
probably damaging |
Het |
Begain |
A |
G |
12: 108,999,278 (GRCm39) |
Y703H |
probably damaging |
Het |
Bspry |
T |
A |
4: 62,414,226 (GRCm39) |
|
probably benign |
Het |
Cct8l1 |
T |
G |
5: 25,721,836 (GRCm39) |
S184A |
probably benign |
Het |
Cdyl2 |
C |
T |
8: 117,306,025 (GRCm39) |
R412Q |
possibly damaging |
Het |
Celf6 |
T |
C |
9: 59,510,808 (GRCm39) |
S205P |
probably damaging |
Het |
Cltc |
G |
A |
11: 86,595,811 (GRCm39) |
A1263V |
possibly damaging |
Het |
Cltc |
C |
A |
11: 86,595,812 (GRCm39) |
A1263S |
possibly damaging |
Het |
Ctnnd2 |
T |
A |
15: 30,480,939 (GRCm39) |
F62L |
probably damaging |
Het |
Dlec1 |
T |
A |
9: 118,972,695 (GRCm39) |
C1473S |
probably benign |
Het |
Dmbt1 |
T |
A |
7: 130,694,986 (GRCm39) |
|
probably benign |
Het |
Dnase1 |
G |
A |
16: 3,856,896 (GRCm39) |
V176I |
probably benign |
Het |
Dusp1 |
G |
T |
17: 26,726,032 (GRCm39) |
Y220* |
probably null |
Het |
Enpp3 |
A |
C |
10: 24,667,881 (GRCm39) |
|
probably benign |
Het |
Exosc10 |
T |
C |
4: 148,649,755 (GRCm39) |
L395P |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,677,693 (GRCm39) |
K533R |
probably damaging |
Het |
Gcm2 |
T |
A |
13: 41,258,125 (GRCm39) |
T168S |
possibly damaging |
Het |
Gm9924 |
C |
A |
5: 31,252,491 (GRCm39) |
|
probably benign |
Het |
Ifrd1 |
A |
G |
12: 40,264,092 (GRCm39) |
V101A |
probably benign |
Het |
Iqsec1 |
G |
T |
6: 90,653,859 (GRCm39) |
Q629K |
probably damaging |
Het |
Kcnma1 |
T |
A |
14: 23,576,881 (GRCm39) |
M254L |
probably benign |
Het |
Krit1 |
T |
C |
5: 3,859,733 (GRCm39) |
|
probably benign |
Het |
Letm1 |
T |
C |
5: 33,902,391 (GRCm39) |
K633E |
probably benign |
Het |
Mfsd1 |
A |
G |
3: 67,503,928 (GRCm39) |
I307V |
probably benign |
Het |
Mtrr |
T |
C |
13: 68,712,476 (GRCm39) |
T637A |
probably benign |
Het |
Naxe |
C |
A |
3: 87,964,305 (GRCm39) |
D212Y |
probably damaging |
Het |
Nlk |
A |
T |
11: 78,477,762 (GRCm39) |
V327D |
probably damaging |
Het |
Or2f1b |
A |
G |
6: 42,739,880 (GRCm39) |
K298R |
probably null |
Het |
Or5w11 |
A |
T |
2: 87,459,715 (GRCm39) |
I187F |
probably benign |
Het |
Pdzd8 |
C |
T |
19: 59,289,060 (GRCm39) |
G780D |
probably damaging |
Het |
Prune1 |
T |
C |
3: 95,166,548 (GRCm39) |
|
probably benign |
Het |
Qser1 |
A |
T |
2: 104,618,606 (GRCm39) |
H645Q |
probably damaging |
Het |
Rd3l |
A |
G |
12: 111,945,901 (GRCm39) |
Y193H |
probably benign |
Het |
Reln |
A |
G |
5: 22,114,956 (GRCm39) |
Y3119H |
probably damaging |
Het |
Scel |
C |
T |
14: 103,802,257 (GRCm39) |
A219V |
probably benign |
Het |
Skint11 |
A |
T |
4: 114,101,833 (GRCm39) |
Q91L |
possibly damaging |
Het |
Slc39a10 |
G |
A |
1: 46,857,288 (GRCm39) |
A696V |
probably damaging |
Het |
Slc5a5 |
C |
A |
8: 71,338,764 (GRCm39) |
D516Y |
possibly damaging |
Het |
Slc8b1 |
G |
A |
5: 120,665,928 (GRCm39) |
|
probably null |
Het |
Slc9a3 |
A |
G |
13: 74,311,233 (GRCm39) |
E576G |
possibly damaging |
Het |
Slco1b2 |
A |
T |
6: 141,580,271 (GRCm39) |
|
probably benign |
Het |
Smc5 |
A |
G |
19: 23,209,223 (GRCm39) |
V647A |
probably damaging |
Het |
Snph |
T |
C |
2: 151,436,263 (GRCm39) |
N222D |
possibly damaging |
Het |
Srbd1 |
A |
G |
17: 86,416,659 (GRCm39) |
F500L |
probably benign |
Het |
Stxbp6 |
T |
C |
12: 44,948,806 (GRCm39) |
D101G |
probably damaging |
Het |
Taar7b |
A |
G |
10: 23,875,879 (GRCm39) |
I15V |
probably benign |
Het |
Tdrd12 |
G |
T |
7: 35,200,826 (GRCm39) |
N338K |
probably damaging |
Het |
Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
Tmem219 |
A |
T |
7: 126,495,988 (GRCm39) |
D128E |
probably benign |
Het |
Togaram2 |
A |
G |
17: 71,992,166 (GRCm39) |
T3A |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,724,627 (GRCm39) |
|
probably benign |
Het |
Uchl1 |
C |
A |
5: 66,834,382 (GRCm39) |
C47* |
probably null |
Het |
Unc79 |
T |
G |
12: 102,977,542 (GRCm39) |
S182A |
probably benign |
Het |
Vmn2r1 |
A |
G |
3: 63,989,138 (GRCm39) |
T26A |
probably benign |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Vps54 |
T |
C |
11: 21,256,947 (GRCm39) |
V685A |
probably damaging |
Het |
Zcchc7 |
T |
G |
4: 44,762,250 (GRCm39) |
V126G |
possibly damaging |
Het |
Zmym2 |
A |
G |
14: 57,180,808 (GRCm39) |
T907A |
probably benign |
Het |
|
Other mutations in Cdk13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Cdk13
|
APN |
13 |
17,895,683 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00800:Cdk13
|
APN |
13 |
17,902,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02447:Cdk13
|
APN |
13 |
17,947,001 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02494:Cdk13
|
APN |
13 |
17,913,710 (GRCm39) |
nonsense |
probably null |
|
IGL02542:Cdk13
|
APN |
13 |
17,902,763 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02602:Cdk13
|
APN |
13 |
17,901,745 (GRCm39) |
missense |
probably damaging |
0.99 |
Vortex
|
UTSW |
13 |
17,913,739 (GRCm39) |
missense |
probably damaging |
1.00 |
Whirlpool
|
UTSW |
13 |
17,946,988 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0115:Cdk13
|
UTSW |
13 |
17,894,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R0421:Cdk13
|
UTSW |
13 |
17,937,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R0481:Cdk13
|
UTSW |
13 |
17,894,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R0681:Cdk13
|
UTSW |
13 |
17,895,882 (GRCm39) |
splice site |
probably benign |
|
R1432:Cdk13
|
UTSW |
13 |
17,893,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Cdk13
|
UTSW |
13 |
17,913,748 (GRCm39) |
nonsense |
probably null |
|
R2221:Cdk13
|
UTSW |
13 |
17,894,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R2332:Cdk13
|
UTSW |
13 |
17,893,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R2389:Cdk13
|
UTSW |
13 |
17,926,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4546:Cdk13
|
UTSW |
13 |
17,941,159 (GRCm39) |
missense |
probably damaging |
0.98 |
R4753:Cdk13
|
UTSW |
13 |
17,937,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R4855:Cdk13
|
UTSW |
13 |
17,895,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Cdk13
|
UTSW |
13 |
17,894,319 (GRCm39) |
missense |
probably benign |
|
R4861:Cdk13
|
UTSW |
13 |
17,941,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4861:Cdk13
|
UTSW |
13 |
17,941,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Cdk13
|
UTSW |
13 |
17,894,319 (GRCm39) |
missense |
probably benign |
|
R4909:Cdk13
|
UTSW |
13 |
17,946,988 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5152:Cdk13
|
UTSW |
13 |
17,893,110 (GRCm39) |
missense |
probably benign |
0.13 |
R5308:Cdk13
|
UTSW |
13 |
17,946,898 (GRCm39) |
missense |
probably damaging |
0.98 |
R5350:Cdk13
|
UTSW |
13 |
17,978,515 (GRCm39) |
unclassified |
probably benign |
|
R5412:Cdk13
|
UTSW |
13 |
17,941,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R5493:Cdk13
|
UTSW |
13 |
17,978,147 (GRCm39) |
unclassified |
probably benign |
|
R5719:Cdk13
|
UTSW |
13 |
17,894,240 (GRCm39) |
missense |
probably damaging |
0.98 |
R6052:Cdk13
|
UTSW |
13 |
17,895,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Cdk13
|
UTSW |
13 |
17,926,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6415:Cdk13
|
UTSW |
13 |
17,913,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7665:Cdk13
|
UTSW |
13 |
17,947,138 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7666:Cdk13
|
UTSW |
13 |
17,947,161 (GRCm39) |
start gained |
probably benign |
|
R7764:Cdk13
|
UTSW |
13 |
17,895,890 (GRCm39) |
splice site |
probably null |
|
R8100:Cdk13
|
UTSW |
13 |
17,978,101 (GRCm39) |
missense |
unknown |
|
R9089:Cdk13
|
UTSW |
13 |
17,978,444 (GRCm39) |
missense |
unknown |
|
R9224:Cdk13
|
UTSW |
13 |
17,941,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Cdk13
|
UTSW |
13 |
17,902,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Cdk13
|
UTSW |
13 |
17,902,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Cdk13
|
UTSW |
13 |
17,926,440 (GRCm39) |
missense |
|
|
R9685:Cdk13
|
UTSW |
13 |
17,978,542 (GRCm39) |
missense |
unknown |
|
RF009:Cdk13
|
UTSW |
13 |
17,978,329 (GRCm39) |
missense |
unknown |
|
|