Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,231,357 (GRCm39) |
S1038R |
probably benign |
Het |
Aar2 |
T |
C |
2: 156,392,745 (GRCm39) |
F45L |
probably damaging |
Het |
Abcg2 |
A |
G |
6: 58,641,533 (GRCm39) |
Y122C |
probably damaging |
Het |
Arfgef1 |
A |
T |
1: 10,243,427 (GRCm39) |
W1041R |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,873,373 (GRCm39) |
N52S |
probably benign |
Het |
Asrgl1 |
T |
A |
19: 9,093,974 (GRCm39) |
T185S |
probably damaging |
Het |
Astl |
T |
A |
2: 127,192,146 (GRCm39) |
S234T |
probably damaging |
Het |
Atp5mf |
T |
C |
5: 145,120,656 (GRCm39) |
Y87C |
probably damaging |
Het |
Atxn7l1 |
A |
T |
12: 33,396,062 (GRCm39) |
R264W |
probably damaging |
Het |
Axin2 |
T |
C |
11: 108,840,180 (GRCm39) |
Y828H |
probably damaging |
Het |
Bnipl |
T |
C |
3: 95,153,140 (GRCm39) |
D145G |
possibly damaging |
Het |
C8b |
A |
T |
4: 104,640,191 (GRCm39) |
M165L |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,541,944 (GRCm39) |
L87P |
possibly damaging |
Het |
Cnot1 |
T |
C |
8: 96,455,772 (GRCm39) |
E1995G |
probably damaging |
Het |
Csf2rb2 |
G |
A |
15: 78,169,196 (GRCm39) |
A653V |
probably benign |
Het |
Cutc |
A |
G |
19: 43,756,699 (GRCm39) |
N264D |
probably benign |
Het |
Cxcr4 |
C |
T |
1: 128,516,884 (GRCm39) |
W259* |
probably null |
Het |
Dnah8 |
T |
C |
17: 30,980,104 (GRCm39) |
|
probably null |
Het |
Dsp |
T |
C |
13: 38,367,937 (GRCm39) |
I652T |
probably benign |
Het |
Dstyk |
A |
T |
1: 132,381,859 (GRCm39) |
M538L |
probably benign |
Het |
Eppk1 |
T |
A |
15: 75,993,219 (GRCm39) |
I1221F |
probably benign |
Het |
Ern2 |
T |
A |
7: 121,769,485 (GRCm39) |
Y847F |
probably damaging |
Het |
Exosc7 |
T |
A |
9: 122,959,990 (GRCm39) |
V197D |
probably damaging |
Het |
Gabra1 |
T |
C |
11: 42,024,352 (GRCm39) |
Y441C |
probably damaging |
Het |
Garem1 |
G |
A |
18: 21,262,985 (GRCm39) |
P610S |
possibly damaging |
Het |
Garem2 |
T |
A |
5: 30,319,330 (GRCm39) |
V264E |
probably damaging |
Het |
Gata2 |
G |
A |
6: 88,177,272 (GRCm39) |
G101S |
probably benign |
Het |
Gcnt4 |
A |
G |
13: 97,083,429 (GRCm39) |
T242A |
probably benign |
Het |
Ghitm |
A |
C |
14: 36,852,719 (GRCm39) |
Y120* |
probably null |
Het |
Gimap7 |
A |
G |
6: 48,700,470 (GRCm39) |
S19G |
probably damaging |
Het |
Gm5475 |
G |
A |
15: 100,324,881 (GRCm39) |
G103E |
unknown |
Het |
Gstcd |
A |
T |
3: 132,790,357 (GRCm39) |
C137S |
probably damaging |
Het |
Gtf2b |
AATCATC |
AATC |
3: 142,477,178 (GRCm39) |
|
probably benign |
Het |
Hfm1 |
T |
C |
5: 107,065,346 (GRCm39) |
D111G |
probably benign |
Het |
Ighg2b |
A |
G |
12: 113,270,304 (GRCm39) |
I238T |
|
Het |
Il2ra |
A |
C |
2: 11,685,161 (GRCm39) |
M166L |
probably benign |
Het |
Itga1 |
A |
T |
13: 115,171,820 (GRCm39) |
L95* |
probably null |
Het |
Itpr3 |
A |
G |
17: 27,308,915 (GRCm39) |
T373A |
probably benign |
Het |
Klhl28 |
A |
G |
12: 64,996,871 (GRCm39) |
V490A |
probably damaging |
Het |
Kntc1 |
A |
T |
5: 123,898,706 (GRCm39) |
N200I |
possibly damaging |
Het |
L3mbtl4 |
A |
G |
17: 68,766,794 (GRCm39) |
K167R |
probably benign |
Het |
Lgals1 |
A |
T |
15: 78,813,930 (GRCm39) |
T63S |
probably benign |
Het |
Lnpep |
C |
A |
17: 17,795,596 (GRCm39) |
C305F |
probably damaging |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Mcmbp |
A |
G |
7: 128,311,583 (GRCm39) |
I310T |
possibly damaging |
Het |
Mical2 |
G |
A |
7: 111,945,996 (GRCm39) |
R986H |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,415,330 (GRCm39) |
S2759C |
possibly damaging |
Het |
Myh7 |
A |
G |
14: 55,229,384 (GRCm39) |
V138A |
possibly damaging |
Het |
Ncr1 |
T |
G |
7: 4,344,300 (GRCm39) |
|
probably null |
Het |
Ndufa10 |
A |
T |
1: 92,397,610 (GRCm39) |
D145E |
possibly damaging |
Het |
Neo1 |
T |
A |
9: 58,801,307 (GRCm39) |
|
probably null |
Het |
Ninl |
A |
T |
2: 150,791,701 (GRCm39) |
S941T |
probably benign |
Het |
Nrm |
T |
A |
17: 36,172,411 (GRCm39) |
|
probably null |
Het |
Nup214 |
T |
C |
2: 31,907,227 (GRCm39) |
V1018A |
possibly damaging |
Het |
Odf1 |
A |
G |
15: 38,219,716 (GRCm39) |
I15V |
probably benign |
Het |
Or10al2 |
T |
A |
17: 37,983,059 (GRCm39) |
N48K |
probably damaging |
Het |
Or10j7 |
C |
T |
1: 173,011,458 (GRCm39) |
R181H |
probably benign |
Het |
Or1e1c |
A |
T |
11: 73,265,710 (GRCm39) |
N48I |
probably damaging |
Het |
Or4b1d |
T |
A |
2: 89,969,004 (GRCm39) |
T160S |
probably benign |
Het |
Or52e18 |
A |
T |
7: 104,609,657 (GRCm39) |
I94N |
probably damaging |
Het |
Or5m10 |
C |
T |
2: 85,717,338 (GRCm39) |
H65Y |
probably damaging |
Het |
Or5p66 |
A |
T |
7: 107,885,898 (GRCm39) |
V145D |
probably benign |
Het |
Or7g32 |
C |
A |
9: 19,389,382 (GRCm39) |
D55Y |
probably benign |
Het |
Osgin2 |
A |
T |
4: 15,998,957 (GRCm39) |
Y222N |
probably damaging |
Het |
Pcdhga10 |
T |
C |
18: 37,882,363 (GRCm39) |
V708A |
probably benign |
Het |
Pfn3 |
T |
C |
13: 55,562,900 (GRCm39) |
D27G |
possibly damaging |
Het |
Plch2 |
A |
G |
4: 155,095,322 (GRCm39) |
|
probably null |
Het |
Plin2 |
C |
A |
4: 86,576,914 (GRCm39) |
Q270H |
probably damaging |
Het |
Polk |
A |
G |
13: 96,630,403 (GRCm39) |
F386S |
probably damaging |
Het |
Prkar1a |
G |
A |
11: 109,556,778 (GRCm39) |
G286E |
probably damaging |
Het |
Prodh |
A |
T |
16: 17,898,049 (GRCm39) |
L276Q |
probably damaging |
Het |
Ranbp10 |
T |
C |
8: 106,513,306 (GRCm39) |
N202S |
probably damaging |
Het |
Rapgef6 |
C |
A |
11: 54,540,097 (GRCm39) |
T724K |
probably benign |
Het |
Rnf144a |
T |
A |
12: 26,377,574 (GRCm39) |
K56N |
probably benign |
Het |
Rpa1 |
T |
A |
11: 75,203,938 (GRCm39) |
K303I |
probably damaging |
Het |
Slc16a9 |
A |
C |
10: 70,118,340 (GRCm39) |
N220H |
possibly damaging |
Het |
Slc28a3 |
T |
C |
13: 58,724,664 (GRCm39) |
I197V |
probably benign |
Het |
Slc35d1 |
A |
T |
4: 103,071,946 (GRCm39) |
F19I |
|
Het |
Sohlh2 |
A |
T |
3: 55,099,721 (GRCm39) |
E164D |
probably damaging |
Het |
Sord |
A |
T |
2: 122,093,765 (GRCm39) |
K295* |
probably null |
Het |
Spata31d1b |
A |
G |
13: 59,860,196 (GRCm39) |
Y23C |
probably benign |
Het |
Stard9 |
T |
A |
2: 120,510,417 (GRCm39) |
Y333N |
probably damaging |
Het |
Tas2r107 |
A |
G |
6: 131,636,753 (GRCm39) |
F99L |
probably damaging |
Het |
Thap12 |
C |
T |
7: 98,352,592 (GRCm39) |
|
probably benign |
Het |
Tmprss9 |
A |
T |
10: 80,730,993 (GRCm39) |
T840S |
probably benign |
Het |
Trim16 |
T |
A |
11: 62,720,026 (GRCm39) |
|
probably null |
Het |
Ttc16 |
C |
T |
2: 32,664,805 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Unc80 |
A |
T |
1: 66,651,371 (GRCm39) |
Y1572F |
possibly damaging |
Het |
Usp42 |
G |
T |
5: 143,706,060 (GRCm39) |
A320D |
possibly damaging |
Het |
Vmn2r94 |
T |
C |
17: 18,464,038 (GRCm39) |
T751A |
probably damaging |
Het |
Zbtb41 |
C |
T |
1: 139,368,084 (GRCm39) |
L591F |
probably damaging |
Het |
Zdhhc5 |
T |
A |
2: 84,524,662 (GRCm39) |
E219D |
probably damaging |
Het |
Zfp248 |
A |
T |
6: 118,406,012 (GRCm39) |
F526I |
probably damaging |
Het |
Zfp322a |
T |
C |
13: 23,540,558 (GRCm39) |
K395E |
possibly damaging |
Het |
Zfp423 |
G |
A |
8: 88,506,877 (GRCm39) |
P1156S |
probably benign |
Het |
Zfp644 |
T |
C |
5: 106,786,131 (GRCm39) |
T139A |
possibly damaging |
Het |
|
Other mutations in Cdk17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Cdk17
|
APN |
10 |
93,062,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00781:Cdk17
|
APN |
10 |
93,068,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01622:Cdk17
|
APN |
10 |
93,074,824 (GRCm39) |
unclassified |
probably benign |
|
IGL01623:Cdk17
|
APN |
10 |
93,074,824 (GRCm39) |
unclassified |
probably benign |
|
IGL01732:Cdk17
|
APN |
10 |
93,053,907 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01768:Cdk17
|
APN |
10 |
93,044,123 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02942:Cdk17
|
APN |
10 |
93,074,830 (GRCm39) |
missense |
probably benign |
|
IGL03308:Cdk17
|
APN |
10 |
93,057,506 (GRCm39) |
critical splice donor site |
probably null |
|
delude
|
UTSW |
10 |
93,053,823 (GRCm39) |
splice site |
probably null |
|
Imagine
|
UTSW |
10 |
93,068,277 (GRCm39) |
missense |
probably damaging |
1.00 |
Magician
|
UTSW |
10 |
93,064,565 (GRCm39) |
missense |
probably damaging |
1.00 |
prestidigitator
|
UTSW |
10 |
93,061,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4436_Cdk17_536
|
UTSW |
10 |
93,047,758 (GRCm39) |
splice site |
probably null |
|
R0039:Cdk17
|
UTSW |
10 |
93,062,640 (GRCm39) |
splice site |
probably benign |
|
R0398:Cdk17
|
UTSW |
10 |
93,073,702 (GRCm39) |
missense |
probably benign |
0.01 |
R0432:Cdk17
|
UTSW |
10 |
93,073,652 (GRCm39) |
unclassified |
probably benign |
|
R0609:Cdk17
|
UTSW |
10 |
93,052,334 (GRCm39) |
missense |
probably benign |
|
R0781:Cdk17
|
UTSW |
10 |
93,074,895 (GRCm39) |
nonsense |
probably null |
|
R1110:Cdk17
|
UTSW |
10 |
93,074,895 (GRCm39) |
nonsense |
probably null |
|
R1604:Cdk17
|
UTSW |
10 |
93,068,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Cdk17
|
UTSW |
10 |
93,057,492 (GRCm39) |
missense |
probably benign |
0.21 |
R1758:Cdk17
|
UTSW |
10 |
93,044,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R1797:Cdk17
|
UTSW |
10 |
93,044,114 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1864:Cdk17
|
UTSW |
10 |
93,061,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Cdk17
|
UTSW |
10 |
93,061,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Cdk17
|
UTSW |
10 |
93,064,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Cdk17
|
UTSW |
10 |
93,053,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R2207:Cdk17
|
UTSW |
10 |
93,064,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Cdk17
|
UTSW |
10 |
93,047,820 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2262:Cdk17
|
UTSW |
10 |
93,047,820 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3737:Cdk17
|
UTSW |
10 |
93,057,506 (GRCm39) |
critical splice donor site |
probably null |
|
R3883:Cdk17
|
UTSW |
10 |
93,047,939 (GRCm39) |
critical splice donor site |
probably null |
|
R4436:Cdk17
|
UTSW |
10 |
93,047,758 (GRCm39) |
splice site |
probably null |
|
R5372:Cdk17
|
UTSW |
10 |
93,061,901 (GRCm39) |
missense |
probably benign |
0.03 |
R5444:Cdk17
|
UTSW |
10 |
93,053,823 (GRCm39) |
splice site |
probably null |
|
R5488:Cdk17
|
UTSW |
10 |
93,068,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Cdk17
|
UTSW |
10 |
93,068,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R5815:Cdk17
|
UTSW |
10 |
93,064,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Cdk17
|
UTSW |
10 |
93,071,331 (GRCm39) |
missense |
probably benign |
0.26 |
R6209:Cdk17
|
UTSW |
10 |
93,044,093 (GRCm39) |
missense |
probably benign |
0.05 |
R6384:Cdk17
|
UTSW |
10 |
93,047,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R6627:Cdk17
|
UTSW |
10 |
93,068,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Cdk17
|
UTSW |
10 |
93,064,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Cdk17
|
UTSW |
10 |
93,068,343 (GRCm39) |
missense |
probably benign |
0.07 |
R8096:Cdk17
|
UTSW |
10 |
93,052,229 (GRCm39) |
missense |
probably damaging |
0.98 |
R8118:Cdk17
|
UTSW |
10 |
93,052,252 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8459:Cdk17
|
UTSW |
10 |
93,068,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R8670:Cdk17
|
UTSW |
10 |
93,061,958 (GRCm39) |
nonsense |
probably null |
|
R8722:Cdk17
|
UTSW |
10 |
93,064,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R8829:Cdk17
|
UTSW |
10 |
93,042,920 (GRCm39) |
unclassified |
probably benign |
|
R9077:Cdk17
|
UTSW |
10 |
93,068,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Cdk17
|
UTSW |
10 |
93,044,066 (GRCm39) |
missense |
probably damaging |
0.98 |
|