Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
A |
3: 137,775,751 (GRCm39) |
Q1647K |
possibly damaging |
Het |
Abcf3 |
A |
G |
16: 20,369,326 (GRCm39) |
E236G |
probably damaging |
Het |
Adamts17 |
A |
G |
7: 66,654,218 (GRCm39) |
T483A |
probably damaging |
Het |
Ankrd26 |
G |
T |
6: 118,517,426 (GRCm39) |
P465Q |
probably null |
Het |
Babam2 |
C |
T |
5: 31,859,391 (GRCm39) |
|
probably benign |
Het |
Bpifb1 |
T |
A |
2: 154,058,200 (GRCm39) |
|
probably benign |
Het |
Ccnb1ip1 |
T |
A |
14: 51,031,122 (GRCm39) |
T64S |
possibly damaging |
Het |
Cdhr3 |
A |
G |
12: 33,136,102 (GRCm39) |
V46A |
probably damaging |
Het |
Cep170 |
A |
T |
1: 176,584,254 (GRCm39) |
D708E |
probably benign |
Het |
Cpsf6 |
A |
T |
10: 117,197,273 (GRCm39) |
|
probably benign |
Het |
Dgka |
A |
T |
10: 128,572,528 (GRCm39) |
F42I |
probably benign |
Het |
Dip2a |
A |
T |
10: 76,112,491 (GRCm39) |
V1059E |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dock4 |
T |
A |
12: 40,496,364 (GRCm39) |
I3K |
probably benign |
Het |
Dsc2 |
A |
T |
18: 20,171,279 (GRCm39) |
N573K |
probably damaging |
Het |
Eif2b4 |
G |
A |
5: 31,348,575 (GRCm39) |
R213* |
probably null |
Het |
Eif3b |
A |
G |
5: 140,426,856 (GRCm39) |
D704G |
probably benign |
Het |
Epn2 |
T |
C |
11: 61,437,197 (GRCm39) |
E125G |
probably damaging |
Het |
F830016B08Rik |
A |
G |
18: 60,434,153 (GRCm39) |
N412S |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,233,225 (GRCm39) |
M570V |
probably benign |
Het |
Gm16686 |
A |
T |
4: 88,673,725 (GRCm39) |
|
probably benign |
Het |
Hook2 |
C |
T |
8: 85,729,349 (GRCm39) |
Q632* |
probably null |
Het |
Ipcef1 |
A |
T |
10: 6,929,573 (GRCm39) |
W56R |
probably damaging |
Het |
Krt78 |
T |
C |
15: 101,856,637 (GRCm39) |
I418M |
probably benign |
Het |
Limk1 |
G |
A |
5: 134,699,295 (GRCm39) |
T154I |
probably damaging |
Het |
Lyl1 |
A |
T |
8: 85,430,910 (GRCm39) |
T271S |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,336,895 (GRCm39) |
I333V |
probably damaging |
Het |
Meioc |
A |
G |
11: 102,565,259 (GRCm39) |
T236A |
probably benign |
Het |
Nbas |
A |
G |
12: 13,532,538 (GRCm39) |
T1749A |
possibly damaging |
Het |
Nfib |
T |
A |
4: 82,215,016 (GRCm39) |
Q529L |
probably damaging |
Het |
Nfkb2 |
G |
T |
19: 46,296,006 (GRCm39) |
E170D |
probably benign |
Het |
Nisch |
A |
T |
14: 30,914,545 (GRCm39) |
F42L |
probably damaging |
Het |
Nomo1 |
T |
A |
7: 45,706,626 (GRCm39) |
Y547N |
probably damaging |
Het |
Or10g3 |
C |
T |
14: 52,609,764 (GRCm39) |
V249I |
probably damaging |
Het |
Or13a24 |
T |
C |
7: 140,154,515 (GRCm39) |
S150P |
possibly damaging |
Het |
Or5l14 |
A |
G |
2: 87,792,693 (GRCm39) |
L181P |
probably damaging |
Het |
Or8g51 |
T |
C |
9: 38,609,266 (GRCm39) |
Y136C |
probably damaging |
Het |
Pcdh18 |
T |
A |
3: 49,709,563 (GRCm39) |
N117I |
probably damaging |
Het |
Prkn |
T |
C |
17: 12,223,010 (GRCm39) |
S387P |
probably benign |
Het |
Prl3c1 |
A |
T |
13: 27,387,508 (GRCm39) |
K164N |
probably benign |
Het |
Prr23a3 |
T |
A |
9: 98,747,700 (GRCm39) |
L218Q |
probably damaging |
Het |
Prss43 |
A |
G |
9: 110,656,836 (GRCm39) |
H114R |
possibly damaging |
Het |
Ptcd3 |
A |
T |
6: 71,878,296 (GRCm39) |
M142K |
probably damaging |
Het |
Shisa7 |
G |
A |
7: 4,837,249 (GRCm39) |
T89I |
possibly damaging |
Het |
Slco1a1 |
C |
T |
6: 141,892,340 (GRCm39) |
A9T |
possibly damaging |
Het |
Srcap |
C |
T |
7: 127,158,172 (GRCm39) |
|
probably benign |
Het |
Tdg-ps |
G |
A |
15: 82,400,572 (GRCm39) |
|
noncoding transcript |
Het |
Tgm4 |
A |
G |
9: 122,880,451 (GRCm39) |
D284G |
probably damaging |
Het |
Tmc1 |
T |
A |
19: 20,804,013 (GRCm39) |
I355F |
probably benign |
Het |
Tmem121b |
A |
T |
6: 120,469,995 (GRCm39) |
F241I |
possibly damaging |
Het |
Tmem200c |
T |
A |
17: 69,149,235 (GRCm39) |
V606E |
probably benign |
Het |
Ttc39c |
A |
G |
18: 12,861,782 (GRCm39) |
K370R |
probably benign |
Het |
Vmn2r87 |
G |
A |
10: 130,314,336 (GRCm39) |
Q417* |
probably null |
Het |
Vps45 |
T |
C |
3: 95,955,699 (GRCm39) |
Y97C |
possibly damaging |
Het |
Zfp407 |
A |
G |
18: 84,581,039 (GRCm39) |
S25P |
probably benign |
Het |
Zfp566 |
A |
G |
7: 29,777,306 (GRCm39) |
S292P |
probably damaging |
Het |
|
Other mutations in Cryzl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00808:Cryzl2
|
APN |
1 |
157,298,246 (GRCm39) |
missense |
probably benign |
|
IGL01481:Cryzl2
|
APN |
1 |
157,298,309 (GRCm39) |
splice site |
probably null |
|
IGL01878:Cryzl2
|
APN |
1 |
157,299,970 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02596:Cryzl2
|
APN |
1 |
157,292,539 (GRCm39) |
missense |
probably damaging |
1.00 |
G5030:Cryzl2
|
UTSW |
1 |
157,292,580 (GRCm39) |
nonsense |
probably null |
|
R0399:Cryzl2
|
UTSW |
1 |
157,289,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Cryzl2
|
UTSW |
1 |
157,292,014 (GRCm39) |
missense |
probably benign |
0.00 |
R0518:Cryzl2
|
UTSW |
1 |
157,292,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Cryzl2
|
UTSW |
1 |
157,293,294 (GRCm39) |
missense |
probably benign |
0.15 |
R1104:Cryzl2
|
UTSW |
1 |
157,298,174 (GRCm39) |
splice site |
probably benign |
|
R1471:Cryzl2
|
UTSW |
1 |
157,298,291 (GRCm39) |
missense |
probably benign |
0.01 |
R1773:Cryzl2
|
UTSW |
1 |
157,298,292 (GRCm39) |
missense |
probably benign |
0.01 |
R5046:Cryzl2
|
UTSW |
1 |
157,292,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Cryzl2
|
UTSW |
1 |
157,289,546 (GRCm39) |
nonsense |
probably null |
|
R5778:Cryzl2
|
UTSW |
1 |
157,298,357 (GRCm39) |
missense |
probably benign |
0.00 |
R6928:Cryzl2
|
UTSW |
1 |
157,298,357 (GRCm39) |
missense |
probably benign |
0.00 |
R7037:Cryzl2
|
UTSW |
1 |
157,298,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R7099:Cryzl2
|
UTSW |
1 |
157,316,154 (GRCm39) |
critical splice donor site |
probably benign |
|
R7911:Cryzl2
|
UTSW |
1 |
157,299,925 (GRCm39) |
missense |
probably benign |
|
R8854:Cryzl2
|
UTSW |
1 |
157,286,370 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9618:Cryzl2
|
UTSW |
1 |
157,289,578 (GRCm39) |
missense |
probably benign |
0.00 |
R9667:Cryzl2
|
UTSW |
1 |
157,316,038 (GRCm39) |
missense |
probably benign |
|
Z1088:Cryzl2
|
UTSW |
1 |
157,293,359 (GRCm39) |
missense |
probably benign |
0.22 |
|