Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
T |
C |
3: 59,659,513 (GRCm39) |
V322A |
probably benign |
Het |
Abca8b |
G |
T |
11: 109,825,407 (GRCm39) |
L1598M |
probably benign |
Het |
Adam4 |
T |
C |
12: 81,466,348 (GRCm39) |
T758A |
probably benign |
Het |
B3galnt2 |
T |
C |
13: 14,169,814 (GRCm39) |
I424T |
probably damaging |
Het |
Cacna1g |
T |
C |
11: 94,321,312 (GRCm39) |
Y1316C |
probably damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,517,517 (GRCm39) |
S388P |
probably damaging |
Het |
Cdh8 |
A |
G |
8: 99,757,498 (GRCm39) |
I700T |
possibly damaging |
Het |
Cdhr3 |
G |
T |
12: 33,098,985 (GRCm39) |
Y535* |
probably null |
Het |
Clasp2 |
T |
C |
9: 113,641,836 (GRCm39) |
|
probably null |
Het |
Col16a1 |
T |
A |
4: 129,947,151 (GRCm39) |
D165E |
probably damaging |
Het |
Col9a1 |
A |
T |
1: 24,234,436 (GRCm39) |
|
probably benign |
Het |
Cpa3 |
A |
T |
3: 20,296,307 (GRCm39) |
I10N |
possibly damaging |
Het |
Cstf3 |
T |
A |
2: 104,439,347 (GRCm39) |
|
probably benign |
Het |
Dnah3 |
C |
A |
7: 119,570,689 (GRCm39) |
|
probably null |
Het |
E2f6 |
T |
C |
12: 16,874,706 (GRCm39) |
C263R |
probably benign |
Het |
Eps8l2 |
C |
A |
7: 140,936,534 (GRCm39) |
Q288K |
possibly damaging |
Het |
Fam193a |
T |
A |
5: 34,578,199 (GRCm39) |
V231D |
probably damaging |
Het |
Gjd3 |
C |
T |
11: 102,691,029 (GRCm39) |
G325S |
probably benign |
Het |
Gpatch8 |
T |
A |
11: 102,429,111 (GRCm39) |
E39D |
unknown |
Het |
Gpr107 |
C |
T |
2: 31,042,375 (GRCm39) |
A2V |
probably damaging |
Het |
Kansl3 |
G |
T |
1: 36,385,045 (GRCm39) |
H629N |
possibly damaging |
Het |
Kcna10 |
C |
A |
3: 107,101,545 (GRCm39) |
H59N |
probably benign |
Het |
Kitl |
A |
T |
10: 99,915,886 (GRCm39) |
E138D |
possibly damaging |
Het |
Kpna2 |
T |
C |
11: 106,881,571 (GRCm39) |
K353R |
probably damaging |
Het |
M1ap |
T |
A |
6: 82,958,798 (GRCm39) |
I143N |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,420,538 (GRCm39) |
S239P |
possibly damaging |
Het |
Med13l |
T |
A |
5: 118,880,105 (GRCm39) |
S1066T |
probably damaging |
Het |
Mettl23 |
G |
T |
11: 116,739,865 (GRCm39) |
E47* |
probably null |
Het |
Or52i2 |
T |
C |
7: 102,319,433 (GRCm39) |
F102S |
probably damaging |
Het |
Or5af1 |
C |
T |
11: 58,722,039 (GRCm39) |
Q20* |
probably null |
Het |
Proca1 |
T |
A |
11: 78,092,699 (GRCm39) |
D48E |
possibly damaging |
Het |
Rab34 |
T |
G |
11: 78,082,458 (GRCm39) |
V227G |
probably damaging |
Het |
Rab7 |
A |
T |
6: 87,990,632 (GRCm39) |
L14Q |
probably damaging |
Het |
Rasgef1c |
C |
T |
11: 49,847,934 (GRCm39) |
S23F |
probably benign |
Het |
Rit1 |
A |
G |
3: 88,633,457 (GRCm39) |
|
probably benign |
Het |
Scin |
T |
C |
12: 40,174,568 (GRCm39) |
T172A |
probably benign |
Het |
Scmh1 |
C |
A |
4: 120,325,575 (GRCm39) |
N97K |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,846,162 (GRCm39) |
E655G |
possibly damaging |
Het |
Slc22a15 |
A |
G |
3: 101,771,905 (GRCm39) |
V243A |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,789,042 (GRCm39) |
|
probably benign |
Het |
Smim7 |
C |
T |
8: 73,324,867 (GRCm39) |
G3R |
probably damaging |
Het |
Snurf |
C |
T |
7: 59,645,282 (GRCm39) |
R44H |
possibly damaging |
Het |
Snx13 |
G |
A |
12: 35,174,471 (GRCm39) |
A667T |
possibly damaging |
Het |
Sowaha |
T |
G |
11: 53,369,590 (GRCm39) |
H382P |
probably damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tmem259 |
G |
T |
10: 79,814,442 (GRCm39) |
|
probably null |
Het |
Topbp1 |
A |
G |
9: 103,211,277 (GRCm39) |
T945A |
probably damaging |
Het |
Tor1aip2 |
T |
C |
1: 155,939,307 (GRCm39) |
|
probably benign |
Het |
Ube3b |
T |
C |
5: 114,527,136 (GRCm39) |
V118A |
probably damaging |
Het |
Usp38 |
T |
C |
8: 81,711,717 (GRCm39) |
K773E |
probably damaging |
Het |
Wnk1 |
G |
A |
6: 119,925,852 (GRCm39) |
|
probably benign |
Het |
Zfp871 |
A |
G |
17: 32,994,842 (GRCm39) |
V111A |
possibly damaging |
Het |
|
Other mutations in Ccdc157 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01599:Ccdc157
|
APN |
11 |
4,098,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02267:Ccdc157
|
APN |
11 |
4,094,035 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03182:Ccdc157
|
APN |
11 |
4,101,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:Ccdc157
|
UTSW |
11 |
4,096,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R0360:Ccdc157
|
UTSW |
11 |
4,096,663 (GRCm39) |
missense |
probably damaging |
0.98 |
R1349:Ccdc157
|
UTSW |
11 |
4,099,056 (GRCm39) |
missense |
probably benign |
0.20 |
R1527:Ccdc157
|
UTSW |
11 |
4,101,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Ccdc157
|
UTSW |
11 |
4,099,030 (GRCm39) |
missense |
probably benign |
0.07 |
R1932:Ccdc157
|
UTSW |
11 |
4,096,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Ccdc157
|
UTSW |
11 |
4,100,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R4361:Ccdc157
|
UTSW |
11 |
4,096,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R4754:Ccdc157
|
UTSW |
11 |
4,098,994 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4786:Ccdc157
|
UTSW |
11 |
4,101,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Ccdc157
|
UTSW |
11 |
4,100,078 (GRCm39) |
nonsense |
probably null |
|
R5625:Ccdc157
|
UTSW |
11 |
4,101,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Ccdc157
|
UTSW |
11 |
4,094,538 (GRCm39) |
missense |
probably benign |
0.23 |
R6193:Ccdc157
|
UTSW |
11 |
4,101,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6936:Ccdc157
|
UTSW |
11 |
4,094,030 (GRCm39) |
missense |
probably benign |
|
R7057:Ccdc157
|
UTSW |
11 |
4,094,586 (GRCm39) |
missense |
probably benign |
0.33 |
R7113:Ccdc157
|
UTSW |
11 |
4,098,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7136:Ccdc157
|
UTSW |
11 |
4,098,592 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9601:Ccdc157
|
UTSW |
11 |
4,094,598 (GRCm39) |
missense |
probably damaging |
0.97 |
T0975:Ccdc157
|
UTSW |
11 |
4,096,246 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ccdc157
|
UTSW |
11 |
4,096,547 (GRCm39) |
nonsense |
probably null |
|
|