Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg3 |
A |
G |
17: 57,189,954 (GRCm39) |
K327E |
probably damaging |
Het |
Adamts14 |
G |
A |
10: 61,054,307 (GRCm39) |
A572V |
possibly damaging |
Het |
Add2 |
A |
G |
6: 86,075,597 (GRCm39) |
N249D |
probably benign |
Het |
Adgrb2 |
A |
T |
4: 129,915,904 (GRCm39) |
M1503L |
probably benign |
Het |
Alms1 |
A |
G |
6: 85,586,407 (GRCm39) |
K421E |
unknown |
Het |
B3galt5 |
A |
G |
16: 96,116,916 (GRCm39) |
K183R |
possibly damaging |
Het |
Braf |
T |
C |
6: 39,665,187 (GRCm39) |
I94M |
probably damaging |
Het |
Cacna1a |
A |
G |
8: 85,294,311 (GRCm39) |
E1158G |
possibly damaging |
Het |
Ccdc38 |
C |
A |
10: 93,398,662 (GRCm39) |
L147I |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,886,130 (GRCm39) |
N210D |
possibly damaging |
Het |
Cdh20 |
T |
C |
1: 109,925,583 (GRCm39) |
|
probably benign |
Het |
Coro1b |
T |
A |
19: 4,202,525 (GRCm39) |
Y338N |
probably damaging |
Het |
Crlf3 |
A |
C |
11: 79,954,812 (GRCm39) |
|
probably null |
Het |
Crnn |
A |
T |
3: 93,056,723 (GRCm39) |
K503M |
probably damaging |
Het |
Cul5 |
T |
A |
9: 53,537,269 (GRCm39) |
N521I |
probably damaging |
Het |
Cyp2c50 |
T |
A |
19: 40,080,634 (GRCm39) |
|
probably null |
Het |
Dis3 |
T |
C |
14: 99,337,042 (GRCm39) |
H23R |
possibly damaging |
Het |
Dock7 |
A |
T |
4: 98,949,519 (GRCm39) |
L441H |
|
Het |
Dock7 |
C |
A |
4: 98,967,992 (GRCm39) |
E162* |
probably null |
Het |
Dpp9 |
A |
T |
17: 56,512,611 (GRCm39) |
M174K |
possibly damaging |
Het |
Dtd1 |
A |
G |
2: 144,459,147 (GRCm39) |
D57G |
probably benign |
Het |
F3 |
A |
G |
3: 121,525,206 (GRCm39) |
E149G |
probably damaging |
Het |
Glp2r |
C |
T |
11: 67,648,417 (GRCm39) |
R95K |
probably damaging |
Het |
Gpr107 |
T |
A |
2: 31,068,358 (GRCm39) |
F273L |
probably benign |
Het |
Gria1 |
A |
T |
11: 57,174,451 (GRCm39) |
I647F |
probably damaging |
Het |
Heatr5a |
A |
C |
12: 51,926,217 (GRCm39) |
I1878S |
possibly damaging |
Het |
Hsf2 |
G |
T |
10: 57,380,653 (GRCm39) |
C230F |
probably benign |
Het |
Igfbp2 |
T |
G |
1: 72,891,164 (GRCm39) |
M254R |
probably damaging |
Het |
Kifc2 |
C |
A |
15: 76,545,537 (GRCm39) |
Q95K |
possibly damaging |
Het |
Lnx1 |
T |
G |
5: 74,780,972 (GRCm39) |
N183T |
probably benign |
Het |
Ltn1 |
G |
T |
16: 87,205,716 (GRCm39) |
T983K |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,367,093 (GRCm39) |
V2556D |
possibly damaging |
Het |
Map4k3 |
A |
G |
17: 80,905,077 (GRCm39) |
V738A |
possibly damaging |
Het |
Mtmr12 |
T |
G |
15: 12,265,681 (GRCm39) |
Y466D |
possibly damaging |
Het |
Musk |
A |
G |
4: 58,333,672 (GRCm39) |
I256V |
probably benign |
Het |
Ociad1 |
T |
C |
5: 73,452,338 (GRCm39) |
F43S |
probably damaging |
Het |
Or10g9b |
A |
T |
9: 39,918,229 (GRCm39) |
S5R |
possibly damaging |
Het |
Or4k5 |
A |
G |
14: 50,385,713 (GRCm39) |
L206P |
probably damaging |
Het |
Pah |
G |
A |
10: 87,390,249 (GRCm39) |
A132T |
probably damaging |
Het |
Pak5 |
G |
A |
2: 135,925,244 (GRCm39) |
S686F |
possibly damaging |
Het |
Pi4kb |
T |
C |
3: 94,896,623 (GRCm39) |
S307P |
probably benign |
Het |
Plxna1 |
T |
C |
6: 89,318,889 (GRCm39) |
T645A |
possibly damaging |
Het |
Pold1 |
C |
T |
7: 44,191,614 (GRCm39) |
R124K |
possibly damaging |
Het |
Pramel27 |
T |
A |
4: 143,573,116 (GRCm39) |
I3N |
possibly damaging |
Het |
Prdm10 |
T |
C |
9: 31,289,777 (GRCm39) |
Y1153H |
probably damaging |
Het |
Ptk2b |
T |
C |
14: 66,391,693 (GRCm39) |
N947S |
possibly damaging |
Het |
Rad54b |
A |
G |
4: 11,578,956 (GRCm39) |
|
probably null |
Het |
S1pr4 |
A |
G |
10: 81,335,623 (GRCm39) |
|
probably benign |
Het |
Sec23b |
A |
G |
2: 144,432,269 (GRCm39) |
K760E |
probably benign |
Het |
Sergef |
T |
A |
7: 46,264,170 (GRCm39) |
N239I |
probably damaging |
Het |
Serpinb9 |
C |
A |
13: 33,192,054 (GRCm39) |
N78K |
probably benign |
Het |
Sntb1 |
G |
T |
15: 55,511,347 (GRCm39) |
F412L |
possibly damaging |
Het |
Stradb |
T |
A |
1: 59,032,108 (GRCm39) |
F294L |
probably damaging |
Het |
Ttll11 |
G |
A |
2: 35,793,046 (GRCm39) |
R266C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,624,882 (GRCm39) |
M15232K |
possibly damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,584,793 (GRCm39) |
I547M |
probably benign |
Het |
Vgf |
C |
A |
5: 137,060,245 (GRCm39) |
P136T |
unknown |
Het |
Vmn1r36 |
T |
A |
6: 66,693,914 (GRCm39) |
|
probably benign |
Het |
Vmn2r102 |
T |
C |
17: 19,901,405 (GRCm39) |
S511P |
probably damaging |
Het |
Wdr27 |
C |
T |
17: 15,103,965 (GRCm39) |
V714I |
probably benign |
Het |
Zbed6 |
T |
A |
1: 133,586,981 (GRCm39) |
I119L |
probably benign |
Het |
Zfp229 |
A |
G |
17: 21,964,045 (GRCm39) |
S92G |
probably benign |
Het |
Zfp710 |
C |
T |
7: 79,732,250 (GRCm39) |
Q476* |
probably null |
Het |
Zfp808 |
A |
G |
13: 62,320,637 (GRCm39) |
N622S |
probably benign |
Het |
|
Other mutations in Ccdc177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01598:Ccdc177
|
APN |
12 |
80,805,519 (GRCm39) |
missense |
unknown |
|
IGL02433:Ccdc177
|
APN |
12 |
80,804,372 (GRCm39) |
missense |
unknown |
|
R0829:Ccdc177
|
UTSW |
12 |
80,806,253 (GRCm39) |
missense |
probably damaging |
0.96 |
R1739:Ccdc177
|
UTSW |
12 |
80,806,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Ccdc177
|
UTSW |
12 |
80,805,486 (GRCm39) |
missense |
unknown |
|
R2337:Ccdc177
|
UTSW |
12 |
80,805,465 (GRCm39) |
missense |
unknown |
|
R5001:Ccdc177
|
UTSW |
12 |
80,804,160 (GRCm39) |
missense |
unknown |
|
R5164:Ccdc177
|
UTSW |
12 |
80,805,336 (GRCm39) |
missense |
unknown |
|
R5249:Ccdc177
|
UTSW |
12 |
80,805,282 (GRCm39) |
missense |
unknown |
|
R5461:Ccdc177
|
UTSW |
12 |
80,804,816 (GRCm39) |
missense |
unknown |
|
R6802:Ccdc177
|
UTSW |
12 |
80,806,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Ccdc177
|
UTSW |
12 |
80,805,927 (GRCm39) |
missense |
probably damaging |
0.98 |
R7412:Ccdc177
|
UTSW |
12 |
80,805,792 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7510:Ccdc177
|
UTSW |
12 |
80,804,457 (GRCm39) |
missense |
unknown |
|
R7712:Ccdc177
|
UTSW |
12 |
80,804,712 (GRCm39) |
nonsense |
probably null |
|
R8036:Ccdc177
|
UTSW |
12 |
80,804,897 (GRCm39) |
missense |
unknown |
|
R8693:Ccdc177
|
UTSW |
12 |
80,804,582 (GRCm39) |
missense |
unknown |
|
R8708:Ccdc177
|
UTSW |
12 |
80,805,891 (GRCm39) |
missense |
probably benign |
0.08 |
R8862:Ccdc177
|
UTSW |
12 |
80,804,208 (GRCm39) |
missense |
unknown |
|
R8894:Ccdc177
|
UTSW |
12 |
80,806,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9423:Ccdc177
|
UTSW |
12 |
80,804,162 (GRCm39) |
missense |
unknown |
|
R9727:Ccdc177
|
UTSW |
12 |
80,806,044 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Ccdc177
|
UTSW |
12 |
80,804,510 (GRCm39) |
missense |
unknown |
|
|