Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
A |
8: 73,198,923 (GRCm39) |
A110D |
probably benign |
Het |
4930407I10Rik |
A |
G |
15: 81,947,615 (GRCm39) |
E504G |
probably benign |
Het |
4931406B18Rik |
C |
A |
7: 43,148,702 (GRCm39) |
A170S |
|
Het |
Apbb2 |
T |
C |
5: 66,609,018 (GRCm39) |
K210E |
probably benign |
Het |
Arid4a |
C |
A |
12: 71,122,129 (GRCm39) |
L515I |
probably damaging |
Het |
Atp13a3 |
A |
G |
16: 30,134,716 (GRCm39) |
S1186P |
possibly damaging |
Het |
Brf1 |
A |
G |
12: 112,927,011 (GRCm39) |
Y500H |
probably damaging |
Het |
Btaf1 |
A |
G |
19: 36,964,114 (GRCm39) |
Y895C |
probably benign |
Het |
Cenpf |
T |
C |
1: 189,391,571 (GRCm39) |
T737A |
probably benign |
Het |
Cmklr1 |
G |
C |
5: 113,752,043 (GRCm39) |
H319Q |
probably benign |
Het |
Col18a1 |
G |
A |
10: 76,893,204 (GRCm39) |
T1057M |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,515,260 (GRCm39) |
|
probably null |
Het |
Csmd3 |
A |
C |
15: 47,617,187 (GRCm39) |
H1000Q |
|
Het |
Cyp4a29 |
T |
A |
4: 115,108,395 (GRCm39) |
M373K |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,333,173 (GRCm39) |
E215G |
probably damaging |
Het |
Dusp19 |
T |
C |
2: 80,447,729 (GRCm39) |
M1T |
probably null |
Het |
Etv4 |
A |
G |
11: 101,664,492 (GRCm39) |
Y253H |
probably benign |
Het |
Exosc6 |
G |
A |
8: 111,783,513 (GRCm39) |
A171T |
probably damaging |
Het |
Fam219a |
G |
A |
4: 41,521,870 (GRCm39) |
T70M |
probably damaging |
Het |
Fau |
G |
A |
19: 6,108,297 (GRCm39) |
R6H |
probably benign |
Het |
Flrt3 |
T |
C |
2: 140,501,879 (GRCm39) |
D583G |
probably damaging |
Het |
Gm14443 |
A |
T |
2: 175,011,869 (GRCm39) |
C192* |
probably null |
Het |
Gm4353 |
T |
A |
7: 115,682,843 (GRCm39) |
N246I |
probably benign |
Het |
Igfn1 |
A |
G |
1: 135,926,327 (GRCm39) |
L41P |
probably benign |
Het |
Jakmip3 |
A |
T |
7: 138,622,560 (GRCm39) |
I307F |
probably damaging |
Het |
Kcnt2 |
T |
A |
1: 140,353,035 (GRCm39) |
V248D |
probably damaging |
Het |
Kctd14 |
A |
G |
7: 97,107,243 (GRCm39) |
K166R |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,528,493 (GRCm39) |
|
probably null |
Het |
Kif5c |
A |
G |
2: 49,620,151 (GRCm39) |
D461G |
probably damaging |
Het |
Lpin2 |
T |
C |
17: 71,538,516 (GRCm39) |
|
probably null |
Het |
Mettl22 |
G |
A |
16: 8,305,231 (GRCm39) |
D295N |
probably damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Or10a5 |
A |
T |
7: 106,635,640 (GRCm39) |
I93F |
probably damaging |
Het |
Or5b95 |
T |
A |
19: 12,658,190 (GRCm39) |
C239* |
probably null |
Het |
Or5k8 |
A |
T |
16: 58,644,677 (GRCm39) |
Y132N |
probably damaging |
Het |
Pecam1 |
G |
T |
11: 106,586,587 (GRCm39) |
N309K |
probably damaging |
Het |
Pigc |
C |
T |
1: 161,798,032 (GRCm39) |
R5C |
probably benign |
Het |
Pih1d1 |
T |
C |
7: 44,809,193 (GRCm39) |
V259A |
possibly damaging |
Het |
Ptpre |
A |
G |
7: 135,271,508 (GRCm39) |
I374M |
probably benign |
Het |
Rnps1 |
A |
G |
17: 24,637,573 (GRCm39) |
S72G |
unknown |
Het |
S100pbp |
A |
G |
4: 129,044,847 (GRCm39) |
Y363H |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,619,040 (GRCm39) |
T523A |
probably benign |
Het |
Slc38a8 |
A |
G |
8: 120,212,851 (GRCm39) |
F270S |
possibly damaging |
Het |
Slc4a1ap |
T |
C |
5: 31,693,538 (GRCm39) |
S491P |
probably damaging |
Het |
Slc66a2 |
T |
C |
18: 80,300,300 (GRCm39) |
L57P |
probably damaging |
Het |
Slc7a6 |
T |
C |
8: 106,922,534 (GRCm39) |
V440A |
probably damaging |
Het |
Sobp |
A |
T |
10: 42,898,902 (GRCm39) |
C228S |
probably damaging |
Het |
Sox8 |
T |
C |
17: 25,787,813 (GRCm39) |
D212G |
possibly damaging |
Het |
Specc1 |
A |
G |
11: 62,102,464 (GRCm39) |
|
probably null |
Het |
Svop |
G |
A |
5: 114,168,231 (GRCm39) |
T456M |
probably benign |
Het |
Synrg |
A |
G |
11: 83,900,278 (GRCm39) |
D750G |
probably damaging |
Het |
Syt14 |
C |
A |
1: 192,612,944 (GRCm39) |
E336* |
probably null |
Het |
Tcp10c |
A |
T |
17: 13,576,650 (GRCm39) |
Q76H |
probably damaging |
Het |
Tcp11l1 |
C |
T |
2: 104,528,897 (GRCm39) |
V134I |
possibly damaging |
Het |
Tex51 |
T |
C |
18: 32,594,029 (GRCm39) |
R110G |
possibly damaging |
Het |
Tle3 |
T |
A |
9: 61,319,562 (GRCm39) |
H443Q |
possibly damaging |
Het |
Unc13a |
C |
T |
8: 72,108,335 (GRCm39) |
R506Q |
possibly damaging |
Het |
Vmn2r27 |
T |
C |
6: 124,174,224 (GRCm39) |
Y542C |
possibly damaging |
Het |
Vmn2r5 |
T |
G |
3: 64,411,411 (GRCm39) |
N386H |
possibly damaging |
Het |
Vmn2r91 |
A |
G |
17: 18,327,905 (GRCm39) |
I500V |
probably damaging |
Het |
Wdfy4 |
A |
T |
14: 32,760,704 (GRCm39) |
|
probably null |
Het |
Zfp709 |
A |
T |
8: 72,644,648 (GRCm39) |
E692D |
possibly damaging |
Het |
Zglp1 |
A |
T |
9: 20,977,482 (GRCm39) |
L111Q |
probably benign |
Het |
|
Other mutations in Cdhr17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6134:Cdhr17
|
UTSW |
5 |
17,029,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R6261:Cdhr17
|
UTSW |
5 |
17,017,183 (GRCm39) |
splice site |
noncoding transcript |
|
R6288:Cdhr17
|
UTSW |
5 |
17,061,283 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6826:Cdhr17
|
UTSW |
5 |
17,013,292 (GRCm39) |
missense |
unknown |
|
R6980:Cdhr17
|
UTSW |
5 |
17,031,944 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7224:Cdhr17
|
UTSW |
5 |
17,041,592 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7310:Cdhr17
|
UTSW |
5 |
17,075,246 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7411:Cdhr17
|
UTSW |
5 |
17,029,763 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7798:Cdhr17
|
UTSW |
5 |
17,061,656 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7915:Cdhr17
|
UTSW |
5 |
17,032,012 (GRCm39) |
missense |
probably benign |
0.00 |
R8347:Cdhr17
|
UTSW |
5 |
17,006,572 (GRCm39) |
missense |
probably benign |
0.00 |
R8868:Cdhr17
|
UTSW |
5 |
17,028,152 (GRCm39) |
missense |
probably benign |
0.09 |
R9153:Cdhr17
|
UTSW |
5 |
17,040,916 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9200:Cdhr17
|
UTSW |
5 |
17,006,659 (GRCm39) |
critical splice donor site |
probably null |
|
R9261:Cdhr17
|
UTSW |
5 |
17,006,547 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9298:Cdhr17
|
UTSW |
5 |
16,996,855 (GRCm39) |
nonsense |
probably null |
|
R9462:Cdhr17
|
UTSW |
5 |
17,027,213 (GRCm39) |
missense |
|
|
Z1177:Cdhr17
|
UTSW |
5 |
17,061,722 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cdhr17
|
UTSW |
5 |
17,040,977 (GRCm39) |
missense |
possibly damaging |
0.92 |
|