Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
C |
6: 128,545,675 (GRCm39) |
F484C |
probably damaging |
Het |
Aoc1l1 |
A |
C |
6: 48,953,535 (GRCm39) |
I487L |
probably benign |
Het |
Ctnnal1 |
T |
C |
4: 56,812,349 (GRCm39) |
T726A |
probably benign |
Het |
Cyp2j11 |
T |
A |
4: 96,236,853 (GRCm39) |
|
probably benign |
Het |
Ddx60 |
T |
A |
8: 62,476,275 (GRCm39) |
M1541K |
probably null |
Het |
Dnah14 |
C |
T |
1: 181,536,616 (GRCm39) |
P2420S |
probably damaging |
Het |
Fhit |
T |
C |
14: 9,573,435 (GRCm38) |
E205G |
probably benign |
Het |
Glipr1l1 |
C |
T |
10: 111,912,075 (GRCm39) |
T203M |
probably benign |
Het |
Gm4353 |
T |
A |
7: 115,683,504 (GRCm39) |
D97V |
probably benign |
Het |
Gprc6a |
A |
T |
10: 51,491,907 (GRCm39) |
I543K |
probably damaging |
Het |
Ifi205 |
T |
C |
1: 173,854,830 (GRCm39) |
T110A |
possibly damaging |
Het |
Med27 |
T |
A |
2: 29,399,453 (GRCm39) |
S95T |
probably damaging |
Het |
Mocs1 |
T |
C |
17: 49,757,341 (GRCm39) |
S308P |
probably damaging |
Het |
Mrpl11 |
C |
T |
19: 5,013,397 (GRCm39) |
S88F |
possibly damaging |
Het |
Nav3 |
A |
T |
10: 109,702,845 (GRCm39) |
Y229* |
probably null |
Het |
Or2f1b |
A |
T |
6: 42,739,899 (GRCm39) |
L304F |
probably damaging |
Het |
Or2n1e |
A |
G |
17: 38,585,772 (GRCm39) |
M37V |
probably benign |
Het |
Or52n2c |
C |
T |
7: 104,574,599 (GRCm39) |
R124H |
probably benign |
Het |
Or52r1 |
C |
A |
7: 102,537,158 (GRCm39) |
L67F |
probably benign |
Het |
Or5g27 |
T |
A |
2: 85,409,886 (GRCm39) |
M101K |
possibly damaging |
Het |
Pear1 |
A |
G |
3: 87,663,238 (GRCm39) |
I460T |
probably benign |
Het |
Phc3 |
T |
A |
3: 30,968,678 (GRCm39) |
K816N |
probably damaging |
Het |
Phf19 |
T |
A |
2: 34,787,129 (GRCm39) |
D445V |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,563,742 (GRCm39) |
F486L |
probably damaging |
Het |
Plagl1 |
G |
T |
10: 13,003,639 (GRCm39) |
|
probably benign |
Het |
Prkca |
A |
G |
11: 107,948,671 (GRCm39) |
I106T |
probably benign |
Het |
Ptpn3 |
C |
T |
4: 57,248,681 (GRCm39) |
G218R |
probably damaging |
Het |
Ptx3 |
A |
G |
3: 66,132,130 (GRCm39) |
D217G |
possibly damaging |
Het |
Rab3d |
T |
C |
9: 21,821,815 (GRCm39) |
T209A |
probably benign |
Het |
Rfx2 |
A |
G |
17: 57,084,473 (GRCm39) |
F642S |
possibly damaging |
Het |
Rhpn2 |
T |
A |
7: 35,075,636 (GRCm39) |
M271K |
possibly damaging |
Het |
Serpinb6b |
A |
G |
13: 33,161,977 (GRCm39) |
T259A |
probably damaging |
Het |
Speer3 |
G |
A |
5: 13,844,705 (GRCm39) |
V123M |
possibly damaging |
Het |
Svil |
T |
G |
18: 5,106,724 (GRCm39) |
V1855G |
probably damaging |
Het |
Thbs4 |
A |
G |
13: 92,888,303 (GRCm39) |
F950L |
probably benign |
Het |
Tiparp |
T |
C |
3: 65,460,664 (GRCm39) |
V551A |
probably damaging |
Het |
Vmn2r71 |
T |
A |
7: 85,268,482 (GRCm39) |
D228E |
probably benign |
Het |
Vmn2r85 |
T |
C |
10: 130,261,531 (GRCm39) |
I269V |
probably benign |
Het |
Vps9d1 |
A |
T |
8: 123,972,410 (GRCm39) |
M497K |
probably damaging |
Het |
Wnt5b |
A |
G |
6: 119,410,603 (GRCm39) |
V241A |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,228,342 (GRCm39) |
N353S |
probably damaging |
Het |
Zfp526 |
C |
T |
7: 24,925,757 (GRCm39) |
T672M |
probably damaging |
Het |
|
Other mutations in Cdsn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Cdsn
|
APN |
17 |
35,865,740 (GRCm39) |
missense |
unknown |
|
IGL02851:Cdsn
|
APN |
17 |
35,866,791 (GRCm39) |
missense |
possibly damaging |
0.66 |
E7848:Cdsn
|
UTSW |
17 |
35,867,004 (GRCm39) |
missense |
probably benign |
0.05 |
R0032:Cdsn
|
UTSW |
17 |
35,866,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R0105:Cdsn
|
UTSW |
17 |
35,867,035 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0105:Cdsn
|
UTSW |
17 |
35,867,035 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0696:Cdsn
|
UTSW |
17 |
35,866,893 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2070:Cdsn
|
UTSW |
17 |
35,865,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R2071:Cdsn
|
UTSW |
17 |
35,865,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Cdsn
|
UTSW |
17 |
35,866,326 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5254:Cdsn
|
UTSW |
17 |
35,863,099 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R6117:Cdsn
|
UTSW |
17 |
35,865,931 (GRCm39) |
missense |
unknown |
|
R7828:Cdsn
|
UTSW |
17 |
35,865,878 (GRCm39) |
missense |
unknown |
|
R8174:Cdsn
|
UTSW |
17 |
35,866,529 (GRCm39) |
nonsense |
probably null |
|
R8337:Cdsn
|
UTSW |
17 |
35,866,415 (GRCm39) |
missense |
possibly damaging |
0.83 |
RF020:Cdsn
|
UTSW |
17 |
35,865,876 (GRCm39) |
small insertion |
probably benign |
|
RF023:Cdsn
|
UTSW |
17 |
35,865,876 (GRCm39) |
small insertion |
probably benign |
|
RF045:Cdsn
|
UTSW |
17 |
35,865,865 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Cdsn
|
UTSW |
17 |
35,866,968 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Cdsn
|
UTSW |
17 |
35,866,722 (GRCm39) |
missense |
possibly damaging |
0.90 |
|