Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt1 |
A |
T |
12: 112,628,735 (GRCm39) |
Y18* |
probably null |
Het |
Ank2 |
C |
A |
3: 126,806,393 (GRCm39) |
A583S |
probably damaging |
Het |
Aoc1l3 |
T |
C |
6: 48,965,546 (GRCm39) |
V518A |
possibly damaging |
Het |
Atp8b4 |
T |
C |
2: 126,214,115 (GRCm39) |
N706S |
probably benign |
Het |
Bace2 |
A |
G |
16: 97,200,865 (GRCm39) |
N111S |
probably damaging |
Het |
Cnp |
A |
T |
11: 100,471,184 (GRCm39) |
R275S |
probably benign |
Het |
Cs |
T |
A |
10: 128,188,586 (GRCm39) |
M104K |
probably benign |
Het |
Ctcfl |
G |
A |
2: 172,954,167 (GRCm39) |
T310I |
probably damaging |
Het |
Cyp2d40 |
T |
C |
15: 82,645,763 (GRCm39) |
I81V |
probably benign |
Het |
Ddx19a |
A |
G |
8: 111,719,706 (GRCm39) |
V30A |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dock6 |
G |
A |
9: 21,733,107 (GRCm39) |
A1062V |
probably damaging |
Het |
Dpysl2 |
T |
C |
14: 67,067,395 (GRCm39) |
D172G |
probably benign |
Het |
Eml2 |
A |
G |
7: 18,935,504 (GRCm39) |
D638G |
probably damaging |
Het |
Epb41l4b |
C |
A |
4: 57,103,522 (GRCm39) |
A105S |
possibly damaging |
Het |
Fat4 |
A |
G |
3: 38,942,750 (GRCm39) |
I548V |
probably benign |
Het |
Gabrb2 |
G |
A |
11: 42,484,758 (GRCm39) |
A272T |
probably damaging |
Het |
Gask1a |
T |
C |
9: 121,794,707 (GRCm39) |
L287P |
probably damaging |
Het |
Hcn1 |
C |
T |
13: 118,111,998 (GRCm39) |
P654L |
unknown |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Hk1 |
C |
A |
10: 62,122,349 (GRCm39) |
G477C |
probably damaging |
Het |
Hspa5 |
C |
T |
2: 34,663,204 (GRCm39) |
P127L |
probably damaging |
Het |
Kiss1r |
A |
G |
10: 79,755,259 (GRCm39) |
|
probably null |
Het |
L3mbtl4 |
G |
T |
17: 68,768,561 (GRCm39) |
R223L |
probably benign |
Het |
Loxl4 |
G |
T |
19: 42,595,074 (GRCm39) |
N200K |
probably damaging |
Het |
Lrba |
T |
C |
3: 86,192,398 (GRCm39) |
V104A |
probably benign |
Het |
Lyst |
T |
A |
13: 13,809,485 (GRCm39) |
V385D |
probably benign |
Het |
Lyst |
T |
A |
13: 13,812,293 (GRCm39) |
C902S |
probably damaging |
Het |
Mrpl28 |
T |
C |
17: 26,345,261 (GRCm39) |
F227S |
probably benign |
Het |
Mtmr3 |
A |
T |
11: 4,448,896 (GRCm39) |
V289E |
possibly damaging |
Het |
Ndst3 |
A |
G |
3: 123,465,732 (GRCm39) |
V80A |
probably damaging |
Het |
Nid2 |
C |
T |
14: 19,829,749 (GRCm39) |
A680V |
possibly damaging |
Het |
Nup210 |
A |
T |
6: 91,031,433 (GRCm39) |
I812N |
probably damaging |
Het |
Or2ak6 |
A |
T |
11: 58,592,495 (GRCm39) |
|
probably benign |
Het |
Or2g7 |
C |
T |
17: 38,378,862 (GRCm39) |
H267Y |
probably benign |
Het |
Or2y17 |
A |
T |
11: 49,231,757 (GRCm39) |
T133S |
probably damaging |
Het |
Or52n4b |
A |
G |
7: 108,144,452 (GRCm39) |
K238R |
probably damaging |
Het |
Or5b114-ps1 |
C |
A |
19: 13,352,336 (GRCm39) |
N3K |
probably damaging |
Het |
Or8c11 |
T |
A |
9: 38,289,729 (GRCm39) |
M184K |
probably damaging |
Het |
Or8k16 |
A |
G |
2: 85,520,255 (GRCm39) |
S161G |
possibly damaging |
Het |
Pcdhb6 |
A |
C |
18: 37,469,329 (GRCm39) |
Q750P |
possibly damaging |
Het |
Plppr4 |
T |
C |
3: 117,153,683 (GRCm39) |
Y72C |
probably damaging |
Het |
Rasgrf2 |
G |
T |
13: 92,159,100 (GRCm39) |
|
probably benign |
Het |
Sbk2 |
A |
G |
7: 4,961,905 (GRCm39) |
I127T |
probably damaging |
Het |
Smchd1 |
A |
C |
17: 71,722,039 (GRCm39) |
S817A |
probably benign |
Het |
Speer4b |
A |
T |
5: 27,705,123 (GRCm39) |
N83K |
probably damaging |
Het |
Strc |
A |
T |
2: 121,201,207 (GRCm39) |
L1296Q |
probably damaging |
Het |
Thap11 |
C |
A |
8: 106,582,215 (GRCm39) |
R75S |
possibly damaging |
Het |
Unc13a |
A |
C |
8: 72,111,407 (GRCm39) |
L268R |
possibly damaging |
Het |
Zfp39 |
A |
T |
11: 58,781,269 (GRCm39) |
C498S |
unknown |
Het |
Zfp507 |
T |
C |
7: 35,494,978 (GRCm39) |
T22A |
possibly damaging |
Het |
Zfp85 |
T |
C |
13: 67,897,712 (GRCm39) |
Y120C |
probably benign |
Het |
Zfp882 |
G |
A |
8: 72,667,093 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Nudcd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Nudcd1
|
APN |
15 |
44,284,222 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01956:Nudcd1
|
APN |
15 |
44,263,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Nudcd1
|
APN |
15 |
44,269,357 (GRCm39) |
missense |
probably benign |
0.41 |
R0333:Nudcd1
|
UTSW |
15 |
44,264,683 (GRCm39) |
missense |
probably benign |
|
R0960:Nudcd1
|
UTSW |
15 |
44,291,047 (GRCm39) |
unclassified |
probably benign |
|
R3409:Nudcd1
|
UTSW |
15 |
44,284,207 (GRCm39) |
missense |
probably benign |
0.17 |
R3410:Nudcd1
|
UTSW |
15 |
44,284,207 (GRCm39) |
missense |
probably benign |
0.17 |
R4771:Nudcd1
|
UTSW |
15 |
44,268,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R4970:Nudcd1
|
UTSW |
15 |
44,240,039 (GRCm39) |
nonsense |
probably null |
|
R5112:Nudcd1
|
UTSW |
15 |
44,240,039 (GRCm39) |
nonsense |
probably null |
|
R5789:Nudcd1
|
UTSW |
15 |
44,251,879 (GRCm39) |
nonsense |
probably null |
|
R6353:Nudcd1
|
UTSW |
15 |
44,284,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Nudcd1
|
UTSW |
15 |
44,269,253 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7742:Nudcd1
|
UTSW |
15 |
44,268,754 (GRCm39) |
missense |
probably benign |
0.06 |
R8949:Nudcd1
|
UTSW |
15 |
44,251,971 (GRCm39) |
missense |
probably benign |
0.00 |
R9066:Nudcd1
|
UTSW |
15 |
44,243,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Nudcd1
|
UTSW |
15 |
44,263,473 (GRCm39) |
missense |
probably benign |
0.00 |
R9438:Nudcd1
|
UTSW |
15 |
44,269,321 (GRCm39) |
missense |
probably benign |
0.15 |
Z1177:Nudcd1
|
UTSW |
15 |
44,268,828 (GRCm39) |
missense |
probably benign |
0.01 |
|