Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
A |
T |
11: 110,100,927 (GRCm39) |
V953D |
probably damaging |
Het |
Abcb8 |
T |
C |
5: 24,610,879 (GRCm39) |
|
probably benign |
Het |
Acad12 |
A |
T |
5: 121,742,243 (GRCm39) |
|
probably benign |
Het |
Adam2 |
A |
T |
14: 66,283,595 (GRCm39) |
C436S |
probably damaging |
Het |
Aebp2 |
T |
C |
6: 140,569,943 (GRCm39) |
|
probably benign |
Het |
Akap8 |
A |
T |
17: 32,536,159 (GRCm39) |
C85S |
possibly damaging |
Het |
Aldh1a3 |
C |
A |
7: 66,068,927 (GRCm39) |
R19L |
probably damaging |
Het |
Baz2a |
A |
G |
10: 127,955,559 (GRCm39) |
T848A |
possibly damaging |
Het |
Bud13 |
C |
T |
9: 46,199,350 (GRCm39) |
A237V |
probably benign |
Het |
Cbarp |
CGCCTCTGCTGCCTCT |
CGCCTCT |
10: 79,968,067 (GRCm39) |
|
probably benign |
Het |
Ccdc187 |
G |
A |
2: 26,166,104 (GRCm39) |
P775L |
possibly damaging |
Het |
Ccz1 |
C |
T |
5: 143,929,328 (GRCm39) |
G367R |
probably damaging |
Het |
Cep104 |
T |
C |
4: 154,065,681 (GRCm39) |
V56A |
possibly damaging |
Het |
Chd6 |
C |
A |
2: 160,798,998 (GRCm39) |
R2362S |
probably damaging |
Het |
Chd6 |
C |
T |
2: 160,798,999 (GRCm39) |
R2362K |
probably damaging |
Het |
Cmc1 |
T |
C |
9: 117,944,443 (GRCm39) |
E25G |
probably benign |
Het |
Cntnap5b |
T |
C |
1: 100,374,619 (GRCm39) |
S1123P |
probably damaging |
Het |
Col4a3 |
T |
A |
1: 82,693,778 (GRCm39) |
L66* |
probably null |
Het |
Crmp1 |
A |
G |
5: 37,440,212 (GRCm39) |
T329A |
probably benign |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Cyp3a16 |
A |
G |
5: 145,378,843 (GRCm39) |
S393P |
possibly damaging |
Het |
Cyp4f18 |
T |
A |
8: 72,749,975 (GRCm39) |
I225F |
probably damaging |
Het |
Ecpas |
T |
C |
4: 58,853,131 (GRCm39) |
I401M |
probably damaging |
Het |
Foxq1 |
G |
A |
13: 31,743,314 (GRCm39) |
A139T |
probably damaging |
Het |
Gm10428 |
G |
T |
11: 62,644,169 (GRCm39) |
|
probably benign |
Het |
Gpr89 |
A |
G |
3: 96,800,196 (GRCm39) |
L134P |
probably damaging |
Het |
Hjv |
T |
C |
3: 96,435,938 (GRCm39) |
S399P |
probably benign |
Het |
Hrc |
A |
T |
7: 44,986,025 (GRCm39) |
|
probably null |
Het |
Igf1r |
T |
A |
7: 67,857,001 (GRCm39) |
Y988N |
probably damaging |
Het |
Igf2r |
A |
C |
17: 12,917,239 (GRCm39) |
|
probably null |
Het |
Itga2b |
A |
G |
11: 102,357,100 (GRCm39) |
F260S |
probably benign |
Het |
Kif2a |
T |
A |
13: 107,098,672 (GRCm39) |
N698I |
probably benign |
Het |
Lap3 |
A |
C |
5: 45,662,147 (GRCm39) |
I316L |
probably benign |
Het |
Map2k6 |
T |
G |
11: 110,290,197 (GRCm39) |
|
probably benign |
Het |
Mtrex |
T |
A |
13: 113,054,196 (GRCm39) |
I146F |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,110,078 (GRCm39) |
E1422G |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,250,061 (GRCm39) |
V1081A |
probably benign |
Het |
Nom1 |
A |
G |
5: 29,642,639 (GRCm39) |
E380G |
probably damaging |
Het |
Nwd2 |
A |
T |
5: 63,882,573 (GRCm39) |
Y75F |
probably damaging |
Het |
Or3a1b |
T |
A |
11: 74,012,335 (GRCm39) |
D73E |
probably damaging |
Het |
Or51a24 |
G |
A |
7: 103,733,376 (GRCm39) |
R304W |
probably benign |
Het |
Pkd1l1 |
A |
G |
11: 8,866,301 (GRCm39) |
V518A |
probably damaging |
Het |
Ptgs2 |
A |
G |
1: 149,981,279 (GRCm39) |
M521V |
probably benign |
Het |
Qsox1 |
T |
A |
1: 155,655,274 (GRCm39) |
M630L |
probably benign |
Het |
Spty2d1 |
A |
G |
7: 46,648,032 (GRCm39) |
L299P |
probably damaging |
Het |
St6gal1 |
T |
G |
16: 23,139,805 (GRCm39) |
|
probably benign |
Het |
Sult2a6 |
T |
C |
7: 13,984,283 (GRCm39) |
Y149C |
probably damaging |
Het |
Tlr3 |
G |
A |
8: 45,855,808 (GRCm39) |
T124M |
probably benign |
Het |
Tmem171 |
A |
G |
13: 98,829,019 (GRCm39) |
Y44H |
probably damaging |
Het |
Usp35 |
C |
T |
7: 96,961,558 (GRCm39) |
V623I |
probably benign |
Het |
Vangl2 |
T |
A |
1: 171,833,694 (GRCm39) |
H463L |
probably damaging |
Het |
Vmn1r175 |
A |
C |
7: 23,507,905 (GRCm39) |
L241V |
probably benign |
Het |
Vmn1r19 |
A |
T |
6: 57,382,338 (GRCm39) |
K297I |
unknown |
Het |
Vmn2r23 |
C |
A |
6: 123,689,718 (GRCm39) |
T198K |
probably benign |
Het |
Vmn2r-ps69 |
T |
A |
7: 84,953,223 (GRCm39) |
|
noncoding transcript |
Het |
Xirp2 |
A |
G |
2: 67,341,311 (GRCm39) |
Y1184C |
probably benign |
Het |
Ythdc1 |
A |
G |
5: 86,983,810 (GRCm39) |
|
probably benign |
Het |
Zbtb39 |
C |
T |
10: 127,578,515 (GRCm39) |
A363V |
probably damaging |
Het |
Zmiz1 |
T |
A |
14: 25,651,728 (GRCm39) |
I527K |
possibly damaging |
Het |
Zmiz1 |
C |
A |
14: 25,651,730 (GRCm39) |
P534T |
probably damaging |
Het |
|
Other mutations in Ddhd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01501:Ddhd2
|
APN |
8 |
26,225,857 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01629:Ddhd2
|
APN |
8 |
26,225,855 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01656:Ddhd2
|
APN |
8 |
26,217,739 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01723:Ddhd2
|
APN |
8 |
26,225,038 (GRCm39) |
nonsense |
probably null |
|
IGL01820:Ddhd2
|
APN |
8 |
26,239,781 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01901:Ddhd2
|
APN |
8 |
26,238,621 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02619:Ddhd2
|
APN |
8 |
26,236,981 (GRCm39) |
critical splice acceptor site |
probably null |
|
PIT4362001:Ddhd2
|
UTSW |
8 |
26,225,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Ddhd2
|
UTSW |
8 |
26,229,617 (GRCm39) |
splice site |
probably null |
|
R0240:Ddhd2
|
UTSW |
8 |
26,229,617 (GRCm39) |
splice site |
probably null |
|
R0408:Ddhd2
|
UTSW |
8 |
26,229,614 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0732:Ddhd2
|
UTSW |
8 |
26,231,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1483:Ddhd2
|
UTSW |
8 |
26,243,155 (GRCm39) |
missense |
probably benign |
0.01 |
R1597:Ddhd2
|
UTSW |
8 |
26,239,768 (GRCm39) |
missense |
probably benign |
0.09 |
R1881:Ddhd2
|
UTSW |
8 |
26,217,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R1927:Ddhd2
|
UTSW |
8 |
26,231,688 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2044:Ddhd2
|
UTSW |
8 |
26,242,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Ddhd2
|
UTSW |
8 |
26,228,261 (GRCm39) |
missense |
probably benign |
0.01 |
R4728:Ddhd2
|
UTSW |
8 |
26,242,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Ddhd2
|
UTSW |
8 |
26,242,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R5138:Ddhd2
|
UTSW |
8 |
26,217,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Ddhd2
|
UTSW |
8 |
26,229,587 (GRCm39) |
missense |
probably benign |
0.00 |
R5799:Ddhd2
|
UTSW |
8 |
26,238,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Ddhd2
|
UTSW |
8 |
26,243,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Ddhd2
|
UTSW |
8 |
26,225,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Ddhd2
|
UTSW |
8 |
26,238,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Ddhd2
|
UTSW |
8 |
26,242,144 (GRCm39) |
missense |
probably benign |
0.00 |
R6791:Ddhd2
|
UTSW |
8 |
26,242,242 (GRCm39) |
missense |
probably benign |
0.04 |
R7386:Ddhd2
|
UTSW |
8 |
26,244,318 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7470:Ddhd2
|
UTSW |
8 |
26,225,087 (GRCm39) |
missense |
probably benign |
0.06 |
R7911:Ddhd2
|
UTSW |
8 |
26,238,563 (GRCm39) |
critical splice donor site |
probably null |
|
R8153:Ddhd2
|
UTSW |
8 |
26,240,816 (GRCm39) |
missense |
probably benign |
0.16 |
R8385:Ddhd2
|
UTSW |
8 |
26,225,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R9190:Ddhd2
|
UTSW |
8 |
26,244,495 (GRCm39) |
missense |
probably benign |
0.18 |
R9381:Ddhd2
|
UTSW |
8 |
26,239,849 (GRCm39) |
missense |
probably benign |
0.17 |
R9497:Ddhd2
|
UTSW |
8 |
26,217,731 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1176:Ddhd2
|
UTSW |
8 |
26,225,856 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1177:Ddhd2
|
UTSW |
8 |
26,244,413 (GRCm39) |
missense |
unknown |
|
Z1177:Ddhd2
|
UTSW |
8 |
26,244,402 (GRCm39) |
missense |
probably benign |
|
|