Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
A |
T |
7: 29,274,214 (GRCm39) |
|
noncoding transcript |
Het |
Abca14 |
A |
G |
7: 119,850,431 (GRCm39) |
E761G |
probably benign |
Het |
Apc |
C |
T |
18: 34,394,179 (GRCm39) |
T35I |
probably damaging |
Het |
Arhgef2 |
T |
A |
3: 88,541,723 (GRCm39) |
I228N |
probably damaging |
Het |
Atp6v1g2 |
A |
G |
17: 35,456,638 (GRCm39) |
E74G |
probably damaging |
Het |
Ccdc70 |
A |
G |
8: 22,463,447 (GRCm39) |
E79G |
probably damaging |
Het |
Cdc42ep4 |
A |
G |
11: 113,619,528 (GRCm39) |
S288P |
probably damaging |
Het |
Cip2a |
C |
T |
16: 48,837,828 (GRCm39) |
Q843* |
probably null |
Het |
Cpn2 |
T |
C |
16: 30,078,321 (GRCm39) |
D460G |
probably benign |
Het |
Crtam |
A |
G |
9: 40,884,811 (GRCm39) |
*393Q |
probably null |
Het |
Cwc22 |
A |
G |
2: 77,757,591 (GRCm39) |
I179T |
probably damaging |
Het |
Dnah8 |
A |
T |
17: 30,896,178 (GRCm39) |
D864V |
probably benign |
Het |
Map3k7 |
T |
C |
4: 31,964,302 (GRCm39) |
S14P |
unknown |
Het |
Med25 |
A |
G |
7: 44,534,566 (GRCm39) |
S150P |
probably damaging |
Het |
Mex3b |
T |
C |
7: 82,517,070 (GRCm39) |
V71A |
probably benign |
Het |
Morc3 |
T |
C |
16: 93,638,275 (GRCm39) |
L19S |
probably damaging |
Het |
Morn1 |
T |
A |
4: 155,176,770 (GRCm39) |
S98T |
probably damaging |
Het |
Mthfd1l |
G |
T |
10: 4,006,771 (GRCm39) |
A678S |
probably damaging |
Het |
Napa |
A |
G |
7: 15,848,083 (GRCm39) |
Y200C |
probably damaging |
Het |
Nr5a2 |
T |
C |
1: 136,876,565 (GRCm39) |
I33V |
probably benign |
Het |
Or14j6 |
A |
G |
17: 38,215,345 (GRCm39) |
K303E |
possibly damaging |
Het |
Pcnx1 |
A |
G |
12: 81,996,960 (GRCm39) |
D952G |
probably damaging |
Het |
Phf20l1 |
G |
A |
15: 66,466,769 (GRCm39) |
R66Q |
probably damaging |
Het |
Resf1 |
A |
G |
6: 149,236,145 (GRCm39) |
I1488M |
probably benign |
Het |
Rfk |
A |
G |
19: 17,375,960 (GRCm39) |
T85A |
probably benign |
Het |
Sbno2 |
T |
C |
10: 79,893,855 (GRCm39) |
D1179G |
possibly damaging |
Het |
Serpina3k |
C |
T |
12: 104,307,166 (GRCm39) |
Q133* |
probably null |
Het |
Setd4 |
T |
C |
16: 93,383,122 (GRCm39) |
|
probably benign |
Het |
Sh2d4b |
C |
T |
14: 40,582,548 (GRCm39) |
|
probably null |
Het |
Slc1a6 |
G |
A |
10: 78,648,718 (GRCm39) |
V480I |
possibly damaging |
Het |
Slc39a3 |
A |
T |
10: 80,867,104 (GRCm39) |
V214E |
possibly damaging |
Het |
Tll1 |
A |
G |
8: 64,504,435 (GRCm39) |
Y654H |
probably damaging |
Het |
Traf3ip1 |
T |
A |
1: 91,427,374 (GRCm39) |
C115S |
unknown |
Het |
Vmn1r209 |
T |
A |
13: 22,989,836 (GRCm39) |
I285F |
probably damaging |
Het |
Vmn2r87 |
G |
T |
10: 130,315,631 (GRCm39) |
T145K |
probably damaging |
Het |
Zan |
T |
C |
5: 137,394,388 (GRCm39) |
T4484A |
unknown |
Het |
Zfp768 |
T |
C |
7: 126,943,810 (GRCm39) |
E106G |
probably benign |
Het |
Zfp984 |
A |
G |
4: 147,839,234 (GRCm39) |
I539T |
possibly damaging |
Het |
|
Other mutations in Cyp3a41b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00538:Cyp3a41b
|
APN |
5 |
145,515,010 (GRCm39) |
splice site |
probably benign |
|
IGL02341:Cyp3a41b
|
APN |
5 |
145,510,461 (GRCm39) |
missense |
probably benign |
0.34 |
R0284:Cyp3a41b
|
UTSW |
5 |
145,515,014 (GRCm39) |
splice site |
probably benign |
|
R1857:Cyp3a41b
|
UTSW |
5 |
145,503,660 (GRCm39) |
missense |
probably benign |
0.06 |
R2269:Cyp3a41b
|
UTSW |
5 |
145,514,976 (GRCm39) |
missense |
probably benign |
0.10 |
R4299:Cyp3a41b
|
UTSW |
5 |
145,510,487 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4801:Cyp3a41b
|
UTSW |
5 |
145,510,461 (GRCm39) |
missense |
probably benign |
0.34 |
R4802:Cyp3a41b
|
UTSW |
5 |
145,510,461 (GRCm39) |
missense |
probably benign |
0.34 |
R5911:Cyp3a41b
|
UTSW |
5 |
145,519,349 (GRCm39) |
missense |
probably benign |
0.01 |
R6363:Cyp3a41b
|
UTSW |
5 |
145,507,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7198:Cyp3a41b
|
UTSW |
5 |
145,519,330 (GRCm39) |
missense |
probably benign |
0.00 |
R7410:Cyp3a41b
|
UTSW |
5 |
145,514,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R8221:Cyp3a41b
|
UTSW |
5 |
145,506,190 (GRCm39) |
missense |
probably benign |
0.01 |
R8923:Cyp3a41b
|
UTSW |
5 |
145,521,448 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9064:Cyp3a41b
|
UTSW |
5 |
145,514,910 (GRCm39) |
missense |
probably damaging |
0.97 |
R9091:Cyp3a41b
|
UTSW |
5 |
145,514,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9270:Cyp3a41b
|
UTSW |
5 |
145,514,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|