Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
A |
T |
2: 103,535,417 (GRCm39) |
Y528F |
possibly damaging |
Het |
Acad10 |
G |
A |
5: 121,787,604 (GRCm39) |
T115I |
possibly damaging |
Het |
Adam19 |
T |
C |
11: 46,018,092 (GRCm39) |
F385L |
probably damaging |
Het |
Adgb |
T |
C |
10: 10,318,357 (GRCm39) |
N162D |
probably benign |
Het |
Arhgap20 |
C |
A |
9: 51,757,570 (GRCm39) |
P521T |
probably damaging |
Het |
Arsa |
A |
T |
15: 89,359,380 (GRCm39) |
L134Q |
probably damaging |
Het |
Atp5f1b |
A |
G |
10: 127,925,921 (GRCm39) |
Y508C |
probably damaging |
Het |
AW554918 |
G |
A |
18: 25,553,067 (GRCm39) |
M287I |
probably benign |
Het |
Bmp4 |
T |
C |
14: 46,621,360 (GRCm39) |
K395E |
probably damaging |
Het |
Cacna2d4 |
A |
G |
6: 119,277,294 (GRCm39) |
Y669C |
probably damaging |
Het |
Casq2 |
T |
C |
3: 102,051,550 (GRCm39) |
|
probably null |
Het |
Cdk5rap1 |
A |
T |
2: 154,202,519 (GRCm39) |
I237N |
possibly damaging |
Het |
Cerk |
G |
C |
15: 86,033,565 (GRCm39) |
S286C |
possibly damaging |
Het |
Cir1 |
A |
C |
2: 73,117,987 (GRCm39) |
L186R |
probably damaging |
Het |
Csf3r |
A |
T |
4: 125,936,781 (GRCm39) |
|
probably null |
Het |
Cyp8b1 |
A |
G |
9: 121,744,348 (GRCm39) |
F328S |
possibly damaging |
Het |
Dzank1 |
A |
T |
2: 144,355,365 (GRCm39) |
V110D |
probably benign |
Het |
Gm6729 |
T |
A |
10: 86,376,799 (GRCm39) |
|
noncoding transcript |
Het |
Gnpat |
T |
C |
8: 125,604,246 (GRCm39) |
F246L |
probably benign |
Het |
Gnpat |
T |
A |
8: 125,605,255 (GRCm39) |
L248H |
probably damaging |
Het |
Gstm7 |
T |
C |
3: 107,834,266 (GRCm39) |
T163A |
probably benign |
Het |
Hspa5 |
A |
G |
2: 34,665,110 (GRCm39) |
T424A |
probably damaging |
Het |
Itgb1 |
T |
G |
8: 129,439,786 (GRCm39) |
D158E |
probably damaging |
Het |
Kif21a |
A |
G |
15: 90,819,853 (GRCm39) |
V1637A |
probably benign |
Het |
Kl |
G |
T |
5: 150,905,985 (GRCm39) |
V452F |
probably damaging |
Het |
Krt23 |
T |
C |
11: 99,369,045 (GRCm39) |
N416S |
probably benign |
Het |
Lama4 |
A |
T |
10: 38,968,241 (GRCm39) |
H1461L |
possibly damaging |
Het |
Lamc3 |
A |
G |
2: 31,818,814 (GRCm39) |
T1180A |
probably benign |
Het |
Mboat2 |
T |
C |
12: 24,996,527 (GRCm39) |
Y145H |
probably damaging |
Het |
Mlxipl |
T |
A |
5: 135,142,564 (GRCm39) |
I126N |
probably damaging |
Het |
Myo16 |
T |
A |
8: 10,620,181 (GRCm39) |
N1577K |
possibly damaging |
Het |
Nlrp4f |
A |
G |
13: 65,332,897 (GRCm39) |
V87A |
possibly damaging |
Het |
Or5al5 |
A |
G |
2: 85,961,915 (GRCm39) |
F31L |
probably benign |
Het |
Or6p1 |
A |
T |
1: 174,258,701 (GRCm39) |
K236* |
probably null |
Het |
Pask |
A |
T |
1: 93,258,549 (GRCm39) |
D266E |
probably benign |
Het |
Pcdhb17 |
A |
G |
18: 37,619,899 (GRCm39) |
Y563C |
probably damaging |
Het |
Pdlim3 |
T |
A |
8: 46,349,837 (GRCm39) |
I49N |
probably damaging |
Het |
Pla2g4c |
T |
A |
7: 13,077,334 (GRCm39) |
V292E |
possibly damaging |
Het |
Pramel23 |
T |
C |
4: 143,423,477 (GRCm39) |
I437M |
possibly damaging |
Het |
Prrt4 |
G |
T |
6: 29,169,813 (GRCm39) |
Q880K |
possibly damaging |
Het |
Pygb |
A |
G |
2: 150,628,858 (GRCm39) |
D24G |
probably benign |
Het |
R3hcc1l |
T |
A |
19: 42,552,093 (GRCm39) |
D363E |
probably damaging |
Het |
Rif1 |
A |
C |
2: 52,001,574 (GRCm39) |
Q1676P |
probably benign |
Het |
Ryr1 |
C |
A |
7: 28,795,683 (GRCm39) |
R1069L |
probably damaging |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Slc2a13 |
A |
G |
15: 91,296,363 (GRCm39) |
V317A |
probably damaging |
Het |
Slc35b4 |
A |
T |
6: 34,138,619 (GRCm39) |
F197I |
probably damaging |
Het |
Tchhl1 |
G |
A |
3: 93,377,520 (GRCm39) |
V75I |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,182,771 (GRCm39) |
S3521P |
possibly damaging |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp335 |
GTCCTCCTCCTCCTCCTC |
GTCCTCCTCCTCCTC |
2: 164,749,388 (GRCm39) |
|
probably benign |
Het |
Zfp874a |
T |
G |
13: 67,590,539 (GRCm39) |
I382L |
possibly damaging |
Het |
|
Other mutations in Cyp3a41a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02284:Cyp3a41a
|
APN |
5 |
145,641,673 (GRCm39) |
splice site |
probably benign |
|
IGL03003:Cyp3a41a
|
APN |
5 |
145,642,640 (GRCm39) |
missense |
probably benign |
|
R0006:Cyp3a41a
|
UTSW |
5 |
145,641,606 (GRCm39) |
missense |
probably benign |
0.01 |
R0515:Cyp3a41a
|
UTSW |
5 |
145,654,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3708:Cyp3a41a
|
UTSW |
5 |
145,654,733 (GRCm39) |
critical splice donor site |
probably null |
|
R4049:Cyp3a41a
|
UTSW |
5 |
145,650,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Cyp3a41a
|
UTSW |
5 |
145,652,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Cyp3a41a
|
UTSW |
5 |
145,656,858 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R6519:Cyp3a41a
|
UTSW |
5 |
145,652,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Cyp3a41a
|
UTSW |
5 |
145,642,639 (GRCm39) |
missense |
probably benign |
0.00 |
R7184:Cyp3a41a
|
UTSW |
5 |
145,642,663 (GRCm39) |
missense |
probably benign |
0.01 |
R7372:Cyp3a41a
|
UTSW |
5 |
145,650,374 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7451:Cyp3a41a
|
UTSW |
5 |
145,636,550 (GRCm39) |
missense |
probably benign |
0.10 |
R7463:Cyp3a41a
|
UTSW |
5 |
145,650,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7766:Cyp3a41a
|
UTSW |
5 |
145,654,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R9179:Cyp3a41a
|
UTSW |
5 |
145,642,654 (GRCm39) |
missense |
probably benign |
|
R9225:Cyp3a41a
|
UTSW |
5 |
145,650,414 (GRCm39) |
missense |
probably benign |
0.03 |
R9300:Cyp3a41a
|
UTSW |
5 |
145,656,906 (GRCm39) |
start gained |
probably benign |
|
R9308:Cyp3a41a
|
UTSW |
5 |
145,656,858 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9403:Cyp3a41a
|
UTSW |
5 |
145,639,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R9635:Cyp3a41a
|
UTSW |
5 |
145,652,320 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9682:Cyp3a41a
|
UTSW |
5 |
145,652,326 (GRCm39) |
missense |
possibly damaging |
0.66 |
|