Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
T |
A |
18: 6,635,934 (GRCm39) |
L329Q |
probably damaging |
Het |
Adam26b |
A |
T |
8: 43,974,009 (GRCm39) |
M331K |
possibly damaging |
Het |
Ak3 |
T |
C |
19: 29,025,118 (GRCm39) |
S38G |
probably damaging |
Het |
Ankrd10 |
A |
T |
8: 11,665,788 (GRCm39) |
C271S |
possibly damaging |
Het |
Ap1s3 |
A |
G |
1: 79,601,494 (GRCm39) |
Y66H |
probably damaging |
Het |
Ap4b1 |
A |
T |
3: 103,729,065 (GRCm39) |
I736L |
probably benign |
Het |
Arpp19 |
T |
A |
9: 74,963,948 (GRCm39) |
M67K |
possibly damaging |
Het |
Brf1 |
T |
G |
12: 112,951,589 (GRCm39) |
H130P |
probably damaging |
Het |
Cacna1s |
C |
G |
1: 136,045,392 (GRCm39) |
T1680S |
probably benign |
Het |
Cckar |
C |
T |
5: 53,864,583 (GRCm39) |
|
probably benign |
Het |
Cd93 |
T |
C |
2: 148,283,532 (GRCm39) |
K605E |
probably benign |
Het |
Cdcp3 |
T |
C |
7: 130,867,566 (GRCm39) |
M1409T |
unknown |
Het |
Ces1h |
C |
T |
8: 94,080,093 (GRCm39) |
V474I |
unknown |
Het |
Cfap70 |
A |
T |
14: 20,493,669 (GRCm39) |
|
probably null |
Het |
Ch25h |
G |
A |
19: 34,452,441 (GRCm39) |
T29I |
possibly damaging |
Het |
Csmd3 |
T |
A |
15: 48,222,739 (GRCm39) |
T329S |
probably benign |
Het |
Cux1 |
T |
C |
5: 136,315,623 (GRCm39) |
N1139S |
probably damaging |
Het |
Cyp2j6 |
G |
T |
4: 96,414,087 (GRCm39) |
H393N |
probably benign |
Het |
Dchs2 |
T |
G |
3: 83,036,720 (GRCm39) |
L489R |
probably damaging |
Het |
Dip2a |
T |
C |
10: 76,110,098 (GRCm39) |
T1173A |
probably benign |
Het |
Exoc3l2 |
T |
G |
7: 19,203,931 (GRCm39) |
|
probably null |
Het |
Fastkd3 |
G |
A |
13: 68,732,303 (GRCm39) |
R208H |
probably damaging |
Het |
Fbxo16 |
C |
A |
14: 65,531,287 (GRCm39) |
R64S |
probably benign |
Het |
Frem3 |
A |
T |
8: 81,339,419 (GRCm39) |
I571F |
probably damaging |
Het |
Ftsj3 |
T |
A |
11: 106,144,602 (GRCm39) |
D129V |
probably damaging |
Het |
Gm6370 |
A |
G |
5: 146,430,447 (GRCm39) |
T211A |
probably benign |
Het |
Gpr171 |
A |
T |
3: 59,005,116 (GRCm39) |
S220T |
probably benign |
Het |
Gsta3 |
T |
C |
1: 21,330,370 (GRCm39) |
I124T |
probably benign |
Het |
Hydin |
A |
G |
8: 111,316,112 (GRCm39) |
I4335V |
probably benign |
Het |
Ift80 |
T |
C |
3: 68,857,809 (GRCm39) |
I279V |
probably benign |
Het |
Ighv1-13 |
T |
A |
12: 114,594,439 (GRCm39) |
M47K |
unknown |
Het |
Il22ra2 |
A |
G |
10: 19,507,401 (GRCm39) |
N138S |
probably damaging |
Het |
Impact |
A |
G |
18: 13,123,551 (GRCm39) |
D298G |
probably benign |
Het |
Ipo7 |
T |
C |
7: 109,643,943 (GRCm39) |
|
probably null |
Het |
Kif5b |
T |
C |
18: 6,225,437 (GRCm39) |
N198D |
probably damaging |
Het |
Klhl36 |
A |
G |
8: 120,597,279 (GRCm39) |
T327A |
probably benign |
Het |
Lepr |
A |
G |
4: 101,649,233 (GRCm39) |
N878S |
probably damaging |
Het |
Lpxn |
T |
A |
19: 12,802,525 (GRCm39) |
F244L |
probably damaging |
Het |
Lrriq4 |
C |
A |
3: 30,709,807 (GRCm39) |
L384I |
probably damaging |
Het |
Ltbp4 |
A |
C |
7: 27,026,119 (GRCm39) |
I629S |
probably benign |
Het |
Lypd5 |
T |
C |
7: 24,051,015 (GRCm39) |
V42A |
probably benign |
Het |
Mc4r |
A |
G |
18: 66,992,304 (GRCm39) |
S270P |
probably damaging |
Het |
Mctp2 |
T |
G |
7: 71,909,311 (GRCm39) |
M1L |
probably benign |
Het |
Myh4 |
G |
A |
11: 67,137,362 (GRCm39) |
E528K |
possibly damaging |
Het |
Nes |
T |
A |
3: 87,886,653 (GRCm39) |
H1637Q |
possibly damaging |
Het |
Or4f7 |
T |
C |
2: 111,644,576 (GRCm39) |
D165G |
probably benign |
Het |
Or5g25 |
A |
T |
2: 85,478,187 (GRCm39) |
H159Q |
possibly damaging |
Het |
Or8b3b |
C |
T |
9: 38,584,147 (GRCm39) |
V198I |
probably damaging |
Het |
Pan3 |
T |
C |
5: 147,387,472 (GRCm39) |
M147T |
probably benign |
Het |
Pcdhga6 |
G |
T |
18: 37,841,642 (GRCm39) |
R454L |
probably benign |
Het |
Pdss2 |
A |
G |
10: 43,221,663 (GRCm39) |
S192G |
probably damaging |
Het |
Pld6 |
A |
T |
11: 59,678,382 (GRCm39) |
M27K |
probably benign |
Het |
Plec |
C |
T |
15: 76,057,598 (GRCm39) |
R4113H |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,467,953 (GRCm39) |
S1379P |
probably damaging |
Het |
Rapgef2 |
T |
C |
3: 79,019,566 (GRCm39) |
H35R |
probably damaging |
Het |
Rasgrp2 |
A |
G |
19: 6,453,100 (GRCm39) |
T75A |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,378,437 (GRCm39) |
L1172P |
probably damaging |
Het |
Rfx7 |
C |
T |
9: 72,525,123 (GRCm39) |
S771L |
probably benign |
Het |
Rpap3 |
A |
G |
15: 97,585,998 (GRCm39) |
I331T |
probably benign |
Het |
Scn2a |
A |
G |
2: 65,546,002 (GRCm39) |
|
probably null |
Het |
Sec23ip |
T |
A |
7: 128,354,467 (GRCm39) |
V241D |
probably benign |
Het |
Sez6l |
C |
A |
5: 112,588,744 (GRCm39) |
Q656H |
possibly damaging |
Het |
Sh3gl2 |
A |
T |
4: 85,273,597 (GRCm39) |
I50L |
probably benign |
Het |
Tab2 |
T |
C |
10: 7,786,897 (GRCm39) |
D605G |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,845,374 (GRCm39) |
V135D |
probably damaging |
Het |
Thap12 |
T |
C |
7: 98,364,534 (GRCm39) |
M234T |
probably benign |
Het |
Trhr |
C |
A |
15: 44,060,736 (GRCm39) |
D85E |
probably benign |
Het |
Trim67 |
A |
G |
8: 125,552,718 (GRCm39) |
I607V |
probably benign |
Het |
Trpm4 |
C |
T |
7: 44,960,055 (GRCm39) |
C760Y |
probably benign |
Het |
Ttll9 |
T |
C |
2: 152,844,841 (GRCm39) |
V403A |
probably damaging |
Het |
Uhrf1 |
T |
C |
17: 56,617,817 (GRCm39) |
Y180H |
probably damaging |
Het |
Unc119b |
C |
T |
5: 115,272,977 (GRCm39) |
|
probably benign |
Het |
Vmn2r44 |
T |
A |
7: 8,381,242 (GRCm39) |
D217V |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,979,137 (GRCm39) |
L425F |
probably damaging |
Het |
Zscan4-ps3 |
A |
T |
7: 11,346,767 (GRCm39) |
R268* |
probably null |
Het |
|
Other mutations in Cyp8b1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01527:Cyp8b1
|
APN |
9 |
121,744,061 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01874:Cyp8b1
|
APN |
9 |
121,744,969 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02004:Cyp8b1
|
APN |
9 |
121,744,058 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02218:Cyp8b1
|
APN |
9 |
121,744,183 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Cyp8b1
|
APN |
9 |
121,744,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02724:Cyp8b1
|
APN |
9 |
121,744,453 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02796:Cyp8b1
|
UTSW |
9 |
121,744,564 (GRCm39) |
missense |
probably benign |
|
R1052:Cyp8b1
|
UTSW |
9 |
121,744,348 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1223:Cyp8b1
|
UTSW |
9 |
121,744,070 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1572:Cyp8b1
|
UTSW |
9 |
121,744,024 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1639:Cyp8b1
|
UTSW |
9 |
121,743,956 (GRCm39) |
missense |
probably benign |
0.01 |
R3833:Cyp8b1
|
UTSW |
9 |
121,745,109 (GRCm39) |
missense |
probably benign |
0.00 |
R3938:Cyp8b1
|
UTSW |
9 |
121,744,684 (GRCm39) |
missense |
probably benign |
0.05 |
R4151:Cyp8b1
|
UTSW |
9 |
121,745,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R4615:Cyp8b1
|
UTSW |
9 |
121,745,164 (GRCm39) |
nonsense |
probably null |
|
R4625:Cyp8b1
|
UTSW |
9 |
121,744,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R5327:Cyp8b1
|
UTSW |
9 |
121,743,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R6391:Cyp8b1
|
UTSW |
9 |
121,744,864 (GRCm39) |
nonsense |
probably null |
|
R6998:Cyp8b1
|
UTSW |
9 |
121,745,059 (GRCm39) |
missense |
probably benign |
|
R7086:Cyp8b1
|
UTSW |
9 |
121,744,355 (GRCm39) |
missense |
probably benign |
0.02 |
R7162:Cyp8b1
|
UTSW |
9 |
121,744,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R7210:Cyp8b1
|
UTSW |
9 |
121,744,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Cyp8b1
|
UTSW |
9 |
121,744,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Cyp8b1
|
UTSW |
9 |
121,744,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R8392:Cyp8b1
|
UTSW |
9 |
121,744,300 (GRCm39) |
missense |
probably damaging |
0.98 |
R8452:Cyp8b1
|
UTSW |
9 |
121,744,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R8672:Cyp8b1
|
UTSW |
9 |
121,743,986 (GRCm39) |
missense |
probably benign |
0.00 |
R9484:Cyp8b1
|
UTSW |
9 |
121,744,983 (GRCm39) |
missense |
probably benign |
0.00 |
R9764:Cyp8b1
|
UTSW |
9 |
121,744,294 (GRCm39) |
missense |
probably benign |
0.03 |
RF013:Cyp8b1
|
UTSW |
9 |
121,744,561 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1177:Cyp8b1
|
UTSW |
9 |
121,745,212 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cyp8b1
|
UTSW |
9 |
121,744,597 (GRCm39) |
missense |
probably benign |
0.06 |
|