Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
A |
G |
11: 59,099,528 (GRCm39) |
|
probably benign |
Het |
A730015C16Rik |
G |
A |
4: 108,705,205 (GRCm39) |
V40M |
probably damaging |
Het |
Abcg2 |
A |
G |
6: 58,655,322 (GRCm39) |
D419G |
probably benign |
Het |
Adamts17 |
A |
C |
7: 66,725,091 (GRCm39) |
E777A |
probably damaging |
Het |
Ak1 |
A |
G |
2: 32,523,478 (GRCm39) |
K166R |
probably benign |
Het |
Ankrd12 |
T |
C |
17: 66,293,300 (GRCm39) |
K711R |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,020,301 (GRCm39) |
|
probably null |
Het |
Atp5f1a |
A |
G |
18: 77,869,625 (GRCm39) |
H519R |
probably benign |
Het |
Best1 |
G |
T |
19: 9,967,853 (GRCm39) |
Y284* |
probably null |
Het |
C2cd6 |
A |
G |
1: 59,115,887 (GRCm39) |
|
probably benign |
Het |
Casz1 |
G |
T |
4: 149,030,628 (GRCm39) |
V1216L |
probably benign |
Het |
Cdc42bpg |
A |
G |
19: 6,363,812 (GRCm39) |
D493G |
probably damaging |
Het |
Ces2f |
A |
G |
8: 105,679,134 (GRCm39) |
D317G |
possibly damaging |
Het |
Chst15 |
A |
T |
7: 131,872,002 (GRCm39) |
M93K |
possibly damaging |
Het |
Cntnap5a |
T |
C |
1: 115,828,750 (GRCm39) |
L58P |
probably damaging |
Het |
Crip3 |
T |
C |
17: 46,741,702 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
G |
A |
4: 128,380,794 (GRCm39) |
E2117K |
probably benign |
Het |
Cstf3 |
A |
G |
2: 104,478,564 (GRCm39) |
D212G |
possibly damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,434,220 (GRCm39) |
K546R |
probably damaging |
Het |
Cubn |
A |
G |
2: 13,480,931 (GRCm39) |
I308T |
probably benign |
Het |
Cxcl9 |
T |
A |
5: 92,472,972 (GRCm39) |
D75V |
probably damaging |
Het |
Dcdc5 |
C |
T |
2: 106,188,977 (GRCm39) |
|
noncoding transcript |
Het |
Defa30 |
C |
A |
8: 21,624,752 (GRCm39) |
T25K |
possibly damaging |
Het |
Dock7 |
A |
T |
4: 98,967,672 (GRCm39) |
H239Q |
possibly damaging |
Het |
Dpp4 |
A |
G |
2: 62,178,245 (GRCm39) |
V629A |
possibly damaging |
Het |
Fam83a |
T |
C |
15: 57,873,341 (GRCm39) |
M390T |
probably benign |
Het |
Fem1c |
A |
G |
18: 46,657,552 (GRCm39) |
L54P |
probably damaging |
Het |
Fntb |
T |
A |
12: 76,957,007 (GRCm39) |
M282K |
probably benign |
Het |
Galnt2l |
A |
G |
8: 122,996,323 (GRCm39) |
|
probably benign |
Het |
Gm11099 |
G |
A |
2: 58,749,482 (GRCm39) |
|
probably benign |
Het |
Gm1527 |
T |
C |
3: 28,980,705 (GRCm39) |
S602P |
probably benign |
Het |
Gm5478 |
T |
A |
15: 101,553,080 (GRCm39) |
I331F |
probably damaging |
Het |
Gm7853 |
C |
A |
14: 35,811,540 (GRCm39) |
|
noncoding transcript |
Het |
Gsta2 |
A |
T |
9: 78,249,147 (GRCm39) |
C18S |
probably benign |
Het |
H1f8 |
T |
C |
6: 115,924,701 (GRCm39) |
V69A |
possibly damaging |
Het |
Hecw1 |
T |
C |
13: 14,480,671 (GRCm39) |
E465G |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,415,548 (GRCm39) |
D4841G |
probably damaging |
Het |
Hus1b |
A |
G |
13: 31,130,984 (GRCm39) |
V225A |
probably benign |
Het |
Keg1 |
A |
T |
19: 12,693,387 (GRCm39) |
M137L |
probably benign |
Het |
Kmt2a |
C |
T |
9: 44,735,932 (GRCm39) |
|
probably benign |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mga |
T |
A |
2: 119,772,156 (GRCm39) |
V1672E |
probably damaging |
Het |
Mios |
T |
C |
6: 8,234,237 (GRCm39) |
S803P |
probably benign |
Het |
Mrtfa |
T |
C |
15: 80,902,409 (GRCm39) |
|
probably benign |
Het |
Msh4 |
A |
T |
3: 153,569,021 (GRCm39) |
Y851N |
probably damaging |
Het |
Mybl1 |
A |
C |
1: 9,742,886 (GRCm39) |
|
probably null |
Het |
Myo5c |
A |
G |
9: 75,183,221 (GRCm39) |
Y865C |
probably damaging |
Het |
Naip1 |
T |
C |
13: 100,563,378 (GRCm39) |
S596G |
probably benign |
Het |
Nek5 |
G |
T |
8: 22,586,747 (GRCm39) |
Q355K |
possibly damaging |
Het |
Nphp3 |
G |
T |
9: 103,903,126 (GRCm39) |
R701L |
possibly damaging |
Het |
Or52n2 |
A |
T |
7: 104,542,444 (GRCm39) |
Y130* |
probably null |
Het |
Or5j3 |
T |
C |
2: 86,128,823 (GRCm39) |
I221T |
probably damaging |
Het |
Or5m10 |
T |
A |
2: 85,717,592 (GRCm39) |
Y149* |
probably null |
Het |
Or5t9 |
T |
C |
2: 86,659,542 (GRCm39) |
S149P |
probably benign |
Het |
Or9g4 |
T |
A |
2: 85,505,262 (GRCm39) |
T78S |
possibly damaging |
Het |
Palm |
A |
G |
10: 79,651,021 (GRCm39) |
N149D |
possibly damaging |
Het |
Pot1b |
T |
C |
17: 55,960,451 (GRCm39) |
I626M |
possibly damaging |
Het |
Ptprt |
T |
A |
2: 161,769,404 (GRCm39) |
D487V |
probably damaging |
Het |
Qpct |
A |
G |
17: 79,378,201 (GRCm39) |
I124V |
probably benign |
Het |
Rbm12b1 |
T |
A |
4: 12,145,817 (GRCm39) |
D596E |
possibly damaging |
Het |
Rnf169 |
A |
G |
7: 99,574,535 (GRCm39) |
S687P |
possibly damaging |
Het |
Sfxn1 |
T |
A |
13: 54,246,469 (GRCm39) |
|
probably null |
Het |
Slc6a21 |
T |
C |
7: 44,922,052 (GRCm39) |
V649A |
probably benign |
Het |
Slit3 |
A |
T |
11: 35,577,126 (GRCm39) |
T1120S |
probably damaging |
Het |
Spem2 |
A |
T |
11: 69,708,896 (GRCm39) |
M58K |
probably benign |
Het |
Sprr2k |
T |
A |
3: 92,340,703 (GRCm39) |
|
probably benign |
Het |
Sspo |
T |
C |
6: 48,440,334 (GRCm39) |
|
probably null |
Het |
Sv2b |
A |
T |
7: 74,769,791 (GRCm39) |
F584I |
possibly damaging |
Het |
Tkfc |
A |
T |
19: 10,572,690 (GRCm39) |
M317K |
probably null |
Het |
Tnni3k |
C |
T |
3: 154,735,942 (GRCm39) |
G134S |
probably benign |
Het |
Ttn |
C |
T |
2: 76,570,124 (GRCm39) |
R26923H |
probably damaging |
Het |
Tuba3b |
T |
C |
6: 145,564,179 (GRCm39) |
V75A |
possibly damaging |
Het |
Unc79 |
T |
C |
12: 103,149,784 (GRCm39) |
L2626P |
probably damaging |
Het |
Usp24 |
A |
T |
4: 106,219,130 (GRCm39) |
I491F |
probably damaging |
Het |
V1ra8 |
A |
T |
6: 90,180,132 (GRCm39) |
I112F |
probably damaging |
Het |
Vmn1r29 |
T |
G |
6: 58,284,663 (GRCm39) |
F128V |
probably benign |
Het |
Wdr87-ps |
A |
G |
7: 29,234,315 (GRCm39) |
|
noncoding transcript |
Het |
Zfp157 |
T |
A |
5: 138,453,357 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rnf157 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00487:Rnf157
|
APN |
11 |
116,253,181 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01146:Rnf157
|
APN |
11 |
116,240,912 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01955:Rnf157
|
APN |
11 |
116,250,722 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02010:Rnf157
|
APN |
11 |
116,287,052 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Rnf157
|
APN |
11 |
116,237,858 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03092:Rnf157
|
APN |
11 |
116,238,795 (GRCm39) |
critical splice acceptor site |
probably null |
|
PIT4362001:Rnf157
|
UTSW |
11 |
116,251,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Rnf157
|
UTSW |
11 |
116,240,276 (GRCm39) |
unclassified |
probably benign |
|
R0022:Rnf157
|
UTSW |
11 |
116,240,276 (GRCm39) |
unclassified |
probably benign |
|
R0036:Rnf157
|
UTSW |
11 |
116,287,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Rnf157
|
UTSW |
11 |
116,245,636 (GRCm39) |
splice site |
probably benign |
|
R1509:Rnf157
|
UTSW |
11 |
116,237,921 (GRCm39) |
missense |
probably benign |
|
R1544:Rnf157
|
UTSW |
11 |
116,245,188 (GRCm39) |
splice site |
probably null |
|
R1654:Rnf157
|
UTSW |
11 |
116,249,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Rnf157
|
UTSW |
11 |
116,245,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Rnf157
|
UTSW |
11 |
116,249,520 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4017:Rnf157
|
UTSW |
11 |
116,250,067 (GRCm39) |
critical splice donor site |
probably null |
|
R4590:Rnf157
|
UTSW |
11 |
116,250,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R4872:Rnf157
|
UTSW |
11 |
116,246,298 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4891:Rnf157
|
UTSW |
11 |
116,249,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Rnf157
|
UTSW |
11 |
116,287,146 (GRCm39) |
splice site |
probably null |
|
R5870:Rnf157
|
UTSW |
11 |
116,237,900 (GRCm39) |
missense |
probably benign |
|
R7171:Rnf157
|
UTSW |
11 |
116,253,199 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7376:Rnf157
|
UTSW |
11 |
116,251,192 (GRCm39) |
missense |
probably benign |
0.35 |
R8178:Rnf157
|
UTSW |
11 |
116,238,307 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8356:Rnf157
|
UTSW |
11 |
116,240,246 (GRCm39) |
missense |
probably benign |
0.11 |
R8456:Rnf157
|
UTSW |
11 |
116,240,246 (GRCm39) |
missense |
probably benign |
0.11 |
R8714:Rnf157
|
UTSW |
11 |
116,237,891 (GRCm39) |
missense |
probably benign |
0.00 |
R9312:Rnf157
|
UTSW |
11 |
116,240,158 (GRCm39) |
critical splice donor site |
probably null |
|
R9313:Rnf157
|
UTSW |
11 |
116,250,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R9579:Rnf157
|
UTSW |
11 |
116,240,822 (GRCm39) |
missense |
probably benign |
|
R9641:Rnf157
|
UTSW |
11 |
116,303,576 (GRCm39) |
missense |
probably benign |
0.12 |
X0020:Rnf157
|
UTSW |
11 |
116,251,134 (GRCm39) |
missense |
probably damaging |
1.00 |
|