Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
A |
G |
15: 101,100,959 (GRCm39) |
R374G |
probably damaging |
Het |
Apob |
C |
A |
12: 8,047,883 (GRCm39) |
P941Q |
probably damaging |
Het |
Armc9 |
T |
A |
1: 86,127,638 (GRCm39) |
|
probably null |
Het |
Arpc5l |
T |
C |
2: 38,903,730 (GRCm39) |
|
probably benign |
Het |
Atg2b |
C |
A |
12: 105,592,621 (GRCm39) |
D1745Y |
probably damaging |
Het |
Atp9a |
A |
G |
2: 168,494,552 (GRCm39) |
V651A |
probably damaging |
Het |
Ccnyl1 |
T |
C |
1: 64,747,631 (GRCm39) |
I148T |
possibly damaging |
Het |
Cfap95 |
T |
A |
19: 23,630,017 (GRCm39) |
D25V |
unknown |
Het |
Chrna6 |
A |
T |
8: 27,903,682 (GRCm39) |
W17R |
possibly damaging |
Het |
Cpne1 |
G |
A |
2: 155,919,917 (GRCm39) |
H244Y |
probably damaging |
Het |
Cpxm2 |
A |
G |
7: 131,650,807 (GRCm39) |
Y618H |
possibly damaging |
Het |
Csf1r |
T |
C |
18: 61,243,473 (GRCm39) |
I163T |
probably benign |
Het |
Ctdsp1 |
T |
C |
1: 74,434,606 (GRCm39) |
|
probably benign |
Het |
Ctsb |
T |
A |
14: 63,370,806 (GRCm39) |
I6N |
probably benign |
Het |
Dcbld1 |
A |
G |
10: 52,160,244 (GRCm39) |
N44S |
probably damaging |
Het |
Dnah11 |
C |
T |
12: 117,976,112 (GRCm39) |
C2769Y |
probably benign |
Het |
Efemp2 |
C |
A |
19: 5,530,093 (GRCm39) |
Q187K |
probably damaging |
Het |
Elavl3 |
A |
T |
9: 21,947,612 (GRCm39) |
I109N |
probably damaging |
Het |
Elovl5 |
G |
T |
9: 77,890,066 (GRCm39) |
K292N |
probably benign |
Het |
Epb41 |
G |
T |
4: 131,731,105 (GRCm39) |
P1T |
probably damaging |
Het |
Gm44865 |
G |
T |
7: 108,165,007 (GRCm39) |
|
probably benign |
Het |
Gnat2 |
C |
A |
3: 108,007,368 (GRCm39) |
T262K |
probably damaging |
Het |
Katnip |
T |
C |
7: 125,451,174 (GRCm39) |
C1102R |
probably benign |
Het |
Kmt2e |
A |
T |
5: 23,702,540 (GRCm39) |
I951F |
probably damaging |
Het |
Large2 |
T |
C |
2: 92,197,927 (GRCm39) |
H258R |
probably damaging |
Het |
Lnx1 |
G |
A |
5: 74,846,420 (GRCm39) |
P10L |
probably benign |
Het |
Lrp6 |
G |
A |
6: 134,497,380 (GRCm39) |
S209L |
possibly damaging |
Het |
Mc3r |
A |
G |
2: 172,091,716 (GRCm39) |
I313V |
probably benign |
Het |
Med1 |
T |
C |
11: 98,051,859 (GRCm39) |
D468G |
possibly damaging |
Het |
Mlxip |
T |
C |
5: 123,584,014 (GRCm39) |
S526P |
probably benign |
Het |
Myo15a |
T |
C |
11: 60,400,357 (GRCm39) |
|
probably benign |
Het |
Nedd1 |
T |
C |
10: 92,525,503 (GRCm39) |
D602G |
possibly damaging |
Het |
Nol7 |
C |
T |
13: 43,554,769 (GRCm39) |
|
probably benign |
Het |
Or8c10 |
T |
C |
9: 38,279,364 (GRCm39) |
I174T |
possibly damaging |
Het |
Piezo2 |
T |
C |
18: 63,257,731 (GRCm39) |
D329G |
probably benign |
Het |
Pkia |
G |
T |
3: 7,507,142 (GRCm39) |
E75* |
probably null |
Het |
Pramel26 |
A |
C |
4: 143,538,330 (GRCm39) |
F214V |
possibly damaging |
Het |
Ptpn14 |
A |
T |
1: 189,571,754 (GRCm39) |
T282S |
probably damaging |
Het |
Ptprg |
C |
T |
14: 12,219,029 (GRCm38) |
P408S |
probably damaging |
Het |
Rpa2 |
A |
G |
4: 132,502,358 (GRCm39) |
I147V |
probably benign |
Het |
Serpina12 |
T |
C |
12: 103,997,397 (GRCm39) |
T375A |
possibly damaging |
Het |
Slc18a1 |
T |
C |
8: 69,491,515 (GRCm39) |
T500A |
probably benign |
Het |
Tapt1 |
A |
G |
5: 44,350,529 (GRCm39) |
F247L |
possibly damaging |
Het |
Trav8d-2 |
A |
G |
14: 53,280,218 (GRCm39) |
I69M |
possibly damaging |
Het |
|
Other mutations in Serpinb11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01487:Serpinb11
|
APN |
1 |
107,307,568 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Serpinb11
|
APN |
1 |
107,305,388 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01893:Serpinb11
|
APN |
1 |
107,305,387 (GRCm39) |
missense |
probably benign |
|
IGL03126:Serpinb11
|
APN |
1 |
107,307,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Serpinb11
|
UTSW |
1 |
107,305,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R0153:Serpinb11
|
UTSW |
1 |
107,299,933 (GRCm39) |
missense |
probably benign |
0.07 |
R0419:Serpinb11
|
UTSW |
1 |
107,304,590 (GRCm39) |
nonsense |
probably null |
|
R1550:Serpinb11
|
UTSW |
1 |
107,307,418 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1764:Serpinb11
|
UTSW |
1 |
107,304,532 (GRCm39) |
missense |
probably benign |
0.03 |
R1972:Serpinb11
|
UTSW |
1 |
107,297,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Serpinb11
|
UTSW |
1 |
107,305,338 (GRCm39) |
missense |
probably benign |
0.07 |
R3768:Serpinb11
|
UTSW |
1 |
107,305,392 (GRCm39) |
critical splice donor site |
probably null |
|
R4332:Serpinb11
|
UTSW |
1 |
107,297,294 (GRCm39) |
critical splice donor site |
probably null |
|
R5001:Serpinb11
|
UTSW |
1 |
107,304,598 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5010:Serpinb11
|
UTSW |
1 |
107,307,379 (GRCm39) |
missense |
probably benign |
|
R5043:Serpinb11
|
UTSW |
1 |
107,297,195 (GRCm39) |
missense |
probably damaging |
0.97 |
R5186:Serpinb11
|
UTSW |
1 |
107,307,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5833:Serpinb11
|
UTSW |
1 |
107,305,392 (GRCm39) |
critical splice donor site |
probably null |
|
R5907:Serpinb11
|
UTSW |
1 |
107,299,919 (GRCm39) |
missense |
probably benign |
0.12 |
R6244:Serpinb11
|
UTSW |
1 |
107,299,972 (GRCm39) |
missense |
probably damaging |
0.99 |
R6395:Serpinb11
|
UTSW |
1 |
107,299,781 (GRCm39) |
splice site |
probably null |
|
R7111:Serpinb11
|
UTSW |
1 |
107,304,614 (GRCm39) |
missense |
probably benign |
0.00 |
R7354:Serpinb11
|
UTSW |
1 |
107,305,263 (GRCm39) |
missense |
probably benign |
0.03 |
R7664:Serpinb11
|
UTSW |
1 |
107,307,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R8075:Serpinb11
|
UTSW |
1 |
107,298,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Serpinb11
|
UTSW |
1 |
107,305,262 (GRCm39) |
missense |
probably benign |
0.01 |
R9091:Serpinb11
|
UTSW |
1 |
107,304,533 (GRCm39) |
missense |
probably benign |
0.15 |
R9270:Serpinb11
|
UTSW |
1 |
107,304,533 (GRCm39) |
missense |
probably benign |
0.15 |
|