Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
G |
3: 121,881,126 (GRCm39) |
N514D |
probably benign |
Het |
Adgre1 |
G |
A |
17: 57,757,101 (GRCm39) |
R786H |
probably null |
Het |
Ankrd7 |
G |
A |
6: 18,868,024 (GRCm39) |
V97I |
probably damaging |
Het |
Bltp1 |
A |
G |
3: 37,065,889 (GRCm39) |
I54M |
|
Het |
Bmper |
C |
T |
9: 23,318,009 (GRCm39) |
P543S |
possibly damaging |
Het |
Brwd1 |
A |
T |
16: 95,795,015 (GRCm39) |
M2233K |
possibly damaging |
Het |
C1s2 |
G |
T |
6: 124,602,553 (GRCm39) |
P553T |
probably damaging |
Het |
Cachd1 |
G |
A |
4: 100,823,438 (GRCm39) |
V497I |
possibly damaging |
Het |
Cacng4 |
A |
G |
11: 107,626,019 (GRCm39) |
S191P |
probably damaging |
Het |
Cd109 |
C |
A |
9: 78,605,442 (GRCm39) |
T1015K |
probably damaging |
Het |
Clstn2 |
A |
G |
9: 97,339,703 (GRCm39) |
L756P |
probably damaging |
Het |
Crybg3 |
A |
T |
16: 59,377,887 (GRCm39) |
D1122E |
possibly damaging |
Het |
Csf2 |
A |
T |
11: 54,140,420 (GRCm39) |
L6* |
probably null |
Het |
Csnk1g2 |
T |
A |
10: 80,473,745 (GRCm39) |
Y71N |
possibly damaging |
Het |
Dlg2 |
C |
A |
7: 90,564,731 (GRCm39) |
H116N |
probably benign |
Het |
Dnah14 |
C |
T |
1: 181,619,610 (GRCm39) |
S3978L |
probably damaging |
Het |
Dpp8 |
C |
T |
9: 64,960,453 (GRCm39) |
T328I |
probably null |
Het |
Dync2i1 |
T |
A |
12: 116,205,403 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
C |
6: 84,163,450 (GRCm39) |
V1625A |
probably damaging |
Het |
Efcab3 |
G |
A |
11: 104,783,911 (GRCm39) |
G2754E |
probably benign |
Het |
Egf |
C |
A |
3: 129,548,538 (GRCm39) |
V26F |
probably damaging |
Het |
Eif1ad19 |
T |
C |
12: 87,740,526 (GRCm39) |
N11S |
possibly damaging |
Het |
Fam20a |
T |
A |
11: 109,565,992 (GRCm39) |
Y414F |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,818,241 (GRCm39) |
I4658T |
probably benign |
Het |
Hycc1 |
C |
T |
5: 24,196,748 (GRCm39) |
E47K |
probably benign |
Het |
Igflr1 |
A |
T |
7: 30,266,653 (GRCm39) |
Q167L |
possibly damaging |
Het |
Map3k6 |
A |
G |
4: 132,979,168 (GRCm39) |
|
probably null |
Het |
Mcpt4 |
A |
G |
14: 56,297,511 (GRCm39) |
I215T |
probably damaging |
Het |
Med13 |
T |
C |
11: 86,189,984 (GRCm39) |
Y975C |
probably damaging |
Het |
Meioc |
T |
A |
11: 102,566,419 (GRCm39) |
Y678* |
probably null |
Het |
Myof |
T |
C |
19: 37,924,818 (GRCm39) |
T1190A |
probably benign |
Het |
Nap1l4 |
A |
C |
7: 143,088,132 (GRCm39) |
|
probably benign |
Het |
Ncapg |
T |
C |
5: 45,851,195 (GRCm39) |
V796A |
probably damaging |
Het |
Or4c10b |
C |
T |
2: 89,711,956 (GRCm39) |
T262I |
probably benign |
Het |
Or4c119 |
C |
T |
2: 88,986,782 (GRCm39) |
V246M |
possibly damaging |
Het |
Or5d39 |
T |
A |
2: 87,979,614 (GRCm39) |
I250L |
probably benign |
Het |
Or5d40 |
T |
A |
2: 88,015,260 (GRCm39) |
V13E |
possibly damaging |
Het |
Or5p68 |
T |
C |
7: 107,945,645 (GRCm39) |
Y181C |
probably benign |
Het |
Paxbp1 |
A |
G |
16: 90,824,188 (GRCm39) |
S515P |
probably benign |
Het |
Pip4p1 |
A |
G |
14: 51,165,436 (GRCm39) |
V257A |
probably benign |
Het |
Plce1 |
C |
T |
19: 38,717,414 (GRCm39) |
S1401F |
probably damaging |
Het |
Rptor |
A |
G |
11: 119,777,964 (GRCm39) |
K1043E |
probably benign |
Het |
Rtn4rl2 |
T |
G |
2: 84,711,039 (GRCm39) |
N75T |
probably damaging |
Het |
Slc35f4 |
A |
G |
14: 49,536,291 (GRCm39) |
I448T |
possibly damaging |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Tas2r115 |
A |
G |
6: 132,714,918 (GRCm39) |
I11T |
possibly damaging |
Het |
Tbc1d5 |
A |
G |
17: 51,181,680 (GRCm39) |
V351A |
possibly damaging |
Het |
Trim43b |
A |
T |
9: 88,971,570 (GRCm39) |
D195E |
probably benign |
Het |
Trim65 |
C |
A |
11: 116,021,564 (GRCm39) |
A90S |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,850,765 (GRCm39) |
V1100I |
possibly damaging |
Het |
Tyrp1 |
A |
G |
4: 80,759,012 (GRCm39) |
E295G |
probably null |
Het |
Ube2g2 |
G |
A |
10: 77,480,307 (GRCm39) |
V138I |
probably benign |
Het |
|
Other mutations in Krt79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Krt79
|
APN |
15 |
101,848,601 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00546:Krt79
|
APN |
15 |
101,838,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01595:Krt79
|
APN |
15 |
101,840,206 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02193:Krt79
|
APN |
15 |
101,848,340 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0639:Krt79
|
UTSW |
15 |
101,839,983 (GRCm39) |
nonsense |
probably null |
|
R0980:Krt79
|
UTSW |
15 |
101,846,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1839:Krt79
|
UTSW |
15 |
101,846,373 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4624:Krt79
|
UTSW |
15 |
101,848,241 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4745:Krt79
|
UTSW |
15 |
101,839,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5203:Krt79
|
UTSW |
15 |
101,838,175 (GRCm39) |
missense |
unknown |
|
R5382:Krt79
|
UTSW |
15 |
101,839,875 (GRCm39) |
missense |
probably benign |
0.09 |
R5568:Krt79
|
UTSW |
15 |
101,838,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R6902:Krt79
|
UTSW |
15 |
101,840,314 (GRCm39) |
missense |
probably benign |
0.08 |
R6916:Krt79
|
UTSW |
15 |
101,844,605 (GRCm39) |
missense |
probably benign |
0.01 |
R6998:Krt79
|
UTSW |
15 |
101,846,307 (GRCm39) |
missense |
probably benign |
|
R7009:Krt79
|
UTSW |
15 |
101,839,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Krt79
|
UTSW |
15 |
101,840,278 (GRCm39) |
missense |
probably damaging |
0.97 |
R8161:Krt79
|
UTSW |
15 |
101,839,137 (GRCm39) |
missense |
probably damaging |
0.96 |
R8184:Krt79
|
UTSW |
15 |
101,838,187 (GRCm39) |
missense |
unknown |
|
R8206:Krt79
|
UTSW |
15 |
101,848,705 (GRCm39) |
start gained |
probably null |
|
R8705:Krt79
|
UTSW |
15 |
101,846,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R8993:Krt79
|
UTSW |
15 |
101,839,441 (GRCm39) |
intron |
probably benign |
|
R9055:Krt79
|
UTSW |
15 |
101,839,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R9322:Krt79
|
UTSW |
15 |
101,840,245 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9456:Krt79
|
UTSW |
15 |
101,839,904 (GRCm39) |
missense |
probably benign |
0.02 |
R9495:Krt79
|
UTSW |
15 |
101,840,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9514:Krt79
|
UTSW |
15 |
101,840,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9533:Krt79
|
UTSW |
15 |
101,848,417 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9560:Krt79
|
UTSW |
15 |
101,846,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R9705:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
R9706:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
R9707:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
R9714:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
R9750:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
R9753:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
R9772:Krt79
|
UTSW |
15 |
101,839,196 (GRCm39) |
missense |
probably benign |
|
|