Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,087,930 (GRCm39) |
I1066V |
probably benign |
Het |
Abcd2 |
T |
C |
15: 91,033,197 (GRCm39) |
T740A |
probably benign |
Het |
Amigo1 |
T |
C |
3: 108,094,852 (GRCm39) |
L117P |
probably damaging |
Het |
Ankar |
A |
T |
1: 72,686,160 (GRCm39) |
S1347T |
probably damaging |
Het |
Apol7e |
T |
C |
15: 77,601,956 (GRCm39) |
S185P |
probably damaging |
Het |
Ash1l |
G |
A |
3: 88,942,734 (GRCm39) |
C2088Y |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,630,895 (GRCm39) |
T221A |
probably benign |
Het |
Caln1 |
A |
G |
5: 130,851,825 (GRCm39) |
S205G |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,704,672 (GRCm39) |
I2803V |
unknown |
Het |
Cfh |
A |
C |
1: 140,047,753 (GRCm39) |
F477V |
possibly damaging |
Het |
Cldn23 |
A |
G |
8: 36,293,056 (GRCm39) |
V144A |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 17,077,310 (GRCm39) |
S116P |
probably damaging |
Het |
Dgkd |
A |
T |
1: 87,845,689 (GRCm39) |
T299S |
possibly damaging |
Het |
Fam20b |
T |
G |
1: 156,518,072 (GRCm39) |
T241P |
probably damaging |
Het |
Fndc3b |
A |
T |
3: 27,505,493 (GRCm39) |
M925K |
probably benign |
Het |
Ftdc1 |
C |
A |
16: 58,437,211 (GRCm39) |
M32I |
probably benign |
Het |
Ints3 |
C |
T |
3: 90,299,607 (GRCm39) |
R987Q |
probably damaging |
Het |
Kctd10 |
A |
G |
5: 114,505,316 (GRCm39) |
V226A |
probably damaging |
Het |
Lypd2 |
A |
G |
15: 74,604,881 (GRCm39) |
V38A |
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,909,156 (GRCm39) |
R265G |
possibly damaging |
Het |
Mcc |
C |
T |
18: 44,601,500 (GRCm39) |
V610M |
possibly damaging |
Het |
Mocs1 |
C |
T |
17: 49,756,547 (GRCm39) |
R244C |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,103,232 (GRCm39) |
T677A |
probably damaging |
Het |
Ngp |
A |
G |
9: 110,251,421 (GRCm39) |
N150D |
probably benign |
Het |
Nipbl |
C |
T |
15: 8,388,696 (GRCm39) |
R308Q |
probably benign |
Het |
Nsrp1 |
A |
G |
11: 76,939,177 (GRCm39) |
|
probably null |
Het |
Or2y16 |
A |
T |
11: 49,334,953 (GRCm39) |
I92F |
probably damaging |
Het |
Or4f47 |
T |
A |
2: 111,972,908 (GRCm39) |
I206N |
probably damaging |
Het |
Or52n20 |
A |
T |
7: 104,320,061 (GRCm39) |
I51F |
probably damaging |
Het |
Pbld2 |
A |
T |
10: 62,889,656 (GRCm39) |
D146V |
probably benign |
Het |
Ptprd |
G |
T |
4: 76,047,263 (GRCm39) |
S87R |
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Slc25a35 |
T |
C |
11: 68,862,798 (GRCm39) |
L251S |
probably benign |
Het |
Slx4 |
A |
T |
16: 3,803,136 (GRCm39) |
L1226* |
probably null |
Het |
Smarca4 |
T |
C |
9: 21,558,922 (GRCm39) |
V651A |
possibly damaging |
Het |
Smarcad1 |
T |
C |
6: 65,071,303 (GRCm39) |
F583L |
probably benign |
Het |
Taf2 |
T |
C |
15: 54,894,526 (GRCm39) |
K932E |
probably benign |
Het |
Trav8d-1 |
A |
T |
14: 53,016,425 (GRCm39) |
T104S |
probably benign |
Het |
Trmt9b |
G |
A |
8: 36,965,576 (GRCm39) |
W32* |
probably null |
Het |
Trpm4 |
A |
T |
7: 44,976,552 (GRCm39) |
V155D |
probably damaging |
Het |
Ttc6 |
A |
T |
12: 57,752,429 (GRCm39) |
Y1445F |
possibly damaging |
Het |
Ttll5 |
C |
A |
12: 86,067,322 (GRCm39) |
N1270K |
probably damaging |
Het |
Usp40 |
G |
T |
1: 87,895,400 (GRCm39) |
|
probably null |
Het |
Vmn2r74 |
T |
C |
7: 85,610,690 (GRCm39) |
M1V |
probably null |
Het |
Wwox |
T |
C |
8: 115,433,108 (GRCm39) |
V258A |
probably damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp770 |
G |
A |
2: 114,027,508 (GRCm39) |
T187I |
probably damaging |
Het |
Zranb2 |
A |
G |
3: 157,241,969 (GRCm39) |
|
probably null |
Het |
Zscan4-ps3 |
A |
G |
7: 11,344,267 (GRCm39) |
Q75R |
probably damaging |
Het |
|
Other mutations in Prss22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02112:Prss22
|
APN |
17 |
24,212,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02247:Prss22
|
APN |
17 |
24,215,363 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02952:Prss22
|
APN |
17 |
24,215,697 (GRCm39) |
missense |
probably damaging |
1.00 |
G1Funyon:Prss22
|
UTSW |
17 |
24,212,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Prss22
|
UTSW |
17 |
24,215,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Prss22
|
UTSW |
17 |
24,212,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Prss22
|
UTSW |
17 |
24,215,662 (GRCm39) |
missense |
probably benign |
0.05 |
R1767:Prss22
|
UTSW |
17 |
24,215,331 (GRCm39) |
missense |
probably benign |
0.34 |
R1851:Prss22
|
UTSW |
17 |
24,215,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Prss22
|
UTSW |
17 |
24,215,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Prss22
|
UTSW |
17 |
24,213,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:Prss22
|
UTSW |
17 |
24,215,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R4108:Prss22
|
UTSW |
17 |
24,212,847 (GRCm39) |
missense |
probably benign |
|
R6299:Prss22
|
UTSW |
17 |
24,215,408 (GRCm39) |
missense |
probably damaging |
0.96 |
R7358:Prss22
|
UTSW |
17 |
24,215,419 (GRCm39) |
missense |
probably benign |
0.06 |
R7487:Prss22
|
UTSW |
17 |
24,216,971 (GRCm39) |
missense |
probably damaging |
0.98 |
R7765:Prss22
|
UTSW |
17 |
24,213,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R7857:Prss22
|
UTSW |
17 |
24,212,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8301:Prss22
|
UTSW |
17 |
24,212,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R8466:Prss22
|
UTSW |
17 |
24,215,802 (GRCm39) |
missense |
probably benign |
0.22 |
R8815:Prss22
|
UTSW |
17 |
24,215,662 (GRCm39) |
missense |
probably benign |
0.05 |
R9183:Prss22
|
UTSW |
17 |
24,213,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R9447:Prss22
|
UTSW |
17 |
24,212,837 (GRCm39) |
missense |
probably benign |
|
R9483:Prss22
|
UTSW |
17 |
24,215,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|