Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610030E20Rik |
C |
T |
6: 72,324,635 (GRCm39) |
T56M |
probably damaging |
Het |
Adamtsl5 |
C |
T |
10: 80,181,372 (GRCm39) |
S36N |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,750,704 (GRCm39) |
|
probably benign |
Het |
Ago1 |
A |
G |
4: 126,354,210 (GRCm39) |
F200S |
probably damaging |
Het |
Akr1cl |
T |
C |
1: 65,063,865 (GRCm39) |
D108G |
possibly damaging |
Het |
Aopep |
A |
G |
13: 63,208,954 (GRCm39) |
D357G |
probably benign |
Het |
Arhgef3 |
A |
T |
14: 27,123,743 (GRCm39) |
D468V |
probably benign |
Het |
Aspn |
T |
C |
13: 49,705,353 (GRCm39) |
C72R |
possibly damaging |
Het |
Baz2b |
T |
C |
2: 59,792,485 (GRCm39) |
T548A |
possibly damaging |
Het |
Birc6 |
G |
A |
17: 74,906,368 (GRCm39) |
|
probably null |
Het |
Btnl2 |
A |
T |
17: 34,577,249 (GRCm39) |
T135S |
possibly damaging |
Het |
Ccnl1 |
T |
A |
3: 65,865,282 (GRCm39) |
I90F |
possibly damaging |
Het |
Ccnt1 |
T |
C |
15: 98,463,024 (GRCm39) |
|
probably null |
Het |
Cemip |
C |
A |
7: 83,652,616 (GRCm39) |
|
probably benign |
Het |
Cfap45 |
A |
G |
1: 172,357,501 (GRCm39) |
D85G |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,737,941 (GRCm39) |
D2319V |
unknown |
Het |
Cma1 |
T |
C |
14: 56,181,989 (GRCm39) |
M14V |
possibly damaging |
Het |
Cmtm1 |
T |
C |
8: 105,036,774 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
A |
G |
4: 63,249,559 (GRCm39) |
H1738R |
unknown |
Het |
Colq |
T |
A |
14: 31,275,794 (GRCm39) |
D41V |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,337,166 (GRCm39) |
T2437A |
probably benign |
Het |
Dnah14 |
A |
G |
1: 181,611,139 (GRCm39) |
D3755G |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,150,545 (GRCm39) |
Y1349C |
probably damaging |
Het |
Eps8 |
C |
T |
6: 137,505,569 (GRCm39) |
R53Q |
possibly damaging |
Het |
Fbf1 |
T |
C |
11: 116,043,594 (GRCm39) |
D405G |
probably benign |
Het |
Fen1 |
C |
T |
19: 10,177,674 (GRCm39) |
E257K |
possibly damaging |
Het |
Gstm7 |
A |
T |
3: 107,834,271 (GRCm39) |
M198K |
possibly damaging |
Het |
Hook3 |
A |
T |
8: 26,563,675 (GRCm39) |
S190T |
probably benign |
Het |
Htra4 |
A |
C |
8: 25,520,526 (GRCm39) |
|
probably null |
Het |
Ighv1-15 |
T |
C |
12: 114,621,116 (GRCm39) |
I70V |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,470,324 (GRCm39) |
N452Y |
probably damaging |
Het |
Insyn2a |
T |
G |
7: 134,519,427 (GRCm39) |
K368Q |
probably damaging |
Het |
Iqcf5 |
T |
A |
9: 106,393,020 (GRCm39) |
N92K |
possibly damaging |
Het |
Itk |
A |
G |
11: 46,246,661 (GRCm39) |
Y186H |
probably damaging |
Het |
Klhdc10 |
T |
C |
6: 30,446,690 (GRCm39) |
S282P |
probably benign |
Het |
Klhl18 |
T |
A |
9: 110,305,577 (GRCm39) |
E29V |
possibly damaging |
Het |
Ky |
T |
C |
9: 102,402,614 (GRCm39) |
S140P |
probably damaging |
Het |
Lmntd2 |
T |
C |
7: 140,793,550 (GRCm39) |
E112G |
unknown |
Het |
Lrrc36 |
C |
A |
8: 106,178,718 (GRCm39) |
D304E |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,400,273 (GRCm39) |
F674Y |
probably damaging |
Het |
Notch1 |
C |
T |
2: 26,361,013 (GRCm39) |
D1111N |
probably benign |
Het |
Osbpl8 |
T |
G |
10: 111,107,941 (GRCm39) |
N312K |
possibly damaging |
Het |
Otogl |
C |
T |
10: 107,731,637 (GRCm39) |
C168Y |
probably damaging |
Het |
Phldb2 |
T |
G |
16: 45,645,934 (GRCm39) |
T171P |
probably benign |
Het |
Ppef2 |
A |
T |
5: 92,386,841 (GRCm39) |
F365L |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Ryr1 |
G |
A |
7: 28,795,596 (GRCm39) |
T1105I |
probably benign |
Het |
Sclt1 |
T |
A |
3: 41,617,889 (GRCm39) |
*29L |
probably null |
Het |
Scn11a |
T |
C |
9: 119,594,503 (GRCm39) |
K1297E |
probably damaging |
Het |
Setd1a |
T |
A |
7: 127,385,366 (GRCm39) |
M691K |
probably benign |
Het |
Sftpc |
T |
C |
14: 70,760,059 (GRCm39) |
E66G |
probably damaging |
Het |
Spata31h1 |
T |
C |
10: 82,131,934 (GRCm39) |
I359V |
probably benign |
Het |
Thnsl2 |
T |
C |
6: 71,118,303 (GRCm39) |
T42A |
probably benign |
Het |
Tram1 |
T |
C |
1: 13,640,199 (GRCm39) |
D285G |
probably benign |
Het |
Ttn |
G |
A |
2: 76,675,374 (GRCm39) |
P11137L |
unknown |
Het |
Ttn |
C |
A |
2: 76,727,103 (GRCm39) |
V5821F |
unknown |
Het |
Ttn |
A |
T |
2: 76,566,584 (GRCm39) |
I28103K |
probably damaging |
Het |
Usp38 |
T |
A |
8: 81,740,945 (GRCm39) |
M41L |
probably benign |
Het |
Zcwpw1 |
T |
G |
5: 137,815,753 (GRCm39) |
Y419D |
possibly damaging |
Het |
Zfp407 |
G |
A |
18: 84,577,525 (GRCm39) |
A1196V |
possibly damaging |
Het |
Zfp446 |
T |
A |
7: 12,712,970 (GRCm39) |
S103T |
possibly damaging |
Het |
|
Other mutations in Serpinb9c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00791:Serpinb9c
|
APN |
13 |
33,335,867 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01357:Serpinb9c
|
APN |
13 |
33,335,862 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01413:Serpinb9c
|
APN |
13 |
33,335,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R1411:Serpinb9c
|
UTSW |
13 |
33,335,817 (GRCm39) |
missense |
probably benign |
0.02 |
R1926:Serpinb9c
|
UTSW |
13 |
33,334,218 (GRCm39) |
missense |
probably benign |
0.00 |
R2057:Serpinb9c
|
UTSW |
13 |
33,340,854 (GRCm39) |
nonsense |
probably null |
|
R2058:Serpinb9c
|
UTSW |
13 |
33,340,854 (GRCm39) |
nonsense |
probably null |
|
R2059:Serpinb9c
|
UTSW |
13 |
33,340,854 (GRCm39) |
nonsense |
probably null |
|
R2272:Serpinb9c
|
UTSW |
13 |
33,338,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R3948:Serpinb9c
|
UTSW |
13 |
33,334,077 (GRCm39) |
missense |
probably benign |
|
R4520:Serpinb9c
|
UTSW |
13 |
33,335,840 (GRCm39) |
splice site |
probably null |
|
R4558:Serpinb9c
|
UTSW |
13 |
33,338,482 (GRCm39) |
missense |
probably benign |
0.12 |
R4735:Serpinb9c
|
UTSW |
13 |
33,334,254 (GRCm39) |
missense |
probably benign |
0.13 |
R5004:Serpinb9c
|
UTSW |
13 |
33,334,338 (GRCm39) |
missense |
probably benign |
0.00 |
R5009:Serpinb9c
|
UTSW |
13 |
33,338,414 (GRCm39) |
missense |
probably benign |
0.18 |
R6345:Serpinb9c
|
UTSW |
13 |
33,333,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6801:Serpinb9c
|
UTSW |
13 |
33,341,807 (GRCm39) |
start codon destroyed |
probably benign |
0.00 |
R6886:Serpinb9c
|
UTSW |
13 |
33,334,310 (GRCm39) |
missense |
probably benign |
0.04 |
R7082:Serpinb9c
|
UTSW |
13 |
33,338,390 (GRCm39) |
missense |
probably benign |
0.40 |
R7288:Serpinb9c
|
UTSW |
13 |
33,335,883 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8309:Serpinb9c
|
UTSW |
13 |
33,334,094 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8465:Serpinb9c
|
UTSW |
13 |
33,334,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R8543:Serpinb9c
|
UTSW |
13 |
33,340,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R8750:Serpinb9c
|
UTSW |
13 |
33,335,793 (GRCm39) |
missense |
probably null |
0.93 |
R9002:Serpinb9c
|
UTSW |
13 |
33,334,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R9412:Serpinb9c
|
UTSW |
13 |
33,334,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|