Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
G |
A |
16: 88,424,096 (GRCm39) |
Q132* |
probably null |
Het |
Aadacl4 |
T |
A |
4: 144,349,889 (GRCm39) |
L382* |
probably null |
Het |
Afg3l2 |
A |
G |
18: 67,540,493 (GRCm39) |
I672T |
probably benign |
Het |
Aftph |
A |
T |
11: 20,676,762 (GRCm39) |
D282E |
probably benign |
Het |
Agpat5 |
A |
G |
8: 18,920,930 (GRCm39) |
N161S |
probably benign |
Het |
Alpk2 |
C |
T |
18: 65,414,030 (GRCm39) |
E1562K |
probably damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Apobr |
A |
G |
7: 126,186,723 (GRCm39) |
R745G |
probably benign |
Het |
Arrdc5 |
T |
C |
17: 56,607,144 (GRCm39) |
T34A |
possibly damaging |
Het |
Astl |
T |
C |
2: 127,189,163 (GRCm39) |
L163P |
probably damaging |
Het |
Atf7ip2 |
A |
T |
16: 10,027,005 (GRCm39) |
H91L |
probably damaging |
Het |
Atp13a3 |
A |
T |
16: 30,151,092 (GRCm39) |
S1073T |
possibly damaging |
Het |
Bcl2a1a |
A |
T |
9: 88,839,503 (GRCm39) |
I134L |
probably damaging |
Het |
Brinp1 |
T |
C |
4: 68,747,520 (GRCm39) |
|
probably null |
Het |
Capn9 |
A |
G |
8: 125,340,570 (GRCm39) |
N578S |
probably benign |
Het |
Casp2 |
T |
A |
6: 42,245,842 (GRCm39) |
D166E |
probably damaging |
Het |
Ccr1l1 |
A |
T |
9: 123,777,544 (GRCm39) |
I301N |
probably damaging |
Het |
Chtop |
T |
A |
3: 90,414,874 (GRCm39) |
T15S |
probably damaging |
Het |
Coq5 |
T |
A |
5: 115,417,975 (GRCm39) |
|
probably null |
Het |
Crbn |
G |
A |
6: 106,772,886 (GRCm39) |
P34L |
probably damaging |
Het |
Crisp1 |
G |
T |
17: 40,619,760 (GRCm39) |
D59E |
possibly damaging |
Het |
Cyp4f14 |
A |
T |
17: 33,128,210 (GRCm39) |
D268E |
probably benign |
Het |
D5Ertd579e |
T |
C |
5: 36,770,621 (GRCm39) |
D1258G |
possibly damaging |
Het |
Dcp1b |
T |
C |
6: 119,194,872 (GRCm39) |
S531P |
probably benign |
Het |
Defb25 |
T |
C |
2: 152,464,410 (GRCm39) |
M45V |
probably benign |
Het |
Dffa |
T |
C |
4: 149,190,702 (GRCm39) |
L77P |
probably damaging |
Het |
Dixdc1 |
T |
C |
9: 50,601,164 (GRCm39) |
Q361R |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 30,998,157 (GRCm39) |
L2560P |
probably damaging |
Het |
Fabp5 |
A |
G |
3: 10,080,601 (GRCm39) |
T108A |
probably benign |
Het |
Fam149a |
T |
G |
8: 45,792,411 (GRCm39) |
|
probably null |
Het |
Fam20c |
A |
G |
5: 138,793,056 (GRCm39) |
Y430C |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,489,872 (GRCm39) |
T3595A |
probably damaging |
Het |
Fbp1 |
A |
G |
13: 63,015,245 (GRCm39) |
Y245H |
probably damaging |
Het |
Frem1 |
C |
T |
4: 82,917,128 (GRCm39) |
R605H |
probably benign |
Het |
Fscb |
A |
G |
12: 64,518,292 (GRCm39) |
I1058T |
unknown |
Het |
Fyb2 |
A |
G |
4: 104,808,059 (GRCm39) |
K373R |
probably benign |
Het |
Ggta1 |
A |
T |
2: 35,292,145 (GRCm39) |
Y387* |
probably null |
Het |
Gm18856 |
T |
C |
13: 14,140,342 (GRCm39) |
|
probably benign |
Het |
Gm572 |
T |
C |
4: 148,752,966 (GRCm39) |
S282P |
possibly damaging |
Het |
Gpd2 |
A |
T |
2: 57,247,712 (GRCm39) |
I552F |
probably damaging |
Het |
Grk5 |
T |
C |
19: 61,074,653 (GRCm39) |
|
probably null |
Het |
Hivep1 |
T |
C |
13: 42,313,760 (GRCm39) |
V2000A |
probably damaging |
Het |
Ipo5 |
C |
T |
14: 121,170,714 (GRCm39) |
L466F |
probably damaging |
Het |
Itgb1 |
G |
A |
8: 129,458,526 (GRCm39) |
S785N |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,307,987 (GRCm39) |
R258K |
probably benign |
Het |
Kcnk12 |
A |
G |
17: 88,053,747 (GRCm39) |
V305A |
probably benign |
Het |
Klf5 |
C |
T |
14: 99,538,986 (GRCm39) |
T133I |
probably damaging |
Het |
Lrig2 |
A |
G |
3: 104,399,128 (GRCm39) |
I178T |
probably damaging |
Het |
Lyrm4 |
A |
T |
13: 36,276,907 (GRCm39) |
M30K |
probably benign |
Het |
Mpv17 |
A |
G |
5: 31,311,063 (GRCm39) |
Y7H |
probably damaging |
Het |
Mrps22 |
T |
C |
9: 98,478,869 (GRCm39) |
|
probably null |
Het |
Myof |
A |
T |
19: 37,931,927 (GRCm39) |
W967R |
probably damaging |
Het |
Naip1 |
C |
T |
13: 100,559,657 (GRCm39) |
D1116N |
probably benign |
Het |
Or1e33 |
T |
C |
11: 73,738,781 (GRCm39) |
T57A |
probably benign |
Het |
Or6c66b |
C |
A |
10: 129,376,561 (GRCm39) |
H52N |
probably benign |
Het |
Or8g50 |
G |
A |
9: 39,648,492 (GRCm39) |
C127Y |
probably damaging |
Het |
Or9k2b |
T |
C |
10: 130,016,261 (GRCm39) |
T163A |
probably benign |
Het |
Ovol2 |
T |
C |
2: 144,147,710 (GRCm39) |
Y180C |
probably damaging |
Het |
Pacs1 |
T |
C |
19: 5,202,337 (GRCm39) |
S418G |
probably benign |
Het |
Pcdh1 |
T |
C |
18: 38,325,233 (GRCm39) |
E903G |
probably damaging |
Het |
Pcdhb15 |
A |
T |
18: 37,607,713 (GRCm39) |
Y315F |
probably damaging |
Het |
Pex1 |
T |
C |
5: 3,676,085 (GRCm39) |
L891P |
probably damaging |
Het |
Potefam1 |
T |
A |
2: 111,051,119 (GRCm39) |
M226L |
probably benign |
Het |
Ppfia2 |
G |
A |
10: 106,666,429 (GRCm39) |
M378I |
possibly damaging |
Het |
Ppp1r9a |
T |
A |
6: 5,143,491 (GRCm39) |
|
probably null |
Het |
Prm3 |
T |
C |
16: 10,608,563 (GRCm39) |
E64G |
possibly damaging |
Het |
Prmt6 |
T |
C |
3: 110,157,887 (GRCm39) |
D134G |
possibly damaging |
Het |
Prss42 |
G |
A |
9: 110,629,996 (GRCm39) |
G250D |
probably damaging |
Het |
Pwwp2b |
G |
A |
7: 138,834,747 (GRCm39) |
V63I |
probably benign |
Het |
Rbm17 |
T |
C |
2: 11,590,530 (GRCm39) |
D375G |
possibly damaging |
Het |
Rhbdl1 |
A |
T |
17: 26,055,383 (GRCm39) |
|
probably null |
Het |
Rims2 |
T |
A |
15: 39,155,584 (GRCm39) |
D128E |
probably benign |
Het |
Rock2 |
A |
G |
12: 17,015,653 (GRCm39) |
K850R |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,114,513 (GRCm39) |
I624T |
probably benign |
Het |
Rrp36 |
A |
T |
17: 46,983,340 (GRCm39) |
D91E |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,527,944 (GRCm39) |
D849N |
possibly damaging |
Het |
Sec24a |
A |
T |
11: 51,634,775 (GRCm39) |
Y50* |
probably null |
Het |
Sh2d4b |
A |
G |
14: 40,614,921 (GRCm39) |
M1T |
probably null |
Het |
Slc4a7 |
A |
G |
14: 14,760,247 (GRCm38) |
I561V |
possibly damaging |
Het |
Slc7a12 |
T |
C |
3: 14,564,337 (GRCm39) |
V70A |
possibly damaging |
Het |
Slfnl1 |
A |
T |
4: 120,392,972 (GRCm39) |
I355F |
probably damaging |
Het |
Spata2 |
C |
T |
2: 167,325,439 (GRCm39) |
R460H |
probably damaging |
Het |
Stk11ip |
C |
T |
1: 75,505,629 (GRCm39) |
Q433* |
probably null |
Het |
Susd1 |
T |
C |
4: 59,411,395 (GRCm39) |
Y146C |
probably damaging |
Het |
Susd5 |
A |
T |
9: 113,897,890 (GRCm39) |
D115V |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,845,029 (GRCm39) |
V20E |
probably damaging |
Het |
Tbc1d4 |
T |
C |
14: 101,712,651 (GRCm39) |
Y694C |
possibly damaging |
Het |
Tmem131 |
T |
C |
1: 36,863,840 (GRCm39) |
E640G |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,068,342 (GRCm39) |
T1782A |
probably benign |
Het |
Trim24 |
T |
C |
6: 37,892,214 (GRCm39) |
L249P |
probably damaging |
Het |
Ttf1 |
T |
C |
2: 28,957,164 (GRCm39) |
I478T |
probably damaging |
Het |
Upf2 |
T |
A |
2: 6,044,908 (GRCm39) |
|
probably null |
Het |
Urb1 |
A |
T |
16: 90,584,285 (GRCm39) |
C566S |
probably damaging |
Het |
Vmn1r191 |
T |
C |
13: 22,363,262 (GRCm39) |
N164S |
probably benign |
Het |
Vmn2r81 |
T |
A |
10: 79,104,112 (GRCm39) |
V245E |
probably damaging |
Het |
Wnt8b |
T |
C |
19: 44,499,715 (GRCm39) |
F155L |
probably damaging |
Het |
Xrra1 |
A |
T |
7: 99,547,647 (GRCm39) |
I279F |
probably benign |
Het |
Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
Zfp607b |
C |
T |
7: 27,391,948 (GRCm39) |
H8Y |
possibly damaging |
Het |
Zfp933 |
A |
T |
4: 147,910,476 (GRCm39) |
H373Q |
probably damaging |
Het |
Zfp938 |
A |
G |
10: 82,060,982 (GRCm39) |
L546P |
probably benign |
Het |
Zfp988 |
C |
T |
4: 147,415,739 (GRCm39) |
R58C |
probably benign |
Het |
Zkscan14 |
C |
T |
5: 145,138,464 (GRCm39) |
V8I |
probably benign |
Het |
|
Other mutations in Vwce |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Vwce
|
APN |
19 |
10,641,875 (GRCm39) |
splice site |
probably null |
|
IGL01358:Vwce
|
APN |
19 |
10,641,773 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02330:Vwce
|
APN |
19 |
10,624,165 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02477:Vwce
|
APN |
19 |
10,641,982 (GRCm39) |
splice site |
probably null |
|
IGL02551:Vwce
|
APN |
19 |
10,622,400 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02606:Vwce
|
APN |
19 |
10,632,712 (GRCm39) |
splice site |
probably benign |
|
IGL02633:Vwce
|
APN |
19 |
10,625,858 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02656:Vwce
|
APN |
19 |
10,641,716 (GRCm39) |
missense |
probably benign |
|
IGL02884:Vwce
|
APN |
19 |
10,623,943 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02973:Vwce
|
APN |
19 |
10,632,764 (GRCm39) |
nonsense |
probably null |
|
IGL03038:Vwce
|
APN |
19 |
10,624,035 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03329:Vwce
|
APN |
19 |
10,637,360 (GRCm39) |
missense |
possibly damaging |
0.73 |
PIT4403001:Vwce
|
UTSW |
19 |
10,615,461 (GRCm39) |
missense |
possibly damaging |
0.53 |
PIT4431001:Vwce
|
UTSW |
19 |
10,641,946 (GRCm39) |
missense |
possibly damaging |
0.53 |
PIT4519001:Vwce
|
UTSW |
19 |
10,641,946 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0042:Vwce
|
UTSW |
19 |
10,624,177 (GRCm39) |
missense |
probably benign |
|
R0081:Vwce
|
UTSW |
19 |
10,641,453 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0142:Vwce
|
UTSW |
19 |
10,641,976 (GRCm39) |
missense |
probably damaging |
0.97 |
R0165:Vwce
|
UTSW |
19 |
10,637,337 (GRCm39) |
splice site |
probably benign |
|
R0948:Vwce
|
UTSW |
19 |
10,630,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1053:Vwce
|
UTSW |
19 |
10,641,463 (GRCm39) |
missense |
probably benign |
0.18 |
R1505:Vwce
|
UTSW |
19 |
10,641,608 (GRCm39) |
missense |
probably benign |
|
R1623:Vwce
|
UTSW |
19 |
10,624,108 (GRCm39) |
nonsense |
probably null |
|
R1882:Vwce
|
UTSW |
19 |
10,615,520 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3849:Vwce
|
UTSW |
19 |
10,624,269 (GRCm39) |
missense |
probably damaging |
0.97 |
R4292:Vwce
|
UTSW |
19 |
10,636,996 (GRCm39) |
missense |
probably benign |
0.00 |
R4293:Vwce
|
UTSW |
19 |
10,636,996 (GRCm39) |
missense |
probably benign |
0.00 |
R4531:Vwce
|
UTSW |
19 |
10,641,710 (GRCm39) |
missense |
probably benign |
0.01 |
R4678:Vwce
|
UTSW |
19 |
10,642,012 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4720:Vwce
|
UTSW |
19 |
10,625,831 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4737:Vwce
|
UTSW |
19 |
10,627,943 (GRCm39) |
missense |
probably benign |
0.33 |
R4864:Vwce
|
UTSW |
19 |
10,628,000 (GRCm39) |
missense |
probably benign |
0.01 |
R4916:Vwce
|
UTSW |
19 |
10,624,243 (GRCm39) |
missense |
probably damaging |
0.98 |
R4939:Vwce
|
UTSW |
19 |
10,622,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R5605:Vwce
|
UTSW |
19 |
10,635,402 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5735:Vwce
|
UTSW |
19 |
10,624,431 (GRCm39) |
missense |
probably benign |
0.08 |
R5780:Vwce
|
UTSW |
19 |
10,627,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Vwce
|
UTSW |
19 |
10,621,585 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6383:Vwce
|
UTSW |
19 |
10,636,956 (GRCm39) |
nonsense |
probably null |
|
R6920:Vwce
|
UTSW |
19 |
10,642,057 (GRCm39) |
missense |
probably benign |
|
R7201:Vwce
|
UTSW |
19 |
10,615,479 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7276:Vwce
|
UTSW |
19 |
10,641,538 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7423:Vwce
|
UTSW |
19 |
10,641,704 (GRCm39) |
missense |
probably benign |
0.02 |
R7474:Vwce
|
UTSW |
19 |
10,624,305 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7843:Vwce
|
UTSW |
19 |
10,641,647 (GRCm39) |
missense |
probably benign |
0.01 |
R8254:Vwce
|
UTSW |
19 |
10,627,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R8782:Vwce
|
UTSW |
19 |
10,615,491 (GRCm39) |
missense |
probably benign |
0.33 |
R9154:Vwce
|
UTSW |
19 |
10,625,850 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9369:Vwce
|
UTSW |
19 |
10,624,061 (GRCm39) |
missense |
probably benign |
0.04 |
R9458:Vwce
|
UTSW |
19 |
10,631,688 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9664:Vwce
|
UTSW |
19 |
10,615,481 (GRCm39) |
missense |
probably benign |
0.33 |
RF020:Vwce
|
UTSW |
19 |
10,630,449 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Vwce
|
UTSW |
19 |
10,634,026 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1177:Vwce
|
UTSW |
19 |
10,624,227 (GRCm39) |
missense |
possibly damaging |
0.70 |
|