Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430531B16Rik |
A |
T |
7: 139,978,545 (GRCm38) |
|
probably null |
Het |
Abcb4 |
T |
C |
5: 8,934,226 (GRCm38) |
V652A |
probably benign |
Het |
Acvrl1 |
G |
T |
15: 101,141,072 (GRCm38) |
V417L |
probably damaging |
Het |
Add1 |
A |
G |
5: 34,619,371 (GRCm38) |
R479G |
probably benign |
Het |
Adgb |
A |
T |
10: 10,400,574 (GRCm38) |
L350Q |
possibly damaging |
Het |
Adgrl2 |
A |
T |
3: 148,846,870 (GRCm38) |
S666T |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,045,930 (GRCm38) |
D2268E |
possibly damaging |
Het |
Amigo3 |
C |
A |
9: 108,054,066 (GRCm38) |
H229Q |
probably benign |
Het |
Ano6 |
G |
C |
15: 95,864,244 (GRCm38) |
Q31H |
possibly damaging |
Het |
Ap4m1 |
G |
A |
5: 138,175,019 (GRCm38) |
D180N |
probably damaging |
Het |
Apc2 |
A |
T |
10: 80,311,740 (GRCm38) |
D876V |
probably damaging |
Het |
Apcdd1 |
T |
A |
18: 62,952,188 (GRCm38) |
Y485* |
probably null |
Het |
Aqp1 |
G |
T |
6: 55,336,851 (GRCm38) |
D121Y |
probably benign |
Het |
Bicd2 |
C |
A |
13: 49,369,609 (GRCm38) |
R141S |
probably benign |
Het |
Brpf3 |
C |
A |
17: 28,806,293 (GRCm38) |
H113Q |
probably benign |
Het |
Cacng2 |
A |
T |
15: 78,013,320 (GRCm38) |
Y96* |
probably null |
Het |
Catsperg1 |
G |
T |
7: 29,210,759 (GRCm38) |
N52K |
possibly damaging |
Het |
Celsr2 |
A |
C |
3: 108,394,995 (GRCm38) |
F2606V |
possibly damaging |
Het |
Cerkl |
A |
T |
2: 79,332,605 (GRCm38) |
N516K |
probably benign |
Het |
Ciita |
G |
A |
16: 10,512,288 (GRCm38) |
R812H |
probably damaging |
Het |
Cldn3 |
T |
A |
5: 134,986,983 (GRCm38) |
L180Q |
probably damaging |
Het |
Cnot6l |
T |
C |
5: 96,077,299 (GRCm38) |
I512V |
probably benign |
Het |
Col5a2 |
A |
T |
1: 45,442,867 (GRCm38) |
D32E |
unknown |
Het |
Coro7 |
A |
G |
16: 4,632,048 (GRCm38) |
V616A |
probably damaging |
Het |
Cyp4f18 |
T |
C |
8: 71,988,654 (GRCm38) |
D494G |
probably benign |
Het |
Ddx39 |
T |
A |
8: 83,722,471 (GRCm38) |
V296E |
probably benign |
Het |
Dgkg |
A |
T |
16: 22,548,690 (GRCm38) |
H593Q |
probably damaging |
Het |
Dhx16 |
T |
C |
17: 35,886,160 (GRCm38) |
L645P |
probably damaging |
Het |
Dnah14 |
A |
G |
1: 181,598,403 (GRCm38) |
M171V |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,720,930 (GRCm38) |
V4521I |
probably damaging |
Het |
Dok7 |
A |
T |
5: 35,064,522 (GRCm38) |
M60L |
probably benign |
Het |
Donson |
A |
T |
16: 91,688,711 (GRCm38) |
M1K |
probably null |
Het |
Dsp |
C |
T |
13: 38,192,883 (GRCm38) |
T1548M |
probably benign |
Het |
Dyrk1a |
A |
G |
16: 94,692,043 (GRCm38) |
T712A |
probably damaging |
Het |
Eef2 |
A |
G |
10: 81,181,282 (GRCm38) |
T708A |
probably benign |
Het |
Epn3 |
G |
A |
11: 94,493,780 (GRCm38) |
T289I |
probably benign |
Het |
Fam171a1 |
C |
T |
2: 3,226,472 (GRCm38) |
R881* |
probably null |
Het |
Fam71a |
G |
A |
1: 191,164,353 (GRCm38) |
T31M |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,282,304 (GRCm38) |
R2528W |
probably damaging |
Het |
Fgfr1 |
T |
G |
8: 25,573,839 (GRCm38) |
F707C |
probably damaging |
Het |
Frem2 |
G |
C |
3: 53,654,753 (GRCm38) |
P778A |
probably damaging |
Het |
Ganc |
A |
G |
2: 120,430,599 (GRCm38) |
Y255C |
probably damaging |
Het |
Ginm1 |
A |
T |
10: 7,777,850 (GRCm38) |
Y65* |
probably null |
Het |
Gm11559 |
T |
A |
11: 99,864,881 (GRCm38) |
C119S |
unknown |
Het |
Gnai1 |
T |
A |
5: 18,289,551 (GRCm38) |
H188L |
|
Het |
H6pd |
C |
T |
4: 149,996,350 (GRCm38) |
A13T |
probably benign |
Het |
Hist1h2be |
T |
C |
13: 23,585,923 (GRCm38) |
K12E |
probably benign |
Het |
Hoxd12 |
A |
T |
2: 74,675,246 (GRCm38) |
T54S |
possibly damaging |
Het |
Hs3st5 |
T |
A |
10: 36,833,194 (GRCm38) |
L242M |
probably damaging |
Het |
Il9r |
C |
A |
11: 32,194,389 (GRCm38) |
V139L |
possibly damaging |
Het |
Immt |
A |
G |
6: 71,846,369 (GRCm38) |
D68G |
probably damaging |
Het |
Itsn2 |
A |
G |
12: 4,632,985 (GRCm38) |
I304V |
unknown |
Het |
Lgr4 |
G |
A |
2: 109,996,629 (GRCm38) |
W159* |
probably null |
Het |
Lin52 |
G |
A |
12: 84,457,954 (GRCm38) |
G38S |
probably damaging |
Het |
Lpgat1 |
A |
T |
1: 191,719,453 (GRCm38) |
M64L |
probably benign |
Het |
Lrrc10b |
G |
T |
19: 10,456,778 (GRCm38) |
R180S |
possibly damaging |
Het |
Lrrc29 |
T |
C |
8: 105,312,898 (GRCm38) |
D127G |
probably damaging |
Het |
Lrrc36 |
A |
T |
8: 105,449,769 (GRCm38) |
L258F |
possibly damaging |
Het |
Ltbp4 |
T |
A |
7: 27,329,755 (GRCm38) |
Q235L |
unknown |
Het |
Maml2 |
A |
G |
9: 13,621,607 (GRCm38) |
M706V |
|
Het |
Mc5r |
G |
T |
18: 68,339,668 (GRCm38) |
C366F |
probably damaging |
Het |
Mlip |
T |
C |
9: 77,164,842 (GRCm38) |
R244G |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,585,013 (GRCm38) |
R6658S |
probably benign |
Het |
Mup4 |
G |
T |
4: 59,960,046 (GRCm38) |
H73N |
possibly damaging |
Het |
Nf1 |
A |
G |
11: 79,564,943 (GRCm38) |
M565V |
probably benign |
Het |
Nphp1 |
G |
A |
2: 127,761,217 (GRCm38) |
T382I |
possibly damaging |
Het |
Nrcam |
C |
T |
12: 44,564,026 (GRCm38) |
T503I |
possibly damaging |
Het |
Nwd2 |
A |
T |
5: 63,800,409 (GRCm38) |
N361Y |
probably damaging |
Het |
Olfr1045 |
A |
G |
2: 86,198,573 (GRCm38) |
Y60H |
probably damaging |
Het |
Olfr1309 |
A |
T |
2: 111,983,327 (GRCm38) |
L249* |
probably null |
Het |
Olfr308 |
A |
G |
7: 86,321,574 (GRCm38) |
I126T |
probably damaging |
Het |
Olfr461 |
G |
T |
6: 40,544,895 (GRCm38) |
A28E |
probably damaging |
Het |
Olfr518 |
A |
T |
7: 108,880,816 (GRCm38) |
H263Q |
probably damaging |
Het |
Olfr836 |
A |
G |
9: 19,121,669 (GRCm38) |
Y235C |
probably benign |
Het |
Olfr993 |
A |
T |
2: 85,414,444 (GRCm38) |
V145E |
probably damaging |
Het |
Orc5 |
A |
G |
5: 22,523,584 (GRCm38) |
F308L |
probably benign |
Het |
Padi1 |
T |
A |
4: 140,832,404 (GRCm38) |
Y54F |
probably benign |
Het |
Parp1 |
A |
G |
1: 180,569,100 (GRCm38) |
K23E |
possibly damaging |
Het |
Pate1 |
A |
T |
9: 35,685,972 (GRCm38) |
V79D |
possibly damaging |
Het |
Pcdh18 |
T |
C |
3: 49,756,860 (GRCm38) |
H2R |
probably benign |
Het |
Pcnx2 |
G |
A |
8: 125,887,083 (GRCm38) |
S543F |
probably damaging |
Het |
Pcp4l1 |
G |
A |
1: 171,174,465 (GRCm38) |
A42V |
possibly damaging |
Het |
Pnkp |
T |
A |
7: 44,859,734 (GRCm38) |
F169L |
probably damaging |
Het |
Ppp6r3 |
A |
T |
19: 3,507,325 (GRCm38) |
N254K |
probably damaging |
Het |
Psd |
A |
G |
19: 46,324,454 (GRCm38) |
L159P |
probably benign |
Het |
Ptprf |
A |
G |
4: 118,231,669 (GRCm38) |
Y646H |
probably damaging |
Het |
Rab3ip |
A |
T |
10: 116,937,633 (GRCm38) |
S92T |
probably benign |
Het |
Rabgef1 |
A |
G |
5: 130,187,351 (GRCm38) |
|
probably benign |
Het |
Ralgapa1 |
C |
A |
12: 55,709,004 (GRCm38) |
W1129L |
probably damaging |
Het |
Rhpn2 |
T |
A |
7: 35,385,463 (GRCm38) |
L594Q |
probably benign |
Het |
Rnf38 |
C |
A |
4: 44,158,989 (GRCm38) |
|
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,738,194 (GRCm38) |
H1747L |
possibly damaging |
Het |
Sec16a |
A |
G |
2: 26,439,717 (GRCm38) |
L13P |
unknown |
Het |
Srgap2 |
A |
T |
1: 131,291,613 (GRCm38) |
Y264* |
probably null |
Het |
Stxbp2 |
T |
C |
8: 3,641,151 (GRCm38) |
M465T |
|
Het |
Sumf2 |
A |
G |
5: 129,862,710 (GRCm38) |
K305R |
probably benign |
Het |
Susd2 |
T |
A |
10: 75,642,565 (GRCm38) |
Y59F |
probably benign |
Het |
Taco1 |
T |
C |
11: 106,072,617 (GRCm38) |
V198A |
probably benign |
Het |
Tas2r136 |
A |
T |
6: 132,777,906 (GRCm38) |
M86K |
possibly damaging |
Het |
Tbc1d10c |
T |
C |
19: 4,184,898 (GRCm38) |
E388G |
possibly damaging |
Het |
Tmem132c |
C |
T |
5: 127,564,059 (GRCm38) |
T1098I |
possibly damaging |
Het |
Trim3 |
G |
T |
7: 105,617,800 (GRCm38) |
Y457* |
probably null |
Het |
Ttc38 |
A |
G |
15: 85,852,861 (GRCm38) |
T316A |
probably benign |
Het |
Ubqln4 |
T |
A |
3: 88,555,910 (GRCm38) |
N127K |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,904,626 (GRCm38) |
F262Y |
probably damaging |
Het |
Zdhhc6 |
A |
T |
19: 55,302,755 (GRCm38) |
C343S |
possibly damaging |
Het |
Zfp248 |
A |
G |
6: 118,430,209 (GRCm38) |
C140R |
probably damaging |
Het |
Zfp266 |
T |
C |
9: 20,502,095 (GRCm38) |
T90A |
probably benign |
Het |
Zfp407 |
A |
T |
18: 84,559,042 (GRCm38) |
D1315E |
possibly damaging |
Het |
Zfp644 |
T |
C |
5: 106,638,277 (GRCm38) |
S135G |
probably benign |
Het |
Zscan29 |
A |
T |
2: 121,160,988 (GRCm38) |
I773N |
probably damaging |
Het |
Zswim5 |
T |
A |
4: 116,980,834 (GRCm38) |
V787E |
possibly damaging |
Het |
|
Other mutations in Sppl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Sppl3
|
APN |
5 |
115,074,876 (GRCm38) |
missense |
probably benign |
|
IGL02302:Sppl3
|
APN |
5 |
115,082,331 (GRCm38) |
missense |
probably benign |
0.43 |
IGL02381:Sppl3
|
APN |
5 |
115,074,910 (GRCm38) |
splice site |
probably null |
|
IGL02592:Sppl3
|
APN |
5 |
115,095,911 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02963:Sppl3
|
APN |
5 |
115,061,603 (GRCm38) |
missense |
probably damaging |
1.00 |
R0119:Sppl3
|
UTSW |
5 |
115,088,994 (GRCm38) |
unclassified |
probably benign |
|
R0299:Sppl3
|
UTSW |
5 |
115,088,994 (GRCm38) |
unclassified |
probably benign |
|
R0827:Sppl3
|
UTSW |
5 |
115,082,333 (GRCm38) |
nonsense |
probably null |
|
R1141:Sppl3
|
UTSW |
5 |
115,088,293 (GRCm38) |
frame shift |
probably null |
|
R1321:Sppl3
|
UTSW |
5 |
115,088,293 (GRCm38) |
frame shift |
probably null |
|
R1322:Sppl3
|
UTSW |
5 |
115,088,293 (GRCm38) |
frame shift |
probably null |
|
R1451:Sppl3
|
UTSW |
5 |
115,088,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R3110:Sppl3
|
UTSW |
5 |
115,074,864 (GRCm38) |
missense |
possibly damaging |
0.78 |
R3112:Sppl3
|
UTSW |
5 |
115,074,864 (GRCm38) |
missense |
possibly damaging |
0.78 |
R4701:Sppl3
|
UTSW |
5 |
115,103,313 (GRCm38) |
splice site |
probably null |
|
R4808:Sppl3
|
UTSW |
5 |
115,083,426 (GRCm38) |
splice site |
probably benign |
|
R4931:Sppl3
|
UTSW |
5 |
115,082,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R6513:Sppl3
|
UTSW |
5 |
115,095,936 (GRCm38) |
missense |
probably damaging |
1.00 |
R6993:Sppl3
|
UTSW |
5 |
115,082,290 (GRCm38) |
missense |
probably damaging |
0.99 |
R7384:Sppl3
|
UTSW |
5 |
115,061,641 (GRCm38) |
critical splice donor site |
probably null |
|
R9012:Sppl3
|
UTSW |
5 |
115,088,928 (GRCm38) |
missense |
probably benign |
0.38 |
R9257:Sppl3
|
UTSW |
5 |
115,083,473 (GRCm38) |
missense |
probably benign |
0.41 |
R9258:Sppl3
|
UTSW |
5 |
115,095,863 (GRCm38) |
missense |
probably damaging |
1.00 |
R9306:Sppl3
|
UTSW |
5 |
115,074,863 (GRCm38) |
missense |
probably benign |
|
|