Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,195,037 (GRCm39) |
F145L |
possibly damaging |
Het |
Aars2 |
T |
A |
17: 45,827,847 (GRCm39) |
D555E |
probably damaging |
Het |
Ago1 |
C |
A |
4: 126,354,185 (GRCm39) |
M208I |
probably benign |
Het |
Ak7 |
G |
A |
12: 105,679,834 (GRCm39) |
V123M |
probably benign |
Het |
Amfr |
A |
G |
8: 94,700,849 (GRCm39) |
L537P |
probably damaging |
Het |
Apob |
A |
G |
12: 8,058,568 (GRCm39) |
D2317G |
probably damaging |
Het |
Asb6 |
T |
A |
2: 30,714,483 (GRCm39) |
D209V |
probably damaging |
Het |
AY358078 |
T |
A |
14: 52,063,532 (GRCm39) |
C393S |
possibly damaging |
Het |
Baz2a |
T |
A |
10: 127,957,052 (GRCm39) |
C932S |
probably damaging |
Het |
Btnl10 |
A |
G |
11: 58,814,426 (GRCm39) |
I369V |
probably benign |
Het |
Ccdc66 |
T |
C |
14: 27,222,377 (GRCm39) |
N122S |
probably damaging |
Het |
Cfap96 |
A |
T |
8: 46,423,505 (GRCm39) |
I69N |
probably damaging |
Het |
Clic4 |
A |
T |
4: 134,966,300 (GRCm39) |
|
probably null |
Het |
Col6a3 |
A |
G |
1: 90,709,626 (GRCm39) |
S1857P |
unknown |
Het |
Cracr2a |
A |
C |
6: 127,580,851 (GRCm39) |
D9A |
probably benign |
Het |
Cspg4b |
A |
G |
13: 113,455,783 (GRCm39) |
R610G |
possibly damaging |
Het |
Dcst1 |
T |
C |
3: 89,263,643 (GRCm39) |
E384G |
probably benign |
Het |
Ddx4 |
T |
C |
13: 112,748,594 (GRCm39) |
K435E |
probably damaging |
Het |
Deaf1 |
T |
A |
7: 140,890,884 (GRCm39) |
T433S |
possibly damaging |
Het |
Dnah3 |
T |
A |
7: 119,689,169 (GRCm39) |
M82L |
probably benign |
Het |
Dnhd1 |
G |
T |
7: 105,352,851 (GRCm39) |
R2668L |
probably damaging |
Het |
Efcab6 |
C |
T |
15: 83,831,126 (GRCm39) |
G596D |
probably benign |
Het |
Ercc3 |
G |
A |
18: 32,378,624 (GRCm39) |
A202T |
probably benign |
Het |
Fam181b |
C |
A |
7: 92,729,992 (GRCm39) |
A255E |
possibly damaging |
Het |
Fam83e |
T |
A |
7: 45,372,924 (GRCm39) |
D178E |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,455,228 (GRCm39) |
L2116S |
possibly damaging |
Het |
Gm16494 |
T |
A |
17: 47,327,723 (GRCm39) |
K54* |
probably null |
Het |
Golgb1 |
A |
G |
16: 36,738,987 (GRCm39) |
D2442G |
probably damaging |
Het |
Greb1l |
G |
A |
18: 10,553,705 (GRCm39) |
A1569T |
probably damaging |
Het |
Grik5 |
C |
G |
7: 24,767,489 (GRCm39) |
E64Q |
probably damaging |
Het |
Gstm5 |
A |
G |
3: 107,805,302 (GRCm39) |
Y130C |
probably damaging |
Het |
Gucy2e |
C |
G |
11: 69,126,994 (GRCm39) |
A160P |
possibly damaging |
Het |
Hydin |
A |
T |
8: 111,293,582 (GRCm39) |
T3510S |
probably benign |
Het |
Ift70a1 |
T |
C |
2: 75,810,977 (GRCm39) |
T369A |
probably benign |
Het |
Itgb2 |
A |
G |
10: 77,381,949 (GRCm39) |
I84V |
probably benign |
Het |
Itsn1 |
A |
G |
16: 91,696,475 (GRCm39) |
Q26R |
probably damaging |
Het |
Kat6a |
A |
G |
8: 23,429,327 (GRCm39) |
S1561G |
probably benign |
Het |
Khnyn |
G |
A |
14: 56,124,438 (GRCm39) |
V231I |
probably benign |
Het |
Kif21b |
A |
G |
1: 136,075,602 (GRCm39) |
D243G |
probably benign |
Het |
Klk4 |
T |
A |
7: 43,534,762 (GRCm39) |
N240K |
probably damaging |
Het |
Knl1 |
T |
C |
2: 118,901,025 (GRCm39) |
S909P |
possibly damaging |
Het |
Lamb1 |
A |
C |
12: 31,373,528 (GRCm39) |
D1419A |
probably benign |
Het |
Lin9 |
T |
A |
1: 180,508,759 (GRCm39) |
V421D |
probably damaging |
Het |
Lipt2 |
T |
C |
7: 99,809,519 (GRCm39) |
L202P |
probably benign |
Het |
Mbd5 |
T |
G |
2: 49,147,209 (GRCm39) |
M473R |
probably benign |
Het |
Mcc |
A |
T |
18: 44,652,587 (GRCm39) |
I279N |
probably damaging |
Het |
Mcpt9 |
C |
T |
14: 56,266,049 (GRCm39) |
V60M |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Mylk2 |
G |
A |
2: 152,759,476 (GRCm39) |
V389M |
probably damaging |
Het |
Ndufs7 |
T |
A |
10: 80,092,501 (GRCm39) |
Y203* |
probably null |
Het |
Nup160 |
T |
A |
2: 90,515,541 (GRCm39) |
|
probably null |
Het |
Nup88 |
G |
A |
11: 70,860,522 (GRCm39) |
R62* |
probably null |
Het |
Or2g7 |
T |
C |
17: 38,378,853 (GRCm39) |
S264P |
probably damaging |
Het |
Or51af1 |
T |
A |
7: 103,141,788 (GRCm39) |
Q99L |
probably damaging |
Het |
Or6c207 |
G |
A |
10: 129,104,274 (GRCm39) |
A306V |
probably benign |
Het |
Or8b8 |
T |
A |
9: 37,809,622 (GRCm39) |
S307R |
probably benign |
Het |
Or8g33 |
A |
G |
9: 39,337,731 (GRCm39) |
M212T |
probably benign |
Het |
Os9 |
T |
C |
10: 126,934,223 (GRCm39) |
N471S |
probably benign |
Het |
Otof |
C |
T |
5: 30,529,244 (GRCm39) |
V1757M |
probably damaging |
Het |
Pakap |
A |
T |
4: 57,709,954 (GRCm39) |
T300S |
probably benign |
Het |
Pald1 |
T |
C |
10: 61,184,395 (GRCm39) |
T241A |
probably benign |
Het |
Pappa2 |
G |
A |
1: 158,642,015 (GRCm39) |
S1347L |
probably damaging |
Het |
Pccb |
T |
C |
9: 100,916,832 (GRCm39) |
T27A |
probably benign |
Het |
Pde4dip |
A |
T |
3: 97,603,260 (GRCm39) |
V2243D |
probably damaging |
Het |
Pkd2l2 |
C |
A |
18: 34,571,254 (GRCm39) |
Q590K |
probably benign |
Het |
Pmepa1 |
G |
A |
2: 173,070,120 (GRCm39) |
P145L |
possibly damaging |
Het |
Ppp3cb |
T |
C |
14: 20,570,714 (GRCm39) |
N339S |
possibly damaging |
Het |
Rnf133 |
T |
C |
6: 23,649,041 (GRCm39) |
E296G |
possibly damaging |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Serpinb12 |
T |
A |
1: 106,876,883 (GRCm39) |
D66E |
probably benign |
Het |
Slc46a2 |
C |
T |
4: 59,911,886 (GRCm39) |
C442Y |
probably damaging |
Het |
Slc7a1 |
A |
G |
5: 148,278,869 (GRCm39) |
L301P |
probably damaging |
Het |
Spg21 |
A |
G |
9: 65,383,257 (GRCm39) |
T148A |
probably benign |
Het |
Stox2 |
A |
G |
8: 47,645,970 (GRCm39) |
S497P |
probably damaging |
Het |
Sult1c2 |
C |
A |
17: 54,280,983 (GRCm39) |
W40L |
probably benign |
Het |
Sytl2 |
T |
C |
7: 90,024,977 (GRCm39) |
S322P |
probably benign |
Het |
Telo2 |
C |
A |
17: 25,324,122 (GRCm39) |
R531L |
possibly damaging |
Het |
Thbs3 |
T |
C |
3: 89,131,897 (GRCm39) |
V719A |
probably damaging |
Het |
Tlr9 |
T |
A |
9: 106,101,732 (GRCm39) |
L341Q |
probably damaging |
Het |
Tmprss5 |
A |
G |
9: 49,024,548 (GRCm39) |
N230D |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tpo |
C |
T |
12: 30,148,228 (GRCm39) |
V558M |
probably benign |
Het |
Trex1 |
T |
G |
9: 108,887,352 (GRCm39) |
Q213P |
possibly damaging |
Het |
Ttc7b |
G |
A |
12: 100,466,376 (GRCm39) |
R79C |
probably damaging |
Het |
Ugt1a6a |
A |
G |
1: 88,066,586 (GRCm39) |
K131E |
probably benign |
Het |
Vipr1 |
T |
A |
9: 121,494,202 (GRCm39) |
|
probably null |
Het |
Vmn1r22 |
T |
C |
6: 57,877,860 (GRCm39) |
D39G |
probably damaging |
Het |
Vmn2r58 |
A |
T |
7: 41,522,046 (GRCm39) |
C17S |
probably benign |
Het |
Vps41 |
T |
C |
13: 18,929,453 (GRCm39) |
Y63H |
probably damaging |
Het |
Xdh |
G |
T |
17: 74,217,195 (GRCm39) |
T691N |
probably benign |
Het |
Zfp518b |
T |
C |
5: 38,830,970 (GRCm39) |
N345S |
probably damaging |
Het |
Zfp536 |
T |
A |
7: 37,267,918 (GRCm39) |
K499N |
probably damaging |
Het |
Zfp963 |
A |
T |
8: 70,195,510 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Slc35e2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01919:Slc35e2
|
APN |
4 |
155,697,187 (GRCm39) |
missense |
probably benign |
|
IGL02244:Slc35e2
|
APN |
4 |
155,703,019 (GRCm39) |
missense |
probably damaging |
0.97 |
R1774:Slc35e2
|
UTSW |
4 |
155,694,621 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1856:Slc35e2
|
UTSW |
4 |
155,696,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Slc35e2
|
UTSW |
4 |
155,702,106 (GRCm39) |
missense |
probably benign |
0.04 |
R4603:Slc35e2
|
UTSW |
4 |
155,702,106 (GRCm39) |
missense |
probably benign |
0.04 |
R4610:Slc35e2
|
UTSW |
4 |
155,702,106 (GRCm39) |
missense |
probably benign |
0.04 |
R4917:Slc35e2
|
UTSW |
4 |
155,700,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Slc35e2
|
UTSW |
4 |
155,700,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5440:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5468:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5469:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5470:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5512:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5513:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5514:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5689:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5692:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5711:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5714:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5799:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R5872:Slc35e2
|
UTSW |
4 |
155,697,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Slc35e2
|
UTSW |
4 |
155,696,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Slc35e2
|
UTSW |
4 |
155,696,171 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6044:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6063:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6065:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6066:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6188:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6243:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6273:Slc35e2
|
UTSW |
4 |
155,694,483 (GRCm39) |
missense |
probably benign |
|
R6484:Slc35e2
|
UTSW |
4 |
155,697,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R6867:Slc35e2
|
UTSW |
4 |
155,703,157 (GRCm39) |
missense |
probably benign |
0.00 |
R7143:Slc35e2
|
UTSW |
4 |
155,703,051 (GRCm39) |
missense |
probably benign |
0.01 |
R7384:Slc35e2
|
UTSW |
4 |
155,695,089 (GRCm39) |
missense |
probably benign |
0.01 |
R8463:Slc35e2
|
UTSW |
4 |
155,694,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R8737:Slc35e2
|
UTSW |
4 |
155,695,042 (GRCm39) |
missense |
probably benign |
0.01 |
R8940:Slc35e2
|
UTSW |
4 |
155,694,542 (GRCm39) |
missense |
probably damaging |
0.99 |
|