Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acod1 |
T |
A |
14: 103,287,075 (GRCm39) |
W69R |
probably damaging |
Het |
Adamtsl4 |
C |
T |
3: 95,584,426 (GRCm39) |
R990Q |
possibly damaging |
Het |
Ahdc1 |
T |
A |
4: 132,792,743 (GRCm39) |
V1328E |
possibly damaging |
Het |
Bpifb2 |
A |
G |
2: 153,731,356 (GRCm39) |
H244R |
possibly damaging |
Het |
Camk1 |
C |
A |
6: 113,315,109 (GRCm39) |
V199L |
probably damaging |
Het |
Ccdc18 |
A |
T |
5: 108,328,283 (GRCm39) |
K661I |
possibly damaging |
Het |
Cdh16 |
C |
T |
8: 105,344,874 (GRCm39) |
V444I |
probably benign |
Het |
Cep295 |
A |
T |
9: 15,243,715 (GRCm39) |
Y1580* |
probably null |
Het |
Cntnap5c |
A |
T |
17: 58,362,663 (GRCm39) |
N339Y |
probably damaging |
Het |
Col6a3 |
C |
G |
1: 90,695,328 (GRCm39) |
|
probably benign |
Het |
Deup1 |
T |
A |
9: 15,503,721 (GRCm39) |
D280V |
probably damaging |
Het |
Dlat |
G |
T |
9: 50,560,967 (GRCm39) |
A360E |
probably damaging |
Het |
Evpl |
T |
A |
11: 116,113,019 (GRCm39) |
D1557V |
probably benign |
Het |
Ext1 |
A |
G |
15: 53,208,065 (GRCm39) |
V232A |
possibly damaging |
Het |
Gdpd5 |
T |
C |
7: 99,105,726 (GRCm39) |
I514T |
possibly damaging |
Het |
Gm14443 |
A |
T |
2: 175,010,693 (GRCm39) |
C584* |
probably null |
Het |
Gm2696 |
T |
A |
10: 77,672,034 (GRCm39) |
C78S |
unknown |
Het |
Gm4131 |
T |
C |
14: 62,701,300 (GRCm39) |
D276G |
possibly damaging |
Het |
Gm5114 |
C |
T |
7: 39,060,657 (GRCm39) |
G64D |
probably benign |
Het |
Gsx2 |
G |
T |
5: 75,236,755 (GRCm39) |
A112S |
probably benign |
Het |
Hebp1 |
G |
T |
6: 135,114,919 (GRCm39) |
R181S |
probably damaging |
Het |
Hectd4 |
G |
A |
5: 121,488,557 (GRCm39) |
G3616D |
probably damaging |
Het |
Hemgn |
T |
G |
4: 46,394,638 (GRCm39) |
T491P |
probably benign |
Het |
Idh2 |
TCCCAGGGCC |
TCC |
7: 79,748,079 (GRCm39) |
|
probably null |
Het |
Itsn1 |
T |
C |
16: 91,636,721 (GRCm39) |
S723P |
unknown |
Het |
Kat6a |
G |
A |
8: 23,398,293 (GRCm39) |
G287D |
probably damaging |
Het |
Ktn1 |
T |
G |
14: 47,907,757 (GRCm39) |
|
probably benign |
Het |
Lrrc56 |
C |
A |
7: 140,778,246 (GRCm39) |
D79E |
possibly damaging |
Het |
Lrrn1 |
C |
T |
6: 107,544,303 (GRCm39) |
Q34* |
probably null |
Het |
Mlxipl |
A |
G |
5: 135,157,483 (GRCm39) |
M340V |
probably benign |
Het |
Mroh6 |
T |
C |
15: 75,756,563 (GRCm39) |
T604A |
possibly damaging |
Het |
Or13a26 |
G |
T |
7: 140,284,607 (GRCm39) |
V148L |
probably benign |
Het |
Or1n1 |
T |
A |
2: 36,749,610 (GRCm39) |
Y250F |
probably damaging |
Het |
Or4c122 |
A |
T |
2: 89,079,658 (GRCm39) |
S115T |
probably benign |
Het |
Palb2 |
A |
C |
7: 121,710,884 (GRCm39) |
V1022G |
unknown |
Het |
Pank1 |
T |
G |
19: 34,855,989 (GRCm39) |
H163P |
possibly damaging |
Het |
Pcdha12 |
A |
G |
18: 37,154,736 (GRCm39) |
Q485R |
probably benign |
Het |
Pcdhb15 |
T |
A |
18: 37,608,734 (GRCm39) |
S655R |
probably damaging |
Het |
Pcdhgb1 |
T |
A |
18: 37,814,467 (GRCm39) |
C319* |
probably null |
Het |
Pipox |
A |
T |
11: 77,774,804 (GRCm39) |
L93* |
probably null |
Het |
Pkd1l1 |
A |
C |
11: 8,911,482 (GRCm39) |
V265G |
|
Het |
Pld3 |
G |
A |
7: 27,239,079 (GRCm39) |
Q149* |
probably null |
Het |
Pramel34 |
A |
T |
5: 93,784,316 (GRCm39) |
Y383N |
probably damaging |
Het |
Prpf3 |
T |
A |
3: 95,748,021 (GRCm39) |
T415S |
possibly damaging |
Het |
Rasgef1b |
G |
A |
5: 99,447,895 (GRCm39) |
T105I |
unknown |
Het |
Rere |
G |
T |
4: 150,701,792 (GRCm39) |
E24* |
probably null |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Ric3 |
A |
T |
7: 108,637,924 (GRCm39) |
D277E |
probably benign |
Het |
Rnf44 |
A |
T |
13: 54,831,826 (GRCm39) |
M82K |
probably damaging |
Het |
Rsph14 |
T |
C |
10: 74,795,516 (GRCm39) |
N223S |
probably benign |
Het |
Rusc2 |
A |
G |
4: 43,415,396 (GRCm39) |
E234G |
probably damaging |
Het |
Scfd2 |
T |
C |
5: 74,642,900 (GRCm39) |
N349S |
probably benign |
Het |
Sema3d |
G |
A |
5: 12,555,822 (GRCm39) |
C183Y |
probably damaging |
Het |
Slc39a12 |
T |
C |
2: 14,454,670 (GRCm39) |
S563P |
probably damaging |
Het |
Slc9a8 |
A |
T |
2: 167,315,454 (GRCm39) |
D526V |
probably damaging |
Het |
Smpdl3b |
G |
T |
4: 132,461,060 (GRCm39) |
T339N |
probably damaging |
Het |
Speer1e |
A |
T |
5: 11,236,408 (GRCm39) |
Q147L |
probably benign |
Het |
Spi1 |
G |
A |
2: 90,945,516 (GRCm39) |
G199D |
probably damaging |
Het |
Stx2 |
T |
C |
5: 129,070,564 (GRCm39) |
T118A |
probably damaging |
Het |
Synj2 |
C |
A |
17: 6,088,015 (GRCm39) |
S1355R |
possibly damaging |
Het |
Taf15 |
A |
G |
11: 83,389,964 (GRCm39) |
T245A |
probably benign |
Het |
Tnrc6b |
C |
T |
15: 80,760,653 (GRCm39) |
A120V |
probably damaging |
Het |
Usp19 |
G |
T |
9: 108,370,934 (GRCm39) |
G198W |
probably damaging |
Het |
Wdtc1 |
G |
T |
4: 133,041,114 (GRCm39) |
H46N |
probably damaging |
Het |
Zbtb1 |
C |
A |
12: 76,432,646 (GRCm39) |
R211S |
probably damaging |
Het |
Zc3h8 |
A |
G |
2: 128,775,207 (GRCm39) |
V151A |
probably benign |
Het |
Zfp219 |
T |
C |
14: 52,244,899 (GRCm39) |
T499A |
possibly damaging |
Het |
Zfp689 |
A |
G |
7: 127,047,940 (GRCm39) |
F31L |
probably damaging |
Het |
Zfp879 |
C |
T |
11: 50,729,321 (GRCm39) |
D26N |
probably damaging |
Het |
|
Other mutations in Setd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00722:Setd2
|
APN |
9 |
110,380,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01023:Setd2
|
APN |
9 |
110,376,581 (GRCm39) |
nonsense |
probably null |
|
IGL01063:Setd2
|
APN |
9 |
110,402,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01745:Setd2
|
APN |
9 |
110,423,779 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01911:Setd2
|
APN |
9 |
110,446,499 (GRCm39) |
splice site |
probably null |
|
IGL01955:Setd2
|
APN |
9 |
110,378,386 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02023:Setd2
|
APN |
9 |
110,423,704 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02080:Setd2
|
APN |
9 |
110,376,518 (GRCm39) |
splice site |
probably null |
|
IGL02412:Setd2
|
APN |
9 |
110,379,842 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02519:Setd2
|
APN |
9 |
110,382,184 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02631:Setd2
|
APN |
9 |
110,379,644 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02754:Setd2
|
APN |
9 |
110,379,124 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02828:Setd2
|
APN |
9 |
110,390,282 (GRCm39) |
missense |
probably benign |
0.31 |
IGL03033:Setd2
|
APN |
9 |
110,380,343 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03140:Setd2
|
APN |
9 |
110,444,020 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03378:Setd2
|
APN |
9 |
110,382,220 (GRCm39) |
missense |
unknown |
|
American_samoa
|
UTSW |
9 |
110,396,826 (GRCm39) |
nonsense |
probably null |
|
slingshot
|
UTSW |
9 |
110,378,575 (GRCm39) |
missense |
probably benign |
0.00 |
P0028:Setd2
|
UTSW |
9 |
110,403,022 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4544001:Setd2
|
UTSW |
9 |
110,380,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Setd2
|
UTSW |
9 |
110,423,494 (GRCm39) |
missense |
probably damaging |
0.98 |
R0058:Setd2
|
UTSW |
9 |
110,423,494 (GRCm39) |
missense |
probably damaging |
0.98 |
R0167:Setd2
|
UTSW |
9 |
110,402,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R0408:Setd2
|
UTSW |
9 |
110,423,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R0452:Setd2
|
UTSW |
9 |
110,382,168 (GRCm39) |
splice site |
probably null |
|
R0541:Setd2
|
UTSW |
9 |
110,402,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R0947:Setd2
|
UTSW |
9 |
110,377,579 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1249:Setd2
|
UTSW |
9 |
110,402,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R1294:Setd2
|
UTSW |
9 |
110,378,575 (GRCm39) |
missense |
probably benign |
0.00 |
R1518:Setd2
|
UTSW |
9 |
110,431,306 (GRCm39) |
missense |
probably damaging |
0.98 |
R1585:Setd2
|
UTSW |
9 |
110,380,464 (GRCm39) |
missense |
unknown |
|
R1647:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R1649:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R1651:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R1652:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R1673:Setd2
|
UTSW |
9 |
110,433,248 (GRCm39) |
missense |
probably damaging |
0.97 |
R1703:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R1706:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R1709:Setd2
|
UTSW |
9 |
110,378,925 (GRCm39) |
missense |
probably benign |
0.00 |
R1752:Setd2
|
UTSW |
9 |
110,423,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Setd2
|
UTSW |
9 |
110,446,884 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1796:Setd2
|
UTSW |
9 |
110,379,413 (GRCm39) |
missense |
probably benign |
0.01 |
R1812:Setd2
|
UTSW |
9 |
110,379,170 (GRCm39) |
missense |
probably damaging |
0.99 |
R1884:Setd2
|
UTSW |
9 |
110,385,486 (GRCm39) |
critical splice donor site |
probably null |
|
R2024:Setd2
|
UTSW |
9 |
110,378,201 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2051:Setd2
|
UTSW |
9 |
110,379,958 (GRCm39) |
missense |
probably benign |
|
R2117:Setd2
|
UTSW |
9 |
110,433,212 (GRCm39) |
frame shift |
probably null |
|
R2120:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R2124:Setd2
|
UTSW |
9 |
110,378,932 (GRCm39) |
missense |
probably benign |
0.12 |
R2172:Setd2
|
UTSW |
9 |
110,378,912 (GRCm39) |
missense |
probably benign |
0.10 |
R2179:Setd2
|
UTSW |
9 |
110,423,756 (GRCm39) |
nonsense |
probably null |
|
R2262:Setd2
|
UTSW |
9 |
110,390,311 (GRCm39) |
intron |
probably benign |
|
R2411:Setd2
|
UTSW |
9 |
110,379,497 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2413:Setd2
|
UTSW |
9 |
110,376,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R2419:Setd2
|
UTSW |
9 |
110,378,065 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2424:Setd2
|
UTSW |
9 |
110,446,590 (GRCm39) |
missense |
probably benign |
0.37 |
R3757:Setd2
|
UTSW |
9 |
110,402,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R3765:Setd2
|
UTSW |
9 |
110,423,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R3796:Setd2
|
UTSW |
9 |
110,378,639 (GRCm39) |
missense |
probably benign |
0.00 |
R3797:Setd2
|
UTSW |
9 |
110,378,639 (GRCm39) |
missense |
probably benign |
0.00 |
R3799:Setd2
|
UTSW |
9 |
110,378,639 (GRCm39) |
missense |
probably benign |
0.00 |
R3899:Setd2
|
UTSW |
9 |
110,421,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R3900:Setd2
|
UTSW |
9 |
110,421,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Setd2
|
UTSW |
9 |
110,380,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R4010:Setd2
|
UTSW |
9 |
110,428,263 (GRCm39) |
missense |
probably null |
1.00 |
R4580:Setd2
|
UTSW |
9 |
110,403,311 (GRCm39) |
missense |
probably benign |
0.06 |
R4614:Setd2
|
UTSW |
9 |
110,398,881 (GRCm39) |
critical splice donor site |
probably null |
|
R4651:Setd2
|
UTSW |
9 |
110,423,200 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4652:Setd2
|
UTSW |
9 |
110,423,200 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4855:Setd2
|
UTSW |
9 |
110,401,022 (GRCm39) |
missense |
probably benign |
0.02 |
R4970:Setd2
|
UTSW |
9 |
110,377,226 (GRCm39) |
missense |
probably benign |
0.28 |
R5112:Setd2
|
UTSW |
9 |
110,377,226 (GRCm39) |
missense |
probably benign |
0.28 |
R5123:Setd2
|
UTSW |
9 |
110,446,595 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5140:Setd2
|
UTSW |
9 |
110,380,197 (GRCm39) |
missense |
probably benign |
0.00 |
R5202:Setd2
|
UTSW |
9 |
110,380,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Setd2
|
UTSW |
9 |
110,446,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Setd2
|
UTSW |
9 |
110,378,907 (GRCm39) |
nonsense |
probably null |
|
R5604:Setd2
|
UTSW |
9 |
110,433,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R5678:Setd2
|
UTSW |
9 |
110,431,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R5708:Setd2
|
UTSW |
9 |
110,377,891 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5763:Setd2
|
UTSW |
9 |
110,385,343 (GRCm39) |
splice site |
probably null |
|
R5814:Setd2
|
UTSW |
9 |
110,396,826 (GRCm39) |
nonsense |
probably null |
|
R5924:Setd2
|
UTSW |
9 |
110,403,112 (GRCm39) |
missense |
probably benign |
0.23 |
R6244:Setd2
|
UTSW |
9 |
110,377,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6313:Setd2
|
UTSW |
9 |
110,385,434 (GRCm39) |
missense |
unknown |
|
R6431:Setd2
|
UTSW |
9 |
110,379,453 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6526:Setd2
|
UTSW |
9 |
110,361,785 (GRCm39) |
missense |
probably benign |
0.33 |
R6579:Setd2
|
UTSW |
9 |
110,378,846 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6996:Setd2
|
UTSW |
9 |
110,379,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R7012:Setd2
|
UTSW |
9 |
110,376,751 (GRCm39) |
missense |
probably damaging |
0.97 |
R7105:Setd2
|
UTSW |
9 |
110,377,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R7134:Setd2
|
UTSW |
9 |
110,377,865 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7222:Setd2
|
UTSW |
9 |
110,380,530 (GRCm39) |
missense |
|
|
R7359:Setd2
|
UTSW |
9 |
110,392,012 (GRCm39) |
missense |
|
|
R7492:Setd2
|
UTSW |
9 |
110,423,700 (GRCm39) |
missense |
|
|
R7643:Setd2
|
UTSW |
9 |
110,396,908 (GRCm39) |
splice site |
probably null |
|
R7869:Setd2
|
UTSW |
9 |
110,379,082 (GRCm39) |
nonsense |
probably null |
|
R7903:Setd2
|
UTSW |
9 |
110,446,905 (GRCm39) |
missense |
|
|
R8004:Setd2
|
UTSW |
9 |
110,421,613 (GRCm39) |
missense |
|
|
R8017:Setd2
|
UTSW |
9 |
110,431,255 (GRCm39) |
missense |
|
|
R8019:Setd2
|
UTSW |
9 |
110,431,255 (GRCm39) |
missense |
|
|
R8366:Setd2
|
UTSW |
9 |
110,377,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R8460:Setd2
|
UTSW |
9 |
110,423,338 (GRCm39) |
missense |
|
|
R8498:Setd2
|
UTSW |
9 |
110,378,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R8870:Setd2
|
UTSW |
9 |
110,423,321 (GRCm39) |
missense |
|
|
R8878:Setd2
|
UTSW |
9 |
110,421,467 (GRCm39) |
missense |
probably benign |
|
R9132:Setd2
|
UTSW |
9 |
110,374,385 (GRCm39) |
critical splice donor site |
probably null |
|
R9159:Setd2
|
UTSW |
9 |
110,374,385 (GRCm39) |
critical splice donor site |
probably null |
|
R9198:Setd2
|
UTSW |
9 |
110,378,168 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9277:Setd2
|
UTSW |
9 |
110,379,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R9326:Setd2
|
UTSW |
9 |
110,378,671 (GRCm39) |
missense |
probably benign |
0.00 |
R9558:Setd2
|
UTSW |
9 |
110,376,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R9664:Setd2
|
UTSW |
9 |
110,377,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R9673:Setd2
|
UTSW |
9 |
110,378,138 (GRCm39) |
missense |
probably damaging |
1.00 |
RF009:Setd2
|
UTSW |
9 |
110,379,779 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Setd2
|
UTSW |
9 |
110,376,343 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Setd2
|
UTSW |
9 |
110,361,794 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Setd2
|
UTSW |
9 |
110,376,647 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Setd2
|
UTSW |
9 |
110,376,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|