Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
4930568D16Rik |
A |
T |
2: 35,244,939 (GRCm39) |
Y138N |
probably benign |
Het |
Abca4 |
T |
C |
3: 121,838,197 (GRCm39) |
M1T |
probably null |
Het |
Acer3 |
A |
G |
7: 97,908,621 (GRCm39) |
V104A |
probably damaging |
Het |
Agpat4 |
A |
G |
17: 12,435,597 (GRCm39) |
E287G |
probably benign |
Het |
Akip1 |
C |
T |
7: 109,308,156 (GRCm39) |
A146V |
unknown |
Het |
Ank2 |
T |
C |
3: 126,738,678 (GRCm39) |
N2402S |
unknown |
Het |
Arhgdig |
A |
T |
17: 26,418,451 (GRCm39) |
Y177* |
probably null |
Het |
Arhgef38 |
T |
A |
3: 132,847,998 (GRCm39) |
T355S |
unknown |
Het |
Atp8a2 |
C |
A |
14: 60,249,827 (GRCm39) |
|
probably null |
Het |
Atp8b4 |
A |
G |
2: 126,216,430 (GRCm39) |
I672T |
probably damaging |
Het |
Baat |
T |
A |
4: 49,503,008 (GRCm39) |
D38V |
probably damaging |
Het |
Bcl9 |
T |
C |
3: 97,117,861 (GRCm39) |
S278G |
probably benign |
Het |
Ccdc150 |
C |
T |
1: 54,324,760 (GRCm39) |
L350F |
probably damaging |
Het |
Ceacam20 |
T |
G |
7: 19,705,533 (GRCm39) |
S175A |
probably damaging |
Het |
Chd6 |
A |
T |
2: 160,871,784 (GRCm39) |
I217K |
possibly damaging |
Het |
Cnppd1 |
T |
C |
1: 75,117,617 (GRCm39) |
I35V |
probably benign |
Het |
Col15a1 |
T |
C |
4: 47,245,603 (GRCm39) |
I118T |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,567,564 (GRCm39) |
Y1289N |
|
Het |
Dio2 |
T |
C |
12: 90,696,587 (GRCm39) |
T134A |
probably benign |
Het |
Dnaaf9 |
A |
T |
2: 130,581,380 (GRCm39) |
N678K |
probably benign |
Het |
Dnah17 |
A |
G |
11: 117,987,464 (GRCm39) |
V1282A |
possibly damaging |
Het |
Dnah17 |
A |
G |
11: 118,012,212 (GRCm39) |
S517P |
possibly damaging |
Het |
Dync2h1 |
C |
T |
9: 7,125,730 (GRCm39) |
|
probably null |
Het |
Echdc2 |
C |
A |
4: 108,036,111 (GRCm39) |
P274Q |
probably damaging |
Het |
Fam117a |
T |
A |
11: 95,271,570 (GRCm39) |
C381S |
probably damaging |
Het |
Fbxl12 |
A |
G |
9: 20,550,130 (GRCm39) |
F122S |
probably damaging |
Het |
Gen1 |
G |
A |
12: 11,291,309 (GRCm39) |
Q892* |
probably null |
Het |
Gimap4 |
A |
G |
6: 48,667,746 (GRCm39) |
Y167C |
probably damaging |
Het |
Gle1 |
T |
A |
2: 29,839,014 (GRCm39) |
F476L |
probably damaging |
Het |
Gpr135 |
A |
T |
12: 72,117,473 (GRCm39) |
V98E |
possibly damaging |
Het |
Greb1l |
A |
T |
18: 10,522,130 (GRCm39) |
H742L |
probably benign |
Het |
Habp2 |
G |
T |
19: 56,304,781 (GRCm39) |
C392F |
probably damaging |
Het |
Hapln3 |
G |
T |
7: 78,771,455 (GRCm39) |
R145S |
probably damaging |
Het |
Ikbkb |
A |
G |
8: 23,171,711 (GRCm39) |
C179R |
probably damaging |
Het |
Kat6a |
A |
T |
8: 23,400,156 (GRCm39) |
I306L |
possibly damaging |
Het |
Lmo3 |
A |
T |
6: 138,342,958 (GRCm39) |
Y140* |
probably null |
Het |
Lrrc32 |
T |
A |
7: 98,148,937 (GRCm39) |
N572K |
probably damaging |
Het |
Lrrn1 |
T |
A |
6: 107,545,093 (GRCm39) |
M297K |
probably damaging |
Het |
Magi2 |
G |
A |
5: 20,766,308 (GRCm39) |
V676I |
probably damaging |
Het |
Mdga1 |
T |
C |
17: 30,051,282 (GRCm39) |
*957W |
probably null |
Het |
Mip |
G |
T |
10: 128,063,029 (GRCm39) |
G158V |
probably damaging |
Het |
Mmp14 |
T |
C |
14: 54,677,960 (GRCm39) |
I527T |
probably benign |
Het |
Mmp27 |
G |
A |
9: 7,573,550 (GRCm39) |
G188D |
probably damaging |
Het |
Mylk4 |
A |
T |
13: 32,960,236 (GRCm39) |
C17S |
possibly damaging |
Het |
Naa50 |
T |
G |
16: 43,977,554 (GRCm39) |
I94R |
probably damaging |
Het |
Nyap1 |
A |
T |
5: 137,734,248 (GRCm39) |
Y262N |
probably damaging |
Het |
Obsl1 |
A |
G |
1: 75,466,177 (GRCm39) |
V1517A |
probably benign |
Het |
P4htm |
T |
A |
9: 108,459,147 (GRCm39) |
M262L |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,784,542 (GRCm39) |
E156G |
probably benign |
Het |
Pcdhb15 |
A |
T |
18: 37,607,971 (GRCm39) |
Y401F |
possibly damaging |
Het |
Pde2a |
G |
A |
7: 101,160,361 (GRCm39) |
R845H |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Penk |
C |
T |
4: 4,134,097 (GRCm39) |
M183I |
probably benign |
Het |
Pole |
T |
C |
5: 110,444,955 (GRCm39) |
V437A |
probably damaging |
Het |
Ppp1r7 |
T |
C |
1: 93,279,262 (GRCm39) |
I114T |
probably damaging |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
Pwp2 |
G |
A |
10: 78,014,827 (GRCm39) |
Q386* |
probably null |
Het |
Rad17 |
A |
T |
13: 100,769,720 (GRCm39) |
S280T |
possibly damaging |
Het |
Rhebl1 |
C |
T |
15: 98,776,414 (GRCm39) |
E128K |
possibly damaging |
Het |
Sema3e |
G |
T |
5: 14,291,084 (GRCm39) |
V615L |
probably benign |
Het |
Ssu2 |
A |
G |
6: 112,357,975 (GRCm39) |
S123P |
probably damaging |
Het |
Stk10 |
A |
G |
11: 32,538,878 (GRCm39) |
E239G |
|
Het |
Surf6 |
G |
T |
2: 26,782,380 (GRCm39) |
Q316K |
probably damaging |
Het |
Tcerg1 |
G |
A |
18: 42,685,573 (GRCm39) |
D637N |
possibly damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tnxb |
C |
A |
17: 34,931,993 (GRCm39) |
F2175L |
probably damaging |
Het |
Trp53i11 |
G |
C |
2: 93,029,273 (GRCm39) |
V91L |
probably benign |
Het |
Tspan9 |
A |
G |
6: 127,944,102 (GRCm39) |
V66A |
probably damaging |
Het |
Usp16 |
C |
T |
16: 87,261,669 (GRCm39) |
T95M |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,324,982 (GRCm39) |
F1691Y |
probably damaging |
Het |
Uty |
A |
T |
Y: 1,099,584 (GRCm39) |
L1204I |
possibly damaging |
Het |
Vmn1r192 |
A |
T |
13: 22,371,800 (GRCm39) |
V140D |
possibly damaging |
Het |
Vps54 |
T |
C |
11: 21,250,234 (GRCm39) |
V552A |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,340,668 (GRCm39) |
V804A |
possibly damaging |
Het |
Zfp869 |
A |
C |
8: 70,161,057 (GRCm39) |
L33R |
probably damaging |
Het |
|
Other mutations in Slc22a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00592:Slc22a2
|
APN |
17 |
12,827,305 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00658:Slc22a2
|
APN |
17 |
12,834,202 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01073:Slc22a2
|
APN |
17 |
12,803,236 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01573:Slc22a2
|
APN |
17 |
12,824,848 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02000:Slc22a2
|
APN |
17 |
12,803,270 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02943:Slc22a2
|
APN |
17 |
12,828,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03301:Slc22a2
|
APN |
17 |
12,824,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Slc22a2
|
UTSW |
17 |
12,834,159 (GRCm39) |
missense |
probably benign |
0.00 |
R0835:Slc22a2
|
UTSW |
17 |
12,831,318 (GRCm39) |
missense |
probably benign |
0.01 |
R1330:Slc22a2
|
UTSW |
17 |
12,805,699 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1432:Slc22a2
|
UTSW |
17 |
12,803,195 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1559:Slc22a2
|
UTSW |
17 |
12,803,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Slc22a2
|
UTSW |
17 |
12,805,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R1884:Slc22a2
|
UTSW |
17 |
12,833,713 (GRCm39) |
splice site |
probably benign |
|
R2042:Slc22a2
|
UTSW |
17 |
12,818,012 (GRCm39) |
missense |
probably benign |
0.01 |
R2197:Slc22a2
|
UTSW |
17 |
12,817,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Slc22a2
|
UTSW |
17 |
12,818,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Slc22a2
|
UTSW |
17 |
12,805,692 (GRCm39) |
missense |
probably benign |
|
R4003:Slc22a2
|
UTSW |
17 |
12,831,337 (GRCm39) |
missense |
probably benign |
0.01 |
R4021:Slc22a2
|
UTSW |
17 |
12,803,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4093:Slc22a2
|
UTSW |
17 |
12,831,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4404:Slc22a2
|
UTSW |
17 |
12,833,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R4419:Slc22a2
|
UTSW |
17 |
12,831,473 (GRCm39) |
nonsense |
probably null |
|
R4564:Slc22a2
|
UTSW |
17 |
12,828,943 (GRCm39) |
missense |
probably benign |
0.08 |
R4866:Slc22a2
|
UTSW |
17 |
12,803,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Slc22a2
|
UTSW |
17 |
12,833,702 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5224:Slc22a2
|
UTSW |
17 |
12,805,719 (GRCm39) |
missense |
probably damaging |
0.97 |
R5668:Slc22a2
|
UTSW |
17 |
12,827,296 (GRCm39) |
missense |
probably benign |
|
R6326:Slc22a2
|
UTSW |
17 |
12,831,297 (GRCm39) |
nonsense |
probably null |
|
R7137:Slc22a2
|
UTSW |
17 |
12,803,228 (GRCm39) |
missense |
probably benign |
|
R7211:Slc22a2
|
UTSW |
17 |
12,805,770 (GRCm39) |
critical splice donor site |
probably null |
|
R7378:Slc22a2
|
UTSW |
17 |
12,831,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7521:Slc22a2
|
UTSW |
17 |
12,805,710 (GRCm39) |
missense |
probably benign |
0.14 |
R7524:Slc22a2
|
UTSW |
17 |
12,824,944 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7735:Slc22a2
|
UTSW |
17 |
12,828,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R8136:Slc22a2
|
UTSW |
17 |
12,824,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R8671:Slc22a2
|
UTSW |
17 |
12,824,863 (GRCm39) |
nonsense |
probably null |
|
R8799:Slc22a2
|
UTSW |
17 |
12,831,425 (GRCm39) |
missense |
probably benign |
0.14 |
R8874:Slc22a2
|
UTSW |
17 |
12,828,866 (GRCm39) |
missense |
probably benign |
0.37 |
R9046:Slc22a2
|
UTSW |
17 |
12,834,234 (GRCm39) |
missense |
probably null |
0.15 |
R9220:Slc22a2
|
UTSW |
17 |
12,838,757 (GRCm39) |
missense |
probably benign |
0.03 |
R9410:Slc22a2
|
UTSW |
17 |
12,805,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R9511:Slc22a2
|
UTSW |
17 |
12,828,916 (GRCm39) |
missense |
probably damaging |
0.98 |
R9580:Slc22a2
|
UTSW |
17 |
12,803,177 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Slc22a2
|
UTSW |
17 |
12,833,663 (GRCm39) |
missense |
probably benign |
0.36 |
Z1176:Slc22a2
|
UTSW |
17 |
12,803,512 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1177:Slc22a2
|
UTSW |
17 |
12,824,897 (GRCm39) |
missense |
probably benign |
0.00 |
|