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 |
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 |
Slc22a2 |
A |
T |
17: 12,824,837 (GRCm39) |
Y233F |
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 Arhgef38 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Arhgef38
|
APN |
3 |
132,837,812 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00533:Arhgef38
|
APN |
3 |
132,822,220 (GRCm39) |
nonsense |
probably null |
|
IGL03031:Arhgef38
|
APN |
3 |
132,837,828 (GRCm39) |
missense |
possibly damaging |
0.90 |
F5770:Arhgef38
|
UTSW |
3 |
132,855,301 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4362001:Arhgef38
|
UTSW |
3 |
132,866,591 (GRCm39) |
missense |
|
|
R0050:Arhgef38
|
UTSW |
3 |
132,837,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R0050:Arhgef38
|
UTSW |
3 |
132,837,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R0076:Arhgef38
|
UTSW |
3 |
132,866,507 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0515:Arhgef38
|
UTSW |
3 |
132,855,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Arhgef38
|
UTSW |
3 |
132,843,232 (GRCm39) |
missense |
probably benign |
0.25 |
R0765:Arhgef38
|
UTSW |
3 |
132,822,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Arhgef38
|
UTSW |
3 |
132,822,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R1261:Arhgef38
|
UTSW |
3 |
132,866,624 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1568:Arhgef38
|
UTSW |
3 |
132,838,225 (GRCm39) |
missense |
probably damaging |
0.98 |
R1580:Arhgef38
|
UTSW |
3 |
132,839,465 (GRCm39) |
missense |
probably benign |
0.24 |
R1716:Arhgef38
|
UTSW |
3 |
132,846,598 (GRCm39) |
missense |
probably benign |
0.35 |
R1875:Arhgef38
|
UTSW |
3 |
132,839,501 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2118:Arhgef38
|
UTSW |
3 |
132,866,514 (GRCm39) |
missense |
probably benign |
0.31 |
R2119:Arhgef38
|
UTSW |
3 |
132,866,514 (GRCm39) |
missense |
probably benign |
0.31 |
R2122:Arhgef38
|
UTSW |
3 |
132,866,514 (GRCm39) |
missense |
probably benign |
0.31 |
R2417:Arhgef38
|
UTSW |
3 |
132,852,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R3832:Arhgef38
|
UTSW |
3 |
132,912,686 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4657:Arhgef38
|
UTSW |
3 |
132,940,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Arhgef38
|
UTSW |
3 |
132,846,533 (GRCm39) |
critical splice donor site |
probably null |
|
R4732:Arhgef38
|
UTSW |
3 |
132,838,030 (GRCm39) |
nonsense |
probably null |
|
R4733:Arhgef38
|
UTSW |
3 |
132,838,030 (GRCm39) |
nonsense |
probably null |
|
R5059:Arhgef38
|
UTSW |
3 |
132,843,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5108:Arhgef38
|
UTSW |
3 |
132,843,029 (GRCm39) |
missense |
probably benign |
0.14 |
R5310:Arhgef38
|
UTSW |
3 |
132,822,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R5820:Arhgef38
|
UTSW |
3 |
132,866,560 (GRCm39) |
missense |
probably benign |
0.44 |
R5987:Arhgef38
|
UTSW |
3 |
132,912,719 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6115:Arhgef38
|
UTSW |
3 |
132,838,374 (GRCm39) |
splice site |
probably null |
|
R6313:Arhgef38
|
UTSW |
3 |
132,940,469 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6339:Arhgef38
|
UTSW |
3 |
132,839,423 (GRCm39) |
missense |
probably benign |
0.35 |
R6356:Arhgef38
|
UTSW |
3 |
132,846,638 (GRCm39) |
missense |
probably benign |
0.01 |
R6648:Arhgef38
|
UTSW |
3 |
132,838,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Arhgef38
|
UTSW |
3 |
132,839,388 (GRCm39) |
start gained |
probably benign |
|
R7083:Arhgef38
|
UTSW |
3 |
132,838,197 (GRCm39) |
missense |
unknown |
|
R7561:Arhgef38
|
UTSW |
3 |
132,866,489 (GRCm39) |
missense |
|
|
R7769:Arhgef38
|
UTSW |
3 |
132,855,383 (GRCm39) |
missense |
unknown |
|
R8050:Arhgef38
|
UTSW |
3 |
132,843,323 (GRCm39) |
nonsense |
probably null |
|
R8471:Arhgef38
|
UTSW |
3 |
132,940,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R8835:Arhgef38
|
UTSW |
3 |
132,837,832 (GRCm39) |
missense |
unknown |
|
R9151:Arhgef38
|
UTSW |
3 |
132,912,706 (GRCm39) |
missense |
|
|
R9154:Arhgef38
|
UTSW |
3 |
132,837,924 (GRCm39) |
missense |
unknown |
|
R9263:Arhgef38
|
UTSW |
3 |
132,866,529 (GRCm39) |
missense |
|
|
R9628:Arhgef38
|
UTSW |
3 |
132,838,025 (GRCm39) |
missense |
unknown |
|
R9799:Arhgef38
|
UTSW |
3 |
132,855,391 (GRCm39) |
missense |
unknown |
|
Z1177:Arhgef38
|
UTSW |
3 |
132,912,722 (GRCm39) |
nonsense |
probably null |
|
|