Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
A |
G |
15: 64,618,744 (GRCm39) |
|
probably null |
Het |
Ap5z1 |
G |
A |
5: 142,462,644 (GRCm39) |
|
probably null |
Het |
Cdhr5 |
T |
G |
7: 140,854,416 (GRCm39) |
I120L |
possibly damaging |
Het |
Chd5 |
C |
T |
4: 152,456,588 (GRCm39) |
S975F |
probably damaging |
Het |
Cts3 |
G |
T |
13: 61,715,871 (GRCm39) |
Q132K |
probably damaging |
Het |
Cylc2 |
T |
A |
4: 51,216,698 (GRCm39) |
|
probably benign |
Het |
Defb39 |
A |
G |
8: 19,102,891 (GRCm39) |
V68A |
probably benign |
Het |
Dgki |
A |
G |
6: 36,839,421 (GRCm39) |
|
probably benign |
Het |
Dhtkd1 |
G |
A |
2: 5,904,783 (GRCm39) |
P867L |
probably damaging |
Het |
Gata5 |
C |
T |
2: 179,969,544 (GRCm39) |
|
probably benign |
Het |
Glt28d2 |
T |
A |
3: 85,779,423 (GRCm39) |
I17F |
probably damaging |
Het |
Gstm2 |
T |
C |
3: 107,892,378 (GRCm39) |
Y82C |
possibly damaging |
Het |
Hs6st1 |
T |
A |
1: 36,142,893 (GRCm39) |
L276* |
probably null |
Het |
Kdm4c |
T |
C |
4: 74,323,058 (GRCm39) |
S997P |
probably damaging |
Het |
Ksr1 |
G |
A |
11: 78,927,551 (GRCm39) |
T289I |
probably damaging |
Het |
Lingo4 |
T |
C |
3: 94,309,124 (GRCm39) |
|
probably benign |
Het |
Ncapd2 |
A |
G |
6: 125,153,694 (GRCm39) |
S674P |
probably damaging |
Het |
Nek1 |
G |
A |
8: 61,557,218 (GRCm39) |
V841I |
probably benign |
Het |
Or10a48 |
T |
C |
7: 108,424,952 (GRCm39) |
T85A |
probably benign |
Het |
Or8i2 |
T |
C |
2: 86,852,346 (GRCm39) |
T181A |
probably benign |
Het |
Pigx |
A |
G |
16: 31,906,201 (GRCm39) |
V40A |
probably damaging |
Het |
Pla2g2d |
T |
G |
4: 138,506,006 (GRCm39) |
M5R |
possibly damaging |
Het |
Ppa2 |
G |
T |
3: 133,073,644 (GRCm39) |
R234I |
probably damaging |
Het |
Rbms1 |
A |
C |
2: 60,592,650 (GRCm39) |
L221R |
probably damaging |
Het |
Rnasel |
C |
A |
1: 153,629,857 (GRCm39) |
N124K |
probably damaging |
Het |
Serpinb9h |
A |
G |
13: 33,588,513 (GRCm39) |
N366S |
possibly damaging |
Het |
Sigirr |
T |
A |
7: 140,674,707 (GRCm39) |
|
probably benign |
Het |
Tas2r136 |
A |
T |
6: 132,754,671 (GRCm39) |
V152E |
probably damaging |
Het |
Tlnrd1 |
C |
T |
7: 83,532,027 (GRCm39) |
V135M |
possibly damaging |
Het |
Tlnrd1 |
A |
G |
7: 83,531,744 (GRCm39) |
L229S |
probably damaging |
Het |
Top1mt |
A |
G |
15: 75,540,554 (GRCm39) |
V239A |
probably damaging |
Het |
Tpd52 |
A |
T |
3: 9,009,775 (GRCm39) |
|
probably null |
Het |
Trim16 |
T |
A |
11: 62,731,383 (GRCm39) |
L331Q |
possibly damaging |
Het |
Ttll4 |
A |
G |
1: 74,726,390 (GRCm39) |
|
probably null |
Het |
Vmn1r27 |
T |
A |
6: 58,192,272 (GRCm39) |
D244V |
probably damaging |
Het |
Vmn2r72 |
A |
C |
7: 85,387,391 (GRCm39) |
D724E |
probably benign |
Het |
Zfp563 |
T |
C |
17: 33,321,253 (GRCm39) |
W18R |
probably damaging |
Het |
Zswim8 |
T |
C |
14: 20,763,142 (GRCm39) |
V347A |
probably benign |
Het |
|
Other mutations in Iqgap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Iqgap1
|
APN |
7 |
80,409,592 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00984:Iqgap1
|
APN |
7 |
80,376,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01570:Iqgap1
|
APN |
7 |
80,372,809 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01738:Iqgap1
|
APN |
7 |
80,373,648 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02141:Iqgap1
|
APN |
7 |
80,387,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Iqgap1
|
APN |
7 |
80,402,041 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02416:Iqgap1
|
APN |
7 |
80,375,786 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Iqgap1
|
APN |
7 |
80,373,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Iqgap1
|
APN |
7 |
80,401,636 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03189:Iqgap1
|
APN |
7 |
80,363,590 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03216:Iqgap1
|
APN |
7 |
80,392,836 (GRCm39) |
missense |
probably benign |
0.33 |
R0024:Iqgap1
|
UTSW |
7 |
80,401,687 (GRCm39) |
missense |
probably benign |
|
R0126:Iqgap1
|
UTSW |
7 |
80,388,070 (GRCm39) |
missense |
probably benign |
0.00 |
R0144:Iqgap1
|
UTSW |
7 |
80,401,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Iqgap1
|
UTSW |
7 |
80,401,678 (GRCm39) |
missense |
probably benign |
0.01 |
R0376:Iqgap1
|
UTSW |
7 |
80,373,627 (GRCm39) |
missense |
probably benign |
0.01 |
R0650:Iqgap1
|
UTSW |
7 |
80,386,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Iqgap1
|
UTSW |
7 |
80,386,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0741:Iqgap1
|
UTSW |
7 |
80,370,735 (GRCm39) |
missense |
probably benign |
0.03 |
R0751:Iqgap1
|
UTSW |
7 |
80,375,321 (GRCm39) |
unclassified |
probably benign |
|
R1067:Iqgap1
|
UTSW |
7 |
80,373,576 (GRCm39) |
missense |
probably benign |
0.01 |
R1389:Iqgap1
|
UTSW |
7 |
80,409,504 (GRCm39) |
critical splice donor site |
probably null |
|
R1473:Iqgap1
|
UTSW |
7 |
80,383,759 (GRCm39) |
missense |
probably benign |
0.00 |
R1613:Iqgap1
|
UTSW |
7 |
80,418,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:Iqgap1
|
UTSW |
7 |
80,410,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Iqgap1
|
UTSW |
7 |
80,393,576 (GRCm39) |
missense |
probably benign |
|
R2062:Iqgap1
|
UTSW |
7 |
80,373,727 (GRCm39) |
nonsense |
probably null |
|
R2149:Iqgap1
|
UTSW |
7 |
80,412,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Iqgap1
|
UTSW |
7 |
80,409,651 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2153:Iqgap1
|
UTSW |
7 |
80,401,701 (GRCm39) |
missense |
probably benign |
0.00 |
R3160:Iqgap1
|
UTSW |
7 |
80,402,086 (GRCm39) |
missense |
probably benign |
|
R3162:Iqgap1
|
UTSW |
7 |
80,402,086 (GRCm39) |
missense |
probably benign |
|
R3605:Iqgap1
|
UTSW |
7 |
80,373,537 (GRCm39) |
missense |
probably benign |
0.02 |
R3709:Iqgap1
|
UTSW |
7 |
80,366,835 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3935:Iqgap1
|
UTSW |
7 |
80,393,585 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3979:Iqgap1
|
UTSW |
7 |
80,409,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R4545:Iqgap1
|
UTSW |
7 |
80,412,315 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4787:Iqgap1
|
UTSW |
7 |
80,385,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Iqgap1
|
UTSW |
7 |
80,415,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Iqgap1
|
UTSW |
7 |
80,373,524 (GRCm39) |
splice site |
probably null |
|
R5037:Iqgap1
|
UTSW |
7 |
80,383,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Iqgap1
|
UTSW |
7 |
80,392,816 (GRCm39) |
missense |
probably benign |
0.02 |
R5183:Iqgap1
|
UTSW |
7 |
80,372,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5262:Iqgap1
|
UTSW |
7 |
80,376,490 (GRCm39) |
missense |
probably benign |
0.00 |
R5271:Iqgap1
|
UTSW |
7 |
80,383,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5289:Iqgap1
|
UTSW |
7 |
80,388,472 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5359:Iqgap1
|
UTSW |
7 |
80,416,707 (GRCm39) |
missense |
probably benign |
0.00 |
R5423:Iqgap1
|
UTSW |
7 |
80,449,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Iqgap1
|
UTSW |
7 |
80,375,828 (GRCm39) |
missense |
probably benign |
0.03 |
R5849:Iqgap1
|
UTSW |
7 |
80,452,906 (GRCm39) |
missense |
probably benign |
|
R6164:Iqgap1
|
UTSW |
7 |
80,458,854 (GRCm39) |
missense |
unknown |
|
R6315:Iqgap1
|
UTSW |
7 |
80,449,638 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6335:Iqgap1
|
UTSW |
7 |
80,377,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Iqgap1
|
UTSW |
7 |
80,380,074 (GRCm39) |
missense |
probably benign |
0.00 |
R6723:Iqgap1
|
UTSW |
7 |
80,373,570 (GRCm39) |
missense |
probably benign |
0.01 |
R6800:Iqgap1
|
UTSW |
7 |
80,378,729 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6815:Iqgap1
|
UTSW |
7 |
80,416,632 (GRCm39) |
critical splice donor site |
probably null |
|
R7240:Iqgap1
|
UTSW |
7 |
80,409,587 (GRCm39) |
missense |
probably benign |
0.22 |
R7386:Iqgap1
|
UTSW |
7 |
80,375,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R7387:Iqgap1
|
UTSW |
7 |
80,370,738 (GRCm39) |
missense |
probably benign |
0.03 |
R7410:Iqgap1
|
UTSW |
7 |
80,372,778 (GRCm39) |
nonsense |
probably null |
|
R7429:Iqgap1
|
UTSW |
7 |
80,401,188 (GRCm39) |
missense |
probably benign |
0.00 |
R7452:Iqgap1
|
UTSW |
7 |
80,410,577 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7615:Iqgap1
|
UTSW |
7 |
80,401,094 (GRCm39) |
missense |
probably benign |
|
R7615:Iqgap1
|
UTSW |
7 |
80,379,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7726:Iqgap1
|
UTSW |
7 |
80,407,204 (GRCm39) |
missense |
probably benign |
0.37 |
R7783:Iqgap1
|
UTSW |
7 |
80,458,807 (GRCm39) |
missense |
probably benign |
0.01 |
R7785:Iqgap1
|
UTSW |
7 |
80,387,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Iqgap1
|
UTSW |
7 |
80,393,636 (GRCm39) |
missense |
probably benign |
0.04 |
R8270:Iqgap1
|
UTSW |
7 |
80,379,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Iqgap1
|
UTSW |
7 |
80,375,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Iqgap1
|
UTSW |
7 |
80,401,141 (GRCm39) |
missense |
probably benign |
|
R9520:Iqgap1
|
UTSW |
7 |
80,393,869 (GRCm39) |
missense |
probably benign |
|
R9533:Iqgap1
|
UTSW |
7 |
80,383,929 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9536:Iqgap1
|
UTSW |
7 |
80,458,840 (GRCm39) |
missense |
|
|
R9730:Iqgap1
|
UTSW |
7 |
80,401,124 (GRCm39) |
missense |
possibly damaging |
0.63 |
RF004:Iqgap1
|
UTSW |
7 |
80,370,623 (GRCm39) |
missense |
probably benign |
|
RF063:Iqgap1
|
UTSW |
7 |
80,373,499 (GRCm39) |
frame shift |
probably null |
|
X0064:Iqgap1
|
UTSW |
7 |
80,370,679 (GRCm39) |
nonsense |
probably null |
|
X0067:Iqgap1
|
UTSW |
7 |
80,416,651 (GRCm39) |
missense |
probably benign |
|
Z1176:Iqgap1
|
UTSW |
7 |
80,418,057 (GRCm39) |
missense |
probably benign |
0.00 |
|