Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add2 |
A |
T |
6: 86,063,899 (GRCm39) |
E66V |
probably damaging |
Het |
Aldh1a3 |
T |
C |
7: 66,062,658 (GRCm39) |
I156V |
probably benign |
Het |
Ang4 |
T |
A |
14: 52,001,725 (GRCm39) |
K74N |
probably benign |
Het |
Arcn1 |
A |
T |
9: 44,670,172 (GRCm39) |
|
probably benign |
Het |
Atn1 |
A |
G |
6: 124,720,188 (GRCm39) |
|
probably benign |
Het |
Bmal2 |
A |
G |
6: 146,724,185 (GRCm39) |
H359R |
probably damaging |
Het |
Bmerb1 |
T |
C |
16: 13,911,795 (GRCm39) |
L47P |
probably damaging |
Het |
Brip1 |
T |
C |
11: 86,083,653 (GRCm39) |
T123A |
probably benign |
Het |
Camkv |
A |
G |
9: 107,823,045 (GRCm39) |
Y95C |
probably damaging |
Het |
Cdk12 |
T |
A |
11: 98,095,211 (GRCm39) |
S340T |
probably benign |
Het |
Ckap2l |
G |
A |
2: 129,138,224 (GRCm39) |
|
probably benign |
Het |
Clmn |
A |
T |
12: 104,738,085 (GRCm39) |
L1042Q |
probably damaging |
Het |
Clmn |
G |
T |
12: 104,738,086 (GRCm39) |
L1042M |
probably damaging |
Het |
Cluh |
T |
C |
11: 74,554,631 (GRCm39) |
V737A |
probably benign |
Het |
Cpne8 |
A |
G |
15: 90,424,462 (GRCm39) |
V309A |
probably benign |
Het |
Cpxm2 |
T |
A |
7: 131,756,342 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,747,073 (GRCm39) |
|
probably benign |
Het |
Ctr9 |
T |
A |
7: 110,650,159 (GRCm39) |
S818T |
probably benign |
Het |
Cyp26a1 |
C |
T |
19: 37,688,405 (GRCm39) |
A309V |
probably damaging |
Het |
Dbndd2 |
C |
T |
2: 164,332,122 (GRCm39) |
T115I |
possibly damaging |
Het |
Dhcr7 |
A |
G |
7: 143,394,964 (GRCm39) |
N157S |
probably benign |
Het |
Dlx2 |
C |
A |
2: 71,375,859 (GRCm39) |
V155F |
probably damaging |
Het |
Duox1 |
A |
T |
2: 122,176,982 (GRCm39) |
I1470F |
probably damaging |
Het |
Esrrb |
A |
T |
12: 86,517,071 (GRCm39) |
I68F |
probably benign |
Het |
Fhod3 |
T |
A |
18: 25,248,862 (GRCm39) |
L1347* |
probably null |
Het |
Fip1l1 |
T |
C |
5: 74,755,721 (GRCm39) |
|
probably benign |
Het |
Frem3 |
A |
G |
8: 81,413,637 (GRCm39) |
Y1966C |
probably damaging |
Het |
Gatd3a |
T |
C |
10: 77,998,539 (GRCm39) |
D229G |
probably damaging |
Het |
Ggt5 |
C |
T |
10: 75,440,604 (GRCm39) |
R242C |
possibly damaging |
Het |
Gm14496 |
G |
A |
2: 181,637,480 (GRCm39) |
V185I |
probably benign |
Het |
Gnptab |
T |
C |
10: 88,265,814 (GRCm39) |
V409A |
probably damaging |
Het |
Gramd1a |
A |
G |
7: 30,837,589 (GRCm39) |
F390S |
possibly damaging |
Het |
Helz2 |
A |
G |
2: 180,872,570 (GRCm39) |
S2477P |
probably damaging |
Het |
Hsd17b3 |
T |
C |
13: 64,236,936 (GRCm39) |
K3E |
probably benign |
Het |
Ift172 |
T |
C |
5: 31,414,715 (GRCm39) |
H1395R |
probably benign |
Het |
Jam2 |
T |
A |
16: 84,609,855 (GRCm39) |
C180S |
probably damaging |
Het |
Kalrn |
A |
C |
16: 33,870,289 (GRCm39) |
S160A |
possibly damaging |
Het |
Kcnk3 |
T |
C |
5: 30,779,979 (GRCm39) |
I343T |
probably damaging |
Het |
Kif13a |
T |
C |
13: 46,967,712 (GRCm39) |
E334G |
probably damaging |
Het |
Klhl41 |
A |
G |
2: 69,508,491 (GRCm39) |
K482E |
possibly damaging |
Het |
Lig3 |
A |
G |
11: 82,689,113 (GRCm39) |
E794G |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,240,436 (GRCm39) |
M780T |
possibly damaging |
Het |
Ndst2 |
A |
G |
14: 20,779,761 (GRCm39) |
Y160H |
probably damaging |
Het |
Ndufb10 |
T |
C |
17: 24,941,648 (GRCm39) |
M90V |
probably damaging |
Het |
Obscn |
T |
C |
11: 59,024,104 (GRCm39) |
K522R |
probably benign |
Het |
Olfml2b |
T |
C |
1: 170,475,413 (GRCm39) |
S113P |
probably benign |
Het |
Or14a257 |
T |
A |
7: 86,138,698 (GRCm39) |
E20D |
probably benign |
Het |
Or4a78 |
A |
G |
2: 89,497,423 (GRCm39) |
I269T |
probably benign |
Het |
Or4d10b |
T |
A |
19: 12,036,979 (GRCm39) |
M46L |
probably benign |
Het |
Or51v14 |
T |
C |
7: 103,261,444 (GRCm39) |
T39A |
probably benign |
Het |
Or6k2 |
T |
A |
1: 173,986,930 (GRCm39) |
M197K |
possibly damaging |
Het |
Parg |
T |
C |
14: 31,936,511 (GRCm39) |
|
probably benign |
Het |
Pde7a |
C |
T |
3: 19,284,482 (GRCm39) |
C367Y |
probably damaging |
Het |
Pigr |
T |
A |
1: 130,772,281 (GRCm39) |
C166* |
probably null |
Het |
Pip4k2c |
A |
T |
10: 127,036,704 (GRCm39) |
|
probably benign |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Prkd2 |
A |
T |
7: 16,599,602 (GRCm39) |
|
probably benign |
Het |
Ptprt |
G |
T |
2: 161,654,059 (GRCm39) |
|
probably null |
Het |
Rapgef5 |
C |
T |
12: 117,610,741 (GRCm39) |
|
probably benign |
Het |
Retreg1 |
T |
C |
15: 25,971,756 (GRCm39) |
L356P |
probably benign |
Het |
Rigi |
T |
A |
4: 40,239,596 (GRCm39) |
E34V |
possibly damaging |
Het |
Rnf43 |
A |
G |
11: 87,622,077 (GRCm39) |
T393A |
probably benign |
Het |
Samd3 |
T |
C |
10: 26,147,725 (GRCm39) |
S467P |
probably benign |
Het |
Scarf1 |
C |
A |
11: 75,405,229 (GRCm39) |
C89* |
probably null |
Het |
Sdk1 |
T |
C |
5: 141,227,779 (GRCm39) |
L59S |
probably benign |
Het |
Sgca |
C |
T |
11: 94,861,512 (GRCm39) |
W244* |
probably null |
Het |
Sh3d21 |
T |
C |
4: 126,045,065 (GRCm39) |
K538R |
probably benign |
Het |
Smyd4 |
T |
A |
11: 75,281,958 (GRCm39) |
L477Q |
possibly damaging |
Het |
Sra1 |
A |
G |
18: 36,801,829 (GRCm39) |
M87T |
probably benign |
Het |
Ssh2 |
T |
C |
11: 77,328,459 (GRCm39) |
Y336H |
possibly damaging |
Het |
Steap1 |
T |
C |
5: 5,790,357 (GRCm39) |
Y197C |
probably damaging |
Het |
Strn3 |
A |
G |
12: 51,673,879 (GRCm39) |
|
probably benign |
Het |
Tgm3 |
A |
G |
2: 129,868,677 (GRCm39) |
T205A |
probably benign |
Het |
Tll2 |
G |
A |
19: 41,101,512 (GRCm39) |
T374I |
probably damaging |
Het |
Tmem63b |
C |
A |
17: 45,971,870 (GRCm39) |
D782Y |
possibly damaging |
Het |
Trim10 |
G |
A |
17: 37,183,283 (GRCm39) |
S193N |
probably benign |
Het |
Ttf1 |
A |
T |
2: 28,963,962 (GRCm39) |
K613* |
probably null |
Het |
Tube1 |
T |
A |
10: 39,010,168 (GRCm39) |
|
probably null |
Het |
Uimc1 |
T |
A |
13: 55,224,222 (GRCm39) |
|
probably null |
Het |
Wwp2 |
G |
T |
8: 108,283,428 (GRCm39) |
|
probably benign |
Het |
Zfp101 |
C |
T |
17: 33,601,418 (GRCm39) |
V113I |
probably benign |
Het |
Zfp292 |
T |
C |
4: 34,809,114 (GRCm39) |
D1310G |
probably benign |
Het |
Zfp575 |
A |
T |
7: 24,285,245 (GRCm39) |
L132H |
probably damaging |
Het |
Zmym2 |
T |
C |
14: 57,194,420 (GRCm39) |
F1226S |
probably damaging |
Het |
Zswim6 |
A |
C |
13: 107,862,989 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Arhgef33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00783:Arhgef33
|
APN |
17 |
80,675,659 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00784:Arhgef33
|
APN |
17 |
80,675,659 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01601:Arhgef33
|
APN |
17 |
80,655,112 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01647:Arhgef33
|
APN |
17 |
80,672,695 (GRCm39) |
splice site |
probably benign |
|
IGL02654:Arhgef33
|
APN |
17 |
80,677,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02712:Arhgef33
|
APN |
17 |
80,667,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R0195:Arhgef33
|
UTSW |
17 |
80,688,863 (GRCm39) |
missense |
probably damaging |
0.96 |
R0732:Arhgef33
|
UTSW |
17 |
80,688,783 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1144:Arhgef33
|
UTSW |
17 |
80,662,473 (GRCm39) |
missense |
probably benign |
|
R1465:Arhgef33
|
UTSW |
17 |
80,674,730 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1465:Arhgef33
|
UTSW |
17 |
80,674,730 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1513:Arhgef33
|
UTSW |
17 |
80,678,818 (GRCm39) |
missense |
probably benign |
|
R1680:Arhgef33
|
UTSW |
17 |
80,655,080 (GRCm39) |
missense |
probably damaging |
0.96 |
R1696:Arhgef33
|
UTSW |
17 |
80,656,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Arhgef33
|
UTSW |
17 |
80,681,172 (GRCm39) |
missense |
probably benign |
0.05 |
R2046:Arhgef33
|
UTSW |
17 |
80,680,895 (GRCm39) |
missense |
probably benign |
0.08 |
R3933:Arhgef33
|
UTSW |
17 |
80,680,749 (GRCm39) |
missense |
probably benign |
0.01 |
R4573:Arhgef33
|
UTSW |
17 |
80,672,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Arhgef33
|
UTSW |
17 |
80,644,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Arhgef33
|
UTSW |
17 |
80,677,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Arhgef33
|
UTSW |
17 |
80,644,709 (GRCm39) |
missense |
probably benign |
|
R6460:Arhgef33
|
UTSW |
17 |
80,657,018 (GRCm39) |
splice site |
probably null |
|
R7307:Arhgef33
|
UTSW |
17 |
80,654,549 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7594:Arhgef33
|
UTSW |
17 |
80,677,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R7746:Arhgef33
|
UTSW |
17 |
80,654,549 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7895:Arhgef33
|
UTSW |
17 |
80,680,914 (GRCm39) |
missense |
probably benign |
0.00 |
R7956:Arhgef33
|
UTSW |
17 |
80,662,477 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8508:Arhgef33
|
UTSW |
17 |
80,674,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Arhgef33
|
UTSW |
17 |
80,680,615 (GRCm39) |
missense |
probably damaging |
0.96 |
R8743:Arhgef33
|
UTSW |
17 |
80,667,882 (GRCm39) |
critical splice donor site |
probably null |
|
R8768:Arhgef33
|
UTSW |
17 |
80,681,148 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9322:Arhgef33
|
UTSW |
17 |
80,677,818 (GRCm39) |
nonsense |
probably null |
|
R9349:Arhgef33
|
UTSW |
17 |
80,644,736 (GRCm39) |
nonsense |
probably null |
|
R9625:Arhgef33
|
UTSW |
17 |
80,654,707 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9727:Arhgef33
|
UTSW |
17 |
80,678,720 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arhgef33
|
UTSW |
17 |
80,691,659 (GRCm39) |
missense |
unknown |
|
|