Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,771,971 (GRCm39) |
N387Y |
probably damaging |
Het |
Abhd17a |
T |
C |
10: 80,422,421 (GRCm39) |
E87G |
probably damaging |
Het |
Aco1 |
T |
A |
4: 40,188,330 (GRCm39) |
|
probably null |
Het |
Adcy6 |
T |
C |
15: 98,494,086 (GRCm39) |
N817S |
probably benign |
Het |
Ak8 |
T |
A |
2: 28,599,957 (GRCm39) |
L63* |
probably null |
Het |
Asap1 |
A |
G |
15: 63,966,261 (GRCm39) |
L891S |
possibly damaging |
Het |
Cacng5 |
C |
A |
11: 107,768,379 (GRCm39) |
M209I |
probably benign |
Het |
Casr |
T |
C |
16: 36,335,950 (GRCm39) |
I120V |
probably benign |
Het |
Ccnq |
T |
C |
11: 78,641,950 (GRCm39) |
Y180C |
probably damaging |
Het |
Chd7 |
T |
C |
4: 8,833,866 (GRCm39) |
Y1207H |
probably damaging |
Het |
Chrnb2 |
A |
T |
3: 89,668,883 (GRCm39) |
F144Y |
probably damaging |
Het |
Cyp4a14 |
T |
A |
4: 115,348,391 (GRCm39) |
H362L |
probably damaging |
Het |
Dnaaf4 |
A |
G |
9: 72,869,257 (GRCm39) |
T156A |
probably benign |
Het |
Dym |
G |
A |
18: 75,419,718 (GRCm39) |
V630M |
probably damaging |
Het |
Dync2i1 |
A |
T |
12: 116,177,076 (GRCm39) |
V842E |
possibly damaging |
Het |
Dyrk1b |
C |
A |
7: 27,886,134 (GRCm39) |
P619Q |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,831,659 (GRCm39) |
D433G |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,561,086 (GRCm39) |
S1140R |
probably damaging |
Het |
Gabra5 |
T |
C |
7: 57,068,082 (GRCm39) |
R255G |
probably damaging |
Het |
Galnt17 |
T |
A |
5: 131,110,428 (GRCm39) |
I304F |
probably damaging |
Het |
Gpc5 |
A |
G |
14: 115,607,363 (GRCm39) |
S322G |
probably benign |
Het |
Herc1 |
TCCC |
TCC |
9: 66,408,470 (GRCm39) |
|
probably null |
Het |
Hmcn1 |
T |
A |
1: 150,610,269 (GRCm39) |
N1467Y |
probably damaging |
Het |
Ifna6 |
T |
C |
4: 88,745,987 (GRCm39) |
L112P |
probably damaging |
Het |
Ifrd1 |
C |
T |
12: 40,253,913 (GRCm39) |
|
probably null |
Het |
Il17f |
A |
G |
1: 20,849,713 (GRCm39) |
M17T |
probably benign |
Het |
Itga11 |
G |
A |
9: 62,675,866 (GRCm39) |
V892I |
probably benign |
Het |
Nckap5l |
A |
G |
15: 99,321,042 (GRCm39) |
L1246P |
probably damaging |
Het |
Nlrp4f |
A |
T |
13: 65,342,243 (GRCm39) |
H467Q |
probably damaging |
Het |
Ntng2 |
A |
G |
2: 29,118,055 (GRCm39) |
V131A |
possibly damaging |
Het |
Or51r1 |
G |
A |
7: 102,227,706 (GRCm39) |
M1I |
probably null |
Het |
Or8b40 |
T |
G |
9: 38,027,271 (GRCm39) |
Y60D |
probably damaging |
Het |
Or8g37 |
T |
A |
9: 39,731,193 (GRCm39) |
V86E |
probably benign |
Het |
Or8g55 |
T |
C |
9: 39,784,976 (GRCm39) |
V135A |
probably benign |
Het |
Osbpl8 |
T |
C |
10: 111,110,874 (GRCm39) |
Y459H |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,597,778 (GRCm39) |
V537D |
possibly damaging |
Het |
Pde4b |
A |
T |
4: 102,459,868 (GRCm39) |
M583L |
probably damaging |
Het |
Phlda1 |
T |
C |
10: 111,342,555 (GRCm39) |
V97A |
possibly damaging |
Het |
Pik3cb |
G |
T |
9: 98,976,574 (GRCm39) |
H174Q |
probably benign |
Het |
Plxdc2 |
A |
T |
2: 16,552,952 (GRCm39) |
I117F |
probably benign |
Het |
Psapl1 |
C |
A |
5: 36,362,303 (GRCm39) |
C298* |
probably null |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Homo |
Rtkn2 |
T |
A |
10: 67,877,283 (GRCm39) |
F448I |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,500,617 (GRCm39) |
R221G |
probably damaging |
Het |
Serpina3c |
A |
G |
12: 104,117,759 (GRCm39) |
L193P |
probably damaging |
Het |
Sox12 |
T |
C |
2: 152,238,678 (GRCm39) |
Y314C |
probably damaging |
Het |
Spata31h1 |
A |
G |
10: 82,119,331 (GRCm39) |
S4560P |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,067,859 (GRCm39) |
E1772G |
probably damaging |
Het |
Supt6 |
A |
G |
11: 78,099,775 (GRCm39) |
V1570A |
probably benign |
Het |
Synrg |
T |
C |
11: 83,872,251 (GRCm39) |
F125S |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,494,919 (GRCm39) |
I1116F |
possibly damaging |
Het |
Tfap2a |
T |
A |
13: 40,882,230 (GRCm39) |
N25I |
probably damaging |
Het |
Tfap2d |
C |
A |
1: 19,173,507 (GRCm39) |
H10N |
possibly damaging |
Het |
Trpm8 |
T |
C |
1: 88,312,428 (GRCm39) |
I1103T |
possibly damaging |
Het |
Vmn1r158 |
C |
T |
7: 22,489,306 (GRCm39) |
C301Y |
probably damaging |
Het |
Vmn2r56 |
T |
C |
7: 12,428,719 (GRCm39) |
I516V |
probably benign |
Het |
Vmn2r71 |
G |
A |
7: 85,269,095 (GRCm39) |
|
probably null |
Het |
Vnn3 |
C |
T |
10: 23,745,523 (GRCm39) |
R491C |
probably benign |
Het |
Vps50 |
A |
G |
6: 3,600,274 (GRCm39) |
Y911C |
probably damaging |
Het |
Zfp772 |
C |
T |
7: 7,206,716 (GRCm39) |
R325Q |
possibly damaging |
Het |
Zranb3 |
T |
A |
1: 127,887,556 (GRCm39) |
H957L |
probably benign |
Het |
Zscan20 |
G |
T |
4: 128,479,668 (GRCm39) |
T941K |
probably damaging |
Het |
Zscan25 |
T |
A |
5: 145,227,373 (GRCm39) |
F346I |
probably damaging |
Het |
|
Other mutations in Arhgef28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00426:Arhgef28
|
APN |
13 |
98,124,785 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00945:Arhgef28
|
APN |
13 |
98,103,907 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01099:Arhgef28
|
APN |
13 |
98,090,480 (GRCm39) |
splice site |
probably benign |
|
IGL01328:Arhgef28
|
APN |
13 |
98,106,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01396:Arhgef28
|
APN |
13 |
98,090,401 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02067:Arhgef28
|
APN |
13 |
98,213,825 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02147:Arhgef28
|
APN |
13 |
98,097,822 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02285:Arhgef28
|
APN |
13 |
98,187,536 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02439:Arhgef28
|
APN |
13 |
98,067,647 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02499:Arhgef28
|
APN |
13 |
98,090,291 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02532:Arhgef28
|
APN |
13 |
98,166,391 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02634:Arhgef28
|
APN |
13 |
98,187,566 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02902:Arhgef28
|
APN |
13 |
98,083,383 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03067:Arhgef28
|
APN |
13 |
98,124,794 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03081:Arhgef28
|
APN |
13 |
98,165,881 (GRCm39) |
splice site |
probably benign |
|
IGL03106:Arhgef28
|
APN |
13 |
98,094,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03195:Arhgef28
|
APN |
13 |
98,088,071 (GRCm39) |
splice site |
probably null |
|
IGL03325:Arhgef28
|
APN |
13 |
98,036,324 (GRCm39) |
missense |
probably benign |
0.03 |
H8786:Arhgef28
|
UTSW |
13 |
98,083,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Arhgef28
|
UTSW |
13 |
98,082,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0027:Arhgef28
|
UTSW |
13 |
98,082,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0062:Arhgef28
|
UTSW |
13 |
98,093,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0062:Arhgef28
|
UTSW |
13 |
98,093,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0090:Arhgef28
|
UTSW |
13 |
98,211,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R0096:Arhgef28
|
UTSW |
13 |
98,067,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Arhgef28
|
UTSW |
13 |
98,067,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Arhgef28
|
UTSW |
13 |
98,094,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Arhgef28
|
UTSW |
13 |
98,106,863 (GRCm39) |
missense |
probably benign |
0.21 |
R0711:Arhgef28
|
UTSW |
13 |
98,067,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Arhgef28
|
UTSW |
13 |
98,075,987 (GRCm39) |
missense |
probably benign |
0.16 |
R0790:Arhgef28
|
UTSW |
13 |
98,117,914 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1240:Arhgef28
|
UTSW |
13 |
98,066,000 (GRCm39) |
missense |
probably benign |
0.00 |
R1365:Arhgef28
|
UTSW |
13 |
98,211,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Arhgef28
|
UTSW |
13 |
98,211,510 (GRCm39) |
missense |
probably benign |
0.01 |
R1490:Arhgef28
|
UTSW |
13 |
98,114,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Arhgef28
|
UTSW |
13 |
98,102,054 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1660:Arhgef28
|
UTSW |
13 |
98,117,884 (GRCm39) |
missense |
probably benign |
0.05 |
R1671:Arhgef28
|
UTSW |
13 |
98,067,542 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1747:Arhgef28
|
UTSW |
13 |
98,073,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Arhgef28
|
UTSW |
13 |
98,067,694 (GRCm39) |
missense |
probably benign |
0.03 |
R1864:Arhgef28
|
UTSW |
13 |
98,130,640 (GRCm39) |
missense |
probably benign |
0.00 |
R1887:Arhgef28
|
UTSW |
13 |
98,282,081 (GRCm39) |
missense |
probably damaging |
0.97 |
R1924:Arhgef28
|
UTSW |
13 |
98,073,324 (GRCm39) |
splice site |
probably benign |
|
R1987:Arhgef28
|
UTSW |
13 |
98,103,604 (GRCm39) |
missense |
probably benign |
|
R2215:Arhgef28
|
UTSW |
13 |
98,187,529 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2342:Arhgef28
|
UTSW |
13 |
98,130,537 (GRCm39) |
missense |
probably benign |
0.00 |
R2495:Arhgef28
|
UTSW |
13 |
98,165,881 (GRCm39) |
splice site |
probably benign |
|
R3897:Arhgef28
|
UTSW |
13 |
98,093,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R3922:Arhgef28
|
UTSW |
13 |
98,130,452 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4063:Arhgef28
|
UTSW |
13 |
98,130,575 (GRCm39) |
missense |
probably benign |
0.16 |
R4086:Arhgef28
|
UTSW |
13 |
98,103,712 (GRCm39) |
missense |
probably damaging |
0.98 |
R4543:Arhgef28
|
UTSW |
13 |
98,211,508 (GRCm39) |
missense |
probably benign |
0.00 |
R4730:Arhgef28
|
UTSW |
13 |
98,114,650 (GRCm39) |
missense |
probably benign |
0.00 |
R4735:Arhgef28
|
UTSW |
13 |
98,036,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Arhgef28
|
UTSW |
13 |
98,066,062 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5069:Arhgef28
|
UTSW |
13 |
98,211,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R5558:Arhgef28
|
UTSW |
13 |
98,097,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Arhgef28
|
UTSW |
13 |
98,065,999 (GRCm39) |
missense |
probably benign |
0.01 |
R5594:Arhgef28
|
UTSW |
13 |
98,076,000 (GRCm39) |
missense |
probably benign |
0.00 |
R5937:Arhgef28
|
UTSW |
13 |
98,076,051 (GRCm39) |
missense |
probably benign |
0.00 |
R5987:Arhgef28
|
UTSW |
13 |
98,073,368 (GRCm39) |
nonsense |
probably null |
|
R6015:Arhgef28
|
UTSW |
13 |
98,211,530 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6193:Arhgef28
|
UTSW |
13 |
98,121,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Arhgef28
|
UTSW |
13 |
98,065,917 (GRCm39) |
critical splice donor site |
probably null |
|
R6306:Arhgef28
|
UTSW |
13 |
98,121,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Arhgef28
|
UTSW |
13 |
98,130,527 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6562:Arhgef28
|
UTSW |
13 |
98,124,647 (GRCm39) |
critical splice donor site |
probably null |
|
R6646:Arhgef28
|
UTSW |
13 |
98,076,002 (GRCm39) |
missense |
probably benign |
0.09 |
R6655:Arhgef28
|
UTSW |
13 |
98,036,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R6707:Arhgef28
|
UTSW |
13 |
98,211,624 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6707:Arhgef28
|
UTSW |
13 |
98,073,224 (GRCm39) |
missense |
probably damaging |
0.96 |
R6940:Arhgef28
|
UTSW |
13 |
98,102,038 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7018:Arhgef28
|
UTSW |
13 |
98,101,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:Arhgef28
|
UTSW |
13 |
98,124,769 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7120:Arhgef28
|
UTSW |
13 |
98,081,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R7266:Arhgef28
|
UTSW |
13 |
98,101,960 (GRCm39) |
missense |
probably benign |
|
R7353:Arhgef28
|
UTSW |
13 |
98,211,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Arhgef28
|
UTSW |
13 |
98,133,370 (GRCm39) |
missense |
probably benign |
0.34 |
R7491:Arhgef28
|
UTSW |
13 |
98,081,194 (GRCm39) |
missense |
probably benign |
0.03 |
R7500:Arhgef28
|
UTSW |
13 |
98,115,003 (GRCm39) |
missense |
probably benign |
0.00 |
R7653:Arhgef28
|
UTSW |
13 |
98,105,821 (GRCm39) |
missense |
probably benign |
0.04 |
R7813:Arhgef28
|
UTSW |
13 |
98,082,189 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7989:Arhgef28
|
UTSW |
13 |
98,036,243 (GRCm39) |
missense |
probably benign |
|
R8064:Arhgef28
|
UTSW |
13 |
98,115,002 (GRCm39) |
missense |
probably benign |
0.13 |
R8221:Arhgef28
|
UTSW |
13 |
98,282,064 (GRCm39) |
missense |
probably benign |
0.00 |
R8293:Arhgef28
|
UTSW |
13 |
98,079,029 (GRCm39) |
missense |
probably benign |
0.00 |
R8328:Arhgef28
|
UTSW |
13 |
98,187,517 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8348:Arhgef28
|
UTSW |
13 |
98,190,375 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8432:Arhgef28
|
UTSW |
13 |
98,088,091 (GRCm39) |
missense |
probably benign |
0.29 |
R8843:Arhgef28
|
UTSW |
13 |
98,130,557 (GRCm39) |
missense |
probably benign |
|
R8859:Arhgef28
|
UTSW |
13 |
98,082,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Arhgef28
|
UTSW |
13 |
98,066,141 (GRCm39) |
missense |
probably benign |
0.03 |
R8987:Arhgef28
|
UTSW |
13 |
98,190,472 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9253:Arhgef28
|
UTSW |
13 |
98,124,779 (GRCm39) |
missense |
probably benign |
0.09 |
R9351:Arhgef28
|
UTSW |
13 |
98,130,576 (GRCm39) |
missense |
probably benign |
0.11 |
R9381:Arhgef28
|
UTSW |
13 |
98,036,269 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9395:Arhgef28
|
UTSW |
13 |
98,103,692 (GRCm39) |
frame shift |
probably null |
|
R9466:Arhgef28
|
UTSW |
13 |
98,124,825 (GRCm39) |
missense |
|
|
R9529:Arhgef28
|
UTSW |
13 |
98,213,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Arhgef28
|
UTSW |
13 |
98,078,983 (GRCm39) |
missense |
probably benign |
0.00 |
R9662:Arhgef28
|
UTSW |
13 |
98,065,969 (GRCm39) |
missense |
probably benign |
0.20 |
R9744:Arhgef28
|
UTSW |
13 |
98,094,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9776:Arhgef28
|
UTSW |
13 |
98,133,415 (GRCm39) |
missense |
probably benign |
0.19 |
Z1088:Arhgef28
|
UTSW |
13 |
98,082,199 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arhgef28
|
UTSW |
13 |
98,036,264 (GRCm39) |
missense |
probably benign |
0.43 |
|