Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
G |
A |
5: 114,368,781 (GRCm39) |
M1666I |
possibly damaging |
Het |
Adamts13 |
A |
T |
2: 26,874,153 (GRCm39) |
Q434L |
probably damaging |
Het |
Adgrg3 |
G |
A |
8: 95,762,562 (GRCm39) |
R204H |
probably benign |
Het |
AU041133 |
T |
A |
10: 81,987,101 (GRCm39) |
C251* |
probably null |
Het |
Axin2 |
T |
A |
11: 108,833,794 (GRCm39) |
N580K |
probably benign |
Het |
C4b |
A |
G |
17: 34,948,631 (GRCm39) |
C1560R |
probably damaging |
Het |
Cacna1g |
A |
G |
11: 94,334,880 (GRCm39) |
I809T |
possibly damaging |
Het |
Cacna1s |
C |
A |
1: 136,016,755 (GRCm39) |
|
probably null |
Het |
Cadps2 |
T |
C |
6: 23,688,857 (GRCm39) |
S151G |
probably damaging |
Het |
Capn1 |
T |
C |
19: 6,040,086 (GRCm39) |
|
probably null |
Het |
Capn9 |
A |
G |
8: 125,302,965 (GRCm39) |
S28G |
probably benign |
Het |
Ccdc73 |
A |
G |
2: 104,822,637 (GRCm39) |
D862G |
probably damaging |
Het |
Cdk17 |
T |
C |
10: 93,061,979 (GRCm39) |
L237P |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,440,802 (GRCm39) |
I1120V |
possibly damaging |
Het |
Chad |
A |
C |
11: 94,456,384 (GRCm39) |
N154T |
possibly damaging |
Het |
Cog1 |
C |
T |
11: 113,547,038 (GRCm39) |
T544I |
probably benign |
Het |
Cracd |
A |
T |
5: 77,006,470 (GRCm39) |
T944S |
unknown |
Het |
Ctnna2 |
T |
C |
6: 76,931,830 (GRCm39) |
E590G |
possibly damaging |
Het |
Dapk2 |
T |
A |
9: 66,072,642 (GRCm39) |
M6K |
probably benign |
Het |
Dchs1 |
T |
C |
7: 105,421,487 (GRCm39) |
E311G |
possibly damaging |
Het |
Ddr2 |
T |
A |
1: 169,809,641 (GRCm39) |
T779S |
probably benign |
Het |
Dhtkd1 |
A |
G |
2: 5,916,744 (GRCm39) |
V644A |
probably damaging |
Het |
Dock2 |
A |
G |
11: 34,414,934 (GRCm39) |
V147A |
possibly damaging |
Het |
Ear10 |
A |
T |
14: 44,160,357 (GRCm39) |
*157K |
probably null |
Het |
Gm10801 |
T |
C |
2: 98,494,197 (GRCm39) |
I113T |
probably damaging |
Het |
Gmps |
T |
G |
3: 63,906,049 (GRCm39) |
C449G |
probably damaging |
Het |
Grin3a |
A |
G |
4: 49,844,988 (GRCm39) |
S32P |
possibly damaging |
Het |
Igkv1-115 |
A |
T |
6: 68,138,592 (GRCm39) |
D65V |
probably damaging |
Het |
Klk1b4 |
A |
G |
7: 43,859,105 (GRCm39) |
N41S |
probably benign |
Het |
Krt26 |
CTAGTA |
CTA |
11: 99,224,352 (GRCm39) |
|
probably benign |
Het |
Lrrc8a |
T |
A |
2: 30,145,262 (GRCm39) |
D25E |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,421,960 (GRCm39) |
R4426G |
possibly damaging |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Myo5a |
G |
T |
9: 75,023,489 (GRCm39) |
D17Y |
probably damaging |
Het |
Nat1 |
C |
G |
8: 67,944,076 (GRCm39) |
L154V |
probably benign |
Het |
Nek3 |
T |
A |
8: 22,647,047 (GRCm39) |
T163S |
probably damaging |
Het |
Or2w25 |
G |
T |
11: 59,503,949 (GRCm39) |
R53L |
possibly damaging |
Het |
Or5p80 |
A |
G |
7: 108,229,562 (GRCm39) |
D121G |
probably damaging |
Het |
Or6c204 |
A |
G |
10: 129,023,044 (GRCm39) |
I82T |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,789,147 (GRCm39) |
I225N |
probably damaging |
Het |
Or8g32 |
A |
T |
9: 39,305,163 (GRCm39) |
E22D |
possibly damaging |
Het |
Or9s13 |
T |
C |
1: 92,548,525 (GRCm39) |
L299P |
probably damaging |
Het |
Osr1 |
T |
G |
12: 9,629,268 (GRCm39) |
L47R |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pik3ap1 |
T |
A |
19: 41,291,053 (GRCm39) |
N493I |
possibly damaging |
Het |
Polr3e |
T |
A |
7: 120,539,820 (GRCm39) |
N522K |
probably damaging |
Het |
Rabgap1 |
T |
A |
2: 37,385,771 (GRCm39) |
|
probably null |
Het |
Rp1l1 |
C |
A |
14: 64,268,992 (GRCm39) |
A1526E |
probably benign |
Het |
Scn3a |
T |
A |
2: 65,291,878 (GRCm39) |
I1623F |
probably damaging |
Het |
Serpinb9e |
A |
G |
13: 33,437,428 (GRCm39) |
T104A |
probably benign |
Het |
Sh3rf3 |
T |
C |
10: 58,939,989 (GRCm39) |
|
probably benign |
Het |
Slc30a3 |
A |
G |
5: 31,245,748 (GRCm39) |
Y213H |
probably damaging |
Het |
Sptbn4 |
C |
T |
7: 27,106,563 (GRCm39) |
R955H |
probably damaging |
Het |
Tfb1m |
A |
T |
17: 3,569,946 (GRCm39) |
Y307N |
probably damaging |
Het |
Tnrc6b |
G |
T |
15: 80,768,407 (GRCm39) |
|
probably null |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Ulk1 |
A |
G |
5: 110,938,936 (GRCm39) |
Y501H |
probably damaging |
Het |
Zbtb17 |
A |
G |
4: 141,191,914 (GRCm39) |
H315R |
probably damaging |
Het |
Zeb2 |
A |
G |
2: 44,892,624 (GRCm39) |
Y142H |
probably damaging |
Het |
Zfr |
T |
C |
15: 12,160,715 (GRCm39) |
S763P |
possibly 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 |
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 |
R6751:Arhgef28
|
UTSW |
13 |
98,211,755 (GRCm39) |
missense |
probably damaging |
0.97 |
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 |
|