Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
A |
G |
16: 88,555,938 (GRCm39) |
T51A |
probably benign |
Het |
Abcc8 |
A |
G |
7: 45,754,886 (GRCm39) |
|
probably null |
Het |
Accs |
A |
T |
2: 93,674,602 (GRCm39) |
M123K |
probably damaging |
Het |
Ace |
G |
A |
11: 105,863,880 (GRCm39) |
G443S |
possibly damaging |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Arhgef18 |
T |
C |
8: 3,482,775 (GRCm39) |
L160P |
probably damaging |
Het |
Arnt |
T |
G |
3: 95,381,837 (GRCm39) |
|
probably null |
Het |
Art3 |
A |
G |
5: 92,540,359 (GRCm39) |
N34S |
possibly damaging |
Het |
Avl9 |
A |
T |
6: 56,700,526 (GRCm39) |
E53D |
possibly damaging |
Het |
AW209491 |
A |
T |
13: 14,811,447 (GRCm39) |
E100V |
probably benign |
Het |
Axin2 |
T |
C |
11: 108,814,529 (GRCm39) |
I139T |
probably damaging |
Het |
Birc7 |
G |
T |
2: 180,575,103 (GRCm39) |
V280L |
probably damaging |
Het |
Bmal1 |
T |
C |
7: 112,886,353 (GRCm39) |
Y137H |
probably damaging |
Het |
C1ra |
A |
G |
6: 124,494,338 (GRCm39) |
N262D |
probably benign |
Het |
Cacna1g |
A |
G |
11: 94,348,001 (GRCm39) |
F696L |
probably benign |
Het |
Casp14 |
T |
A |
10: 78,550,079 (GRCm39) |
|
probably null |
Het |
Ciao2a |
A |
G |
9: 66,045,684 (GRCm39) |
I151V |
probably benign |
Het |
Crlf1 |
T |
C |
8: 70,951,862 (GRCm39) |
Y176H |
probably damaging |
Het |
Dnajb4 |
A |
T |
3: 151,892,468 (GRCm39) |
S122T |
probably benign |
Het |
Dthd1 |
G |
A |
5: 62,971,653 (GRCm39) |
D159N |
possibly damaging |
Het |
Erich6 |
A |
T |
3: 58,528,699 (GRCm39) |
I517N |
possibly damaging |
Het |
Fam118b |
T |
A |
9: 35,129,239 (GRCm39) |
H343L |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,178,560 (GRCm39) |
D1500V |
probably damaging |
Het |
Fcgbp |
T |
C |
7: 27,803,595 (GRCm39) |
|
probably null |
Het |
Fgfrl1 |
A |
G |
5: 108,853,142 (GRCm39) |
D255G |
probably damaging |
Het |
Gm9611 |
G |
A |
14: 42,118,087 (GRCm39) |
Q82* |
probably null |
Het |
Ifit3 |
G |
T |
19: 34,565,359 (GRCm39) |
E302* |
probably null |
Het |
Igkv3-9 |
G |
A |
6: 70,565,737 (GRCm39) |
C112Y |
probably damaging |
Het |
Ints4 |
A |
G |
7: 97,148,792 (GRCm39) |
T233A |
probably benign |
Het |
Khnyn |
A |
T |
14: 56,125,059 (GRCm39) |
S438C |
probably damaging |
Het |
Kifc1 |
T |
C |
17: 34,102,849 (GRCm39) |
R192G |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,919,951 (GRCm39) |
S98P |
unknown |
Het |
Krt1c |
A |
T |
15: 101,724,769 (GRCm39) |
D280E |
probably damaging |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Macf1 |
T |
C |
4: 123,295,200 (GRCm39) |
I5344V |
probably damaging |
Het |
Mcf2l |
A |
T |
8: 13,053,529 (GRCm39) |
|
probably null |
Het |
Mms22l |
A |
C |
4: 24,505,373 (GRCm39) |
H211P |
probably damaging |
Het |
Nipsnap1 |
A |
G |
11: 4,839,145 (GRCm39) |
R163G |
possibly damaging |
Het |
Nusap1 |
A |
G |
2: 119,477,616 (GRCm39) |
N375S |
possibly damaging |
Het |
Or51t4 |
A |
G |
7: 102,598,278 (GRCm39) |
Y202C |
probably damaging |
Het |
Or52e19b |
A |
T |
7: 103,032,735 (GRCm39) |
V158D |
possibly damaging |
Het |
Or8g17 |
A |
G |
9: 38,930,747 (GRCm39) |
L30P |
probably damaging |
Het |
Phf14 |
G |
A |
6: 11,933,306 (GRCm39) |
G56D |
unknown |
Het |
Phykpl |
G |
A |
11: 51,477,408 (GRCm39) |
V67M |
probably damaging |
Het |
Pigk |
A |
G |
3: 152,453,404 (GRCm39) |
D374G |
probably benign |
Het |
Pirb |
A |
G |
7: 3,722,857 (GRCm39) |
V45A |
probably damaging |
Het |
Prm3 |
CTCTTCTTCTTCTTC |
CTCTTCTTCTTC |
16: 10,608,565 (GRCm39) |
|
probably benign |
Het |
Rb1cc1 |
T |
C |
1: 6,318,786 (GRCm39) |
V735A |
probably damaging |
Het |
Rcor2 |
A |
G |
19: 7,251,225 (GRCm39) |
T333A |
possibly damaging |
Het |
Ret |
A |
G |
6: 118,151,305 (GRCm39) |
V593A |
probably benign |
Het |
Scgb1b10 |
A |
T |
7: 31,800,570 (GRCm39) |
D53V |
probably damaging |
Het |
Sec61a2 |
G |
A |
2: 5,881,794 (GRCm39) |
A212V |
probably damaging |
Het |
Sgpl1 |
A |
T |
10: 60,942,121 (GRCm39) |
F245I |
probably damaging |
Het |
Sh2d4b |
A |
C |
14: 40,542,723 (GRCm39) |
V351G |
probably damaging |
Het |
Shld2 |
C |
T |
14: 33,990,436 (GRCm39) |
V157I |
probably benign |
Het |
Slc22a1 |
T |
A |
17: 12,871,310 (GRCm39) |
M484L |
probably benign |
Het |
Slit1 |
C |
G |
19: 41,599,247 (GRCm39) |
G1066R |
probably damaging |
Het |
Slit1 |
A |
T |
19: 41,599,248 (GRCm39) |
D1065E |
probably benign |
Het |
Spg11 |
G |
A |
2: 121,922,803 (GRCm39) |
A882V |
probably damaging |
Het |
Stab2 |
A |
C |
10: 86,681,897 (GRCm39) |
F2501L |
probably benign |
Het |
Stim2 |
A |
T |
5: 54,275,671 (GRCm39) |
K607N |
probably damaging |
Het |
Syde1 |
C |
T |
10: 78,425,916 (GRCm39) |
V84M |
probably damaging |
Het |
Tepsin |
A |
T |
11: 119,985,061 (GRCm39) |
N202K |
probably benign |
Het |
Tmem207 |
T |
A |
16: 26,335,495 (GRCm39) |
I81F |
possibly damaging |
Het |
Tnc |
C |
A |
4: 63,935,580 (GRCm39) |
G452V |
probably damaging |
Het |
Tshz1 |
G |
T |
18: 84,033,782 (GRCm39) |
Q209K |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,773,696 (GRCm39) |
N2308K |
unknown |
Het |
Zfp266 |
A |
G |
9: 20,410,548 (GRCm39) |
I543T |
probably benign |
Het |
Zfp777 |
G |
T |
6: 48,001,645 (GRCm39) |
P815Q |
probably damaging |
Het |
Zhx3 |
A |
G |
2: 160,623,015 (GRCm39) |
I384T |
probably damaging |
Het |
|
Other mutations in Arhgap25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01454:Arhgap25
|
APN |
6 |
87,473,058 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02112:Arhgap25
|
APN |
6 |
87,444,919 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03051:Arhgap25
|
APN |
6 |
87,472,896 (GRCm39) |
missense |
probably null |
1.00 |
R0462:Arhgap25
|
UTSW |
6 |
87,436,942 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1636:Arhgap25
|
UTSW |
6 |
87,472,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Arhgap25
|
UTSW |
6 |
87,440,289 (GRCm39) |
missense |
probably benign |
0.41 |
R2077:Arhgap25
|
UTSW |
6 |
87,436,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R2845:Arhgap25
|
UTSW |
6 |
87,436,949 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4091:Arhgap25
|
UTSW |
6 |
87,440,017 (GRCm39) |
missense |
probably benign |
|
R4435:Arhgap25
|
UTSW |
6 |
87,439,920 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4773:Arhgap25
|
UTSW |
6 |
87,473,053 (GRCm39) |
missense |
probably benign |
|
R5121:Arhgap25
|
UTSW |
6 |
87,509,846 (GRCm39) |
missense |
probably benign |
0.01 |
R5169:Arhgap25
|
UTSW |
6 |
87,440,252 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5334:Arhgap25
|
UTSW |
6 |
87,440,243 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5726:Arhgap25
|
UTSW |
6 |
87,440,441 (GRCm39) |
missense |
probably benign |
|
R6696:Arhgap25
|
UTSW |
6 |
87,443,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R6696:Arhgap25
|
UTSW |
6 |
87,442,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R8113:Arhgap25
|
UTSW |
6 |
87,465,287 (GRCm39) |
nonsense |
probably null |
|
R9110:Arhgap25
|
UTSW |
6 |
87,453,254 (GRCm39) |
missense |
probably benign |
0.07 |
R9500:Arhgap25
|
UTSW |
6 |
87,469,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9591:Arhgap25
|
UTSW |
6 |
87,440,102 (GRCm39) |
missense |
probably benign |
|
Z1176:Arhgap25
|
UTSW |
6 |
87,453,168 (GRCm39) |
missense |
probably damaging |
1.00 |
|