Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
A |
G |
3: 59,947,066 (GRCm39) |
T255A |
possibly damaging |
Het |
Acat3 |
C |
T |
17: 13,146,294 (GRCm39) |
A230T |
probably benign |
Het |
Acsl1 |
C |
A |
8: 46,986,663 (GRCm39) |
P650Q |
probably benign |
Het |
Adgrl3 |
T |
A |
5: 81,660,383 (GRCm39) |
I316N |
probably damaging |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
AI429214 |
T |
A |
8: 37,461,362 (GRCm39) |
V170E |
probably benign |
Het |
Akap13 |
G |
A |
7: 75,375,052 (GRCm39) |
G1895S |
possibly damaging |
Het |
Alpk2 |
G |
A |
18: 65,483,439 (GRCm39) |
Q190* |
probably null |
Het |
Aox3 |
C |
A |
1: 58,197,375 (GRCm39) |
Q574K |
probably benign |
Het |
Apeh |
A |
G |
9: 107,962,866 (GRCm39) |
Y702H |
probably damaging |
Het |
Aqp11 |
A |
G |
7: 97,386,692 (GRCm39) |
I151T |
probably benign |
Het |
Arhgef18 |
A |
G |
8: 3,501,939 (GRCm39) |
N699S |
probably damaging |
Het |
Asnsd1 |
A |
G |
1: 53,386,476 (GRCm39) |
S384P |
probably benign |
Het |
Atl1 |
G |
T |
12: 69,978,431 (GRCm39) |
|
probably null |
Het |
Atp13a2 |
A |
T |
4: 140,722,702 (GRCm39) |
D203V |
possibly damaging |
Het |
Axdnd1 |
A |
T |
1: 156,160,784 (GRCm39) |
N164K |
probably benign |
Het |
Bnipl |
T |
A |
3: 95,152,994 (GRCm39) |
I162F |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,845,120 (GRCm39) |
L655I |
probably damaging |
Het |
Canx |
T |
C |
11: 50,195,185 (GRCm39) |
I294M |
probably damaging |
Het |
Casz1 |
T |
C |
4: 149,030,521 (GRCm39) |
F1180S |
probably damaging |
Het |
Cav3 |
T |
C |
6: 112,449,344 (GRCm39) |
Y121H |
probably benign |
Het |
Cd4 |
A |
C |
6: 124,847,499 (GRCm39) |
S222A |
probably benign |
Het |
Cds1 |
T |
C |
5: 101,960,416 (GRCm39) |
I289T |
probably benign |
Het |
Cep112 |
T |
C |
11: 108,399,084 (GRCm39) |
F328L |
probably damaging |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Cfap44 |
A |
T |
16: 44,230,838 (GRCm39) |
D273V |
probably benign |
Het |
Cfap91 |
T |
C |
16: 38,162,124 (GRCm39) |
T6A |
probably benign |
Het |
Clec7a |
C |
T |
6: 129,447,918 (GRCm39) |
G49D |
probably benign |
Het |
Col22a1 |
G |
A |
15: 71,729,102 (GRCm39) |
Q599* |
probably null |
Het |
Col6a5 |
T |
A |
9: 105,822,799 (GRCm39) |
H186L |
unknown |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dnah12 |
A |
T |
14: 26,445,613 (GRCm39) |
R725* |
probably null |
Het |
Dnajc10 |
G |
A |
2: 80,181,078 (GRCm39) |
|
probably null |
Het |
Edem3 |
A |
T |
1: 151,670,482 (GRCm39) |
H337L |
possibly damaging |
Het |
Eif2ak4 |
A |
T |
2: 118,252,604 (GRCm39) |
H392L |
probably benign |
Het |
Ercc6l2 |
G |
A |
13: 63,996,585 (GRCm39) |
V365I |
probably damaging |
Het |
Fan1 |
T |
C |
7: 63,996,636 (GRCm39) |
E978G |
probably damaging |
Het |
Fcrl6 |
C |
T |
1: 172,426,815 (GRCm39) |
V44M |
probably benign |
Het |
Gaa |
G |
A |
11: 119,161,108 (GRCm39) |
W50* |
probably null |
Het |
Gm10032 |
T |
C |
14: 67,030,227 (GRCm39) |
|
noncoding transcript |
Het |
Gm10985 |
CTCTAT |
CT |
3: 53,752,670 (GRCm39) |
|
probably null |
Het |
Gprc5b |
G |
T |
7: 118,583,398 (GRCm39) |
P157Q |
probably damaging |
Het |
Gsdmc3 |
G |
A |
15: 63,730,383 (GRCm39) |
Q394* |
probably null |
Het |
Gucd1 |
A |
G |
10: 75,347,922 (GRCm39) |
S38P |
probably damaging |
Het |
Higd1a |
A |
T |
9: 121,679,313 (GRCm39) |
I58N |
probably damaging |
Het |
Hmx3 |
G |
C |
7: 131,146,278 (GRCm39) |
V329L |
possibly damaging |
Het |
Hnrnpul2 |
A |
T |
19: 8,801,802 (GRCm39) |
R337* |
probably null |
Het |
Idua |
T |
A |
5: 108,829,304 (GRCm39) |
H368Q |
possibly damaging |
Het |
Ifih1 |
A |
G |
2: 62,453,811 (GRCm39) |
V218A |
probably benign |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Kif1b |
G |
A |
4: 149,272,097 (GRCm39) |
S1568L |
possibly damaging |
Het |
Klhl30 |
T |
A |
1: 91,286,499 (GRCm39) |
|
probably null |
Het |
Lasp1 |
T |
A |
11: 97,726,960 (GRCm39) |
D227E |
probably benign |
Het |
Lhx6 |
A |
G |
2: 35,981,336 (GRCm39) |
I85T |
possibly damaging |
Het |
Limch1 |
A |
G |
5: 67,187,103 (GRCm39) |
D840G |
probably damaging |
Het |
Loxl4 |
C |
G |
19: 42,592,402 (GRCm39) |
E385D |
probably damaging |
Het |
Lrrtm4 |
A |
T |
6: 79,998,722 (GRCm39) |
I44F |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,832,483 (GRCm39) |
|
probably null |
Het |
Lyg1 |
T |
C |
1: 37,989,755 (GRCm39) |
Y44C |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,129,122 (GRCm39) |
I129V |
probably damaging |
Het |
Med27 |
C |
T |
2: 29,414,442 (GRCm39) |
Q150* |
probably null |
Het |
Ms4a5 |
A |
T |
19: 11,256,732 (GRCm39) |
I55N |
probably damaging |
Het |
Muc5ac |
T |
C |
7: 141,364,479 (GRCm39) |
S2597P |
possibly damaging |
Het |
Mxd1 |
A |
C |
6: 86,628,422 (GRCm39) |
|
probably null |
Het |
Myo3a |
A |
G |
2: 22,468,186 (GRCm39) |
D480G |
probably benign |
Het |
Neb |
T |
C |
2: 52,200,650 (GRCm39) |
Y343C |
probably damaging |
Het |
Niban1 |
A |
C |
1: 151,571,886 (GRCm39) |
E277A |
probably damaging |
Het |
Niban1 |
A |
G |
1: 151,584,884 (GRCm39) |
I494V |
possibly damaging |
Het |
Nrn1 |
A |
C |
13: 36,914,180 (GRCm39) |
V34G |
probably damaging |
Het |
Or4k52 |
A |
G |
2: 111,610,841 (GRCm39) |
M59V |
probably damaging |
Het |
Or4n5 |
A |
G |
14: 50,132,524 (GRCm39) |
I245T |
probably benign |
Het |
Or52b1 |
C |
T |
7: 104,978,459 (GRCm39) |
W313* |
probably null |
Het |
Or56a3 |
A |
G |
7: 104,735,822 (GRCm39) |
T300A |
probably damaging |
Het |
Or8b39 |
G |
T |
9: 37,996,572 (GRCm39) |
V147L |
probably benign |
Het |
Or8h9 |
T |
C |
2: 86,789,442 (GRCm39) |
Y120C |
possibly damaging |
Het |
Or8k40 |
A |
T |
2: 86,584,796 (GRCm39) |
N95K |
probably benign |
Het |
Pdia4 |
A |
T |
6: 47,773,771 (GRCm39) |
V526E |
probably damaging |
Het |
Pdia6 |
T |
C |
12: 17,328,546 (GRCm39) |
V167A |
probably damaging |
Het |
Pgk2 |
A |
G |
17: 40,518,400 (GRCm39) |
F343L |
probably damaging |
Het |
Piwil1 |
T |
C |
5: 128,831,160 (GRCm39) |
V827A |
probably damaging |
Het |
Plag1 |
A |
T |
4: 3,904,169 (GRCm39) |
Y341N |
possibly damaging |
Het |
Plch2 |
T |
C |
4: 155,083,456 (GRCm39) |
E393G |
probably damaging |
Het |
Ptprg |
T |
A |
14: 12,154,355 (GRCm38) |
M692K |
probably benign |
Het |
Rassf8 |
G |
A |
6: 145,760,908 (GRCm39) |
R78H |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,341,027 (GRCm39) |
Q3556R |
probably damaging |
Het |
Rpa2 |
T |
C |
4: 132,496,099 (GRCm39) |
|
probably null |
Het |
Rpe |
T |
G |
1: 66,755,139 (GRCm39) |
F174V |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 110,159,502 (GRCm39) |
D36G |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,582,423 (GRCm39) |
Y1590* |
probably null |
Het |
Slc24a4 |
T |
C |
12: 102,189,018 (GRCm39) |
V151A |
probably damaging |
Het |
Slc30a8 |
A |
T |
15: 52,159,330 (GRCm39) |
M17L |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,579,506 (GRCm39) |
Y1228H |
probably damaging |
Het |
Smad4 |
G |
A |
18: 73,795,815 (GRCm39) |
T193M |
probably benign |
Het |
Smtn |
T |
A |
11: 3,480,045 (GRCm39) |
H392L |
probably benign |
Het |
St8sia3 |
A |
G |
18: 64,402,745 (GRCm39) |
D128G |
probably damaging |
Het |
Sucla2 |
A |
T |
14: 73,830,108 (GRCm39) |
M382L |
possibly damaging |
Het |
Tbx5 |
A |
G |
5: 119,974,988 (GRCm39) |
T4A |
probably benign |
Het |
Tdrd5 |
T |
C |
1: 156,104,143 (GRCm39) |
R528G |
probably damaging |
Het |
Tex44 |
T |
C |
1: 86,354,811 (GRCm39) |
L240P |
probably benign |
Het |
Tns4 |
A |
T |
11: 98,970,904 (GRCm39) |
|
probably null |
Het |
Trappc10 |
A |
T |
10: 78,039,758 (GRCm39) |
V731E |
possibly damaging |
Het |
Ttf1 |
A |
G |
2: 28,961,357 (GRCm39) |
K582E |
probably damaging |
Het |
Ttf2 |
C |
A |
3: 100,855,509 (GRCm39) |
Q895H |
possibly damaging |
Het |
Ttll6 |
A |
G |
11: 96,038,358 (GRCm39) |
E402G |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,720,436 (GRCm39) |
|
probably null |
Het |
Ugt8a |
T |
C |
3: 125,669,195 (GRCm39) |
D303G |
probably damaging |
Het |
Ulk1 |
G |
T |
5: 110,940,302 (GRCm39) |
A373D |
probably benign |
Het |
Vmn2r13 |
A |
G |
5: 109,306,058 (GRCm39) |
S507P |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,293,033 (GRCm39) |
D358E |
possibly damaging |
Het |
Vmn2r88 |
T |
C |
14: 51,651,264 (GRCm39) |
S201P |
probably benign |
Het |
Zfp36l2 |
A |
G |
17: 84,494,403 (GRCm39) |
F78S |
probably damaging |
Het |
Zfp454 |
A |
C |
11: 50,764,822 (GRCm39) |
S203R |
probably benign |
Het |
Zfp616 |
C |
A |
11: 73,976,229 (GRCm39) |
Q833K |
probably benign |
Het |
Znhit2 |
A |
G |
19: 6,112,091 (GRCm39) |
T279A |
probably benign |
Het |
Zswim3 |
T |
A |
2: 164,661,913 (GRCm39) |
I131N |
probably benign |
Het |
|
Other mutations in Arhgap28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00435:Arhgap28
|
APN |
17 |
68,152,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01388:Arhgap28
|
APN |
17 |
68,160,034 (GRCm39) |
unclassified |
probably benign |
|
IGL01560:Arhgap28
|
APN |
17 |
68,203,066 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01578:Arhgap28
|
APN |
17 |
68,165,195 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01650:Arhgap28
|
APN |
17 |
68,180,127 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02383:Arhgap28
|
APN |
17 |
68,203,084 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02403:Arhgap28
|
APN |
17 |
68,180,154 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02652:Arhgap28
|
APN |
17 |
68,191,795 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03102:Arhgap28
|
APN |
17 |
68,203,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Arhgap28
|
APN |
17 |
68,175,951 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03306:Arhgap28
|
APN |
17 |
68,159,930 (GRCm39) |
missense |
probably damaging |
1.00 |
K3955:Arhgap28
|
UTSW |
17 |
68,311,001 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4445001:Arhgap28
|
UTSW |
17 |
68,203,230 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0135:Arhgap28
|
UTSW |
17 |
68,171,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Arhgap28
|
UTSW |
17 |
68,208,424 (GRCm39) |
missense |
probably benign |
0.13 |
R0385:Arhgap28
|
UTSW |
17 |
68,171,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R0412:Arhgap28
|
UTSW |
17 |
68,203,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Arhgap28
|
UTSW |
17 |
68,203,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Arhgap28
|
UTSW |
17 |
68,203,108 (GRCm39) |
splice site |
probably null |
|
R0691:Arhgap28
|
UTSW |
17 |
68,203,159 (GRCm39) |
splice site |
probably null |
|
R0811:Arhgap28
|
UTSW |
17 |
68,208,294 (GRCm39) |
small deletion |
probably benign |
|
R1150:Arhgap28
|
UTSW |
17 |
68,164,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1151:Arhgap28
|
UTSW |
17 |
68,164,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1152:Arhgap28
|
UTSW |
17 |
68,164,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Arhgap28
|
UTSW |
17 |
68,164,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1427:Arhgap28
|
UTSW |
17 |
68,164,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1632:Arhgap28
|
UTSW |
17 |
68,156,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R1747:Arhgap28
|
UTSW |
17 |
68,208,304 (GRCm39) |
missense |
probably benign |
0.02 |
R1951:Arhgap28
|
UTSW |
17 |
68,208,336 (GRCm39) |
missense |
probably benign |
0.00 |
R2031:Arhgap28
|
UTSW |
17 |
68,203,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R2181:Arhgap28
|
UTSW |
17 |
68,203,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R3700:Arhgap28
|
UTSW |
17 |
68,208,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R3800:Arhgap28
|
UTSW |
17 |
68,180,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R3811:Arhgap28
|
UTSW |
17 |
68,203,088 (GRCm39) |
missense |
probably benign |
|
R4213:Arhgap28
|
UTSW |
17 |
68,178,988 (GRCm39) |
missense |
probably benign |
0.04 |
R4347:Arhgap28
|
UTSW |
17 |
68,180,137 (GRCm39) |
missense |
probably benign |
|
R4954:Arhgap28
|
UTSW |
17 |
68,176,008 (GRCm39) |
nonsense |
probably null |
|
R5592:Arhgap28
|
UTSW |
17 |
68,165,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R5610:Arhgap28
|
UTSW |
17 |
68,203,235 (GRCm39) |
nonsense |
probably null |
|
R5758:Arhgap28
|
UTSW |
17 |
68,180,154 (GRCm39) |
missense |
probably benign |
0.04 |
R5774:Arhgap28
|
UTSW |
17 |
68,188,487 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6413:Arhgap28
|
UTSW |
17 |
68,182,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6661:Arhgap28
|
UTSW |
17 |
68,152,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7255:Arhgap28
|
UTSW |
17 |
68,159,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R7324:Arhgap28
|
UTSW |
17 |
68,202,879 (GRCm39) |
splice site |
probably null |
|
R7338:Arhgap28
|
UTSW |
17 |
68,203,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Arhgap28
|
UTSW |
17 |
68,178,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R7860:Arhgap28
|
UTSW |
17 |
68,208,277 (GRCm39) |
nonsense |
probably null |
|
R8516:Arhgap28
|
UTSW |
17 |
68,180,068 (GRCm39) |
missense |
probably benign |
0.08 |
R9210:Arhgap28
|
UTSW |
17 |
68,162,430 (GRCm39) |
missense |
probably benign |
0.00 |
R9212:Arhgap28
|
UTSW |
17 |
68,162,430 (GRCm39) |
missense |
probably benign |
0.00 |
R9779:Arhgap28
|
UTSW |
17 |
68,152,764 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Arhgap28
|
UTSW |
17 |
68,168,272 (GRCm39) |
missense |
possibly damaging |
0.62 |
|