Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatf |
T |
C |
11: 84,402,339 (GRCm39) |
I116V |
probably benign |
Het |
Abhd18 |
T |
C |
3: 40,871,123 (GRCm39) |
F94S |
probably damaging |
Het |
Afg2a |
G |
C |
3: 37,486,312 (GRCm39) |
D345H |
possibly damaging |
Het |
Amn1 |
A |
T |
6: 149,086,634 (GRCm39) |
|
probably benign |
Het |
Arhgap32 |
T |
C |
9: 32,170,199 (GRCm39) |
V993A |
probably damaging |
Het |
Arhgap33 |
A |
T |
7: 30,223,921 (GRCm39) |
S703T |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,618,785 (GRCm39) |
|
probably benign |
Het |
Atg2a |
A |
G |
19: 6,303,407 (GRCm39) |
Y1083C |
probably damaging |
Het |
Atp2a3 |
T |
C |
11: 72,872,731 (GRCm39) |
F760L |
probably damaging |
Het |
B9d1 |
A |
G |
11: 61,403,271 (GRCm39) |
|
probably benign |
Het |
Batf |
C |
T |
12: 85,733,636 (GRCm39) |
|
probably benign |
Het |
BC051019 |
T |
A |
7: 109,317,182 (GRCm39) |
Y170F |
probably benign |
Het |
Bphl |
T |
C |
13: 34,221,754 (GRCm39) |
*37Q |
probably null |
Het |
Cab39l |
T |
C |
14: 59,737,008 (GRCm39) |
S43P |
probably damaging |
Het |
Cad |
A |
G |
5: 31,234,856 (GRCm39) |
|
probably benign |
Het |
Cct4 |
T |
G |
11: 22,946,014 (GRCm39) |
S119A |
probably benign |
Het |
Cd163 |
G |
A |
6: 124,288,408 (GRCm39) |
V280M |
probably damaging |
Het |
Cd86 |
A |
G |
16: 36,438,999 (GRCm39) |
|
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,152,375 (GRCm39) |
|
probably benign |
Het |
Cdhr5 |
A |
G |
7: 140,852,431 (GRCm39) |
F145S |
probably damaging |
Het |
Cdt1 |
T |
C |
8: 123,298,799 (GRCm39) |
S479P |
possibly damaging |
Het |
Ces2g |
T |
C |
8: 105,693,199 (GRCm39) |
V372A |
probably benign |
Het |
Chrna3 |
T |
C |
9: 54,929,562 (GRCm39) |
D92G |
probably damaging |
Het |
Cndp1 |
A |
G |
18: 84,637,658 (GRCm39) |
S359P |
probably benign |
Het |
Cops4 |
A |
G |
5: 100,676,528 (GRCm39) |
Q93R |
probably damaging |
Het |
Dgka |
G |
C |
10: 128,556,952 (GRCm39) |
|
probably benign |
Het |
Dmp1 |
A |
T |
5: 104,360,074 (GRCm39) |
D250V |
probably damaging |
Het |
Dnajb2 |
C |
T |
1: 75,216,278 (GRCm39) |
|
probably benign |
Het |
Dock9 |
T |
C |
14: 121,899,996 (GRCm39) |
T113A |
possibly damaging |
Het |
Egln3 |
T |
A |
12: 54,250,107 (GRCm39) |
I81F |
probably benign |
Het |
Elapor2 |
G |
A |
5: 9,470,723 (GRCm39) |
|
probably null |
Het |
Elovl5 |
T |
C |
9: 77,868,199 (GRCm39) |
V37A |
probably benign |
Het |
Esco1 |
A |
T |
18: 10,594,940 (GRCm39) |
N115K |
probably benign |
Het |
Fat1 |
A |
T |
8: 45,403,579 (GRCm39) |
N110I |
probably damaging |
Het |
Fezf1 |
T |
A |
6: 23,246,054 (GRCm39) |
K370N |
probably damaging |
Het |
Galnt18 |
T |
A |
7: 111,153,771 (GRCm39) |
K284N |
probably damaging |
Het |
Glt8d1 |
C |
A |
14: 30,733,580 (GRCm39) |
T355K |
possibly damaging |
Het |
Gm17455 |
G |
A |
10: 60,239,014 (GRCm39) |
R93H |
possibly damaging |
Het |
Gng8 |
T |
A |
7: 16,629,213 (GRCm39) |
D46E |
probably benign |
Het |
Gpx4 |
T |
C |
10: 79,892,011 (GRCm39) |
|
probably benign |
Het |
Grk2 |
A |
T |
19: 4,341,347 (GRCm39) |
N189K |
probably damaging |
Het |
Grm5 |
T |
C |
7: 87,779,989 (GRCm39) |
V1143A |
probably benign |
Het |
Hibch |
A |
G |
1: 52,942,055 (GRCm39) |
E237G |
possibly damaging |
Het |
Hipk2 |
C |
T |
6: 38,706,924 (GRCm39) |
A682T |
probably benign |
Het |
Hmcn1 |
G |
T |
1: 150,608,543 (GRCm39) |
|
probably benign |
Het |
Htt |
A |
G |
5: 34,979,188 (GRCm39) |
D857G |
possibly damaging |
Het |
Idh2 |
C |
T |
7: 79,748,005 (GRCm39) |
A232T |
probably damaging |
Het |
Igsf8 |
A |
G |
1: 172,146,265 (GRCm39) |
E421G |
probably benign |
Het |
Kif26a |
T |
A |
12: 112,145,905 (GRCm39) |
|
probably null |
Het |
Klhl26 |
T |
C |
8: 70,904,251 (GRCm39) |
Y519C |
probably damaging |
Het |
Lamc1 |
A |
C |
1: 153,122,682 (GRCm39) |
|
probably null |
Het |
Mical3 |
A |
T |
6: 120,936,162 (GRCm39) |
S1455T |
possibly damaging |
Het |
Mitf |
G |
A |
6: 97,971,390 (GRCm39) |
G186S |
probably benign |
Het |
Ms4a15 |
G |
A |
19: 10,958,722 (GRCm39) |
|
probably benign |
Het |
Myo5b |
A |
G |
18: 74,787,038 (GRCm39) |
E481G |
probably damaging |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Nbeal2 |
C |
A |
9: 110,456,255 (GRCm39) |
V1686L |
probably damaging |
Het |
Nedd4l |
T |
G |
18: 65,306,092 (GRCm39) |
S335A |
possibly damaging |
Het |
Nos1 |
A |
T |
5: 118,043,539 (GRCm39) |
N605Y |
probably damaging |
Het |
Nyx |
C |
A |
X: 13,353,508 (GRCm39) |
T454K |
probably benign |
Het |
Or52n2 |
A |
G |
7: 104,542,478 (GRCm39) |
L119P |
probably damaging |
Het |
Or8g55 |
T |
A |
9: 39,784,698 (GRCm39) |
N42K |
probably damaging |
Het |
Pcdhb12 |
T |
A |
18: 37,571,148 (GRCm39) |
F765I |
probably benign |
Het |
Pex3 |
C |
T |
10: 13,403,532 (GRCm39) |
G330R |
probably damaging |
Het |
Pfkfb1 |
T |
C |
X: 149,417,609 (GRCm39) |
Y339H |
probably damaging |
Het |
Pias1 |
G |
A |
9: 62,794,593 (GRCm39) |
Q26* |
probably null |
Het |
Pik3cg |
C |
A |
12: 32,254,545 (GRCm39) |
V481L |
possibly damaging |
Het |
Plcg2 |
C |
T |
8: 118,282,843 (GRCm39) |
T108M |
probably damaging |
Het |
Pon2 |
G |
A |
6: 5,267,059 (GRCm39) |
|
probably benign |
Het |
Ppef2 |
A |
T |
5: 92,400,952 (GRCm39) |
|
probably benign |
Het |
Pramel21 |
G |
T |
4: 143,342,726 (GRCm39) |
V278F |
probably benign |
Het |
Ptpn22 |
A |
G |
3: 103,767,771 (GRCm39) |
K18E |
probably damaging |
Het |
Pum2 |
C |
T |
12: 8,771,736 (GRCm39) |
Q360* |
probably null |
Het |
Rab10 |
A |
C |
12: 3,302,723 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
T |
G |
10: 58,303,254 (GRCm39) |
S809A |
possibly damaging |
Het |
Rbms2 |
A |
G |
10: 127,969,539 (GRCm39) |
V348A |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,316,838 (GRCm39) |
E988G |
possibly damaging |
Het |
Rnf213 |
A |
T |
11: 119,333,946 (GRCm39) |
M3052L |
probably damaging |
Het |
Rpl14 |
C |
A |
9: 120,403,428 (GRCm39) |
|
probably benign |
Het |
Rplp0 |
A |
G |
5: 115,697,931 (GRCm39) |
Y13C |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,703,218 (GRCm39) |
|
probably benign |
Het |
Sac3d1 |
T |
C |
19: 6,168,324 (GRCm39) |
E98G |
probably damaging |
Het |
Scn10a |
T |
A |
9: 119,453,166 (GRCm39) |
D1242V |
probably damaging |
Het |
Scnn1b |
T |
C |
7: 121,498,681 (GRCm39) |
Y74H |
probably damaging |
Het |
Serpinb3a |
C |
T |
1: 106,975,212 (GRCm39) |
W198* |
probably null |
Het |
Sf3b4 |
C |
A |
3: 96,081,017 (GRCm39) |
D108E |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,032,935 (GRCm39) |
V307A |
probably damaging |
Het |
Slc2a2 |
A |
G |
3: 28,781,426 (GRCm39) |
D458G |
probably benign |
Het |
Strc |
T |
C |
2: 121,210,014 (GRCm39) |
D103G |
probably damaging |
Het |
Synrg |
T |
C |
11: 83,910,369 (GRCm39) |
I923T |
probably benign |
Het |
Tango6 |
G |
T |
8: 107,462,314 (GRCm39) |
|
probably benign |
Het |
Tas2r106 |
A |
G |
6: 131,655,539 (GRCm39) |
L104P |
probably damaging |
Het |
Tat |
C |
T |
8: 110,718,316 (GRCm39) |
P67L |
probably damaging |
Het |
Tln2 |
A |
C |
9: 67,262,479 (GRCm39) |
S593A |
probably benign |
Het |
Tmem94 |
A |
G |
11: 115,685,607 (GRCm39) |
|
probably null |
Het |
Tppp3 |
G |
A |
8: 106,194,804 (GRCm39) |
A109V |
probably benign |
Het |
Trank1 |
T |
C |
9: 111,220,361 (GRCm39) |
F2366S |
probably benign |
Het |
Trpc5 |
T |
A |
X: 143,264,392 (GRCm39) |
Y155F |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,151,268 (GRCm39) |
T451A |
probably benign |
Het |
Ttc9 |
C |
A |
12: 81,678,423 (GRCm39) |
A82E |
probably damaging |
Het |
Ttll11 |
T |
A |
2: 35,834,886 (GRCm39) |
N180I |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,566,743 (GRCm39) |
N28050S |
possibly damaging |
Het |
Vmn2r73 |
G |
T |
7: 85,522,140 (GRCm39) |
H66Q |
probably benign |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Wnt3 |
G |
A |
11: 103,703,141 (GRCm39) |
C208Y |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,978,325 (GRCm39) |
C696F |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,979,927 (GRCm39) |
D162G |
probably damaging |
Het |
Zfp869 |
A |
T |
8: 70,159,054 (GRCm39) |
H506Q |
probably damaging |
Het |
|
Other mutations in Adam28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Adam28
|
APN |
14 |
68,859,569 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL00654:Adam28
|
APN |
14 |
68,886,877 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01021:Adam28
|
APN |
14 |
68,879,563 (GRCm39) |
missense |
probably benign |
|
IGL01099:Adam28
|
APN |
14 |
68,874,778 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01349:Adam28
|
APN |
14 |
68,848,455 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01744:Adam28
|
APN |
14 |
68,844,956 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01805:Adam28
|
APN |
14 |
68,879,540 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02007:Adam28
|
APN |
14 |
68,870,668 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02828:Adam28
|
APN |
14 |
68,884,319 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03180:Adam28
|
APN |
14 |
68,874,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Adam28
|
APN |
14 |
68,872,252 (GRCm39) |
splice site |
probably benign |
|
IGL02980:Adam28
|
UTSW |
14 |
68,857,255 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4453001:Adam28
|
UTSW |
14 |
68,872,325 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:Adam28
|
UTSW |
14 |
68,874,822 (GRCm39) |
missense |
probably benign |
0.33 |
R0321:Adam28
|
UTSW |
14 |
68,855,200 (GRCm39) |
missense |
probably damaging |
0.97 |
R0329:Adam28
|
UTSW |
14 |
68,855,188 (GRCm39) |
missense |
probably damaging |
0.96 |
R0605:Adam28
|
UTSW |
14 |
68,844,049 (GRCm39) |
unclassified |
probably benign |
|
R0732:Adam28
|
UTSW |
14 |
68,874,796 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Adam28
|
UTSW |
14 |
68,845,387 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1319:Adam28
|
UTSW |
14 |
68,846,578 (GRCm39) |
missense |
probably benign |
0.28 |
R1745:Adam28
|
UTSW |
14 |
68,870,620 (GRCm39) |
missense |
probably benign |
0.04 |
R1836:Adam28
|
UTSW |
14 |
68,886,870 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1838:Adam28
|
UTSW |
14 |
68,876,659 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1839:Adam28
|
UTSW |
14 |
68,876,659 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1850:Adam28
|
UTSW |
14 |
68,876,644 (GRCm39) |
missense |
probably benign |
0.01 |
R1912:Adam28
|
UTSW |
14 |
68,881,780 (GRCm39) |
missense |
probably benign |
0.24 |
R2830:Adam28
|
UTSW |
14 |
68,864,363 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2889:Adam28
|
UTSW |
14 |
68,872,294 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3977:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R3978:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R3979:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R4282:Adam28
|
UTSW |
14 |
68,885,155 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4416:Adam28
|
UTSW |
14 |
68,859,531 (GRCm39) |
critical splice donor site |
probably null |
|
R4690:Adam28
|
UTSW |
14 |
68,879,497 (GRCm39) |
missense |
probably benign |
0.01 |
R4724:Adam28
|
UTSW |
14 |
68,864,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R4768:Adam28
|
UTSW |
14 |
68,872,264 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4883:Adam28
|
UTSW |
14 |
68,875,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R5054:Adam28
|
UTSW |
14 |
68,855,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R5710:Adam28
|
UTSW |
14 |
68,847,357 (GRCm39) |
missense |
probably damaging |
0.96 |
R5835:Adam28
|
UTSW |
14 |
68,893,130 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6002:Adam28
|
UTSW |
14 |
68,879,511 (GRCm39) |
missense |
probably benign |
|
R6054:Adam28
|
UTSW |
14 |
68,879,601 (GRCm39) |
missense |
probably benign |
0.01 |
R6349:Adam28
|
UTSW |
14 |
68,870,621 (GRCm39) |
missense |
probably benign |
0.29 |
R6449:Adam28
|
UTSW |
14 |
68,868,116 (GRCm39) |
missense |
probably benign |
0.31 |
R6455:Adam28
|
UTSW |
14 |
68,870,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Adam28
|
UTSW |
14 |
68,855,576 (GRCm39) |
missense |
probably benign |
0.04 |
R6833:Adam28
|
UTSW |
14 |
68,855,576 (GRCm39) |
missense |
probably benign |
0.04 |
R7212:Adam28
|
UTSW |
14 |
68,874,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R7411:Adam28
|
UTSW |
14 |
68,864,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Adam28
|
UTSW |
14 |
68,864,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Adam28
|
UTSW |
14 |
68,868,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R7649:Adam28
|
UTSW |
14 |
68,872,282 (GRCm39) |
missense |
probably benign |
0.12 |
R7765:Adam28
|
UTSW |
14 |
68,846,555 (GRCm39) |
critical splice donor site |
probably null |
|
R8469:Adam28
|
UTSW |
14 |
68,844,029 (GRCm39) |
missense |
probably benign |
0.16 |
R8520:Adam28
|
UTSW |
14 |
68,879,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R9026:Adam28
|
UTSW |
14 |
68,846,593 (GRCm39) |
missense |
probably benign |
0.16 |
R9163:Adam28
|
UTSW |
14 |
68,866,531 (GRCm39) |
missense |
probably damaging |
0.98 |
R9264:Adam28
|
UTSW |
14 |
68,844,914 (GRCm39) |
missense |
probably benign |
|
R9304:Adam28
|
UTSW |
14 |
68,874,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Adam28
|
UTSW |
14 |
68,879,479 (GRCm39) |
missense |
probably benign |
0.36 |
R9441:Adam28
|
UTSW |
14 |
68,874,943 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Adam28
|
UTSW |
14 |
68,864,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|