Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
A |
T |
7: 40,642,480 (GRCm39) |
T141S |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,333,132 (GRCm39) |
I625N |
possibly damaging |
Het |
Adam33 |
C |
A |
2: 130,893,391 (GRCm39) |
|
probably benign |
Het |
Adgrl2 |
A |
T |
3: 148,528,617 (GRCm39) |
I1185N |
probably damaging |
Het |
Afp |
A |
T |
5: 90,649,486 (GRCm39) |
|
probably benign |
Het |
Aggf1 |
A |
G |
13: 95,501,356 (GRCm39) |
V342A |
probably benign |
Het |
Ankrd11 |
A |
T |
8: 123,619,789 (GRCm39) |
S1333R |
probably benign |
Het |
Arhgef11 |
C |
A |
3: 87,640,776 (GRCm39) |
S1311* |
probably null |
Het |
Atp6v1g1 |
T |
C |
4: 63,466,878 (GRCm39) |
Y47H |
probably benign |
Het |
Atp8b4 |
T |
C |
2: 126,165,013 (GRCm39) |
|
probably null |
Het |
Barx2 |
A |
G |
9: 31,770,327 (GRCm39) |
L67P |
probably damaging |
Het |
Bbs7 |
G |
A |
3: 36,627,706 (GRCm39) |
P694S |
probably benign |
Het |
Btbd10 |
A |
T |
7: 112,946,266 (GRCm39) |
V33E |
probably benign |
Het |
C2 |
T |
C |
17: 35,091,457 (GRCm39) |
T69A |
possibly damaging |
Het |
C8b |
T |
G |
4: 104,641,679 (GRCm39) |
L205R |
possibly damaging |
Het |
Cct4 |
T |
G |
11: 22,944,333 (GRCm39) |
N72K |
probably damaging |
Het |
Cd300lg |
C |
A |
11: 101,944,981 (GRCm39) |
P353H |
possibly damaging |
Het |
Cdh20 |
A |
T |
1: 104,875,222 (GRCm39) |
I335L |
possibly damaging |
Het |
Cfhr2 |
T |
A |
1: 139,738,757 (GRCm39) |
H268L |
probably benign |
Het |
Chia1 |
T |
A |
3: 106,036,255 (GRCm39) |
D278E |
probably benign |
Het |
Cntn6 |
A |
G |
6: 104,781,359 (GRCm39) |
T482A |
possibly damaging |
Het |
Cst13 |
T |
A |
2: 148,665,016 (GRCm39) |
F4I |
probably benign |
Het |
Ctsc |
T |
A |
7: 87,930,706 (GRCm39) |
V95E |
probably damaging |
Het |
Ddhd1 |
A |
T |
14: 45,842,508 (GRCm39) |
|
probably null |
Het |
Dmxl2 |
A |
T |
9: 54,322,712 (GRCm39) |
|
probably null |
Het |
Dnah5 |
A |
C |
15: 28,402,059 (GRCm39) |
T3407P |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,735,665 (GRCm39) |
Y1344* |
probably null |
Het |
Eif4g3 |
T |
C |
4: 137,933,395 (GRCm39) |
V1740A |
probably damaging |
Het |
Epb41l5 |
A |
G |
1: 119,506,634 (GRCm39) |
|
probably benign |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Fnbp1l |
C |
T |
3: 122,339,955 (GRCm39) |
R499Q |
probably damaging |
Het |
Gm10033 |
T |
C |
8: 69,826,022 (GRCm39) |
|
noncoding transcript |
Het |
Gm12790 |
A |
G |
4: 101,825,396 (GRCm39) |
L6P |
probably benign |
Het |
Gramd4 |
A |
G |
15: 86,009,397 (GRCm39) |
D210G |
probably damaging |
Het |
Hectd3 |
T |
C |
4: 116,859,466 (GRCm39) |
S697P |
possibly damaging |
Het |
Hsf4 |
T |
C |
8: 106,002,235 (GRCm39) |
V399A |
probably benign |
Het |
Hyal6 |
T |
A |
6: 24,743,434 (GRCm39) |
C377S |
probably damaging |
Het |
Myb |
C |
T |
10: 21,028,844 (GRCm39) |
V85M |
probably damaging |
Het |
Mypn |
A |
G |
10: 62,988,636 (GRCm39) |
V463A |
probably damaging |
Het |
Nav1 |
T |
A |
1: 135,388,163 (GRCm39) |
I1144L |
probably benign |
Het |
Nckap5 |
A |
G |
1: 125,942,398 (GRCm39) |
|
probably benign |
Het |
Nipbl |
A |
T |
15: 8,401,657 (GRCm39) |
S30T |
probably damaging |
Het |
Nmt1 |
T |
C |
11: 102,948,307 (GRCm39) |
F277S |
probably damaging |
Het |
Nploc4 |
A |
C |
11: 120,274,115 (GRCm39) |
|
probably benign |
Het |
Nup54 |
C |
A |
5: 92,576,080 (GRCm39) |
R137I |
probably damaging |
Het |
Or52n2b |
T |
C |
7: 104,565,963 (GRCm39) |
Y180C |
probably damaging |
Het |
Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
Pkd1l1 |
G |
T |
11: 8,804,487 (GRCm39) |
Y1701* |
probably null |
Het |
Plekhg6 |
T |
C |
6: 125,340,072 (GRCm39) |
T763A |
probably damaging |
Het |
Pmepa1 |
C |
T |
2: 173,070,368 (GRCm39) |
|
probably null |
Het |
Ppfia2 |
A |
G |
10: 106,666,518 (GRCm39) |
E408G |
possibly damaging |
Het |
Pramel13 |
G |
A |
4: 144,121,658 (GRCm39) |
T122M |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
Shisal2b |
A |
T |
13: 105,000,113 (GRCm39) |
C37S |
probably damaging |
Het |
Slc13a1 |
A |
T |
6: 24,118,082 (GRCm39) |
|
probably null |
Het |
Slc17a8 |
T |
A |
10: 89,427,076 (GRCm39) |
T342S |
probably damaging |
Het |
Slc30a9 |
A |
G |
5: 67,510,005 (GRCm39) |
E519G |
probably benign |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Slc39a5 |
G |
A |
10: 128,233,610 (GRCm39) |
L296F |
probably damaging |
Het |
Slco6b1 |
A |
C |
1: 96,857,610 (GRCm39) |
|
noncoding transcript |
Het |
Slco6d1 |
G |
A |
1: 98,418,341 (GRCm39) |
G509D |
probably damaging |
Het |
Spen |
A |
G |
4: 141,199,132 (GRCm39) |
V3142A |
probably damaging |
Het |
Spta1 |
T |
A |
1: 174,050,250 (GRCm39) |
H1763Q |
probably damaging |
Het |
Srcap |
T |
C |
7: 127,159,124 (GRCm39) |
|
probably benign |
Het |
Stard9 |
T |
C |
2: 120,543,328 (GRCm39) |
|
probably benign |
Het |
Stat4 |
A |
G |
1: 52,111,106 (GRCm39) |
|
probably benign |
Het |
Svbp |
T |
A |
4: 119,053,225 (GRCm39) |
|
probably benign |
Het |
Tm2d1 |
A |
T |
4: 98,258,833 (GRCm39) |
|
probably benign |
Het |
Trpv1 |
C |
A |
11: 73,130,952 (GRCm39) |
|
probably null |
Het |
Trrap |
A |
G |
5: 144,794,232 (GRCm39) |
D3713G |
possibly damaging |
Het |
Ubr1 |
T |
A |
2: 120,786,125 (GRCm39) |
D165V |
probably benign |
Het |
Utrn |
C |
A |
10: 12,524,897 (GRCm39) |
M2195I |
probably benign |
Het |
Vmn1r229 |
G |
A |
17: 21,034,904 (GRCm39) |
V50I |
possibly damaging |
Het |
Vmn1r44 |
A |
T |
6: 89,870,632 (GRCm39) |
H126L |
probably benign |
Het |
Vmn2r116 |
T |
C |
17: 23,605,570 (GRCm39) |
|
probably benign |
Het |
Vmn2r27 |
A |
C |
6: 124,168,591 (GRCm39) |
Y846* |
probably null |
Het |
Vmn2r84 |
T |
A |
10: 130,227,859 (GRCm39) |
S126C |
possibly damaging |
Het |
Xylb |
T |
A |
9: 119,197,133 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
A |
T |
6: 47,867,108 (GRCm39) |
K232* |
probably null |
Het |
Zfp39 |
C |
A |
11: 58,781,149 (GRCm39) |
V538L |
probably benign |
Het |
Zfp560 |
T |
C |
9: 20,263,149 (GRCm39) |
N76D |
possibly damaging |
Het |
Zmym4 |
C |
T |
4: 126,804,962 (GRCm39) |
V433I |
probably benign |
Het |
Zscan5b |
A |
G |
7: 6,233,425 (GRCm39) |
E83G |
probably damaging |
Het |
|
Other mutations in Prl8a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02654:Prl8a2
|
APN |
13 |
27,536,780 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL03268:Prl8a2
|
APN |
13 |
27,537,938 (GRCm39) |
missense |
probably benign |
0.09 |
R0557:Prl8a2
|
UTSW |
13 |
27,536,875 (GRCm39) |
nonsense |
probably null |
|
R0574:Prl8a2
|
UTSW |
13 |
27,532,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R1166:Prl8a2
|
UTSW |
13 |
27,537,935 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1875:Prl8a2
|
UTSW |
13 |
27,535,037 (GRCm39) |
missense |
probably benign |
0.02 |
R2420:Prl8a2
|
UTSW |
13 |
27,532,896 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4152:Prl8a2
|
UTSW |
13 |
27,534,985 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5285:Prl8a2
|
UTSW |
13 |
27,534,116 (GRCm39) |
splice site |
probably null |
|
R6452:Prl8a2
|
UTSW |
13 |
27,536,780 (GRCm39) |
missense |
probably benign |
0.08 |
R6906:Prl8a2
|
UTSW |
13 |
27,532,900 (GRCm39) |
missense |
probably benign |
0.03 |
R7217:Prl8a2
|
UTSW |
13 |
27,534,998 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7490:Prl8a2
|
UTSW |
13 |
27,536,753 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8170:Prl8a2
|
UTSW |
13 |
27,536,794 (GRCm39) |
missense |
probably benign |
|
R9099:Prl8a2
|
UTSW |
13 |
27,536,794 (GRCm39) |
missense |
probably benign |
0.01 |
R9099:Prl8a2
|
UTSW |
13 |
27,536,793 (GRCm39) |
nonsense |
probably null |
|
R9244:Prl8a2
|
UTSW |
13 |
27,534,982 (GRCm39) |
missense |
probably benign |
0.00 |
|