Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt2 |
A |
C |
7: 27,337,499 (GRCm39) |
D417A |
probably benign |
Het |
Ap1b1 |
T |
A |
11: 4,969,336 (GRCm39) |
S231T |
possibly damaging |
Het |
Arhgap31 |
G |
A |
16: 38,421,935 (GRCm39) |
T1377I |
probably damaging |
Het |
Cdkl3 |
A |
G |
11: 51,895,896 (GRCm39) |
T48A |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,251,501 (GRCm39) |
Y510C |
probably damaging |
Het |
Chml |
A |
G |
1: 175,515,751 (GRCm39) |
S57P |
probably damaging |
Het |
Cpxm1 |
G |
T |
2: 130,236,060 (GRCm39) |
C367* |
probably null |
Het |
D930020B18Rik |
A |
G |
10: 121,528,319 (GRCm39) |
T428A |
probably damaging |
Het |
Dnaja3 |
A |
T |
16: 4,519,033 (GRCm39) |
I325F |
probably damaging |
Het |
Efcab3 |
A |
T |
11: 104,612,258 (GRCm39) |
|
probably benign |
Het |
Erbb3 |
A |
G |
10: 128,407,519 (GRCm39) |
V943A |
probably benign |
Het |
Fam110b |
A |
G |
4: 5,799,481 (GRCm39) |
I300V |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,588,537 (GRCm39) |
E76G |
probably damaging |
Het |
Fbxl3 |
G |
A |
14: 103,332,900 (GRCm39) |
T26M |
possibly damaging |
Het |
Furin |
A |
G |
7: 80,042,647 (GRCm39) |
L380P |
probably damaging |
Het |
Fxr2 |
A |
C |
11: 69,541,328 (GRCm39) |
I354L |
possibly damaging |
Het |
Garnl3 |
G |
T |
2: 32,887,741 (GRCm39) |
N756K |
probably damaging |
Het |
Gimap1 |
A |
G |
6: 48,720,258 (GRCm39) |
Y290C |
probably damaging |
Het |
Gm5592 |
G |
A |
7: 40,935,795 (GRCm39) |
W99* |
probably null |
Het |
Hexd |
G |
T |
11: 121,107,819 (GRCm39) |
S183I |
possibly damaging |
Het |
Hmg20a |
C |
T |
9: 56,384,514 (GRCm39) |
P95S |
probably damaging |
Het |
Jhy |
A |
T |
9: 40,806,842 (GRCm39) |
I769N |
probably damaging |
Het |
Lrrd1 |
G |
T |
5: 3,901,267 (GRCm39) |
C524F |
probably damaging |
Het |
Musk |
C |
A |
4: 58,296,629 (GRCm39) |
S76R |
probably damaging |
Het |
Myom3 |
C |
T |
4: 135,513,160 (GRCm39) |
R613* |
probably null |
Het |
Naa16 |
T |
A |
14: 79,618,956 (GRCm39) |
E172D |
probably benign |
Het |
Or5al5 |
A |
T |
2: 85,961,174 (GRCm39) |
Y278N |
probably benign |
Het |
Pam |
C |
T |
1: 97,762,166 (GRCm39) |
V700M |
probably damaging |
Het |
Phf8-ps |
C |
T |
17: 33,286,628 (GRCm39) |
G58E |
probably damaging |
Het |
Pkd1l2 |
C |
A |
8: 117,743,655 (GRCm39) |
R1978L |
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,593,791 (GRCm39) |
T1441S |
possibly damaging |
Het |
Plg |
A |
G |
17: 12,621,934 (GRCm39) |
|
probably benign |
Het |
Pot1a |
A |
G |
6: 25,750,099 (GRCm39) |
L521P |
probably damaging |
Het |
Pramel14 |
G |
A |
4: 143,720,924 (GRCm39) |
P6S |
probably damaging |
Het |
Ptprj |
A |
T |
2: 90,270,256 (GRCm39) |
V1280E |
probably damaging |
Het |
Rcbtb2 |
T |
C |
14: 73,402,222 (GRCm39) |
S136P |
possibly damaging |
Het |
Rtl1 |
C |
T |
12: 109,558,369 (GRCm39) |
E1157K |
possibly damaging |
Het |
Sell |
G |
A |
1: 163,893,195 (GRCm39) |
R137Q |
probably benign |
Het |
Shisa9 |
A |
T |
16: 12,062,522 (GRCm39) |
M248L |
probably benign |
Het |
Spag17 |
A |
G |
3: 99,966,149 (GRCm39) |
E1144G |
probably benign |
Het |
Sphk2 |
G |
T |
7: 45,360,157 (GRCm39) |
Q616K |
probably benign |
Het |
Tecrl |
T |
C |
5: 83,442,453 (GRCm39) |
T207A |
probably benign |
Het |
Ubr5 |
T |
C |
15: 37,996,842 (GRCm39) |
T1885A |
probably benign |
Het |
Usp24 |
T |
C |
4: 106,232,965 (GRCm39) |
|
probably benign |
Het |
Usp32 |
A |
G |
11: 84,927,350 (GRCm39) |
M622T |
probably benign |
Het |
Vangl1 |
A |
G |
3: 102,091,607 (GRCm39) |
F160L |
probably damaging |
Het |
Vps13d |
T |
C |
4: 144,813,317 (GRCm39) |
S3289G |
probably damaging |
Het |
Wdfy4 |
A |
G |
14: 32,855,673 (GRCm39) |
F647S |
probably damaging |
Het |
Wdhd1 |
A |
G |
14: 47,498,907 (GRCm39) |
L509P |
probably damaging |
Het |
Zcchc2 |
A |
G |
1: 105,955,229 (GRCm39) |
E640G |
probably damaging |
Het |
Zfp563 |
T |
A |
17: 33,324,383 (GRCm39) |
I326N |
probably benign |
Het |
|
Other mutations in Obox6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00705:Obox6
|
APN |
7 |
15,567,662 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02066:Obox6
|
APN |
7 |
15,568,628 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02070:Obox6
|
APN |
7 |
15,568,804 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02450:Obox6
|
APN |
7 |
15,567,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R0091:Obox6
|
UTSW |
7 |
15,568,364 (GRCm39) |
missense |
probably benign |
0.38 |
R0512:Obox6
|
UTSW |
7 |
15,567,874 (GRCm39) |
missense |
probably benign |
0.42 |
R1686:Obox6
|
UTSW |
7 |
15,567,750 (GRCm39) |
missense |
probably damaging |
0.99 |
R1727:Obox6
|
UTSW |
7 |
15,568,502 (GRCm39) |
missense |
probably benign |
0.04 |
R1755:Obox6
|
UTSW |
7 |
15,568,445 (GRCm39) |
missense |
probably damaging |
0.98 |
R1813:Obox6
|
UTSW |
7 |
15,568,770 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1896:Obox6
|
UTSW |
7 |
15,568,770 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2086:Obox6
|
UTSW |
7 |
15,567,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Obox6
|
UTSW |
7 |
15,568,738 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4732:Obox6
|
UTSW |
7 |
15,568,697 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4733:Obox6
|
UTSW |
7 |
15,568,697 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4790:Obox6
|
UTSW |
7 |
15,568,502 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5830:Obox6
|
UTSW |
7 |
15,568,382 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6838:Obox6
|
UTSW |
7 |
15,567,664 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7275:Obox6
|
UTSW |
7 |
15,567,805 (GRCm39) |
missense |
probably benign |
0.19 |
R7347:Obox6
|
UTSW |
7 |
15,568,571 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7485:Obox6
|
UTSW |
7 |
15,567,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Obox6
|
UTSW |
7 |
15,567,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8438:Obox6
|
UTSW |
7 |
15,567,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8802:Obox6
|
UTSW |
7 |
15,567,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R9274:Obox6
|
UTSW |
7 |
15,567,766 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9340:Obox6
|
UTSW |
7 |
15,567,722 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9566:Obox6
|
UTSW |
7 |
15,568,352 (GRCm39) |
missense |
|
|
R9641:Obox6
|
UTSW |
7 |
15,568,742 (GRCm39) |
nonsense |
probably null |
|
R9722:Obox6
|
UTSW |
7 |
15,568,831 (GRCm39) |
missense |
probably benign |
0.01 |
|