Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
A |
T |
14: 35,533,418 (GRCm39) |
|
probably null |
Het |
Abcb4 |
T |
A |
5: 8,997,376 (GRCm39) |
C952S |
probably damaging |
Het |
Adamtsl2 |
A |
G |
2: 26,979,647 (GRCm39) |
D272G |
probably benign |
Het |
Aim2 |
G |
A |
1: 173,289,530 (GRCm39) |
D158N |
probably damaging |
Het |
Aldh3b1 |
C |
T |
19: 3,964,024 (GRCm39) |
R426H |
probably damaging |
Het |
Apoc2 |
A |
G |
7: 19,407,278 (GRCm39) |
S28P |
probably benign |
Het |
Arfgef3 |
G |
A |
10: 18,473,179 (GRCm39) |
T1628I |
probably benign |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
Bmp8b |
T |
A |
4: 123,015,692 (GRCm39) |
D226E |
probably benign |
Het |
Brsk2 |
T |
C |
7: 141,552,229 (GRCm39) |
Y618H |
probably damaging |
Het |
Casp12 |
T |
A |
9: 5,346,554 (GRCm39) |
F27Y |
probably damaging |
Het |
Casp8 |
T |
A |
1: 58,883,951 (GRCm39) |
N439K |
probably benign |
Het |
Ccdc175 |
T |
A |
12: 72,204,281 (GRCm39) |
K253N |
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 179,867,744 (GRCm39) |
H193R |
probably damaging |
Het |
Cdk17 |
T |
C |
10: 93,052,334 (GRCm39) |
M105T |
probably benign |
Het |
Cdon |
C |
A |
9: 35,389,907 (GRCm39) |
P854T |
probably damaging |
Het |
Cep44 |
A |
G |
8: 56,997,187 (GRCm39) |
M117T |
possibly damaging |
Het |
Cep89 |
A |
T |
7: 35,134,955 (GRCm39) |
E674D |
probably damaging |
Het |
Cit |
C |
T |
5: 116,012,002 (GRCm39) |
A203V |
probably damaging |
Het |
Clstn1 |
C |
A |
4: 149,713,757 (GRCm39) |
|
probably null |
Het |
Col7a1 |
T |
A |
9: 108,787,215 (GRCm39) |
D565E |
unknown |
Het |
Cpb1 |
T |
A |
3: 20,316,638 (GRCm39) |
Y304F |
probably damaging |
Het |
Cps1 |
T |
G |
1: 67,211,961 (GRCm39) |
Y710D |
probably damaging |
Het |
Creb3l1 |
T |
C |
2: 91,817,398 (GRCm39) |
T372A |
possibly damaging |
Het |
Dars1 |
A |
G |
1: 128,333,118 (GRCm39) |
V102A |
probably benign |
Het |
Dhx35 |
C |
T |
2: 158,659,335 (GRCm39) |
T168I |
possibly damaging |
Het |
Dnah5 |
T |
C |
15: 28,327,925 (GRCm39) |
S2100P |
probably benign |
Het |
Dst |
T |
C |
1: 34,306,041 (GRCm39) |
|
probably null |
Het |
Egflam |
A |
C |
15: 7,283,004 (GRCm39) |
L351R |
possibly damaging |
Het |
Elp2 |
T |
A |
18: 24,759,213 (GRCm39) |
D523E |
probably benign |
Het |
Exo5 |
C |
A |
4: 120,778,881 (GRCm39) |
G328V |
probably damaging |
Het |
Fut9 |
A |
G |
4: 25,620,811 (GRCm39) |
M1T |
probably null |
Het |
Galnt5 |
A |
G |
2: 57,914,637 (GRCm39) |
N584S |
possibly damaging |
Het |
Gbp3 |
T |
C |
3: 142,273,533 (GRCm39) |
V360A |
probably damaging |
Het |
Gdf6 |
G |
A |
4: 9,859,977 (GRCm39) |
C353Y |
probably damaging |
Het |
Hace1 |
A |
G |
10: 45,524,965 (GRCm39) |
T244A |
probably damaging |
Het |
Hr |
T |
C |
14: 70,797,097 (GRCm39) |
I500T |
probably benign |
Het |
Ifnl2 |
A |
T |
7: 28,208,707 (GRCm39) |
L115Q |
probably damaging |
Het |
Iigp1 |
T |
C |
18: 60,522,896 (GRCm39) |
F5L |
probably benign |
Het |
Inhbb |
A |
G |
1: 119,345,146 (GRCm39) |
L381P |
probably damaging |
Het |
Irx3 |
A |
T |
8: 92,527,721 (GRCm39) |
S50T |
probably benign |
Het |
Ivns1abp |
C |
T |
1: 151,235,896 (GRCm39) |
T363I |
probably benign |
Het |
Izumo1 |
A |
T |
7: 45,272,323 (GRCm39) |
T35S |
probably benign |
Het |
Kank4 |
A |
G |
4: 98,665,342 (GRCm39) |
S651P |
probably damaging |
Het |
Kit |
T |
C |
5: 75,771,539 (GRCm39) |
V232A |
probably benign |
Het |
Klhl11 |
T |
C |
11: 100,354,540 (GRCm39) |
Y427C |
probably damaging |
Het |
Laptm4b |
T |
A |
15: 34,258,835 (GRCm39) |
N36K |
probably damaging |
Het |
Lrrk1 |
T |
C |
7: 65,916,363 (GRCm39) |
|
probably null |
Het |
Mamdc4 |
G |
T |
2: 25,454,205 (GRCm39) |
Q1042K |
probably benign |
Het |
Mical2 |
A |
G |
7: 111,920,647 (GRCm39) |
|
probably null |
Het |
Ms4a3 |
C |
A |
19: 11,608,725 (GRCm39) |
V176F |
possibly damaging |
Het |
Myo3a |
T |
C |
2: 22,338,324 (GRCm39) |
V427A |
probably benign |
Het |
Myo3a |
A |
C |
2: 22,401,110 (GRCm39) |
E626D |
possibly damaging |
Het |
Nckap5 |
A |
T |
1: 125,955,025 (GRCm39) |
L509* |
probably null |
Het |
Ndufa5 |
A |
T |
6: 24,519,248 (GRCm39) |
D64E |
possibly damaging |
Het |
Nedd4l |
T |
C |
18: 65,341,532 (GRCm39) |
Y753H |
probably damaging |
Het |
Nynrin |
T |
C |
14: 56,110,218 (GRCm39) |
V1775A |
probably damaging |
Het |
Oplah |
A |
G |
15: 76,187,192 (GRCm39) |
S570P |
probably benign |
Het |
Or14c39 |
T |
C |
7: 86,344,084 (GRCm39) |
V140A |
possibly damaging |
Het |
Or2ag1b |
A |
T |
7: 106,288,205 (GRCm39) |
H244Q |
probably damaging |
Het |
Or4q3 |
T |
C |
14: 50,583,383 (GRCm39) |
Y141C |
probably damaging |
Het |
Or5t18 |
A |
G |
2: 86,637,205 (GRCm39) |
L46S |
probably damaging |
Het |
Or9r3 |
G |
A |
10: 129,948,449 (GRCm39) |
S70F |
probably damaging |
Het |
Osbpl11 |
C |
A |
16: 33,054,814 (GRCm39) |
Y632* |
probably null |
Het |
Osbpl5 |
A |
T |
7: 143,248,558 (GRCm39) |
L644Q |
probably damaging |
Het |
Pcdhb19 |
T |
C |
18: 37,631,005 (GRCm39) |
W267R |
probably benign |
Het |
Pkhd1l1 |
A |
C |
15: 44,330,820 (GRCm39) |
S132R |
possibly damaging |
Het |
Pramel23 |
A |
T |
4: 143,425,073 (GRCm39) |
D123E |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,704,011 (GRCm39) |
S1348T |
probably benign |
Het |
Rc3h1 |
T |
A |
1: 160,757,705 (GRCm39) |
W8R |
probably damaging |
Het |
Rgs3 |
T |
G |
4: 62,544,173 (GRCm39) |
V315G |
probably damaging |
Het |
Rora |
T |
A |
9: 69,269,151 (GRCm39) |
M82K |
probably damaging |
Het |
Rph3al |
T |
C |
11: 75,799,795 (GRCm39) |
I55V |
probably benign |
Het |
Sag |
T |
C |
1: 87,740,713 (GRCm39) |
V45A |
probably damaging |
Het |
Scn3a |
T |
C |
2: 65,366,854 (GRCm39) |
E56G |
probably damaging |
Het |
Sec24c |
T |
G |
14: 20,737,016 (GRCm39) |
V324G |
probably damaging |
Het |
Sptbn1 |
A |
G |
11: 30,088,979 (GRCm39) |
L748S |
probably damaging |
Het |
Stard9 |
A |
T |
2: 120,536,787 (GRCm39) |
D4186V |
probably damaging |
Het |
Stk39 |
T |
C |
2: 68,196,511 (GRCm39) |
E306G |
probably damaging |
Het |
Sycp1 |
C |
A |
3: 102,806,165 (GRCm39) |
|
probably null |
Het |
Taf2 |
A |
C |
15: 54,923,446 (GRCm39) |
L277R |
probably damaging |
Het |
Tasor |
C |
T |
14: 27,183,707 (GRCm39) |
T722I |
probably benign |
Het |
Tbc1d23 |
T |
A |
16: 56,993,469 (GRCm39) |
I566F |
possibly damaging |
Het |
Tekt5 |
T |
C |
16: 10,179,168 (GRCm39) |
T400A |
possibly damaging |
Het |
Tgfbrap1 |
T |
C |
1: 43,099,301 (GRCm39) |
H401R |
probably benign |
Het |
Tie1 |
T |
A |
4: 118,333,344 (GRCm39) |
I841L |
possibly damaging |
Het |
Tln1 |
T |
G |
4: 43,544,645 (GRCm39) |
T1095P |
possibly damaging |
Het |
Tmem147 |
A |
G |
7: 30,427,527 (GRCm39) |
Y72H |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,419,941 (GRCm39) |
N691S |
probably benign |
Het |
Trim24 |
G |
A |
6: 37,934,718 (GRCm39) |
C811Y |
probably damaging |
Het |
Trim30b |
T |
A |
7: 104,007,183 (GRCm39) |
|
probably benign |
Het |
Trpc4 |
T |
G |
3: 54,102,189 (GRCm39) |
L29R |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,803,226 (GRCm39) |
I890F |
probably damaging |
Het |
Ttc23l |
C |
T |
15: 10,504,622 (GRCm39) |
E442K |
probably benign |
Het |
Tut7 |
A |
T |
13: 59,947,596 (GRCm39) |
C506* |
probably null |
Het |
Uggt2 |
A |
G |
14: 119,332,748 (GRCm39) |
V62A |
probably damaging |
Het |
Ugt1a6a |
C |
A |
1: 88,066,606 (GRCm39) |
S137R |
probably benign |
Het |
Unc13a |
A |
G |
8: 72,111,111 (GRCm39) |
Y367H |
probably damaging |
Het |
Vmn2r49 |
A |
G |
7: 9,710,233 (GRCm39) |
I833T |
probably benign |
Het |
Vmn2r7 |
T |
C |
3: 64,623,900 (GRCm39) |
D231G |
probably benign |
Het |
Ythdc2 |
A |
T |
18: 44,997,424 (GRCm39) |
M994L |
probably benign |
Het |
Zfp804a |
G |
A |
2: 82,087,932 (GRCm39) |
S587N |
probably damaging |
Het |
Zswim2 |
A |
G |
2: 83,754,003 (GRCm39) |
I219T |
probably benign |
Het |
|
Other mutations in Atp10a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00649:Atp10a
|
APN |
7 |
58,444,230 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00973:Atp10a
|
APN |
7 |
58,457,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00984:Atp10a
|
APN |
7 |
58,308,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01086:Atp10a
|
APN |
7 |
58,474,066 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01296:Atp10a
|
APN |
7 |
58,463,373 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01731:Atp10a
|
APN |
7 |
58,447,310 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02081:Atp10a
|
APN |
7 |
58,477,604 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02095:Atp10a
|
APN |
7 |
58,457,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02549:Atp10a
|
APN |
7 |
58,469,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02558:Atp10a
|
APN |
7 |
58,469,390 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02659:Atp10a
|
APN |
7 |
58,463,379 (GRCm39) |
missense |
probably benign |
|
IGL02986:Atp10a
|
APN |
7 |
58,478,469 (GRCm39) |
missense |
probably benign |
|
IGL03218:Atp10a
|
APN |
7 |
58,438,196 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4260001:Atp10a
|
UTSW |
7 |
58,440,866 (GRCm39) |
nonsense |
probably null |
|
PIT4445001:Atp10a
|
UTSW |
7 |
58,453,215 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4810001:Atp10a
|
UTSW |
7 |
58,463,596 (GRCm39) |
missense |
probably damaging |
0.99 |
R0091:Atp10a
|
UTSW |
7 |
58,423,794 (GRCm39) |
splice site |
probably benign |
|
R0349:Atp10a
|
UTSW |
7 |
58,453,215 (GRCm39) |
missense |
probably damaging |
0.98 |
R0426:Atp10a
|
UTSW |
7 |
58,434,482 (GRCm39) |
missense |
probably benign |
0.00 |
R0722:Atp10a
|
UTSW |
7 |
58,465,931 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0741:Atp10a
|
UTSW |
7 |
58,478,337 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1172:Atp10a
|
UTSW |
7 |
58,453,514 (GRCm39) |
missense |
probably benign |
0.05 |
R1342:Atp10a
|
UTSW |
7 |
58,465,894 (GRCm39) |
splice site |
probably benign |
|
R1648:Atp10a
|
UTSW |
7 |
58,434,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R1715:Atp10a
|
UTSW |
7 |
58,436,253 (GRCm39) |
missense |
probably damaging |
0.98 |
R1737:Atp10a
|
UTSW |
7 |
58,476,986 (GRCm39) |
splice site |
probably benign |
|
R1799:Atp10a
|
UTSW |
7 |
58,474,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Atp10a
|
UTSW |
7 |
58,478,460 (GRCm39) |
missense |
probably benign |
0.12 |
R1918:Atp10a
|
UTSW |
7 |
58,477,683 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2031:Atp10a
|
UTSW |
7 |
58,477,678 (GRCm39) |
nonsense |
probably null |
|
R2080:Atp10a
|
UTSW |
7 |
58,474,075 (GRCm39) |
missense |
probably damaging |
0.97 |
R2424:Atp10a
|
UTSW |
7 |
58,444,303 (GRCm39) |
missense |
probably benign |
0.16 |
R2696:Atp10a
|
UTSW |
7 |
58,463,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3932:Atp10a
|
UTSW |
7 |
58,476,852 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4198:Atp10a
|
UTSW |
7 |
58,463,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4453:Atp10a
|
UTSW |
7 |
58,308,248 (GRCm39) |
small deletion |
probably benign |
|
R4632:Atp10a
|
UTSW |
7 |
58,457,186 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4661:Atp10a
|
UTSW |
7 |
58,308,248 (GRCm39) |
small deletion |
probably benign |
|
R4782:Atp10a
|
UTSW |
7 |
58,440,843 (GRCm39) |
missense |
probably benign |
|
R4888:Atp10a
|
UTSW |
7 |
58,435,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R4935:Atp10a
|
UTSW |
7 |
58,463,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5051:Atp10a
|
UTSW |
7 |
58,389,994 (GRCm39) |
frame shift |
probably null |
|
R5213:Atp10a
|
UTSW |
7 |
58,423,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R5617:Atp10a
|
UTSW |
7 |
58,453,423 (GRCm39) |
missense |
probably benign |
0.06 |
R5834:Atp10a
|
UTSW |
7 |
58,308,366 (GRCm39) |
missense |
probably benign |
0.01 |
R5885:Atp10a
|
UTSW |
7 |
58,463,548 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6013:Atp10a
|
UTSW |
7 |
58,447,538 (GRCm39) |
missense |
probably benign |
0.05 |
R6136:Atp10a
|
UTSW |
7 |
58,478,088 (GRCm39) |
missense |
probably benign |
|
R6269:Atp10a
|
UTSW |
7 |
58,453,487 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6380:Atp10a
|
UTSW |
7 |
58,469,432 (GRCm39) |
nonsense |
probably null |
|
R6743:Atp10a
|
UTSW |
7 |
58,447,562 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6875:Atp10a
|
UTSW |
7 |
58,447,100 (GRCm39) |
missense |
probably benign |
0.01 |
R6975:Atp10a
|
UTSW |
7 |
58,423,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7082:Atp10a
|
UTSW |
7 |
58,308,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Atp10a
|
UTSW |
7 |
58,436,221 (GRCm39) |
missense |
probably benign |
|
R7224:Atp10a
|
UTSW |
7 |
58,447,219 (GRCm39) |
missense |
probably benign |
0.00 |
R7287:Atp10a
|
UTSW |
7 |
58,477,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Atp10a
|
UTSW |
7 |
58,308,288 (GRCm39) |
missense |
unknown |
|
R7474:Atp10a
|
UTSW |
7 |
58,308,275 (GRCm39) |
missense |
unknown |
|
R7530:Atp10a
|
UTSW |
7 |
58,423,724 (GRCm39) |
missense |
probably benign |
0.02 |
R7561:Atp10a
|
UTSW |
7 |
58,476,881 (GRCm39) |
missense |
probably damaging |
0.98 |
R7743:Atp10a
|
UTSW |
7 |
58,453,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Atp10a
|
UTSW |
7 |
58,308,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Atp10a
|
UTSW |
7 |
58,438,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R7903:Atp10a
|
UTSW |
7 |
58,308,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R8015:Atp10a
|
UTSW |
7 |
58,453,245 (GRCm39) |
missense |
probably benign |
0.00 |
R8166:Atp10a
|
UTSW |
7 |
58,457,270 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8201:Atp10a
|
UTSW |
7 |
58,469,424 (GRCm39) |
nonsense |
probably null |
|
R8465:Atp10a
|
UTSW |
7 |
58,478,058 (GRCm39) |
missense |
probably benign |
0.32 |
R8858:Atp10a
|
UTSW |
7 |
58,465,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8985:Atp10a
|
UTSW |
7 |
58,438,092 (GRCm39) |
missense |
probably benign |
0.03 |
R9003:Atp10a
|
UTSW |
7 |
58,457,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9274:Atp10a
|
UTSW |
7 |
58,478,369 (GRCm39) |
missense |
probably benign |
0.22 |
R9385:Atp10a
|
UTSW |
7 |
58,477,887 (GRCm39) |
missense |
probably benign |
0.00 |
R9432:Atp10a
|
UTSW |
7 |
58,469,418 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9454:Atp10a
|
UTSW |
7 |
58,308,339 (GRCm39) |
missense |
probably benign |
|
R9596:Atp10a
|
UTSW |
7 |
58,477,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Atp10a
|
UTSW |
7 |
58,474,078 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Atp10a
|
UTSW |
7 |
58,438,195 (GRCm39) |
critical splice donor site |
probably null |
|
|