Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam7 |
A |
G |
14: 68,763,773 (GRCm39) |
C126R |
probably damaging |
Het |
Agpat5 |
G |
A |
8: 18,928,043 (GRCm39) |
V203I |
possibly damaging |
Het |
Ankrd12 |
T |
A |
17: 66,293,904 (GRCm39) |
R510* |
probably null |
Het |
Anxa6 |
C |
T |
11: 54,904,696 (GRCm39) |
A22T |
probably benign |
Het |
Barx2 |
A |
T |
9: 31,770,309 (GRCm39) |
L73Q |
probably damaging |
Het |
BC024139 |
T |
C |
15: 76,004,333 (GRCm39) |
K702R |
possibly damaging |
Het |
Cc2d1a |
T |
C |
8: 84,861,605 (GRCm39) |
K739R |
probably benign |
Het |
Cdk12 |
A |
G |
11: 98,141,111 (GRCm39) |
T1451A |
unknown |
Het |
Chd7 |
A |
G |
4: 8,858,675 (GRCm39) |
E2367G |
probably damaging |
Het |
Cp |
A |
G |
3: 20,025,193 (GRCm39) |
Y384C |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,468,979 (GRCm39) |
W1270R |
probably benign |
Het |
Dyrk2 |
G |
T |
10: 118,696,567 (GRCm39) |
S230R |
probably damaging |
Het |
Epn3 |
A |
T |
11: 94,384,602 (GRCm39) |
S290R |
probably damaging |
Het |
Fas |
C |
T |
19: 34,304,626 (GRCm39) |
R296C |
probably benign |
Het |
Fmnl1 |
A |
T |
11: 103,084,859 (GRCm39) |
N659I |
unknown |
Het |
Gas8 |
T |
C |
8: 124,257,777 (GRCm39) |
|
probably null |
Het |
Gpr156 |
A |
G |
16: 37,768,598 (GRCm39) |
T40A |
probably benign |
Het |
Hey1 |
G |
C |
3: 8,729,836 (GRCm39) |
A207G |
probably benign |
Het |
Htr3b |
C |
A |
9: 48,876,177 (GRCm39) |
|
probably benign |
Het |
Itgal |
C |
T |
7: 126,928,607 (GRCm39) |
T1044I |
probably benign |
Het |
Itprid2 |
A |
G |
2: 79,475,208 (GRCm39) |
Q389R |
probably benign |
Het |
Kcnip4 |
T |
G |
5: 48,639,997 (GRCm39) |
D38A |
possibly damaging |
Het |
Kcnma1 |
G |
T |
14: 23,641,706 (GRCm39) |
Q216K |
probably benign |
Het |
Kdsr |
T |
A |
1: 106,671,400 (GRCm39) |
E203V |
probably null |
Het |
Lrp1b |
T |
C |
2: 41,298,387 (GRCm39) |
E999G |
|
Het |
Malt1 |
T |
A |
18: 65,603,594 (GRCm39) |
W577R |
probably damaging |
Het |
Mroh2b |
A |
C |
15: 4,978,572 (GRCm39) |
T1373P |
probably damaging |
Het |
Mymk |
A |
G |
2: 26,952,712 (GRCm39) |
|
probably null |
Het |
Myo1f |
T |
A |
17: 33,816,992 (GRCm39) |
H707Q |
probably benign |
Het |
Ncam2 |
C |
A |
16: 81,309,867 (GRCm39) |
H452Q |
possibly damaging |
Het |
Ndrg4 |
A |
G |
8: 96,404,975 (GRCm39) |
M1V |
probably null |
Het |
Nps |
C |
T |
7: 134,874,079 (GRCm39) |
S83L |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,177,044 (GRCm39) |
Y1040* |
probably null |
Het |
Or1j15 |
T |
C |
2: 36,459,443 (GRCm39) |
Y278H |
probably damaging |
Het |
Or2ak4 |
C |
T |
11: 58,648,985 (GRCm39) |
Q165* |
probably null |
Het |
Or4f7 |
T |
C |
2: 111,645,051 (GRCm39) |
T7A |
probably benign |
Het |
Or5h22 |
C |
T |
16: 58,895,243 (GRCm39) |
V67M |
possibly damaging |
Het |
Pak1ip1 |
G |
A |
13: 41,162,770 (GRCm39) |
R191Q |
probably benign |
Het |
Pcdh17 |
G |
A |
14: 84,683,384 (GRCm39) |
|
probably benign |
Het |
Pcdhgc5 |
G |
T |
18: 37,952,945 (GRCm39) |
R73L |
probably benign |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Plxnd1 |
A |
T |
6: 115,943,866 (GRCm39) |
N1144K |
probably damaging |
Het |
Ppp1r1b |
G |
T |
11: 98,246,310 (GRCm39) |
E133D |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,705,815 (GRCm39) |
E1396G |
probably damaging |
Het |
Reps1 |
T |
C |
10: 17,970,218 (GRCm39) |
S272P |
probably damaging |
Het |
Ric8b |
T |
C |
10: 84,816,039 (GRCm39) |
V430A |
probably damaging |
Het |
Sgms1 |
A |
T |
19: 32,137,109 (GRCm39) |
F152L |
probably benign |
Het |
Snapc1 |
C |
A |
12: 74,011,506 (GRCm39) |
F57L |
probably damaging |
Het |
Spidr |
A |
G |
16: 15,786,540 (GRCm39) |
L401P |
probably damaging |
Het |
Spn |
C |
T |
7: 126,735,728 (GRCm39) |
V260M |
probably damaging |
Het |
Sptan1 |
G |
A |
2: 29,916,596 (GRCm39) |
A2095T |
probably damaging |
Het |
Tbc1d15 |
A |
G |
10: 115,038,407 (GRCm39) |
|
probably null |
Het |
Thsd7b |
T |
A |
1: 129,605,790 (GRCm39) |
F510L |
probably benign |
Het |
Trpm5 |
T |
A |
7: 142,632,050 (GRCm39) |
I920F |
probably damaging |
Het |
Tspear |
C |
A |
10: 77,710,898 (GRCm39) |
H507N |
probably benign |
Het |
Vmn2r108 |
T |
A |
17: 20,683,195 (GRCm39) |
K670* |
probably null |
Het |
Vmn2r75 |
A |
T |
7: 85,797,685 (GRCm39) |
C709* |
probably null |
Het |
Wdfy3 |
G |
T |
5: 102,020,767 (GRCm39) |
S2494R |
probably benign |
Het |
Zfp456 |
A |
T |
13: 67,515,108 (GRCm39) |
F199L |
probably damaging |
Het |
Zfp830 |
A |
G |
11: 82,655,529 (GRCm39) |
Q111R |
probably benign |
Het |
Znrf1 |
G |
A |
8: 112,263,842 (GRCm39) |
A24T |
probably damaging |
Het |
|
Other mutations in Septin10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00852:Septin10
|
APN |
10 |
59,028,642 (GRCm39) |
splice site |
probably benign |
|
IGL01296:Septin10
|
APN |
10 |
59,002,422 (GRCm39) |
missense |
probably benign |
|
IGL02402:Septin10
|
APN |
10 |
59,006,758 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02992:Septin10
|
APN |
10 |
59,028,000 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03010:Septin10
|
APN |
10 |
59,006,777 (GRCm39) |
splice site |
probably benign |
|
IGL03164:Septin10
|
APN |
10 |
59,016,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Septin10
|
UTSW |
10 |
59,002,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Septin10
|
UTSW |
10 |
59,016,841 (GRCm39) |
critical splice donor site |
probably null |
|
R3772:Septin10
|
UTSW |
10 |
59,012,709 (GRCm39) |
missense |
probably damaging |
0.97 |
R4086:Septin10
|
UTSW |
10 |
59,028,045 (GRCm39) |
nonsense |
probably null |
|
R4560:Septin10
|
UTSW |
10 |
59,019,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R4573:Septin10
|
UTSW |
10 |
59,028,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R4968:Septin10
|
UTSW |
10 |
59,016,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Septin10
|
UTSW |
10 |
59,012,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Septin10
|
UTSW |
10 |
59,012,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Septin10
|
UTSW |
10 |
59,006,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R6475:Septin10
|
UTSW |
10 |
59,028,133 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7895:Septin10
|
UTSW |
10 |
59,016,871 (GRCm39) |
missense |
probably benign |
0.08 |
|