Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
T |
7: 130,945,335 (GRCm39) |
Y433* |
probably null |
Het |
Apba2 |
C |
T |
7: 64,364,215 (GRCm39) |
R331C |
probably damaging |
Het |
Apod |
T |
C |
16: 31,116,211 (GRCm39) |
D173G |
probably benign |
Het |
B3gnt5 |
A |
T |
16: 19,588,632 (GRCm39) |
M284L |
probably benign |
Het |
Birc6 |
A |
C |
17: 74,947,145 (GRCm39) |
T2955P |
probably benign |
Het |
Blvra |
T |
C |
2: 126,938,885 (GRCm39) |
I287T |
probably damaging |
Het |
Capn5 |
T |
C |
7: 97,778,578 (GRCm39) |
Y347C |
probably damaging |
Het |
Cdh2 |
A |
G |
18: 16,781,665 (GRCm39) |
V85A |
probably benign |
Het |
Cdk5rap2 |
A |
G |
4: 70,184,943 (GRCm39) |
I1169T |
probably benign |
Het |
Cenpj |
A |
G |
14: 56,772,911 (GRCm39) |
V1043A |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,805,619 (GRCm39) |
H1497L |
probably benign |
Het |
Chat |
A |
G |
14: 32,175,775 (GRCm39) |
M95T |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,052,694 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
C |
15: 47,449,149 (GRCm39) |
E3615G |
probably benign |
Het |
Cyp2c68 |
A |
T |
19: 39,701,006 (GRCm39) |
|
probably null |
Het |
Dll1 |
C |
T |
17: 15,590,828 (GRCm39) |
A332T |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,577,021 (GRCm39) |
Q159L |
probably benign |
Het |
Dnai3 |
A |
T |
3: 145,748,564 (GRCm39) |
L850Q |
probably damaging |
Het |
Eci3 |
A |
T |
13: 35,132,741 (GRCm39) |
M212K |
probably damaging |
Het |
Eml4 |
T |
C |
17: 83,768,962 (GRCm39) |
F557L |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,908,190 (GRCm39) |
V2604D |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,395,586 (GRCm39) |
V1871A |
possibly damaging |
Het |
Gart |
T |
C |
16: 91,422,321 (GRCm39) |
N732S |
probably damaging |
Het |
Gas2l2 |
T |
C |
11: 83,313,924 (GRCm39) |
I463V |
probably benign |
Het |
H2-M3 |
C |
A |
17: 37,583,310 (GRCm39) |
T257K |
probably damaging |
Het |
Hdgf |
A |
G |
3: 87,821,883 (GRCm39) |
N166S |
possibly damaging |
Het |
Hoxb3 |
A |
T |
11: 96,236,599 (GRCm39) |
N226Y |
probably damaging |
Het |
Itgav |
T |
C |
2: 83,586,246 (GRCm39) |
Y169H |
probably benign |
Het |
Kalrn |
T |
G |
16: 33,849,075 (GRCm39) |
I426L |
probably damaging |
Het |
Kcnh3 |
G |
A |
15: 99,131,982 (GRCm39) |
V646M |
probably damaging |
Het |
Kif6 |
T |
C |
17: 50,208,324 (GRCm39) |
V735A |
probably benign |
Het |
Krt1c |
T |
A |
15: 101,726,026 (GRCm39) |
I171F |
probably damaging |
Het |
Megf8 |
G |
A |
7: 25,054,523 (GRCm39) |
A1880T |
possibly damaging |
Het |
Miox |
A |
T |
15: 89,220,324 (GRCm39) |
Y172F |
probably benign |
Het |
Myo18a |
G |
A |
11: 77,708,773 (GRCm39) |
R48H |
possibly damaging |
Het |
Ndufb7 |
T |
C |
8: 84,293,487 (GRCm39) |
S14P |
probably damaging |
Het |
Npepps |
A |
T |
11: 97,129,070 (GRCm39) |
H371Q |
probably damaging |
Het |
Or10d5j |
C |
T |
9: 39,868,205 (GRCm39) |
V9M |
probably damaging |
Het |
Or52e15 |
T |
A |
7: 104,645,830 (GRCm39) |
I94F |
probably damaging |
Het |
Or52e19 |
C |
T |
7: 102,959,165 (GRCm39) |
T79I |
probably benign |
Het |
Or8b12c |
A |
G |
9: 37,716,115 (GRCm39) |
T303A |
probably benign |
Het |
Orc5 |
A |
T |
5: 22,734,174 (GRCm39) |
D203E |
probably damaging |
Het |
Pappa |
A |
G |
4: 65,245,265 (GRCm39) |
T1518A |
probably benign |
Het |
Pde6a |
A |
G |
18: 61,395,563 (GRCm39) |
D602G |
probably damaging |
Het |
Pnliprp2 |
G |
A |
19: 58,750,718 (GRCm39) |
V136I |
possibly damaging |
Het |
Postn |
A |
C |
3: 54,284,414 (GRCm39) |
D627A |
probably damaging |
Het |
Prpf39 |
T |
C |
12: 65,089,337 (GRCm39) |
V25A |
probably benign |
Het |
Pxdc1 |
A |
G |
13: 34,836,297 (GRCm39) |
I41T |
probably damaging |
Het |
Rab11fip1 |
T |
A |
8: 27,644,243 (GRCm39) |
E514V |
probably damaging |
Het |
Rag1 |
A |
T |
2: 101,474,025 (GRCm39) |
H372Q |
probably damaging |
Het |
Ranbp1 |
A |
G |
16: 18,057,968 (GRCm39) |
|
probably benign |
Het |
Rexo5 |
A |
G |
7: 119,426,526 (GRCm39) |
I317V |
probably benign |
Het |
Rragc |
A |
G |
4: 123,818,622 (GRCm39) |
Q279R |
probably damaging |
Het |
Sbf1 |
A |
G |
15: 89,191,129 (GRCm39) |
S187P |
probably damaging |
Het |
Senp3 |
T |
A |
11: 69,567,944 (GRCm39) |
Y432F |
probably benign |
Het |
Slfn5 |
G |
A |
11: 82,852,478 (GRCm39) |
C868Y |
probably damaging |
Het |
Sorcs2 |
C |
T |
5: 36,194,838 (GRCm39) |
A722T |
probably benign |
Het |
Sptb |
A |
T |
12: 76,630,581 (GRCm39) |
C2244* |
probably null |
Het |
Srbd1 |
A |
T |
17: 86,416,693 (GRCm39) |
F488L |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,190 (GRCm39) |
I239M |
possibly damaging |
Het |
Themis2 |
A |
G |
4: 132,513,333 (GRCm39) |
W298R |
probably damaging |
Het |
Tmem168 |
T |
G |
6: 13,594,952 (GRCm39) |
N37T |
probably benign |
Het |
Tmem62 |
A |
G |
2: 120,826,845 (GRCm39) |
|
probably benign |
Het |
Tmprss15 |
T |
C |
16: 78,818,358 (GRCm39) |
D524G |
probably damaging |
Het |
Trav5-4 |
G |
T |
14: 53,941,853 (GRCm39) |
M75I |
probably benign |
Het |
Trio |
T |
A |
15: 27,871,257 (GRCm39) |
H620L |
probably damaging |
Het |
Ubap2 |
C |
T |
4: 41,233,698 (GRCm39) |
G64E |
probably damaging |
Het |
Usp32 |
C |
A |
11: 84,949,953 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
T |
5: 102,054,011 (GRCm39) |
F1603Y |
probably damaging |
Het |
Xpo4 |
A |
T |
14: 57,867,782 (GRCm39) |
L155Q |
probably damaging |
Het |
Zbtb21 |
T |
C |
16: 97,751,092 (GRCm39) |
T1092A |
possibly damaging |
Het |
Zfp780b |
A |
T |
7: 27,662,178 (GRCm39) |
Y792* |
probably null |
Het |
|
Other mutations in Cdcp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01149:Cdcp2
|
APN |
4 |
106,964,308 (GRCm39) |
missense |
probably benign |
|
IGL02041:Cdcp2
|
APN |
4 |
106,964,386 (GRCm39) |
intron |
probably benign |
|
IGL03396:Cdcp2
|
APN |
4 |
106,964,369 (GRCm39) |
nonsense |
probably null |
|
R0128:Cdcp2
|
UTSW |
4 |
106,963,904 (GRCm39) |
splice site |
probably benign |
|
R0130:Cdcp2
|
UTSW |
4 |
106,963,904 (GRCm39) |
splice site |
probably benign |
|
R0519:Cdcp2
|
UTSW |
4 |
106,964,389 (GRCm39) |
intron |
probably benign |
|
R0543:Cdcp2
|
UTSW |
4 |
106,954,873 (GRCm39) |
splice site |
probably null |
|
R1376:Cdcp2
|
UTSW |
4 |
106,959,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1376:Cdcp2
|
UTSW |
4 |
106,959,956 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1606:Cdcp2
|
UTSW |
4 |
106,959,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Cdcp2
|
UTSW |
4 |
106,964,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R1887:Cdcp2
|
UTSW |
4 |
106,959,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Cdcp2
|
UTSW |
4 |
106,959,755 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4816:Cdcp2
|
UTSW |
4 |
106,963,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5298:Cdcp2
|
UTSW |
4 |
106,964,182 (GRCm39) |
missense |
probably benign |
0.01 |
R5646:Cdcp2
|
UTSW |
4 |
106,962,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Cdcp2
|
UTSW |
4 |
106,962,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Cdcp2
|
UTSW |
4 |
106,959,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Cdcp2
|
UTSW |
4 |
106,964,283 (GRCm39) |
missense |
probably benign |
|
R8114:Cdcp2
|
UTSW |
4 |
106,962,555 (GRCm39) |
missense |
probably damaging |
0.99 |
R8472:Cdcp2
|
UTSW |
4 |
106,959,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Cdcp2
|
UTSW |
4 |
106,964,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9726:Cdcp2
|
UTSW |
4 |
106,959,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Cdcp2
|
UTSW |
4 |
106,964,262 (GRCm39) |
missense |
possibly damaging |
0.63 |
|