Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
A |
G |
4: 144,401,268 (GRCm39) |
I72T |
probably benign |
Het |
Abca1 |
A |
T |
4: 53,127,626 (GRCm39) |
M131K |
probably benign |
Het |
Agbl1 |
C |
T |
7: 76,416,232 (GRCm39) |
T751M |
possibly damaging |
Het |
Asb14 |
A |
G |
14: 26,636,146 (GRCm39) |
I510V |
possibly damaging |
Het |
Bard1 |
A |
G |
1: 71,127,390 (GRCm39) |
V73A |
possibly damaging |
Het |
C6 |
T |
C |
15: 4,769,355 (GRCm39) |
I187T |
probably damaging |
Het |
Catsper3 |
T |
C |
13: 55,956,709 (GRCm39) |
S376P |
unknown |
Het |
Ccdc150 |
A |
G |
1: 54,328,001 (GRCm39) |
N361S |
possibly damaging |
Het |
Cntn5 |
A |
G |
9: 10,419,076 (GRCm39) |
L7P |
probably benign |
Het |
Cplane1 |
T |
C |
15: 8,280,491 (GRCm39) |
S2805P |
unknown |
Het |
Cxcr6 |
A |
T |
9: 123,639,529 (GRCm39) |
I177F |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,307,869 (GRCm39) |
D3061G |
possibly damaging |
Het |
Epas1 |
T |
C |
17: 87,138,409 (GRCm39) |
F835S |
probably damaging |
Het |
Fat3 |
C |
T |
9: 15,871,792 (GRCm39) |
R3533H |
probably benign |
Het |
Fxr1 |
A |
G |
3: 34,103,333 (GRCm39) |
E221G |
probably damaging |
Het |
Gpatch11 |
A |
G |
17: 79,151,272 (GRCm39) |
T228A |
probably damaging |
Het |
Greb1 |
G |
T |
12: 16,738,592 (GRCm39) |
T1457K |
probably damaging |
Het |
Ighm |
T |
A |
12: 113,382,596 (GRCm39) |
|
probably benign |
Het |
Ints12 |
G |
A |
3: 132,815,126 (GRCm39) |
M444I |
possibly damaging |
Het |
Lmx1b |
G |
A |
2: 33,457,297 (GRCm39) |
Q168* |
probably null |
Het |
Ltbp3 |
C |
A |
19: 5,801,434 (GRCm39) |
N659K |
probably benign |
Het |
Micos13 |
A |
G |
17: 56,915,889 (GRCm39) |
F55S |
probably damaging |
Het |
Mrpl20 |
G |
T |
4: 155,888,329 (GRCm39) |
V43F |
possibly damaging |
Het |
Nlgn1 |
T |
C |
3: 25,487,860 (GRCm39) |
N825S |
possibly damaging |
Het |
Or5d36 |
T |
A |
2: 87,901,583 (GRCm39) |
T48S |
probably benign |
Het |
Or5p67 |
A |
T |
7: 107,922,757 (GRCm39) |
V42E |
possibly damaging |
Het |
Or8k3b |
C |
A |
2: 86,520,896 (GRCm39) |
C141F |
possibly damaging |
Het |
Pccb |
C |
T |
9: 100,912,250 (GRCm39) |
R79Q |
probably damaging |
Het |
Peg10 |
G |
A |
6: 4,755,029 (GRCm39) |
R270H |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Slc4a4 |
T |
C |
5: 89,373,807 (GRCm39) |
V971A |
probably damaging |
Het |
Timm29 |
T |
C |
9: 21,504,887 (GRCm39) |
M185T |
probably damaging |
Het |
Tmem92 |
C |
T |
11: 94,669,873 (GRCm39) |
C86Y |
probably benign |
Het |
Tnfrsf8 |
C |
T |
4: 145,011,895 (GRCm39) |
|
probably null |
Het |
Tnks1bp1 |
T |
A |
2: 84,900,344 (GRCm39) |
C1433* |
probably null |
Het |
Utp14b |
T |
A |
1: 78,642,442 (GRCm39) |
D113E |
possibly damaging |
Het |
Vmn2r110 |
T |
A |
17: 20,803,360 (GRCm39) |
Y405F |
probably damaging |
Het |
Wiz |
A |
G |
17: 32,576,671 (GRCm39) |
S628P |
probably benign |
Het |
Xrcc4 |
T |
C |
13: 90,210,196 (GRCm39) |
T83A |
probably benign |
Het |
|
Other mutations in Pttg1ip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02125:Pttg1ip2
|
APN |
5 |
5,500,644 (GRCm39) |
makesense |
probably null |
|
IGL02701:Pttg1ip2
|
APN |
5 |
5,516,623 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02821:Pttg1ip2
|
APN |
5 |
5,502,039 (GRCm39) |
nonsense |
probably null |
|
R1029:Pttg1ip2
|
UTSW |
5 |
5,505,919 (GRCm39) |
missense |
probably benign |
0.21 |
R1463:Pttg1ip2
|
UTSW |
5 |
5,502,073 (GRCm39) |
splice site |
probably benign |
|
R1525:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1550:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1764:Pttg1ip2
|
UTSW |
5 |
5,528,943 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1911:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1912:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1930:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R1931:Pttg1ip2
|
UTSW |
5 |
5,502,019 (GRCm39) |
missense |
probably benign |
0.00 |
R2013:Pttg1ip2
|
UTSW |
5 |
5,505,964 (GRCm39) |
missense |
probably benign |
0.00 |
R2014:Pttg1ip2
|
UTSW |
5 |
5,505,964 (GRCm39) |
missense |
probably benign |
0.00 |
R2015:Pttg1ip2
|
UTSW |
5 |
5,505,964 (GRCm39) |
missense |
probably benign |
0.00 |
R2151:Pttg1ip2
|
UTSW |
5 |
5,528,875 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2420:Pttg1ip2
|
UTSW |
5 |
5,505,912 (GRCm39) |
missense |
probably benign |
0.00 |
R2421:Pttg1ip2
|
UTSW |
5 |
5,505,912 (GRCm39) |
missense |
probably benign |
0.00 |
R4012:Pttg1ip2
|
UTSW |
5 |
5,528,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7136:Pttg1ip2
|
UTSW |
5 |
5,516,631 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7448:Pttg1ip2
|
UTSW |
5 |
5,505,952 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Pttg1ip2
|
UTSW |
5 |
5,507,284 (GRCm39) |
critical splice donor site |
probably null |
|
|