Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
A |
G |
11: 30,376,177 (GRCm39) |
L230S |
probably damaging |
Het |
4930505A04Rik |
A |
G |
11: 30,396,389 (GRCm39) |
|
probably benign |
Het |
Atg2b |
A |
G |
12: 105,602,032 (GRCm39) |
I1648T |
probably damaging |
Het |
Ccdc110 |
T |
C |
8: 46,394,817 (GRCm39) |
F236S |
probably damaging |
Het |
Ccdc178 |
T |
C |
18: 22,230,782 (GRCm39) |
D363G |
possibly damaging |
Het |
Cntn5 |
T |
A |
9: 9,831,577 (GRCm39) |
D601V |
probably damaging |
Het |
Cog7 |
C |
T |
7: 121,529,752 (GRCm39) |
|
probably null |
Het |
Dnah7c |
A |
G |
1: 46,651,881 (GRCm39) |
K1365E |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,837,096 (GRCm39) |
|
probably null |
Het |
Ehd3 |
T |
A |
17: 74,123,321 (GRCm39) |
I108N |
probably benign |
Het |
Erbb4 |
A |
G |
1: 68,348,773 (GRCm39) |
S535P |
probably damaging |
Het |
Fam170a |
T |
C |
18: 50,414,741 (GRCm39) |
V129A |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,823,892 (GRCm39) |
T361A |
probably benign |
Het |
Gm10295 |
A |
T |
7: 71,000,448 (GRCm39) |
I44K |
unknown |
Het |
Gm10553 |
T |
C |
1: 85,078,170 (GRCm39) |
S96P |
probably benign |
Het |
Gm21738 |
T |
A |
14: 19,415,957 (GRCm38) |
Y194F |
probably benign |
Het |
Hspa13 |
A |
T |
16: 75,562,125 (GRCm39) |
Y25N |
probably damaging |
Het |
Lrfn3 |
G |
A |
7: 30,055,347 (GRCm39) |
P533S |
probably damaging |
Het |
Lrp4 |
A |
G |
2: 91,317,372 (GRCm39) |
|
probably benign |
Het |
Mical3 |
T |
C |
6: 120,911,639 (GRCm39) |
D1991G |
probably benign |
Het |
Myoz1 |
A |
G |
14: 20,700,600 (GRCm39) |
Y206H |
probably damaging |
Het |
Or2at1 |
A |
T |
7: 99,416,431 (GRCm39) |
I21F |
probably benign |
Het |
Otog |
A |
G |
7: 45,924,019 (GRCm39) |
E1126G |
probably damaging |
Het |
Pak3 |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
X: 142,526,889 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,472,613 (GRCm39) |
|
probably benign |
Het |
Rab7 |
A |
G |
6: 87,990,624 (GRCm39) |
S17P |
probably damaging |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Sppl2a |
A |
G |
2: 126,765,514 (GRCm39) |
S203P |
probably benign |
Het |
Taar7a |
A |
G |
10: 23,868,439 (GRCm39) |
I314T |
possibly damaging |
Het |
Tgs1 |
T |
C |
4: 3,593,471 (GRCm39) |
I453T |
probably damaging |
Het |
Tmem117 |
C |
A |
15: 94,909,217 (GRCm39) |
T210N |
probably benign |
Het |
Trim55 |
A |
G |
3: 19,698,906 (GRCm39) |
N45S |
probably damaging |
Het |
Ugt2b34 |
G |
C |
5: 87,052,246 (GRCm39) |
S250* |
probably null |
Het |
Vmn2r67 |
G |
A |
7: 84,785,974 (GRCm39) |
T677I |
probably damaging |
Het |
Zfp335 |
C |
G |
2: 164,734,598 (GRCm39) |
|
probably benign |
Het |
Znrf1 |
T |
A |
8: 112,263,986 (GRCm39) |
Y72N |
probably damaging |
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 |
|
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 |
R3056:Pttg1ip2
|
UTSW |
5 |
5,507,283 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|
|