Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
A |
G |
7: 45,654,668 (GRCm39) |
V551A |
probably benign |
Het |
Acss1 |
A |
T |
2: 150,484,715 (GRCm39) |
L176Q |
probably damaging |
Het |
Aldh7a1 |
A |
G |
18: 56,683,454 (GRCm39) |
I117T |
possibly damaging |
Het |
Arf5 |
C |
T |
6: 28,426,152 (GRCm39) |
R180C |
probably damaging |
Het |
Arhgap21 |
A |
T |
2: 20,886,576 (GRCm39) |
Y39* |
probably null |
Het |
Arrdc1 |
A |
G |
2: 24,816,351 (GRCm39) |
L206P |
probably damaging |
Het |
Cby3 |
A |
T |
11: 50,250,313 (GRCm39) |
Y173F |
probably damaging |
Het |
Cdh18 |
T |
A |
15: 23,436,634 (GRCm39) |
C497S |
probably damaging |
Het |
Cyp11b2 |
T |
C |
15: 74,725,442 (GRCm39) |
I226V |
probably benign |
Het |
Ddit4l |
T |
A |
3: 137,330,036 (GRCm39) |
|
probably null |
Het |
Ddx11 |
C |
T |
17: 66,445,215 (GRCm39) |
T405I |
probably benign |
Het |
Dhx40 |
A |
T |
11: 86,667,565 (GRCm39) |
|
probably null |
Het |
Dlgap2 |
A |
G |
8: 14,872,499 (GRCm39) |
D659G |
probably damaging |
Het |
Eef2 |
A |
G |
10: 81,016,681 (GRCm39) |
E586G |
probably benign |
Het |
Fam161a |
A |
G |
11: 22,970,470 (GRCm39) |
Q216R |
possibly damaging |
Het |
Fbxw24 |
G |
T |
9: 109,436,112 (GRCm39) |
R307S |
probably benign |
Het |
Gbp2b |
G |
T |
3: 142,312,591 (GRCm39) |
A325S |
probably damaging |
Het |
Gli1 |
A |
T |
10: 127,174,385 (GRCm39) |
F2Y |
probably damaging |
Het |
Gnl2 |
T |
C |
4: 124,938,027 (GRCm39) |
V269A |
probably damaging |
Het |
Grin1 |
A |
G |
2: 25,195,143 (GRCm39) |
V292A |
probably benign |
Het |
Heg1 |
T |
A |
16: 33,555,923 (GRCm39) |
V1001E |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,785,406 (GRCm39) |
I1552N |
probably damaging |
Het |
Htr1a |
A |
G |
13: 105,581,788 (GRCm39) |
T343A |
probably benign |
Het |
Itk |
G |
T |
11: 46,280,153 (GRCm39) |
R29S |
probably damaging |
Het |
Ivns1abp |
G |
T |
1: 151,237,242 (GRCm39) |
G469C |
probably damaging |
Het |
Jph3 |
A |
T |
8: 122,511,598 (GRCm39) |
N529Y |
possibly damaging |
Het |
Kdm2b |
A |
G |
5: 123,019,120 (GRCm39) |
L829P |
probably damaging |
Het |
Kprp |
T |
A |
3: 92,732,033 (GRCm39) |
Y339F |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,333,005 (GRCm39) |
V1504A |
possibly damaging |
Het |
Lypd6b |
A |
G |
2: 49,833,615 (GRCm39) |
D85G |
probably damaging |
Het |
Mansc4 |
T |
C |
6: 146,977,136 (GRCm39) |
Y160C |
probably damaging |
Het |
Mgll |
C |
A |
6: 88,790,871 (GRCm39) |
H164N |
probably benign |
Het |
Mtmr4 |
A |
T |
11: 87,504,342 (GRCm39) |
D1097V |
probably damaging |
Het |
Nfasc |
T |
C |
1: 132,536,241 (GRCm39) |
K571E |
probably damaging |
Het |
Nfat5 |
A |
T |
8: 108,097,205 (GRCm39) |
N1527Y |
probably damaging |
Het |
Nlgn1 |
A |
G |
3: 25,966,808 (GRCm39) |
L215P |
probably damaging |
Het |
Or6b9 |
T |
A |
7: 106,555,235 (GRCm39) |
I303L |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,627,020 (GRCm39) |
S1173G |
probably damaging |
Het |
Prrt3 |
A |
T |
6: 113,472,468 (GRCm39) |
V568E |
probably damaging |
Het |
Ptpra |
G |
A |
2: 130,383,313 (GRCm39) |
R503Q |
possibly damaging |
Het |
Rnf7l |
A |
G |
10: 63,257,427 (GRCm39) |
L31P |
probably damaging |
Het |
Sema5a |
G |
A |
15: 32,618,995 (GRCm39) |
A508T |
probably benign |
Het |
Serpinb11 |
T |
C |
1: 107,307,418 (GRCm39) |
I283T |
possibly damaging |
Het |
Setbp1 |
A |
T |
18: 78,901,807 (GRCm39) |
L620Q |
probably damaging |
Het |
Sipa1l3 |
A |
T |
7: 29,082,628 (GRCm39) |
C756S |
probably benign |
Het |
Sirpa |
A |
T |
2: 129,471,961 (GRCm39) |
I463F |
probably damaging |
Het |
Slc13a2 |
G |
T |
11: 78,293,990 (GRCm39) |
N257K |
probably damaging |
Het |
Slc4a5 |
C |
A |
6: 83,248,039 (GRCm39) |
T530N |
probably damaging |
Het |
Stab2 |
A |
T |
10: 86,714,790 (GRCm39) |
F125L |
probably benign |
Het |
Tet2 |
G |
T |
3: 133,175,280 (GRCm39) |
Q1356K |
probably benign |
Het |
Tet3 |
A |
T |
6: 83,363,010 (GRCm39) |
S856T |
probably damaging |
Het |
Tg |
C |
T |
15: 66,565,279 (GRCm39) |
T1207I |
possibly damaging |
Het |
Tkt |
A |
G |
14: 30,287,525 (GRCm39) |
Y173C |
probably damaging |
Het |
Tlr6 |
T |
A |
5: 65,110,754 (GRCm39) |
I718F |
probably damaging |
Het |
Tnfrsf11b |
A |
G |
15: 54,117,454 (GRCm39) |
V267A |
possibly damaging |
Het |
Ubqln3 |
T |
A |
7: 103,790,753 (GRCm39) |
N446Y |
probably damaging |
Het |
Vmn2r118 |
C |
T |
17: 55,915,083 (GRCm39) |
C521Y |
probably damaging |
Het |
Vps16 |
A |
G |
2: 130,282,260 (GRCm39) |
D394G |
probably benign |
Het |
Zfp236 |
A |
T |
18: 82,692,549 (GRCm39) |
M142K |
possibly damaging |
Het |
Zfp780b |
T |
C |
7: 27,664,282 (GRCm39) |
D91G |
probably benign |
Het |
Zfp97 |
T |
A |
17: 17,365,468 (GRCm39) |
Y322* |
probably null |
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 |
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 |
|
|