Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb1 |
A |
T |
6: 88,816,434 (GRCm39) |
V120E |
probably benign |
Het |
Acot11 |
G |
A |
4: 106,615,599 (GRCm39) |
T284M |
probably damaging |
Het |
Adk |
G |
T |
14: 21,102,739 (GRCm39) |
K11N |
probably damaging |
Het |
Akr1c14 |
T |
A |
13: 4,138,966 (GRCm39) |
N316K |
probably benign |
Het |
AL732309.1 |
A |
T |
2: 25,135,851 (GRCm39) |
V121D |
probably benign |
Het |
Amh |
C |
A |
10: 80,642,487 (GRCm39) |
Q257K |
probably benign |
Het |
Antxrl |
T |
G |
14: 33,787,806 (GRCm39) |
H276Q |
probably benign |
Het |
Atp5po |
G |
A |
16: 91,723,755 (GRCm39) |
T105M |
probably damaging |
Het |
Atxn2 |
T |
G |
5: 121,923,880 (GRCm39) |
N734K |
possibly damaging |
Het |
B3gat3 |
T |
A |
19: 8,903,102 (GRCm39) |
V153D |
probably benign |
Het |
Brd2 |
A |
G |
17: 34,332,796 (GRCm39) |
V528A |
probably damaging |
Het |
Camk2g |
T |
C |
14: 20,797,907 (GRCm39) |
S335G |
probably benign |
Het |
Cbln2 |
T |
A |
18: 86,734,859 (GRCm39) |
W211R |
probably damaging |
Het |
Cry2 |
A |
T |
2: 92,243,326 (GRCm39) |
I505N |
possibly damaging |
Het |
Ddx55 |
T |
A |
5: 124,698,784 (GRCm39) |
C249S |
possibly damaging |
Het |
Dglucy |
A |
G |
12: 100,808,997 (GRCm39) |
T232A |
probably damaging |
Het |
Dhx32 |
A |
G |
7: 133,361,206 (GRCm39) |
Y76H |
probably benign |
Het |
Dmac2l |
T |
C |
12: 69,788,443 (GRCm39) |
I114T |
probably damaging |
Het |
Dock7 |
T |
A |
4: 98,861,649 (GRCm39) |
N1356I |
unknown |
Het |
Dock8 |
T |
A |
19: 25,104,449 (GRCm39) |
N710K |
probably benign |
Het |
Dync1i2 |
T |
A |
2: 71,079,700 (GRCm39) |
N391K |
possibly damaging |
Het |
Ect2 |
A |
G |
3: 27,192,684 (GRCm39) |
S420P |
probably damaging |
Het |
Efcab5 |
T |
A |
11: 77,028,605 (GRCm39) |
E242V |
probably damaging |
Het |
Fam83g |
T |
A |
11: 61,575,579 (GRCm39) |
Y74N |
probably damaging |
Het |
Fbxo34 |
T |
A |
14: 47,738,329 (GRCm39) |
|
probably null |
Het |
Flt4 |
A |
G |
11: 49,516,836 (GRCm39) |
T208A |
probably benign |
Het |
Fxyd5 |
T |
A |
7: 30,734,576 (GRCm39) |
H183L |
unknown |
Het |
Gpr150 |
T |
G |
13: 76,204,585 (GRCm39) |
D120A |
probably benign |
Het |
Grm7 |
A |
G |
6: 110,623,079 (GRCm39) |
Y84C |
probably damaging |
Het |
Ighmbp2 |
A |
G |
19: 3,316,405 (GRCm39) |
S562P |
probably damaging |
Het |
Itga7 |
A |
G |
10: 128,780,282 (GRCm39) |
Y530C |
possibly damaging |
Het |
Itpr3 |
T |
A |
17: 27,337,535 (GRCm39) |
D2448E |
probably benign |
Het |
Mmp17 |
C |
A |
5: 129,672,697 (GRCm39) |
H216Q |
probably benign |
Het |
Mns1 |
C |
T |
9: 72,360,097 (GRCm39) |
R416W |
probably damaging |
Het |
Mog |
A |
G |
17: 37,334,019 (GRCm39) |
S25P |
unknown |
Het |
Myh2 |
A |
G |
11: 67,071,976 (GRCm39) |
K568R |
possibly damaging |
Het |
Myh7 |
A |
T |
14: 55,209,947 (GRCm39) |
|
probably null |
Het |
Mymk |
A |
T |
2: 26,957,380 (GRCm39) |
W79R |
probably damaging |
Het |
Ncoa4 |
T |
G |
14: 31,899,326 (GRCm39) |
L623R |
probably damaging |
Het |
Oca2 |
G |
A |
7: 55,929,286 (GRCm39) |
|
probably benign |
Het |
Odam |
A |
C |
5: 88,035,404 (GRCm39) |
S123R |
probably benign |
Het |
Or14c39 |
T |
A |
7: 86,344,012 (GRCm39) |
M116K |
probably damaging |
Het |
Or2w1 |
A |
G |
13: 21,317,427 (GRCm39) |
T161A |
probably benign |
Het |
Or51f1d |
T |
C |
7: 102,700,837 (GRCm39) |
F111L |
probably benign |
Het |
Or5d16 |
A |
G |
2: 87,773,915 (GRCm39) |
F19S |
probably damaging |
Het |
Or6c69 |
T |
A |
10: 129,748,156 (GRCm39) |
|
probably benign |
Het |
Or6c8b |
C |
T |
10: 128,882,324 (GRCm39) |
V203M |
probably benign |
Het |
Ovch2 |
C |
T |
7: 107,393,640 (GRCm39) |
C162Y |
probably damaging |
Het |
Padi1 |
C |
A |
4: 140,556,782 (GRCm39) |
G142C |
probably damaging |
Het |
Pcdhga4 |
A |
G |
18: 37,820,451 (GRCm39) |
I667V |
probably damaging |
Het |
Pfas |
A |
T |
11: 68,883,785 (GRCm39) |
V624E |
probably damaging |
Het |
Phb1 |
A |
T |
11: 95,568,917 (GRCm39) |
E184V |
probably damaging |
Het |
Pip5kl1 |
T |
C |
2: 32,470,443 (GRCm39) |
|
probably null |
Het |
Pitpnm2 |
T |
A |
5: 124,263,419 (GRCm39) |
I824F |
possibly damaging |
Het |
Pla2g4c |
G |
A |
7: 13,059,669 (GRCm39) |
S2N |
possibly damaging |
Het |
Pla2r1 |
A |
T |
2: 60,257,969 (GRCm39) |
|
probably null |
Het |
Pole2 |
T |
C |
12: 69,249,684 (GRCm39) |
D521G |
probably damaging |
Het |
Ptch1 |
T |
C |
13: 63,721,108 (GRCm39) |
K54E |
not run |
Het |
Rapgef2 |
A |
T |
3: 78,989,934 (GRCm39) |
L931Q |
probably damaging |
Het |
Rassf3 |
G |
A |
10: 121,248,924 (GRCm39) |
Q206* |
probably null |
Het |
Rnf123 |
T |
A |
9: 107,946,228 (GRCm39) |
T316S |
probably damaging |
Het |
Rnf138 |
T |
A |
18: 21,141,750 (GRCm39) |
|
probably null |
Het |
Septin3 |
G |
A |
15: 82,173,414 (GRCm39) |
A249T |
probably damaging |
Het |
Slc35a4 |
A |
T |
18: 36,812,669 (GRCm39) |
D3V |
unknown |
Het |
Sltm |
T |
A |
9: 70,451,247 (GRCm39) |
|
probably null |
Het |
Smarca2 |
C |
T |
19: 26,631,864 (GRCm39) |
Q560* |
probably null |
Het |
Tcl1b1 |
A |
T |
12: 105,130,790 (GRCm39) |
D91V |
probably damaging |
Het |
Tirap |
A |
T |
9: 35,100,330 (GRCm39) |
V118E |
probably damaging |
Het |
Tlr5 |
T |
A |
1: 182,801,798 (GRCm39) |
Y367* |
probably null |
Het |
Tmcc1 |
A |
G |
6: 116,084,299 (GRCm39) |
F5L |
probably benign |
Het |
Tnxb |
A |
G |
17: 34,935,475 (GRCm39) |
M2592V |
probably benign |
Het |
Trim66 |
T |
A |
7: 109,059,451 (GRCm39) |
E931V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,571,438 (GRCm39) |
I26485T |
probably damaging |
Het |
Veph1 |
C |
A |
3: 66,065,703 (GRCm39) |
V455L |
probably benign |
Het |
Vmn1r125 |
A |
T |
7: 21,006,750 (GRCm39) |
H216L |
probably damaging |
Het |
Wdr17 |
T |
A |
8: 55,085,522 (GRCm39) |
E1200D |
probably benign |
Het |
Zbtb37 |
T |
A |
1: 160,860,231 (GRCm39) |
N25Y |
probably damaging |
Het |
|
Other mutations in Phlpp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Phlpp2
|
APN |
8 |
110,652,422 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01363:Phlpp2
|
APN |
8 |
110,663,729 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01535:Phlpp2
|
APN |
8 |
110,660,697 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01815:Phlpp2
|
APN |
8 |
110,666,491 (GRCm39) |
missense |
probably benign |
|
IGL02105:Phlpp2
|
APN |
8 |
110,631,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02257:Phlpp2
|
APN |
8 |
110,646,731 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02318:Phlpp2
|
APN |
8 |
110,666,505 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02500:Phlpp2
|
APN |
8 |
110,640,250 (GRCm39) |
missense |
probably benign |
|
IGL03356:Phlpp2
|
APN |
8 |
110,662,249 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03366:Phlpp2
|
APN |
8 |
110,667,467 (GRCm39) |
missense |
probably benign |
0.44 |
R0142:Phlpp2
|
UTSW |
8 |
110,634,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Phlpp2
|
UTSW |
8 |
110,634,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Phlpp2
|
UTSW |
8 |
110,634,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Phlpp2
|
UTSW |
8 |
110,666,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R0426:Phlpp2
|
UTSW |
8 |
110,655,095 (GRCm39) |
missense |
probably benign |
0.01 |
R0477:Phlpp2
|
UTSW |
8 |
110,622,138 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0529:Phlpp2
|
UTSW |
8 |
110,603,603 (GRCm39) |
missense |
probably benign |
0.00 |
R0605:Phlpp2
|
UTSW |
8 |
110,659,843 (GRCm39) |
missense |
probably benign |
0.00 |
R0655:Phlpp2
|
UTSW |
8 |
110,622,219 (GRCm39) |
missense |
probably benign |
0.00 |
R0833:Phlpp2
|
UTSW |
8 |
110,663,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Phlpp2
|
UTSW |
8 |
110,663,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:Phlpp2
|
UTSW |
8 |
110,603,662 (GRCm39) |
nonsense |
probably null |
|
R1417:Phlpp2
|
UTSW |
8 |
110,667,313 (GRCm39) |
nonsense |
probably null |
|
R1602:Phlpp2
|
UTSW |
8 |
110,660,655 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1650:Phlpp2
|
UTSW |
8 |
110,660,587 (GRCm39) |
splice site |
probably benign |
|
R1815:Phlpp2
|
UTSW |
8 |
110,666,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Phlpp2
|
UTSW |
8 |
110,634,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Phlpp2
|
UTSW |
8 |
110,655,124 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2074:Phlpp2
|
UTSW |
8 |
110,655,124 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2075:Phlpp2
|
UTSW |
8 |
110,655,124 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2433:Phlpp2
|
UTSW |
8 |
110,666,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R3028:Phlpp2
|
UTSW |
8 |
110,634,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Phlpp2
|
UTSW |
8 |
110,603,515 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4718:Phlpp2
|
UTSW |
8 |
110,667,452 (GRCm39) |
missense |
probably benign |
0.31 |
R4739:Phlpp2
|
UTSW |
8 |
110,667,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Phlpp2
|
UTSW |
8 |
110,603,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R5020:Phlpp2
|
UTSW |
8 |
110,666,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R5047:Phlpp2
|
UTSW |
8 |
110,640,251 (GRCm39) |
missense |
probably benign |
0.04 |
R5074:Phlpp2
|
UTSW |
8 |
110,652,461 (GRCm39) |
missense |
probably damaging |
0.99 |
R5330:Phlpp2
|
UTSW |
8 |
110,660,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R5663:Phlpp2
|
UTSW |
8 |
110,630,976 (GRCm39) |
missense |
probably benign |
0.01 |
R5668:Phlpp2
|
UTSW |
8 |
110,655,205 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6433:Phlpp2
|
UTSW |
8 |
110,661,317 (GRCm39) |
missense |
probably benign |
|
R6470:Phlpp2
|
UTSW |
8 |
110,663,826 (GRCm39) |
missense |
probably benign |
0.45 |
R6804:Phlpp2
|
UTSW |
8 |
110,655,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7012:Phlpp2
|
UTSW |
8 |
110,603,486 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7183:Phlpp2
|
UTSW |
8 |
110,666,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R7312:Phlpp2
|
UTSW |
8 |
110,666,785 (GRCm39) |
missense |
probably damaging |
0.96 |
R7349:Phlpp2
|
UTSW |
8 |
110,655,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R7801:Phlpp2
|
UTSW |
8 |
110,652,474 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8059:Phlpp2
|
UTSW |
8 |
110,622,189 (GRCm39) |
missense |
probably benign |
0.00 |
R8174:Phlpp2
|
UTSW |
8 |
110,595,321 (GRCm39) |
missense |
unknown |
|
R8242:Phlpp2
|
UTSW |
8 |
110,666,834 (GRCm39) |
missense |
probably benign |
0.03 |
R8488:Phlpp2
|
UTSW |
8 |
110,640,202 (GRCm39) |
missense |
probably benign |
|
R8688:Phlpp2
|
UTSW |
8 |
110,631,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8843:Phlpp2
|
UTSW |
8 |
110,652,431 (GRCm39) |
missense |
probably benign |
0.18 |
R9154:Phlpp2
|
UTSW |
8 |
110,666,590 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9556:Phlpp2
|
UTSW |
8 |
110,666,758 (GRCm39) |
missense |
probably benign |
|
R9737:Phlpp2
|
UTSW |
8 |
110,663,714 (GRCm39) |
missense |
probably damaging |
0.99 |
R9781:Phlpp2
|
UTSW |
8 |
110,662,178 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9786:Phlpp2
|
UTSW |
8 |
110,660,655 (GRCm39) |
nonsense |
probably null |
|
X0018:Phlpp2
|
UTSW |
8 |
110,639,001 (GRCm39) |
missense |
probably damaging |
1.00 |
|