Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts5 |
A |
G |
16: 85,659,923 (GRCm39) |
Y790H |
probably damaging |
Het |
Bend3 |
A |
C |
10: 43,369,667 (GRCm39) |
S7R |
probably benign |
Het |
Ccdc106 |
A |
G |
7: 5,063,325 (GRCm39) |
T277A |
probably damaging |
Het |
Ccdc162 |
G |
A |
10: 41,431,997 (GRCm39) |
A1832V |
probably damaging |
Het |
Ccser1 |
A |
G |
6: 61,288,851 (GRCm39) |
E338G |
probably benign |
Het |
Cd86 |
CA |
CAA |
16: 36,426,917 (GRCm39) |
|
probably null |
Het |
Cecr2 |
T |
C |
6: 120,739,490 (GRCm39) |
S1406P |
probably benign |
Het |
Cep290 |
A |
G |
10: 100,382,360 (GRCm39) |
T208A |
probably damaging |
Het |
Cep85l |
A |
C |
10: 53,172,351 (GRCm39) |
C569W |
probably damaging |
Het |
Ces5a |
G |
A |
8: 94,226,154 (GRCm39) |
T527I |
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,796,608 (GRCm39) |
I200F |
probably damaging |
Het |
Cmas |
G |
A |
6: 142,716,312 (GRCm39) |
D251N |
probably damaging |
Het |
Ctcfl |
G |
T |
2: 172,960,268 (GRCm39) |
A105E |
probably benign |
Het |
Dclk2 |
C |
T |
3: 86,700,566 (GRCm39) |
R638H |
probably damaging |
Het |
Dctn6 |
A |
T |
8: 34,557,962 (GRCm39) |
I170N |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,321,920 (GRCm39) |
Y3800C |
probably damaging |
Het |
Dsg2 |
G |
A |
18: 20,724,988 (GRCm39) |
V465I |
possibly damaging |
Het |
Dzip1 |
T |
C |
14: 119,123,058 (GRCm39) |
T646A |
probably benign |
Het |
Etv4 |
T |
A |
11: 101,675,151 (GRCm39) |
|
probably null |
Het |
Exoc3l2 |
T |
C |
7: 19,218,628 (GRCm39) |
V549A |
unknown |
Het |
Ficd |
G |
T |
5: 113,876,880 (GRCm39) |
A352S |
probably damaging |
Het |
Fry |
T |
G |
5: 150,390,251 (GRCm39) |
I179S |
|
Het |
Galntl5 |
A |
G |
5: 25,400,298 (GRCm39) |
H109R |
probably benign |
Het |
Garem1 |
C |
A |
18: 21,281,811 (GRCm39) |
G182W |
probably damaging |
Het |
Gm5916 |
A |
T |
9: 36,032,285 (GRCm39) |
Y50N |
possibly damaging |
Het |
Gtf2h2 |
A |
T |
13: 100,615,709 (GRCm39) |
F271I |
probably benign |
Het |
Hivep2 |
G |
T |
10: 14,004,845 (GRCm39) |
S481I |
probably benign |
Het |
Homez |
T |
A |
14: 55,094,877 (GRCm39) |
Q277L |
probably damaging |
Het |
Hoxb4 |
C |
A |
11: 96,210,722 (GRCm39) |
|
probably null |
Het |
Igll1 |
A |
G |
16: 16,678,957 (GRCm39) |
S118P |
probably damaging |
Het |
Ikzf2 |
A |
C |
1: 69,617,212 (GRCm39) |
|
probably null |
Het |
Kif5b |
A |
G |
18: 6,225,340 (GRCm39) |
V230A |
probably damaging |
Het |
Ldlr |
T |
A |
9: 21,657,040 (GRCm39) |
V719E |
probably benign |
Het |
Lsm7 |
G |
A |
10: 80,689,565 (GRCm39) |
R66W |
possibly damaging |
Het |
Map3k13 |
T |
A |
16: 21,710,988 (GRCm39) |
D90E |
probably benign |
Het |
Mmrn1 |
A |
G |
6: 60,953,098 (GRCm39) |
K460E |
probably damaging |
Het |
Myh10 |
A |
C |
11: 68,681,515 (GRCm39) |
N1061H |
probably damaging |
Het |
Nepn |
A |
G |
10: 52,277,089 (GRCm39) |
Q275R |
probably benign |
Het |
Noc3l |
A |
T |
19: 38,800,800 (GRCm39) |
D227E |
probably benign |
Het |
Nploc4 |
G |
T |
11: 120,319,376 (GRCm39) |
S61R |
probably benign |
Het |
Nr4a2 |
T |
C |
2: 57,002,381 (GRCm39) |
Y24C |
probably damaging |
Het |
Nup160 |
T |
A |
2: 90,553,699 (GRCm39) |
I1143N |
probably damaging |
Het |
Or14a256 |
G |
T |
7: 86,264,873 (GRCm39) |
H327N |
probably benign |
Het |
Or4a15 |
A |
T |
2: 89,192,838 (GRCm39) |
Y312N |
probably benign |
Het |
Or8c17 |
T |
A |
9: 38,180,004 (GRCm39) |
M57K |
probably damaging |
Het |
Or8h7 |
A |
G |
2: 86,720,956 (GRCm39) |
S188P |
probably damaging |
Het |
Papola |
T |
A |
12: 105,775,604 (GRCm39) |
C204S |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
A |
G |
13: 6,606,633 (GRCm39) |
H229R |
probably damaging |
Het |
Plcl1 |
A |
G |
1: 55,737,377 (GRCm39) |
Q906R |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 44,991,167 (GRCm39) |
N1018S |
probably benign |
Het |
Pramel24 |
T |
A |
4: 143,452,849 (GRCm39) |
D93E |
probably benign |
Het |
Prkd1 |
A |
G |
12: 50,435,125 (GRCm39) |
V534A |
possibly damaging |
Het |
Pygm |
A |
T |
19: 6,435,926 (GRCm39) |
I126F |
probably benign |
Het |
Rag1 |
T |
C |
2: 101,472,415 (GRCm39) |
Y909C |
probably damaging |
Het |
Rasgrf2 |
G |
A |
13: 92,032,637 (GRCm39) |
Q560* |
probably null |
Het |
Rbp3 |
A |
T |
14: 33,684,540 (GRCm39) |
I1190F |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,183,921 (GRCm39) |
K1693E |
probably benign |
Het |
Rgl2 |
T |
C |
17: 34,153,964 (GRCm39) |
F457L |
possibly damaging |
Het |
Rsph3a |
A |
G |
17: 8,165,002 (GRCm39) |
T121A |
probably benign |
Het |
Rufy3 |
A |
G |
5: 88,762,806 (GRCm39) |
N112S |
possibly damaging |
Het |
Ryr3 |
G |
A |
2: 112,502,591 (GRCm39) |
Q3548* |
probably null |
Het |
Sardh |
A |
T |
2: 27,108,824 (GRCm39) |
V637D |
probably benign |
Het |
Spata16 |
T |
C |
3: 26,722,016 (GRCm39) |
V179A |
probably benign |
Het |
Spopfm2 |
T |
C |
3: 94,083,667 (GRCm39) |
E48G |
probably benign |
Het |
Tbc1d30 |
G |
A |
10: 121,124,870 (GRCm39) |
T319I |
probably damaging |
Het |
Tlr2 |
T |
A |
3: 83,744,913 (GRCm39) |
Q390L |
possibly damaging |
Het |
Tmem53 |
C |
T |
4: 117,109,237 (GRCm39) |
|
probably null |
Het |
Vmn1r113 |
T |
A |
7: 20,521,370 (GRCm39) |
I54N |
probably damaging |
Het |
Vmn1r223 |
A |
C |
13: 23,434,036 (GRCm39) |
Y210S |
probably damaging |
Het |
Zbbx |
A |
T |
3: 74,947,205 (GRCm39) |
H670Q |
probably benign |
Het |
|
Other mutations in Pgap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00846:Pgap1
|
APN |
1 |
54,531,180 (GRCm39) |
splice site |
probably benign |
|
IGL01111:Pgap1
|
APN |
1 |
54,570,102 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01406:Pgap1
|
APN |
1 |
54,572,573 (GRCm39) |
splice site |
probably null |
|
IGL01592:Pgap1
|
APN |
1 |
54,560,470 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02005:Pgap1
|
APN |
1 |
54,590,214 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02026:Pgap1
|
APN |
1 |
54,533,978 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02086:Pgap1
|
APN |
1 |
54,587,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Pgap1
|
APN |
1 |
54,551,975 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02361:Pgap1
|
APN |
1 |
54,551,975 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02995:Pgap1
|
APN |
1 |
54,532,509 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03012:Pgap1
|
APN |
1 |
54,572,572 (GRCm39) |
splice site |
probably benign |
|
R0044:Pgap1
|
UTSW |
1 |
54,532,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Pgap1
|
UTSW |
1 |
54,533,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Pgap1
|
UTSW |
1 |
54,533,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Pgap1
|
UTSW |
1 |
54,575,110 (GRCm39) |
splice site |
probably null |
|
R0241:Pgap1
|
UTSW |
1 |
54,575,110 (GRCm39) |
splice site |
probably null |
|
R0352:Pgap1
|
UTSW |
1 |
54,525,617 (GRCm39) |
splice site |
probably benign |
|
R1297:Pgap1
|
UTSW |
1 |
54,567,682 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1429:Pgap1
|
UTSW |
1 |
54,534,020 (GRCm39) |
missense |
probably benign |
0.01 |
R1465:Pgap1
|
UTSW |
1 |
54,567,714 (GRCm39) |
missense |
probably benign |
0.11 |
R1465:Pgap1
|
UTSW |
1 |
54,567,714 (GRCm39) |
missense |
probably benign |
0.11 |
R1542:Pgap1
|
UTSW |
1 |
54,531,249 (GRCm39) |
missense |
probably benign |
0.16 |
R1816:Pgap1
|
UTSW |
1 |
54,531,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R1817:Pgap1
|
UTSW |
1 |
54,575,128 (GRCm39) |
missense |
probably benign |
0.15 |
R1905:Pgap1
|
UTSW |
1 |
54,551,120 (GRCm39) |
missense |
probably benign |
0.26 |
R2006:Pgap1
|
UTSW |
1 |
54,590,220 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3551:Pgap1
|
UTSW |
1 |
54,569,302 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3833:Pgap1
|
UTSW |
1 |
54,596,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R3901:Pgap1
|
UTSW |
1 |
54,532,507 (GRCm39) |
missense |
probably benign |
|
R4487:Pgap1
|
UTSW |
1 |
54,567,751 (GRCm39) |
missense |
probably benign |
0.26 |
R4874:Pgap1
|
UTSW |
1 |
54,569,296 (GRCm39) |
missense |
probably damaging |
0.96 |
R5184:Pgap1
|
UTSW |
1 |
54,521,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Pgap1
|
UTSW |
1 |
54,551,936 (GRCm39) |
missense |
probably benign |
0.05 |
R6212:Pgap1
|
UTSW |
1 |
54,554,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6269:Pgap1
|
UTSW |
1 |
54,587,167 (GRCm39) |
nonsense |
probably null |
|
R6525:Pgap1
|
UTSW |
1 |
54,521,048 (GRCm39) |
missense |
probably benign |
0.00 |
R6944:Pgap1
|
UTSW |
1 |
54,569,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7214:Pgap1
|
UTSW |
1 |
54,582,220 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7290:Pgap1
|
UTSW |
1 |
54,587,225 (GRCm39) |
missense |
possibly damaging |
0.45 |
R7356:Pgap1
|
UTSW |
1 |
54,569,293 (GRCm39) |
missense |
probably benign |
0.10 |
R7525:Pgap1
|
UTSW |
1 |
54,570,081 (GRCm39) |
missense |
probably benign |
0.26 |
R7602:Pgap1
|
UTSW |
1 |
54,582,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R7897:Pgap1
|
UTSW |
1 |
54,590,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8278:Pgap1
|
UTSW |
1 |
54,529,430 (GRCm39) |
missense |
probably benign |
|
R9189:Pgap1
|
UTSW |
1 |
54,519,908 (GRCm39) |
missense |
probably benign |
0.31 |
R9238:Pgap1
|
UTSW |
1 |
54,550,570 (GRCm39) |
missense |
probably benign |
|
R9428:Pgap1
|
UTSW |
1 |
54,575,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Pgap1
|
UTSW |
1 |
54,582,275 (GRCm39) |
nonsense |
probably null |
|
X0025:Pgap1
|
UTSW |
1 |
54,521,029 (GRCm39) |
missense |
probably benign |
0.26 |
X0060:Pgap1
|
UTSW |
1 |
54,575,193 (GRCm39) |
missense |
probably damaging |
1.00 |
|