Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg5 |
C |
T |
8: 95,660,646 (GRCm39) |
T95I |
|
Het |
Arap2 |
C |
T |
5: 62,906,681 (GRCm39) |
V113I |
probably benign |
Het |
Atraid |
C |
T |
5: 31,209,590 (GRCm39) |
Q85* |
probably null |
Het |
Bcdin3d |
T |
C |
15: 99,368,344 (GRCm39) |
D285G |
probably benign |
Het |
Bmal1 |
T |
A |
7: 112,898,610 (GRCm39) |
I346K |
probably benign |
Het |
Carmil3 |
T |
C |
14: 55,736,069 (GRCm39) |
W604R |
probably damaging |
Het |
Ccl6 |
C |
T |
11: 83,480,582 (GRCm39) |
|
probably null |
Het |
Cct4 |
C |
T |
11: 22,940,616 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
C |
T |
17: 43,156,285 (GRCm39) |
R84Q |
possibly damaging |
Het |
Cdt1 |
T |
A |
8: 123,295,012 (GRCm39) |
|
probably null |
Het |
Cln3 |
C |
T |
7: 126,181,942 (GRCm39) |
G40D |
probably damaging |
Het |
Crlf3 |
T |
C |
11: 79,955,216 (GRCm39) |
S47G |
possibly damaging |
Het |
Csrp3 |
T |
C |
7: 48,480,385 (GRCm39) |
K193R |
probably benign |
Het |
Cxcl3 |
A |
C |
5: 90,934,219 (GRCm39) |
E33A |
probably damaging |
Het |
Cyp11b1 |
T |
C |
15: 74,708,708 (GRCm39) |
D362G |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,321,935 (GRCm39) |
D3795G |
probably damaging |
Het |
Dnah3 |
G |
A |
7: 119,521,965 (GRCm39) |
A4076V |
probably damaging |
Het |
Dnaja3 |
T |
A |
16: 4,519,046 (GRCm39) |
I380N |
possibly damaging |
Het |
Dock10 |
T |
A |
1: 80,546,246 (GRCm39) |
H785L |
probably benign |
Het |
Dop1b |
T |
G |
16: 93,607,023 (GRCm39) |
F2226V |
possibly damaging |
Het |
Dscaml1 |
A |
T |
9: 45,581,437 (GRCm39) |
I419F |
probably benign |
Het |
Dyrk4 |
T |
A |
6: 126,862,200 (GRCm39) |
I431F |
probably benign |
Het |
Endog |
C |
T |
2: 30,062,902 (GRCm39) |
R181C |
probably damaging |
Het |
Fam90a1a |
A |
T |
8: 22,453,641 (GRCm39) |
Y332F |
probably benign |
Het |
Fastkd3 |
T |
C |
13: 68,737,499 (GRCm39) |
I588T |
probably benign |
Het |
Galnt9 |
G |
A |
5: 110,737,694 (GRCm39) |
V217I |
probably benign |
Het |
Gm973 |
A |
T |
1: 59,601,888 (GRCm39) |
R501* |
probably null |
Het |
Gnptab |
C |
T |
10: 88,215,019 (GRCm39) |
|
probably benign |
Het |
Gpn1 |
T |
C |
5: 31,660,761 (GRCm39) |
F184S |
probably damaging |
Het |
Imp3 |
G |
T |
9: 56,845,007 (GRCm39) |
V73L |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,032,365 (GRCm39) |
D259G |
probably null |
Het |
Jag1 |
T |
C |
2: 136,948,802 (GRCm39) |
S142G |
probably benign |
Het |
Klhl5 |
A |
T |
5: 65,289,098 (GRCm39) |
E120V |
probably benign |
Het |
Lct |
C |
A |
1: 128,228,197 (GRCm39) |
V1099L |
probably benign |
Het |
Lrba |
G |
C |
3: 86,235,633 (GRCm39) |
W912C |
probably damaging |
Het |
Lss |
C |
T |
10: 76,383,305 (GRCm39) |
T535I |
probably damaging |
Het |
Mcts2 |
T |
C |
2: 152,529,297 (GRCm39) |
I36T |
probably benign |
Het |
Meikin |
T |
A |
11: 54,302,738 (GRCm39) |
N383K |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,461,055 (GRCm39) |
Y663C |
probably damaging |
Het |
Nadk2 |
T |
A |
15: 9,108,342 (GRCm39) |
M419K |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nfat5 |
T |
C |
8: 108,020,515 (GRCm39) |
S20P |
probably damaging |
Het |
Nlrp1a |
C |
T |
11: 71,014,119 (GRCm39) |
C377Y |
probably damaging |
Het |
Nlrp9a |
T |
C |
7: 26,250,463 (GRCm39) |
V76A |
probably damaging |
Het |
Nrap |
C |
A |
19: 56,366,567 (GRCm39) |
A341S |
probably benign |
Het |
Ntng2 |
T |
C |
2: 29,117,732 (GRCm39) |
S239G |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,197,566 (GRCm39) |
C207S |
possibly damaging |
Het |
Or10a4 |
T |
C |
7: 106,697,619 (GRCm39) |
*316R |
probably null |
Het |
Or10ak7 |
T |
A |
4: 118,791,146 (GRCm39) |
I300F |
possibly damaging |
Het |
Or1j17 |
T |
C |
2: 36,578,107 (GRCm39) |
I31T |
probably benign |
Het |
Or2ag1 |
T |
C |
7: 106,473,474 (GRCm39) |
|
probably benign |
Het |
Or5b118 |
T |
A |
19: 13,448,337 (GRCm39) |
M1K |
probably null |
Het |
Or8c13 |
A |
C |
9: 38,091,318 (GRCm39) |
V267G |
probably damaging |
Het |
Or8k31-ps1 |
C |
T |
2: 86,356,150 (GRCm39) |
V124I |
probably damaging |
Het |
Pcdhgb2 |
C |
A |
18: 37,823,159 (GRCm39) |
A50E |
probably damaging |
Het |
Plbd1 |
T |
A |
6: 136,589,829 (GRCm39) |
D463V |
probably damaging |
Het |
Plcg2 |
T |
A |
8: 118,310,288 (GRCm39) |
I380N |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,087,285 (GRCm39) |
W184R |
probably damaging |
Het |
Pptc7 |
G |
A |
5: 122,451,840 (GRCm39) |
V202I |
probably benign |
Het |
Prpf6 |
C |
T |
2: 181,282,389 (GRCm39) |
A510V |
probably damaging |
Het |
Prr5l |
T |
C |
2: 101,559,777 (GRCm39) |
Y235C |
probably benign |
Het |
Ptprk |
T |
C |
10: 28,450,905 (GRCm39) |
V1022A |
probably benign |
Het |
Rbl2 |
T |
C |
8: 91,810,057 (GRCm39) |
|
probably null |
Het |
Rmnd1 |
T |
C |
10: 4,360,753 (GRCm39) |
K348E |
probably benign |
Het |
Rsf1 |
CGGCGGC |
CGGCGGCGGGGGCGGC |
7: 97,229,136 (GRCm39) |
|
probably benign |
Het |
Sacs |
T |
A |
14: 61,429,241 (GRCm39) |
N433K |
probably benign |
Het |
Scyl1 |
T |
C |
19: 5,810,057 (GRCm39) |
T590A |
probably benign |
Het |
Sdhd |
A |
G |
9: 50,508,533 (GRCm39) |
V111A |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,827,509 (GRCm39) |
P330Q |
probably benign |
Het |
Serpinb6d |
C |
T |
13: 33,848,128 (GRCm39) |
P31S |
probably damaging |
Het |
Slc26a9 |
A |
T |
1: 131,687,211 (GRCm39) |
R457W |
probably damaging |
Het |
Slc5a8 |
G |
A |
10: 88,755,364 (GRCm39) |
M490I |
probably benign |
Het |
Slx4 |
A |
G |
16: 3,806,844 (GRCm39) |
I533T |
probably benign |
Het |
Slx4ip |
T |
A |
2: 136,888,650 (GRCm39) |
F110L |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,652,359 (GRCm39) |
R2000G |
probably benign |
Het |
Snx8 |
T |
C |
5: 140,346,008 (GRCm39) |
E75G |
possibly damaging |
Het |
Stab2 |
C |
A |
10: 86,735,705 (GRCm39) |
C1292F |
probably damaging |
Het |
Swt1 |
A |
T |
1: 151,270,364 (GRCm39) |
M617K |
possibly damaging |
Het |
Thoc2l |
A |
G |
5: 104,670,229 (GRCm39) |
T1584A |
probably benign |
Het |
Tiam2 |
T |
A |
17: 3,568,687 (GRCm39) |
I1611N |
possibly damaging |
Het |
Tmem63b |
T |
G |
17: 45,972,748 (GRCm39) |
N682T |
probably benign |
Het |
Trio |
C |
T |
15: 27,871,273 (GRCm39) |
V674M |
probably damaging |
Het |
Trpc3 |
G |
A |
3: 36,704,286 (GRCm39) |
T557M |
possibly damaging |
Het |
Vac14 |
T |
G |
8: 111,397,674 (GRCm39) |
L463R |
probably damaging |
Het |
Vmn2r43 |
C |
T |
7: 8,256,379 (GRCm39) |
|
probably null |
Het |
Wdr49 |
A |
T |
3: 75,265,751 (GRCm39) |
Y232N |
possibly damaging |
Het |
Wdr90 |
T |
C |
17: 26,064,367 (GRCm39) |
M1835V |
probably benign |
Het |
Xpc |
T |
C |
6: 91,469,320 (GRCm39) |
E809G |
probably damaging |
Het |
Zfhx3 |
A |
T |
8: 109,675,493 (GRCm39) |
Q2181L |
probably damaging |
Het |
Zfp442 |
T |
C |
2: 150,251,201 (GRCm39) |
T234A |
probably benign |
Het |
Zfp764 |
A |
T |
7: 127,004,450 (GRCm39) |
M227K |
probably benign |
Het |
Zfp764l1 |
A |
G |
7: 126,990,695 (GRCm39) |
S431P |
probably benign |
Het |
Zfp957 |
A |
G |
14: 79,450,750 (GRCm39) |
S350P |
unknown |
Het |
Zscan29 |
T |
A |
2: 120,999,761 (GRCm39) |
K147* |
probably null |
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 |
R7256:Pgap1
|
UTSW |
1 |
54,532,366 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|