Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,214,257 (GRCm39) |
Y191H |
probably damaging |
Het |
Abcc4 |
C |
A |
14: 118,848,871 (GRCm39) |
V494L |
possibly damaging |
Het |
Abcc4 |
C |
A |
14: 118,848,868 (GRCm39) |
G495C |
probably damaging |
Het |
Acsm4 |
T |
C |
7: 119,307,963 (GRCm39) |
Y367H |
probably benign |
Het |
Adam21 |
A |
T |
12: 81,606,282 (GRCm39) |
Y493* |
probably null |
Het |
Add2 |
T |
C |
6: 86,073,738 (GRCm39) |
F209S |
probably damaging |
Het |
Adgre4 |
T |
C |
17: 56,098,497 (GRCm39) |
S136P |
probably benign |
Het |
Aff4 |
T |
G |
11: 53,263,826 (GRCm39) |
L282R |
probably damaging |
Het |
Akt3 |
A |
G |
1: 176,924,561 (GRCm39) |
I178T |
probably damaging |
Het |
Ap3m1 |
T |
C |
14: 21,091,083 (GRCm39) |
Y174C |
probably damaging |
Het |
Arb2a |
C |
A |
13: 78,050,839 (GRCm39) |
H50N |
probably benign |
Het |
Atl1 |
A |
G |
12: 70,000,274 (GRCm39) |
E308G |
probably benign |
Het |
Atp8b5 |
T |
G |
4: 43,369,688 (GRCm39) |
V942G |
probably damaging |
Het |
B3gntl1 |
A |
G |
11: 121,535,351 (GRCm39) |
|
probably null |
Het |
Btrc |
T |
G |
19: 45,515,782 (GRCm39) |
I480S |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,607,283 (GRCm39) |
I1366N |
probably benign |
Het |
Ccdc113 |
T |
A |
8: 96,267,459 (GRCm39) |
N141K |
probably benign |
Het |
Ccdc167 |
T |
C |
17: 29,923,405 (GRCm39) |
N77D |
possibly damaging |
Het |
Ccser1 |
T |
C |
6: 61,290,630 (GRCm39) |
|
probably benign |
Het |
Cenpe |
A |
G |
3: 134,948,254 (GRCm39) |
E1230G |
probably damaging |
Het |
Clec12a |
A |
C |
6: 129,327,444 (GRCm39) |
T21P |
possibly damaging |
Het |
Cyp26c1 |
T |
A |
19: 37,675,825 (GRCm39) |
F230I |
probably damaging |
Het |
Exog |
A |
G |
9: 119,281,332 (GRCm39) |
E190G |
possibly damaging |
Het |
Fam162b |
A |
G |
10: 51,466,430 (GRCm39) |
W30R |
probably benign |
Het |
Fndc3b |
G |
A |
3: 27,510,600 (GRCm39) |
Q841* |
probably null |
Het |
Frzb |
T |
A |
2: 80,254,945 (GRCm39) |
Y197F |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gabrb1 |
G |
A |
5: 71,857,679 (GRCm39) |
R43Q |
probably benign |
Het |
Gm21060 |
A |
T |
19: 61,285,445 (GRCm39) |
H21Q |
possibly damaging |
Het |
Gm4825 |
A |
G |
15: 85,395,245 (GRCm39) |
|
noncoding transcript |
Het |
Gm5581 |
A |
C |
6: 131,145,125 (GRCm39) |
|
noncoding transcript |
Het |
Gm9894 |
T |
C |
13: 67,912,034 (GRCm39) |
|
noncoding transcript |
Het |
Gpr15 |
T |
A |
16: 58,538,370 (GRCm39) |
I240L |
probably benign |
Het |
Gria4 |
A |
T |
9: 4,519,546 (GRCm39) |
|
probably benign |
Het |
Grid2 |
T |
C |
6: 63,885,877 (GRCm39) |
L91S |
probably damaging |
Het |
Igsf5 |
A |
C |
16: 96,179,551 (GRCm39) |
T215P |
probably damaging |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Kif21a |
G |
A |
15: 90,855,051 (GRCm39) |
A703V |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,440,937 (GRCm39) |
R1159S |
probably benign |
Het |
Kifc2 |
T |
A |
15: 76,547,025 (GRCm39) |
L226H |
probably damaging |
Het |
Klf10 |
T |
C |
15: 38,296,240 (GRCm39) |
H435R |
probably damaging |
Het |
Masp1 |
T |
C |
16: 23,271,682 (GRCm39) |
Y623C |
probably damaging |
Het |
Megf10 |
T |
A |
18: 57,345,426 (GRCm39) |
C118S |
probably damaging |
Het |
Mical3 |
A |
G |
6: 120,959,568 (GRCm39) |
V909A |
possibly damaging |
Het |
Mmrn2 |
A |
G |
14: 34,120,432 (GRCm39) |
|
probably null |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,330,737 (GRCm39) |
E553G |
probably damaging |
Het |
Nmi |
A |
T |
2: 51,838,632 (GRCm39) |
S301T |
probably benign |
Het |
Nr2f2 |
G |
T |
7: 70,007,903 (GRCm39) |
T193K |
possibly damaging |
Het |
Ntng2 |
T |
C |
2: 29,087,110 (GRCm39) |
N404S |
probably damaging |
Het |
Nup50l |
A |
G |
6: 96,142,250 (GRCm39) |
S265P |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or1x2 |
T |
G |
11: 50,918,302 (GRCm39) |
S158A |
probably benign |
Het |
Or52e3 |
T |
C |
7: 102,869,204 (GRCm39) |
V93A |
probably benign |
Het |
Otoa |
T |
A |
7: 120,717,792 (GRCm39) |
D336E |
probably benign |
Het |
Pde4b |
A |
G |
4: 102,454,657 (GRCm39) |
E108G |
probably damaging |
Het |
Pdgfrb |
G |
A |
18: 61,194,577 (GRCm39) |
R118H |
possibly damaging |
Het |
Phactr4 |
G |
A |
4: 132,104,559 (GRCm39) |
T256I |
probably benign |
Het |
Pla2g3 |
C |
T |
11: 3,440,983 (GRCm39) |
T316I |
probably benign |
Het |
Plekhg4 |
A |
G |
8: 106,108,096 (GRCm39) |
E982G |
probably damaging |
Het |
Pot1b |
A |
T |
17: 55,969,531 (GRCm39) |
Y546N |
probably damaging |
Het |
Pphln1-ps1 |
T |
A |
16: 13,495,592 (GRCm39) |
H230Q |
probably benign |
Het |
Rab11fip5 |
C |
A |
6: 85,325,973 (GRCm39) |
Q144H |
possibly damaging |
Het |
Reep3 |
A |
T |
10: 66,875,278 (GRCm39) |
|
probably null |
Het |
Rgl2 |
T |
C |
17: 34,152,589 (GRCm39) |
L400P |
probably damaging |
Het |
Rnf122 |
A |
G |
8: 31,614,874 (GRCm39) |
|
probably benign |
Het |
Scgb1b21 |
G |
T |
7: 33,226,803 (GRCm39) |
|
noncoding transcript |
Het |
Sec63 |
A |
T |
10: 42,699,882 (GRCm39) |
K647N |
probably damaging |
Het |
Sema4a |
C |
T |
3: 88,345,483 (GRCm39) |
|
probably benign |
Het |
Serpinf1 |
C |
T |
11: 75,307,245 (GRCm39) |
V31I |
probably benign |
Het |
Sez6l |
C |
T |
5: 112,572,481 (GRCm39) |
|
probably benign |
Het |
Shank3 |
T |
C |
15: 89,442,167 (GRCm39) |
S1612P |
possibly damaging |
Het |
Slc19a3 |
G |
A |
1: 83,000,519 (GRCm39) |
T166M |
probably benign |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc38a11 |
A |
T |
2: 65,160,683 (GRCm39) |
F304I |
possibly damaging |
Het |
Slitrk1 |
T |
A |
14: 109,149,622 (GRCm39) |
N363I |
probably damaging |
Het |
Slx4ip |
A |
G |
2: 136,909,601 (GRCm39) |
T129A |
probably benign |
Het |
Spop |
T |
C |
11: 95,382,537 (GRCm39) |
V332A |
possibly damaging |
Het |
Sptlc1 |
A |
C |
13: 53,512,916 (GRCm39) |
D147E |
probably benign |
Het |
Tnpo1 |
T |
C |
13: 98,989,440 (GRCm39) |
Y754C |
probably damaging |
Het |
Tox |
C |
A |
4: 6,688,886 (GRCm39) |
V493L |
probably damaging |
Het |
Ttbk1 |
A |
C |
17: 46,791,150 (GRCm39) |
F45V |
probably damaging |
Het |
Ttc27 |
T |
A |
17: 75,087,851 (GRCm39) |
M472K |
probably damaging |
Het |
Ttll7 |
A |
G |
3: 146,621,550 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,552,104 (GRCm39) |
C22851S |
probably benign |
Het |
Ttn |
T |
A |
2: 76,628,556 (GRCm39) |
M14535L |
possibly damaging |
Het |
Txlna |
T |
C |
4: 129,534,055 (GRCm39) |
T54A |
probably benign |
Het |
Usp33 |
T |
C |
3: 152,086,265 (GRCm39) |
V668A |
probably damaging |
Het |
Vmn2r28 |
C |
A |
7: 5,484,070 (GRCm39) |
C710F |
possibly damaging |
Het |
Vmn2r8 |
T |
A |
5: 108,945,961 (GRCm39) |
M549L |
probably benign |
Het |
Vwa5b2 |
T |
C |
16: 20,420,941 (GRCm39) |
|
probably null |
Het |
Wnk1 |
T |
C |
6: 119,946,208 (GRCm39) |
I648M |
probably damaging |
Het |
|
Other mutations in Pmfbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01021:Pmfbp1
|
APN |
8 |
110,264,625 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01505:Pmfbp1
|
APN |
8 |
110,240,543 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Pmfbp1
|
APN |
8 |
110,254,348 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02066:Pmfbp1
|
APN |
8 |
110,268,365 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02926:Pmfbp1
|
APN |
8 |
110,246,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03374:Pmfbp1
|
APN |
8 |
110,269,046 (GRCm39) |
utr 3 prime |
probably benign |
|
R0022:Pmfbp1
|
UTSW |
8 |
110,252,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Pmfbp1
|
UTSW |
8 |
110,252,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Pmfbp1
|
UTSW |
8 |
110,262,617 (GRCm39) |
splice site |
probably benign |
|
R0068:Pmfbp1
|
UTSW |
8 |
110,269,011 (GRCm39) |
splice site |
probably benign |
|
R0211:Pmfbp1
|
UTSW |
8 |
110,268,372 (GRCm39) |
missense |
probably benign |
0.03 |
R0244:Pmfbp1
|
UTSW |
8 |
110,268,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R0468:Pmfbp1
|
UTSW |
8 |
110,240,600 (GRCm39) |
splice site |
probably null |
|
R0479:Pmfbp1
|
UTSW |
8 |
110,257,105 (GRCm39) |
splice site |
probably benign |
|
R1124:Pmfbp1
|
UTSW |
8 |
110,257,115 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1332:Pmfbp1
|
UTSW |
8 |
110,256,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R1336:Pmfbp1
|
UTSW |
8 |
110,256,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R1621:Pmfbp1
|
UTSW |
8 |
110,226,170 (GRCm39) |
missense |
probably benign |
0.04 |
R2069:Pmfbp1
|
UTSW |
8 |
110,258,735 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2125:Pmfbp1
|
UTSW |
8 |
110,246,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2889:Pmfbp1
|
UTSW |
8 |
110,252,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R3034:Pmfbp1
|
UTSW |
8 |
110,247,553 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3956:Pmfbp1
|
UTSW |
8 |
110,256,801 (GRCm39) |
missense |
probably benign |
0.25 |
R4085:Pmfbp1
|
UTSW |
8 |
110,221,579 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4191:Pmfbp1
|
UTSW |
8 |
110,254,260 (GRCm39) |
missense |
probably benign |
0.00 |
R4410:Pmfbp1
|
UTSW |
8 |
110,258,695 (GRCm39) |
missense |
probably benign |
0.07 |
R4418:Pmfbp1
|
UTSW |
8 |
110,257,265 (GRCm39) |
missense |
probably benign |
0.36 |
R4888:Pmfbp1
|
UTSW |
8 |
110,258,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R4937:Pmfbp1
|
UTSW |
8 |
110,262,498 (GRCm39) |
missense |
probably benign |
|
R5070:Pmfbp1
|
UTSW |
8 |
110,256,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R5184:Pmfbp1
|
UTSW |
8 |
110,254,399 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5552:Pmfbp1
|
UTSW |
8 |
110,258,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R5609:Pmfbp1
|
UTSW |
8 |
110,251,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R5760:Pmfbp1
|
UTSW |
8 |
110,247,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R5818:Pmfbp1
|
UTSW |
8 |
110,265,311 (GRCm39) |
splice site |
probably null |
|
R6378:Pmfbp1
|
UTSW |
8 |
110,256,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R6496:Pmfbp1
|
UTSW |
8 |
110,258,789 (GRCm39) |
missense |
probably null |
0.04 |
R6550:Pmfbp1
|
UTSW |
8 |
110,246,839 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6565:Pmfbp1
|
UTSW |
8 |
110,252,060 (GRCm39) |
nonsense |
probably null |
|
R6624:Pmfbp1
|
UTSW |
8 |
110,256,822 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6684:Pmfbp1
|
UTSW |
8 |
110,262,462 (GRCm39) |
missense |
probably benign |
0.10 |
R6823:Pmfbp1
|
UTSW |
8 |
110,256,939 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6833:Pmfbp1
|
UTSW |
8 |
110,265,307 (GRCm39) |
critical splice donor site |
probably null |
|
R6940:Pmfbp1
|
UTSW |
8 |
110,251,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R7000:Pmfbp1
|
UTSW |
8 |
110,257,221 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7411:Pmfbp1
|
UTSW |
8 |
110,240,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R7563:Pmfbp1
|
UTSW |
8 |
110,252,006 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7782:Pmfbp1
|
UTSW |
8 |
110,254,412 (GRCm39) |
missense |
probably damaging |
0.96 |
R8115:Pmfbp1
|
UTSW |
8 |
110,263,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8712:Pmfbp1
|
UTSW |
8 |
110,265,309 (GRCm39) |
splice site |
probably benign |
|
R8954:Pmfbp1
|
UTSW |
8 |
110,258,433 (GRCm39) |
missense |
probably benign |
0.00 |
R9054:Pmfbp1
|
UTSW |
8 |
110,247,661 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9067:Pmfbp1
|
UTSW |
8 |
110,263,244 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9211:Pmfbp1
|
UTSW |
8 |
110,262,445 (GRCm39) |
missense |
probably benign |
0.04 |
R9237:Pmfbp1
|
UTSW |
8 |
110,246,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Pmfbp1
|
UTSW |
8 |
110,262,471 (GRCm39) |
missense |
probably benign |
0.03 |
R9293:Pmfbp1
|
UTSW |
8 |
110,263,205 (GRCm39) |
missense |
probably benign |
0.38 |
R9302:Pmfbp1
|
UTSW |
8 |
110,268,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R9539:Pmfbp1
|
UTSW |
8 |
110,240,537 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Pmfbp1
|
UTSW |
8 |
110,262,499 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Pmfbp1
|
UTSW |
8 |
110,240,576 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Pmfbp1
|
UTSW |
8 |
110,258,383 (GRCm39) |
missense |
probably damaging |
0.98 |
|