Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
A |
G |
3: 59,947,066 (GRCm39) |
T255A |
possibly damaging |
Het |
Abcb10 |
A |
C |
8: 124,691,831 (GRCm39) |
V378G |
probably benign |
Het |
Ackr2 |
C |
T |
9: 121,737,852 (GRCm39) |
R76* |
probably null |
Het |
Acly |
T |
C |
11: 100,414,322 (GRCm39) |
T35A |
probably benign |
Het |
Acp7 |
A |
C |
7: 28,328,974 (GRCm39) |
F69V |
probably damaging |
Het |
Acsl3 |
T |
A |
1: 78,659,678 (GRCm39) |
I110N |
probably damaging |
Het |
Adam5 |
C |
T |
8: 25,305,134 (GRCm39) |
V107M |
probably damaging |
Het |
Adck2 |
T |
C |
6: 39,552,076 (GRCm39) |
V281A |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,567,654 (GRCm39) |
V5173A |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,568,069 (GRCm39) |
S5035T |
probably benign |
Het |
Arl10 |
T |
A |
13: 54,726,937 (GRCm39) |
|
probably null |
Het |
B3gnt3 |
A |
G |
8: 72,146,002 (GRCm39) |
W176R |
probably damaging |
Het |
B4galt4 |
T |
C |
16: 38,586,300 (GRCm39) |
I3T |
probably damaging |
Het |
Casr |
T |
C |
16: 36,315,614 (GRCm39) |
I819V |
possibly damaging |
Het |
Cdh1 |
T |
C |
8: 107,383,472 (GRCm39) |
V237A |
probably damaging |
Het |
Col22a1 |
G |
A |
15: 71,720,426 (GRCm39) |
R605C |
unknown |
Het |
Crlf3 |
A |
G |
11: 79,950,081 (GRCm39) |
V183A |
probably benign |
Het |
Crtac1 |
C |
A |
19: 42,312,171 (GRCm39) |
V181L |
probably damaging |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dnah12 |
A |
T |
14: 26,445,613 (GRCm39) |
R725* |
probably null |
Het |
Dnhd1 |
A |
T |
7: 105,327,178 (GRCm39) |
H709L |
probably benign |
Het |
Dop1a |
A |
G |
9: 86,403,099 (GRCm39) |
Y1431C |
probably damaging |
Het |
Ecpas |
T |
C |
4: 58,833,978 (GRCm39) |
H834R |
probably benign |
Het |
Eif2ak4 |
A |
T |
2: 118,252,604 (GRCm39) |
H392L |
probably benign |
Het |
Entpd3 |
T |
C |
9: 120,384,720 (GRCm39) |
I99T |
probably damaging |
Het |
Epha6 |
T |
C |
16: 59,503,051 (GRCm39) |
D952G |
probably damaging |
Het |
Exoc6 |
T |
C |
19: 37,579,389 (GRCm39) |
L429P |
probably damaging |
Het |
F13a1 |
A |
G |
13: 37,076,815 (GRCm39) |
S625P |
probably benign |
Het |
Fcgbpl1 |
A |
T |
7: 27,857,447 (GRCm39) |
Y2265F |
probably benign |
Het |
Fcho2 |
T |
C |
13: 98,912,406 (GRCm39) |
N240S |
possibly damaging |
Het |
Fcrl6 |
C |
T |
1: 172,426,815 (GRCm39) |
V44M |
probably benign |
Het |
Fmo6 |
A |
T |
1: 162,757,527 (GRCm39) |
M82K |
possibly damaging |
Het |
Gabrr2 |
T |
G |
4: 33,095,548 (GRCm39) |
I479R |
probably damaging |
Het |
Gnl2 |
T |
A |
4: 124,947,278 (GRCm39) |
F633L |
probably benign |
Het |
Greb1l |
C |
T |
18: 10,511,422 (GRCm39) |
S648F |
probably damaging |
Het |
Gsap |
T |
A |
5: 21,447,811 (GRCm39) |
C290S |
probably damaging |
Het |
Gusb |
A |
G |
5: 130,028,288 (GRCm39) |
V268A |
probably benign |
Het |
H2-D1 |
G |
A |
17: 35,483,091 (GRCm39) |
|
probably null |
Het |
Hebp2 |
T |
A |
10: 18,417,008 (GRCm39) |
E164D |
probably benign |
Het |
Higd1a |
A |
T |
9: 121,679,313 (GRCm39) |
I58N |
probably damaging |
Het |
Hoxc13 |
G |
T |
15: 102,835,658 (GRCm39) |
R262L |
probably damaging |
Het |
Ifih1 |
A |
G |
2: 62,453,811 (GRCm39) |
V218A |
probably benign |
Het |
Impg2 |
T |
A |
16: 56,085,427 (GRCm39) |
Y1045N |
probably damaging |
Het |
Kcnk1 |
A |
G |
8: 126,722,395 (GRCm39) |
E66G |
probably damaging |
Het |
Klkb1 |
A |
G |
8: 45,728,541 (GRCm39) |
V406A |
possibly damaging |
Het |
Klra10 |
G |
A |
6: 130,256,241 (GRCm39) |
R138W |
probably damaging |
Het |
Lama2 |
A |
C |
10: 26,920,449 (GRCm39) |
Y193* |
probably null |
Het |
Larp7 |
T |
C |
3: 127,336,779 (GRCm39) |
T428A |
probably benign |
Het |
Lipg |
T |
C |
18: 75,078,956 (GRCm39) |
N432S |
probably benign |
Het |
Loxl1 |
T |
C |
9: 58,200,995 (GRCm39) |
D489G |
probably damaging |
Het |
Lrguk |
A |
G |
6: 34,069,837 (GRCm39) |
K571E |
probably benign |
Het |
Map3k13 |
C |
T |
16: 21,710,894 (GRCm39) |
T59I |
probably benign |
Het |
Mertk |
T |
A |
2: 128,604,058 (GRCm39) |
D397E |
probably benign |
Het |
Mgat3 |
G |
A |
15: 80,096,087 (GRCm39) |
V305I |
probably benign |
Het |
Mrtfb |
T |
C |
16: 13,218,668 (GRCm39) |
V449A |
possibly damaging |
Het |
Mybpc1 |
G |
A |
10: 88,409,299 (GRCm39) |
Q66* |
probably null |
Het |
Myo3a |
A |
G |
2: 22,468,186 (GRCm39) |
D480G |
probably benign |
Het |
Ndufaf3 |
C |
T |
9: 108,443,936 (GRCm39) |
R31Q |
probably benign |
Het |
Neb |
T |
C |
2: 52,200,650 (GRCm39) |
Y343C |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,227,290 (GRCm39) |
|
probably null |
Het |
Or4c10b |
A |
G |
2: 89,711,982 (GRCm39) |
M271V |
probably benign |
Het |
Or8k40 |
A |
T |
2: 86,584,796 (GRCm39) |
N95K |
probably benign |
Het |
Pcsk4 |
T |
C |
10: 80,159,713 (GRCm39) |
M379V |
probably benign |
Het |
Pdzd2 |
A |
T |
15: 12,373,676 (GRCm39) |
V2153E |
probably benign |
Het |
Pkd2l1 |
T |
C |
19: 44,142,939 (GRCm39) |
D427G |
possibly damaging |
Het |
Plcd4 |
A |
G |
1: 74,604,311 (GRCm39) |
Y763C |
probably damaging |
Het |
Plekhh1 |
T |
C |
12: 79,125,774 (GRCm39) |
F1270S |
probably damaging |
Het |
Ptprg |
T |
C |
14: 12,179,283 (GRCm38) |
S767P |
possibly damaging |
Het |
Rabl3 |
T |
G |
16: 37,377,175 (GRCm39) |
|
probably null |
Het |
Rffl |
T |
A |
11: 82,709,264 (GRCm39) |
H53L |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,560,355 (GRCm39) |
V495I |
possibly damaging |
Het |
Scaf11 |
A |
T |
15: 96,317,196 (GRCm39) |
D789E |
possibly damaging |
Het |
Scn2a |
T |
A |
2: 65,582,423 (GRCm39) |
Y1590* |
probably null |
Het |
Siglech |
T |
A |
7: 55,421,434 (GRCm39) |
F190I |
probably benign |
Het |
Slc22a22 |
C |
A |
15: 57,117,636 (GRCm39) |
A302S |
probably damaging |
Het |
Slc46a3 |
T |
A |
5: 147,815,954 (GRCm39) |
T458S |
probably benign |
Het |
Spta1 |
G |
T |
1: 174,035,910 (GRCm39) |
R1072L |
possibly damaging |
Het |
Tbx5 |
A |
G |
5: 119,974,988 (GRCm39) |
T4A |
probably benign |
Het |
Tdrd5 |
T |
C |
1: 156,104,143 (GRCm39) |
R528G |
probably damaging |
Het |
Tfip11 |
T |
C |
5: 112,483,529 (GRCm39) |
V648A |
possibly damaging |
Het |
Thumpd3 |
T |
C |
6: 113,043,749 (GRCm39) |
V388A |
probably benign |
Het |
Tmem131l |
C |
T |
3: 83,850,058 (GRCm39) |
|
probably null |
Het |
Ttf2 |
C |
A |
3: 100,855,509 (GRCm39) |
Q895H |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,720,436 (GRCm39) |
|
probably null |
Het |
Vmn2r13 |
A |
G |
5: 109,306,058 (GRCm39) |
S507P |
probably benign |
Het |
Vtn |
A |
G |
11: 78,391,049 (GRCm39) |
T210A |
probably damaging |
Het |
Zfp1010 |
C |
A |
2: 176,957,195 (GRCm39) |
C101F |
probably damaging |
Het |
Znhit2 |
A |
G |
19: 6,112,091 (GRCm39) |
T279A |
probably benign |
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 |
R1961:Pmfbp1
|
UTSW |
8 |
110,256,776 (GRCm39) |
splice site |
probably benign |
|
R2069:Pmfbp1
|
UTSW |
8 |
110,258,735 (GRCm39) |
missense |
possibly damaging |
0.68 |
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 |
|