Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
G |
2: 35,252,348 (GRCm39) |
T50P |
possibly damaging |
Het |
Adad1 |
A |
G |
3: 37,139,118 (GRCm39) |
E396G |
possibly damaging |
Het |
Adamtsl3 |
T |
A |
7: 82,114,829 (GRCm39) |
C232S |
probably damaging |
Het |
AI606181 |
T |
C |
19: 41,582,063 (GRCm39) |
S78P |
unknown |
Het |
Amph |
T |
A |
13: 19,309,293 (GRCm39) |
M457K |
probably benign |
Het |
Ano1 |
A |
T |
7: 144,223,171 (GRCm39) |
M174K |
probably benign |
Het |
C3 |
T |
A |
17: 57,528,967 (GRCm39) |
K632* |
probably null |
Het |
Cep170 |
C |
T |
1: 176,583,397 (GRCm39) |
G994D |
probably damaging |
Het |
Chd7 |
T |
C |
4: 8,751,875 (GRCm39) |
V124A |
probably damaging |
Het |
Chd9 |
A |
G |
8: 91,761,691 (GRCm39) |
K2259E |
probably damaging |
Het |
Col7a1 |
A |
G |
9: 108,784,402 (GRCm39) |
T137A |
unknown |
Het |
Dcc |
C |
T |
18: 71,942,185 (GRCm39) |
V311I |
probably benign |
Het |
Ddx42 |
A |
T |
11: 106,125,796 (GRCm39) |
Q282L |
probably damaging |
Het |
Fcgbp |
A |
G |
7: 27,804,390 (GRCm39) |
T1833A |
possibly damaging |
Het |
Fpr-rs3 |
A |
G |
17: 20,844,532 (GRCm39) |
I203T |
probably benign |
Het |
Frem1 |
A |
G |
4: 82,818,796 (GRCm39) |
I2139T |
probably benign |
Het |
Gbp11 |
G |
T |
5: 105,479,254 (GRCm39) |
T123N |
possibly damaging |
Het |
Hs3st1 |
G |
A |
5: 39,772,007 (GRCm39) |
P212L |
probably damaging |
Het |
Ifnb1 |
T |
A |
4: 88,440,813 (GRCm39) |
M67L |
probably benign |
Het |
Ighv1-54 |
T |
C |
12: 115,157,497 (GRCm39) |
N50S |
probably benign |
Het |
Ikzf4 |
G |
A |
10: 128,470,542 (GRCm39) |
T326I |
probably benign |
Het |
Ints2 |
A |
T |
11: 86,127,429 (GRCm39) |
V501E |
probably damaging |
Het |
Mfsd1 |
C |
A |
3: 67,507,270 (GRCm39) |
|
probably null |
Het |
Mroh2a |
GCCC |
GC |
1: 88,159,979 (GRCm39) |
|
probably null |
Het |
Mrps11 |
G |
A |
7: 78,438,466 (GRCm39) |
A73T |
possibly damaging |
Het |
Mterf4 |
T |
C |
1: 93,229,291 (GRCm39) |
E311G |
probably damaging |
Het |
Mx2 |
A |
G |
16: 97,347,635 (GRCm39) |
T176A |
probably damaging |
Het |
Mycbp2 |
A |
C |
14: 103,460,482 (GRCm39) |
L1495R |
probably damaging |
Het |
Myo3b |
A |
G |
2: 70,069,113 (GRCm39) |
T451A |
probably benign |
Het |
Myrfl |
T |
C |
10: 116,685,111 (GRCm39) |
T90A |
probably benign |
Het |
Nbeal1 |
A |
G |
1: 60,220,715 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
A |
G |
11: 62,310,443 (GRCm39) |
L201P |
probably damaging |
Het |
Nfxl1 |
G |
T |
5: 72,671,533 (GRCm39) |
L909I |
probably benign |
Het |
Nr3c1 |
GGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGC |
GGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGC |
18: 39,620,011 (GRCm39) |
|
probably benign |
Het |
Or5aq1b |
T |
A |
2: 86,901,705 (GRCm39) |
S258C |
probably benign |
Het |
Plscr5 |
A |
G |
9: 92,086,437 (GRCm39) |
T136A |
probably benign |
Het |
Ppp1r3a |
G |
A |
6: 14,719,339 (GRCm39) |
T525I |
probably benign |
Het |
Ptprg |
G |
A |
14: 12,215,979 (GRCm38) |
G1143R |
probably damaging |
Het |
Rbm47 |
G |
C |
5: 66,183,626 (GRCm39) |
R326G |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,771,398 (GRCm39) |
T2541A |
probably benign |
Het |
Sall1 |
A |
G |
8: 89,755,247 (GRCm39) |
L1244P |
probably damaging |
Het |
Sec16a |
G |
A |
2: 26,316,482 (GRCm39) |
H1673Y |
probably damaging |
Het |
Slc22a19 |
A |
G |
19: 7,688,428 (GRCm39) |
I44T |
probably benign |
Het |
Snap91 |
T |
A |
9: 86,721,681 (GRCm39) |
N53Y |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,276,539 (GRCm39) |
T338A |
possibly damaging |
Het |
Taf6l |
T |
C |
19: 8,755,920 (GRCm39) |
T243A |
probably benign |
Het |
Tex10 |
T |
C |
4: 48,459,891 (GRCm39) |
R487G |
probably damaging |
Het |
Tfcp2 |
G |
T |
15: 100,410,194 (GRCm39) |
T391N |
probably damaging |
Het |
Tnxb |
G |
A |
17: 34,929,338 (GRCm39) |
V2794M |
probably damaging |
Het |
Ush2a |
T |
G |
1: 188,132,000 (GRCm39) |
C741G |
probably damaging |
Het |
Vmn1r3 |
T |
A |
4: 3,184,684 (GRCm39) |
I208F |
probably damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,496,790 (GRCm39) |
I21F |
possibly damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,545,958 (GRCm39) |
D610G |
probably benign |
Het |
Wbp1 |
T |
C |
6: 83,096,468 (GRCm39) |
S229G |
probably benign |
Het |
Xirp1 |
A |
G |
9: 119,847,029 (GRCm39) |
V618A |
probably benign |
Het |
Zbtb32 |
A |
G |
7: 30,291,254 (GRCm39) |
S14P |
possibly damaging |
Het |
Zfp24 |
A |
G |
18: 24,147,269 (GRCm39) |
S348P |
probably damaging |
Het |
|
Other mutations in Frmpd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
D4216:Frmpd2
|
UTSW |
14 |
33,274,014 (GRCm39) |
missense |
probably damaging |
0.97 |
FR4304:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4342:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4589:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6266:Frmpd2
|
UTSW |
14 |
33,287,864 (GRCm39) |
missense |
probably benign |
0.03 |
R6562:Frmpd2
|
UTSW |
14 |
33,293,872 (GRCm39) |
missense |
probably benign |
0.22 |
R7138:Frmpd2
|
UTSW |
14 |
33,293,761 (GRCm39) |
missense |
probably benign |
0.01 |
R7220:Frmpd2
|
UTSW |
14 |
33,229,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Frmpd2
|
UTSW |
14 |
33,274,034 (GRCm39) |
missense |
probably benign |
0.00 |
R7269:Frmpd2
|
UTSW |
14 |
33,244,838 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7412:Frmpd2
|
UTSW |
14 |
33,293,926 (GRCm39) |
missense |
probably benign |
0.00 |
R7432:Frmpd2
|
UTSW |
14 |
33,229,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7635:Frmpd2
|
UTSW |
14 |
33,222,920 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7699:Frmpd2
|
UTSW |
14 |
33,264,895 (GRCm39) |
missense |
probably benign |
|
R7938:Frmpd2
|
UTSW |
14 |
33,260,246 (GRCm39) |
missense |
probably benign |
0.02 |
R7940:Frmpd2
|
UTSW |
14 |
33,276,850 (GRCm39) |
nonsense |
probably null |
|
R8134:Frmpd2
|
UTSW |
14 |
33,227,452 (GRCm39) |
missense |
probably benign |
0.02 |
R8152:Frmpd2
|
UTSW |
14 |
33,265,244 (GRCm39) |
splice site |
probably null |
|
R8232:Frmpd2
|
UTSW |
14 |
33,261,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Frmpd2
|
UTSW |
14 |
33,224,934 (GRCm39) |
missense |
probably benign |
0.23 |
R8304:Frmpd2
|
UTSW |
14 |
33,274,066 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8326:Frmpd2
|
UTSW |
14 |
33,232,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R8410:Frmpd2
|
UTSW |
14 |
33,217,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R8851:Frmpd2
|
UTSW |
14 |
33,217,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Frmpd2
|
UTSW |
14 |
33,248,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Frmpd2
|
UTSW |
14 |
33,252,407 (GRCm39) |
missense |
probably benign |
0.01 |
R9428:Frmpd2
|
UTSW |
14 |
33,272,010 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Frmpd2
|
UTSW |
14 |
33,266,432 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9502:Frmpd2
|
UTSW |
14 |
33,227,404 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Frmpd2
|
UTSW |
14 |
33,252,462 (GRCm39) |
nonsense |
probably null |
|
Z1177:Frmpd2
|
UTSW |
14 |
33,252,461 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Frmpd2
|
UTSW |
14 |
33,252,408 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1177:Frmpd2
|
UTSW |
14 |
33,264,983 (GRCm39) |
missense |
probably benign |
0.02 |
|