Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
T |
A |
13: 59,837,342 (GRCm39) |
T248S |
possibly damaging |
Het |
AA986860 |
T |
C |
1: 130,671,092 (GRCm39) |
V438A |
probably benign |
Het |
Adam25 |
G |
T |
8: 41,207,163 (GRCm39) |
C143F |
probably damaging |
Het |
Aox1 |
T |
A |
1: 58,398,116 (GRCm39) |
F1286I |
possibly damaging |
Het |
Apobec4 |
A |
G |
1: 152,632,001 (GRCm39) |
T10A |
probably benign |
Het |
Arhgap5 |
C |
T |
12: 52,564,366 (GRCm39) |
P446S |
probably damaging |
Het |
Arhgef40 |
A |
G |
14: 52,239,767 (GRCm39) |
N1327S |
probably damaging |
Het |
Armc12 |
A |
G |
17: 28,751,336 (GRCm39) |
D110G |
probably benign |
Het |
Ascc1 |
A |
G |
10: 59,885,624 (GRCm39) |
Y225C |
probably damaging |
Het |
Aspscr1 |
A |
T |
11: 120,579,771 (GRCm39) |
K39N |
possibly damaging |
Het |
B4galnt1 |
G |
T |
10: 127,003,394 (GRCm39) |
V172F |
possibly damaging |
Het |
B4galt1 |
A |
G |
4: 40,823,569 (GRCm39) |
V174A |
probably benign |
Het |
Bcl11a |
C |
A |
11: 24,113,725 (GRCm39) |
A356E |
possibly damaging |
Het |
Bri3bp |
C |
T |
5: 125,528,830 (GRCm39) |
L110F |
probably damaging |
Het |
Cacna1b |
T |
C |
2: 24,544,475 (GRCm39) |
D1231G |
probably damaging |
Het |
Ccdc33 |
T |
A |
9: 57,940,953 (GRCm39) |
I430F |
possibly damaging |
Het |
Cgn |
A |
G |
3: 94,683,405 (GRCm39) |
|
probably benign |
Het |
Crbn |
T |
A |
6: 106,759,883 (GRCm39) |
I317F |
possibly damaging |
Het |
Cyp2d22 |
A |
C |
15: 82,260,118 (GRCm39) |
L22R |
probably damaging |
Het |
Dnah7a |
C |
T |
1: 53,486,476 (GRCm39) |
|
probably null |
Het |
Dnajc12 |
A |
G |
10: 63,222,429 (GRCm39) |
|
probably null |
Het |
Dntt |
T |
A |
19: 41,028,242 (GRCm39) |
D179E |
probably benign |
Het |
Enam |
T |
A |
5: 88,651,650 (GRCm39) |
L1053* |
probably null |
Het |
Epn1 |
T |
A |
7: 5,098,147 (GRCm39) |
D319E |
probably damaging |
Het |
Evpl |
C |
G |
11: 116,113,331 (GRCm39) |
R1453P |
probably damaging |
Het |
Focad |
T |
A |
4: 88,260,558 (GRCm39) |
|
probably null |
Het |
Foxp2 |
A |
T |
6: 15,411,247 (GRCm39) |
M542L |
probably benign |
Het |
Gak |
T |
A |
5: 108,717,743 (GRCm39) |
Q1299L |
probably damaging |
Het |
Galnt5 |
G |
T |
2: 57,888,919 (GRCm39) |
R173I |
possibly damaging |
Het |
Gli1 |
G |
T |
10: 127,166,724 (GRCm39) |
P843Q |
possibly damaging |
Het |
Gm5422 |
G |
T |
10: 31,125,608 (GRCm39) |
|
noncoding transcript |
Het |
Gna14 |
T |
G |
19: 16,576,344 (GRCm39) |
V117G |
possibly damaging |
Het |
Gpr6 |
T |
C |
10: 40,947,037 (GRCm39) |
T182A |
probably damaging |
Het |
Ifi204 |
C |
A |
1: 173,587,927 (GRCm39) |
|
probably benign |
Het |
Ifih1 |
A |
T |
2: 62,429,220 (GRCm39) |
L906H |
probably benign |
Het |
Ighd |
A |
G |
12: 113,379,661 (GRCm39) |
|
probably benign |
Het |
Ighv11-1 |
A |
C |
12: 113,945,622 (GRCm39) |
I77R |
possibly damaging |
Het |
Il22 |
A |
T |
10: 118,041,511 (GRCm39) |
I75F |
probably damaging |
Het |
Il23r |
A |
T |
6: 67,467,686 (GRCm39) |
I27K |
probably damaging |
Het |
Inpp5a |
A |
C |
7: 139,138,839 (GRCm39) |
N261T |
probably damaging |
Het |
Ints8 |
T |
G |
4: 11,223,785 (GRCm39) |
Q686P |
possibly damaging |
Het |
Iqcf4 |
T |
C |
9: 106,445,519 (GRCm39) |
|
probably null |
Het |
Irf2bp1 |
C |
T |
7: 18,739,496 (GRCm39) |
R379C |
possibly damaging |
Het |
Iws1 |
C |
T |
18: 32,213,066 (GRCm39) |
P165S |
probably benign |
Het |
Kalrn |
T |
C |
16: 34,024,327 (GRCm39) |
D610G |
probably damaging |
Het |
Kcna10 |
A |
T |
3: 107,101,926 (GRCm39) |
I186F |
probably benign |
Het |
Limk2 |
C |
A |
11: 3,297,586 (GRCm39) |
E329* |
probably null |
Het |
Nadk |
C |
A |
4: 155,669,684 (GRCm39) |
P157T |
probably benign |
Het |
Notch1 |
T |
G |
2: 26,361,170 (GRCm39) |
K1107Q |
probably benign |
Het |
Nsd1 |
T |
A |
13: 55,361,876 (GRCm39) |
D281E |
probably damaging |
Het |
Obi1 |
A |
G |
14: 104,743,644 (GRCm39) |
L145P |
probably benign |
Het |
Olfml2a |
T |
A |
2: 38,841,250 (GRCm39) |
L262Q |
probably damaging |
Het |
Or1ab2 |
T |
A |
8: 72,864,044 (GRCm39) |
F211L |
probably damaging |
Het |
Or4k44 |
T |
A |
2: 111,368,113 (GRCm39) |
I174L |
probably benign |
Het |
Or51d1 |
A |
T |
7: 102,347,477 (GRCm39) |
T11S |
probably benign |
Het |
Or6k6 |
A |
G |
1: 173,944,964 (GRCm39) |
I206T |
possibly damaging |
Het |
Or7c19 |
A |
G |
8: 85,957,237 (GRCm39) |
T38A |
possibly damaging |
Het |
Otogl |
A |
C |
10: 107,657,785 (GRCm39) |
D1048E |
probably damaging |
Het |
Oxnad1 |
T |
C |
14: 31,817,427 (GRCm39) |
W96R |
probably damaging |
Het |
Pcdh15 |
A |
T |
10: 74,285,995 (GRCm39) |
D743V |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,726,494 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
C |
T |
12: 81,941,938 (GRCm39) |
T112I |
probably benign |
Het |
Pctp |
T |
C |
11: 89,878,099 (GRCm39) |
E145G |
possibly damaging |
Het |
Pip5k1b |
T |
C |
19: 24,332,517 (GRCm39) |
K389R |
probably damaging |
Het |
Pla2g15 |
T |
A |
8: 106,889,691 (GRCm39) |
M321K |
probably benign |
Het |
Pnlip |
T |
A |
19: 58,664,899 (GRCm39) |
D242E |
probably damaging |
Het |
Ptpn21 |
T |
C |
12: 98,645,651 (GRCm39) |
T1096A |
probably benign |
Het |
Rims3 |
A |
T |
4: 120,740,494 (GRCm39) |
|
probably benign |
Het |
Scfd2 |
T |
A |
5: 74,680,256 (GRCm39) |
Q299L |
probably benign |
Het |
Selplg |
T |
C |
5: 113,957,094 (GRCm39) |
D404G |
probably benign |
Het |
Slc15a5 |
T |
C |
6: 138,032,643 (GRCm39) |
D237G |
probably benign |
Het |
Slc16a12 |
T |
A |
19: 34,652,291 (GRCm39) |
H285L |
possibly damaging |
Het |
Sox2 |
C |
A |
3: 34,704,862 (GRCm39) |
R100S |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,477,387 (GRCm39) |
C4969Y |
probably damaging |
Het |
Stxbp2 |
A |
G |
8: 3,682,521 (GRCm39) |
S37G |
probably damaging |
Het |
Tbxas1 |
T |
C |
6: 39,060,791 (GRCm39) |
|
probably null |
Het |
Tcf4 |
A |
G |
18: 69,790,981 (GRCm39) |
Y307C |
probably damaging |
Het |
Thsd7b |
A |
T |
1: 129,977,646 (GRCm39) |
|
probably benign |
Het |
Tnn |
G |
T |
1: 159,943,815 (GRCm39) |
D999E |
possibly damaging |
Het |
Trmt13 |
C |
A |
3: 116,388,247 (GRCm39) |
W63L |
probably benign |
Het |
Tsc2 |
T |
C |
17: 24,823,883 (GRCm39) |
N915S |
probably benign |
Het |
Tyrp1 |
T |
A |
4: 80,759,043 (GRCm39) |
|
probably null |
Het |
Uvrag |
A |
T |
7: 98,638,794 (GRCm39) |
I315N |
probably damaging |
Het |
Vmn1r31 |
C |
A |
6: 58,448,953 (GRCm39) |
*304L |
probably null |
Het |
Vmn2r59 |
T |
A |
7: 41,661,686 (GRCm39) |
I710L |
probably benign |
Het |
Vmn2r82 |
A |
T |
10: 79,214,641 (GRCm39) |
H208L |
probably damaging |
Het |
Wtap |
T |
C |
17: 13,199,711 (GRCm39) |
T91A |
probably benign |
Het |
Xirp1 |
A |
T |
9: 119,846,093 (GRCm39) |
V930E |
probably damaging |
Het |
Xpo4 |
T |
G |
14: 57,827,565 (GRCm39) |
H877P |
probably benign |
Het |
|
Other mutations in Ift88 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00742:Ift88
|
APN |
14 |
57,718,843 (GRCm39) |
unclassified |
probably benign |
|
IGL00886:Ift88
|
APN |
14 |
57,715,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00901:Ift88
|
APN |
14 |
57,681,902 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01148:Ift88
|
APN |
14 |
57,677,189 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01346:Ift88
|
APN |
14 |
57,681,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01474:Ift88
|
APN |
14 |
57,715,531 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02213:Ift88
|
APN |
14 |
57,715,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02391:Ift88
|
APN |
14 |
57,718,871 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03087:Ift88
|
APN |
14 |
57,715,414 (GRCm39) |
missense |
probably benign |
0.00 |
R0392:Ift88
|
UTSW |
14 |
57,733,617 (GRCm39) |
splice site |
probably benign |
|
R0608:Ift88
|
UTSW |
14 |
57,733,678 (GRCm39) |
missense |
probably benign |
|
R0718:Ift88
|
UTSW |
14 |
57,754,870 (GRCm39) |
missense |
probably benign |
0.02 |
R1128:Ift88
|
UTSW |
14 |
57,754,476 (GRCm39) |
nonsense |
probably null |
|
R1422:Ift88
|
UTSW |
14 |
57,710,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R1422:Ift88
|
UTSW |
14 |
57,675,758 (GRCm39) |
splice site |
probably benign |
|
R1432:Ift88
|
UTSW |
14 |
57,674,736 (GRCm39) |
missense |
probably benign |
|
R1518:Ift88
|
UTSW |
14 |
57,668,085 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1566:Ift88
|
UTSW |
14 |
57,678,468 (GRCm39) |
missense |
probably benign |
0.36 |
R1819:Ift88
|
UTSW |
14 |
57,692,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Ift88
|
UTSW |
14 |
57,692,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Ift88
|
UTSW |
14 |
57,726,393 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2926:Ift88
|
UTSW |
14 |
57,726,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R3033:Ift88
|
UTSW |
14 |
57,715,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Ift88
|
UTSW |
14 |
57,668,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R3815:Ift88
|
UTSW |
14 |
57,678,438 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4411:Ift88
|
UTSW |
14 |
57,715,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R4704:Ift88
|
UTSW |
14 |
57,718,307 (GRCm39) |
unclassified |
probably benign |
|
R4822:Ift88
|
UTSW |
14 |
57,679,326 (GRCm39) |
splice site |
probably null |
|
R5355:Ift88
|
UTSW |
14 |
57,675,699 (GRCm39) |
missense |
probably benign |
0.34 |
R5618:Ift88
|
UTSW |
14 |
57,718,965 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6602:Ift88
|
UTSW |
14 |
57,744,716 (GRCm39) |
missense |
probably benign |
0.00 |
R6907:Ift88
|
UTSW |
14 |
57,683,067 (GRCm39) |
missense |
probably benign |
0.23 |
R7241:Ift88
|
UTSW |
14 |
57,717,454 (GRCm39) |
missense |
probably damaging |
0.97 |
R7243:Ift88
|
UTSW |
14 |
57,667,993 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7736:Ift88
|
UTSW |
14 |
57,683,121 (GRCm39) |
missense |
probably benign |
0.18 |
R7766:Ift88
|
UTSW |
14 |
57,685,111 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8526:Ift88
|
UTSW |
14 |
57,683,126 (GRCm39) |
nonsense |
probably null |
|
R9018:Ift88
|
UTSW |
14 |
57,675,702 (GRCm39) |
missense |
probably benign |
0.20 |
R9289:Ift88
|
UTSW |
14 |
57,718,199 (GRCm39) |
missense |
probably benign |
|
R9340:Ift88
|
UTSW |
14 |
57,718,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Ift88
|
UTSW |
14 |
57,685,137 (GRCm39) |
missense |
probably benign |
0.10 |
R9399:Ift88
|
UTSW |
14 |
57,717,385 (GRCm39) |
missense |
probably benign |
0.00 |
R9485:Ift88
|
UTSW |
14 |
57,675,724 (GRCm39) |
missense |
probably benign |
0.00 |
R9712:Ift88
|
UTSW |
14 |
57,718,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R9759:Ift88
|
UTSW |
14 |
57,672,256 (GRCm39) |
nonsense |
probably null |
|
|