Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930480E11Rik |
G |
T |
X: 77,414,311 (GRCm39) |
M345I |
probably benign |
Het |
Abcc2 |
T |
A |
19: 43,816,388 (GRCm39) |
I1226N |
probably damaging |
Het |
Adarb2 |
A |
G |
13: 8,620,216 (GRCm39) |
E234G |
probably benign |
Het |
Ankrd52 |
T |
C |
10: 128,217,865 (GRCm39) |
S282P |
probably damaging |
Het |
Arhgef12 |
A |
T |
9: 42,927,205 (GRCm39) |
S306R |
probably benign |
Het |
Baiap2 |
G |
T |
11: 119,893,865 (GRCm39) |
A514S |
probably benign |
Het |
BC030500 |
T |
A |
8: 59,364,838 (GRCm39) |
|
probably null |
Het |
C1qtnf12 |
T |
A |
4: 156,047,072 (GRCm39) |
W13R |
unknown |
Het |
Ccdc158 |
A |
G |
5: 92,798,647 (GRCm39) |
V351A |
probably benign |
Het |
Cct8 |
T |
C |
16: 87,281,807 (GRCm39) |
E485G |
probably benign |
Het |
Cep85 |
T |
C |
4: 133,875,342 (GRCm39) |
D542G |
probably benign |
Het |
Clhc1 |
T |
A |
11: 29,513,937 (GRCm39) |
S340R |
probably benign |
Het |
Cnot4 |
A |
T |
6: 35,046,362 (GRCm39) |
D168E |
probably damaging |
Het |
Cntn5 |
G |
A |
9: 9,831,640 (GRCm39) |
T375I |
probably benign |
Het |
Ctc1 |
T |
A |
11: 68,917,000 (GRCm39) |
I298N |
probably damaging |
Het |
Dchs2 |
T |
A |
3: 83,232,610 (GRCm39) |
N2198K |
probably benign |
Het |
Ddx6 |
G |
A |
9: 44,535,050 (GRCm39) |
|
probably null |
Het |
Defb11 |
A |
G |
8: 22,395,473 (GRCm39) |
I68T |
probably benign |
Het |
Dip2a |
C |
T |
10: 76,109,036 (GRCm39) |
V1212I |
not run |
Het |
Dop1a |
T |
A |
9: 86,382,874 (GRCm39) |
I269N |
probably damaging |
Het |
Efna3 |
C |
T |
3: 89,223,971 (GRCm39) |
G73S |
possibly damaging |
Het |
Fam98b |
C |
G |
2: 117,094,373 (GRCm39) |
R228G |
probably damaging |
Het |
Fancd2 |
A |
T |
6: 113,533,246 (GRCm39) |
N521I |
probably damaging |
Het |
Farsa |
A |
G |
8: 85,587,957 (GRCm39) |
D134G |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,202,088 (GRCm39) |
F329I |
probably damaging |
Het |
Gm14399 |
A |
T |
2: 174,974,991 (GRCm39) |
I43K |
probably damaging |
Het |
Gpr15 |
A |
G |
16: 58,538,760 (GRCm39) |
S110P |
probably damaging |
Het |
Gpr157 |
T |
C |
4: 150,183,331 (GRCm39) |
V167A |
probably benign |
Het |
Hacd4 |
A |
G |
4: 88,345,000 (GRCm39) |
I134T |
possibly damaging |
Het |
Hpgd |
T |
A |
8: 56,751,461 (GRCm39) |
N96K |
probably damaging |
Het |
Insm2 |
A |
T |
12: 55,647,305 (GRCm39) |
T350S |
probably benign |
Het |
Kmt2d |
A |
G |
15: 98,742,147 (GRCm39) |
S4338P |
unknown |
Het |
Krtap9-3 |
A |
G |
11: 99,488,796 (GRCm39) |
S29P |
probably benign |
Het |
Kyat3 |
T |
A |
3: 142,426,219 (GRCm39) |
S87T |
probably benign |
Het |
Minar2 |
A |
G |
18: 59,199,980 (GRCm39) |
|
probably null |
Het |
Mrpl46 |
T |
C |
7: 78,430,336 (GRCm39) |
T145A |
probably benign |
Het |
Neb |
A |
G |
2: 52,214,973 (GRCm39) |
|
probably null |
Het |
Or2aj5 |
A |
T |
16: 19,425,249 (GRCm39) |
H55Q |
probably damaging |
Het |
Or4c124 |
T |
A |
2: 89,156,629 (GRCm39) |
|
probably benign |
Het |
Or6x1 |
C |
T |
9: 40,098,657 (GRCm39) |
T82I |
probably benign |
Het |
Or7g17 |
A |
G |
9: 18,768,548 (GRCm39) |
Y200C |
probably damaging |
Het |
Or9a7 |
A |
G |
6: 40,521,703 (GRCm39) |
I70T |
probably benign |
Het |
Otogl |
T |
C |
10: 107,657,804 (GRCm39) |
D1042G |
probably benign |
Het |
Paxip1 |
C |
T |
5: 27,965,084 (GRCm39) |
V659I |
probably damaging |
Het |
Pfkl |
A |
G |
10: 77,829,263 (GRCm39) |
W382R |
probably damaging |
Het |
Pfn1 |
A |
G |
11: 70,545,297 (GRCm39) |
W4R |
probably damaging |
Het |
Pik3c2b |
G |
A |
1: 133,022,472 (GRCm39) |
R1138H |
probably benign |
Het |
Pkd1l3 |
A |
G |
8: 110,387,330 (GRCm39) |
D1758G |
probably benign |
Het |
Pmpca |
G |
C |
2: 26,285,046 (GRCm39) |
E424Q |
possibly damaging |
Het |
Pramel29 |
T |
C |
4: 143,939,510 (GRCm39) |
D9G |
possibly damaging |
Het |
Prdm12 |
A |
G |
2: 31,532,386 (GRCm39) |
N132S |
possibly damaging |
Het |
Prokr2 |
T |
A |
2: 132,223,360 (GRCm39) |
M61L |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,184,671 (GRCm39) |
|
probably null |
Het |
Ralgps1 |
A |
T |
2: 33,058,200 (GRCm39) |
D301E |
probably benign |
Het |
Rcbtb2 |
T |
C |
14: 73,404,220 (GRCm39) |
Y231H |
probably damaging |
Het |
Rcc2 |
G |
A |
4: 140,429,586 (GRCm39) |
C40Y |
probably benign |
Het |
Relb |
C |
A |
7: 19,346,538 (GRCm39) |
E345* |
probably null |
Het |
Rhbdl3 |
A |
C |
11: 80,228,411 (GRCm39) |
M294L |
possibly damaging |
Het |
Rpl24 |
G |
A |
16: 55,790,479 (GRCm39) |
A112T |
possibly damaging |
Het |
Rsbn1l |
C |
T |
5: 21,113,196 (GRCm39) |
R442Q |
probably damaging |
Het |
Rxfp3 |
A |
T |
15: 11,036,025 (GRCm39) |
I449N |
probably benign |
Het |
Sema4c |
A |
C |
1: 36,589,096 (GRCm39) |
C677G |
probably damaging |
Het |
Sf3b3 |
A |
C |
8: 111,566,562 (GRCm39) |
I256S |
probably damaging |
Het |
Shank1 |
C |
T |
7: 43,976,585 (GRCm39) |
A561V |
unknown |
Het |
Slc39a6 |
G |
T |
18: 24,734,442 (GRCm39) |
N82K |
possibly damaging |
Het |
Slc3a2 |
T |
C |
19: 8,700,521 (GRCm39) |
|
probably benign |
Het |
Stard13 |
T |
C |
5: 150,986,634 (GRCm39) |
Q292R |
probably benign |
Het |
Tgm6 |
A |
G |
2: 129,986,884 (GRCm39) |
R451G |
probably damaging |
Het |
Tspo |
G |
T |
15: 83,456,466 (GRCm39) |
G83V |
probably damaging |
Het |
Ubxn10 |
T |
C |
4: 138,448,187 (GRCm39) |
Q163R |
probably benign |
Het |
Ushbp1 |
A |
G |
8: 71,847,246 (GRCm39) |
S129P |
probably benign |
Het |
Vmn2r23 |
T |
A |
6: 123,718,540 (GRCm39) |
V631D |
probably damaging |
Het |
Vmn2r24 |
T |
C |
6: 123,764,191 (GRCm39) |
I356T |
possibly damaging |
Het |
Vmn2r84 |
C |
T |
10: 130,222,279 (GRCm39) |
C647Y |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,638,428 (GRCm39) |
E2356G |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,603,240 (GRCm39) |
T614A |
probably benign |
Het |
Zdhhc16 |
G |
T |
19: 41,929,990 (GRCm39) |
W271L |
probably damaging |
Het |
Zer1 |
A |
C |
2: 29,991,904 (GRCm39) |
S652A |
probably damaging |
Het |
Zfp287 |
A |
G |
11: 62,615,655 (GRCm39) |
V224A |
probably damaging |
Het |
Zfp438 |
A |
T |
18: 5,214,874 (GRCm39) |
L28* |
probably null |
Het |
Zfp830 |
G |
A |
11: 82,655,534 (GRCm39) |
A113T |
probably benign |
Het |
Zfp865 |
G |
T |
7: 5,037,416 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Iqch |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00326:Iqch
|
APN |
9 |
63,387,936 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01472:Iqch
|
APN |
9 |
63,455,216 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01553:Iqch
|
APN |
9 |
63,408,199 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01611:Iqch
|
APN |
9 |
63,403,519 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02608:Iqch
|
APN |
9 |
63,329,110 (GRCm39) |
unclassified |
probably benign |
|
IGL03060:Iqch
|
APN |
9 |
63,432,196 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Iqch
|
APN |
9 |
63,361,964 (GRCm39) |
missense |
probably damaging |
0.97 |
museum
|
UTSW |
9 |
63,432,421 (GRCm39) |
nonsense |
probably null |
|
I2288:Iqch
|
UTSW |
9 |
63,408,172 (GRCm39) |
missense |
probably benign |
0.01 |
R0002:Iqch
|
UTSW |
9 |
63,502,025 (GRCm39) |
splice site |
probably benign |
|
R0350:Iqch
|
UTSW |
9 |
63,408,158 (GRCm39) |
missense |
probably benign |
0.43 |
R0532:Iqch
|
UTSW |
9 |
63,415,514 (GRCm39) |
splice site |
probably benign |
|
R0629:Iqch
|
UTSW |
9 |
63,332,664 (GRCm39) |
missense |
probably benign |
0.22 |
R0710:Iqch
|
UTSW |
9 |
63,432,418 (GRCm39) |
missense |
probably benign |
|
R0766:Iqch
|
UTSW |
9 |
63,389,965 (GRCm39) |
missense |
probably benign |
0.02 |
R1797:Iqch
|
UTSW |
9 |
63,495,659 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1856:Iqch
|
UTSW |
9 |
63,441,619 (GRCm39) |
splice site |
probably null |
|
R1954:Iqch
|
UTSW |
9 |
63,455,298 (GRCm39) |
missense |
probably benign |
0.00 |
R1955:Iqch
|
UTSW |
9 |
63,455,298 (GRCm39) |
missense |
probably benign |
0.00 |
R2184:Iqch
|
UTSW |
9 |
63,432,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R2264:Iqch
|
UTSW |
9 |
63,419,581 (GRCm39) |
missense |
probably benign |
0.27 |
R4614:Iqch
|
UTSW |
9 |
63,389,863 (GRCm39) |
missense |
probably benign |
|
R4643:Iqch
|
UTSW |
9 |
63,502,084 (GRCm39) |
missense |
probably benign |
0.00 |
R4654:Iqch
|
UTSW |
9 |
63,432,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R4665:Iqch
|
UTSW |
9 |
63,352,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R5027:Iqch
|
UTSW |
9 |
63,432,294 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5042:Iqch
|
UTSW |
9 |
63,403,516 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5551:Iqch
|
UTSW |
9 |
63,403,535 (GRCm39) |
splice site |
probably null |
|
R5829:Iqch
|
UTSW |
9 |
63,332,639 (GRCm39) |
critical splice donor site |
probably null |
|
R5878:Iqch
|
UTSW |
9 |
63,455,272 (GRCm39) |
missense |
probably damaging |
0.99 |
R6816:Iqch
|
UTSW |
9 |
63,388,041 (GRCm39) |
missense |
probably benign |
0.02 |
R6930:Iqch
|
UTSW |
9 |
63,387,856 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7000:Iqch
|
UTSW |
9 |
63,361,892 (GRCm39) |
missense |
probably benign |
|
R7026:Iqch
|
UTSW |
9 |
63,432,421 (GRCm39) |
nonsense |
probably null |
|
R7066:Iqch
|
UTSW |
9 |
63,432,027 (GRCm39) |
missense |
probably benign |
0.24 |
R7111:Iqch
|
UTSW |
9 |
63,419,599 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7129:Iqch
|
UTSW |
9 |
63,329,191 (GRCm39) |
missense |
probably benign |
0.09 |
R7177:Iqch
|
UTSW |
9 |
63,329,117 (GRCm39) |
makesense |
probably null |
|
R7485:Iqch
|
UTSW |
9 |
63,415,599 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7541:Iqch
|
UTSW |
9 |
63,352,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7805:Iqch
|
UTSW |
9 |
63,329,002 (GRCm39) |
splice site |
probably null |
|
R7973:Iqch
|
UTSW |
9 |
63,432,228 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8113:Iqch
|
UTSW |
9 |
63,361,855 (GRCm39) |
missense |
probably benign |
0.00 |
R8170:Iqch
|
UTSW |
9 |
63,336,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R8218:Iqch
|
UTSW |
9 |
63,389,915 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8687:Iqch
|
UTSW |
9 |
63,432,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R8811:Iqch
|
UTSW |
9 |
63,452,195 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9020:Iqch
|
UTSW |
9 |
63,432,526 (GRCm39) |
missense |
probably benign |
|
R9194:Iqch
|
UTSW |
9 |
63,479,961 (GRCm39) |
missense |
probably benign |
0.00 |
R9232:Iqch
|
UTSW |
9 |
63,329,200 (GRCm39) |
missense |
probably benign |
0.00 |
R9532:Iqch
|
UTSW |
9 |
63,389,935 (GRCm39) |
missense |
|
|
X0066:Iqch
|
UTSW |
9 |
63,336,340 (GRCm39) |
missense |
probably damaging |
0.98 |
|