Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025F22Rik |
C |
T |
19: 11,142,401 |
G14D |
probably damaging |
Het |
4932438A13Rik |
G |
A |
3: 36,908,228 |
A493T |
probably damaging |
Het |
Acaa1a |
C |
A |
9: 119,341,564 |
S17* |
probably null |
Het |
Adamts16 |
T |
A |
13: 70,836,203 |
S114C |
probably damaging |
Het |
Agpat5 |
T |
C |
8: 18,846,708 |
V50A |
probably benign |
Het |
Agrn |
T |
C |
4: 156,179,434 |
N124S |
probably benign |
Het |
AI481877 |
T |
C |
4: 59,069,317 |
D703G |
probably benign |
Het |
Ak8 |
T |
C |
2: 28,735,626 |
I227T |
probably benign |
Het |
Akap6 |
A |
G |
12: 53,142,025 |
E2074G |
probably damaging |
Het |
Apc |
T |
A |
18: 34,312,212 |
S702R |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,720,673 |
I1233T |
probably damaging |
Het |
Asphd2 |
A |
T |
5: 112,385,832 |
F318I |
probably damaging |
Het |
Bnc2 |
T |
C |
4: 84,293,143 |
T397A |
probably benign |
Het |
Bpifb4 |
C |
T |
2: 153,957,134 |
T528I |
probably damaging |
Het |
Brinp3 |
A |
G |
1: 146,901,585 |
E590G |
probably damaging |
Het |
Ccdc149 |
A |
G |
5: 52,385,135 |
S372P |
probably benign |
Het |
Cdhr2 |
A |
G |
13: 54,726,776 |
H887R |
probably benign |
Het |
Clcn6 |
C |
T |
4: 148,017,500 |
V376I |
probably benign |
Het |
Cntln |
T |
G |
4: 85,115,354 |
C1305W |
probably damaging |
Het |
Cspg4 |
A |
G |
9: 56,892,644 |
D1564G |
probably benign |
Het |
Cux1 |
A |
T |
5: 136,309,792 |
S582T |
probably damaging |
Het |
Cwh43 |
G |
A |
5: 73,411,905 |
A97T |
possibly damaging |
Het |
Dsc1 |
A |
T |
18: 20,086,769 |
F781L |
probably damaging |
Het |
Dsc3 |
G |
T |
18: 19,966,291 |
H723N |
probably benign |
Het |
Ear10 |
A |
T |
14: 43,923,055 |
V105D |
probably damaging |
Het |
Ecel1 |
A |
G |
1: 87,149,509 |
V659A |
possibly damaging |
Het |
Eogt |
A |
T |
6: 97,120,194 |
F316I |
probably damaging |
Het |
Etaa1 |
T |
C |
11: 17,947,188 |
N310D |
possibly damaging |
Het |
Exoc3l2 |
G |
A |
7: 19,469,708 |
R75Q |
possibly damaging |
Het |
Fam186a |
A |
C |
15: 99,941,742 |
L2207R |
probably damaging |
Het |
Fam187b |
T |
C |
7: 30,977,599 |
Y178H |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,033,495 |
Q3362L |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,938,398 |
S3903T |
probably damaging |
Het |
Gabra5 |
T |
C |
7: 57,413,780 |
T299A |
probably damaging |
Het |
Gbp11 |
T |
C |
5: 105,327,598 |
T295A |
probably benign |
Het |
Glcci1 |
C |
T |
6: 8,573,203 |
Q44* |
probably null |
Het |
Gpc5 |
A |
T |
14: 115,399,200 |
T432S |
probably benign |
Het |
Grhl1 |
G |
A |
12: 24,584,858 |
E228K |
probably damaging |
Het |
Hyal5 |
T |
C |
6: 24,891,709 |
|
probably null |
Het |
Idh2 |
TCCCAGG |
T |
7: 80,098,331 |
|
probably benign |
Het |
Ints9 |
A |
G |
14: 64,993,007 |
I128V |
probably damaging |
Het |
Kcnt2 |
A |
T |
1: 140,375,112 |
N130I |
probably damaging |
Het |
Krba1 |
T |
C |
6: 48,414,128 |
V717A |
probably benign |
Het |
Lrp12 |
T |
A |
15: 39,878,188 |
D377V |
probably damaging |
Het |
Magi1 |
G |
T |
6: 93,943,229 |
D135E |
possibly damaging |
Het |
Map10 |
T |
A |
8: 125,671,245 |
L459Q |
probably damaging |
Het |
Mitf |
A |
G |
6: 98,003,912 |
D238G |
possibly damaging |
Het |
Mylk |
G |
T |
16: 34,921,971 |
R951L |
probably benign |
Het |
Nacad |
T |
A |
11: 6,599,235 |
D1272V |
probably damaging |
Het |
Nacad |
T |
A |
11: 6,600,165 |
K1009* |
probably null |
Het |
Ncor1 |
T |
C |
11: 62,373,298 |
D786G |
probably benign |
Het |
Oas2 |
G |
A |
5: 120,748,538 |
R188C |
probably benign |
Het |
Odf2l |
A |
G |
3: 145,135,718 |
I300V |
probably benign |
Het |
Olfr1502 |
A |
G |
19: 13,861,822 |
T10A |
probably benign |
Het |
Olfr338 |
T |
A |
2: 36,377,196 |
V140D |
possibly damaging |
Het |
Olfr484 |
A |
G |
7: 108,124,430 |
S278P |
probably damaging |
Het |
Olfr624 |
A |
G |
7: 103,670,956 |
I25T |
possibly damaging |
Het |
Olfr64 |
A |
T |
7: 103,893,135 |
L200* |
probably null |
Het |
Pes1 |
T |
A |
11: 3,978,865 |
D574E |
probably benign |
Het |
Phf20 |
C |
T |
2: 156,294,210 |
R650C |
possibly damaging |
Het |
Pias4 |
G |
A |
10: 81,157,264 |
T248I |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,211,951 |
T2889A |
probably benign |
Het |
Plcxd1 |
C |
A |
5: 110,102,167 |
|
probably null |
Het |
Plekha7 |
A |
G |
7: 116,176,898 |
F194L |
probably damaging |
Het |
Plxnb2 |
T |
C |
15: 89,157,770 |
N1642S |
possibly damaging |
Het |
Pnpla7 |
A |
T |
2: 25,011,564 |
D534V |
probably damaging |
Het |
Ppp2r5c |
A |
T |
12: 110,554,879 |
S279C |
probably damaging |
Het |
Ptprq |
T |
A |
10: 107,708,668 |
T334S |
probably damaging |
Het |
Rab39 |
T |
C |
9: 53,686,521 |
D148G |
probably benign |
Het |
Reep3 |
A |
T |
10: 67,034,653 |
F121L |
probably benign |
Het |
Reln |
G |
T |
5: 21,901,663 |
C3236* |
probably null |
Het |
Rrp8 |
C |
T |
7: 105,734,809 |
C162Y |
probably damaging |
Het |
Scrib |
C |
A |
15: 76,064,986 |
Q399H |
possibly damaging |
Het |
Sertad1 |
T |
A |
7: 27,489,799 |
Y182N |
possibly damaging |
Het |
Sfrp5 |
A |
G |
19: 42,201,824 |
V63A |
possibly damaging |
Het |
Slc46a1 |
T |
C |
11: 78,467,159 |
M346T |
probably benign |
Het |
Sycp2 |
A |
G |
2: 178,363,416 |
L886S |
probably damaging |
Het |
Teddm1b |
A |
T |
1: 153,874,759 |
I105F |
probably benign |
Het |
Thumpd1 |
A |
T |
7: 119,720,605 |
I46N |
possibly damaging |
Het |
Tmod4 |
A |
G |
3: 95,127,853 |
N223S |
probably damaging |
Het |
Tnfrsf10b |
G |
C |
14: 69,773,401 |
C85S |
probably damaging |
Het |
Tox |
T |
C |
4: 6,697,439 |
T455A |
probably benign |
Het |
Tox |
T |
C |
4: 6,741,536 |
Q148R |
probably benign |
Het |
Trp53bp1 |
A |
C |
2: 121,269,945 |
S109R |
probably damaging |
Het |
Tshz2 |
A |
T |
2: 169,884,968 |
T26S |
probably benign |
Het |
Tubb4a |
T |
A |
17: 57,081,016 |
N337Y |
probably damaging |
Het |
Tubb6 |
T |
A |
18: 67,401,388 |
V119E |
probably damaging |
Het |
Unk |
C |
T |
11: 116,054,946 |
T481I |
probably benign |
Het |
Vmn2r112 |
C |
T |
17: 22,601,278 |
T44I |
probably benign |
Het |
Vstm5 |
G |
A |
9: 15,257,533 |
G131D |
probably damaging |
Het |
Wscd1 |
T |
C |
11: 71,759,883 |
L12P |
probably damaging |
Het |
Zfp369 |
T |
A |
13: 65,296,230 |
S396T |
possibly damaging |
Het |
Zfp932 |
T |
A |
5: 110,009,343 |
C302* |
probably null |
Het |
Zfp972 |
A |
T |
2: 177,906,935 |
|
probably null |
Het |
Zfyve21 |
C |
A |
12: 111,827,594 |
A212E |
probably benign |
Het |
|