Other mutations in this stock |
Total: 119 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
C |
7: 27,274,017 (GRCm39) |
L86P |
unknown |
Het |
Aimp1 |
C |
T |
3: 132,382,808 (GRCm39) |
E23K |
probably damaging |
Het |
Ap2b1 |
A |
T |
11: 83,288,605 (GRCm39) |
N884I |
probably benign |
Het |
Apoe |
G |
T |
7: 19,431,423 (GRCm39) |
Q65K |
possibly damaging |
Het |
Arhgef1 |
T |
A |
7: 24,611,996 (GRCm39) |
D93E |
probably benign |
Het |
Arhgef12 |
G |
T |
9: 42,888,958 (GRCm39) |
T1085K |
probably damaging |
Het |
Arid5a |
T |
C |
1: 36,356,745 (GRCm39) |
|
probably null |
Het |
Atp9a |
A |
T |
2: 168,531,280 (GRCm39) |
|
probably null |
Het |
Baz1a |
T |
C |
12: 54,969,325 (GRCm39) |
I635V |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
Cckar |
T |
A |
5: 53,857,124 (GRCm39) |
M429L |
probably benign |
Het |
Ccl3 |
A |
T |
11: 83,539,164 (GRCm39) |
L65Q |
probably benign |
Het |
Ccr3 |
A |
G |
9: 123,829,477 (GRCm39) |
T271A |
probably benign |
Het |
Cd8b1 |
T |
A |
6: 71,303,081 (GRCm39) |
I52N |
probably damaging |
Het |
Cdh15 |
G |
A |
8: 123,591,767 (GRCm39) |
E551K |
probably damaging |
Het |
Cdh17 |
A |
G |
4: 11,810,466 (GRCm39) |
K719R |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,825,655 (GRCm39) |
R38G |
probably null |
Het |
Chd6 |
T |
C |
2: 160,856,114 (GRCm39) |
E715G |
probably damaging |
Het |
Cldn34b2 |
T |
A |
X: 153,908,625 (GRCm39) |
R68* |
probably null |
Het |
Col19a1 |
T |
G |
1: 24,600,410 (GRCm39) |
D44A |
unknown |
Het |
Colgalt2 |
C |
T |
1: 152,382,627 (GRCm39) |
S493F |
probably damaging |
Het |
Cr1l |
T |
C |
1: 194,812,139 (GRCm39) |
I99M |
probably damaging |
Het |
Crybg1 |
T |
C |
10: 43,873,616 (GRCm39) |
E1164G |
probably damaging |
Het |
Cym |
G |
T |
3: 107,118,718 (GRCm39) |
D367E |
probably damaging |
Het |
Dennd2a |
G |
T |
6: 39,499,776 (GRCm39) |
T263K |
probably damaging |
Het |
Dhx9 |
T |
A |
1: 153,336,049 (GRCm39) |
M869L |
probably damaging |
Het |
Dnm2 |
A |
G |
9: 21,415,742 (GRCm39) |
H692R |
probably damaging |
Het |
Ern1 |
A |
T |
11: 106,298,031 (GRCm39) |
S697T |
probably damaging |
Het |
F12 |
G |
A |
13: 55,568,943 (GRCm39) |
T273I |
probably benign |
Het |
Fam151b |
A |
T |
13: 92,604,617 (GRCm39) |
L124Q |
probably damaging |
Het |
Fancg |
A |
G |
4: 43,002,991 (GRCm39) |
V622A |
probably benign |
Het |
Fbxo2 |
T |
A |
4: 148,249,356 (GRCm39) |
N159K |
possibly damaging |
Het |
Fgd2 |
C |
A |
17: 29,586,052 (GRCm39) |
T212K |
possibly damaging |
Het |
Fhl3 |
T |
A |
4: 124,601,342 (GRCm39) |
D178E |
probably benign |
Het |
Filip1 |
G |
T |
9: 79,723,091 (GRCm39) |
A1176D |
possibly damaging |
Het |
Fndc1 |
T |
C |
17: 7,958,081 (GRCm39) |
Y1722C |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,340,143 (GRCm39) |
V812A |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,809,017 (GRCm39) |
I1779V |
probably benign |
Het |
Gli2 |
C |
T |
1: 118,769,798 (GRCm39) |
V585I |
probably benign |
Het |
Gm15056 |
C |
G |
8: 21,390,697 (GRCm39) |
S80T |
probably benign |
Het |
Gm5145 |
A |
G |
17: 20,790,715 (GRCm39) |
E31G |
probably benign |
Het |
Gmfg |
A |
G |
7: 28,145,369 (GRCm39) |
Y71C |
probably damaging |
Het |
Grk1 |
A |
G |
8: 13,459,322 (GRCm39) |
E291G |
probably damaging |
Het |
Gtpbp1 |
A |
G |
15: 79,600,152 (GRCm39) |
E393G |
possibly damaging |
Het |
Gtpbp2 |
A |
G |
17: 46,472,071 (GRCm39) |
D2G |
probably damaging |
Het |
Hc |
A |
T |
2: 34,918,189 (GRCm39) |
V698E |
probably benign |
Het |
Helz |
G |
A |
11: 107,536,895 (GRCm39) |
R249H |
probably damaging |
Het |
Hmcn2 |
A |
G |
2: 31,303,277 (GRCm39) |
I2973V |
possibly damaging |
Het |
Hnrnpa3 |
A |
G |
2: 75,493,950 (GRCm39) |
R286G |
probably benign |
Het |
Hus1b |
A |
T |
13: 31,131,501 (GRCm39) |
W53R |
probably damaging |
Het |
Hydin |
C |
T |
8: 111,321,857 (GRCm39) |
T4503I |
probably benign |
Het |
Ighmbp2 |
G |
C |
19: 3,315,324 (GRCm39) |
P699A |
probably benign |
Het |
Igkv1-122 |
A |
T |
6: 67,994,442 (GRCm39) |
Y110F |
probably benign |
Het |
Igkv8-28 |
T |
C |
6: 70,120,604 (GRCm39) |
Y113C |
probably damaging |
Het |
Iigp1c |
T |
C |
18: 60,379,152 (GRCm39) |
I229T |
possibly damaging |
Het |
Il16 |
A |
G |
7: 83,332,107 (GRCm39) |
S158P |
probably damaging |
Het |
Kalrn |
T |
A |
16: 34,055,637 (GRCm39) |
H876L |
probably damaging |
Het |
Kdm5d |
T |
A |
Y: 914,134 (GRCm39) |
L357H |
probably damaging |
Het |
Krt78 |
T |
C |
15: 101,855,055 (GRCm39) |
T919A |
possibly damaging |
Het |
L3mbtl2 |
T |
C |
15: 81,569,107 (GRCm39) |
C594R |
probably damaging |
Het |
Lcorl |
A |
T |
5: 45,890,931 (GRCm39) |
L474* |
probably null |
Het |
Lgals3 |
A |
T |
14: 47,619,144 (GRCm39) |
|
probably null |
Het |
Lnx1 |
C |
T |
5: 74,771,457 (GRCm39) |
V350I |
probably benign |
Het |
Lpcat3 |
T |
G |
6: 124,680,286 (GRCm39) |
W429G |
possibly damaging |
Het |
Lrp1 |
T |
C |
10: 127,377,241 (GRCm39) |
T4149A |
probably benign |
Het |
Memo1 |
G |
A |
17: 74,565,456 (GRCm39) |
Q36* |
probably null |
Het |
Mical2 |
A |
G |
7: 112,012,154 (GRCm39) |
N668S |
probably benign |
Het |
Ms4a10 |
A |
T |
19: 10,945,553 (GRCm39) |
I76N |
possibly damaging |
Het |
Mthfr |
T |
G |
4: 148,136,329 (GRCm39) |
L362V |
possibly damaging |
Het |
Myh3 |
T |
A |
11: 66,987,279 (GRCm39) |
Y1376* |
probably null |
Het |
Mymk |
C |
A |
2: 26,952,292 (GRCm39) |
V192F |
probably benign |
Het |
Myo1c |
A |
G |
11: 75,562,688 (GRCm39) |
D966G |
possibly damaging |
Het |
Nmnat1 |
T |
C |
4: 149,553,608 (GRCm39) |
N168S |
possibly damaging |
Het |
Nmur1 |
C |
T |
1: 86,314,367 (GRCm39) |
V323M |
possibly damaging |
Het |
Npr2 |
C |
A |
4: 43,633,522 (GRCm39) |
|
probably null |
Het |
Nsd3 |
T |
A |
8: 26,200,703 (GRCm39) |
M1265K |
probably benign |
Het |
Or13c7 |
A |
G |
4: 43,855,262 (GRCm39) |
T318A |
probably benign |
Het |
Or1e34 |
T |
C |
11: 73,778,629 (GRCm39) |
T190A |
probably damaging |
Het |
Or1j16 |
A |
C |
2: 36,530,626 (GRCm39) |
T192P |
probably damaging |
Het |
Or4c107 |
T |
A |
2: 88,789,556 (GRCm39) |
F249I |
probably damaging |
Het |
Or4c11 |
G |
T |
2: 88,695,838 (GRCm39) |
M296I |
probably benign |
Het |
Or5b108 |
T |
A |
19: 13,168,062 (GRCm39) |
F10L |
probably damaging |
Het |
Or5i1 |
T |
C |
2: 87,613,565 (GRCm39) |
V227A |
possibly damaging |
Het |
Or6c216 |
T |
C |
10: 129,678,344 (GRCm39) |
D189G |
probably damaging |
Het |
Otub1 |
G |
A |
19: 7,181,801 (GRCm39) |
A25V |
possibly damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,069 (GRCm39) |
R102* |
probably null |
Het |
Patl2 |
A |
G |
2: 121,957,226 (GRCm39) |
S103P |
probably benign |
Het |
Pcdhb15 |
A |
T |
18: 37,608,628 (GRCm39) |
H620L |
possibly damaging |
Het |
Pdgfc |
A |
T |
3: 81,048,835 (GRCm39) |
D81V |
possibly damaging |
Het |
Pdia2 |
T |
C |
17: 26,415,476 (GRCm39) |
D447G |
probably damaging |
Het |
Pold1 |
C |
A |
7: 44,188,337 (GRCm39) |
A514S |
probably damaging |
Het |
Pomgnt1 |
C |
T |
4: 116,015,691 (GRCm39) |
T552I |
probably benign |
Het |
Ppl |
T |
C |
16: 4,922,400 (GRCm39) |
E294G |
probably benign |
Het |
Pramel12 |
A |
G |
4: 143,143,324 (GRCm39) |
Y30C |
probably damaging |
Het |
Prkcb |
A |
G |
7: 122,056,447 (GRCm39) |
S100G |
probably benign |
Het |
Psg16 |
T |
G |
7: 16,829,097 (GRCm39) |
I227S |
probably benign |
Het |
Rbbp6 |
AAAGAAGAAGAAGAAGAAG |
AAAGAAGAAGAAGAAG |
7: 122,601,175 (GRCm39) |
|
probably benign |
Het |
Reck |
T |
C |
4: 43,931,062 (GRCm39) |
|
probably null |
Het |
Rrbp1 |
C |
T |
2: 143,830,671 (GRCm39) |
G499S |
probably benign |
Het |
Sema6d |
G |
T |
2: 124,506,082 (GRCm39) |
R630L |
probably damaging |
Het |
Slc29a1 |
A |
G |
17: 45,900,882 (GRCm39) |
V94A |
possibly damaging |
Het |
Slc35a1 |
T |
A |
4: 34,664,146 (GRCm39) |
Q324L |
probably benign |
Het |
Slc35c1 |
A |
T |
2: 92,289,266 (GRCm39) |
L80Q |
probably damaging |
Het |
Slc7a10 |
G |
T |
7: 34,897,377 (GRCm39) |
|
probably null |
Het |
Srrm2 |
C |
T |
17: 24,038,593 (GRCm39) |
|
probably benign |
Het |
Stk38 |
T |
G |
17: 29,201,130 (GRCm39) |
D182A |
probably damaging |
Het |
Tas2r104 |
C |
T |
6: 131,662,398 (GRCm39) |
G104S |
probably benign |
Het |
Tmem121b |
T |
C |
6: 120,469,055 (GRCm39) |
E554G |
probably damaging |
Het |
Tor1aip2 |
A |
G |
1: 155,940,888 (GRCm39) |
H398R |
probably benign |
Het |
Tram2 |
C |
T |
1: 21,083,673 (GRCm39) |
V83I |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,935,811 (GRCm39) |
T565I |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,108,164 (GRCm39) |
V56A |
possibly damaging |
Het |
Vmn1r128 |
T |
C |
7: 21,083,644 (GRCm39) |
V116A |
possibly damaging |
Het |
Vmn1r170 |
C |
T |
7: 23,306,087 (GRCm39) |
T163I |
probably benign |
Het |
Vmn2r75 |
T |
A |
7: 85,813,290 (GRCm39) |
D504V |
possibly damaging |
Het |
Vps36 |
G |
A |
8: 22,708,436 (GRCm39) |
M363I |
probably benign |
Het |
Wdsub1 |
A |
G |
2: 59,708,661 (GRCm39) |
S71P |
probably damaging |
Het |
Zdhhc12 |
A |
G |
2: 29,981,496 (GRCm39) |
F189L |
probably benign |
Het |
Zfp521 |
T |
C |
18: 13,977,387 (GRCm39) |
M1009V |
probably benign |
Het |
|
Other mutations in Ncam2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01138:Ncam2
|
APN |
16 |
81,314,467 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01369:Ncam2
|
APN |
16 |
81,258,459 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01554:Ncam2
|
APN |
16 |
81,309,823 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01892:Ncam2
|
APN |
16 |
81,386,587 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02320:Ncam2
|
APN |
16 |
81,231,725 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02669:Ncam2
|
APN |
16 |
81,314,429 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03073:Ncam2
|
APN |
16 |
81,418,235 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03353:Ncam2
|
APN |
16 |
81,231,788 (GRCm39) |
missense |
probably benign |
0.04 |
BB009:Ncam2
|
UTSW |
16 |
81,412,708 (GRCm39) |
missense |
probably damaging |
0.99 |
BB019:Ncam2
|
UTSW |
16 |
81,412,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R0087:Ncam2
|
UTSW |
16 |
81,231,789 (GRCm39) |
missense |
probably benign |
0.11 |
R0097:Ncam2
|
UTSW |
16 |
81,314,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Ncam2
|
UTSW |
16 |
81,314,517 (GRCm39) |
splice site |
probably benign |
|
R0279:Ncam2
|
UTSW |
16 |
81,420,225 (GRCm39) |
splice site |
probably benign |
|
R0471:Ncam2
|
UTSW |
16 |
80,997,772 (GRCm39) |
start gained |
probably benign |
|
R0523:Ncam2
|
UTSW |
16 |
81,258,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R1353:Ncam2
|
UTSW |
16 |
80,997,803 (GRCm39) |
start codon destroyed |
probably null |
|
R1646:Ncam2
|
UTSW |
16 |
81,262,594 (GRCm39) |
critical splice donor site |
probably benign |
|
R1884:Ncam2
|
UTSW |
16 |
81,234,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Ncam2
|
UTSW |
16 |
81,386,586 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2157:Ncam2
|
UTSW |
16 |
81,287,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R2330:Ncam2
|
UTSW |
16 |
81,309,809 (GRCm39) |
missense |
probably benign |
0.17 |
R2404:Ncam2
|
UTSW |
16 |
81,287,128 (GRCm39) |
splice site |
probably benign |
|
R2434:Ncam2
|
UTSW |
16 |
81,392,113 (GRCm39) |
missense |
probably benign |
0.01 |
R3104:Ncam2
|
UTSW |
16 |
81,262,598 (GRCm39) |
splice site |
probably benign |
|
R3842:Ncam2
|
UTSW |
16 |
81,231,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R3954:Ncam2
|
UTSW |
16 |
81,386,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4039:Ncam2
|
UTSW |
16 |
81,287,211 (GRCm39) |
missense |
probably benign |
0.02 |
R4210:Ncam2
|
UTSW |
16 |
81,323,991 (GRCm39) |
missense |
probably benign |
0.02 |
R4514:Ncam2
|
UTSW |
16 |
81,309,884 (GRCm39) |
missense |
probably benign |
0.13 |
R4586:Ncam2
|
UTSW |
16 |
81,262,457 (GRCm39) |
missense |
probably benign |
0.06 |
R4710:Ncam2
|
UTSW |
16 |
81,262,594 (GRCm39) |
critical splice donor site |
probably null |
|
R4732:Ncam2
|
UTSW |
16 |
81,231,772 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4733:Ncam2
|
UTSW |
16 |
81,231,772 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4876:Ncam2
|
UTSW |
16 |
81,287,234 (GRCm39) |
missense |
probably benign |
0.27 |
R4923:Ncam2
|
UTSW |
16 |
81,386,679 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5131:Ncam2
|
UTSW |
16 |
81,234,550 (GRCm39) |
missense |
probably benign |
0.44 |
R5329:Ncam2
|
UTSW |
16 |
81,231,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R5478:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5479:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5481:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5519:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5522:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5523:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5524:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5526:Ncam2
|
UTSW |
16 |
81,231,766 (GRCm39) |
nonsense |
probably null |
|
R5718:Ncam2
|
UTSW |
16 |
81,386,702 (GRCm39) |
splice site |
probably null |
|
R5793:Ncam2
|
UTSW |
16 |
81,372,991 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6050:Ncam2
|
UTSW |
16 |
81,240,054 (GRCm39) |
nonsense |
probably null |
|
R6212:Ncam2
|
UTSW |
16 |
81,229,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R6847:Ncam2
|
UTSW |
16 |
81,229,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R6935:Ncam2
|
UTSW |
16 |
81,323,879 (GRCm39) |
missense |
probably benign |
0.24 |
R7159:Ncam2
|
UTSW |
16 |
81,287,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Ncam2
|
UTSW |
16 |
81,386,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Ncam2
|
UTSW |
16 |
81,309,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Ncam2
|
UTSW |
16 |
81,420,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R7568:Ncam2
|
UTSW |
16 |
81,386,689 (GRCm39) |
missense |
probably benign |
0.19 |
R7686:Ncam2
|
UTSW |
16 |
81,418,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R7759:Ncam2
|
UTSW |
16 |
81,412,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Ncam2
|
UTSW |
16 |
81,287,267 (GRCm39) |
missense |
probably benign |
|
R7932:Ncam2
|
UTSW |
16 |
81,412,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R8078:Ncam2
|
UTSW |
16 |
81,240,136 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8287:Ncam2
|
UTSW |
16 |
81,323,883 (GRCm39) |
missense |
probably benign |
0.07 |
R8354:Ncam2
|
UTSW |
16 |
81,309,847 (GRCm39) |
missense |
probably benign |
0.00 |
R8429:Ncam2
|
UTSW |
16 |
81,386,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Ncam2
|
UTSW |
16 |
81,309,867 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8546:Ncam2
|
UTSW |
16 |
81,314,419 (GRCm39) |
missense |
probably benign |
0.21 |
R8775:Ncam2
|
UTSW |
16 |
81,314,429 (GRCm39) |
missense |
probably benign |
0.18 |
R8775-TAIL:Ncam2
|
UTSW |
16 |
81,314,429 (GRCm39) |
missense |
probably benign |
0.18 |
R9082:Ncam2
|
UTSW |
16 |
81,412,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Ncam2
|
UTSW |
16 |
81,252,204 (GRCm39) |
missense |
probably benign |
0.07 |
R9386:Ncam2
|
UTSW |
16 |
81,252,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Ncam2
|
UTSW |
16 |
81,309,887 (GRCm39) |
missense |
probably benign |
0.03 |
R9510:Ncam2
|
UTSW |
16 |
81,420,341 (GRCm39) |
makesense |
probably null |
|
R9587:Ncam2
|
UTSW |
16 |
81,262,501 (GRCm39) |
missense |
probably benign |
0.00 |
R9616:Ncam2
|
UTSW |
16 |
81,240,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Ncam2
|
UTSW |
16 |
81,418,251 (GRCm39) |
missense |
probably benign |
0.00 |
|