Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
T |
11: 109,840,957 (GRCm39) |
I1072N |
probably damaging |
Het |
Atp1a2 |
T |
C |
1: 172,112,438 (GRCm39) |
T517A |
probably benign |
Het |
Blk |
T |
G |
14: 63,617,236 (GRCm39) |
N257T |
probably benign |
Het |
Brd4 |
A |
T |
17: 32,417,372 (GRCm39) |
|
probably benign |
Het |
Calr4 |
C |
T |
4: 109,092,994 (GRCm39) |
Q25* |
probably null |
Het |
Cbl |
T |
C |
9: 44,065,696 (GRCm39) |
|
probably null |
Het |
Ccdc30 |
T |
G |
4: 119,250,824 (GRCm39) |
H6P |
possibly damaging |
Het |
Cd101 |
A |
C |
3: 100,911,139 (GRCm39) |
Y840D |
probably damaging |
Het |
Cd68 |
T |
A |
11: 69,556,165 (GRCm39) |
N178Y |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,803,952 (GRCm39) |
T1044A |
probably benign |
Het |
Cfap46 |
A |
G |
7: 139,207,291 (GRCm39) |
V1876A |
probably benign |
Het |
Clec2g |
T |
A |
6: 128,925,765 (GRCm39) |
M58K |
probably benign |
Het |
Clip1 |
T |
C |
5: 123,755,793 (GRCm39) |
E860G |
probably damaging |
Het |
Col18a1 |
C |
T |
10: 76,906,794 (GRCm39) |
|
probably null |
Het |
Cul7 |
A |
G |
17: 46,966,868 (GRCm39) |
*650W |
probably null |
Het |
Dkk4 |
C |
T |
8: 23,115,315 (GRCm39) |
A55V |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dnai7 |
T |
C |
6: 145,128,992 (GRCm39) |
E407G |
probably damaging |
Het |
Dnase1 |
C |
A |
16: 3,856,880 (GRCm39) |
Y170* |
probably null |
Het |
Dnmt1 |
A |
C |
9: 20,823,550 (GRCm39) |
I1019S |
probably benign |
Het |
Epha6 |
T |
A |
16: 59,486,942 (GRCm39) |
H1035L |
probably benign |
Het |
Fam124b |
T |
C |
1: 80,177,776 (GRCm39) |
T408A |
probably benign |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Galnt7 |
T |
C |
8: 57,998,414 (GRCm39) |
E305G |
probably damaging |
Het |
Garin1b |
C |
T |
6: 29,326,723 (GRCm39) |
|
probably benign |
Het |
Git1 |
T |
A |
11: 77,389,821 (GRCm39) |
V28E |
probably damaging |
Het |
Gm10010 |
C |
T |
6: 128,177,556 (GRCm39) |
|
noncoding transcript |
Het |
Gm4956 |
T |
C |
1: 21,363,821 (GRCm39) |
|
noncoding transcript |
Het |
Gpr152 |
T |
G |
19: 4,193,506 (GRCm39) |
V349G |
probably benign |
Het |
Gtsf1l |
C |
T |
2: 162,929,112 (GRCm39) |
V124I |
probably damaging |
Het |
Gucy1b1 |
C |
G |
3: 81,953,974 (GRCm39) |
G114A |
probably benign |
Het |
Hk2 |
T |
C |
6: 82,720,936 (GRCm39) |
Q166R |
possibly damaging |
Het |
Hook2 |
A |
G |
8: 85,718,006 (GRCm39) |
I44M |
probably damaging |
Het |
Ildr1 |
T |
A |
16: 36,541,921 (GRCm39) |
M222K |
probably damaging |
Het |
Ints6 |
A |
T |
14: 62,997,640 (GRCm39) |
F55Y |
probably benign |
Het |
Kcnh1 |
A |
G |
1: 191,959,388 (GRCm39) |
N314S |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,746,748 (GRCm39) |
F748L |
probably damaging |
Het |
Lrsam1 |
T |
C |
2: 32,826,407 (GRCm39) |
|
probably benign |
Het |
Msh2 |
A |
T |
17: 88,025,004 (GRCm39) |
K627N |
possibly damaging |
Het |
Myrip |
A |
G |
9: 120,251,534 (GRCm39) |
Q219R |
probably damaging |
Het |
Ndufb3 |
T |
A |
1: 58,630,401 (GRCm39) |
W51R |
probably damaging |
Het |
Nfasc |
A |
T |
1: 132,512,185 (GRCm39) |
|
probably benign |
Het |
Or2c1 |
T |
A |
16: 3,656,912 (GRCm39) |
I25N |
probably benign |
Het |
Or2h2 |
T |
A |
17: 37,396,446 (GRCm39) |
I204F |
probably benign |
Het |
Or8s8 |
T |
C |
15: 98,354,857 (GRCm39) |
V222A |
possibly damaging |
Het |
P3h3 |
T |
A |
6: 124,832,199 (GRCm39) |
E229V |
probably damaging |
Het |
Ppfia2 |
T |
A |
10: 106,701,224 (GRCm39) |
L837* |
probably null |
Het |
Ppp2r1a |
G |
A |
17: 21,179,101 (GRCm39) |
|
probably null |
Het |
Rabgap1 |
T |
A |
2: 37,377,152 (GRCm39) |
V328E |
probably damaging |
Het |
Ralgapb |
G |
A |
2: 158,337,455 (GRCm39) |
R1138Q |
probably damaging |
Het |
Ranbp2 |
A |
T |
10: 58,299,942 (GRCm39) |
Q498L |
probably benign |
Het |
Rbx1 |
T |
A |
15: 81,355,161 (GRCm39) |
C56S |
probably damaging |
Het |
Rcan2 |
T |
C |
17: 44,328,704 (GRCm39) |
F45S |
probably damaging |
Het |
Rgs20 |
T |
C |
1: 4,980,770 (GRCm39) |
Y185C |
probably damaging |
Het |
Rorc |
T |
G |
3: 94,298,460 (GRCm39) |
L315R |
probably damaging |
Het |
Skic2 |
A |
G |
17: 35,066,401 (GRCm39) |
V194A |
probably benign |
Het |
Slc13a2 |
T |
C |
11: 78,290,987 (GRCm39) |
K406E |
possibly damaging |
Het |
Slc35g3 |
T |
A |
11: 69,651,866 (GRCm39) |
K62* |
probably null |
Het |
Sox30 |
T |
C |
11: 45,882,736 (GRCm39) |
S589P |
probably benign |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Ssh2 |
T |
A |
11: 77,346,102 (GRCm39) |
C1362* |
probably null |
Het |
Tecta |
C |
T |
9: 42,284,538 (GRCm39) |
C849Y |
probably damaging |
Het |
Thbs1 |
T |
A |
2: 117,950,518 (GRCm39) |
|
probably null |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tut4 |
T |
C |
4: 108,384,043 (GRCm39) |
|
probably benign |
Het |
Tyk2 |
C |
T |
9: 21,027,126 (GRCm39) |
|
probably null |
Het |
Tyw5 |
C |
A |
1: 57,446,004 (GRCm39) |
|
probably benign |
Het |
Vcp |
T |
C |
4: 42,980,828 (GRCm39) |
T761A |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,822,897 (GRCm39) |
C1401S |
probably benign |
Het |
Wiz |
T |
C |
17: 32,578,340 (GRCm39) |
N391D |
probably damaging |
Het |
Ylpm1 |
G |
A |
12: 85,061,523 (GRCm39) |
E475K |
unknown |
Het |
Zfp108 |
G |
T |
7: 23,960,163 (GRCm39) |
K251N |
probably benign |
Het |
Zfp184 |
A |
G |
13: 22,142,594 (GRCm39) |
D100G |
probably benign |
Het |
Zfp990 |
T |
A |
4: 145,264,669 (GRCm39) |
C556S |
possibly damaging |
Het |
Zkscan16 |
C |
T |
4: 58,951,892 (GRCm39) |
P189L |
probably damaging |
Het |
|
Other mutations in A2ml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00513:A2ml1
|
APN |
6 |
128,555,119 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00596:A2ml1
|
APN |
6 |
128,547,030 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00912:A2ml1
|
APN |
6 |
128,529,270 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01320:A2ml1
|
APN |
6 |
128,552,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01470:A2ml1
|
APN |
6 |
128,557,375 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01576:A2ml1
|
APN |
6 |
128,531,293 (GRCm39) |
splice site |
probably benign |
|
IGL01761:A2ml1
|
APN |
6 |
128,523,300 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01792:A2ml1
|
APN |
6 |
128,537,642 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01843:A2ml1
|
APN |
6 |
128,530,301 (GRCm39) |
splice site |
probably benign |
|
IGL01946:A2ml1
|
APN |
6 |
128,547,442 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02016:A2ml1
|
APN |
6 |
128,535,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:A2ml1
|
APN |
6 |
128,524,173 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02269:A2ml1
|
APN |
6 |
128,530,301 (GRCm39) |
splice site |
probably benign |
|
IGL02589:A2ml1
|
APN |
6 |
128,558,463 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02959:A2ml1
|
APN |
6 |
128,544,023 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02970:A2ml1
|
APN |
6 |
128,546,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03206:A2ml1
|
APN |
6 |
128,530,239 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03298:A2ml1
|
APN |
6 |
128,520,923 (GRCm39) |
missense |
probably benign |
0.00 |
1mM(1):A2ml1
|
UTSW |
6 |
128,557,923 (GRCm39) |
missense |
probably benign |
0.02 |
R0055:A2ml1
|
UTSW |
6 |
128,547,057 (GRCm39) |
splice site |
probably benign |
|
R0055:A2ml1
|
UTSW |
6 |
128,547,057 (GRCm39) |
splice site |
probably benign |
|
R0069:A2ml1
|
UTSW |
6 |
128,538,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0069:A2ml1
|
UTSW |
6 |
128,538,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:A2ml1
|
UTSW |
6 |
128,552,602 (GRCm39) |
splice site |
probably benign |
|
R0299:A2ml1
|
UTSW |
6 |
128,530,195 (GRCm39) |
splice site |
probably benign |
|
R0523:A2ml1
|
UTSW |
6 |
128,535,289 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0565:A2ml1
|
UTSW |
6 |
128,545,706 (GRCm39) |
nonsense |
probably null |
|
R0599:A2ml1
|
UTSW |
6 |
128,529,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:A2ml1
|
UTSW |
6 |
128,527,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R0732:A2ml1
|
UTSW |
6 |
128,523,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:A2ml1
|
UTSW |
6 |
128,537,609 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1070:A2ml1
|
UTSW |
6 |
128,520,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1166:A2ml1
|
UTSW |
6 |
128,547,880 (GRCm39) |
missense |
probably benign |
0.00 |
R1278:A2ml1
|
UTSW |
6 |
128,535,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:A2ml1
|
UTSW |
6 |
128,520,923 (GRCm39) |
missense |
probably benign |
0.00 |
R1536:A2ml1
|
UTSW |
6 |
128,524,196 (GRCm39) |
nonsense |
probably null |
|
R1786:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:A2ml1
|
UTSW |
6 |
128,520,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:A2ml1
|
UTSW |
6 |
128,543,236 (GRCm39) |
missense |
probably benign |
0.34 |
R1863:A2ml1
|
UTSW |
6 |
128,527,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R2007:A2ml1
|
UTSW |
6 |
128,519,855 (GRCm39) |
missense |
probably benign |
0.13 |
R2062:A2ml1
|
UTSW |
6 |
128,529,271 (GRCm39) |
missense |
probably benign |
0.08 |
R2127:A2ml1
|
UTSW |
6 |
128,535,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:A2ml1
|
UTSW |
6 |
128,553,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:A2ml1
|
UTSW |
6 |
128,524,268 (GRCm39) |
missense |
probably null |
0.34 |
R2319:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2321:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2322:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2369:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2370:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2371:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2372:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2375:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2893:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R2894:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R3438:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R3615:A2ml1
|
UTSW |
6 |
128,535,257 (GRCm39) |
missense |
probably benign |
0.07 |
R3616:A2ml1
|
UTSW |
6 |
128,535,257 (GRCm39) |
missense |
probably benign |
0.07 |
R3773:A2ml1
|
UTSW |
6 |
128,532,046 (GRCm39) |
missense |
probably benign |
0.02 |
R3785:A2ml1
|
UTSW |
6 |
128,521,887 (GRCm39) |
critical splice donor site |
probably null |
|
R3803:A2ml1
|
UTSW |
6 |
128,522,033 (GRCm39) |
missense |
probably benign |
0.17 |
R3824:A2ml1
|
UTSW |
6 |
128,545,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R3878:A2ml1
|
UTSW |
6 |
128,531,324 (GRCm39) |
missense |
probably benign |
0.05 |
R4176:A2ml1
|
UTSW |
6 |
128,522,000 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4229:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4230:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4348:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4351:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4352:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4353:A2ml1
|
UTSW |
6 |
128,557,349 (GRCm39) |
missense |
probably benign |
0.01 |
R4427:A2ml1
|
UTSW |
6 |
128,522,009 (GRCm39) |
missense |
probably benign |
0.00 |
R4971:A2ml1
|
UTSW |
6 |
128,524,190 (GRCm39) |
missense |
probably damaging |
0.98 |
R5369:A2ml1
|
UTSW |
6 |
128,545,796 (GRCm39) |
missense |
probably damaging |
0.97 |
R5532:A2ml1
|
UTSW |
6 |
128,530,293 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5860:A2ml1
|
UTSW |
6 |
128,518,024 (GRCm39) |
missense |
probably benign |
0.15 |
R5872:A2ml1
|
UTSW |
6 |
128,538,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5926:A2ml1
|
UTSW |
6 |
128,537,608 (GRCm39) |
missense |
probably benign |
|
R5977:A2ml1
|
UTSW |
6 |
128,558,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R5980:A2ml1
|
UTSW |
6 |
128,544,018 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6014:A2ml1
|
UTSW |
6 |
128,548,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:A2ml1
|
UTSW |
6 |
128,526,799 (GRCm39) |
nonsense |
probably null |
|
R6032:A2ml1
|
UTSW |
6 |
128,526,799 (GRCm39) |
nonsense |
probably null |
|
R6061:A2ml1
|
UTSW |
6 |
128,545,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6327:A2ml1
|
UTSW |
6 |
128,535,655 (GRCm39) |
splice site |
probably null |
|
R6331:A2ml1
|
UTSW |
6 |
128,529,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6465:A2ml1
|
UTSW |
6 |
128,518,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R6640:A2ml1
|
UTSW |
6 |
128,530,248 (GRCm39) |
missense |
probably benign |
0.41 |
R6792:A2ml1
|
UTSW |
6 |
128,523,292 (GRCm39) |
nonsense |
probably null |
|
R6793:A2ml1
|
UTSW |
6 |
128,523,292 (GRCm39) |
nonsense |
probably null |
|
R7207:A2ml1
|
UTSW |
6 |
128,527,734 (GRCm39) |
missense |
probably benign |
0.04 |
R7378:A2ml1
|
UTSW |
6 |
128,523,210 (GRCm39) |
critical splice donor site |
probably null |
|
R7556:A2ml1
|
UTSW |
6 |
128,546,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:A2ml1
|
UTSW |
6 |
128,557,303 (GRCm39) |
missense |
probably benign |
0.08 |
R8017:A2ml1
|
UTSW |
6 |
128,558,410 (GRCm39) |
critical splice donor site |
probably null |
|
R8019:A2ml1
|
UTSW |
6 |
128,558,410 (GRCm39) |
critical splice donor site |
probably null |
|
R8035:A2ml1
|
UTSW |
6 |
128,530,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R8094:A2ml1
|
UTSW |
6 |
128,549,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R8144:A2ml1
|
UTSW |
6 |
128,546,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8365:A2ml1
|
UTSW |
6 |
128,557,918 (GRCm39) |
nonsense |
probably null |
|
R8382:A2ml1
|
UTSW |
6 |
128,537,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8388:A2ml1
|
UTSW |
6 |
128,548,937 (GRCm39) |
missense |
probably benign |
0.03 |
R8717:A2ml1
|
UTSW |
6 |
128,543,958 (GRCm39) |
missense |
probably benign |
0.00 |
R8947:A2ml1
|
UTSW |
6 |
128,529,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:A2ml1
|
UTSW |
6 |
128,545,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R9025:A2ml1
|
UTSW |
6 |
128,534,545 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9083:A2ml1
|
UTSW |
6 |
128,534,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9129:A2ml1
|
UTSW |
6 |
128,523,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:A2ml1
|
UTSW |
6 |
128,536,032 (GRCm39) |
missense |
probably benign |
|
R9165:A2ml1
|
UTSW |
6 |
128,537,632 (GRCm39) |
missense |
probably benign |
|
R9285:A2ml1
|
UTSW |
6 |
128,526,756 (GRCm39) |
missense |
probably benign |
|
R9408:A2ml1
|
UTSW |
6 |
128,522,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R9486:A2ml1
|
UTSW |
6 |
128,546,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R9781:A2ml1
|
UTSW |
6 |
128,519,860 (GRCm39) |
missense |
probably benign |
0.01 |
RF014:A2ml1
|
UTSW |
6 |
128,547,031 (GRCm39) |
missense |
probably damaging |
0.96 |
X0063:A2ml1
|
UTSW |
6 |
128,548,975 (GRCm39) |
missense |
probably benign |
|
Z1176:A2ml1
|
UTSW |
6 |
128,548,940 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:A2ml1
|
UTSW |
6 |
128,552,570 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:A2ml1
|
UTSW |
6 |
128,538,579 (GRCm39) |
nonsense |
probably null |
|
Z1177:A2ml1
|
UTSW |
6 |
128,522,039 (GRCm39) |
missense |
probably benign |
|
|