Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
A |
T |
9: 124,058,052 (GRCm39) |
N19K |
possibly damaging |
Het |
Abraxas2 |
T |
C |
7: 132,476,563 (GRCm39) |
I98T |
probably damaging |
Het |
Ankrd17 |
G |
A |
5: 90,413,371 (GRCm39) |
T1181I |
probably damaging |
Het |
Bsn |
T |
A |
9: 107,991,814 (GRCm39) |
K1313* |
probably null |
Het |
Chst4 |
A |
T |
8: 110,756,699 (GRCm39) |
V388D |
probably damaging |
Het |
Ckap5 |
T |
G |
2: 91,399,054 (GRCm39) |
W613G |
probably damaging |
Het |
Clock |
GACTCACT |
GACT |
5: 76,384,967 (GRCm39) |
|
probably null |
Het |
Enpp1 |
T |
C |
10: 24,531,723 (GRCm39) |
D520G |
probably damaging |
Het |
Epha3 |
T |
C |
16: 63,593,818 (GRCm39) |
N90S |
probably benign |
Het |
Esp36 |
A |
T |
17: 38,728,005 (GRCm39) |
M92K |
unknown |
Het |
Fam135a |
A |
G |
1: 24,107,006 (GRCm39) |
V44A |
possibly damaging |
Het |
Fndc8 |
T |
C |
11: 82,788,412 (GRCm39) |
S81P |
probably damaging |
Het |
Fsip2 |
T |
G |
2: 82,819,838 (GRCm39) |
N5190K |
probably benign |
Het |
Gabrr1 |
T |
G |
4: 33,162,712 (GRCm39) |
V426G |
possibly damaging |
Het |
Igkv6-15 |
T |
A |
6: 70,383,976 (GRCm39) |
M1L |
probably benign |
Het |
Lrrc36 |
A |
G |
8: 106,185,065 (GRCm39) |
E614G |
probably damaging |
Het |
Man1a2 |
A |
T |
3: 100,539,913 (GRCm39) |
I176K |
possibly damaging |
Het |
Mapk4 |
T |
A |
18: 74,063,539 (GRCm39) |
N561I |
probably damaging |
Het |
Med15 |
A |
T |
16: 17,470,567 (GRCm39) |
|
probably benign |
Het |
Mfsd2a |
A |
G |
4: 122,844,498 (GRCm39) |
V258A |
probably benign |
Het |
Micu3 |
G |
A |
8: 40,833,736 (GRCm39) |
V457I |
probably damaging |
Het |
Mov10l1 |
T |
A |
15: 88,880,387 (GRCm39) |
V291E |
possibly damaging |
Het |
Naip2 |
T |
C |
13: 100,291,468 (GRCm39) |
S1157G |
probably benign |
Het |
Ncbp1 |
T |
C |
4: 46,157,827 (GRCm39) |
I355T |
probably damaging |
Het |
Or51s1 |
A |
G |
7: 102,558,935 (GRCm39) |
V37A |
probably benign |
Het |
Or52ad1 |
T |
C |
7: 102,995,473 (GRCm39) |
T221A |
probably benign |
Het |
Otub2 |
A |
G |
12: 103,355,278 (GRCm39) |
|
probably benign |
Het |
Pcdh15 |
T |
C |
10: 74,466,971 (GRCm39) |
S1666P |
probably damaging |
Het |
Pcdha12 |
T |
A |
18: 37,155,234 (GRCm39) |
V651E |
probably damaging |
Het |
Pomt1 |
T |
C |
2: 32,132,961 (GRCm39) |
F186L |
probably damaging |
Het |
Prl3d3 |
G |
A |
13: 27,345,044 (GRCm39) |
A140T |
probably benign |
Het |
Ptprn |
G |
A |
1: 75,234,786 (GRCm39) |
T267I |
probably benign |
Het |
Qrfprl |
C |
T |
6: 65,358,405 (GRCm39) |
A43V |
probably benign |
Het |
Rhbdd2 |
T |
A |
5: 135,665,008 (GRCm39) |
I113N |
probably damaging |
Het |
Saraf |
T |
A |
8: 34,635,767 (GRCm39) |
|
probably null |
Het |
Slc41a2 |
T |
C |
10: 83,137,022 (GRCm39) |
|
probably null |
Het |
Slc47a1 |
A |
G |
11: 61,250,229 (GRCm39) |
V352A |
probably benign |
Het |
Tmem237 |
T |
C |
1: 59,153,375 (GRCm39) |
T49A |
probably benign |
Het |
Tmem273 |
A |
C |
14: 32,528,778 (GRCm39) |
I48L |
probably benign |
Het |
Tmprss11e |
C |
T |
5: 86,863,414 (GRCm39) |
C217Y |
probably damaging |
Het |
Ubfd1 |
T |
C |
7: 121,667,103 (GRCm39) |
V140A |
probably benign |
Het |
Utrn |
A |
G |
10: 12,516,669 (GRCm39) |
|
probably null |
Het |
Utrn |
T |
A |
10: 12,574,844 (GRCm39) |
I1028F |
possibly damaging |
Het |
Virma |
C |
T |
4: 11,539,968 (GRCm39) |
T1479M |
probably damaging |
Het |
Vwa7 |
G |
T |
17: 35,243,867 (GRCm39) |
R767L |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,065,297 (GRCm39) |
Y1290* |
probably null |
Het |
Zfp970 |
G |
A |
2: 177,167,338 (GRCm39) |
C304Y |
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 |
R5014:A2ml1
|
UTSW |
6 |
128,520,896 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|
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 |
|
|