Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adss1 |
A |
C |
12: 112,602,831 (GRCm39) |
I341L |
probably benign |
Het |
Aldh1b1 |
T |
A |
4: 45,803,092 (GRCm39) |
M210K |
possibly damaging |
Het |
Ankrd17 |
G |
A |
5: 90,431,451 (GRCm39) |
Q778* |
probably null |
Het |
Bmper |
T |
C |
9: 23,318,106 (GRCm39) |
V575A |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,073,913 (GRCm39) |
V736A |
probably benign |
Het |
Ccdc81 |
A |
T |
7: 89,515,723 (GRCm39) |
L652* |
probably null |
Het |
Cdt1 |
C |
T |
8: 123,298,585 (GRCm39) |
R437W |
probably damaging |
Het |
Ckb |
A |
C |
12: 111,637,466 (GRCm39) |
L165R |
possibly damaging |
Het |
Col25a1 |
G |
T |
3: 130,290,075 (GRCm39) |
G255V |
probably damaging |
Het |
Ddx17 |
A |
G |
15: 79,420,156 (GRCm39) |
|
probably null |
Het |
Dennd4a |
G |
T |
9: 64,759,794 (GRCm39) |
G300W |
possibly damaging |
Het |
Dlg4 |
T |
A |
11: 69,930,008 (GRCm39) |
I316N |
probably damaging |
Het |
Dlgap2 |
C |
T |
8: 14,793,410 (GRCm39) |
P467L |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,732,227 (GRCm39) |
I4226M |
possibly damaging |
Het |
Drc1 |
G |
A |
5: 30,521,829 (GRCm39) |
A734T |
probably benign |
Het |
Entpd1 |
A |
G |
19: 40,600,865 (GRCm39) |
M1V |
probably null |
Het |
Exph5 |
T |
G |
9: 53,287,935 (GRCm39) |
I1672S |
possibly damaging |
Het |
Fam149b |
T |
A |
14: 20,427,852 (GRCm39) |
D379E |
probably damaging |
Het |
Fgfr2 |
T |
C |
7: 129,787,074 (GRCm39) |
T461A |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,919,946 (GRCm39) |
V469A |
probably damaging |
Het |
Frem3 |
A |
T |
8: 81,338,231 (GRCm39) |
K175* |
probably null |
Het |
Fsd2 |
C |
T |
7: 81,209,629 (GRCm39) |
G71E |
probably benign |
Het |
Gcat |
T |
C |
15: 78,919,188 (GRCm39) |
I116T |
probably damaging |
Het |
Gigyf2 |
G |
A |
1: 87,331,458 (GRCm39) |
S202N |
unknown |
Het |
Glra3 |
T |
G |
8: 56,565,911 (GRCm39) |
|
probably null |
Het |
Golga4 |
C |
T |
9: 118,365,836 (GRCm39) |
T296I |
possibly damaging |
Het |
Herc1 |
C |
T |
9: 66,341,552 (GRCm39) |
T1816I |
possibly damaging |
Het |
Igfbpl1 |
C |
A |
4: 45,826,786 (GRCm39) |
R3L |
unknown |
Het |
Ighv15-2 |
A |
T |
12: 114,528,470 (GRCm39) |
S28T |
probably benign |
Het |
Kat2b |
T |
A |
17: 53,955,835 (GRCm39) |
M427K |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,295,906 (GRCm39) |
T882A |
probably damaging |
Het |
Kif1a |
G |
T |
1: 92,967,496 (GRCm39) |
F1138L |
probably damaging |
Het |
Klhl20 |
A |
T |
1: 160,934,307 (GRCm39) |
S237R |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,123,014 (GRCm39) |
N725K |
probably damaging |
Het |
Lmtk3 |
A |
G |
7: 45,444,890 (GRCm39) |
D1191G |
unknown |
Het |
Ltbp1 |
C |
A |
17: 75,670,358 (GRCm39) |
N1466K |
possibly damaging |
Het |
Lyrm1 |
T |
C |
7: 119,515,449 (GRCm39) |
V113A |
probably benign |
Het |
Mfsd13a |
G |
T |
19: 46,360,446 (GRCm39) |
A333S |
probably benign |
Het |
Mllt10 |
T |
C |
2: 18,167,214 (GRCm39) |
S380P |
possibly damaging |
Het |
Mrc2 |
A |
G |
11: 105,238,829 (GRCm39) |
K1295E |
possibly damaging |
Het |
Muc5ac |
A |
T |
7: 141,363,528 (GRCm39) |
I2280F |
unknown |
Het |
Neurod2 |
A |
C |
11: 98,218,023 (GRCm39) |
F380L |
probably damaging |
Het |
Ntrk3 |
G |
A |
7: 78,005,954 (GRCm39) |
A469V |
probably damaging |
Het |
Nup205 |
T |
C |
6: 35,175,888 (GRCm39) |
F584L |
probably damaging |
Het |
Oas1d |
A |
T |
5: 121,057,210 (GRCm39) |
Y272F |
probably damaging |
Het |
Olfm3 |
T |
C |
3: 114,874,794 (GRCm39) |
V30A |
probably benign |
Het |
Or4c110 |
T |
A |
2: 88,831,973 (GRCm39) |
I220F |
probably damaging |
Het |
Or5b117 |
A |
G |
19: 13,431,563 (GRCm39) |
I106T |
probably benign |
Het |
Or8k22 |
A |
G |
2: 86,163,064 (GRCm39) |
V212A |
probably benign |
Het |
Pcdhga12 |
A |
G |
18: 37,901,427 (GRCm39) |
Y753C |
probably damaging |
Het |
Phox2b |
A |
G |
5: 67,253,514 (GRCm39) |
V294A |
unknown |
Het |
Prdm2 |
A |
T |
4: 142,859,812 (GRCm39) |
C1159* |
probably null |
Het |
Ptpn12 |
G |
T |
5: 21,207,631 (GRCm39) |
S275* |
probably null |
Het |
Rigi |
T |
C |
4: 40,209,894 (GRCm39) |
M725V |
probably damaging |
Het |
Rnf223 |
A |
T |
4: 156,216,776 (GRCm39) |
E50D |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,879,548 (GRCm39) |
Y169N |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,757,736 (GRCm39) |
|
probably null |
Het |
Shank2 |
T |
C |
7: 143,964,798 (GRCm39) |
I802T |
probably damaging |
Het |
Skint2 |
A |
T |
4: 112,481,329 (GRCm39) |
N64I |
probably damaging |
Het |
Smpd3 |
A |
C |
8: 106,982,254 (GRCm39) |
C617G |
probably benign |
Het |
Tmem106c |
G |
C |
15: 97,865,985 (GRCm39) |
G192R |
probably damaging |
Het |
Tmem72 |
T |
C |
6: 116,673,800 (GRCm39) |
H106R |
probably damaging |
Het |
Upf2 |
G |
C |
2: 6,030,926 (GRCm39) |
V789L |
unknown |
Het |
Vash1 |
A |
G |
12: 86,726,758 (GRCm39) |
|
probably benign |
Het |
Vmn1r201 |
T |
A |
13: 22,658,875 (GRCm39) |
Y30N |
probably benign |
Het |
Xpr1 |
A |
G |
1: 155,166,035 (GRCm39) |
F571L |
possibly damaging |
Het |
Yif1a |
T |
C |
19: 5,139,815 (GRCm39) |
S87P |
probably damaging |
Het |
Zer1 |
T |
C |
2: 29,997,520 (GRCm39) |
Y462C |
probably damaging |
Het |
Zfp597 |
G |
A |
16: 3,684,375 (GRCm39) |
P127L |
possibly damaging |
Het |
Zxdc |
T |
C |
6: 90,375,749 (GRCm39) |
S742P |
probably benign |
Het |
|
Other mutations in Ly75 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00561:Ly75
|
APN |
2 |
60,206,421 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01072:Ly75
|
APN |
2 |
60,184,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01409:Ly75
|
APN |
2 |
60,152,036 (GRCm39) |
splice site |
probably null |
|
IGL01432:Ly75
|
APN |
2 |
60,206,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01626:Ly75
|
APN |
2 |
60,131,359 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01690:Ly75
|
APN |
2 |
60,168,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01862:Ly75
|
APN |
2 |
60,129,516 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Ly75
|
APN |
2 |
60,142,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02075:Ly75
|
APN |
2 |
60,182,700 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02338:Ly75
|
APN |
2 |
60,184,796 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02364:Ly75
|
APN |
2 |
60,188,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02456:Ly75
|
APN |
2 |
60,124,125 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02474:Ly75
|
APN |
2 |
60,213,526 (GRCm39) |
missense |
probably null |
1.00 |
IGL02608:Ly75
|
APN |
2 |
60,152,244 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02986:Ly75
|
APN |
2 |
60,138,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03015:Ly75
|
APN |
2 |
60,206,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03049:Ly75
|
APN |
2 |
60,182,414 (GRCm39) |
missense |
probably damaging |
0.99 |
euphues
|
UTSW |
2 |
60,129,389 (GRCm39) |
critical splice donor site |
probably null |
|
four_score
|
UTSW |
2 |
60,142,115 (GRCm39) |
missense |
possibly damaging |
0.75 |
lyly
|
UTSW |
2 |
60,158,217 (GRCm39) |
missense |
possibly damaging |
0.49 |
Witty
|
UTSW |
2 |
60,184,844 (GRCm39) |
missense |
probably damaging |
1.00 |
D605:Ly75
|
UTSW |
2 |
60,182,696 (GRCm39) |
critical splice donor site |
probably null |
|
R0046:Ly75
|
UTSW |
2 |
60,169,801 (GRCm39) |
intron |
probably benign |
|
R0055:Ly75
|
UTSW |
2 |
60,152,262 (GRCm39) |
missense |
probably benign |
0.01 |
R0055:Ly75
|
UTSW |
2 |
60,152,262 (GRCm39) |
missense |
probably benign |
0.01 |
R0071:Ly75
|
UTSW |
2 |
60,152,163 (GRCm39) |
missense |
probably benign |
0.01 |
R0071:Ly75
|
UTSW |
2 |
60,152,163 (GRCm39) |
missense |
probably benign |
0.01 |
R0285:Ly75
|
UTSW |
2 |
60,148,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Ly75
|
UTSW |
2 |
60,136,748 (GRCm39) |
missense |
probably benign |
0.20 |
R0492:Ly75
|
UTSW |
2 |
60,138,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R0688:Ly75
|
UTSW |
2 |
60,146,565 (GRCm39) |
missense |
probably benign |
0.41 |
R1367:Ly75
|
UTSW |
2 |
60,124,102 (GRCm39) |
splice site |
probably null |
|
R1463:Ly75
|
UTSW |
2 |
60,199,101 (GRCm39) |
critical splice donor site |
probably null |
|
R1581:Ly75
|
UTSW |
2 |
60,158,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1663:Ly75
|
UTSW |
2 |
60,144,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Ly75
|
UTSW |
2 |
60,142,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Ly75
|
UTSW |
2 |
60,180,284 (GRCm39) |
missense |
probably benign |
0.00 |
R2244:Ly75
|
UTSW |
2 |
60,180,257 (GRCm39) |
missense |
probably benign |
0.01 |
R2905:Ly75
|
UTSW |
2 |
60,164,898 (GRCm39) |
missense |
probably benign |
0.00 |
R3967:Ly75
|
UTSW |
2 |
60,158,217 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3968:Ly75
|
UTSW |
2 |
60,158,217 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4039:Ly75
|
UTSW |
2 |
60,183,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4406:Ly75
|
UTSW |
2 |
60,184,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R4526:Ly75
|
UTSW |
2 |
60,161,117 (GRCm39) |
missense |
probably benign |
0.09 |
R4647:Ly75
|
UTSW |
2 |
60,138,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Ly75
|
UTSW |
2 |
60,180,284 (GRCm39) |
missense |
probably benign |
0.00 |
R4796:Ly75
|
UTSW |
2 |
60,180,284 (GRCm39) |
missense |
probably benign |
0.00 |
R4962:Ly75
|
UTSW |
2 |
60,182,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Ly75
|
UTSW |
2 |
60,206,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Ly75
|
UTSW |
2 |
60,206,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Ly75
|
UTSW |
2 |
60,133,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5373:Ly75
|
UTSW |
2 |
60,142,115 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5374:Ly75
|
UTSW |
2 |
60,142,115 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5384:Ly75
|
UTSW |
2 |
60,164,831 (GRCm39) |
nonsense |
probably null |
|
R5385:Ly75
|
UTSW |
2 |
60,133,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Ly75
|
UTSW |
2 |
60,195,455 (GRCm39) |
missense |
probably benign |
0.41 |
R5531:Ly75
|
UTSW |
2 |
60,195,489 (GRCm39) |
missense |
probably damaging |
0.98 |
R5662:Ly75
|
UTSW |
2 |
60,182,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5667:Ly75
|
UTSW |
2 |
60,138,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R5668:Ly75
|
UTSW |
2 |
60,184,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Ly75
|
UTSW |
2 |
60,138,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Ly75
|
UTSW |
2 |
60,129,426 (GRCm39) |
missense |
probably benign |
0.00 |
R5764:Ly75
|
UTSW |
2 |
60,148,783 (GRCm39) |
missense |
probably benign |
|
R5896:Ly75
|
UTSW |
2 |
60,213,490 (GRCm39) |
missense |
probably benign |
|
R6025:Ly75
|
UTSW |
2 |
60,206,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6113:Ly75
|
UTSW |
2 |
60,199,217 (GRCm39) |
missense |
probably benign |
0.04 |
R6448:Ly75
|
UTSW |
2 |
60,129,389 (GRCm39) |
critical splice donor site |
probably null |
|
R6601:Ly75
|
UTSW |
2 |
60,148,720 (GRCm39) |
missense |
probably benign |
0.11 |
R6745:Ly75
|
UTSW |
2 |
60,138,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R6955:Ly75
|
UTSW |
2 |
60,158,217 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6960:Ly75
|
UTSW |
2 |
60,136,749 (GRCm39) |
missense |
probably benign |
|
R7100:Ly75
|
UTSW |
2 |
60,136,778 (GRCm39) |
missense |
probably benign |
|
R7110:Ly75
|
UTSW |
2 |
60,206,528 (GRCm39) |
missense |
probably benign |
0.31 |
R7203:Ly75
|
UTSW |
2 |
60,154,196 (GRCm39) |
nonsense |
probably null |
|
R7291:Ly75
|
UTSW |
2 |
60,160,337 (GRCm39) |
missense |
probably damaging |
0.98 |
R7308:Ly75
|
UTSW |
2 |
60,164,859 (GRCm39) |
missense |
probably benign |
0.04 |
R7447:Ly75
|
UTSW |
2 |
60,164,818 (GRCm39) |
nonsense |
probably null |
|
R7512:Ly75
|
UTSW |
2 |
60,164,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R7595:Ly75
|
UTSW |
2 |
60,124,171 (GRCm39) |
missense |
probably benign |
0.01 |
R8005:Ly75
|
UTSW |
2 |
60,163,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ly75
|
UTSW |
2 |
60,144,572 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8392:Ly75
|
UTSW |
2 |
60,180,284 (GRCm39) |
missense |
probably benign |
0.00 |
R8705:Ly75
|
UTSW |
2 |
60,148,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R8714:Ly75
|
UTSW |
2 |
60,164,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8798:Ly75
|
UTSW |
2 |
60,154,270 (GRCm39) |
missense |
probably benign |
0.32 |
R8799:Ly75
|
UTSW |
2 |
60,178,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R8834:Ly75
|
UTSW |
2 |
60,161,433 (GRCm39) |
missense |
probably benign |
|
R8990:Ly75
|
UTSW |
2 |
60,188,903 (GRCm39) |
missense |
probably benign |
0.10 |
R9015:Ly75
|
UTSW |
2 |
60,146,442 (GRCm39) |
missense |
probably benign |
|
R9547:Ly75
|
UTSW |
2 |
60,161,069 (GRCm39) |
critical splice donor site |
probably null |
|
R9628:Ly75
|
UTSW |
2 |
60,158,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R9659:Ly75
|
UTSW |
2 |
60,168,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Ly75
|
UTSW |
2 |
60,154,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Ly75
|
UTSW |
2 |
60,136,672 (GRCm39) |
critical splice donor site |
probably null |
|
X0025:Ly75
|
UTSW |
2 |
60,184,819 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ly75
|
UTSW |
2 |
60,182,477 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1177:Ly75
|
UTSW |
2 |
60,180,348 (GRCm39) |
nonsense |
probably null |
|
|