Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
G |
7: 119,953,701 (GRCm39) |
N535S |
probably benign |
Het |
Abcc6 |
A |
T |
7: 45,648,165 (GRCm39) |
L717Q |
probably benign |
Het |
Abraxas2 |
C |
A |
7: 132,484,790 (GRCm39) |
Q278K |
probably benign |
Het |
Acap2 |
A |
T |
16: 30,924,342 (GRCm39) |
D637E |
probably benign |
Het |
AI661453 |
A |
G |
17: 47,777,023 (GRCm39) |
|
probably benign |
Het |
Aoah |
A |
T |
13: 21,024,266 (GRCm39) |
E74V |
probably damaging |
Het |
Aoc1l1 |
A |
T |
6: 48,953,629 (GRCm39) |
D518V |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,671,576 (GRCm39) |
L292S |
possibly damaging |
Het |
Astl |
T |
A |
2: 127,189,109 (GRCm39) |
V166E |
probably damaging |
Het |
Bbs1 |
T |
G |
19: 4,953,735 (GRCm39) |
K143Q |
possibly damaging |
Het |
Bbx |
T |
C |
16: 50,094,907 (GRCm39) |
|
probably benign |
Het |
Birc6 |
A |
T |
17: 74,967,408 (GRCm39) |
Q4103L |
possibly damaging |
Het |
C1qtnf2 |
T |
G |
11: 43,381,811 (GRCm39) |
F178V |
probably damaging |
Het |
Camta2 |
A |
G |
11: 70,562,401 (GRCm39) |
F999L |
probably benign |
Het |
Cfap68 |
T |
C |
9: 50,676,174 (GRCm39) |
Y32C |
probably damaging |
Het |
Clcn7 |
A |
G |
17: 25,363,425 (GRCm39) |
I34V |
probably benign |
Het |
Cntn5 |
G |
T |
9: 9,748,420 (GRCm39) |
P487Q |
probably damaging |
Het |
Ctu2 |
T |
A |
8: 123,205,891 (GRCm39) |
I213K |
probably benign |
Het |
Des |
C |
A |
1: 75,340,108 (GRCm39) |
|
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,098,094 (GRCm39) |
D432E |
probably benign |
Het |
Dlgap5 |
G |
A |
14: 47,633,380 (GRCm39) |
R549* |
probably null |
Het |
Dmac2l |
A |
G |
12: 69,787,828 (GRCm39) |
Q88R |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,323,194 (GRCm39) |
T1397A |
probably damaging |
Het |
Dnmt1 |
T |
A |
9: 20,848,451 (GRCm39) |
|
probably benign |
Het |
Dstyk |
T |
A |
1: 132,391,113 (GRCm39) |
M838K |
probably damaging |
Het |
Dtwd1 |
C |
A |
2: 126,001,904 (GRCm39) |
T208N |
probably damaging |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Dync1i2 |
T |
A |
2: 71,044,907 (GRCm39) |
|
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,499,383 (GRCm39) |
M1251K |
probably benign |
Het |
Fmod |
T |
C |
1: 133,968,256 (GRCm39) |
Y99H |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,645,163 (GRCm39) |
V1552D |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,407,739 (GRCm39) |
S281T |
probably damaging |
Het |
Glb1 |
A |
G |
9: 114,293,233 (GRCm39) |
H536R |
probably benign |
Het |
Glis2 |
T |
A |
16: 4,431,506 (GRCm39) |
S344R |
possibly damaging |
Het |
Gm4847 |
A |
T |
1: 166,462,472 (GRCm39) |
S339R |
probably benign |
Het |
Gpr155 |
A |
G |
2: 73,187,002 (GRCm39) |
S44P |
probably benign |
Het |
Gprin1 |
G |
A |
13: 54,886,445 (GRCm39) |
P610S |
probably damaging |
Het |
Gvin3 |
T |
A |
7: 106,202,215 (GRCm39) |
H343L |
possibly damaging |
Het |
H2-Ob |
A |
T |
17: 34,461,554 (GRCm39) |
M98L |
probably benign |
Het |
H3c6 |
T |
C |
13: 23,746,530 (GRCm39) |
T4A |
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,223,943 (GRCm39) |
|
probably benign |
Het |
Ikbke |
C |
A |
1: 131,201,211 (GRCm39) |
V176L |
probably damaging |
Het |
Il13 |
T |
C |
11: 53,523,351 (GRCm39) |
T85A |
possibly damaging |
Het |
Inpp5k |
A |
T |
11: 75,538,017 (GRCm39) |
|
probably null |
Het |
Irgm2 |
T |
C |
11: 58,111,355 (GRCm39) |
S361P |
possibly damaging |
Het |
Itga11 |
C |
T |
9: 62,639,486 (GRCm39) |
|
probably benign |
Het |
Kalrn |
G |
T |
16: 33,829,632 (GRCm39) |
|
probably benign |
Het |
Kcng1 |
C |
A |
2: 168,110,952 (GRCm39) |
G71C |
probably damaging |
Het |
Kcnq5 |
T |
A |
1: 21,575,573 (GRCm39) |
D291V |
probably damaging |
Het |
Klhl7 |
A |
T |
5: 24,305,861 (GRCm39) |
M37L |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lhx6 |
C |
T |
2: 35,977,478 (GRCm39) |
V325I |
probably benign |
Het |
Lipc |
A |
G |
9: 70,841,817 (GRCm39) |
I9T |
possibly damaging |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Mast1 |
C |
A |
8: 85,648,107 (GRCm39) |
G458V |
probably damaging |
Het |
Mga |
T |
C |
2: 119,794,638 (GRCm39) |
V2565A |
possibly damaging |
Het |
Mpzl2 |
C |
G |
9: 44,955,471 (GRCm39) |
D127E |
probably benign |
Het |
Mrtfb |
T |
C |
16: 13,230,450 (GRCm39) |
I1045T |
probably damaging |
Het |
Myh3 |
T |
A |
11: 66,981,882 (GRCm39) |
C793S |
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,715,928 (GRCm39) |
L765P |
probably damaging |
Het |
Nup210 |
A |
G |
6: 91,005,858 (GRCm39) |
I1335T |
possibly damaging |
Het |
Or52b3 |
T |
C |
7: 102,204,267 (GRCm39) |
|
probably null |
Het |
Oxr1 |
T |
A |
15: 41,683,340 (GRCm39) |
S254R |
probably damaging |
Het |
Pan3 |
A |
G |
5: 147,466,908 (GRCm39) |
I592V |
possibly damaging |
Het |
Pask |
C |
T |
1: 93,249,019 (GRCm39) |
A794T |
probably benign |
Het |
Pex2 |
T |
C |
3: 5,626,650 (GRCm39) |
E53G |
probably damaging |
Het |
Pfkfb2 |
T |
C |
1: 130,626,460 (GRCm39) |
T438A |
probably benign |
Het |
Phactr4 |
T |
C |
4: 132,098,095 (GRCm39) |
E391G |
probably damaging |
Het |
Pira2 |
A |
T |
7: 3,847,344 (GRCm39) |
L115Q |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,376,273 (GRCm39) |
|
probably null |
Het |
Pnlip |
A |
G |
19: 58,664,876 (GRCm39) |
S235G |
probably benign |
Het |
Prkd1 |
A |
G |
12: 50,536,694 (GRCm39) |
V130A |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,703,999 (GRCm39) |
T1344A |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,001,419 (GRCm39) |
Y780C |
probably damaging |
Het |
Pxn |
T |
A |
5: 115,690,815 (GRCm39) |
|
probably benign |
Het |
Rap1gap2 |
G |
A |
11: 74,316,802 (GRCm39) |
T245M |
probably damaging |
Het |
Rc3h1 |
G |
T |
1: 160,757,827 (GRCm39) |
K48N |
probably damaging |
Het |
Rfwd3 |
T |
C |
8: 112,009,245 (GRCm39) |
I444V |
probably benign |
Het |
Rictor |
C |
T |
15: 6,794,588 (GRCm39) |
R293C |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,001,412 (GRCm39) |
I1622N |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,306,019 (GRCm39) |
V609A |
probably benign |
Het |
Scgb1b2 |
G |
T |
7: 30,991,188 (GRCm39) |
|
probably benign |
Het |
Serac1 |
A |
T |
17: 6,101,060 (GRCm39) |
I448N |
probably damaging |
Het |
Sh3kbp1 |
C |
A |
X: 158,607,492 (GRCm39) |
T200K |
probably benign |
Het |
Sned1 |
T |
A |
1: 93,199,406 (GRCm39) |
F495L |
probably damaging |
Het |
Socs7 |
T |
C |
11: 97,263,950 (GRCm39) |
F281L |
probably benign |
Het |
Spta1 |
C |
T |
1: 174,040,180 (GRCm39) |
L1214F |
probably benign |
Het |
Ssu72 |
A |
G |
4: 155,789,900 (GRCm39) |
E21G |
probably damaging |
Het |
Syngr4 |
A |
G |
7: 45,536,464 (GRCm39) |
V186A |
probably benign |
Het |
Tmem130 |
C |
A |
5: 144,680,595 (GRCm39) |
V270L |
probably benign |
Het |
Trim66 |
A |
T |
7: 109,074,320 (GRCm39) |
I647N |
probably damaging |
Het |
Tspyl2 |
A |
T |
X: 151,121,890 (GRCm39) |
D572E |
probably benign |
Het |
Unc45b |
G |
A |
11: 82,808,580 (GRCm39) |
R222H |
probably benign |
Het |
Uxs1 |
T |
C |
1: 43,866,783 (GRCm39) |
Y29C |
probably damaging |
Het |
Virma |
T |
A |
4: 11,548,726 (GRCm39) |
|
probably benign |
Het |
Vmn1r202 |
C |
T |
13: 22,685,953 (GRCm39) |
G155S |
possibly damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,755,972 (GRCm39) |
F15I |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,594,661 (GRCm39) |
T471A |
probably benign |
Het |
Zfa-ps |
T |
A |
10: 52,419,373 (GRCm39) |
|
noncoding transcript |
Het |
Zfp260 |
A |
G |
7: 29,804,765 (GRCm39) |
K222E |
probably damaging |
Het |
Zfp300 |
A |
G |
X: 20,948,190 (GRCm39) |
S525P |
possibly damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,979 (GRCm39) |
D324G |
probably damaging |
Het |
Zfp934 |
T |
C |
13: 62,665,648 (GRCm39) |
D331G |
probably damaging |
Het |
Zscan29 |
T |
C |
2: 121,000,587 (GRCm39) |
R7G |
probably damaging |
Het |
|
Other mutations in Tars3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Tars3
|
APN |
7 |
65,302,007 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00470:Tars3
|
APN |
7 |
65,338,656 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00594:Tars3
|
APN |
7 |
65,325,880 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01352:Tars3
|
APN |
7 |
65,308,658 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01519:Tars3
|
APN |
7 |
65,313,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Tars3
|
APN |
7 |
65,332,566 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02370:Tars3
|
APN |
7 |
65,310,913 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02729:Tars3
|
APN |
7 |
65,332,567 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03234:Tars3
|
APN |
7 |
65,302,026 (GRCm39) |
missense |
probably benign |
0.06 |
gary
|
UTSW |
7 |
65,338,700 (GRCm39) |
critical splice donor site |
probably null |
|
R8254_tarsl2_650
|
UTSW |
7 |
65,325,809 (GRCm39) |
missense |
probably benign |
|
smart_money
|
UTSW |
7 |
65,327,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Tars3
|
UTSW |
7 |
65,314,717 (GRCm39) |
missense |
probably benign |
0.19 |
R0153:Tars3
|
UTSW |
7 |
65,333,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:Tars3
|
UTSW |
7 |
65,327,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Tars3
|
UTSW |
7 |
65,305,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R1450:Tars3
|
UTSW |
7 |
65,297,244 (GRCm39) |
missense |
probably benign |
0.01 |
R1467:Tars3
|
UTSW |
7 |
65,305,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Tars3
|
UTSW |
7 |
65,305,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Tars3
|
UTSW |
7 |
65,308,645 (GRCm39) |
missense |
probably benign |
|
R2143:Tars3
|
UTSW |
7 |
65,305,539 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2144:Tars3
|
UTSW |
7 |
65,305,539 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2208:Tars3
|
UTSW |
7 |
65,332,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Tars3
|
UTSW |
7 |
65,338,700 (GRCm39) |
critical splice donor site |
probably null |
|
R3715:Tars3
|
UTSW |
7 |
65,338,700 (GRCm39) |
critical splice donor site |
probably null |
|
R3914:Tars3
|
UTSW |
7 |
65,333,556 (GRCm39) |
missense |
probably benign |
0.05 |
R3929:Tars3
|
UTSW |
7 |
65,333,791 (GRCm39) |
splice site |
probably null |
|
R4008:Tars3
|
UTSW |
7 |
65,327,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Tars3
|
UTSW |
7 |
65,302,018 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4367:Tars3
|
UTSW |
7 |
65,332,567 (GRCm39) |
missense |
probably damaging |
0.97 |
R4652:Tars3
|
UTSW |
7 |
65,339,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Tars3
|
UTSW |
7 |
65,297,302 (GRCm39) |
missense |
probably benign |
0.38 |
R4901:Tars3
|
UTSW |
7 |
65,341,042 (GRCm39) |
missense |
probably benign |
0.05 |
R4999:Tars3
|
UTSW |
7 |
65,308,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R5423:Tars3
|
UTSW |
7 |
65,333,567 (GRCm39) |
missense |
probably benign |
0.00 |
R5756:Tars3
|
UTSW |
7 |
65,325,724 (GRCm39) |
missense |
probably benign |
0.22 |
R5772:Tars3
|
UTSW |
7 |
65,333,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Tars3
|
UTSW |
7 |
65,332,527 (GRCm39) |
missense |
probably benign |
0.32 |
R6230:Tars3
|
UTSW |
7 |
65,336,184 (GRCm39) |
splice site |
probably null |
|
R6424:Tars3
|
UTSW |
7 |
65,305,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R6615:Tars3
|
UTSW |
7 |
65,327,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6792:Tars3
|
UTSW |
7 |
65,312,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7350:Tars3
|
UTSW |
7 |
65,308,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Tars3
|
UTSW |
7 |
65,297,341 (GRCm39) |
missense |
probably damaging |
0.96 |
R7592:Tars3
|
UTSW |
7 |
65,308,619 (GRCm39) |
missense |
probably benign |
0.01 |
R7634:Tars3
|
UTSW |
7 |
65,325,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R7710:Tars3
|
UTSW |
7 |
65,314,717 (GRCm39) |
missense |
probably benign |
0.19 |
R7808:Tars3
|
UTSW |
7 |
65,302,009 (GRCm39) |
missense |
probably benign |
0.01 |
R7875:Tars3
|
UTSW |
7 |
65,327,899 (GRCm39) |
missense |
probably benign |
0.05 |
R8254:Tars3
|
UTSW |
7 |
65,325,809 (GRCm39) |
missense |
probably benign |
|
R8793:Tars3
|
UTSW |
7 |
65,294,673 (GRCm39) |
start gained |
probably benign |
|
R9162:Tars3
|
UTSW |
7 |
65,332,518 (GRCm39) |
missense |
probably benign |
0.01 |
R9200:Tars3
|
UTSW |
7 |
65,302,013 (GRCm39) |
missense |
probably benign |
|
R9461:Tars3
|
UTSW |
7 |
65,339,719 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9533:Tars3
|
UTSW |
7 |
65,333,808 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Tars3
|
UTSW |
7 |
65,302,012 (GRCm39) |
nonsense |
probably null |
|
|