Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,133,021 (GRCm39) |
N1317D |
probably benign |
Het |
Abhd8 |
T |
A |
8: 71,910,794 (GRCm39) |
Y338F |
possibly damaging |
Het |
Actg2 |
G |
T |
6: 83,493,346 (GRCm39) |
N297K |
probably damaging |
Het |
Agap1 |
A |
G |
1: 89,558,156 (GRCm39) |
D148G |
probably damaging |
Het |
Alox12 |
T |
C |
11: 70,145,417 (GRCm39) |
D52G |
possibly damaging |
Het |
Ano5 |
T |
A |
7: 51,224,573 (GRCm39) |
S496T |
probably damaging |
Het |
Arl6ip4 |
T |
C |
5: 124,255,968 (GRCm39) |
|
probably null |
Het |
Atp4a |
G |
C |
7: 30,421,941 (GRCm39) |
E826Q |
probably damaging |
Het |
Bbs7 |
T |
C |
3: 36,657,060 (GRCm39) |
D256G |
probably damaging |
Het |
Bckdha |
T |
A |
7: 25,330,866 (GRCm39) |
D50V |
probably damaging |
Het |
Cast |
A |
G |
13: 74,844,056 (GRCm39) |
S693P |
possibly damaging |
Het |
Cfap251 |
C |
T |
5: 123,412,267 (GRCm39) |
T532M |
probably damaging |
Het |
Col6a1 |
T |
C |
10: 76,545,700 (GRCm39) |
Y924C |
unknown |
Het |
Crkl |
A |
G |
16: 17,270,604 (GRCm39) |
Y88C |
probably damaging |
Het |
Cse1l |
T |
C |
2: 166,761,541 (GRCm39) |
F32L |
probably benign |
Het |
Dmxl2 |
C |
T |
9: 54,300,957 (GRCm39) |
V2385I |
probably benign |
Het |
Dnah1 |
T |
A |
14: 30,989,984 (GRCm39) |
I3219F |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,916,375 (GRCm39) |
R4266H |
probably benign |
Het |
Efcab5 |
A |
G |
11: 77,012,088 (GRCm39) |
L722P |
probably damaging |
Het |
Emilin3 |
C |
A |
2: 160,751,105 (GRCm39) |
V215L |
probably benign |
Het |
Entr1 |
T |
C |
2: 26,276,983 (GRCm39) |
D249G |
possibly damaging |
Het |
Esr1 |
A |
T |
10: 4,696,622 (GRCm39) |
N157I |
possibly damaging |
Het |
Esrrg |
A |
G |
1: 187,930,904 (GRCm39) |
M309V |
probably benign |
Het |
Fam120b |
G |
A |
17: 15,622,172 (GRCm39) |
R50Q |
probably damaging |
Het |
Fat2 |
G |
T |
11: 55,201,129 (GRCm39) |
Y648* |
probably null |
Het |
Gbp2b |
T |
A |
3: 142,309,414 (GRCm39) |
I175N |
probably benign |
Het |
Gm1043 |
T |
A |
5: 37,311,952 (GRCm39) |
|
probably benign |
Het |
Gm21060 |
A |
G |
19: 61,285,411 (GRCm39) |
C33R |
possibly damaging |
Het |
Gpx6 |
C |
T |
13: 21,496,510 (GRCm39) |
S28L |
probably benign |
Het |
Hyls1 |
G |
A |
9: 35,472,480 (GRCm39) |
S312F |
probably benign |
Het |
Ifi44 |
T |
C |
3: 151,455,195 (GRCm39) |
Q10R |
probably benign |
Het |
Impa2 |
T |
C |
18: 67,451,498 (GRCm39) |
V264A |
probably benign |
Het |
Khdc1a |
A |
T |
1: 21,421,108 (GRCm39) |
M98L |
probably benign |
Het |
Lrrc45 |
T |
A |
11: 120,611,474 (GRCm39) |
L616* |
probably null |
Het |
Mios |
A |
T |
6: 8,215,704 (GRCm39) |
H300L |
probably benign |
Het |
Mllt6 |
A |
T |
11: 97,568,051 (GRCm39) |
T827S |
probably damaging |
Het |
Mrc1 |
C |
A |
2: 14,321,712 (GRCm39) |
D1068E |
probably benign |
Het |
Ndst3 |
T |
C |
3: 123,346,168 (GRCm39) |
Y702C |
probably damaging |
Het |
Nek11 |
T |
A |
9: 105,082,087 (GRCm39) |
|
probably null |
Het |
Nek4 |
T |
C |
14: 30,678,890 (GRCm39) |
F138S |
probably damaging |
Het |
Nfatc4 |
T |
A |
14: 56,069,897 (GRCm39) |
Y688* |
probably null |
Het |
Nlrx1 |
C |
T |
9: 44,175,057 (GRCm39) |
V240M |
probably damaging |
Het |
Npy6r |
A |
T |
18: 44,409,149 (GRCm39) |
Y190F |
probably benign |
Het |
Or10ab5 |
A |
C |
7: 108,245,433 (GRCm39) |
S117A |
possibly damaging |
Het |
Or10d4b |
T |
C |
9: 39,534,637 (GRCm39) |
F71L |
probably damaging |
Het |
Or1j10 |
T |
G |
2: 36,267,556 (GRCm39) |
L256R |
probably damaging |
Het |
Or52b4i |
C |
A |
7: 102,191,817 (GRCm39) |
R225S |
probably benign |
Het |
Or5p52 |
A |
G |
7: 107,502,620 (GRCm39) |
E232G |
probably benign |
Het |
Or6c68 |
A |
T |
10: 129,158,238 (GRCm39) |
T249S |
probably benign |
Het |
Osbpl7 |
A |
C |
11: 96,943,087 (GRCm39) |
H113P |
probably benign |
Het |
Pam16l |
C |
T |
10: 43,400,252 (GRCm39) |
A30V |
probably benign |
Het |
Pck1 |
A |
G |
2: 172,996,650 (GRCm39) |
E188G |
probably benign |
Het |
Pimreg |
A |
G |
11: 71,936,576 (GRCm39) |
D213G |
probably benign |
Het |
Pkd1l2 |
A |
G |
8: 117,769,976 (GRCm39) |
I1160T |
probably damaging |
Het |
Ppargc1b |
G |
A |
18: 61,441,005 (GRCm39) |
Q622* |
probably null |
Het |
Ppfia2 |
T |
A |
10: 106,742,338 (GRCm39) |
C1044S |
probably damaging |
Het |
Ppp4r3a |
A |
G |
12: 101,024,659 (GRCm39) |
V280A |
probably damaging |
Het |
Ptprf |
T |
C |
4: 118,068,245 (GRCm39) |
N1764D |
probably benign |
Het |
Pygm |
C |
T |
19: 6,438,842 (GRCm39) |
R311C |
possibly damaging |
Het |
Rab7b |
A |
G |
1: 131,626,299 (GRCm39) |
K109R |
probably damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCTGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Homo |
Setbp1 |
T |
G |
18: 78,900,926 (GRCm39) |
I914L |
probably benign |
Het |
Shprh |
A |
C |
10: 11,027,735 (GRCm39) |
Q114P |
probably benign |
Het |
Slc5a9 |
T |
C |
4: 111,742,725 (GRCm39) |
I456V |
possibly damaging |
Het |
Slc8b1 |
T |
C |
5: 120,657,985 (GRCm39) |
|
probably null |
Het |
Spin1 |
T |
A |
13: 51,293,552 (GRCm39) |
Y87* |
probably null |
Het |
Spring1 |
T |
C |
5: 118,393,798 (GRCm39) |
W59R |
probably damaging |
Het |
Srebf2 |
T |
C |
15: 82,061,477 (GRCm39) |
|
probably null |
Het |
Sufu |
T |
C |
19: 46,463,978 (GRCm39) |
Y397H |
probably damaging |
Het |
Tgm3 |
A |
T |
2: 129,883,920 (GRCm39) |
Y526F |
probably damaging |
Het |
Tmem209 |
A |
G |
6: 30,482,967 (GRCm39) |
L508P |
probably damaging |
Het |
Tmem67 |
T |
C |
4: 12,063,799 (GRCm39) |
D454G |
probably benign |
Het |
Ttn |
T |
C |
2: 76,646,943 (GRCm39) |
E3280G |
possibly damaging |
Het |
Tusc3 |
G |
C |
8: 39,538,560 (GRCm39) |
G200R |
probably damaging |
Het |
Umps |
A |
G |
16: 33,782,508 (GRCm39) |
V138A |
probably benign |
Het |
Ypel1 |
A |
G |
16: 16,902,377 (GRCm39) |
|
probably null |
Het |
Zdhhc19 |
T |
A |
16: 32,317,860 (GRCm39) |
L63Q |
probably null |
Het |
|
Other mutations in Tgfb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02609:Tgfb3
|
APN |
12 |
86,124,613 (GRCm39) |
missense |
probably benign |
|
IGL02899:Tgfb3
|
APN |
12 |
86,116,550 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03276:Tgfb3
|
APN |
12 |
86,104,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R0050:Tgfb3
|
UTSW |
12 |
86,116,658 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0053:Tgfb3
|
UTSW |
12 |
86,124,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Tgfb3
|
UTSW |
12 |
86,124,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0976:Tgfb3
|
UTSW |
12 |
86,116,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1460:Tgfb3
|
UTSW |
12 |
86,105,841 (GRCm39) |
intron |
probably benign |
|
R1474:Tgfb3
|
UTSW |
12 |
86,116,120 (GRCm39) |
critical splice donor site |
probably null |
|
R1686:Tgfb3
|
UTSW |
12 |
86,116,517 (GRCm39) |
splice site |
probably benign |
|
R1826:Tgfb3
|
UTSW |
12 |
86,108,818 (GRCm39) |
missense |
probably benign |
0.04 |
R2105:Tgfb3
|
UTSW |
12 |
86,116,543 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2294:Tgfb3
|
UTSW |
12 |
86,116,684 (GRCm39) |
missense |
probably benign |
0.17 |
R3159:Tgfb3
|
UTSW |
12 |
86,105,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Tgfb3
|
UTSW |
12 |
86,124,589 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4866:Tgfb3
|
UTSW |
12 |
86,124,588 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4868:Tgfb3
|
UTSW |
12 |
86,108,955 (GRCm39) |
missense |
probably benign |
0.02 |
R5104:Tgfb3
|
UTSW |
12 |
86,105,756 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6030:Tgfb3
|
UTSW |
12 |
86,110,624 (GRCm39) |
missense |
probably benign |
0.03 |
R6213:Tgfb3
|
UTSW |
12 |
86,104,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Tgfb3
|
UTSW |
12 |
86,124,615 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6331:Tgfb3
|
UTSW |
12 |
86,110,638 (GRCm39) |
missense |
probably benign |
0.03 |
R6762:Tgfb3
|
UTSW |
12 |
86,116,237 (GRCm39) |
missense |
probably benign |
0.00 |
R7473:Tgfb3
|
UTSW |
12 |
86,108,923 (GRCm39) |
missense |
possibly damaging |
0.92 |
|