Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
A |
5: 63,898,537 (GRCm38) |
C205* |
probably null |
Het |
2810474O19Rik |
T |
A |
6: 149,326,432 (GRCm38) |
N325K |
probably benign |
Het |
4921539E11Rik |
T |
A |
4: 103,270,764 (GRCm38) |
T55S |
possibly damaging |
Het |
Akap12 |
A |
G |
10: 4,313,855 (GRCm38) |
D88G |
probably benign |
Het |
Ankrd53 |
C |
A |
6: 83,763,203 (GRCm38) |
F84L |
probably damaging |
Het |
Apol7b |
A |
C |
15: 77,423,339 (GRCm38) |
F319V |
probably damaging |
Het |
Bsn |
A |
G |
9: 108,114,549 (GRCm38) |
S1335P |
probably benign |
Het |
Cep192 |
T |
C |
18: 67,803,158 (GRCm38) |
|
probably null |
Het |
Cfap57 |
A |
G |
4: 118,593,132 (GRCm38) |
S598P |
probably benign |
Het |
Commd8 |
T |
C |
5: 72,165,499 (GRCm38) |
H25R |
probably damaging |
Het |
Crisp4 |
T |
C |
1: 18,128,665 (GRCm38) |
I143V |
probably benign |
Het |
Cyp4a12b |
A |
T |
4: 115,438,145 (GRCm38) |
T483S |
probably benign |
Het |
Dbx2 |
C |
T |
15: 95,632,353 (GRCm38) |
M244I |
probably damaging |
Het |
Dnah6 |
T |
G |
6: 73,121,970 (GRCm38) |
H1982P |
possibly damaging |
Het |
Fam220a |
C |
A |
5: 143,563,127 (GRCm38) |
P98Q |
probably damaging |
Het |
Ggnbp1 |
A |
G |
17: 27,029,543 (GRCm38) |
K29E |
possibly damaging |
Het |
Gm14569 |
A |
C |
X: 36,432,128 (GRCm38) |
M976R |
probably benign |
Het |
Gm9573 |
T |
A |
17: 35,622,965 (GRCm38) |
|
probably benign |
Het |
Hck |
G |
T |
2: 153,129,856 (GRCm38) |
W112C |
probably damaging |
Het |
Heatr5a |
A |
T |
12: 51,939,658 (GRCm38) |
S591T |
possibly damaging |
Het |
Hhat |
A |
G |
1: 192,717,107 (GRCm38) |
S242P |
probably benign |
Het |
Hnrnpll |
A |
G |
17: 80,044,518 (GRCm38) |
S333P |
probably benign |
Het |
Hoxc6 |
T |
C |
15: 103,010,007 (GRCm38) |
|
probably null |
Het |
Inpp5j |
G |
A |
11: 3,502,150 (GRCm38) |
P367S |
probably damaging |
Het |
Lamc2 |
A |
G |
1: 153,133,597 (GRCm38) |
|
probably null |
Het |
Loxhd1 |
T |
A |
18: 77,321,642 (GRCm38) |
I194N |
possibly damaging |
Het |
Miga1 |
CCAGGGCAG |
CCAG |
3: 152,335,304 (GRCm38) |
|
probably null |
Het |
Mkln1 |
C |
T |
6: 31,490,530 (GRCm38) |
Q60* |
probably null |
Het |
Mybph |
C |
A |
1: 134,196,996 (GRCm38) |
H185N |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,520,829 (GRCm38) |
D9G |
possibly damaging |
Het |
Myo6 |
A |
T |
9: 80,228,925 (GRCm38) |
D110V |
probably damaging |
Het |
Ncoa7 |
A |
G |
10: 30,691,299 (GRCm38) |
V412A |
probably benign |
Het |
Neb |
T |
C |
2: 52,287,345 (GRCm38) |
K1328R |
probably damaging |
Het |
Olfm5 |
T |
A |
7: 104,164,741 (GRCm38) |
Q22L |
unknown |
Het |
Olfr1106 |
C |
T |
2: 87,048,835 (GRCm38) |
V134M |
possibly damaging |
Het |
Olfr1328 |
A |
T |
4: 118,934,184 (GRCm38) |
Y221* |
probably null |
Het |
Olfr1355 |
A |
G |
10: 78,879,280 (GRCm38) |
Y36C |
probably damaging |
Het |
Olfr1414 |
C |
A |
1: 92,511,777 (GRCm38) |
G84C |
probably damaging |
Het |
Olfr1423 |
T |
C |
19: 12,036,341 (GRCm38) |
T134A |
probably benign |
Het |
Olfr414 |
T |
A |
1: 174,431,091 (GRCm38) |
I221N |
probably damaging |
Het |
P3h1 |
A |
T |
4: 119,247,976 (GRCm38) |
Q717L |
probably null |
Het |
Pclo |
T |
C |
5: 14,713,795 (GRCm38) |
I4094T |
unknown |
Het |
Pfdn6 |
G |
A |
17: 33,939,077 (GRCm38) |
R73W |
probably benign |
Het |
Phyhipl |
A |
C |
10: 70,559,761 (GRCm38) |
M205R |
possibly damaging |
Het |
Pitpnm1 |
C |
T |
19: 4,107,973 (GRCm38) |
|
probably null |
Het |
Plcg1 |
A |
G |
2: 160,752,578 (GRCm38) |
|
probably null |
Het |
Pnldc1 |
A |
G |
17: 12,906,505 (GRCm38) |
S81P |
possibly damaging |
Het |
Pno1 |
T |
C |
11: 17,204,519 (GRCm38) |
I221V |
possibly damaging |
Het |
Porcn |
A |
G |
X: 8,204,301 (GRCm38) |
V75A |
probably damaging |
Het |
Prkcg |
T |
A |
7: 3,305,346 (GRCm38) |
C69S |
probably damaging |
Het |
Rbbp6 |
G |
T |
7: 122,999,488 (GRCm38) |
|
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,110,324 (GRCm38) |
|
probably benign |
Het |
Scly |
A |
G |
1: 91,320,169 (GRCm38) |
D413G |
probably damaging |
Het |
Scn11a |
G |
A |
9: 119,780,795 (GRCm38) |
R996* |
probably null |
Het |
Slc6a13 |
A |
T |
6: 121,332,373 (GRCm38) |
D281V |
probably damaging |
Het |
Slfn5 |
T |
C |
11: 82,956,616 (GRCm38) |
V109A |
probably benign |
Het |
Smyd1 |
A |
T |
6: 71,312,719 (GRCm38) |
|
probably null |
Het |
Snx29 |
T |
A |
16: 11,367,724 (GRCm38) |
M57K |
probably benign |
Het |
Stag1 |
T |
G |
9: 100,888,086 (GRCm38) |
I603S |
probably benign |
Het |
Svep1 |
C |
A |
4: 58,097,292 (GRCm38) |
C1417F |
possibly damaging |
Het |
Tbc1d23 |
T |
C |
16: 57,189,351 (GRCm38) |
I392V |
probably benign |
Het |
Tchh |
T |
C |
3: 93,446,799 (GRCm38) |
L1182P |
unknown |
Het |
Tle3 |
T |
A |
9: 61,394,633 (GRCm38) |
V108E |
probably damaging |
Het |
Tmem144 |
T |
C |
3: 79,825,400 (GRCm38) |
|
probably null |
Het |
Tpr |
T |
G |
1: 150,419,907 (GRCm38) |
L894V |
possibly damaging |
Het |
Trappc9 |
A |
T |
15: 73,000,025 (GRCm38) |
V472E |
probably damaging |
Het |
Ttc37 |
T |
C |
13: 76,134,815 (GRCm38) |
V752A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,811,243 (GRCm38) |
L5176Q |
possibly damaging |
Het |
Vmn1r12 |
T |
A |
6: 57,159,509 (GRCm38) |
I197N |
possibly damaging |
Het |
Vmn1r26 |
T |
C |
6: 58,009,126 (GRCm38) |
Y26C |
possibly damaging |
Het |
Vwa3a |
A |
G |
7: 120,758,954 (GRCm38) |
I83V |
probably null |
Het |
Xirp1 |
C |
T |
9: 120,018,591 (GRCm38) |
E409K |
probably benign |
Het |
Zc3h14 |
T |
G |
12: 98,763,922 (GRCm38) |
I46R |
probably damaging |
Het |
Zfp976 |
A |
G |
7: 42,613,841 (GRCm38) |
C191R |
probably damaging |
Het |
|
Other mutations in Trim38 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00915:Trim38
|
APN |
13 |
23,791,032 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL01592:Trim38
|
APN |
13 |
23,791,427 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL02339:Trim38
|
APN |
13 |
23,788,230 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03062:Trim38
|
APN |
13 |
23,782,963 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03278:Trim38
|
APN |
13 |
23,790,996 (GRCm38) |
missense |
possibly damaging |
0.65 |
R0630:Trim38
|
UTSW |
13 |
23,791,132 (GRCm38) |
nonsense |
probably null |
|
R1263:Trim38
|
UTSW |
13 |
23,791,134 (GRCm38) |
missense |
probably damaging |
1.00 |
R1560:Trim38
|
UTSW |
13 |
23,782,702 (GRCm38) |
missense |
probably benign |
0.02 |
R4407:Trim38
|
UTSW |
13 |
23,791,491 (GRCm38) |
missense |
probably benign |
0.04 |
R4462:Trim38
|
UTSW |
13 |
23,791,452 (GRCm38) |
missense |
probably null |
1.00 |
R4649:Trim38
|
UTSW |
13 |
23,782,969 (GRCm38) |
missense |
probably damaging |
1.00 |
R4651:Trim38
|
UTSW |
13 |
23,782,969 (GRCm38) |
missense |
probably damaging |
1.00 |
R4653:Trim38
|
UTSW |
13 |
23,782,969 (GRCm38) |
missense |
probably damaging |
1.00 |
R4816:Trim38
|
UTSW |
13 |
23,788,281 (GRCm38) |
missense |
probably damaging |
1.00 |
R4970:Trim38
|
UTSW |
13 |
23,791,329 (GRCm38) |
missense |
probably damaging |
0.98 |
R5946:Trim38
|
UTSW |
13 |
23,782,734 (GRCm38) |
missense |
probably benign |
0.04 |
R6538:Trim38
|
UTSW |
13 |
23,785,949 (GRCm38) |
missense |
probably damaging |
0.97 |
R6974:Trim38
|
UTSW |
13 |
23,789,519 (GRCm38) |
missense |
probably benign |
0.05 |
R7227:Trim38
|
UTSW |
13 |
23,785,963 (GRCm38) |
missense |
possibly damaging |
0.88 |
R7319:Trim38
|
UTSW |
13 |
23,791,401 (GRCm38) |
missense |
probably damaging |
1.00 |
R7425:Trim38
|
UTSW |
13 |
23,788,382 (GRCm38) |
missense |
probably benign |
0.02 |
R8243:Trim38
|
UTSW |
13 |
23,791,395 (GRCm38) |
missense |
probably damaging |
1.00 |
R8965:Trim38
|
UTSW |
13 |
23,791,023 (GRCm38) |
missense |
possibly damaging |
0.65 |
R9354:Trim38
|
UTSW |
13 |
23,785,892 (GRCm38) |
missense |
probably benign |
0.09 |
R9573:Trim38
|
UTSW |
13 |
23,782,705 (GRCm38) |
missense |
probably benign |
0.01 |
|