Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
C |
T |
16: 21,513,146 (GRCm39) |
A4T |
probably benign |
Het |
Aacs |
T |
C |
5: 125,583,316 (GRCm39) |
S291P |
probably damaging |
Het |
Abcb1a |
T |
C |
5: 8,752,280 (GRCm39) |
|
probably null |
Het |
Apol10a |
C |
T |
15: 77,372,841 (GRCm39) |
T159I |
possibly damaging |
Het |
Arhgap5 |
A |
T |
12: 52,565,860 (GRCm39) |
M944L |
probably benign |
Het |
Atg16l2 |
A |
G |
7: 100,946,385 (GRCm39) |
L129P |
probably damaging |
Het |
Baiap2l2 |
T |
A |
15: 79,143,951 (GRCm39) |
Y381F |
probably benign |
Het |
Chd6 |
A |
T |
2: 160,812,103 (GRCm39) |
D1363E |
probably benign |
Het |
Ciao3 |
A |
T |
17: 26,000,283 (GRCm39) |
H322L |
probably damaging |
Het |
Cir1 |
T |
C |
2: 73,142,867 (GRCm39) |
|
probably benign |
Het |
Clec4a2 |
T |
C |
6: 123,117,622 (GRCm39) |
I180T |
probably damaging |
Het |
Clec4d |
T |
A |
6: 123,245,072 (GRCm39) |
H117Q |
probably damaging |
Het |
Cntnap2 |
A |
T |
6: 45,037,251 (GRCm39) |
R10W |
possibly damaging |
Het |
Coro6 |
A |
G |
11: 77,360,025 (GRCm39) |
E362G |
possibly damaging |
Het |
Ctr9 |
T |
A |
7: 110,634,578 (GRCm39) |
C196S |
probably benign |
Het |
Cyp2c55 |
A |
G |
19: 39,007,173 (GRCm39) |
K190E |
probably benign |
Het |
Dbt |
T |
C |
3: 116,332,781 (GRCm39) |
I200T |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,084,279 (GRCm39) |
F1242L |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,348,868 (GRCm39) |
W2534R |
probably damaging |
Het |
Dph7 |
T |
C |
2: 24,853,143 (GRCm39) |
S86P |
possibly damaging |
Het |
Dpp9 |
A |
C |
17: 56,505,970 (GRCm39) |
|
probably null |
Het |
Eif4g3 |
T |
A |
4: 137,925,408 (GRCm39) |
S1584T |
probably benign |
Het |
Eml4 |
T |
G |
17: 83,717,459 (GRCm39) |
D10E |
probably damaging |
Het |
Enpp1 |
A |
T |
10: 24,555,146 (GRCm39) |
C67S |
probably null |
Het |
Eps15 |
A |
G |
4: 109,200,387 (GRCm39) |
Y2C |
probably damaging |
Het |
Fam135b |
C |
T |
15: 71,335,920 (GRCm39) |
V425I |
probably benign |
Het |
Frem2 |
G |
A |
3: 53,443,240 (GRCm39) |
A2508V |
probably benign |
Het |
Fzd3 |
T |
A |
14: 65,473,193 (GRCm39) |
M192L |
possibly damaging |
Het |
Gls |
C |
T |
1: 52,271,947 (GRCm39) |
A69T |
probably damaging |
Het |
Gm10051 |
T |
A |
5: 133,504,113 (GRCm39) |
|
noncoding transcript |
Het |
Gm9271 |
A |
G |
7: 39,013,346 (GRCm39) |
|
noncoding transcript |
Het |
Gramd1b |
T |
C |
9: 40,227,128 (GRCm39) |
|
probably null |
Het |
Gvin-ps6 |
G |
A |
7: 106,022,782 (GRCm39) |
|
noncoding transcript |
Het |
H2-T23 |
A |
T |
17: 36,343,016 (GRCm39) |
|
probably benign |
Het |
H2-T5 |
T |
A |
17: 36,478,448 (GRCm39) |
I195F |
probably damaging |
Het |
Hmbox1 |
G |
A |
14: 65,134,483 (GRCm39) |
T39I |
probably damaging |
Het |
Hmx1 |
A |
G |
5: 35,549,115 (GRCm39) |
E136G |
probably damaging |
Het |
Hpdl |
T |
C |
4: 116,678,221 (GRCm39) |
N80S |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,173,071 (GRCm39) |
N918S |
probably benign |
Het |
Igkv5-37 |
T |
A |
6: 69,940,306 (GRCm39) |
S113C |
probably damaging |
Het |
Il36rn |
T |
C |
2: 24,167,503 (GRCm39) |
|
probably benign |
Het |
Mab21l4 |
A |
C |
1: 93,083,890 (GRCm39) |
M189R |
probably benign |
Het |
Marco |
G |
T |
1: 120,422,499 (GRCm39) |
T61K |
probably damaging |
Het |
Med1 |
T |
A |
11: 98,071,090 (GRCm39) |
R86* |
probably null |
Het |
Mertk |
A |
G |
2: 128,593,914 (GRCm39) |
Y306C |
probably damaging |
Het |
Mgat4c |
T |
C |
10: 102,224,265 (GRCm39) |
F160L |
probably damaging |
Het |
Midn |
A |
T |
10: 79,987,238 (GRCm39) |
E88V |
probably null |
Het |
Muc4 |
G |
A |
16: 32,596,277 (GRCm39) |
R3163H |
possibly damaging |
Het |
Naip1 |
T |
C |
13: 100,581,034 (GRCm39) |
D71G |
possibly damaging |
Het |
Nhlrc4 |
T |
C |
17: 26,162,577 (GRCm39) |
T57A |
probably benign |
Het |
Nlrp1a |
T |
C |
11: 71,004,466 (GRCm39) |
|
probably null |
Het |
Npffr2 |
A |
T |
5: 89,730,879 (GRCm39) |
K270* |
probably null |
Het |
Or10a3 |
T |
G |
7: 108,480,689 (GRCm39) |
E41D |
probably benign |
Het |
Or2b6 |
T |
A |
13: 21,823,340 (GRCm39) |
M118L |
possibly damaging |
Het |
Or51e1 |
T |
A |
7: 102,359,378 (GRCm39) |
I304N |
probably damaging |
Het |
Or8g26 |
T |
A |
9: 39,095,664 (GRCm39) |
Y60* |
probably null |
Het |
Or8k40 |
C |
T |
2: 86,584,155 (GRCm39) |
C309Y |
probably benign |
Het |
Otub2 |
T |
A |
12: 103,359,103 (GRCm39) |
L64Q |
probably benign |
Het |
Pabpc4l |
C |
G |
3: 46,400,570 (GRCm39) |
G358A |
possibly damaging |
Het |
Pabpc4l |
C |
T |
3: 46,400,579 (GRCm39) |
R355H |
probably benign |
Het |
Parp1 |
T |
C |
1: 180,417,033 (GRCm39) |
S606P |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,594,354 (GRCm39) |
V1253A |
probably benign |
Het |
Psg29 |
G |
A |
7: 16,942,458 (GRCm39) |
R153H |
probably benign |
Het |
Rbm25 |
A |
G |
12: 83,691,181 (GRCm39) |
M58V |
possibly damaging |
Het |
Rbm28 |
T |
C |
6: 29,125,353 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,671,933 (GRCm39) |
S3436P |
possibly damaging |
Het |
Slc3a1 |
A |
G |
17: 85,354,181 (GRCm39) |
I335V |
probably benign |
Het |
Slc4a4 |
T |
C |
5: 89,373,753 (GRCm39) |
F953S |
probably damaging |
Het |
Spata20 |
A |
G |
11: 94,375,404 (GRCm39) |
I130T |
possibly damaging |
Het |
Spata31h1 |
T |
C |
10: 82,119,481 (GRCm39) |
T4510A |
possibly damaging |
Het |
Srcap |
T |
C |
7: 127,148,471 (GRCm39) |
S1879P |
probably damaging |
Het |
St18 |
G |
C |
1: 6,887,828 (GRCm39) |
V466L |
probably benign |
Het |
Stard3nl |
A |
T |
13: 19,551,948 (GRCm39) |
M166K |
probably benign |
Het |
Stard3nl |
G |
A |
13: 19,560,736 (GRCm39) |
T13M |
probably damaging |
Het |
Stil |
A |
G |
4: 114,863,979 (GRCm39) |
T74A |
probably benign |
Het |
Syt6 |
T |
G |
3: 103,532,972 (GRCm39) |
M367R |
probably damaging |
Het |
Tacc1 |
T |
C |
8: 25,672,581 (GRCm39) |
T125A |
possibly damaging |
Het |
Tbc1d8 |
G |
A |
1: 39,441,959 (GRCm39) |
T211I |
possibly damaging |
Het |
Tcaf1 |
A |
G |
6: 42,663,809 (GRCm39) |
S24P |
probably benign |
Het |
Trim75 |
T |
G |
8: 65,435,199 (GRCm39) |
Y417S |
probably damaging |
Het |
Ttll12 |
T |
C |
15: 83,464,321 (GRCm39) |
Y503C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Unc5c |
A |
T |
3: 141,522,692 (GRCm39) |
Y706F |
probably benign |
Het |
Zfp593 |
T |
C |
4: 133,972,077 (GRCm39) |
|
probably benign |
Het |
Zfp956 |
T |
C |
6: 47,939,476 (GRCm39) |
S175P |
probably damaging |
Het |
|
Other mutations in Epn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02227:Epn1
|
APN |
7 |
5,098,035 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03126:Epn1
|
APN |
7 |
5,098,684 (GRCm39) |
missense |
probably benign |
0.01 |
epsilon
|
UTSW |
7 |
5,098,047 (GRCm39) |
missense |
probably benign |
|
R1074:Epn1
|
UTSW |
7 |
5,098,047 (GRCm39) |
missense |
probably benign |
|
R1365:Epn1
|
UTSW |
7 |
5,096,369 (GRCm39) |
missense |
probably benign |
0.05 |
R1848:Epn1
|
UTSW |
7 |
5,092,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Epn1
|
UTSW |
7 |
5,086,874 (GRCm39) |
missense |
probably damaging |
0.99 |
R2237:Epn1
|
UTSW |
7 |
5,100,601 (GRCm39) |
missense |
probably damaging |
0.98 |
R2238:Epn1
|
UTSW |
7 |
5,100,601 (GRCm39) |
missense |
probably damaging |
0.98 |
R2239:Epn1
|
UTSW |
7 |
5,100,601 (GRCm39) |
missense |
probably damaging |
0.98 |
R4255:Epn1
|
UTSW |
7 |
5,100,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4324:Epn1
|
UTSW |
7 |
5,100,210 (GRCm39) |
missense |
probably benign |
0.07 |
R4542:Epn1
|
UTSW |
7 |
5,096,980 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4703:Epn1
|
UTSW |
7 |
5,098,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R4845:Epn1
|
UTSW |
7 |
5,096,908 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5838:Epn1
|
UTSW |
7 |
5,100,165 (GRCm39) |
nonsense |
probably null |
|
R5952:Epn1
|
UTSW |
7 |
5,096,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Epn1
|
UTSW |
7 |
5,098,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Epn1
|
UTSW |
7 |
5,098,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Epn1
|
UTSW |
7 |
5,093,122 (GRCm39) |
missense |
probably damaging |
0.98 |
R6710:Epn1
|
UTSW |
7 |
5,100,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R6937:Epn1
|
UTSW |
7 |
5,092,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7196:Epn1
|
UTSW |
7 |
5,096,380 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7420:Epn1
|
UTSW |
7 |
5,100,687 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7948:Epn1
|
UTSW |
7 |
5,092,992 (GRCm39) |
nonsense |
probably null |
|
R8766:Epn1
|
UTSW |
7 |
5,095,860 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8843:Epn1
|
UTSW |
7 |
5,096,375 (GRCm39) |
missense |
probably benign |
0.36 |
R9059:Epn1
|
UTSW |
7 |
5,098,067 (GRCm39) |
missense |
probably benign |
0.00 |
R9315:Epn1
|
UTSW |
7 |
5,096,339 (GRCm39) |
missense |
probably benign |
|
R9376:Epn1
|
UTSW |
7 |
5,086,720 (GRCm39) |
unclassified |
probably benign |
|
R9432:Epn1
|
UTSW |
7 |
5,096,369 (GRCm39) |
missense |
probably benign |
0.22 |
X0065:Epn1
|
UTSW |
7 |
5,098,092 (GRCm39) |
missense |
probably benign |
0.02 |
|