Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
A |
G |
4: 144,282,082 (GRCm39) |
Y237H |
probably benign |
Het |
Abca8a |
A |
T |
11: 109,947,167 (GRCm39) |
Y1036* |
probably null |
Het |
Abcg3 |
T |
C |
5: 105,121,973 (GRCm39) |
T135A |
probably damaging |
Het |
Arhgef28 |
G |
A |
13: 98,213,773 (GRCm39) |
A30V |
probably damaging |
Het |
Cald1 |
T |
A |
6: 34,662,947 (GRCm39) |
D3E |
probably damaging |
Het |
Ccdc89 |
T |
A |
7: 90,076,573 (GRCm39) |
L261Q |
probably damaging |
Het |
Ceacam1 |
T |
C |
7: 25,171,231 (GRCm39) |
D411G |
possibly damaging |
Het |
Chil4 |
T |
A |
3: 106,118,656 (GRCm39) |
N87Y |
probably damaging |
Het |
Ciita |
T |
A |
16: 10,328,640 (GRCm39) |
L308Q |
probably benign |
Het |
Clptm1 |
T |
C |
7: 19,371,600 (GRCm39) |
I278V |
probably benign |
Het |
Col5a3 |
A |
T |
9: 20,685,308 (GRCm39) |
|
probably null |
Het |
Ddost |
T |
A |
4: 138,038,780 (GRCm39) |
D336E |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,561,495 (GRCm39) |
Y2054C |
probably damaging |
Het |
Erc2 |
T |
A |
14: 28,197,723 (GRCm39) |
L1000H |
unknown |
Het |
Fhip2b |
T |
C |
14: 70,822,579 (GRCm39) |
E714G |
probably damaging |
Het |
Gdpd4 |
T |
C |
7: 97,610,793 (GRCm39) |
V71A |
possibly damaging |
Het |
Hmcn1 |
A |
G |
1: 150,545,175 (GRCm39) |
Y2811H |
probably damaging |
Het |
Hmox2 |
C |
T |
16: 4,582,818 (GRCm39) |
Q184* |
probably null |
Het |
Igkv9-124 |
G |
T |
6: 67,919,280 (GRCm39) |
T44N |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,737,649 (GRCm39) |
T5149I |
unknown |
Het |
Lamb2 |
T |
A |
9: 108,363,477 (GRCm39) |
D885E |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,407,680 (GRCm39) |
S220P |
probably damaging |
Het |
Muc2 |
A |
T |
7: 141,287,453 (GRCm39) |
T211S |
possibly damaging |
Het |
Mup13 |
A |
T |
4: 61,184,117 (GRCm39) |
C15S |
possibly damaging |
Het |
Myh3 |
T |
C |
11: 66,979,556 (GRCm39) |
|
probably null |
Het |
Nek10 |
A |
G |
14: 14,850,833 (GRCm38) |
I293V |
probably benign |
Het |
Or10d3 |
G |
A |
9: 39,461,723 (GRCm39) |
T148I |
probably benign |
Het |
Or2a52 |
T |
A |
6: 43,144,432 (GRCm39) |
S147T |
possibly damaging |
Het |
Or6c68 |
A |
G |
10: 129,158,205 (GRCm39) |
T238A |
probably damaging |
Het |
Pdss2 |
G |
A |
10: 43,269,990 (GRCm39) |
V278I |
probably benign |
Het |
Prex1 |
T |
C |
2: 166,431,518 (GRCm39) |
K748R |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,174,519 (GRCm39) |
|
probably null |
Het |
Ranbp17 |
G |
A |
11: 33,424,826 (GRCm39) |
S510L |
unknown |
Het |
Rp1 |
T |
A |
1: 4,416,447 (GRCm39) |
H1555L |
probably benign |
Het |
Rsph6a |
A |
G |
7: 18,799,535 (GRCm39) |
K389E |
probably benign |
Het |
Ryk |
T |
C |
9: 102,746,518 (GRCm39) |
V151A |
probably benign |
Het |
Ryr3 |
T |
A |
2: 112,465,660 (GRCm39) |
N4838I |
possibly damaging |
Het |
Sbno1 |
G |
A |
5: 124,517,413 (GRCm39) |
R1233* |
probably null |
Het |
Scn2a |
A |
T |
2: 65,594,932 (GRCm39) |
K1927M |
probably damaging |
Het |
Sec22c |
A |
T |
9: 121,513,860 (GRCm39) |
I259N |
probably damaging |
Het |
Slc6a15 |
A |
T |
10: 103,240,583 (GRCm39) |
D402V |
probably benign |
Het |
Stk38 |
G |
A |
17: 29,207,210 (GRCm39) |
T111I |
probably damaging |
Het |
Tmem237 |
G |
A |
1: 59,147,215 (GRCm39) |
T306I |
probably damaging |
Het |
Tmprss11a |
T |
C |
5: 86,576,501 (GRCm39) |
K117E |
probably benign |
Het |
Tmprss9 |
A |
T |
10: 80,730,640 (GRCm39) |
D722V |
probably damaging |
Het |
Trpc1 |
T |
C |
9: 95,592,250 (GRCm39) |
Y575C |
probably damaging |
Het |
Ube2d2b |
A |
G |
5: 107,978,438 (GRCm39) |
M30V |
probably benign |
Het |
Usp36 |
A |
T |
11: 118,159,461 (GRCm39) |
L661* |
probably null |
Het |
Vmn2r13 |
G |
T |
5: 109,304,064 (GRCm39) |
T789N |
probably damaging |
Het |
Vmn2r5 |
T |
C |
3: 64,400,018 (GRCm39) |
T550A |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,355,540 (GRCm39) |
S3434P |
possibly damaging |
Het |
Zfp106 |
A |
G |
2: 120,351,007 (GRCm39) |
V1571A |
probably damaging |
Het |
Zfp438 |
A |
G |
18: 5,213,501 (GRCm39) |
S486P |
possibly damaging |
Het |
Zfp616 |
A |
G |
11: 73,975,660 (GRCm39) |
H643R |
probably damaging |
Het |
Zfp616 |
A |
G |
11: 73,976,596 (GRCm39) |
K955R |
possibly damaging |
Het |
|
Other mutations in 2900026A02Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02810:2900026A02Rik
|
APN |
5 |
113,249,401 (GRCm39) |
missense |
probably damaging |
1.00 |
oyster
|
UTSW |
5 |
113,330,833 (GRCm39) |
missense |
probably benign |
0.14 |
pimento
|
UTSW |
5 |
113,243,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:2900026A02Rik
|
UTSW |
5 |
113,249,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:2900026A02Rik
|
UTSW |
5 |
113,249,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4329:2900026A02Rik
|
UTSW |
5 |
113,243,455 (GRCm39) |
critical splice donor site |
probably null |
|
R4766:2900026A02Rik
|
UTSW |
5 |
113,245,502 (GRCm39) |
missense |
probably benign |
0.01 |
R6124:2900026A02Rik
|
UTSW |
5 |
113,331,622 (GRCm39) |
missense |
probably benign |
|
R6336:2900026A02Rik
|
UTSW |
5 |
113,331,349 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6365:2900026A02Rik
|
UTSW |
5 |
113,330,510 (GRCm39) |
missense |
probably benign |
0.00 |
R6575:2900026A02Rik
|
UTSW |
5 |
113,330,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6759:2900026A02Rik
|
UTSW |
5 |
113,331,692 (GRCm39) |
missense |
probably benign |
0.00 |
R7117:2900026A02Rik
|
UTSW |
5 |
113,339,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7168:2900026A02Rik
|
UTSW |
5 |
113,285,659 (GRCm39) |
missense |
probably damaging |
0.96 |
R7339:2900026A02Rik
|
UTSW |
5 |
113,330,938 (GRCm39) |
missense |
probably benign |
0.09 |
R7450:2900026A02Rik
|
UTSW |
5 |
113,331,977 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7458:2900026A02Rik
|
UTSW |
5 |
113,338,510 (GRCm39) |
missense |
probably benign |
0.05 |
R7525:2900026A02Rik
|
UTSW |
5 |
113,331,221 (GRCm39) |
missense |
probably damaging |
0.99 |
R7707:2900026A02Rik
|
UTSW |
5 |
113,285,852 (GRCm39) |
start codon destroyed |
probably benign |
0.14 |
R7848:2900026A02Rik
|
UTSW |
5 |
113,340,007 (GRCm39) |
missense |
probably damaging |
0.96 |
R7869:2900026A02Rik
|
UTSW |
5 |
113,332,001 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7871:2900026A02Rik
|
UTSW |
5 |
113,331,092 (GRCm39) |
missense |
probably benign |
0.02 |
R8327:2900026A02Rik
|
UTSW |
5 |
113,331,685 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8411:2900026A02Rik
|
UTSW |
5 |
113,285,588 (GRCm39) |
missense |
probably benign |
|
R8429:2900026A02Rik
|
UTSW |
5 |
113,331,302 (GRCm39) |
missense |
probably benign |
0.29 |
R8940:2900026A02Rik
|
UTSW |
5 |
113,241,068 (GRCm39) |
missense |
probably benign |
0.07 |
R9065:2900026A02Rik
|
UTSW |
5 |
113,323,084 (GRCm39) |
missense |
probably benign |
0.00 |
R9096:2900026A02Rik
|
UTSW |
5 |
113,339,793 (GRCm39) |
missense |
|
|
R9182:2900026A02Rik
|
UTSW |
5 |
113,243,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:2900026A02Rik
|
UTSW |
5 |
113,330,564 (GRCm39) |
missense |
probably benign |
0.34 |
R9330:2900026A02Rik
|
UTSW |
5 |
113,330,833 (GRCm39) |
missense |
probably benign |
0.14 |
R9336:2900026A02Rik
|
UTSW |
5 |
113,240,966 (GRCm39) |
critical splice donor site |
probably null |
|
R9375:2900026A02Rik
|
UTSW |
5 |
113,332,567 (GRCm39) |
missense |
probably benign |
|
R9388:2900026A02Rik
|
UTSW |
5 |
113,338,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9483:2900026A02Rik
|
UTSW |
5 |
113,339,010 (GRCm39) |
missense |
probably benign |
0.01 |
R9675:2900026A02Rik
|
UTSW |
5 |
113,339,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:2900026A02Rik
|
UTSW |
5 |
113,338,527 (GRCm39) |
missense |
possibly damaging |
0.93 |
|