Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
A |
T |
11: 101,304,917 (GRCm39) |
D190E |
probably damaging |
Het |
Acnat2 |
A |
G |
4: 49,383,084 (GRCm39) |
|
probably null |
Het |
Acot10 |
T |
G |
15: 20,666,712 (GRCm39) |
T10P |
possibly damaging |
Het |
Aldh7a1 |
T |
C |
18: 56,667,286 (GRCm39) |
|
probably null |
Het |
Alkbh7 |
G |
A |
17: 57,305,443 (GRCm39) |
V87I |
probably benign |
Het |
Ano2 |
A |
T |
6: 125,689,238 (GRCm39) |
H121L |
probably benign |
Het |
Apob |
A |
T |
12: 8,050,896 (GRCm39) |
Y1040F |
probably damaging |
Het |
Arhgap25 |
A |
T |
6: 87,436,942 (GRCm39) |
V636E |
possibly damaging |
Het |
Atad2b |
A |
T |
12: 4,991,973 (GRCm39) |
T191S |
possibly damaging |
Het |
Atpsckmt |
T |
C |
15: 31,617,018 (GRCm39) |
M161T |
probably damaging |
Het |
Btbd9 |
A |
T |
17: 30,749,191 (GRCm39) |
V41D |
possibly damaging |
Het |
Bzw2 |
G |
A |
12: 36,174,023 (GRCm39) |
R25C |
probably damaging |
Het |
Carmil1 |
T |
C |
13: 24,206,494 (GRCm39) |
S1326G |
probably benign |
Het |
Cdh18 |
A |
G |
15: 23,366,971 (GRCm39) |
R226G |
probably damaging |
Het |
Cdh3 |
A |
G |
8: 107,282,012 (GRCm39) |
N800S |
possibly damaging |
Het |
Cep152 |
A |
T |
2: 125,425,854 (GRCm39) |
V837E |
possibly damaging |
Het |
Cep85 |
G |
A |
4: 133,858,732 (GRCm39) |
T713M |
possibly damaging |
Het |
Chd7 |
T |
C |
4: 8,850,821 (GRCm39) |
Y1736H |
probably damaging |
Het |
Chst3 |
T |
C |
10: 60,022,535 (GRCm39) |
E104G |
probably benign |
Het |
Cic |
T |
A |
7: 24,986,565 (GRCm39) |
S1299T |
probably damaging |
Het |
Cic |
C |
A |
7: 24,986,566 (GRCm39) |
S1299Y |
probably damaging |
Het |
Cmah |
T |
A |
13: 24,620,724 (GRCm39) |
S319R |
possibly damaging |
Het |
Cnbd1 |
A |
G |
4: 18,895,044 (GRCm39) |
F233L |
probably benign |
Het |
Cpne5 |
T |
C |
17: 29,395,163 (GRCm39) |
E251G |
probably benign |
Het |
Csf2rb2 |
G |
A |
15: 78,169,373 (GRCm39) |
P485L |
probably damaging |
Het |
Dimt1 |
T |
C |
13: 107,085,264 (GRCm39) |
M70T |
possibly damaging |
Het |
Dlk2 |
A |
G |
17: 46,614,024 (GRCm39) |
*383W |
probably null |
Het |
Dnah2 |
G |
A |
11: 69,350,027 (GRCm39) |
R2369C |
probably damaging |
Het |
Dock2 |
A |
G |
11: 34,218,052 (GRCm39) |
F1173L |
possibly damaging |
Het |
Dok7 |
A |
G |
5: 35,223,806 (GRCm39) |
H115R |
possibly damaging |
Het |
Dpy19l1 |
A |
G |
9: 24,325,645 (GRCm39) |
I720T |
probably benign |
Het |
Eps8 |
A |
T |
6: 137,491,309 (GRCm39) |
D356E |
probably benign |
Het |
Exoc1 |
A |
G |
5: 76,691,464 (GRCm39) |
N263D |
probably benign |
Het |
Fbxl3 |
T |
C |
14: 103,320,322 (GRCm39) |
D375G |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,836,765 (GRCm39) |
D228V |
probably damaging |
Het |
Flg2 |
A |
T |
3: 93,108,744 (GRCm39) |
E257D |
probably benign |
Het |
Fstl4 |
A |
G |
11: 53,077,229 (GRCm39) |
D662G |
probably benign |
Het |
Gbp10 |
G |
T |
5: 105,366,390 (GRCm39) |
Q505K |
possibly damaging |
Het |
Gemin2 |
C |
T |
12: 59,060,305 (GRCm39) |
P15S |
probably damaging |
Het |
Grhl2 |
A |
G |
15: 37,344,919 (GRCm39) |
M514V |
probably benign |
Het |
Hgs |
A |
G |
11: 120,369,970 (GRCm39) |
N413D |
possibly damaging |
Het |
Il12rb2 |
T |
C |
6: 67,280,594 (GRCm39) |
S538G |
possibly damaging |
Het |
Kdm5a |
A |
G |
6: 120,379,561 (GRCm39) |
D623G |
probably damaging |
Het |
Kifbp |
A |
T |
10: 62,395,235 (GRCm39) |
I469N |
probably damaging |
Het |
Matk |
G |
T |
10: 81,095,527 (GRCm39) |
V116F |
probably damaging |
Het |
Mcm3 |
T |
C |
1: 20,875,556 (GRCm39) |
T694A |
probably benign |
Het |
Mctp1 |
C |
A |
13: 76,949,520 (GRCm39) |
H260Q |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,582,910 (GRCm39) |
Y2562N |
possibly damaging |
Het |
Naip5 |
T |
A |
13: 100,358,240 (GRCm39) |
I999F |
probably damaging |
Het |
Or11h4 |
T |
A |
14: 50,974,554 (GRCm39) |
I22L |
probably benign |
Het |
Or14j7 |
A |
T |
17: 38,234,667 (GRCm39) |
D70V |
probably damaging |
Het |
Or1x6 |
A |
G |
11: 50,939,336 (GRCm39) |
Y134C |
probably damaging |
Het |
Or52a5 |
A |
T |
7: 103,426,770 (GRCm39) |
S261T |
probably benign |
Het |
Or7g12 |
A |
T |
9: 18,900,198 (GRCm39) |
I305F |
probably benign |
Het |
Or8g52 |
T |
A |
9: 39,630,706 (GRCm39) |
F61Y |
probably benign |
Het |
Pafah1b1 |
A |
G |
11: 74,568,541 (GRCm39) |
V396A |
probably benign |
Het |
Pard6b |
T |
A |
2: 167,929,467 (GRCm39) |
I91N |
possibly damaging |
Het |
Pdzd2 |
T |
C |
15: 12,592,246 (GRCm39) |
S133G |
probably damaging |
Het |
Plcg2 |
T |
G |
8: 118,312,044 (GRCm39) |
S445R |
probably benign |
Het |
Plekhd1 |
G |
T |
12: 80,768,352 (GRCm39) |
V396L |
probably damaging |
Het |
Ppp4r2 |
A |
G |
6: 100,843,518 (GRCm39) |
D294G |
possibly damaging |
Het |
Ppwd1 |
T |
C |
13: 104,359,468 (GRCm39) |
|
probably null |
Het |
Prr22 |
A |
G |
17: 57,077,551 (GRCm39) |
|
probably benign |
Het |
Psme4 |
A |
G |
11: 30,798,117 (GRCm39) |
D1370G |
probably damaging |
Het |
Rac3 |
T |
A |
11: 120,613,684 (GRCm39) |
V86D |
probably damaging |
Het |
Rnf207 |
T |
C |
4: 152,397,829 (GRCm39) |
S335G |
possibly damaging |
Het |
Rxfp3 |
A |
G |
15: 11,037,063 (GRCm39) |
L103P |
probably damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Smpdl3a |
G |
T |
10: 57,670,827 (GRCm39) |
C17F |
probably benign |
Het |
Spaca7b |
T |
A |
8: 11,711,749 (GRCm39) |
|
probably benign |
Het |
Spata31g1 |
T |
A |
4: 42,973,429 (GRCm39) |
F921I |
probably benign |
Het |
Spen |
A |
T |
4: 141,200,962 (GRCm39) |
I2555N |
probably damaging |
Het |
Srpk2 |
G |
T |
5: 23,723,424 (GRCm39) |
T564K |
probably damaging |
Het |
Stard4 |
C |
T |
18: 33,338,202 (GRCm39) |
R116H |
probably damaging |
Het |
Supt7l |
A |
T |
5: 31,677,640 (GRCm39) |
S175R |
probably damaging |
Het |
Sycp1 |
A |
T |
3: 102,726,422 (GRCm39) |
Y932N |
possibly damaging |
Het |
Tas2r122 |
T |
C |
6: 132,688,141 (GRCm39) |
M251V |
probably benign |
Het |
Tbx15 |
A |
T |
3: 99,223,634 (GRCm39) |
E274V |
probably damaging |
Het |
Tex52 |
A |
G |
6: 128,361,917 (GRCm39) |
E298G |
probably benign |
Het |
Tmem101 |
T |
C |
11: 102,046,693 (GRCm39) |
M59V |
probably benign |
Het |
Tmem132b |
T |
C |
5: 125,862,990 (GRCm39) |
V665A |
probably damaging |
Het |
Trim23 |
T |
C |
13: 104,334,541 (GRCm39) |
V347A |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,643,136 (GRCm39) |
H4166R |
probably benign |
Het |
Vmn2r101 |
G |
T |
17: 19,810,431 (GRCm39) |
V406L |
probably benign |
Het |
Vrk3 |
A |
G |
7: 44,413,624 (GRCm39) |
D166G |
possibly damaging |
Het |
Washc4 |
T |
A |
10: 83,392,777 (GRCm39) |
M259K |
probably benign |
Het |
Wdr70 |
T |
C |
15: 8,108,645 (GRCm39) |
D167G |
probably benign |
Het |
Zfp1005 |
A |
G |
2: 150,111,122 (GRCm39) |
E604G |
possibly damaging |
Het |
Zfp28 |
A |
T |
7: 6,395,239 (GRCm39) |
Q248L |
possibly damaging |
Het |
Zfp39 |
A |
G |
11: 58,781,232 (GRCm39) |
I510T |
probably benign |
Het |
Zfp710 |
T |
A |
7: 79,740,089 (GRCm39) |
*646R |
probably null |
Het |
Zfp90 |
C |
T |
8: 107,151,892 (GRCm39) |
S535L |
possibly damaging |
Het |
Zfp949 |
C |
T |
9: 88,450,787 (GRCm39) |
T119I |
possibly damaging |
Het |
|
Other mutations in Mios |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01089:Mios
|
APN |
6 |
8,234,363 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01365:Mios
|
APN |
6 |
8,216,089 (GRCm39) |
nonsense |
probably null |
|
IGL01548:Mios
|
APN |
6 |
8,234,252 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01898:Mios
|
APN |
6 |
8,222,668 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02110:Mios
|
APN |
6 |
8,215,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02308:Mios
|
APN |
6 |
8,231,269 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02375:Mios
|
APN |
6 |
8,222,598 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02452:Mios
|
APN |
6 |
8,222,492 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02670:Mios
|
APN |
6 |
8,235,378 (GRCm39) |
splice site |
probably benign |
|
IGL03083:Mios
|
APN |
6 |
8,215,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Mios
|
UTSW |
6 |
8,215,470 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1351:Mios
|
UTSW |
6 |
8,228,120 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1476:Mios
|
UTSW |
6 |
8,234,237 (GRCm39) |
missense |
probably benign |
0.01 |
R1802:Mios
|
UTSW |
6 |
8,216,385 (GRCm39) |
nonsense |
probably null |
|
R1959:Mios
|
UTSW |
6 |
8,215,437 (GRCm39) |
missense |
probably benign |
0.17 |
R1964:Mios
|
UTSW |
6 |
8,215,798 (GRCm39) |
missense |
probably damaging |
0.99 |
R2272:Mios
|
UTSW |
6 |
8,226,865 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2915:Mios
|
UTSW |
6 |
8,214,935 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3852:Mios
|
UTSW |
6 |
8,216,453 (GRCm39) |
missense |
probably benign |
0.09 |
R3876:Mios
|
UTSW |
6 |
8,233,189 (GRCm39) |
missense |
probably damaging |
0.98 |
R3948:Mios
|
UTSW |
6 |
8,215,496 (GRCm39) |
missense |
probably benign |
|
R4698:Mios
|
UTSW |
6 |
8,228,113 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4785:Mios
|
UTSW |
6 |
8,222,464 (GRCm39) |
missense |
probably benign |
|
R4789:Mios
|
UTSW |
6 |
8,235,429 (GRCm39) |
missense |
probably benign |
0.06 |
R4866:Mios
|
UTSW |
6 |
8,214,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Mios
|
UTSW |
6 |
8,215,094 (GRCm39) |
missense |
probably benign |
0.00 |
R4991:Mios
|
UTSW |
6 |
8,215,847 (GRCm39) |
missense |
probably benign |
0.00 |
R5479:Mios
|
UTSW |
6 |
8,215,314 (GRCm39) |
missense |
probably benign |
0.00 |
R5714:Mios
|
UTSW |
6 |
8,215,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R6030:Mios
|
UTSW |
6 |
8,215,704 (GRCm39) |
missense |
probably benign |
0.11 |
R6030:Mios
|
UTSW |
6 |
8,215,704 (GRCm39) |
missense |
probably benign |
0.11 |
R6111:Mios
|
UTSW |
6 |
8,214,836 (GRCm39) |
missense |
probably benign |
0.01 |
R6455:Mios
|
UTSW |
6 |
8,231,239 (GRCm39) |
missense |
probably benign |
0.03 |
R7381:Mios
|
UTSW |
6 |
8,216,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R8350:Mios
|
UTSW |
6 |
8,227,998 (GRCm39) |
missense |
probably benign |
0.00 |
R8708:Mios
|
UTSW |
6 |
8,234,255 (GRCm39) |
missense |
probably benign |
0.17 |
R8913:Mios
|
UTSW |
6 |
8,215,924 (GRCm39) |
missense |
probably benign |
|
R9062:Mios
|
UTSW |
6 |
8,233,221 (GRCm39) |
missense |
probably benign |
0.00 |
R9359:Mios
|
UTSW |
6 |
8,214,894 (GRCm39) |
missense |
probably benign |
0.17 |
R9521:Mios
|
UTSW |
6 |
8,233,171 (GRCm39) |
missense |
probably benign |
0.45 |
|