Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12 |
T |
C |
2: 150,681,698 (GRCm39) |
I231V |
possibly damaging |
Het |
Adsl |
A |
G |
15: 80,845,554 (GRCm39) |
|
probably null |
Het |
Ahnak |
C |
A |
19: 8,991,131 (GRCm39) |
N4138K |
possibly damaging |
Het |
Ahnak |
T |
C |
19: 8,995,575 (GRCm39) |
S5620P |
probably damaging |
Het |
Akap13 |
C |
T |
7: 75,378,894 (GRCm39) |
T2145I |
probably damaging |
Het |
Alpk2 |
T |
A |
18: 65,440,694 (GRCm39) |
Q700L |
probably damaging |
Het |
Apobec1 |
T |
C |
6: 122,557,732 (GRCm39) |
Y159C |
probably damaging |
Het |
Atg9a |
T |
C |
1: 75,162,916 (GRCm39) |
T395A |
probably damaging |
Het |
Atp6v1f |
A |
G |
6: 29,467,957 (GRCm39) |
I48V |
probably benign |
Het |
BC051665 |
A |
C |
13: 60,930,518 (GRCm39) |
V278G |
probably damaging |
Het |
Bicd1 |
A |
T |
6: 149,415,201 (GRCm39) |
H638L |
probably damaging |
Het |
Cacna2d4 |
A |
G |
6: 119,251,192 (GRCm39) |
Y460C |
probably damaging |
Het |
Ccdc157 |
C |
A |
11: 4,094,538 (GRCm39) |
R496L |
probably benign |
Het |
Cdcp3 |
T |
G |
7: 130,843,696 (GRCm39) |
|
probably null |
Het |
Cep44 |
C |
G |
8: 56,994,056 (GRCm39) |
V174L |
probably damaging |
Het |
Clca3a1 |
G |
T |
3: 144,722,522 (GRCm39) |
F283L |
possibly damaging |
Het |
Csk |
T |
C |
9: 57,537,585 (GRCm39) |
T110A |
probably benign |
Het |
Cspg4 |
T |
A |
9: 56,792,506 (GRCm39) |
|
probably null |
Het |
Cutc |
A |
G |
19: 43,748,468 (GRCm39) |
I124V |
probably benign |
Het |
Cyp2d9 |
A |
G |
15: 82,339,725 (GRCm39) |
T104A |
probably benign |
Het |
Cyp2j9 |
G |
T |
4: 96,465,951 (GRCm39) |
T294K |
probably benign |
Het |
D630003M21Rik |
T |
A |
2: 158,046,577 (GRCm39) |
|
probably null |
Het |
Dcaf15 |
G |
T |
8: 84,825,081 (GRCm39) |
F450L |
probably damaging |
Het |
Ddhd1 |
A |
T |
14: 45,840,125 (GRCm39) |
I723K |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 118,005,039 (GRCm39) |
A782T |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,677,724 (GRCm39) |
D399G |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,148,717 (GRCm39) |
N909S |
probably benign |
Het |
Erbin |
A |
G |
13: 103,975,813 (GRCm39) |
|
probably null |
Het |
Fanci |
G |
A |
7: 79,083,069 (GRCm39) |
V682I |
probably benign |
Het |
Fap |
A |
T |
2: 62,403,847 (GRCm39) |
F9L |
probably benign |
Het |
Fat3 |
T |
C |
9: 15,849,757 (GRCm39) |
I3882V |
probably benign |
Het |
Fkbp15 |
A |
T |
4: 62,244,294 (GRCm39) |
|
probably null |
Het |
Fsd2 |
T |
C |
7: 81,186,975 (GRCm39) |
Y601C |
probably damaging |
Het |
Gm5900 |
T |
C |
7: 104,599,468 (GRCm39) |
|
noncoding transcript |
Het |
Gramd4 |
G |
T |
15: 85,984,985 (GRCm39) |
G82V |
probably damaging |
Het |
Hc |
C |
T |
2: 34,887,449 (GRCm39) |
V1352I |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,548,623 (GRCm39) |
N466K |
probably damaging |
Het |
Ice2 |
T |
A |
9: 69,315,544 (GRCm39) |
D133E |
probably benign |
Het |
Ifi213 |
T |
C |
1: 173,396,545 (GRCm39) |
M510V |
probably benign |
Het |
Itpkb |
T |
G |
1: 180,248,880 (GRCm39) |
L861R |
probably damaging |
Het |
Kbtbd3 |
T |
A |
9: 4,330,476 (GRCm39) |
D283E |
probably damaging |
Het |
Man2a1 |
A |
G |
17: 64,932,375 (GRCm39) |
K154R |
probably benign |
Het |
Masp1 |
T |
A |
16: 23,310,677 (GRCm39) |
I252F |
probably damaging |
Het |
Megf11 |
G |
T |
9: 64,593,246 (GRCm39) |
C586F |
probably damaging |
Het |
Myh2 |
C |
A |
11: 67,083,545 (GRCm39) |
A1476E |
possibly damaging |
Het |
Myo18b |
A |
T |
5: 112,950,196 (GRCm39) |
|
probably null |
Het |
Naip6 |
A |
T |
13: 100,435,829 (GRCm39) |
V898E |
possibly damaging |
Het |
Nav1 |
T |
C |
1: 135,512,884 (GRCm39) |
M59V |
probably benign |
Het |
Nlrp3 |
A |
T |
11: 59,437,678 (GRCm39) |
Y119F |
probably benign |
Het |
Oxa1l |
T |
A |
14: 54,600,758 (GRCm39) |
I77N |
possibly damaging |
Het |
Pcdhb8 |
T |
A |
18: 37,490,537 (GRCm39) |
D738E |
possibly damaging |
Het |
Pdia5 |
A |
T |
16: 35,243,335 (GRCm39) |
W269R |
probably damaging |
Het |
Peak1 |
T |
A |
9: 56,114,622 (GRCm39) |
T1440S |
probably benign |
Het |
Piezo1 |
A |
G |
8: 123,214,682 (GRCm39) |
V1547A |
probably benign |
Het |
Pkp1 |
T |
C |
1: 135,810,259 (GRCm39) |
Y437C |
probably damaging |
Het |
Pla2r1 |
T |
C |
2: 60,253,104 (GRCm39) |
D1329G |
probably damaging |
Het |
Ppip5k2 |
T |
C |
1: 97,671,887 (GRCm39) |
|
probably benign |
Het |
Prrg4 |
C |
T |
2: 104,675,378 (GRCm39) |
S75N |
probably benign |
Het |
Psmb9 |
T |
A |
17: 34,401,266 (GRCm39) |
I198F |
probably damaging |
Het |
Rcbtb2 |
T |
A |
14: 73,399,405 (GRCm39) |
L23* |
probably null |
Het |
Sbno1 |
A |
T |
5: 124,524,854 (GRCm39) |
|
probably benign |
Het |
Scn3a |
T |
C |
2: 65,345,039 (GRCm39) |
E483G |
probably damaging |
Het |
Sdccag8 |
T |
A |
1: 176,652,388 (GRCm39) |
D46E |
probably benign |
Het |
Selenov |
A |
G |
7: 27,987,579 (GRCm39) |
F293L |
probably damaging |
Het |
Septin2 |
A |
C |
1: 93,407,023 (GRCm39) |
D20A |
probably benign |
Het |
Shc1 |
T |
A |
3: 89,334,274 (GRCm39) |
Y313* |
probably null |
Het |
Siglec1 |
T |
A |
2: 130,915,553 (GRCm39) |
Y1346F |
probably damaging |
Het |
Slc22a5 |
T |
A |
11: 53,764,559 (GRCm39) |
I296F |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,365,123 (GRCm39) |
N152S |
probably damaging |
Het |
Smoc1 |
C |
T |
12: 81,151,531 (GRCm39) |
R83* |
probably null |
Het |
Ssx2ip |
A |
G |
3: 146,133,586 (GRCm39) |
D227G |
possibly damaging |
Het |
Tbrg4 |
T |
C |
11: 6,567,372 (GRCm39) |
D576G |
probably damaging |
Het |
Tbx20 |
T |
A |
9: 24,670,155 (GRCm39) |
Y226F |
probably damaging |
Het |
Trav10d |
G |
T |
14: 53,048,929 (GRCm39) |
A107S |
probably damaging |
Het |
Trim60 |
A |
T |
8: 65,453,016 (GRCm39) |
L411* |
probably null |
Het |
Ttbk2 |
A |
T |
2: 120,575,521 (GRCm39) |
V1083D |
probably benign |
Het |
Unc93a |
T |
A |
17: 13,344,464 (GRCm39) |
Q26L |
probably damaging |
Het |
Usp14 |
T |
A |
18: 10,022,819 (GRCm39) |
N65I |
possibly damaging |
Het |
Vip |
A |
T |
10: 5,593,988 (GRCm39) |
S114C |
probably damaging |
Het |
Vmn1r237 |
A |
T |
17: 21,534,813 (GRCm39) |
I179F |
probably damaging |
Het |
Wdr47 |
T |
A |
3: 108,545,201 (GRCm39) |
|
probably null |
Het |
Zfp975 |
A |
T |
7: 42,311,963 (GRCm39) |
C217S |
probably damaging |
Het |
|
Other mutations in 1700017N19Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01565:1700017N19Rik
|
APN |
10 |
100,439,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02159:1700017N19Rik
|
APN |
10 |
100,446,527 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:1700017N19Rik
|
APN |
10 |
100,446,579 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02629:1700017N19Rik
|
APN |
10 |
100,445,006 (GRCm39) |
splice site |
probably benign |
|
IGL02692:1700017N19Rik
|
APN |
10 |
100,439,410 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02962:1700017N19Rik
|
APN |
10 |
100,446,455 (GRCm39) |
splice site |
probably null |
|
R0145:1700017N19Rik
|
UTSW |
10 |
100,437,783 (GRCm39) |
missense |
probably damaging |
0.96 |
R0402:1700017N19Rik
|
UTSW |
10 |
100,445,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R1514:1700017N19Rik
|
UTSW |
10 |
100,448,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:1700017N19Rik
|
UTSW |
10 |
100,439,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R1680:1700017N19Rik
|
UTSW |
10 |
100,439,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R1686:1700017N19Rik
|
UTSW |
10 |
100,448,722 (GRCm39) |
missense |
probably damaging |
0.97 |
R3951:1700017N19Rik
|
UTSW |
10 |
100,451,158 (GRCm39) |
splice site |
probably benign |
|
R3952:1700017N19Rik
|
UTSW |
10 |
100,451,158 (GRCm39) |
splice site |
probably benign |
|
R4423:1700017N19Rik
|
UTSW |
10 |
100,441,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R4905:1700017N19Rik
|
UTSW |
10 |
100,448,680 (GRCm39) |
splice site |
probably null |
|
R5507:1700017N19Rik
|
UTSW |
10 |
100,445,095 (GRCm39) |
missense |
probably benign |
0.02 |
R5898:1700017N19Rik
|
UTSW |
10 |
100,448,762 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5977:1700017N19Rik
|
UTSW |
10 |
100,451,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R7034:1700017N19Rik
|
UTSW |
10 |
100,445,118 (GRCm39) |
critical splice donor site |
probably null |
|
R7036:1700017N19Rik
|
UTSW |
10 |
100,445,118 (GRCm39) |
critical splice donor site |
probably null |
|
R7394:1700017N19Rik
|
UTSW |
10 |
100,445,038 (GRCm39) |
missense |
probably benign |
0.01 |
R7412:1700017N19Rik
|
UTSW |
10 |
100,448,691 (GRCm39) |
nonsense |
probably null |
|
R7870:1700017N19Rik
|
UTSW |
10 |
100,441,505 (GRCm39) |
missense |
probably benign |
|
R7914:1700017N19Rik
|
UTSW |
10 |
100,428,538 (GRCm39) |
missense |
probably benign |
|
R8466:1700017N19Rik
|
UTSW |
10 |
100,437,873 (GRCm39) |
missense |
probably benign |
0.00 |
R8558:1700017N19Rik
|
UTSW |
10 |
100,430,497 (GRCm39) |
missense |
probably benign |
0.23 |
R9004:1700017N19Rik
|
UTSW |
10 |
100,454,197 (GRCm39) |
unclassified |
probably benign |
|
R9105:1700017N19Rik
|
UTSW |
10 |
100,439,407 (GRCm39) |
nonsense |
probably null |
|
R9641:1700017N19Rik
|
UTSW |
10 |
100,430,498 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1088:1700017N19Rik
|
UTSW |
10 |
100,441,501 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:1700017N19Rik
|
UTSW |
10 |
100,448,291 (GRCm39) |
missense |
probably damaging |
0.98 |
|