Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430097D07Rik |
A |
T |
2: 32,464,630 (GRCm39) |
|
probably benign |
Het |
Aagab |
G |
C |
9: 63,543,738 (GRCm39) |
A231P |
possibly damaging |
Het |
Adgra3 |
C |
T |
5: 50,156,537 (GRCm39) |
D398N |
probably benign |
Het |
Ap3b1 |
A |
T |
13: 94,609,313 (GRCm39) |
D616V |
possibly damaging |
Het |
Apc2 |
T |
A |
10: 80,150,047 (GRCm39) |
H1700Q |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp2b4 |
T |
A |
1: 133,634,518 (GRCm39) |
I1177L |
probably benign |
Het |
Card6 |
T |
C |
15: 5,134,623 (GRCm39) |
|
probably null |
Het |
Cdk13 |
A |
G |
13: 17,894,319 (GRCm39) |
S1103P |
probably benign |
Het |
Cdk6 |
G |
T |
5: 3,394,444 (GRCm39) |
K26N |
possibly damaging |
Het |
Cfap221 |
T |
C |
1: 119,861,934 (GRCm39) |
T614A |
probably damaging |
Het |
Cfap221 |
T |
A |
1: 119,912,488 (GRCm39) |
Y133F |
probably damaging |
Het |
Clcc1 |
A |
G |
3: 108,584,154 (GRCm39) |
T513A |
probably benign |
Het |
Clec4g |
T |
A |
8: 3,766,419 (GRCm39) |
|
probably benign |
Het |
Cntln |
A |
C |
4: 84,889,466 (GRCm39) |
E316D |
probably benign |
Het |
Col6a4 |
A |
G |
9: 105,937,271 (GRCm39) |
I1415T |
probably benign |
Het |
Cpne2 |
T |
A |
8: 95,290,592 (GRCm39) |
D392E |
probably benign |
Het |
Cpz |
T |
C |
5: 35,664,048 (GRCm39) |
N496D |
probably damaging |
Het |
Cyp3a59 |
A |
G |
5: 146,024,197 (GRCm39) |
D61G |
probably damaging |
Het |
Cyp4a29 |
T |
C |
4: 115,110,078 (GRCm39) |
V440A |
probably benign |
Het |
Dbn1 |
A |
T |
13: 55,625,355 (GRCm39) |
|
probably benign |
Het |
Ddx46 |
A |
G |
13: 55,786,012 (GRCm39) |
D64G |
unknown |
Het |
Dhrs7c |
G |
A |
11: 67,700,620 (GRCm39) |
V56M |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,364,015 (GRCm39) |
H4122Q |
probably benign |
Het |
Ecm2 |
A |
T |
13: 49,676,263 (GRCm39) |
I327F |
possibly damaging |
Het |
Elavl3 |
T |
C |
9: 21,937,614 (GRCm39) |
K189E |
possibly damaging |
Het |
Enam |
A |
T |
5: 88,636,593 (GRCm39) |
R82* |
probably null |
Het |
Fat3 |
T |
A |
9: 15,932,626 (GRCm39) |
I1436F |
probably benign |
Het |
Glt8d2 |
T |
C |
10: 82,487,874 (GRCm39) |
|
probably benign |
Het |
Grin2c |
T |
C |
11: 115,151,616 (GRCm39) |
T115A |
probably damaging |
Het |
H6pd |
C |
T |
4: 150,067,235 (GRCm39) |
V384M |
possibly damaging |
Het |
Hba-x |
A |
G |
11: 32,227,008 (GRCm39) |
E39G |
probably benign |
Het |
Hcar2 |
G |
A |
5: 124,003,260 (GRCm39) |
T81M |
probably benign |
Het |
Herpud2 |
G |
A |
9: 25,036,285 (GRCm39) |
P125L |
probably benign |
Het |
Hnrnpul2 |
C |
T |
19: 8,807,191 (GRCm39) |
P618S |
probably benign |
Het |
Hpse2 |
T |
C |
19: 43,373,203 (GRCm39) |
Y142C |
probably damaging |
Het |
Itih1 |
A |
G |
14: 30,658,658 (GRCm39) |
|
probably null |
Het |
Kcnk10 |
T |
C |
12: 98,401,418 (GRCm39) |
N405S |
possibly damaging |
Het |
Klhl14 |
A |
T |
18: 21,691,029 (GRCm39) |
|
probably null |
Het |
L3mbtl3 |
T |
A |
10: 26,168,668 (GRCm39) |
E587V |
unknown |
Het |
Leap2 |
A |
T |
11: 53,313,653 (GRCm39) |
F40I |
probably damaging |
Het |
Leng8 |
T |
A |
7: 4,147,930 (GRCm39) |
|
probably null |
Het |
Lrrc66 |
A |
G |
5: 73,765,910 (GRCm39) |
F378L |
probably benign |
Het |
Mansc1 |
T |
C |
6: 134,587,625 (GRCm39) |
H184R |
probably benign |
Het |
Map10 |
T |
A |
8: 126,397,431 (GRCm39) |
Y275N |
probably damaging |
Het |
Med23 |
T |
C |
10: 24,750,581 (GRCm39) |
|
probably null |
Het |
Mpp3 |
A |
G |
11: 101,915,962 (GRCm39) |
Y55H |
probably benign |
Het |
Mrpl17 |
T |
C |
7: 105,459,260 (GRCm39) |
N112S |
probably benign |
Het |
Nectin4 |
T |
C |
1: 171,212,383 (GRCm39) |
V327A |
possibly damaging |
Het |
Nlrp14 |
A |
T |
7: 106,781,862 (GRCm39) |
H353L |
probably benign |
Het |
Notch2 |
A |
T |
3: 98,009,735 (GRCm39) |
Y554F |
probably damaging |
Het |
Nphp3 |
T |
C |
9: 103,880,193 (GRCm39) |
S72P |
probably damaging |
Het |
Nrsn2 |
T |
C |
2: 152,211,531 (GRCm39) |
K167E |
probably benign |
Het |
Or14j8 |
A |
T |
17: 38,262,962 (GRCm39) |
S318T |
probably benign |
Het |
Or5b117 |
T |
C |
19: 13,431,885 (GRCm39) |
|
probably null |
Het |
Or8g30 |
T |
C |
9: 39,230,881 (GRCm39) |
T10A |
probably benign |
Het |
Or9i2 |
T |
A |
19: 13,815,643 (GRCm39) |
E298V |
probably damaging |
Het |
Osbpl9 |
T |
C |
4: 108,925,564 (GRCm39) |
N485S |
probably benign |
Het |
Pbk |
T |
A |
14: 66,052,650 (GRCm39) |
H164Q |
probably damaging |
Het |
Pfn2 |
G |
T |
3: 57,754,874 (GRCm39) |
N10K |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,176,225 (GRCm39) |
S405P |
|
Het |
Pik3ca |
A |
G |
3: 32,491,312 (GRCm39) |
D133G |
probably damaging |
Het |
Pramel27 |
G |
T |
4: 143,579,873 (GRCm39) |
R486L |
probably benign |
Het |
Prkar2a |
G |
A |
9: 108,622,823 (GRCm39) |
|
probably null |
Het |
Prl6a1 |
A |
T |
13: 27,502,983 (GRCm39) |
D193V |
probably damaging |
Het |
Psg25 |
A |
T |
7: 18,258,838 (GRCm39) |
D279E |
probably benign |
Het |
Rad21 |
G |
T |
15: 51,831,896 (GRCm39) |
P395Q |
probably damaging |
Het |
Rnf168 |
C |
A |
16: 32,118,014 (GRCm39) |
T525K |
probably benign |
Het |
Rpn2 |
T |
C |
2: 157,159,964 (GRCm39) |
|
probably null |
Het |
Rreb1 |
G |
A |
13: 38,115,034 (GRCm39) |
V798M |
possibly damaging |
Het |
Scgb3a2 |
C |
T |
18: 43,899,819 (GRCm39) |
P36S |
probably damaging |
Het |
Scn3a |
T |
C |
2: 65,291,376 (GRCm39) |
D1790G |
probably damaging |
Het |
Sec24b |
A |
T |
3: 129,777,619 (GRCm39) |
H1226Q |
probably benign |
Het |
Sec63 |
T |
A |
10: 42,665,389 (GRCm39) |
Y106* |
probably null |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slc12a3 |
G |
A |
8: 95,078,438 (GRCm39) |
|
probably null |
Het |
Slc6a1 |
T |
A |
6: 114,279,494 (GRCm39) |
I91N |
possibly damaging |
Het |
Slitrk6 |
T |
C |
14: 110,989,315 (GRCm39) |
T131A |
probably damaging |
Het |
Spata1 |
C |
G |
3: 146,175,529 (GRCm39) |
D326H |
probably damaging |
Het |
St8sia1 |
G |
A |
6: 142,859,860 (GRCm39) |
L90F |
probably damaging |
Het |
Thsd4 |
T |
A |
9: 59,896,313 (GRCm39) |
Y657F |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,327,659 (GRCm39) |
C1404* |
probably null |
Het |
Tma16 |
A |
C |
8: 66,934,129 (GRCm39) |
C75W |
probably damaging |
Het |
Trgv4 |
T |
C |
13: 19,369,236 (GRCm39) |
V29A |
probably benign |
Het |
Trim3 |
T |
A |
7: 105,267,047 (GRCm39) |
H444L |
probably damaging |
Het |
Trmt10a |
A |
T |
3: 137,854,146 (GRCm39) |
K75* |
probably null |
Het |
Ttn |
T |
C |
2: 76,561,644 (GRCm39) |
D28954G |
probably damaging |
Het |
Uggt2 |
A |
G |
14: 119,273,376 (GRCm39) |
|
probably null |
Het |
Vars1 |
T |
A |
17: 35,234,702 (GRCm39) |
V1177E |
probably benign |
Het |
Vmn2r114 |
G |
T |
17: 23,527,008 (GRCm39) |
A508E |
probably benign |
Het |
Vmn2r19 |
G |
T |
6: 123,286,800 (GRCm39) |
K144N |
probably benign |
Het |
Wdr41 |
C |
T |
13: 95,151,682 (GRCm39) |
Q281* |
probably null |
Het |
Zfp938 |
T |
A |
10: 82,061,957 (GRCm39) |
Q221L |
probably benign |
Het |
|
Other mutations in Iqcm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01895:Iqcm
|
APN |
8 |
76,615,188 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Iqcm
|
APN |
8 |
76,281,511 (GRCm39) |
utr 5 prime |
probably benign |
|
R0056:Iqcm
|
UTSW |
8 |
76,480,014 (GRCm39) |
missense |
probably benign |
|
R2146:Iqcm
|
UTSW |
8 |
76,615,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Iqcm
|
UTSW |
8 |
76,441,404 (GRCm39) |
missense |
probably benign |
|
R3801:Iqcm
|
UTSW |
8 |
76,396,021 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3804:Iqcm
|
UTSW |
8 |
76,396,021 (GRCm39) |
missense |
possibly damaging |
0.59 |
R3834:Iqcm
|
UTSW |
8 |
76,304,380 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3897:Iqcm
|
UTSW |
8 |
76,480,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Iqcm
|
UTSW |
8 |
76,356,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4448:Iqcm
|
UTSW |
8 |
76,356,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4450:Iqcm
|
UTSW |
8 |
76,356,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4687:Iqcm
|
UTSW |
8 |
76,489,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Iqcm
|
UTSW |
8 |
76,615,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Iqcm
|
UTSW |
8 |
76,472,980 (GRCm39) |
missense |
probably damaging |
0.99 |
R4856:Iqcm
|
UTSW |
8 |
76,615,228 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5063:Iqcm
|
UTSW |
8 |
76,472,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Iqcm
|
UTSW |
8 |
76,441,417 (GRCm39) |
missense |
probably benign |
|
R6403:Iqcm
|
UTSW |
8 |
76,304,624 (GRCm39) |
critical splice donor site |
probably null |
|
R6667:Iqcm
|
UTSW |
8 |
76,479,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R7187:Iqcm
|
UTSW |
8 |
76,480,044 (GRCm39) |
missense |
probably benign |
0.22 |
R7263:Iqcm
|
UTSW |
8 |
76,489,701 (GRCm39) |
missense |
probably benign |
|
R7701:Iqcm
|
UTSW |
8 |
76,281,539 (GRCm39) |
missense |
probably benign |
0.02 |
R7916:Iqcm
|
UTSW |
8 |
76,304,578 (GRCm39) |
missense |
probably benign |
|
R7938:Iqcm
|
UTSW |
8 |
76,304,596 (GRCm39) |
missense |
probably benign |
|
R7974:Iqcm
|
UTSW |
8 |
76,281,520 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R8039:Iqcm
|
UTSW |
8 |
76,489,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R8311:Iqcm
|
UTSW |
8 |
76,480,118 (GRCm39) |
splice site |
probably benign |
|
R8703:Iqcm
|
UTSW |
8 |
76,615,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9175:Iqcm
|
UTSW |
8 |
76,710,867 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9475:Iqcm
|
UTSW |
8 |
76,480,083 (GRCm39) |
missense |
probably damaging |
1.00 |
RF002:Iqcm
|
UTSW |
8 |
76,304,527 (GRCm39) |
missense |
probably benign |
0.01 |
X0018:Iqcm
|
UTSW |
8 |
76,710,840 (GRCm39) |
nonsense |
probably null |
|
|