Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
A |
T |
5: 113,243,473 (GRCm39) |
M190K |
probably damaging |
Het |
4931406B18Rik |
A |
G |
7: 43,153,640 (GRCm39) |
W3R |
probably damaging |
Het |
Acap3 |
T |
C |
4: 155,989,892 (GRCm39) |
L720P |
probably damaging |
Het |
Actc1 |
T |
C |
2: 113,882,494 (GRCm39) |
T7A |
probably benign |
Het |
Angpt2 |
T |
A |
8: 18,760,658 (GRCm39) |
|
probably null |
Het |
Babam2 |
T |
A |
5: 32,058,401 (GRCm39) |
D228E |
possibly damaging |
Het |
Ccar1 |
G |
A |
10: 62,621,347 (GRCm39) |
L34F |
probably damaging |
Het |
Ccdc83 |
T |
C |
7: 89,886,102 (GRCm39) |
D219G |
probably damaging |
Het |
Cdc20b |
G |
A |
13: 113,208,503 (GRCm39) |
|
probably null |
Het |
Chd7 |
T |
A |
4: 8,838,737 (GRCm39) |
L1312Q |
probably damaging |
Het |
Cltc |
G |
A |
11: 86,595,982 (GRCm39) |
T1252I |
probably damaging |
Het |
Cnpy1 |
G |
T |
5: 28,450,799 (GRCm39) |
D2E |
possibly damaging |
Het |
Crat |
C |
T |
2: 30,298,085 (GRCm39) |
V205M |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,457,358 (GRCm39) |
N1135D |
|
Het |
Dgkb |
T |
C |
12: 38,216,776 (GRCm39) |
|
probably null |
Het |
Dglucy |
T |
C |
12: 100,811,028 (GRCm39) |
V254A |
possibly damaging |
Het |
Disp3 |
A |
G |
4: 148,354,841 (GRCm39) |
S392P |
probably damaging |
Het |
Dlx6 |
A |
T |
6: 6,863,456 (GRCm39) |
Q26L |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,684,351 (GRCm39) |
D258G |
probably damaging |
Het |
Dnah6 |
A |
T |
6: 73,121,688 (GRCm39) |
Y1431* |
probably null |
Het |
Dnah7b |
T |
C |
1: 46,330,038 (GRCm39) |
I3294T |
probably benign |
Het |
Dnai2 |
A |
G |
11: 114,623,839 (GRCm39) |
N34S |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,260,398 (GRCm39) |
K981R |
possibly damaging |
Het |
Entpd8 |
T |
C |
2: 24,971,931 (GRCm39) |
I33T |
probably benign |
Het |
Eppk1 |
A |
G |
15: 75,995,453 (GRCm39) |
L476P |
probably benign |
Het |
Etv1 |
T |
A |
12: 38,830,716 (GRCm39) |
|
probably null |
Het |
Fads2b |
T |
C |
2: 85,330,581 (GRCm39) |
H242R |
probably benign |
Het |
Fam193a |
T |
A |
5: 34,623,361 (GRCm39) |
N1316K |
possibly damaging |
Het |
Fkbp4 |
T |
C |
6: 128,415,382 (GRCm39) |
E31G |
probably benign |
Het |
Fnbp1l |
C |
T |
3: 122,363,345 (GRCm39) |
D81N |
probably damaging |
Het |
Fstl4 |
T |
C |
11: 53,024,905 (GRCm39) |
V259A |
probably damaging |
Het |
Glipr1l1 |
T |
C |
10: 111,912,056 (GRCm39) |
S197P |
probably damaging |
Het |
Gprin3 |
A |
T |
6: 59,331,197 (GRCm39) |
M370K |
probably benign |
Het |
Gsc |
G |
T |
12: 104,439,120 (GRCm39) |
Y85* |
probably null |
Het |
Gys2 |
T |
G |
6: 142,391,735 (GRCm39) |
Y509S |
probably damaging |
Het |
Gys2 |
T |
C |
6: 142,406,978 (GRCm39) |
N126S |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,488,405 (GRCm39) |
W4292R |
probably damaging |
Het |
Hmcn1 |
C |
A |
1: 150,500,337 (GRCm39) |
E3952* |
probably null |
Het |
Hsd3b9 |
C |
T |
3: 98,354,005 (GRCm39) |
A165T |
possibly damaging |
Het |
Htr1f |
T |
C |
16: 64,746,825 (GRCm39) |
M156V |
probably benign |
Het |
Il21r |
G |
A |
7: 125,228,213 (GRCm39) |
G228E |
probably benign |
Het |
Kat6b |
C |
T |
14: 21,567,187 (GRCm39) |
S82L |
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,940,355 (GRCm39) |
L1651Q |
probably damaging |
Het |
Lipi |
G |
T |
16: 75,357,673 (GRCm39) |
Y297* |
probably null |
Het |
Mapre3 |
T |
C |
5: 31,022,016 (GRCm39) |
S190P |
possibly damaging |
Het |
Mmp8 |
T |
A |
9: 7,567,467 (GRCm39) |
Y442* |
probably null |
Het |
Mmut |
A |
G |
17: 41,252,310 (GRCm39) |
E284G |
probably damaging |
Het |
Mt3 |
G |
A |
8: 94,880,615 (GRCm39) |
E62K |
unknown |
Het |
Myh13 |
A |
G |
11: 67,228,579 (GRCm39) |
E373G |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,226,374 (GRCm39) |
Y422C |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,834,016 (GRCm39) |
V53A |
probably damaging |
Het |
Nucb2 |
A |
G |
7: 116,121,070 (GRCm39) |
|
probably null |
Het |
Opn5 |
A |
T |
17: 42,903,890 (GRCm39) |
H148Q |
probably damaging |
Het |
Or13a23-ps1 |
A |
T |
7: 140,118,782 (GRCm39) |
L117F |
probably benign |
Het |
Or51h1 |
A |
T |
7: 102,308,927 (GRCm39) |
I300L |
probably damaging |
Het |
Or51v14 |
T |
C |
7: 103,261,063 (GRCm39) |
K166E |
possibly damaging |
Het |
Or6b1 |
A |
T |
6: 42,815,010 (GRCm39) |
N65I |
probably benign |
Het |
Or7g16 |
G |
T |
9: 18,726,742 (GRCm39) |
Q283K |
probably damaging |
Het |
Or8b56 |
C |
A |
9: 38,739,172 (GRCm39) |
H56N |
probably damaging |
Het |
Osmr |
T |
A |
15: 6,850,569 (GRCm39) |
D679V |
probably damaging |
Het |
Pde4dip |
T |
C |
3: 97,602,314 (GRCm39) |
D2305G |
probably benign |
Het |
Pdgfrl |
A |
T |
8: 41,429,996 (GRCm39) |
Q121L |
probably damaging |
Het |
Pls1 |
C |
A |
9: 95,658,811 (GRCm39) |
V226F |
probably damaging |
Het |
Plxnd1 |
T |
A |
6: 115,970,746 (GRCm39) |
I341F |
probably damaging |
Het |
Ppfia2 |
T |
A |
10: 106,763,640 (GRCm39) |
M1211K |
probably benign |
Het |
Ppfibp2 |
T |
A |
7: 107,308,053 (GRCm39) |
Y229N |
possibly damaging |
Het |
Prss53 |
A |
G |
7: 127,487,554 (GRCm39) |
S266P |
probably benign |
Het |
Pycr2 |
C |
T |
1: 180,734,397 (GRCm39) |
Q226* |
probably null |
Het |
Rad50 |
T |
C |
11: 53,583,590 (GRCm39) |
H397R |
probably benign |
Het |
Raf1 |
T |
C |
6: 115,600,440 (GRCm39) |
E393G |
probably damaging |
Het |
Reln |
T |
C |
5: 22,106,617 (GRCm39) |
D3251G |
probably benign |
Het |
Robo4 |
A |
T |
9: 37,313,206 (GRCm39) |
|
probably benign |
Het |
Sbf1 |
A |
T |
15: 89,173,806 (GRCm39) |
|
probably null |
Het |
Serpinb6a |
T |
C |
13: 34,109,360 (GRCm39) |
D145G |
probably damaging |
Het |
Setx |
T |
A |
2: 29,061,299 (GRCm39) |
M2236K |
probably damaging |
Het |
Sgms1 |
A |
G |
19: 32,101,758 (GRCm39) |
V416A |
probably benign |
Het |
Six5 |
T |
G |
7: 18,830,932 (GRCm39) |
S520A |
probably benign |
Het |
Sox5 |
T |
A |
6: 143,779,118 (GRCm39) |
I722F |
possibly damaging |
Het |
Spag17 |
T |
G |
3: 99,966,158 (GRCm39) |
I1147S |
possibly damaging |
Het |
Spice1 |
C |
T |
16: 44,206,065 (GRCm39) |
T842I |
possibly damaging |
Het |
Ssbp2 |
A |
G |
13: 91,848,800 (GRCm39) |
T358A |
probably damaging |
Het |
Taok3 |
T |
C |
5: 117,355,307 (GRCm39) |
|
probably null |
Het |
Tbc1d2b |
C |
A |
9: 90,152,652 (GRCm39) |
C38F |
probably damaging |
Het |
Tecrl |
C |
A |
5: 83,457,049 (GRCm39) |
|
probably null |
Het |
Tgm7 |
T |
C |
2: 120,926,980 (GRCm39) |
N390D |
probably benign |
Het |
Thsd4 |
T |
G |
9: 59,894,649 (GRCm39) |
M770L |
probably benign |
Het |
Tmod2 |
C |
A |
9: 75,504,624 (GRCm39) |
|
probably benign |
Het |
Tnks |
A |
G |
8: 35,308,905 (GRCm39) |
|
probably null |
Het |
Tox3 |
T |
C |
8: 90,984,507 (GRCm39) |
N224S |
probably benign |
Het |
Trappc10 |
C |
T |
10: 78,050,464 (GRCm39) |
E326K |
probably damaging |
Het |
Usp16 |
T |
A |
16: 87,276,542 (GRCm39) |
F627I |
probably benign |
Het |
Vcam1 |
T |
C |
3: 115,911,004 (GRCm39) |
I465V |
probably benign |
Het |
Vmn1r128 |
T |
C |
7: 21,083,683 (GRCm39) |
I129T |
possibly damaging |
Het |
Vmn1r217 |
T |
A |
13: 23,298,495 (GRCm39) |
I136L |
probably benign |
Het |
Vmn2r2 |
A |
T |
3: 64,044,802 (GRCm39) |
C115S |
probably damaging |
Het |
Vmn2r85 |
A |
C |
10: 130,265,350 (GRCm39) |
S44R |
probably benign |
Het |
Wasf3 |
T |
A |
5: 146,403,635 (GRCm39) |
Y248* |
probably null |
Het |
Yipf5 |
A |
T |
18: 40,343,851 (GRCm39) |
L127M |
probably damaging |
Het |
Zbp1 |
G |
T |
2: 173,050,933 (GRCm39) |
C312* |
probably null |
Het |
Zfp423 |
A |
T |
8: 88,508,742 (GRCm39) |
F534Y |
probably damaging |
Het |
Zfp69 |
T |
G |
4: 120,792,308 (GRCm39) |
Y156S |
probably damaging |
Het |
Zmat4 |
A |
G |
8: 24,419,226 (GRCm39) |
N155S |
probably damaging |
Het |
|
Other mutations in Cct2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02111:Cct2
|
APN |
10 |
116,889,017 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02150:Cct2
|
APN |
10 |
116,898,004 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02349:Cct2
|
APN |
10 |
116,889,044 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03010:Cct2
|
APN |
10 |
116,894,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Cct2
|
APN |
10 |
116,896,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R0507:Cct2
|
UTSW |
10 |
116,891,151 (GRCm39) |
splice site |
probably null |
|
R0742:Cct2
|
UTSW |
10 |
116,891,151 (GRCm39) |
splice site |
probably null |
|
R1102:Cct2
|
UTSW |
10 |
116,896,545 (GRCm39) |
splice site |
probably null |
|
R1438:Cct2
|
UTSW |
10 |
116,890,897 (GRCm39) |
unclassified |
probably benign |
|
R2040:Cct2
|
UTSW |
10 |
116,889,018 (GRCm39) |
missense |
probably benign |
0.00 |
R2157:Cct2
|
UTSW |
10 |
116,898,714 (GRCm39) |
splice site |
probably benign |
|
R2227:Cct2
|
UTSW |
10 |
116,888,922 (GRCm39) |
missense |
probably null |
0.18 |
R3410:Cct2
|
UTSW |
10 |
116,897,968 (GRCm39) |
missense |
probably benign |
0.01 |
R3981:Cct2
|
UTSW |
10 |
116,890,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Cct2
|
UTSW |
10 |
116,890,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4364:Cct2
|
UTSW |
10 |
116,891,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4401:Cct2
|
UTSW |
10 |
116,893,714 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6162:Cct2
|
UTSW |
10 |
116,894,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R6300:Cct2
|
UTSW |
10 |
116,892,064 (GRCm39) |
missense |
probably damaging |
0.96 |
R6312:Cct2
|
UTSW |
10 |
116,891,960 (GRCm39) |
missense |
probably benign |
0.00 |
R7075:Cct2
|
UTSW |
10 |
116,897,370 (GRCm39) |
missense |
unknown |
|
R7198:Cct2
|
UTSW |
10 |
116,889,029 (GRCm39) |
missense |
probably benign |
|
R7236:Cct2
|
UTSW |
10 |
116,897,464 (GRCm39) |
missense |
probably benign |
0.00 |
R8373:Cct2
|
UTSW |
10 |
116,896,729 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8803:Cct2
|
UTSW |
10 |
116,894,090 (GRCm39) |
missense |
probably benign |
0.00 |
R8859:Cct2
|
UTSW |
10 |
116,896,739 (GRCm39) |
missense |
possibly damaging |
0.63 |
|