Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2 |
C |
T |
3: 59,914,511 (GRCm39) |
T38I |
probably benign |
Het |
Ace |
T |
A |
11: 105,861,424 (GRCm39) |
L191* |
probably null |
Het |
Ahctf1 |
G |
A |
1: 179,614,341 (GRCm39) |
H451Y |
probably damaging |
Het |
Amotl1 |
C |
A |
9: 14,466,869 (GRCm39) |
|
probably null |
Het |
Angptl6 |
T |
A |
9: 20,786,940 (GRCm39) |
Y261F |
probably damaging |
Het |
Arhgap1 |
G |
T |
2: 91,499,744 (GRCm39) |
S293I |
probably benign |
Het |
Atg9a |
A |
C |
1: 75,161,867 (GRCm39) |
F560V |
probably damaging |
Het |
B4galnt4 |
G |
A |
7: 140,648,488 (GRCm39) |
G668D |
possibly damaging |
Het |
Btaf1 |
T |
A |
19: 36,935,901 (GRCm39) |
N230K |
probably benign |
Het |
Cdk5rap2 |
A |
T |
4: 70,218,887 (GRCm39) |
D623E |
probably damaging |
Het |
Cenpf |
C |
A |
1: 189,385,430 (GRCm39) |
K2283N |
probably benign |
Het |
Clec16a |
A |
T |
16: 10,462,731 (GRCm39) |
D683V |
probably damaging |
Het |
Clvs2 |
T |
C |
10: 33,404,400 (GRCm39) |
D272G |
probably benign |
Het |
Cnksr1 |
A |
G |
4: 133,959,494 (GRCm39) |
V380A |
probably damaging |
Het |
Col20a1 |
C |
A |
2: 180,655,684 (GRCm39) |
P42T |
|
Het |
Ddx47 |
A |
G |
6: 135,000,356 (GRCm39) |
K451E |
probably benign |
Het |
Dennd4a |
G |
A |
9: 64,819,672 (GRCm39) |
G1761D |
probably benign |
Het |
Dnah11 |
T |
A |
12: 118,156,107 (GRCm39) |
H181L |
probably benign |
Het |
Dync1h1 |
T |
C |
12: 110,602,333 (GRCm39) |
C2074R |
probably damaging |
Het |
Ell2 |
A |
T |
13: 75,917,793 (GRCm39) |
Q574H |
probably damaging |
Het |
Enpp7 |
A |
G |
11: 118,879,191 (GRCm39) |
N50S |
possibly damaging |
Het |
Fbp2 |
T |
C |
13: 62,989,709 (GRCm39) |
K199R |
probably benign |
Het |
Fetub |
A |
T |
16: 22,758,321 (GRCm39) |
E368V |
possibly damaging |
Het |
Flt1 |
A |
T |
5: 147,507,682 (GRCm39) |
D1209E |
probably benign |
Het |
Flt1 |
A |
T |
5: 147,618,460 (GRCm39) |
N260K |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,917,465 (GRCm39) |
H3495R |
|
Het |
Fsip2 |
A |
G |
2: 82,810,521 (GRCm39) |
Q2280R |
probably benign |
Het |
Gja10 |
A |
T |
4: 32,601,573 (GRCm39) |
C270* |
probably null |
Het |
Gpld1 |
A |
G |
13: 25,170,890 (GRCm39) |
T794A |
probably benign |
Het |
Gsk3b |
A |
G |
16: 38,004,900 (GRCm39) |
Y157C |
probably damaging |
Het |
Gsta2 |
T |
C |
9: 78,244,880 (GRCm39) |
K78R |
probably damaging |
Het |
Gtf3a |
A |
G |
5: 146,885,721 (GRCm39) |
D44G |
probably benign |
Het |
Hap1 |
C |
A |
11: 100,246,864 (GRCm39) |
G14W |
probably damaging |
Het |
Hcn4 |
T |
A |
9: 58,765,387 (GRCm39) |
I623N |
unknown |
Het |
Kank1 |
T |
C |
19: 25,388,702 (GRCm39) |
S792P |
possibly damaging |
Het |
Klra5 |
A |
T |
6: 129,880,533 (GRCm39) |
W212R |
probably damaging |
Het |
Kmt2d |
A |
T |
15: 98,754,237 (GRCm39) |
L1622Q |
unknown |
Het |
Lipi |
T |
A |
16: 75,355,481 (GRCm39) |
D343V |
probably damaging |
Het |
Lrp6 |
A |
T |
6: 134,445,785 (GRCm39) |
N1009K |
probably benign |
Het |
Lrrc39 |
T |
A |
3: 116,363,790 (GRCm39) |
I121N |
probably damaging |
Het |
Mamstr |
A |
T |
7: 45,294,403 (GRCm39) |
D419V |
probably benign |
Het |
Map2k7 |
C |
T |
8: 4,293,594 (GRCm39) |
T119I |
probably damaging |
Het |
Mov10l1 |
A |
T |
15: 88,896,169 (GRCm39) |
D671V |
probably benign |
Het |
Mrps24 |
A |
T |
11: 5,654,642 (GRCm39) |
L104Q |
probably damaging |
Het |
Myh1 |
T |
A |
11: 67,102,247 (GRCm39) |
L846H |
probably damaging |
Het |
Ndufaf5 |
T |
A |
2: 140,025,840 (GRCm39) |
I133N |
possibly damaging |
Het |
Ndufs5 |
A |
G |
4: 123,609,655 (GRCm39) |
|
probably null |
Het |
Numa1 |
G |
C |
7: 101,639,835 (GRCm39) |
D62H |
possibly damaging |
Het |
Or10g3 |
A |
T |
14: 52,610,196 (GRCm39) |
Y105N |
probably damaging |
Het |
Or52e19 |
T |
A |
7: 102,959,168 (GRCm39) |
I80N |
probably damaging |
Het |
Or52p2 |
G |
T |
7: 102,237,945 (GRCm39) |
Q2K |
probably benign |
Het |
Or8b12c |
C |
G |
9: 37,715,709 (GRCm39) |
F167L |
probably damaging |
Het |
Pag1 |
T |
C |
3: 9,764,529 (GRCm39) |
K208R |
probably benign |
Het |
Pkd1 |
T |
C |
17: 24,792,051 (GRCm39) |
V1246A |
probably damaging |
Het |
Plekhg2 |
T |
C |
7: 28,069,526 (GRCm39) |
T144A |
probably benign |
Het |
Plekhm2 |
A |
T |
4: 141,361,658 (GRCm39) |
S262T |
probably benign |
Het |
Pramel14 |
A |
T |
4: 143,720,905 (GRCm39) |
L12Q |
probably damaging |
Het |
Prpf4 |
A |
G |
4: 62,334,235 (GRCm39) |
D230G |
probably benign |
Het |
Rbm15b |
C |
T |
9: 106,763,595 (GRCm39) |
R191Q |
probably benign |
Het |
Sec16a |
G |
A |
2: 26,329,852 (GRCm39) |
T721I |
probably benign |
Het |
Serpinb6c |
A |
T |
13: 34,083,309 (GRCm39) |
I35N |
probably damaging |
Het |
Sgk1 |
T |
G |
10: 21,871,726 (GRCm39) |
S181A |
probably benign |
Het |
Slc25a10 |
T |
C |
11: 120,385,795 (GRCm39) |
S74P |
probably damaging |
Het |
Slc30a3 |
C |
A |
5: 31,245,325 (GRCm39) |
V332F |
possibly damaging |
Het |
Smg1 |
A |
G |
7: 117,806,122 (GRCm39) |
S240P |
unknown |
Het |
Snapc4 |
G |
A |
2: 26,264,545 (GRCm39) |
R265W |
probably damaging |
Het |
Taar1 |
C |
T |
10: 23,796,976 (GRCm39) |
R225C |
possibly damaging |
Het |
Tmem74 |
A |
G |
15: 43,730,231 (GRCm39) |
S271P |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,141,289 (GRCm39) |
V127A |
unknown |
Het |
Trim66 |
G |
T |
7: 109,081,188 (GRCm39) |
H244N |
probably damaging |
Het |
Tshz2 |
T |
A |
2: 169,728,425 (GRCm39) |
L1007H |
probably damaging |
Het |
Ttc39c |
A |
T |
18: 12,831,003 (GRCm39) |
S288C |
probably benign |
Het |
Twnk |
C |
T |
19: 45,000,272 (GRCm39) |
Q663* |
probably null |
Het |
Ucn |
T |
A |
5: 31,295,857 (GRCm39) |
Q3L |
probably benign |
Het |
Usp9y |
C |
T |
Y: 1,395,758 (GRCm39) |
R492H |
probably damaging |
Het |
Vars1 |
T |
C |
17: 35,234,620 (GRCm39) |
S1150P |
probably benign |
Het |
Zc3h7b |
G |
A |
15: 81,656,681 (GRCm39) |
R166Q |
probably benign |
Het |
Zfand1 |
T |
C |
3: 10,405,811 (GRCm39) |
D264G |
probably benign |
Het |
Zfp839 |
A |
G |
12: 110,834,848 (GRCm39) |
E701G |
probably benign |
Het |
|
Other mutations in Ccne1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00793:Ccne1
|
APN |
7 |
37,805,726 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02377:Ccne1
|
APN |
7 |
37,798,415 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02800:Ccne1
|
APN |
7 |
37,802,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Ccne1
|
UTSW |
7 |
37,805,747 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1938:Ccne1
|
UTSW |
7 |
37,805,702 (GRCm39) |
critical splice donor site |
probably null |
|
R4810:Ccne1
|
UTSW |
7 |
37,799,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Ccne1
|
UTSW |
7 |
37,798,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Ccne1
|
UTSW |
7 |
37,799,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R6480:Ccne1
|
UTSW |
7 |
37,806,279 (GRCm39) |
start gained |
probably benign |
|
R6981:Ccne1
|
UTSW |
7 |
37,797,998 (GRCm39) |
unclassified |
probably benign |
|
R7165:Ccne1
|
UTSW |
7 |
37,798,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R7398:Ccne1
|
UTSW |
7 |
37,805,702 (GRCm39) |
critical splice donor site |
probably null |
|
R7458:Ccne1
|
UTSW |
7 |
37,800,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R7835:Ccne1
|
UTSW |
7 |
37,802,270 (GRCm39) |
missense |
probably benign |
0.03 |
R8744:Ccne1
|
UTSW |
7 |
37,802,598 (GRCm39) |
missense |
probably benign |
0.17 |
R8866:Ccne1
|
UTSW |
7 |
37,800,046 (GRCm39) |
missense |
probably benign |
|
R9011:Ccne1
|
UTSW |
7 |
37,806,085 (GRCm39) |
missense |
probably benign |
0.05 |
R9185:Ccne1
|
UTSW |
7 |
37,799,255 (GRCm39) |
missense |
probably benign |
0.00 |
|