Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adar |
T |
C |
3: 89,638,147 (GRCm39) |
|
probably null |
Het |
Arpc2 |
A |
G |
1: 74,287,338 (GRCm39) |
T53A |
probably benign |
Het |
Ccdc170 |
C |
A |
10: 4,499,713 (GRCm39) |
L545M |
probably benign |
Het |
Celsr1 |
T |
C |
15: 85,810,391 (GRCm39) |
N2166D |
probably benign |
Het |
Clca4b |
T |
G |
3: 144,634,103 (GRCm39) |
D104A |
probably damaging |
Het |
Clcnka |
C |
T |
4: 141,120,051 (GRCm39) |
|
probably null |
Het |
Clip2 |
A |
T |
5: 134,551,518 (GRCm39) |
N201K |
probably damaging |
Het |
Cyp1a2 |
G |
A |
9: 57,589,485 (GRCm39) |
L110F |
possibly damaging |
Het |
Dhtkd1 |
T |
C |
2: 5,947,467 (GRCm39) |
T6A |
unknown |
Het |
Enthd1 |
A |
C |
15: 80,336,652 (GRCm39) |
L594R |
probably damaging |
Het |
Espnl |
A |
G |
1: 91,272,626 (GRCm39) |
D618G |
probably benign |
Het |
Gm6096 |
A |
T |
7: 33,950,904 (GRCm39) |
I148F |
probably damaging |
Het |
Hsf5 |
C |
T |
11: 87,526,951 (GRCm39) |
T541I |
probably benign |
Het |
Il18r1 |
A |
G |
1: 40,537,563 (GRCm39) |
S443G |
possibly damaging |
Het |
Il1a |
T |
C |
2: 129,146,640 (GRCm39) |
D151G |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,754,166 (GRCm39) |
|
probably benign |
Het |
Kcnh1 |
A |
C |
1: 192,188,164 (GRCm39) |
D875A |
possibly damaging |
Het |
Naip6 |
T |
A |
13: 100,439,760 (GRCm39) |
I336F |
probably benign |
Het |
Napepld |
A |
G |
5: 21,880,657 (GRCm39) |
F246S |
possibly damaging |
Het |
Nova1 |
C |
T |
12: 46,760,280 (GRCm39) |
|
probably null |
Het |
Nsa2 |
C |
A |
13: 97,268,525 (GRCm39) |
A181S |
probably damaging |
Het |
Ntn5 |
C |
A |
7: 45,343,671 (GRCm39) |
R337S |
probably damaging |
Het |
Nynrin |
T |
C |
14: 56,101,611 (GRCm39) |
S427P |
probably benign |
Het |
Or52e5 |
A |
G |
7: 104,718,836 (GRCm39) |
E54G |
probably damaging |
Het |
Pcgf1 |
T |
A |
6: 83,055,867 (GRCm39) |
|
probably null |
Het |
Pfn4 |
T |
A |
12: 4,824,446 (GRCm39) |
L58I |
probably benign |
Het |
Plekha1 |
C |
A |
7: 130,499,059 (GRCm39) |
P116Q |
probably damaging |
Het |
Pou5f2 |
T |
C |
13: 78,173,300 (GRCm39) |
S81P |
possibly damaging |
Het |
Prag1 |
A |
G |
8: 36,570,146 (GRCm39) |
D243G |
probably damaging |
Het |
Rbm26 |
G |
A |
14: 105,389,943 (GRCm39) |
P227L |
probably damaging |
Het |
Rgl1 |
A |
T |
1: 152,394,904 (GRCm39) |
N756K |
probably damaging |
Het |
Rhou |
A |
T |
8: 124,380,880 (GRCm39) |
T66S |
possibly damaging |
Het |
Rspo3 |
A |
T |
10: 29,380,704 (GRCm39) |
D103E |
probably benign |
Het |
Rundc3b |
T |
C |
5: 8,570,902 (GRCm39) |
K306E |
probably benign |
Het |
Slc25a32 |
A |
G |
15: 38,965,466 (GRCm39) |
|
probably benign |
Het |
St6galnac2 |
C |
T |
11: 116,575,945 (GRCm39) |
D169N |
probably damaging |
Het |
Tars3 |
A |
G |
7: 65,332,566 (GRCm39) |
T556A |
possibly damaging |
Het |
Tmem266 |
A |
G |
9: 55,342,486 (GRCm39) |
K324E |
probably benign |
Het |
Tnrc6c |
T |
C |
11: 117,640,161 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
A |
T |
15: 72,817,971 (GRCm39) |
S452T |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,717,121 (GRCm39) |
|
probably benign |
Het |
Ttll5 |
T |
G |
12: 85,965,708 (GRCm39) |
I571S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,797,433 (GRCm39) |
T544A |
probably benign |
Het |
Ubn1 |
T |
C |
16: 4,891,334 (GRCm39) |
|
probably null |
Het |
Ubr2 |
C |
A |
17: 47,303,907 (GRCm39) |
|
probably benign |
Het |
Usp21 |
A |
T |
1: 171,111,574 (GRCm39) |
W360R |
probably damaging |
Het |
Vmn2r62 |
A |
T |
7: 42,414,526 (GRCm39) |
L639H |
probably damaging |
Het |
Zc3h7b |
T |
A |
15: 81,656,000 (GRCm39) |
I116N |
possibly damaging |
Het |
Zfp618 |
C |
T |
4: 63,050,872 (GRCm39) |
T551I |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 7,230,707 (GRCm39) |
|
probably benign |
Het |
Zkscan8 |
T |
C |
13: 21,704,973 (GRCm39) |
H322R |
probably benign |
Het |
Zwint |
T |
G |
10: 72,493,019 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ccm2l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01826:Ccm2l
|
APN |
2 |
152,909,853 (GRCm39) |
splice site |
probably benign |
|
IGL02821:Ccm2l
|
APN |
2 |
152,909,779 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Ccm2l
|
APN |
2 |
152,920,521 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03237:Ccm2l
|
APN |
2 |
152,907,922 (GRCm39) |
utr 5 prime |
probably benign |
|
R0103:Ccm2l
|
UTSW |
2 |
152,909,839 (GRCm39) |
nonsense |
probably null |
|
R0103:Ccm2l
|
UTSW |
2 |
152,909,839 (GRCm39) |
nonsense |
probably null |
|
R0420:Ccm2l
|
UTSW |
2 |
152,912,782 (GRCm39) |
missense |
probably null |
0.08 |
R0617:Ccm2l
|
UTSW |
2 |
152,912,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R0760:Ccm2l
|
UTSW |
2 |
152,914,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R1309:Ccm2l
|
UTSW |
2 |
152,912,844 (GRCm39) |
missense |
probably damaging |
0.97 |
R4787:Ccm2l
|
UTSW |
2 |
152,921,422 (GRCm39) |
missense |
probably benign |
0.00 |
R7106:Ccm2l
|
UTSW |
2 |
152,912,571 (GRCm39) |
missense |
possibly damaging |
0.45 |
R7159:Ccm2l
|
UTSW |
2 |
152,912,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R8141:Ccm2l
|
UTSW |
2 |
152,912,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Ccm2l
|
UTSW |
2 |
152,909,695 (GRCm39) |
missense |
probably benign |
0.43 |
R8852:Ccm2l
|
UTSW |
2 |
152,916,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R8971:Ccm2l
|
UTSW |
2 |
152,909,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Ccm2l
|
UTSW |
2 |
152,916,720 (GRCm39) |
missense |
probably damaging |
0.99 |
|