Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
T |
11: 109,974,326 (GRCm39) |
S203T |
probably damaging |
Het |
Adat1 |
A |
T |
8: 112,716,494 (GRCm39) |
M76K |
probably damaging |
Het |
Ankrd33 |
G |
C |
15: 101,014,780 (GRCm39) |
V56L |
probably benign |
Het |
Ascc3 |
T |
A |
10: 50,592,725 (GRCm39) |
L1134I |
possibly damaging |
Het |
C3 |
T |
G |
17: 57,524,286 (GRCm39) |
D948A |
probably damaging |
Het |
Ccdc121rt3 |
A |
C |
5: 112,503,395 (GRCm39) |
M103R |
probably benign |
Het |
Ccdc40 |
A |
G |
11: 119,122,612 (GRCm39) |
E138G |
possibly damaging |
Het |
Cd80 |
A |
G |
16: 38,306,866 (GRCm39) |
|
probably null |
Het |
Cdca7 |
T |
A |
2: 72,309,873 (GRCm39) |
|
probably null |
Het |
Chit1 |
A |
G |
1: 134,079,030 (GRCm39) |
S447G |
probably benign |
Het |
Cmya5 |
C |
T |
13: 93,205,786 (GRCm39) |
|
probably null |
Het |
Col1a2 |
T |
C |
6: 4,534,639 (GRCm39) |
L881P |
unknown |
Het |
Crebbp |
A |
T |
16: 3,935,187 (GRCm39) |
S901T |
probably damaging |
Het |
Dcun1d2 |
T |
C |
8: 13,321,637 (GRCm39) |
Y158C |
probably damaging |
Het |
Dnhd1 |
C |
T |
7: 105,370,005 (GRCm39) |
P4477S |
probably benign |
Het |
Donson |
A |
G |
16: 91,478,218 (GRCm39) |
Y428H |
probably damaging |
Het |
Dsp |
G |
T |
13: 38,375,716 (GRCm39) |
W1167L |
probably benign |
Het |
Elmo2 |
C |
T |
2: 165,136,961 (GRCm39) |
V592M |
probably damaging |
Het |
Enpp3 |
T |
A |
10: 24,702,093 (GRCm39) |
E60D |
probably damaging |
Het |
Erfl |
A |
T |
7: 24,631,089 (GRCm39) |
|
probably null |
Het |
Fam83b |
TAAGA |
T |
9: 76,409,394 (GRCm39) |
|
probably null |
Het |
Fbxo38 |
A |
G |
18: 62,669,295 (GRCm39) |
C52R |
probably damaging |
Het |
Gm10912 |
T |
C |
2: 103,897,055 (GRCm39) |
W65R |
probably damaging |
Het |
Gm43518 |
A |
T |
5: 124,074,490 (GRCm39) |
M44L |
probably benign |
Het |
Gnb1 |
T |
A |
4: 155,637,913 (GRCm39) |
D212E |
probably damaging |
Het |
Gnl1 |
A |
G |
17: 36,299,620 (GRCm39) |
N597S |
probably damaging |
Het |
Gprin1 |
T |
G |
13: 54,886,855 (GRCm39) |
E473A |
probably benign |
Het |
Ighv1-69 |
T |
A |
12: 115,586,834 (GRCm39) |
M100L |
probably benign |
Het |
Igkv14-100 |
T |
C |
6: 68,496,193 (GRCm39) |
S29P |
probably damaging |
Het |
Ints6 |
A |
G |
14: 62,951,786 (GRCm39) |
V232A |
probably damaging |
Het |
Jup |
A |
G |
11: 100,270,379 (GRCm39) |
L376P |
probably damaging |
Het |
Kdr |
A |
T |
5: 76,132,920 (GRCm39) |
Y119* |
probably null |
Het |
Kif1a |
T |
G |
1: 92,993,820 (GRCm39) |
T377P |
probably benign |
Het |
Lama5 |
C |
A |
2: 179,822,524 (GRCm39) |
V2850L |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,313,552 (GRCm39) |
Y2393C |
probably damaging |
Het |
Mfsd13a |
C |
T |
19: 46,356,763 (GRCm39) |
Q255* |
probably null |
Het |
Msh3 |
A |
C |
13: 92,372,096 (GRCm39) |
D891E |
probably damaging |
Het |
Msl2 |
A |
G |
9: 100,957,335 (GRCm39) |
N2D |
possibly damaging |
Het |
Myo19 |
T |
C |
11: 84,791,373 (GRCm39) |
L476P |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,467,686 (GRCm39) |
R501W |
probably damaging |
Het |
Nfasc |
C |
A |
1: 132,548,787 (GRCm39) |
K293N |
probably damaging |
Het |
Npbwr1 |
A |
T |
1: 5,987,319 (GRCm39) |
L65Q |
probably damaging |
Het |
Nrbp1 |
T |
A |
5: 31,401,825 (GRCm39) |
D34E |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,220,871 (GRCm39) |
V1891D |
probably benign |
Het |
Or51g2 |
T |
A |
7: 102,623,175 (GRCm39) |
N8I |
possibly damaging |
Het |
Or5g29 |
T |
A |
2: 85,420,942 (GRCm39) |
D19E |
probably benign |
Het |
Or5k1b |
T |
C |
16: 58,581,482 (GRCm39) |
N19S |
probably benign |
Het |
Or8g22 |
G |
T |
9: 38,958,379 (GRCm39) |
C156* |
probably null |
Het |
Oscp1 |
G |
A |
4: 125,976,783 (GRCm39) |
|
probably null |
Het |
Pcdhgb7 |
A |
G |
18: 37,886,086 (GRCm39) |
T419A |
probably damaging |
Het |
Pdzph1 |
T |
C |
17: 59,281,121 (GRCm39) |
D387G |
probably benign |
Het |
Phc1 |
A |
G |
6: 122,311,990 (GRCm39) |
F56S |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,599,061 (GRCm39) |
E59G |
possibly damaging |
Het |
Prickle1 |
G |
T |
15: 93,398,752 (GRCm39) |
T692K |
possibly damaging |
Het |
Rbm45 |
T |
A |
2: 76,206,738 (GRCm39) |
L250Q |
probably damaging |
Het |
Ror1 |
T |
A |
4: 100,265,108 (GRCm39) |
M194K |
probably damaging |
Het |
Rrbp1 |
T |
A |
2: 143,799,722 (GRCm39) |
|
probably null |
Het |
Rundc3b |
T |
C |
5: 8,562,348 (GRCm39) |
K340R |
probably null |
Het |
Scn1a |
T |
A |
2: 66,148,243 (GRCm39) |
T1101S |
probably damaging |
Het |
Sdk1 |
C |
G |
5: 142,080,412 (GRCm39) |
|
probably null |
Het |
Skic2 |
A |
G |
17: 35,064,183 (GRCm39) |
F501S |
possibly damaging |
Het |
Slc20a1 |
T |
A |
2: 129,041,979 (GRCm39) |
M114K |
probably damaging |
Het |
Sorl1 |
A |
C |
9: 41,881,047 (GRCm39) |
I2158S |
probably benign |
Het |
Strip1 |
A |
T |
3: 107,534,111 (GRCm39) |
F174L |
probably benign |
Het |
Sucnr1 |
A |
T |
3: 59,993,699 (GRCm39) |
I76L |
probably benign |
Het |
Syt17 |
C |
T |
7: 118,007,242 (GRCm39) |
V412I |
probably benign |
Het |
Tie1 |
T |
A |
4: 118,346,850 (GRCm39) |
H18L |
probably benign |
Het |
Tpp1 |
T |
G |
7: 105,398,129 (GRCm39) |
K345Q |
probably damaging |
Het |
Trcg1 |
G |
A |
9: 57,148,852 (GRCm39) |
M141I |
possibly damaging |
Het |
Trpc4ap |
T |
C |
2: 155,499,742 (GRCm39) |
N260S |
probably benign |
Het |
Vps41 |
C |
A |
13: 19,026,438 (GRCm39) |
T512K |
possibly damaging |
Het |
Vps52 |
A |
T |
17: 34,178,293 (GRCm39) |
M147L |
probably benign |
Het |
Ywhaq |
A |
G |
12: 21,441,752 (GRCm39) |
|
probably benign |
Het |
Zfp619 |
A |
G |
7: 39,184,387 (GRCm39) |
N139S |
probably benign |
Het |
|
Other mutations in Cnnm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Cnnm2
|
APN |
19 |
46,751,659 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01971:Cnnm2
|
APN |
19 |
46,860,115 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02003:Cnnm2
|
APN |
19 |
46,856,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Cnnm2
|
APN |
19 |
46,865,827 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02185:Cnnm2
|
APN |
19 |
46,751,434 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02652:Cnnm2
|
APN |
19 |
46,751,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02682:Cnnm2
|
APN |
19 |
46,750,515 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03009:Cnnm2
|
APN |
19 |
46,865,794 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03378:Cnnm2
|
APN |
19 |
46,866,473 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1581:Cnnm2
|
UTSW |
19 |
46,751,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R3700:Cnnm2
|
UTSW |
19 |
46,750,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Cnnm2
|
UTSW |
19 |
46,750,232 (GRCm39) |
nonsense |
probably null |
|
R3911:Cnnm2
|
UTSW |
19 |
46,866,375 (GRCm39) |
missense |
probably damaging |
0.96 |
R4508:Cnnm2
|
UTSW |
19 |
46,865,709 (GRCm39) |
missense |
probably benign |
0.01 |
R4678:Cnnm2
|
UTSW |
19 |
46,751,685 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4878:Cnnm2
|
UTSW |
19 |
46,847,522 (GRCm39) |
missense |
probably benign |
0.45 |
R5154:Cnnm2
|
UTSW |
19 |
46,751,571 (GRCm39) |
missense |
probably benign |
0.02 |
R5445:Cnnm2
|
UTSW |
19 |
46,865,727 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5771:Cnnm2
|
UTSW |
19 |
46,845,434 (GRCm39) |
splice site |
probably null |
|
R5914:Cnnm2
|
UTSW |
19 |
46,751,616 (GRCm39) |
missense |
probably benign |
0.07 |
R6263:Cnnm2
|
UTSW |
19 |
46,845,344 (GRCm39) |
missense |
probably benign |
0.30 |
R6715:Cnnm2
|
UTSW |
19 |
46,842,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6881:Cnnm2
|
UTSW |
19 |
46,865,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Cnnm2
|
UTSW |
19 |
46,847,379 (GRCm39) |
splice site |
probably null |
|
R7486:Cnnm2
|
UTSW |
19 |
46,750,513 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7600:Cnnm2
|
UTSW |
19 |
46,750,506 (GRCm39) |
missense |
probably benign |
0.02 |
R7648:Cnnm2
|
UTSW |
19 |
46,866,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R7800:Cnnm2
|
UTSW |
19 |
46,866,420 (GRCm39) |
missense |
probably benign |
0.28 |
R8867:Cnnm2
|
UTSW |
19 |
46,750,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R8971:Cnnm2
|
UTSW |
19 |
46,845,362 (GRCm39) |
missense |
probably benign |
0.28 |
R9433:Cnnm2
|
UTSW |
19 |
46,750,807 (GRCm39) |
missense |
probably benign |
0.23 |
R9463:Cnnm2
|
UTSW |
19 |
46,750,990 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Cnnm2
|
UTSW |
19 |
46,750,902 (GRCm39) |
missense |
probably benign |
0.05 |
X0018:Cnnm2
|
UTSW |
19 |
46,751,212 (GRCm39) |
missense |
probably damaging |
1.00 |
|