Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522H14Rik |
T |
G |
4: 109,362,918 (GRCm39) |
S134R |
probably damaging |
Het |
A930033H14Rik |
T |
A |
10: 69,048,679 (GRCm39) |
R53W |
unknown |
Het |
Abca9 |
G |
T |
11: 110,025,024 (GRCm39) |
D1006E |
probably benign |
Het |
Abcc6 |
T |
A |
7: 45,669,660 (GRCm39) |
R132* |
probably null |
Het |
Ankrd40 |
C |
T |
11: 94,229,250 (GRCm39) |
T283I |
probably damaging |
Het |
Atr |
A |
G |
9: 95,747,092 (GRCm39) |
K125E |
possibly damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Cep290 |
A |
T |
10: 100,346,404 (GRCm39) |
L527F |
probably damaging |
Het |
Cep295 |
T |
C |
9: 15,245,262 (GRCm39) |
N1065D |
possibly damaging |
Het |
Clip2 |
C |
T |
5: 134,533,616 (GRCm39) |
R487Q |
probably benign |
Het |
Ddx54 |
C |
T |
5: 120,758,807 (GRCm39) |
A350V |
probably benign |
Het |
Defb23 |
C |
T |
2: 152,301,333 (GRCm39) |
V80I |
probably benign |
Het |
Dennd5b |
G |
A |
6: 148,970,138 (GRCm39) |
T127I |
probably damaging |
Het |
Dnah6 |
G |
T |
6: 73,168,589 (GRCm39) |
Q445K |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,141,166 (GRCm39) |
H1287R |
probably benign |
Het |
Exoc2 |
T |
C |
13: 31,061,233 (GRCm39) |
T554A |
probably benign |
Het |
Fgf8 |
T |
C |
19: 45,730,846 (GRCm39) |
N60D |
probably benign |
Het |
Gdi2 |
A |
G |
13: 3,588,299 (GRCm39) |
M1V |
probably null |
Het |
Glra3 |
G |
T |
8: 56,542,058 (GRCm39) |
R267L |
probably damaging |
Het |
Gm21886 |
ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG |
ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG |
18: 80,133,040 (GRCm39) |
|
probably benign |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Greb1 |
C |
T |
12: 16,738,598 (GRCm39) |
R1455H |
probably damaging |
Het |
Grk6 |
C |
A |
13: 55,607,640 (GRCm39) |
P575T |
possibly damaging |
Het |
Hpgd |
A |
T |
8: 56,751,391 (GRCm39) |
D73V |
probably benign |
Het |
Hpse |
G |
A |
5: 100,842,022 (GRCm39) |
H288Y |
probably damaging |
Het |
Hpse2 |
G |
A |
19: 42,794,826 (GRCm39) |
R506* |
probably null |
Het |
Ing1 |
C |
A |
8: 11,611,649 (GRCm39) |
T123N |
probably benign |
Het |
Kdm2b |
T |
C |
5: 123,125,823 (GRCm39) |
D27G |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,577,956 (GRCm39) |
D773E |
probably benign |
Het |
Lrrc7 |
T |
C |
3: 157,880,888 (GRCm39) |
D516G |
probably benign |
Het |
Lrsam1 |
A |
G |
2: 32,835,452 (GRCm39) |
|
probably null |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Meak7 |
C |
A |
8: 120,498,010 (GRCm39) |
A165S |
probably benign |
Het |
Ndufaf3 |
T |
C |
9: 108,443,158 (GRCm39) |
*186W |
probably null |
Het |
Ndufaf5 |
C |
T |
2: 140,012,807 (GRCm39) |
A59V |
possibly damaging |
Het |
Nphp3 |
T |
C |
9: 103,886,369 (GRCm39) |
L281S |
probably damaging |
Het |
Or10a4 |
T |
G |
7: 106,696,786 (GRCm39) |
V38G |
probably benign |
Het |
Or4c12 |
T |
A |
2: 89,774,316 (GRCm39) |
I48F |
possibly damaging |
Het |
Or8b37 |
A |
T |
9: 37,958,892 (GRCm39) |
I125F |
probably damaging |
Het |
Otogl |
G |
T |
10: 107,735,328 (GRCm39) |
T152K |
probably damaging |
Het |
Oxgr1 |
C |
T |
14: 120,260,094 (GRCm39) |
V38I |
probably benign |
Het |
Polr2a |
G |
A |
11: 69,638,043 (GRCm39) |
T142M |
possibly damaging |
Het |
Pou6f1 |
C |
T |
15: 100,476,206 (GRCm39) |
R560Q |
possibly damaging |
Het |
Ptgr3 |
T |
G |
18: 84,113,128 (GRCm39) |
V268G |
probably damaging |
Het |
Rbm33 |
A |
G |
5: 28,544,242 (GRCm39) |
E166G |
probably damaging |
Het |
Rgs14 |
T |
A |
13: 55,528,784 (GRCm39) |
Y308* |
probably null |
Het |
Rpl10a |
T |
C |
17: 28,547,594 (GRCm39) |
|
probably benign |
Het |
Rras2 |
A |
C |
7: 113,659,593 (GRCm39) |
I57S |
probably damaging |
Het |
Scn1b |
C |
T |
7: 30,824,596 (GRCm39) |
V31M |
probably damaging |
Het |
Sema6d |
G |
A |
2: 124,506,117 (GRCm39) |
A642T |
probably damaging |
Het |
Sis |
T |
A |
3: 72,835,543 (GRCm39) |
T940S |
probably benign |
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc22a27 |
G |
A |
19: 7,904,126 (GRCm39) |
Q4* |
probably null |
Het |
Slc44a2 |
T |
A |
9: 21,263,770 (GRCm39) |
I646N |
possibly damaging |
Het |
Sprtn |
C |
A |
8: 125,629,704 (GRCm39) |
Y332* |
probably null |
Het |
Srpk1 |
A |
G |
17: 28,825,297 (GRCm39) |
I125T |
probably damaging |
Het |
Sv2b |
G |
A |
7: 74,786,068 (GRCm39) |
H451Y |
probably benign |
Het |
Tec |
G |
A |
5: 72,939,439 (GRCm39) |
T192M |
probably benign |
Het |
Tlr3 |
G |
A |
8: 45,850,944 (GRCm39) |
T127M |
probably damaging |
Het |
Trim25 |
C |
A |
11: 88,906,391 (GRCm39) |
P405T |
probably benign |
Het |
Trpm4 |
T |
C |
7: 44,958,054 (GRCm39) |
D952G |
probably damaging |
Het |
Tsc1 |
A |
G |
2: 28,566,486 (GRCm39) |
D635G |
probably benign |
Het |
Ttc7b |
T |
C |
12: 100,461,683 (GRCm39) |
E98G |
possibly damaging |
Het |
Ubr2 |
A |
G |
17: 47,274,071 (GRCm39) |
|
probably null |
Het |
Usp19 |
T |
A |
9: 108,376,885 (GRCm39) |
S1153T |
probably damaging |
Het |
Vmn2r63 |
A |
T |
7: 42,553,361 (GRCm39) |
L632M |
probably benign |
Het |
Vps13c |
C |
T |
9: 67,826,526 (GRCm39) |
T1389I |
probably benign |
Het |
Wasf1 |
T |
A |
10: 40,806,731 (GRCm39) |
Y125N |
probably damaging |
Het |
|
Other mutations in Enpp7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00793:Enpp7
|
APN |
11 |
118,881,371 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Enpp7
|
APN |
11 |
118,879,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02672:Enpp7
|
APN |
11 |
118,883,166 (GRCm39) |
critical splice donor site |
probably null |
|
R0465:Enpp7
|
UTSW |
11 |
118,879,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R1718:Enpp7
|
UTSW |
11 |
118,881,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R2208:Enpp7
|
UTSW |
11 |
118,879,588 (GRCm39) |
splice site |
probably benign |
|
R2970:Enpp7
|
UTSW |
11 |
118,881,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Enpp7
|
UTSW |
11 |
118,881,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R3967:Enpp7
|
UTSW |
11 |
118,881,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R5222:Enpp7
|
UTSW |
11 |
118,881,788 (GRCm39) |
missense |
probably benign |
0.03 |
R5454:Enpp7
|
UTSW |
11 |
118,879,634 (GRCm39) |
missense |
probably benign |
0.03 |
R5577:Enpp7
|
UTSW |
11 |
118,882,953 (GRCm39) |
missense |
probably benign |
0.01 |
R7361:Enpp7
|
UTSW |
11 |
118,882,985 (GRCm39) |
missense |
probably benign |
0.02 |
R8855:Enpp7
|
UTSW |
11 |
118,879,191 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9048:Enpp7
|
UTSW |
11 |
118,881,455 (GRCm39) |
missense |
probably damaging |
1.00 |
|