Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
G |
A |
5: 8,984,327 (GRCm39) |
|
probably null |
Het |
Angptl7 |
C |
G |
4: 148,584,534 (GRCm39) |
Q71H |
probably damaging |
Het |
Arhgap30 |
A |
T |
1: 171,229,822 (GRCm39) |
N176Y |
probably damaging |
Het |
Armc9 |
T |
A |
1: 86,202,256 (GRCm39) |
S805T |
probably damaging |
Het |
Atxn1 |
T |
G |
13: 45,720,407 (GRCm39) |
H496P |
probably damaging |
Het |
Cabin1 |
C |
T |
10: 75,557,197 (GRCm39) |
G1147D |
probably damaging |
Het |
Cabin1 |
A |
G |
10: 75,575,255 (GRCm39) |
S597P |
probably damaging |
Het |
Catsperd |
T |
C |
17: 56,969,744 (GRCm39) |
S613P |
probably damaging |
Het |
Cdh2 |
A |
G |
18: 16,783,466 (GRCm39) |
Y88H |
probably damaging |
Het |
Cntn1 |
C |
A |
15: 92,126,549 (GRCm39) |
P47Q |
probably damaging |
Het |
Col11a2 |
T |
C |
17: 34,261,164 (GRCm39) |
L38P |
possibly damaging |
Het |
Col5a2 |
T |
G |
1: 45,415,855 (GRCm39) |
I1431L |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 16,048,772 (GRCm39) |
G2310D |
probably damaging |
Het |
Dhcr7 |
T |
A |
7: 143,391,528 (GRCm39) |
I39N |
probably damaging |
Het |
Dnajc13 |
C |
T |
9: 104,044,586 (GRCm39) |
|
probably benign |
Het |
Drgx |
G |
T |
14: 32,330,206 (GRCm39) |
Q136H |
probably damaging |
Het |
Folr2 |
T |
C |
7: 101,489,497 (GRCm39) |
|
probably null |
Het |
Galnt11 |
T |
C |
5: 25,470,336 (GRCm39) |
I595T |
probably damaging |
Het |
Gp5 |
G |
A |
16: 30,128,326 (GRCm39) |
A116V |
possibly damaging |
Het |
Gpn3 |
T |
C |
5: 122,520,303 (GRCm39) |
|
probably benign |
Het |
Gprin3 |
T |
C |
6: 59,331,644 (GRCm39) |
N221S |
probably benign |
Het |
Hfm1 |
T |
C |
5: 107,022,079 (GRCm39) |
E989G |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,743,847 (GRCm39) |
|
probably null |
Het |
Josd2 |
T |
C |
7: 44,120,592 (GRCm39) |
S110P |
probably damaging |
Het |
Kat14 |
C |
A |
2: 144,217,873 (GRCm39) |
T123K |
probably damaging |
Het |
Lamtor1 |
C |
T |
7: 101,558,971 (GRCm39) |
T48I |
probably damaging |
Het |
Lrrc24 |
A |
G |
15: 76,602,546 (GRCm39) |
L113P |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,504,286 (GRCm39) |
T2561A |
possibly damaging |
Het |
Mog |
T |
C |
17: 37,331,433 (GRCm39) |
E89G |
probably damaging |
Het |
Mon2 |
A |
G |
10: 122,874,364 (GRCm39) |
|
probably null |
Het |
Mtx1 |
T |
C |
3: 89,121,205 (GRCm39) |
Y143C |
probably benign |
Het |
Nacad |
T |
C |
11: 6,548,507 (GRCm39) |
E1409G |
possibly damaging |
Het |
Ndst3 |
T |
C |
3: 123,400,676 (GRCm39) |
H410R |
probably damaging |
Het |
Nkx6-2 |
T |
C |
7: 139,161,486 (GRCm39) |
E233G |
possibly damaging |
Het |
Or8g22 |
A |
G |
9: 38,958,158 (GRCm39) |
S186P |
probably damaging |
Het |
Ovgp1 |
T |
C |
3: 105,887,269 (GRCm39) |
F222L |
possibly damaging |
Het |
Pkhd1 |
T |
C |
1: 20,358,429 (GRCm39) |
S2716G |
probably null |
Het |
Pla2g4e |
T |
C |
2: 120,001,718 (GRCm39) |
T644A |
probably benign |
Het |
Plxnd1 |
A |
G |
6: 115,932,726 (GRCm39) |
I1918T |
probably damaging |
Het |
Psmg1 |
A |
T |
16: 95,790,812 (GRCm39) |
|
probably benign |
Het |
Ptprd |
G |
A |
4: 76,047,136 (GRCm39) |
R364C |
probably damaging |
Het |
Rgs22 |
T |
C |
15: 36,026,088 (GRCm39) |
I945V |
possibly damaging |
Het |
Rgs7bp |
T |
C |
13: 105,088,072 (GRCm39) |
N234S |
probably benign |
Het |
Rrp7a |
T |
C |
15: 83,004,010 (GRCm39) |
|
probably benign |
Het |
Scg2 |
T |
A |
1: 79,414,193 (GRCm39) |
R177* |
probably null |
Het |
Sema4c |
C |
A |
1: 36,589,392 (GRCm39) |
C578F |
probably damaging |
Het |
Slc1a5 |
T |
A |
7: 16,531,668 (GRCm39) |
|
probably benign |
Het |
Slc5a3 |
A |
G |
16: 91,875,571 (GRCm39) |
T543A |
possibly damaging |
Het |
Slx4ip |
T |
A |
2: 136,888,687 (GRCm39) |
F123I |
probably benign |
Het |
Smtn |
C |
T |
11: 3,472,916 (GRCm39) |
R737H |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,866,300 (GRCm39) |
I14T |
possibly damaging |
Het |
Stradb |
T |
C |
1: 59,019,599 (GRCm39) |
F43L |
probably benign |
Het |
Szt2 |
T |
C |
4: 118,245,866 (GRCm39) |
D1029G |
probably benign |
Het |
Taar6 |
T |
C |
10: 23,860,613 (GRCm39) |
Y311C |
probably damaging |
Het |
Tcea3 |
A |
T |
4: 135,995,404 (GRCm39) |
N249I |
probably damaging |
Het |
Tecta |
A |
G |
9: 42,241,573 (GRCm39) |
M2134T |
probably benign |
Het |
Tg |
G |
A |
15: 66,636,186 (GRCm39) |
G591D |
probably damaging |
Het |
Tm4sf20 |
T |
A |
1: 82,746,084 (GRCm39) |
I19F |
probably benign |
Het |
Top2a |
T |
C |
11: 98,888,676 (GRCm39) |
K1262E |
probably benign |
Het |
Ube2r2 |
A |
G |
4: 41,190,742 (GRCm39) |
|
probably benign |
Het |
Usp29 |
T |
C |
7: 6,964,927 (GRCm39) |
S257P |
possibly damaging |
Het |
Usp40 |
T |
C |
1: 87,880,077 (GRCm39) |
N1038S |
probably benign |
Het |
Utp25 |
A |
T |
1: 192,797,262 (GRCm39) |
M530K |
probably damaging |
Het |
Vmn1r121 |
C |
T |
7: 20,831,538 (GRCm39) |
E301K |
probably benign |
Het |
Vmn2r49 |
T |
A |
7: 9,722,959 (GRCm39) |
H105L |
probably benign |
Het |
Zgrf1 |
C |
T |
3: 127,355,517 (GRCm39) |
Q248* |
probably null |
Het |
|
Other mutations in Oas1h |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01676:Oas1h
|
APN |
5 |
121,009,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01890:Oas1h
|
APN |
5 |
121,000,852 (GRCm39) |
splice site |
probably null |
|
IGL02745:Oas1h
|
APN |
5 |
120,999,542 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02888:Oas1h
|
APN |
5 |
120,999,610 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02970:Oas1h
|
APN |
5 |
120,999,698 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0125:Oas1h
|
UTSW |
5 |
121,000,626 (GRCm39) |
nonsense |
probably null |
|
R1261:Oas1h
|
UTSW |
5 |
121,009,930 (GRCm39) |
missense |
probably benign |
0.01 |
R1506:Oas1h
|
UTSW |
5 |
121,009,951 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1565:Oas1h
|
UTSW |
5 |
121,000,663 (GRCm39) |
missense |
probably damaging |
0.97 |
R1696:Oas1h
|
UTSW |
5 |
121,000,885 (GRCm39) |
critical splice donor site |
probably null |
|
R1750:Oas1h
|
UTSW |
5 |
121,009,840 (GRCm39) |
splice site |
probably null |
|
R3116:Oas1h
|
UTSW |
5 |
120,999,679 (GRCm39) |
nonsense |
probably null |
|
R4814:Oas1h
|
UTSW |
5 |
121,000,728 (GRCm39) |
missense |
probably damaging |
0.99 |
R4906:Oas1h
|
UTSW |
5 |
121,005,172 (GRCm39) |
nonsense |
probably null |
|
R4961:Oas1h
|
UTSW |
5 |
121,009,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5160:Oas1h
|
UTSW |
5 |
121,009,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Oas1h
|
UTSW |
5 |
121,009,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R5903:Oas1h
|
UTSW |
5 |
121,009,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Oas1h
|
UTSW |
5 |
121,005,229 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7062:Oas1h
|
UTSW |
5 |
120,999,528 (GRCm39) |
unclassified |
probably benign |
|
R7966:Oas1h
|
UTSW |
5 |
121,009,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R7975:Oas1h
|
UTSW |
5 |
121,009,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Oas1h
|
UTSW |
5 |
121,005,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777-TAIL:Oas1h
|
UTSW |
5 |
121,005,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R8951:Oas1h
|
UTSW |
5 |
121,000,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Oas1h
|
UTSW |
5 |
121,005,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Oas1h
|
UTSW |
5 |
121,005,088 (GRCm39) |
missense |
probably damaging |
0.99 |
|