Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr1b |
T |
C |
1: 36,740,911 (GRCm39) |
Y171C |
possibly damaging |
Het |
Ap1g1 |
G |
A |
8: 110,560,122 (GRCm39) |
S281N |
probably benign |
Het |
Arfgef3 |
C |
A |
10: 18,506,168 (GRCm39) |
G878V |
probably damaging |
Het |
Ccdc137 |
T |
C |
11: 120,352,844 (GRCm39) |
F196S |
probably damaging |
Het |
Ccdc18 |
C |
T |
5: 108,296,838 (GRCm39) |
Q214* |
probably null |
Het |
Ccrl2 |
T |
C |
9: 110,884,422 (GRCm39) |
I359V |
probably benign |
Het |
Cdh20 |
C |
T |
1: 104,869,868 (GRCm39) |
T196I |
probably damaging |
Het |
Cfap20dc |
T |
C |
14: 8,482,521 (GRCm38) |
T551A |
probably benign |
Het |
Col6a3 |
G |
T |
1: 90,714,361 (GRCm39) |
T1683K |
unknown |
Het |
Copa |
A |
G |
1: 171,938,285 (GRCm39) |
I524V |
probably benign |
Het |
Cyld |
A |
T |
8: 89,457,383 (GRCm39) |
R536* |
probably null |
Het |
Dock10 |
T |
A |
1: 80,544,472 (GRCm39) |
E905V |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,012,031 (GRCm39) |
F1348L |
probably benign |
Het |
Efcab3 |
A |
T |
11: 105,002,629 (GRCm39) |
K5664I |
probably damaging |
Het |
Gm9892 |
A |
T |
8: 52,649,435 (GRCm39) |
|
noncoding transcript |
Het |
Grm4 |
A |
G |
17: 27,721,709 (GRCm39) |
I144T |
probably damaging |
Het |
Kcnv1 |
G |
A |
15: 44,977,840 (GRCm39) |
T66M |
probably damaging |
Het |
Krt28 |
G |
T |
11: 99,265,376 (GRCm39) |
S97Y |
probably damaging |
Het |
Map3k6 |
T |
C |
4: 132,979,258 (GRCm39) |
Y1204H |
possibly damaging |
Het |
Mfsd2b |
G |
T |
12: 4,924,356 (GRCm39) |
|
probably benign |
Het |
Nav3 |
T |
C |
10: 109,605,157 (GRCm39) |
D972G |
probably damaging |
Het |
Or2ak6 |
T |
G |
11: 58,593,277 (GRCm39) |
L250R |
probably damaging |
Het |
Or2y3 |
C |
T |
17: 38,393,321 (GRCm39) |
V183I |
probably benign |
Het |
Or5d39 |
T |
C |
2: 87,979,632 (GRCm39) |
T244A |
probably benign |
Het |
Prex1 |
G |
A |
2: 166,412,256 (GRCm39) |
R392W |
probably damaging |
Het |
Ptpn5 |
C |
T |
7: 46,741,296 (GRCm39) |
W38* |
probably null |
Het |
Rab3gap1 |
T |
C |
1: 127,865,304 (GRCm39) |
|
probably null |
Het |
Rfx7 |
A |
G |
9: 72,499,051 (GRCm39) |
T72A |
possibly damaging |
Het |
Scn7a |
T |
C |
2: 66,572,345 (GRCm39) |
I209V |
probably benign |
Het |
Sh3d21 |
C |
T |
4: 126,044,511 (GRCm39) |
|
probably benign |
Het |
Slc27a1 |
A |
G |
8: 72,037,617 (GRCm39) |
T535A |
probably benign |
Het |
Slc5a5 |
A |
G |
8: 71,342,930 (GRCm39) |
V210A |
probably benign |
Het |
Snx25 |
A |
G |
8: 46,558,291 (GRCm39) |
C239R |
probably damaging |
Het |
Sp5 |
T |
C |
2: 70,307,382 (GRCm39) |
F356L |
probably damaging |
Het |
Spaca9 |
T |
C |
2: 28,582,998 (GRCm39) |
I141V |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,485,107 (GRCm39) |
L763H |
probably damaging |
Het |
Thnsl1 |
A |
G |
2: 21,217,059 (GRCm39) |
E271G |
probably benign |
Het |
Vmn1r79 |
T |
A |
7: 11,910,971 (GRCm39) |
C284* |
probably null |
Het |
Vwa5a |
T |
C |
9: 38,649,112 (GRCm39) |
|
probably benign |
Het |
Zar1 |
T |
C |
5: 72,737,736 (GRCm39) |
E121G |
possibly damaging |
Het |
Zscan29 |
C |
T |
2: 120,995,275 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gm5174 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Laco
|
UTSW |
10 |
86,491,972 (GRCm39) |
unclassified |
noncoding transcript |
|
R1083:Gm5174
|
UTSW |
10 |
86,491,972 (GRCm39) |
unclassified |
noncoding transcript |
|
R1199:Gm5174
|
UTSW |
10 |
86,493,189 (GRCm39) |
unclassified |
noncoding transcript |
|
R1296:Gm5174
|
UTSW |
10 |
86,492,866 (GRCm39) |
unclassified |
noncoding transcript |
|
R1715:Gm5174
|
UTSW |
10 |
86,492,776 (GRCm39) |
unclassified |
noncoding transcript |
|
R1957:Gm5174
|
UTSW |
10 |
86,492,617 (GRCm39) |
unclassified |
noncoding transcript |
|
R2221:Gm5174
|
UTSW |
10 |
86,492,372 (GRCm39) |
unclassified |
noncoding transcript |
|
R2223:Gm5174
|
UTSW |
10 |
86,492,372 (GRCm39) |
unclassified |
noncoding transcript |
|
R3104:Gm5174
|
UTSW |
10 |
86,492,519 (GRCm39) |
unclassified |
noncoding transcript |
|
R4165:Gm5174
|
UTSW |
10 |
86,492,797 (GRCm39) |
unclassified |
noncoding transcript |
|
R4166:Gm5174
|
UTSW |
10 |
86,492,797 (GRCm39) |
unclassified |
noncoding transcript |
|
R4243:Gm5174
|
UTSW |
10 |
86,492,144 (GRCm39) |
unclassified |
noncoding transcript |
|
R5024:Gm5174
|
UTSW |
10 |
86,492,451 (GRCm39) |
unclassified |
noncoding transcript |
|
R5292:Gm5174
|
UTSW |
10 |
86,492,562 (GRCm39) |
unclassified |
noncoding transcript |
|
R5586:Gm5174
|
UTSW |
10 |
86,492,409 (GRCm39) |
unclassified |
noncoding transcript |
|
R5864:Gm5174
|
UTSW |
10 |
86,493,045 (GRCm39) |
unclassified |
noncoding transcript |
|
|