Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438A13Rik |
C |
T |
3: 36,967,305 (GRCm38) |
Q2193* |
probably null |
Het |
Asb1 |
T |
C |
1: 91,546,918 (GRCm38) |
|
probably benign |
Het |
Cnot6 |
G |
A |
11: 49,685,114 (GRCm38) |
Q178* |
probably null |
Het |
Col5a1 |
C |
T |
2: 27,974,715 (GRCm38) |
A737V |
unknown |
Het |
Cyp27b1 |
T |
C |
10: 127,050,358 (GRCm38) |
S303P |
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,409,296 (GRCm38) |
L3620P |
probably damaging |
Het |
Dock7 |
A |
T |
4: 98,966,286 (GRCm38) |
|
probably null |
Het |
Fam161b |
T |
C |
12: 84,357,594 (GRCm38) |
D104G |
probably benign |
Het |
Fam8a1 |
A |
G |
13: 46,673,604 (GRCm38) |
M284V |
possibly damaging |
Het |
Fkbp3 |
T |
A |
12: 65,069,103 (GRCm38) |
K65* |
probably null |
Het |
Gatb |
A |
G |
3: 85,613,551 (GRCm38) |
|
probably null |
Het |
Gm572 |
A |
T |
4: 148,651,228 (GRCm38) |
H38L |
probably benign |
Het |
L2hgdh |
G |
A |
12: 69,692,480 (GRCm38) |
R406W |
possibly damaging |
Het |
Lmo7 |
A |
T |
14: 101,880,980 (GRCm38) |
T214S |
probably damaging |
Het |
Map3k12 |
T |
C |
15: 102,503,546 (GRCm38) |
H361R |
probably benign |
Het |
Mios |
T |
C |
6: 8,235,378 (GRCm38) |
|
probably benign |
Het |
Mta1 |
T |
C |
12: 113,130,121 (GRCm38) |
L315P |
probably damaging |
Het |
Pask |
A |
C |
1: 93,310,818 (GRCm38) |
V1315G |
probably damaging |
Het |
Pias4 |
A |
T |
10: 81,164,070 (GRCm38) |
C50S |
probably damaging |
Het |
Rgs11 |
G |
A |
17: 26,207,631 (GRCm38) |
V279I |
probably benign |
Het |
Sgk1 |
T |
A |
10: 21,928,546 (GRCm38) |
C92S |
probably benign |
Het |
Slc2a13 |
C |
T |
15: 91,497,509 (GRCm38) |
G259E |
probably damaging |
Het |
Slc5a4b |
A |
G |
10: 76,075,100 (GRCm38) |
C301R |
probably damaging |
Het |
Sstr4 |
G |
T |
2: 148,396,533 (GRCm38) |
G355* |
probably null |
Het |
Tnrc6a |
T |
A |
7: 123,171,312 (GRCm38) |
L775Q |
possibly damaging |
Het |
Vmn1r218 |
A |
G |
13: 23,137,004 (GRCm38) |
I94V |
probably benign |
Het |
Xpa |
A |
G |
4: 46,185,682 (GRCm38) |
F99L |
probably benign |
Het |
|
Other mutations in Gm6576 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00232:Gm6576
|
APN |
15 |
27,025,798 (GRCm38) |
exon |
noncoding transcript |
|
IGL01325:Gm6576
|
APN |
15 |
27,025,884 (GRCm38) |
exon |
noncoding transcript |
|
IGL02027:Gm6576
|
APN |
15 |
27,025,866 (GRCm38) |
exon |
noncoding transcript |
|
IGL02416:Gm6576
|
APN |
15 |
27,025,987 (GRCm38) |
exon |
noncoding transcript |
|
R0128:Gm6576
|
UTSW |
15 |
27,026,000 (GRCm38) |
exon |
noncoding transcript |
|
|