Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg7 |
A |
G |
16: 56,582,308 (GRCm39) |
S277P |
possibly damaging |
Het |
Arl6ip4 |
T |
C |
5: 124,254,662 (GRCm39) |
S52P |
probably benign |
Het |
Barx2 |
T |
C |
9: 31,824,383 (GRCm39) |
H2R |
probably damaging |
Het |
Calhm3 |
T |
C |
19: 47,140,404 (GRCm39) |
T230A |
probably damaging |
Het |
Card11 |
C |
T |
5: 140,868,117 (GRCm39) |
V844M |
possibly damaging |
Het |
Dnah6 |
C |
T |
6: 73,126,156 (GRCm39) |
R1327Q |
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,923,549 (GRCm39) |
I427V |
probably benign |
Het |
Ehbp1 |
C |
A |
11: 22,039,524 (GRCm39) |
|
probably null |
Het |
Fgg |
T |
A |
3: 82,921,496 (GRCm39) |
I393N |
possibly damaging |
Het |
Foxq1 |
A |
T |
13: 31,742,516 (GRCm39) |
|
probably benign |
Het |
Hmgxb3 |
T |
C |
18: 61,280,566 (GRCm39) |
T646A |
probably benign |
Het |
Homer3 |
G |
A |
8: 70,745,706 (GRCm39) |
E324K |
possibly damaging |
Het |
Krt80 |
A |
G |
15: 101,257,384 (GRCm39) |
F183L |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,668,354 (GRCm39) |
K647* |
probably null |
Het |
Mcm3ap |
A |
G |
10: 76,325,891 (GRCm39) |
Y1067C |
probably damaging |
Het |
Myh1 |
G |
T |
11: 67,104,097 (GRCm39) |
Q921H |
probably benign |
Het |
Nme8 |
A |
G |
13: 19,862,029 (GRCm39) |
F200S |
probably damaging |
Het |
Nploc4 |
T |
C |
11: 120,309,143 (GRCm39) |
N153S |
possibly damaging |
Het |
Or14c45 |
T |
C |
7: 86,176,591 (GRCm39) |
F209L |
probably damaging |
Het |
Or2ak6 |
T |
C |
11: 58,592,952 (GRCm39) |
C142R |
probably damaging |
Het |
Or4a73 |
A |
G |
2: 89,421,117 (GRCm39) |
V114A |
probably benign |
Het |
Or5k1 |
C |
T |
16: 58,617,607 (GRCm39) |
V201I |
probably benign |
Het |
Pipox |
T |
A |
11: 77,782,943 (GRCm39) |
L86F |
probably damaging |
Het |
Polr3h |
G |
T |
15: 81,801,406 (GRCm39) |
L157I |
probably benign |
Het |
Prex2 |
G |
A |
1: 11,336,376 (GRCm39) |
V1525M |
possibly damaging |
Het |
Rapgef2 |
A |
T |
3: 78,996,079 (GRCm39) |
D561E |
possibly damaging |
Het |
Sacs |
A |
T |
14: 61,440,354 (GRCm39) |
D800V |
possibly damaging |
Het |
Sbsn |
A |
T |
7: 30,451,655 (GRCm39) |
L223F |
possibly damaging |
Het |
Srrm3 |
G |
T |
5: 135,864,030 (GRCm39) |
E43* |
probably null |
Het |
Tcaf3 |
G |
A |
6: 42,570,663 (GRCm39) |
A363V |
probably damaging |
Het |
Tmem138 |
A |
G |
19: 10,552,268 (GRCm39) |
F78S |
probably damaging |
Het |
Tnfrsf17 |
G |
A |
16: 11,137,676 (GRCm39) |
D138N |
probably damaging |
Het |
Tubgcp6 |
C |
T |
15: 88,986,568 (GRCm39) |
V1344I |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,266,842 (GRCm39) |
L1875* |
probably null |
Het |
Vmn2r109 |
C |
A |
17: 20,774,798 (GRCm39) |
G186C |
probably damaging |
Het |
Zfp541 |
A |
G |
7: 15,810,373 (GRCm39) |
N137D |
possibly damaging |
Het |
|
Other mutations in Slc16a9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Slc16a9
|
APN |
10 |
70,118,529 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01725:Slc16a9
|
APN |
10 |
70,119,815 (GRCm39) |
missense |
probably benign |
|
IGL02963:Slc16a9
|
APN |
10 |
70,102,966 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4810001:Slc16a9
|
UTSW |
10 |
70,119,762 (GRCm39) |
nonsense |
probably null |
|
R1301:Slc16a9
|
UTSW |
10 |
70,118,308 (GRCm39) |
missense |
probably benign |
0.07 |
R4036:Slc16a9
|
UTSW |
10 |
70,110,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Slc16a9
|
UTSW |
10 |
70,118,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Slc16a9
|
UTSW |
10 |
70,118,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5868:Slc16a9
|
UTSW |
10 |
70,118,320 (GRCm39) |
missense |
probably benign |
0.01 |
R7313:Slc16a9
|
UTSW |
10 |
70,119,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R9044:Slc16a9
|
UTSW |
10 |
70,110,797 (GRCm39) |
missense |
probably benign |
0.06 |
R9789:Slc16a9
|
UTSW |
10 |
70,118,340 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Slc16a9
|
UTSW |
10 |
70,119,856 (GRCm39) |
missense |
probably benign |
0.15 |
|