Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
T |
C |
10: 10,283,209 (GRCm39) |
I166V |
probably benign |
Het |
Albfm1 |
T |
G |
5: 90,712,096 (GRCm39) |
V63G |
probably damaging |
Het |
Anapc5 |
T |
C |
5: 122,955,968 (GRCm39) |
E154G |
probably benign |
Het |
Anpep |
A |
T |
7: 79,490,744 (GRCm39) |
Y257* |
probably null |
Het |
Atp8b1 |
A |
T |
18: 64,686,118 (GRCm39) |
D688E |
probably damaging |
Het |
Bub1b |
C |
A |
2: 118,461,459 (GRCm39) |
H670Q |
possibly damaging |
Het |
Casp3 |
G |
T |
8: 47,088,423 (GRCm39) |
D107Y |
probably damaging |
Het |
Castor2 |
T |
C |
5: 134,154,783 (GRCm39) |
|
probably null |
Het |
Clcc1 |
A |
T |
3: 108,570,907 (GRCm39) |
Y105F |
possibly damaging |
Het |
Cr2 |
A |
C |
1: 194,838,636 (GRCm39) |
L671R |
probably damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,427,542 (GRCm39) |
V713A |
probably damaging |
Het |
Cyp4a31 |
T |
C |
4: 115,422,210 (GRCm39) |
F65L |
probably benign |
Het |
Dpysl2 |
T |
C |
14: 67,052,926 (GRCm39) |
S308G |
probably damaging |
Het |
Dusp22 |
A |
T |
13: 30,892,726 (GRCm39) |
I168F |
probably benign |
Het |
Ecel1 |
A |
G |
1: 87,079,872 (GRCm39) |
S414P |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,174,810 (GRCm39) |
F1968L |
probably damaging |
Het |
Fsip2 |
C |
T |
2: 82,805,493 (GRCm39) |
T604I |
probably damaging |
Het |
H2-DMb1 |
T |
A |
17: 34,374,547 (GRCm39) |
F66I |
possibly damaging |
Het |
Hgf |
T |
C |
5: 16,819,991 (GRCm39) |
V574A |
probably damaging |
Het |
Hoxa7 |
A |
T |
6: 52,193,605 (GRCm39) |
Y137* |
probably null |
Het |
Ikbke |
T |
A |
1: 131,191,085 (GRCm39) |
I519F |
probably damaging |
Het |
Inpp5j |
T |
G |
11: 3,451,107 (GRCm39) |
H514P |
probably damaging |
Het |
Kmt2d |
A |
G |
15: 98,738,070 (GRCm39) |
|
probably benign |
Het |
Larp7 |
T |
A |
3: 127,340,603 (GRCm39) |
R112S |
probably benign |
Het |
Lepr |
C |
T |
4: 101,590,611 (GRCm39) |
A63V |
probably benign |
Het |
Lmx1a |
G |
T |
1: 167,660,428 (GRCm39) |
V238L |
probably damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mcmbp |
T |
C |
7: 128,317,729 (GRCm39) |
E172G |
possibly damaging |
Het |
Nek8 |
C |
A |
11: 78,061,309 (GRCm39) |
V379L |
probably benign |
Het |
Numa1 |
T |
G |
7: 101,658,945 (GRCm39) |
L356R |
probably damaging |
Het |
Pard6b |
C |
T |
2: 167,940,943 (GRCm39) |
A310V |
probably benign |
Het |
Pcgf5 |
C |
A |
19: 36,414,740 (GRCm39) |
N26K |
possibly damaging |
Het |
Phtf1 |
G |
A |
3: 103,910,919 (GRCm39) |
|
probably null |
Het |
Plch1 |
C |
A |
3: 63,618,640 (GRCm39) |
D675Y |
probably damaging |
Het |
Plk2 |
A |
G |
13: 110,532,871 (GRCm39) |
H144R |
probably damaging |
Het |
Rax |
T |
A |
18: 66,068,152 (GRCm39) |
N318Y |
unknown |
Het |
Slc9a5 |
A |
G |
8: 106,085,103 (GRCm39) |
N535D |
possibly damaging |
Het |
Smarcd2 |
T |
A |
11: 106,157,731 (GRCm39) |
K138* |
probably null |
Het |
Taar7e |
A |
T |
10: 23,913,932 (GRCm39) |
I141F |
probably damaging |
Het |
Taar7f |
T |
A |
10: 23,925,921 (GRCm39) |
W172R |
probably damaging |
Het |
Tango6 |
A |
G |
8: 107,415,856 (GRCm39) |
I226V |
probably benign |
Het |
Tcn2 |
T |
C |
11: 3,872,114 (GRCm39) |
K338E |
possibly damaging |
Het |
Tdp1 |
C |
A |
12: 99,864,588 (GRCm39) |
A243E |
probably damaging |
Het |
Tfpt |
A |
G |
7: 3,623,386 (GRCm39) |
Y240H |
probably damaging |
Het |
Tmod4 |
A |
G |
3: 95,035,140 (GRCm39) |
D215G |
probably benign |
Het |
Top3b |
A |
G |
16: 16,700,396 (GRCm39) |
|
probably null |
Het |
Urgcp |
C |
A |
11: 5,665,878 (GRCm39) |
G820V |
probably damaging |
Het |
Zfand2b |
A |
T |
1: 75,146,454 (GRCm39) |
M110L |
probably benign |
Het |
Zfyve1 |
A |
T |
12: 83,621,909 (GRCm39) |
V162E |
probably damaging |
Het |
|
Other mutations in Mcpt8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01344:Mcpt8
|
APN |
14 |
56,321,402 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01960:Mcpt8
|
APN |
14 |
56,319,864 (GRCm39) |
splice site |
probably null |
|
R0973:Mcpt8
|
UTSW |
14 |
56,321,257 (GRCm39) |
splice site |
probably benign |
|
R1472:Mcpt8
|
UTSW |
14 |
56,319,791 (GRCm39) |
missense |
probably benign |
0.02 |
R1908:Mcpt8
|
UTSW |
14 |
56,321,291 (GRCm39) |
missense |
probably benign |
0.03 |
R2131:Mcpt8
|
UTSW |
14 |
56,319,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R3123:Mcpt8
|
UTSW |
14 |
56,321,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R3124:Mcpt8
|
UTSW |
14 |
56,321,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R3125:Mcpt8
|
UTSW |
14 |
56,321,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R4209:Mcpt8
|
UTSW |
14 |
56,321,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Mcpt8
|
UTSW |
14 |
56,321,285 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4860:Mcpt8
|
UTSW |
14 |
56,319,737 (GRCm39) |
missense |
probably benign |
0.02 |
R4860:Mcpt8
|
UTSW |
14 |
56,319,737 (GRCm39) |
missense |
probably benign |
0.02 |
R5457:Mcpt8
|
UTSW |
14 |
56,319,793 (GRCm39) |
missense |
probably benign |
0.04 |
R5900:Mcpt8
|
UTSW |
14 |
56,319,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R6334:Mcpt8
|
UTSW |
14 |
56,322,604 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6339:Mcpt8
|
UTSW |
14 |
56,319,794 (GRCm39) |
missense |
probably benign |
0.00 |
R7505:Mcpt8
|
UTSW |
14 |
56,320,548 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Mcpt8
|
UTSW |
14 |
56,319,793 (GRCm39) |
missense |
probably benign |
0.02 |
|