Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam23 |
T |
A |
1: 63,586,888 (GRCm39) |
Y416* |
probably null |
Het |
Akr1b10 |
G |
T |
6: 34,369,431 (GRCm39) |
|
probably null |
Het |
Arap2 |
G |
T |
5: 62,906,237 (GRCm39) |
P261T |
possibly damaging |
Het |
Bckdha |
C |
A |
7: 25,330,858 (GRCm39) |
D53Y |
probably damaging |
Het |
Bfsp2 |
A |
G |
9: 103,357,271 (GRCm39) |
V52A |
probably benign |
Het |
Bola3 |
T |
C |
6: 83,328,249 (GRCm39) |
L45P |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,255,134 (GRCm39) |
|
probably null |
Het |
Ccn6 |
C |
G |
10: 39,031,094 (GRCm39) |
C143S |
probably damaging |
Het |
Ceacam16 |
C |
A |
7: 19,587,537 (GRCm39) |
Q410H |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,940,986 (GRCm39) |
|
probably null |
Het |
Cenpe |
T |
C |
3: 134,944,233 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
A |
T |
3: 144,738,400 (GRCm39) |
V36D |
probably damaging |
Het |
Copa |
T |
A |
1: 171,948,812 (GRCm39) |
S1155T |
probably benign |
Het |
Crb2 |
C |
A |
2: 37,683,680 (GRCm39) |
P1061T |
possibly damaging |
Het |
Crot |
T |
C |
5: 9,027,541 (GRCm39) |
T264A |
probably benign |
Het |
Cyp51 |
C |
T |
5: 4,141,877 (GRCm39) |
G346S |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,098,975 (GRCm39) |
S2027P |
possibly damaging |
Het |
Fbh1 |
T |
C |
2: 11,772,021 (GRCm39) |
H220R |
possibly damaging |
Het |
Gdf2 |
T |
A |
14: 33,666,791 (GRCm39) |
V171D |
probably damaging |
Het |
Golgb1 |
T |
G |
16: 36,738,933 (GRCm39) |
V2424G |
probably damaging |
Het |
Gpbp1l1 |
T |
C |
4: 116,428,182 (GRCm39) |
|
probably null |
Het |
Greb1l |
A |
G |
18: 10,522,247 (GRCm39) |
N672S |
possibly damaging |
Het |
Kcnma1 |
C |
T |
14: 24,053,815 (GRCm39) |
|
probably null |
Het |
Lrba |
T |
C |
3: 86,258,562 (GRCm39) |
F1350L |
probably damaging |
Het |
Nat8f4 |
A |
G |
6: 85,878,052 (GRCm39) |
V157A |
possibly damaging |
Het |
Niban1 |
T |
C |
1: 151,525,086 (GRCm39) |
Y164H |
probably damaging |
Het |
Nt5dc2 |
T |
C |
14: 30,860,832 (GRCm39) |
S439P |
probably damaging |
Het |
Or2ag12 |
T |
C |
7: 106,276,992 (GRCm39) |
R234G |
probably damaging |
Het |
Or2n1 |
A |
G |
17: 38,486,386 (GRCm39) |
N137S |
probably benign |
Het |
Or5t18 |
G |
A |
2: 86,636,804 (GRCm39) |
P180S |
possibly damaging |
Het |
Or8k40 |
T |
A |
2: 86,584,887 (GRCm39) |
H65L |
probably damaging |
Het |
Orm3 |
A |
T |
4: 63,274,395 (GRCm39) |
|
probably null |
Het |
Otof |
A |
G |
5: 30,528,056 (GRCm39) |
L1929P |
probably damaging |
Het |
Pex5l |
C |
A |
3: 33,069,164 (GRCm39) |
C111F |
probably damaging |
Het |
Plcl1 |
T |
A |
1: 55,737,374 (GRCm39) |
M905K |
probably benign |
Het |
Prdm6 |
T |
C |
18: 53,673,278 (GRCm39) |
I186T |
possibly damaging |
Het |
Rara |
T |
G |
11: 98,861,395 (GRCm39) |
I236S |
probably damaging |
Het |
Reln |
A |
T |
5: 22,200,364 (GRCm39) |
S1379T |
possibly damaging |
Het |
Rnps1-ps |
A |
T |
6: 7,983,149 (GRCm39) |
|
noncoding transcript |
Het |
Rp1l1 |
T |
A |
14: 64,267,758 (GRCm39) |
Y1115N |
probably damaging |
Het |
Rpe65 |
A |
T |
3: 159,310,222 (GRCm39) |
N135I |
probably damaging |
Het |
Rps6 |
A |
G |
4: 86,775,050 (GRCm39) |
V18A |
probably benign |
Het |
Scrn3 |
T |
C |
2: 73,166,121 (GRCm39) |
S385P |
possibly damaging |
Het |
Sis |
T |
C |
3: 72,850,968 (GRCm39) |
T577A |
probably damaging |
Het |
Slx1b |
G |
A |
7: 126,290,979 (GRCm39) |
L239F |
probably damaging |
Het |
Smad4 |
G |
T |
18: 73,810,807 (GRCm39) |
T59K |
possibly damaging |
Het |
Smad6 |
A |
G |
9: 63,928,212 (GRCm39) |
V32A |
probably benign |
Het |
Smc6 |
T |
A |
12: 11,324,075 (GRCm39) |
F73L |
probably damaging |
Het |
Sorbs2 |
T |
C |
8: 46,225,747 (GRCm39) |
|
probably null |
Het |
Svbp |
T |
A |
4: 119,053,090 (GRCm39) |
F32I |
probably benign |
Het |
Tap1 |
C |
A |
17: 34,408,541 (GRCm39) |
|
probably benign |
Het |
Tesk1 |
C |
T |
4: 43,445,786 (GRCm39) |
P280S |
possibly damaging |
Het |
Thrb |
A |
G |
14: 18,033,456 (GRCm38) |
I406M |
probably damaging |
Het |
Tsc22d1 |
T |
C |
14: 76,656,049 (GRCm39) |
S761P |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,706,997 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
C |
A |
17: 31,203,763 (GRCm39) |
Y525* |
probably null |
Het |
Vmn2r70 |
C |
T |
7: 85,208,540 (GRCm39) |
V646I |
probably benign |
Het |
Wipf1 |
C |
T |
2: 73,267,513 (GRCm39) |
G295D |
probably benign |
Het |
Zim1 |
A |
T |
7: 6,680,129 (GRCm39) |
H511Q |
probably damaging |
Het |
|
Other mutations in Gpx6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00674:Gpx6
|
APN |
13 |
21,497,978 (GRCm39) |
splice site |
probably benign |
|
Jaded
|
UTSW |
13 |
21,501,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Gpx6
|
UTSW |
13 |
21,503,047 (GRCm39) |
missense |
probably benign |
0.44 |
R0835:Gpx6
|
UTSW |
13 |
21,501,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Gpx6
|
UTSW |
13 |
21,503,090 (GRCm39) |
missense |
probably benign |
|
R1538:Gpx6
|
UTSW |
13 |
21,497,822 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1839:Gpx6
|
UTSW |
13 |
21,496,497 (GRCm39) |
missense |
probably benign |
|
R2151:Gpx6
|
UTSW |
13 |
21,503,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R2845:Gpx6
|
UTSW |
13 |
21,503,045 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3785:Gpx6
|
UTSW |
13 |
21,497,956 (GRCm39) |
missense |
probably benign |
0.02 |
R3973:Gpx6
|
UTSW |
13 |
21,501,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R3974:Gpx6
|
UTSW |
13 |
21,501,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4124:Gpx6
|
UTSW |
13 |
21,501,815 (GRCm39) |
nonsense |
probably null |
|
R4707:Gpx6
|
UTSW |
13 |
21,496,434 (GRCm39) |
nonsense |
probably null |
|
R4751:Gpx6
|
UTSW |
13 |
21,501,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Gpx6
|
UTSW |
13 |
21,496,434 (GRCm39) |
nonsense |
probably null |
|
R4785:Gpx6
|
UTSW |
13 |
21,496,434 (GRCm39) |
nonsense |
probably null |
|
R5002:Gpx6
|
UTSW |
13 |
21,497,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Gpx6
|
UTSW |
13 |
21,501,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Gpx6
|
UTSW |
13 |
21,503,239 (GRCm39) |
missense |
probably benign |
|
R6030:Gpx6
|
UTSW |
13 |
21,496,510 (GRCm39) |
missense |
probably benign |
0.01 |
R6030:Gpx6
|
UTSW |
13 |
21,496,510 (GRCm39) |
missense |
probably benign |
0.01 |
R7223:Gpx6
|
UTSW |
13 |
21,501,840 (GRCm39) |
critical splice donor site |
probably null |
|
R9701:Gpx6
|
UTSW |
13 |
21,501,777 (GRCm39) |
missense |
probably benign |
0.13 |
X0017:Gpx6
|
UTSW |
13 |
21,501,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|