Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
A |
T |
14: 59,380,252 (GRCm39) |
N15K |
possibly damaging |
Het |
Adam32 |
A |
T |
8: 25,362,664 (GRCm39) |
I587K |
probably damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,584,843 (GRCm39) |
S942G |
probably benign |
Het |
Adamtsl5 |
A |
G |
10: 80,180,750 (GRCm39) |
F104S |
probably damaging |
Het |
Adgrf5 |
A |
G |
17: 43,761,245 (GRCm39) |
D980G |
probably benign |
Het |
Apba1 |
A |
T |
19: 23,894,950 (GRCm39) |
D462V |
possibly damaging |
Het |
Arhgef11 |
T |
C |
3: 87,634,433 (GRCm39) |
|
probably benign |
Het |
Cd74 |
T |
C |
18: 60,943,393 (GRCm39) |
|
probably benign |
Het |
Cdc16 |
T |
C |
8: 13,831,542 (GRCm39) |
S592P |
probably benign |
Het |
Cenpj |
A |
G |
14: 56,802,502 (GRCm39) |
M21T |
possibly damaging |
Het |
Col28a1 |
A |
G |
6: 8,103,521 (GRCm39) |
L425S |
probably damaging |
Het |
Dbt |
C |
T |
3: 116,313,908 (GRCm39) |
T25I |
possibly damaging |
Het |
Dguok |
C |
A |
6: 83,467,552 (GRCm39) |
M98I |
possibly damaging |
Het |
Dmxl1 |
T |
C |
18: 50,004,781 (GRCm39) |
L943P |
probably damaging |
Het |
Eloa |
G |
A |
4: 135,738,231 (GRCm39) |
S243L |
probably benign |
Het |
Enkur |
C |
A |
2: 21,201,530 (GRCm39) |
A52S |
probably damaging |
Het |
Ezh1 |
T |
C |
11: 101,083,787 (GRCm39) |
E744G |
probably damaging |
Het |
Fbxw11 |
T |
C |
11: 32,672,101 (GRCm39) |
S190P |
possibly damaging |
Het |
Foxb1 |
G |
A |
9: 69,666,550 (GRCm39) |
|
probably benign |
Het |
Gabra5 |
C |
T |
7: 57,058,432 (GRCm39) |
G439S |
probably damaging |
Het |
Gtf2h2 |
A |
T |
13: 100,617,541 (GRCm39) |
V207D |
probably damaging |
Het |
Hoatz |
A |
G |
9: 51,011,358 (GRCm39) |
I93T |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,796,948 (GRCm39) |
V317A |
probably benign |
Het |
Lair1 |
C |
A |
7: 4,012,683 (GRCm39) |
|
probably benign |
Het |
Lrit2 |
T |
A |
14: 36,791,051 (GRCm39) |
H243Q |
probably damaging |
Het |
Mast3 |
C |
T |
8: 71,232,174 (GRCm39) |
A1268T |
probably damaging |
Het |
Matn2 |
G |
A |
15: 34,316,671 (GRCm39) |
M4I |
possibly damaging |
Het |
Mob1b |
T |
A |
5: 88,897,502 (GRCm39) |
F137I |
probably damaging |
Het |
Mreg |
T |
C |
1: 72,203,325 (GRCm39) |
|
probably benign |
Het |
Nom1 |
T |
C |
5: 29,651,272 (GRCm39) |
V684A |
possibly damaging |
Het |
Pla2r1 |
T |
C |
2: 60,271,425 (GRCm39) |
|
probably benign |
Het |
Plxna1 |
A |
G |
6: 89,331,870 (GRCm39) |
F447L |
possibly damaging |
Het |
Pno1 |
A |
T |
11: 17,160,992 (GRCm39) |
I114N |
probably damaging |
Het |
Ppp1r7 |
T |
G |
1: 93,288,540 (GRCm39) |
|
probably benign |
Het |
Pprc1 |
T |
A |
19: 46,059,968 (GRCm39) |
Y1503N |
probably benign |
Het |
Rab30 |
T |
C |
7: 92,484,930 (GRCm39) |
V132A |
probably damaging |
Het |
Slc15a4 |
T |
C |
5: 127,679,024 (GRCm39) |
T439A |
probably benign |
Het |
Slc29a3 |
A |
G |
10: 60,559,596 (GRCm39) |
V186A |
possibly damaging |
Het |
Stxbp5l |
G |
A |
16: 37,165,454 (GRCm39) |
T88I |
possibly damaging |
Het |
Tarbp1 |
A |
G |
8: 127,160,701 (GRCm39) |
V1250A |
probably benign |
Het |
Tcte2 |
A |
T |
17: 13,937,824 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
A |
T |
2: 121,100,800 (GRCm39) |
|
probably null |
Het |
Trpc4 |
A |
T |
3: 54,173,828 (GRCm39) |
L407F |
possibly damaging |
Het |
Vmn1r6 |
T |
C |
6: 56,979,896 (GRCm39) |
F164S |
probably damaging |
Het |
Zfp579 |
C |
A |
7: 4,997,743 (GRCm39) |
R56L |
probably benign |
Het |
|
Other mutations in Pate2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01729:Pate2
|
APN |
9 |
35,581,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03055:Pate2
|
APN |
9 |
35,523,069 (GRCm39) |
splice site |
probably benign |
|
foie_gras
|
UTSW |
9 |
35,581,797 (GRCm39) |
nonsense |
probably null |
|
PIT4576001:Pate2
|
UTSW |
9 |
35,581,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R1229:Pate2
|
UTSW |
9 |
35,580,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R1397:Pate2
|
UTSW |
9 |
35,580,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R2393:Pate2
|
UTSW |
9 |
35,581,036 (GRCm39) |
splice site |
probably benign |
|
R2426:Pate2
|
UTSW |
9 |
35,581,776 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3407:Pate2
|
UTSW |
9 |
35,582,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R4323:Pate2
|
UTSW |
9 |
35,581,767 (GRCm39) |
splice site |
probably benign |
|
R4574:Pate2
|
UTSW |
9 |
35,596,969 (GRCm39) |
intron |
probably benign |
|
R4716:Pate2
|
UTSW |
9 |
35,596,978 (GRCm39) |
intron |
probably benign |
|
R5023:Pate2
|
UTSW |
9 |
35,597,407 (GRCm39) |
intron |
probably benign |
|
R5057:Pate2
|
UTSW |
9 |
35,597,407 (GRCm39) |
intron |
probably benign |
|
R5384:Pate2
|
UTSW |
9 |
35,581,837 (GRCm39) |
missense |
probably damaging |
0.98 |
R5574:Pate2
|
UTSW |
9 |
35,597,411 (GRCm39) |
intron |
probably benign |
|
R5593:Pate2
|
UTSW |
9 |
35,581,778 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5851:Pate2
|
UTSW |
9 |
35,581,797 (GRCm39) |
nonsense |
probably null |
|
R6510:Pate2
|
UTSW |
9 |
35,581,018 (GRCm39) |
missense |
probably null |
0.99 |
R6800:Pate2
|
UTSW |
9 |
35,596,941 (GRCm39) |
intron |
probably benign |
|
R6819:Pate2
|
UTSW |
9 |
35,581,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7531:Pate2
|
UTSW |
9 |
35,582,008 (GRCm39) |
splice site |
probably null |
|
R7765:Pate2
|
UTSW |
9 |
35,581,197 (GRCm39) |
missense |
probably benign |
0.15 |
R7842:Pate2
|
UTSW |
9 |
35,581,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8015:Pate2
|
UTSW |
9 |
35,581,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R8957:Pate2
|
UTSW |
9 |
35,596,911 (GRCm39) |
missense |
probably benign |
0.03 |
R9126:Pate2
|
UTSW |
9 |
35,581,908 (GRCm39) |
critical splice donor site |
probably null |
|
|