Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot11 |
C |
T |
4: 106,617,327 (GRCm39) |
G240R |
probably damaging |
Het |
Arfgef2 |
T |
A |
2: 166,735,540 (GRCm39) |
|
probably null |
Het |
Arsk |
T |
C |
13: 76,222,907 (GRCm39) |
Y230C |
probably damaging |
Het |
Atf7ip |
G |
A |
6: 136,559,389 (GRCm39) |
V737M |
probably damaging |
Het |
Atp6v1e1 |
A |
T |
6: 120,781,011 (GRCm39) |
|
probably null |
Het |
Bbs9 |
T |
C |
9: 22,557,260 (GRCm39) |
V3A |
probably benign |
Het |
Brap |
T |
C |
5: 121,813,365 (GRCm39) |
S243P |
probably damaging |
Het |
Camkmt |
T |
A |
17: 85,702,037 (GRCm39) |
I167N |
probably damaging |
Het |
Ckap2l |
C |
A |
2: 129,111,114 (GRCm39) |
E694D |
probably damaging |
Het |
Crmp1 |
G |
A |
5: 37,441,408 (GRCm39) |
V497I |
probably benign |
Het |
Dbx2 |
A |
G |
15: 95,522,741 (GRCm39) |
V322A |
possibly damaging |
Het |
Dll1 |
C |
A |
17: 15,590,513 (GRCm39) |
C401F |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,490,147 (GRCm39) |
T1991A |
probably damaging |
Het |
Dock3 |
C |
T |
9: 107,036,651 (GRCm39) |
W42* |
probably null |
Het |
Epha6 |
C |
A |
16: 60,245,198 (GRCm39) |
A334S |
possibly damaging |
Het |
Hdac1-ps |
A |
G |
17: 78,800,287 (GRCm39) |
E426G |
probably damaging |
Het |
Insrr |
C |
T |
3: 87,720,873 (GRCm39) |
R1044C |
probably damaging |
Het |
Irs2 |
T |
C |
8: 11,054,961 (GRCm39) |
N1157S |
possibly damaging |
Het |
Kndc1 |
T |
C |
7: 139,502,667 (GRCm39) |
|
probably null |
Het |
Map3k19 |
T |
C |
1: 127,748,185 (GRCm39) |
N1241S |
probably benign |
Het |
Or9g4b |
T |
C |
2: 85,615,906 (GRCm39) |
F17S |
possibly damaging |
Het |
Pcdh17 |
T |
A |
14: 84,683,657 (GRCm39) |
D41E |
probably damaging |
Het |
Plg |
T |
G |
17: 12,597,595 (GRCm39) |
L14R |
probably damaging |
Het |
Prkab1 |
A |
G |
5: 116,158,092 (GRCm39) |
V168A |
probably benign |
Het |
Prr35 |
G |
C |
17: 26,166,689 (GRCm39) |
P283A |
probably benign |
Het |
Ptdss1 |
C |
T |
13: 67,101,595 (GRCm39) |
R95* |
probably null |
Het |
Rab3gap2 |
T |
G |
1: 184,980,062 (GRCm39) |
S327A |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Homo |
Sdr42e2 |
T |
C |
7: 120,425,332 (GRCm39) |
S308P |
probably damaging |
Het |
Senp8 |
C |
A |
9: 59,644,473 (GRCm39) |
V228L |
probably benign |
Het |
Serpina10 |
A |
T |
12: 103,594,628 (GRCm39) |
I197K |
probably benign |
Het |
Serpinb6d |
A |
G |
13: 33,854,718 (GRCm39) |
N231S |
probably benign |
Het |
Sez6l2 |
T |
C |
7: 126,567,177 (GRCm39) |
V869A |
probably damaging |
Het |
Sgo2b |
T |
A |
8: 64,380,769 (GRCm39) |
K688* |
probably null |
Het |
Sh3kbp1 |
A |
T |
X: 158,624,176 (GRCm39) |
E39D |
probably benign |
Homo |
Ufsp2 |
T |
C |
8: 46,438,504 (GRCm39) |
M194T |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,485,881 (GRCm39) |
I2997T |
possibly damaging |
Het |
Vmn2r107 |
G |
A |
17: 20,595,637 (GRCm39) |
G730D |
probably damaging |
Het |
Wdr72 |
T |
C |
9: 74,059,822 (GRCm39) |
Y411H |
possibly damaging |
Het |
Xirp2 |
T |
C |
2: 67,343,212 (GRCm39) |
S1818P |
possibly damaging |
Het |
|
Other mutations in Paqr5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02893:Paqr5
|
APN |
9 |
61,876,150 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03190:Paqr5
|
APN |
9 |
61,880,084 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4480001:Paqr5
|
UTSW |
9 |
61,863,438 (GRCm39) |
missense |
probably benign |
0.09 |
R0528:Paqr5
|
UTSW |
9 |
61,863,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R0686:Paqr5
|
UTSW |
9 |
61,880,076 (GRCm39) |
missense |
probably benign |
0.00 |
R0688:Paqr5
|
UTSW |
9 |
61,880,076 (GRCm39) |
missense |
probably benign |
0.00 |
R1323:Paqr5
|
UTSW |
9 |
61,868,810 (GRCm39) |
critical splice donor site |
probably null |
|
R1323:Paqr5
|
UTSW |
9 |
61,868,810 (GRCm39) |
critical splice donor site |
probably null |
|
R2872:Paqr5
|
UTSW |
9 |
61,876,061 (GRCm39) |
critical splice donor site |
probably null |
|
R2872:Paqr5
|
UTSW |
9 |
61,876,061 (GRCm39) |
critical splice donor site |
probably null |
|
R5663:Paqr5
|
UTSW |
9 |
61,876,144 (GRCm39) |
missense |
probably benign |
0.03 |
R6728:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Paqr5
|
UTSW |
9 |
61,871,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Paqr5
|
UTSW |
9 |
61,876,064 (GRCm39) |
missense |
probably null |
1.00 |
R6857:Paqr5
|
UTSW |
9 |
61,883,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Paqr5
|
UTSW |
9 |
61,880,113 (GRCm39) |
nonsense |
probably null |
|
R7456:Paqr5
|
UTSW |
9 |
61,880,072 (GRCm39) |
missense |
probably benign |
0.13 |
R8362:Paqr5
|
UTSW |
9 |
61,879,945 (GRCm39) |
nonsense |
probably null |
|
R9204:Paqr5
|
UTSW |
9 |
61,868,826 (GRCm39) |
missense |
probably benign |
0.02 |
R9475:Paqr5
|
UTSW |
9 |
61,863,507 (GRCm39) |
missense |
probably damaging |
0.98 |
R9508:Paqr5
|
UTSW |
9 |
61,880,079 (GRCm39) |
missense |
probably benign |
0.00 |
R9549:Paqr5
|
UTSW |
9 |
61,863,543 (GRCm39) |
missense |
possibly damaging |
0.96 |
|