Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
A |
6: 86,941,033 (GRCm39) |
I609N |
unknown |
Het |
Ano10 |
A |
T |
9: 122,090,308 (GRCm39) |
I277N |
probably damaging |
Het |
Ap2b1 |
A |
G |
11: 83,237,499 (GRCm39) |
D483G |
probably damaging |
Het |
As3mt |
T |
A |
19: 46,708,391 (GRCm39) |
F226Y |
probably damaging |
Het |
Atp10a |
G |
A |
7: 58,453,487 (GRCm39) |
R855H |
possibly damaging |
Het |
Bin3 |
T |
A |
14: 70,374,611 (GRCm39) |
H213Q |
probably benign |
Het |
Bora |
T |
C |
14: 99,311,103 (GRCm39) |
C512R |
probably damaging |
Het |
Camk2b |
T |
A |
11: 5,928,497 (GRCm39) |
D414V |
probably damaging |
Het |
Ccdc27 |
A |
T |
4: 154,122,179 (GRCm39) |
L233Q |
unknown |
Het |
Ccdc73 |
T |
C |
2: 104,737,978 (GRCm39) |
S25P |
probably damaging |
Het |
Cenpf |
G |
A |
1: 189,392,117 (GRCm39) |
H572Y |
probably benign |
Het |
Chil4 |
A |
G |
3: 106,111,487 (GRCm39) |
V209A |
probably damaging |
Het |
Clstn1 |
T |
C |
4: 149,728,524 (GRCm39) |
V650A |
probably benign |
Het |
Cox6a2 |
T |
A |
7: 127,805,437 (GRCm39) |
S11C |
probably benign |
Het |
Csf1 |
T |
C |
3: 107,656,317 (GRCm39) |
E238G |
probably benign |
Het |
Cyp4a10 |
T |
A |
4: 115,381,509 (GRCm39) |
M191K |
probably damaging |
Het |
Cyp4a14 |
A |
G |
4: 115,348,328 (GRCm39) |
V383A |
possibly damaging |
Het |
D130052B06Rik |
T |
G |
11: 33,573,916 (GRCm39) |
V171G |
possibly damaging |
Het |
Dlgap2 |
A |
G |
8: 14,872,369 (GRCm39) |
T617A |
probably benign |
Het |
Dyrk4 |
T |
A |
6: 126,863,690 (GRCm39) |
I351F |
probably damaging |
Het |
Epg5 |
T |
C |
18: 77,991,585 (GRCm39) |
V94A |
probably benign |
Het |
Fam111a |
A |
G |
19: 12,565,807 (GRCm39) |
T519A |
probably benign |
Het |
Gdpd4 |
A |
G |
7: 97,623,669 (GRCm39) |
S314G |
probably damaging |
Het |
Gm9758 |
T |
A |
5: 14,962,274 (GRCm39) |
K111N |
possibly damaging |
Het |
Gpr137b |
A |
T |
13: 13,538,096 (GRCm39) |
V285E |
probably damaging |
Het |
Hyls1 |
G |
A |
9: 35,472,480 (GRCm39) |
S312F |
probably benign |
Het |
Itgal |
T |
A |
7: 126,929,389 (GRCm39) |
L1102Q |
probably null |
Het |
Kctd19 |
T |
A |
8: 106,121,992 (GRCm39) |
Y185F |
possibly damaging |
Het |
Kif5b |
A |
G |
18: 6,223,558 (GRCm39) |
L317P |
possibly damaging |
Het |
Klhl42 |
C |
A |
6: 146,993,805 (GRCm39) |
A259E |
probably damaging |
Het |
Lrrc2 |
A |
G |
9: 110,810,017 (GRCm39) |
D351G |
probably damaging |
Het |
Med12l |
A |
G |
3: 59,135,243 (GRCm39) |
E797G |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,489,813 (GRCm39) |
E63G |
probably damaging |
Het |
Nek9 |
T |
C |
12: 85,379,103 (GRCm39) |
|
probably null |
Het |
Or12e8 |
A |
T |
2: 87,677,218 (GRCm39) |
H201L |
possibly damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Parp6 |
G |
A |
9: 59,557,295 (GRCm39) |
V627I |
probably benign |
Het |
Pclo |
C |
T |
5: 14,572,108 (GRCm39) |
Q498* |
probably null |
Het |
Pdlim5 |
T |
C |
3: 142,018,086 (GRCm39) |
T170A |
possibly damaging |
Het |
Pgap1 |
A |
T |
1: 54,587,167 (GRCm39) |
Y136* |
probably null |
Het |
Pgghg |
T |
A |
7: 140,526,097 (GRCm39) |
N563K |
probably damaging |
Het |
Plxnb2 |
A |
G |
15: 89,044,916 (GRCm39) |
M1143T |
probably benign |
Het |
Pnpla1 |
G |
A |
17: 29,100,342 (GRCm39) |
G403E |
probably benign |
Het |
Prc1 |
G |
A |
7: 79,959,175 (GRCm39) |
R381Q |
probably damaging |
Het |
Psph |
A |
T |
5: 129,843,529 (GRCm39) |
I175N |
probably damaging |
Het |
Rbbp8nl |
T |
A |
2: 179,923,305 (GRCm39) |
K131* |
probably null |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Homo |
Sde2 |
G |
A |
1: 180,683,371 (GRCm39) |
V42I |
probably benign |
Het |
Slc25a3 |
G |
A |
10: 90,952,963 (GRCm39) |
R314* |
probably null |
Het |
Spag9 |
A |
G |
11: 93,935,333 (GRCm39) |
N48S |
probably benign |
Het |
Srp54b |
T |
C |
12: 55,302,757 (GRCm39) |
M351T |
possibly damaging |
Het |
Tasor2 |
C |
T |
13: 3,631,891 (GRCm39) |
R870H |
possibly damaging |
Het |
Tcaf2 |
A |
G |
6: 42,604,342 (GRCm39) |
L679P |
probably damaging |
Het |
Tnrc6b |
T |
A |
15: 80,764,944 (GRCm39) |
N815K |
probably benign |
Het |
Usp17la |
A |
T |
7: 104,509,557 (GRCm39) |
Q54L |
possibly damaging |
Het |
Vmn2r92 |
T |
A |
17: 18,387,036 (GRCm39) |
I125K |
probably benign |
Het |
Xrra1 |
T |
C |
7: 99,566,679 (GRCm39) |
Y732H |
probably damaging |
Het |
Zfp131 |
A |
G |
13: 120,227,941 (GRCm39) |
S603P |
possibly damaging |
Het |
Zfp28 |
G |
T |
7: 6,396,612 (GRCm39) |
S349I |
probably benign |
Het |
|
Other mutations in Cyp2c23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01467:Cyp2c23
|
APN |
19 |
44,003,512 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01642:Cyp2c23
|
APN |
19 |
43,993,995 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01782:Cyp2c23
|
APN |
19 |
44,017,554 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01843:Cyp2c23
|
APN |
19 |
43,994,046 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02902:Cyp2c23
|
APN |
19 |
44,009,997 (GRCm39) |
splice site |
probably benign |
|
IGL03382:Cyp2c23
|
APN |
19 |
44,003,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R0196:Cyp2c23
|
UTSW |
19 |
44,000,795 (GRCm39) |
missense |
probably damaging |
0.98 |
R0735:Cyp2c23
|
UTSW |
19 |
44,005,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Cyp2c23
|
UTSW |
19 |
44,002,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Cyp2c23
|
UTSW |
19 |
43,993,947 (GRCm39) |
missense |
probably benign |
0.07 |
R1809:Cyp2c23
|
UTSW |
19 |
44,009,997 (GRCm39) |
splice site |
probably benign |
|
R1872:Cyp2c23
|
UTSW |
19 |
43,993,990 (GRCm39) |
nonsense |
probably null |
|
R2866:Cyp2c23
|
UTSW |
19 |
43,993,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Cyp2c23
|
UTSW |
19 |
43,995,478 (GRCm39) |
missense |
probably benign |
0.11 |
R4234:Cyp2c23
|
UTSW |
19 |
44,017,604 (GRCm39) |
missense |
unknown |
|
R4748:Cyp2c23
|
UTSW |
19 |
44,005,176 (GRCm39) |
splice site |
probably null |
|
R4948:Cyp2c23
|
UTSW |
19 |
44,010,138 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5101:Cyp2c23
|
UTSW |
19 |
44,017,622 (GRCm39) |
missense |
unknown |
|
R5420:Cyp2c23
|
UTSW |
19 |
44,004,103 (GRCm39) |
critical splice donor site |
probably null |
|
R5770:Cyp2c23
|
UTSW |
19 |
44,010,018 (GRCm39) |
missense |
probably damaging |
0.99 |
R5993:Cyp2c23
|
UTSW |
19 |
44,000,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Cyp2c23
|
UTSW |
19 |
43,993,902 (GRCm39) |
missense |
probably benign |
0.03 |
R6610:Cyp2c23
|
UTSW |
19 |
43,995,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R7344:Cyp2c23
|
UTSW |
19 |
44,010,176 (GRCm39) |
splice site |
probably null |
|
R7603:Cyp2c23
|
UTSW |
19 |
44,003,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Cyp2c23
|
UTSW |
19 |
43,995,555 (GRCm39) |
missense |
probably damaging |
0.99 |
R8098:Cyp2c23
|
UTSW |
19 |
44,004,242 (GRCm39) |
missense |
probably benign |
0.29 |
R8157:Cyp2c23
|
UTSW |
19 |
44,010,066 (GRCm39) |
missense |
probably benign |
0.00 |
R8813:Cyp2c23
|
UTSW |
19 |
44,002,054 (GRCm39) |
missense |
probably benign |
0.07 |
R9497:Cyp2c23
|
UTSW |
19 |
44,010,085 (GRCm39) |
missense |
probably damaging |
0.99 |
X0065:Cyp2c23
|
UTSW |
19 |
44,017,610 (GRCm39) |
missense |
unknown |
|
|