Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AB124611 |
C |
G |
9: 21,440,331 (GRCm39) |
Q106E |
probably benign |
Het |
Abi2 |
A |
G |
1: 60,492,888 (GRCm39) |
M387V |
probably null |
Het |
Adra2c |
A |
T |
5: 35,437,707 (GRCm39) |
N160Y |
probably damaging |
Het |
Ager |
G |
A |
17: 34,819,716 (GRCm39) |
R383H |
probably benign |
Het |
Arhgef28 |
C |
T |
13: 98,130,557 (GRCm39) |
R427H |
probably benign |
Het |
Atl1 |
T |
A |
12: 69,972,922 (GRCm39) |
S81T |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,947,470 (GRCm39) |
|
probably benign |
Het |
Cdh10 |
T |
A |
15: 19,013,487 (GRCm39) |
F696I |
possibly damaging |
Het |
Cdk2ap2 |
T |
C |
19: 4,147,429 (GRCm39) |
S2P |
unknown |
Het |
Cela1 |
G |
A |
15: 100,580,821 (GRCm39) |
T145I |
probably benign |
Het |
Celsr2 |
A |
T |
3: 108,303,443 (GRCm39) |
|
probably benign |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Col22a1 |
A |
G |
15: 71,878,503 (GRCm39) |
I218T |
probably damaging |
Het |
Copb1 |
T |
C |
7: 113,820,935 (GRCm39) |
I785V |
possibly damaging |
Het |
Dnajc16 |
A |
T |
4: 141,492,002 (GRCm39) |
V607E |
possibly damaging |
Het |
Dnali1 |
A |
T |
4: 124,957,414 (GRCm39) |
L110Q |
probably damaging |
Het |
Epn1 |
A |
G |
7: 5,096,375 (GRCm39) |
E223G |
probably benign |
Het |
Erbb3 |
A |
G |
10: 128,414,325 (GRCm39) |
L473P |
possibly damaging |
Het |
Fhip1a |
A |
G |
3: 85,568,318 (GRCm39) |
I1067T |
possibly damaging |
Het |
Gadl1 |
T |
A |
9: 115,835,569 (GRCm39) |
D332E |
probably benign |
Het |
Gm10801 |
TC |
TCGAC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Heg1 |
A |
G |
16: 33,570,863 (GRCm39) |
S1188G |
probably null |
Het |
Hipk3 |
G |
A |
2: 104,268,242 (GRCm39) |
A575V |
probably benign |
Het |
Htt |
T |
A |
5: 35,046,809 (GRCm39) |
I2375N |
possibly damaging |
Het |
Klhl24 |
A |
T |
16: 19,938,980 (GRCm39) |
K512* |
probably null |
Het |
Krtdap |
A |
T |
7: 30,488,952 (GRCm39) |
Y40F |
probably damaging |
Het |
Lhx1 |
A |
T |
11: 84,410,455 (GRCm39) |
S381T |
probably benign |
Het |
Lnpep |
G |
A |
17: 17,773,203 (GRCm39) |
P655L |
probably damaging |
Het |
Map6d1 |
A |
G |
16: 20,055,386 (GRCm39) |
V150A |
probably benign |
Het |
Marchf10 |
A |
G |
11: 105,292,802 (GRCm39) |
S202P |
possibly damaging |
Het |
Med1 |
A |
C |
11: 98,080,102 (GRCm39) |
L13R |
possibly damaging |
Het |
Mxi1 |
G |
A |
19: 53,360,126 (GRCm39) |
G283S |
probably damaging |
Het |
Myh7 |
T |
G |
14: 55,212,752 (GRCm39) |
D1431A |
probably damaging |
Het |
Myo3b |
G |
T |
2: 70,088,325 (GRCm39) |
G863W |
probably damaging |
Het |
Nat8f1 |
G |
T |
6: 85,887,907 (GRCm39) |
Q18K |
probably benign |
Het |
Ncaph |
A |
G |
2: 126,950,529 (GRCm39) |
V576A |
probably benign |
Het |
Nfkbia |
T |
G |
12: 55,539,196 (GRCm39) |
D39A |
possibly damaging |
Het |
Nrxn2 |
G |
T |
19: 6,555,057 (GRCm39) |
G1179C |
probably damaging |
Het |
Or12k8 |
A |
C |
2: 36,975,307 (GRCm39) |
V151G |
probably damaging |
Het |
P4ha1 |
A |
G |
10: 59,205,455 (GRCm39) |
D495G |
probably damaging |
Het |
Phf20 |
C |
T |
2: 156,144,843 (GRCm39) |
A817V |
probably benign |
Het |
Phlpp2 |
A |
T |
8: 110,652,431 (GRCm39) |
I592F |
probably benign |
Het |
Polq |
A |
G |
16: 36,832,280 (GRCm39) |
S7G |
unknown |
Het |
Ppfia3 |
G |
T |
7: 44,997,941 (GRCm39) |
Q729K |
probably benign |
Het |
Prmt8 |
A |
C |
6: 127,706,462 (GRCm39) |
F110V |
probably damaging |
Het |
Psca |
A |
T |
15: 74,587,868 (GRCm39) |
|
probably null |
Het |
Pus7 |
G |
T |
5: 23,980,754 (GRCm39) |
D165E |
probably benign |
Het |
Raver2 |
A |
G |
4: 100,994,942 (GRCm39) |
E555G |
probably damaging |
Het |
Rb1cc1 |
G |
A |
1: 6,315,395 (GRCm39) |
V457M |
probably damaging |
Het |
Rbp3 |
A |
G |
14: 33,676,522 (GRCm39) |
R157G |
probably benign |
Het |
Scart2 |
A |
C |
7: 139,828,913 (GRCm39) |
T191P |
possibly damaging |
Het |
Sgk2 |
T |
A |
2: 162,854,890 (GRCm39) |
S334T |
probably damaging |
Het |
Sh2d4b |
T |
C |
14: 40,614,832 (GRCm39) |
M31V |
probably benign |
Het |
Slc23a3 |
G |
A |
1: 75,106,271 (GRCm39) |
T316I |
probably damaging |
Het |
Slc5a4b |
C |
A |
10: 75,910,925 (GRCm39) |
G304C |
probably damaging |
Het |
Slc7a14 |
A |
G |
3: 31,311,759 (GRCm39) |
V87A |
probably damaging |
Het |
Slitrk3 |
A |
T |
3: 72,956,164 (GRCm39) |
N869K |
probably benign |
Het |
St8sia6 |
T |
C |
2: 13,661,896 (GRCm39) |
R312G |
possibly damaging |
Het |
Strip2 |
A |
T |
6: 29,923,968 (GRCm39) |
E94V |
probably benign |
Het |
Sycp2 |
T |
C |
2: 177,990,052 (GRCm39) |
D1398G |
probably damaging |
Het |
Syne1 |
C |
A |
10: 5,143,040 (GRCm39) |
V114F |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,280,204 (GRCm39) |
K1630E |
probably benign |
Het |
Sytl2 |
A |
G |
7: 90,025,334 (GRCm39) |
N441D |
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,501,136 (GRCm39) |
C424R |
|
Het |
Tln2 |
T |
C |
9: 67,302,827 (GRCm39) |
D48G |
probably damaging |
Het |
Treml1 |
A |
G |
17: 48,673,852 (GRCm39) |
T288A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,596,113 (GRCm39) |
I20267V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,679,259 (GRCm39) |
V10821D |
unknown |
Het |
Vmn2r111 |
A |
C |
17: 22,767,011 (GRCm39) |
S829A |
probably benign |
Het |
Xcl1 |
T |
A |
1: 164,763,079 (GRCm39) |
|
probably benign |
Het |
Zdhhc23 |
A |
T |
16: 43,794,227 (GRCm39) |
V149E |
probably damaging |
Het |
Zfp273 |
A |
T |
13: 67,970,387 (GRCm39) |
I12F |
possibly damaging |
Het |
Zfp874a |
A |
T |
13: 67,590,764 (GRCm39) |
C307S |
probably damaging |
Het |
|
Other mutations in Rin3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Rin3
|
APN |
12 |
102,339,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01521:Rin3
|
APN |
12 |
102,335,307 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4495001:Rin3
|
UTSW |
12 |
102,335,295 (GRCm39) |
missense |
probably benign |
0.02 |
R0109:Rin3
|
UTSW |
12 |
102,279,340 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0109:Rin3
|
UTSW |
12 |
102,279,340 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0504:Rin3
|
UTSW |
12 |
102,353,823 (GRCm39) |
nonsense |
probably null |
|
R0699:Rin3
|
UTSW |
12 |
102,335,834 (GRCm39) |
missense |
probably damaging |
0.98 |
R1499:Rin3
|
UTSW |
12 |
102,335,018 (GRCm39) |
missense |
unknown |
|
R1733:Rin3
|
UTSW |
12 |
102,335,589 (GRCm39) |
nonsense |
probably null |
|
R1743:Rin3
|
UTSW |
12 |
102,356,355 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2911:Rin3
|
UTSW |
12 |
102,339,843 (GRCm39) |
missense |
probably benign |
0.43 |
R2961:Rin3
|
UTSW |
12 |
102,279,305 (GRCm39) |
nonsense |
probably null |
|
R3153:Rin3
|
UTSW |
12 |
102,334,800 (GRCm39) |
missense |
unknown |
|
R3932:Rin3
|
UTSW |
12 |
102,356,342 (GRCm39) |
missense |
probably damaging |
0.98 |
R4498:Rin3
|
UTSW |
12 |
102,335,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Rin3
|
UTSW |
12 |
102,327,642 (GRCm39) |
intron |
probably benign |
|
R4985:Rin3
|
UTSW |
12 |
102,334,821 (GRCm39) |
missense |
unknown |
|
R5300:Rin3
|
UTSW |
12 |
102,335,929 (GRCm39) |
missense |
probably benign |
0.29 |
R5363:Rin3
|
UTSW |
12 |
102,292,093 (GRCm39) |
missense |
probably damaging |
0.97 |
R5414:Rin3
|
UTSW |
12 |
102,356,116 (GRCm39) |
nonsense |
probably null |
|
R5458:Rin3
|
UTSW |
12 |
102,339,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5503:Rin3
|
UTSW |
12 |
102,279,314 (GRCm39) |
missense |
probably benign |
0.17 |
R5534:Rin3
|
UTSW |
12 |
102,353,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Rin3
|
UTSW |
12 |
102,356,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5752:Rin3
|
UTSW |
12 |
102,279,378 (GRCm39) |
start gained |
probably benign |
|
R5874:Rin3
|
UTSW |
12 |
102,356,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Rin3
|
UTSW |
12 |
102,335,584 (GRCm39) |
missense |
probably benign |
0.06 |
R7250:Rin3
|
UTSW |
12 |
102,334,893 (GRCm39) |
missense |
unknown |
|
R7264:Rin3
|
UTSW |
12 |
102,356,374 (GRCm39) |
missense |
probably benign |
0.01 |
R7514:Rin3
|
UTSW |
12 |
102,335,909 (GRCm39) |
nonsense |
probably null |
|
R7534:Rin3
|
UTSW |
12 |
102,317,200 (GRCm39) |
missense |
unknown |
|
R7837:Rin3
|
UTSW |
12 |
102,335,024 (GRCm39) |
missense |
unknown |
|
R7875:Rin3
|
UTSW |
12 |
102,335,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Rin3
|
UTSW |
12 |
102,335,418 (GRCm39) |
missense |
probably benign |
0.14 |
R8014:Rin3
|
UTSW |
12 |
102,327,630 (GRCm39) |
nonsense |
probably null |
|
R8187:Rin3
|
UTSW |
12 |
102,292,066 (GRCm39) |
missense |
unknown |
|
R8757:Rin3
|
UTSW |
12 |
102,339,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Rin3
|
UTSW |
12 |
102,339,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Rin3
|
UTSW |
12 |
102,335,537 (GRCm39) |
missense |
probably benign |
0.16 |
R9050:Rin3
|
UTSW |
12 |
102,335,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R9197:Rin3
|
UTSW |
12 |
102,335,306 (GRCm39) |
missense |
probably benign |
0.03 |
R9272:Rin3
|
UTSW |
12 |
102,335,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Rin3
|
UTSW |
12 |
102,335,589 (GRCm39) |
nonsense |
probably null |
|
R9517:Rin3
|
UTSW |
12 |
102,334,895 (GRCm39) |
missense |
unknown |
|
R9576:Rin3
|
UTSW |
12 |
102,335,589 (GRCm39) |
nonsense |
probably null |
|
Z1177:Rin3
|
UTSW |
12 |
102,292,121 (GRCm39) |
missense |
unknown |
|
|