Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
T |
A |
4: 148,029,440 (GRCm39) |
F470Y |
probably damaging |
Het |
Adra1a |
T |
C |
14: 66,875,250 (GRCm39) |
L75P |
probably damaging |
Het |
Agap1 |
T |
C |
1: 89,762,188 (GRCm39) |
S560P |
probably damaging |
Het |
Ahcyl |
T |
C |
16: 45,974,970 (GRCm39) |
T136A |
probably benign |
Het |
Arrdc4 |
T |
A |
7: 68,391,623 (GRCm39) |
I215L |
probably damaging |
Het |
Atad3a |
C |
T |
4: 155,840,610 (GRCm39) |
A97T |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,386,713 (GRCm39) |
T383S |
probably benign |
Het |
C2cd5 |
G |
A |
6: 142,995,951 (GRCm39) |
R379* |
probably null |
Het |
Cacna1e |
G |
T |
1: 154,274,549 (GRCm39) |
H2138N |
probably benign |
Het |
Card14 |
A |
T |
11: 119,216,328 (GRCm39) |
D303V |
possibly damaging |
Het |
Ccdc202 |
T |
C |
14: 96,119,252 (GRCm39) |
V3A |
probably benign |
Het |
Cfhr1 |
T |
C |
1: 139,475,478 (GRCm39) |
Y331C |
unknown |
Het |
Chp1 |
G |
A |
2: 119,415,146 (GRCm39) |
D183N |
probably benign |
Het |
Cntn2 |
T |
C |
1: 132,443,882 (GRCm39) |
T966A |
probably benign |
Het |
Cpne9 |
T |
G |
6: 113,266,965 (GRCm39) |
C133G |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,515,948 (GRCm39) |
T121A |
|
Het |
Cul7 |
C |
T |
17: 46,963,747 (GRCm39) |
Q275* |
probably null |
Het |
Cyp11b1 |
T |
C |
15: 74,710,897 (GRCm39) |
D221G |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 49,979,685 (GRCm39) |
F107I |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,363,170 (GRCm39) |
I3911V |
probably benign |
Het |
Eif1ad16 |
A |
G |
12: 87,985,259 (GRCm39) |
Y95H |
probably damaging |
Het |
Eloa |
T |
C |
4: 135,736,595 (GRCm39) |
H551R |
probably benign |
Het |
Fam171b |
T |
A |
2: 83,709,732 (GRCm39) |
V468D |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,200,666 (GRCm39) |
W803R |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,163,201 (GRCm39) |
D2G |
probably benign |
Het |
Fbxo8 |
A |
G |
8: 57,041,120 (GRCm39) |
T179A |
probably benign |
Het |
Gdap1 |
A |
G |
1: 17,231,623 (GRCm39) |
T323A |
probably damaging |
Het |
Gm136 |
T |
C |
4: 34,743,875 (GRCm39) |
N323S |
probably null |
Het |
Gm6899 |
A |
T |
11: 26,543,819 (GRCm39) |
T129S |
unknown |
Het |
Gnb3 |
A |
T |
6: 124,814,183 (GRCm39) |
C166S |
possibly damaging |
Het |
Gpx8 |
T |
C |
13: 113,179,711 (GRCm39) |
M197V |
probably benign |
Het |
Gse1 |
G |
T |
8: 121,295,217 (GRCm39) |
R446L |
unknown |
Het |
Itch |
A |
T |
2: 155,054,987 (GRCm39) |
T764S |
probably benign |
Het |
Itch |
A |
G |
2: 155,051,922 (GRCm39) |
K614E |
probably damaging |
Het |
Itpkb |
T |
G |
1: 180,241,544 (GRCm39) |
M738R |
probably damaging |
Het |
Jph1 |
T |
A |
1: 17,074,192 (GRCm39) |
K609* |
probably null |
Het |
Kcns1 |
G |
A |
2: 164,010,241 (GRCm39) |
R173C |
probably damaging |
Het |
Larp4b |
C |
T |
13: 9,186,834 (GRCm39) |
S54L |
probably damaging |
Het |
Lonrf1 |
G |
T |
8: 36,715,918 (GRCm39) |
S239* |
probably null |
Het |
Lyst |
T |
G |
13: 13,857,808 (GRCm39) |
|
probably null |
Het |
Mccc1 |
T |
A |
3: 36,015,132 (GRCm39) |
R663* |
probably null |
Het |
Mcm3 |
A |
G |
1: 20,876,997 (GRCm39) |
V646A |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,739,912 (GRCm39) |
L3722P |
probably damaging |
Het |
Mmp27 |
T |
G |
9: 7,579,002 (GRCm39) |
D392E |
probably damaging |
Het |
Ms4a14 |
A |
G |
19: 11,279,906 (GRCm39) |
I884T |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,574,439 (GRCm39) |
T963I |
probably benign |
Het |
Muc6 |
G |
C |
7: 141,217,659 (GRCm39) |
P2338R |
probably damaging |
Het |
Mucl3 |
C |
A |
17: 35,948,969 (GRCm39) |
S210I |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Ndrg2 |
C |
T |
14: 52,147,812 (GRCm39) |
A102T |
possibly damaging |
Het |
Nhsl3 |
T |
C |
4: 129,117,566 (GRCm39) |
N411S |
probably benign |
Het |
Nos1 |
A |
G |
5: 118,035,792 (GRCm39) |
D431G |
probably damaging |
Het |
Oog4 |
CAA |
CA |
4: 143,164,022 (GRCm39) |
|
probably null |
Het |
Otog |
T |
C |
7: 45,901,480 (GRCm39) |
L393P |
probably damaging |
Het |
Plcl1 |
A |
G |
1: 55,736,627 (GRCm39) |
N656S |
probably damaging |
Het |
Pole3 |
C |
A |
4: 62,443,060 (GRCm39) |
V27F |
probably damaging |
Het |
Prrt4 |
T |
A |
6: 29,177,140 (GRCm39) |
I210F |
probably damaging |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Rbpms |
A |
T |
8: 34,354,387 (GRCm39) |
S53T |
possibly damaging |
Het |
Rgs7 |
C |
A |
1: 174,949,296 (GRCm39) |
V203L |
probably benign |
Het |
Riok1 |
A |
T |
13: 38,229,263 (GRCm39) |
D150V |
probably damaging |
Het |
Rrp1b |
T |
C |
17: 32,274,900 (GRCm39) |
L335P |
probably benign |
Het |
Rsph6a |
T |
G |
7: 18,801,962 (GRCm39) |
I592S |
possibly damaging |
Het |
Skor1 |
C |
T |
9: 63,052,661 (GRCm39) |
G436D |
probably damaging |
Het |
Slc17a8 |
T |
C |
10: 89,433,319 (GRCm39) |
T51A |
possibly damaging |
Het |
Slc22a8 |
T |
C |
19: 8,585,248 (GRCm39) |
S266P |
probably damaging |
Het |
Socs2 |
A |
G |
10: 95,250,845 (GRCm39) |
|
probably benign |
Het |
Tas2r106 |
A |
G |
6: 131,655,668 (GRCm39) |
I61T |
possibly damaging |
Het |
Tfap2a |
T |
C |
13: 40,882,051 (GRCm39) |
N77D |
probably damaging |
Het |
Tmem236 |
T |
A |
2: 14,197,076 (GRCm39) |
L88Q |
probably damaging |
Het |
Ttc41 |
A |
G |
10: 86,595,088 (GRCm39) |
E954G |
probably damaging |
Het |
Vmn1r34 |
G |
T |
6: 66,613,994 (GRCm39) |
S248* |
probably null |
Het |
Wipf1 |
T |
C |
2: 73,262,789 (GRCm39) |
R483G |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,476,946 (GRCm39) |
N3187S |
probably benign |
Het |
Zfp202 |
C |
A |
9: 40,121,829 (GRCm39) |
P309T |
probably benign |
Het |
Zfp39 |
T |
C |
11: 58,781,469 (GRCm39) |
H431R |
probably damaging |
Het |
Zfp658 |
T |
A |
7: 43,224,102 (GRCm39) |
H792Q |
probably benign |
Het |
|
Other mutations in Gpr61 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00505:Gpr61
|
APN |
3 |
108,058,514 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Gpr61
|
APN |
3 |
108,057,534 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02878:Gpr61
|
APN |
3 |
108,057,344 (GRCm39) |
missense |
probably damaging |
0.97 |
R1061:Gpr61
|
UTSW |
3 |
108,057,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Gpr61
|
UTSW |
3 |
108,057,797 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1296:Gpr61
|
UTSW |
3 |
108,057,797 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1329:Gpr61
|
UTSW |
3 |
108,057,830 (GRCm39) |
missense |
probably benign |
0.16 |
R1718:Gpr61
|
UTSW |
3 |
108,057,696 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1840:Gpr61
|
UTSW |
3 |
108,057,797 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2139:Gpr61
|
UTSW |
3 |
108,058,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5016:Gpr61
|
UTSW |
3 |
108,057,983 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7042:Gpr61
|
UTSW |
3 |
108,058,647 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8058:Gpr61
|
UTSW |
3 |
108,058,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R8118:Gpr61
|
UTSW |
3 |
108,057,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R8931:Gpr61
|
UTSW |
3 |
108,057,470 (GRCm39) |
missense |
probably benign |
|
R9063:Gpr61
|
UTSW |
3 |
108,057,555 (GRCm39) |
missense |
probably benign |
0.01 |
|