Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
T |
A |
11: 109,921,714 (GRCm39) |
M1447L |
probably benign |
Het |
Adam30 |
G |
A |
3: 98,070,257 (GRCm39) |
V697I |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,277,452 (GRCm39) |
N689D |
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,813,906 (GRCm39) |
K753R |
probably benign |
Het |
Adra2a |
T |
C |
19: 54,034,835 (GRCm39) |
F64L |
probably damaging |
Het |
Ankub1 |
A |
G |
3: 57,580,345 (GRCm39) |
L104P |
probably damaging |
Het |
Arel1 |
A |
G |
12: 84,988,719 (GRCm39) |
V10A |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,962,047 (GRCm39) |
N1165K |
probably benign |
Het |
Atp6v0d2 |
T |
A |
4: 19,880,060 (GRCm39) |
D279V |
probably benign |
Het |
Cadps |
A |
T |
14: 12,616,099 (GRCm38) |
D310E |
probably damaging |
Het |
Caskin2 |
T |
C |
11: 115,695,615 (GRCm39) |
I249V |
possibly damaging |
Het |
Cdh23 |
T |
C |
10: 60,212,620 (GRCm39) |
N1598S |
probably benign |
Het |
Cep250 |
A |
T |
2: 155,834,682 (GRCm39) |
Q2202H |
probably benign |
Het |
Ces5a |
T |
A |
8: 94,261,311 (GRCm39) |
T35S |
probably damaging |
Het |
Cnot11 |
G |
A |
1: 39,579,020 (GRCm39) |
W295* |
probably null |
Het |
Cntnap5a |
G |
T |
1: 116,149,619 (GRCm39) |
W565L |
probably damaging |
Het |
Dgka |
T |
C |
10: 128,569,468 (GRCm39) |
E148G |
probably damaging |
Het |
Dnah14 |
G |
A |
1: 181,455,739 (GRCm39) |
D955N |
probably benign |
Het |
Erbin |
G |
A |
13: 103,998,834 (GRCm39) |
T184I |
probably damaging |
Het |
Fam20c |
G |
T |
5: 138,793,309 (GRCm39) |
G477W |
probably damaging |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fgfr4 |
T |
C |
13: 55,309,262 (GRCm39) |
V433A |
probably benign |
Het |
Gal3st1 |
A |
T |
11: 3,948,093 (GRCm39) |
Q100L |
possibly damaging |
Het |
Gfra2 |
T |
C |
14: 71,163,380 (GRCm39) |
F221S |
probably damaging |
Het |
Gm19965 |
G |
A |
1: 116,748,921 (GRCm39) |
V201M |
|
Het |
Gnb1l |
A |
T |
16: 18,382,806 (GRCm39) |
T282S |
probably benign |
Het |
Greb1 |
G |
A |
12: 16,761,739 (GRCm39) |
T547I |
probably damaging |
Het |
Ifi214 |
A |
T |
1: 173,357,097 (GRCm39) |
V2E |
probably benign |
Het |
Ighv1-71 |
T |
C |
12: 115,706,267 (GRCm39) |
M1V |
probably null |
Het |
Itm2b |
C |
T |
14: 73,605,785 (GRCm39) |
G67D |
probably damaging |
Het |
Kif21a |
A |
T |
15: 90,851,432 (GRCm39) |
C995* |
probably null |
Het |
Kifc2 |
A |
T |
15: 76,544,904 (GRCm39) |
Y13F |
probably damaging |
Het |
Lamb1 |
T |
A |
12: 31,315,595 (GRCm39) |
V59D |
probably benign |
Het |
Lhx1 |
A |
T |
11: 84,412,703 (GRCm39) |
D163E |
probably damaging |
Het |
Lrrc1 |
A |
T |
9: 77,365,121 (GRCm39) |
Y187N |
probably benign |
Het |
Map3k1 |
C |
A |
13: 111,904,645 (GRCm39) |
V380F |
probably damaging |
Het |
Mapk11 |
T |
C |
15: 89,028,511 (GRCm39) |
D283G |
probably damaging |
Het |
Mccc2 |
G |
T |
13: 100,091,207 (GRCm39) |
A430D |
probably damaging |
Het |
Mest |
A |
G |
6: 30,747,158 (GRCm39) |
N340S |
unknown |
Het |
Mms22l |
T |
C |
4: 24,517,139 (GRCm39) |
L340P |
probably benign |
Het |
Mrnip |
A |
G |
11: 50,087,808 (GRCm39) |
Y110C |
possibly damaging |
Het |
Mtmr4 |
A |
G |
11: 87,502,063 (GRCm39) |
T706A |
probably benign |
Het |
Muc21 |
G |
A |
17: 35,929,761 (GRCm39) |
A1475V |
unknown |
Het |
Ncstn |
A |
G |
1: 171,900,373 (GRCm39) |
F234S |
probably benign |
Het |
Nrp1 |
T |
C |
8: 129,202,777 (GRCm39) |
|
probably null |
Het |
Nup37 |
T |
G |
10: 88,010,356 (GRCm39) |
C217G |
probably damaging |
Het |
Or8g22 |
A |
G |
9: 38,958,694 (GRCm39) |
L7P |
unknown |
Het |
Pdzrn3 |
T |
C |
6: 101,128,206 (GRCm39) |
N820S |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,587,225 (GRCm39) |
F117Y |
possibly damaging |
Het |
Phip |
A |
T |
9: 82,753,346 (GRCm39) |
F1799L |
possibly damaging |
Het |
Ppm1f |
T |
A |
16: 16,728,819 (GRCm39) |
F74I |
probably benign |
Het |
Prpf8 |
C |
A |
11: 75,384,783 (GRCm39) |
N775K |
possibly damaging |
Het |
Ptdss2 |
T |
C |
7: 140,731,693 (GRCm39) |
I167T |
possibly damaging |
Het |
Ptpn18 |
G |
A |
1: 34,501,892 (GRCm39) |
|
probably null |
Het |
Rbl2 |
C |
A |
8: 91,841,669 (GRCm39) |
A955D |
probably benign |
Het |
Rgl1 |
A |
G |
1: 152,420,146 (GRCm39) |
S366P |
possibly damaging |
Het |
Rit2 |
A |
T |
18: 31,376,221 (GRCm39) |
M38K |
possibly damaging |
Het |
Robo1 |
A |
G |
16: 72,801,408 (GRCm39) |
M1011V |
probably benign |
Het |
Senp6 |
A |
T |
9: 80,043,797 (GRCm39) |
E809D |
probably benign |
Het |
Stard3 |
G |
A |
11: 98,269,045 (GRCm39) |
|
probably null |
Het |
Taar3 |
T |
G |
10: 23,826,298 (GRCm39) |
Y281* |
probably null |
Het |
Tacc2 |
G |
T |
7: 130,331,103 (GRCm39) |
K352N |
probably benign |
Het |
Tamalin |
G |
A |
15: 101,129,419 (GRCm39) |
S234N |
probably damaging |
Het |
Tasor |
T |
A |
14: 27,160,610 (GRCm39) |
I124N |
probably damaging |
Het |
Tdpoz4 |
G |
A |
3: 93,704,155 (GRCm39) |
V151I |
not run |
Het |
Tenm2 |
A |
G |
11: 35,914,298 (GRCm39) |
L2413P |
probably damaging |
Het |
Tgm6 |
T |
C |
2: 129,983,110 (GRCm39) |
V233A |
probably damaging |
Het |
Tlx3 |
G |
A |
11: 33,153,514 (GRCm39) |
|
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,677,082 (GRCm39) |
R118L |
possibly damaging |
Het |
Trim23 |
C |
A |
13: 104,323,941 (GRCm39) |
H133Q |
probably damaging |
Het |
Unc80 |
A |
T |
1: 66,640,356 (GRCm39) |
D1421V |
probably damaging |
Het |
Vmn1r172 |
A |
G |
7: 23,360,048 (GRCm39) |
N311S |
unknown |
Het |
Vps25 |
T |
A |
11: 101,149,775 (GRCm39) |
L153Q |
probably damaging |
Het |
Wbp1l |
G |
T |
19: 46,611,876 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
A |
G |
18: 44,970,558 (GRCm39) |
I291V |
possibly damaging |
Het |
Zfp2 |
A |
G |
11: 50,791,570 (GRCm39) |
C158R |
probably damaging |
Het |
Zfp786 |
G |
A |
6: 47,796,929 (GRCm39) |
P670S |
probably damaging |
Het |
Zfp827 |
G |
A |
8: 79,916,442 (GRCm39) |
R339H |
possibly damaging |
Het |
Zmym6 |
C |
T |
4: 127,017,294 (GRCm39) |
A1025V |
possibly damaging |
Het |
|
Other mutations in Gpr171 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01808:Gpr171
|
APN |
3 |
59,005,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02635:Gpr171
|
APN |
3 |
59,005,017 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02858:Gpr171
|
APN |
3 |
59,005,288 (GRCm39) |
missense |
probably benign |
0.26 |
R1491:Gpr171
|
UTSW |
3 |
59,005,016 (GRCm39) |
missense |
probably benign |
0.01 |
R1539:Gpr171
|
UTSW |
3 |
59,005,142 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1819:Gpr171
|
UTSW |
3 |
59,005,341 (GRCm39) |
missense |
probably benign |
0.02 |
R2255:Gpr171
|
UTSW |
3 |
59,005,628 (GRCm39) |
missense |
probably benign |
0.01 |
R3721:Gpr171
|
UTSW |
3 |
59,005,091 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3856:Gpr171
|
UTSW |
3 |
59,005,506 (GRCm39) |
missense |
probably damaging |
0.96 |
R4259:Gpr171
|
UTSW |
3 |
59,004,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Gpr171
|
UTSW |
3 |
59,004,887 (GRCm39) |
missense |
probably benign |
0.11 |
R4816:Gpr171
|
UTSW |
3 |
59,005,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Gpr171
|
UTSW |
3 |
59,005,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R6363:Gpr171
|
UTSW |
3 |
59,005,313 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6414:Gpr171
|
UTSW |
3 |
59,005,544 (GRCm39) |
missense |
probably damaging |
0.97 |
R7076:Gpr171
|
UTSW |
3 |
59,005,577 (GRCm39) |
missense |
probably damaging |
0.98 |
R7404:Gpr171
|
UTSW |
3 |
59,005,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R7447:Gpr171
|
UTSW |
3 |
59,005,860 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7721:Gpr171
|
UTSW |
3 |
59,005,320 (GRCm39) |
missense |
probably benign |
0.40 |
R8120:Gpr171
|
UTSW |
3 |
59,005,406 (GRCm39) |
missense |
probably damaging |
0.96 |
R8548:Gpr171
|
UTSW |
3 |
59,005,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Gpr171
|
UTSW |
3 |
59,005,116 (GRCm39) |
missense |
probably benign |
|
R9126:Gpr171
|
UTSW |
3 |
59,005,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Gpr171
|
UTSW |
3 |
59,005,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Gpr171
|
UTSW |
3 |
59,005,311 (GRCm39) |
nonsense |
probably null |
|
R9418:Gpr171
|
UTSW |
3 |
59,004,999 (GRCm39) |
missense |
possibly damaging |
0.82 |
|