Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
C |
2: 69,089,971 (GRCm39) |
Y971C |
probably damaging |
Het |
Actr5 |
T |
A |
2: 158,468,433 (GRCm39) |
S188T |
probably damaging |
Het |
Adamtsl4 |
A |
G |
3: 95,586,896 (GRCm39) |
|
probably null |
Het |
Agbl2 |
A |
G |
2: 90,645,733 (GRCm39) |
N822S |
probably benign |
Het |
Ankdd1b |
T |
A |
13: 96,554,255 (GRCm39) |
|
probably benign |
Het |
Arhgef40 |
C |
T |
14: 52,242,395 (GRCm39) |
|
probably benign |
Het |
Art5 |
A |
G |
7: 101,747,701 (GRCm39) |
|
probably null |
Het |
Atpsckmt |
T |
G |
15: 31,608,243 (GRCm39) |
V98G |
probably damaging |
Het |
Cacna1s |
T |
C |
1: 136,046,390 (GRCm39) |
|
probably benign |
Het |
Car9 |
G |
A |
4: 43,508,616 (GRCm39) |
W42* |
probably null |
Het |
Cdh20 |
T |
C |
1: 104,862,035 (GRCm39) |
Y72H |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,043,718 (GRCm39) |
D407G |
possibly damaging |
Het |
Cngb3 |
T |
A |
4: 19,309,562 (GRCm39) |
D73E |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,945,451 (GRCm39) |
F888I |
probably damaging |
Het |
Dgat2 |
T |
C |
7: 98,807,504 (GRCm39) |
D222G |
probably benign |
Het |
Dscaml1 |
T |
C |
9: 45,583,993 (GRCm39) |
M486T |
probably benign |
Het |
Faim2 |
C |
T |
15: 99,425,460 (GRCm39) |
|
probably null |
Het |
Fance |
T |
C |
17: 28,537,293 (GRCm39) |
|
probably benign |
Het |
Fancm |
G |
T |
12: 65,168,480 (GRCm39) |
M1614I |
possibly damaging |
Het |
Fcrl5 |
A |
T |
3: 87,351,496 (GRCm39) |
N248I |
probably damaging |
Het |
Foxo3 |
G |
A |
10: 42,073,774 (GRCm39) |
R29W |
probably damaging |
Het |
Gabbr2 |
A |
G |
4: 46,718,797 (GRCm39) |
Y74H |
probably damaging |
Het |
Gatd1 |
A |
C |
7: 140,990,981 (GRCm39) |
D55E |
probably benign |
Het |
Havcr1 |
A |
G |
11: 46,643,268 (GRCm39) |
T63A |
probably benign |
Het |
Hltf |
T |
C |
3: 20,118,865 (GRCm39) |
|
probably null |
Het |
Ifit3b |
A |
T |
19: 34,590,030 (GRCm39) |
Q402L |
probably damaging |
Het |
Ints3 |
A |
G |
3: 90,322,828 (GRCm39) |
L134S |
probably benign |
Het |
Kcna10 |
A |
G |
3: 107,102,217 (GRCm39) |
T283A |
probably benign |
Het |
Kmt2e |
A |
C |
5: 23,697,313 (GRCm39) |
R590S |
probably damaging |
Het |
Lefty1 |
A |
T |
1: 180,765,277 (GRCm39) |
N282Y |
probably benign |
Het |
Loxl4 |
T |
A |
19: 42,596,030 (GRCm39) |
Y141F |
probably benign |
Het |
Lrrn2 |
T |
C |
1: 132,866,915 (GRCm39) |
V660A |
probably benign |
Het |
Lyst |
T |
C |
13: 13,824,935 (GRCm39) |
S1517P |
probably benign |
Het |
Mcoln2 |
A |
G |
3: 145,881,468 (GRCm39) |
H208R |
probably benign |
Het |
Mdga2 |
C |
T |
12: 66,517,775 (GRCm39) |
|
probably benign |
Het |
Mpp2 |
T |
A |
11: 101,955,259 (GRCm39) |
E122V |
possibly damaging |
Het |
Mrgprb5 |
T |
C |
7: 47,818,526 (GRCm39) |
N70D |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,343,500 (GRCm39) |
E37D |
possibly damaging |
Het |
Nbeal1 |
T |
A |
1: 60,274,722 (GRCm39) |
|
probably null |
Het |
Ncoa6 |
T |
C |
2: 155,233,081 (GRCm39) |
|
probably benign |
Het |
Nfib |
C |
A |
4: 82,422,967 (GRCm39) |
|
probably null |
Het |
Nostrin |
G |
T |
2: 68,975,156 (GRCm39) |
G24* |
probably null |
Het |
Nudc |
A |
G |
4: 133,260,576 (GRCm39) |
Y293H |
probably damaging |
Het |
Or51a42 |
T |
A |
7: 103,707,940 (GRCm39) |
N290Y |
probably damaging |
Het |
Pcmtd1 |
T |
A |
1: 7,225,325 (GRCm39) |
Y41* |
probably null |
Het |
Pigt |
T |
C |
2: 164,343,544 (GRCm39) |
L340P |
probably damaging |
Het |
Pomgnt1 |
T |
C |
4: 116,012,972 (GRCm39) |
Y420H |
probably damaging |
Het |
Pramel6 |
C |
T |
2: 87,341,096 (GRCm39) |
T476I |
probably benign |
Het |
Ptprn2 |
T |
A |
12: 116,788,016 (GRCm39) |
H118Q |
possibly damaging |
Het |
Rasl10a |
G |
A |
11: 5,008,517 (GRCm39) |
S71N |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,310,893 (GRCm39) |
I804V |
probably benign |
Het |
Rps4l-ps |
T |
C |
7: 114,526,537 (GRCm39) |
|
noncoding transcript |
Het |
Sash1 |
T |
A |
10: 8,605,477 (GRCm39) |
H971L |
probably benign |
Het |
Secisbp2 |
T |
A |
13: 51,806,768 (GRCm39) |
F54L |
possibly damaging |
Het |
Senp1 |
A |
T |
15: 97,954,731 (GRCm39) |
H484Q |
probably benign |
Het |
Slc12a1 |
T |
C |
2: 124,995,913 (GRCm39) |
I22T |
possibly damaging |
Het |
Slc25a36 |
A |
G |
9: 96,972,172 (GRCm39) |
|
probably benign |
Het |
Srcap |
T |
A |
7: 127,140,731 (GRCm39) |
S1443T |
probably benign |
Het |
Sv2c |
T |
C |
13: 96,123,319 (GRCm39) |
T385A |
probably benign |
Het |
Tas2r131 |
T |
A |
6: 132,933,936 (GRCm39) |
H291L |
probably damaging |
Het |
Thbs3 |
A |
G |
3: 89,124,147 (GRCm39) |
D80G |
probably damaging |
Het |
Tnxb |
C |
T |
17: 34,908,394 (GRCm39) |
S1349L |
probably damaging |
Het |
Toporsl |
A |
G |
4: 52,611,996 (GRCm39) |
R630G |
probably benign |
Het |
Vmn1r43 |
C |
A |
6: 89,846,837 (GRCm39) |
M216I |
probably benign |
Het |
Wdr17 |
T |
A |
8: 55,092,911 (GRCm39) |
E1068D |
probably benign |
Het |
Wnt10a |
G |
A |
1: 74,842,762 (GRCm39) |
V413I |
probably damaging |
Het |
Zfp141 |
T |
C |
7: 42,126,111 (GRCm39) |
|
probably null |
Het |
Zfp169 |
T |
C |
13: 48,643,634 (GRCm39) |
I498V |
probably benign |
Het |
|
Other mutations in Gpr152 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Gpr152
|
APN |
19 |
4,193,506 (GRCm39) |
missense |
probably benign |
|
IGL01400:Gpr152
|
APN |
19 |
4,193,626 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01538:Gpr152
|
APN |
19 |
4,192,951 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02288:Gpr152
|
APN |
19 |
4,193,694 (GRCm39) |
missense |
probably benign |
|
IGL02513:Gpr152
|
APN |
19 |
4,192,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03335:Gpr152
|
APN |
19 |
4,193,770 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0318:Gpr152
|
UTSW |
19 |
4,193,541 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1216:Gpr152
|
UTSW |
19 |
4,193,554 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1936:Gpr152
|
UTSW |
19 |
4,192,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Gpr152
|
UTSW |
19 |
4,193,805 (GRCm39) |
missense |
probably benign |
0.00 |
R3161:Gpr152
|
UTSW |
19 |
4,192,713 (GRCm39) |
missense |
probably benign |
0.00 |
R4193:Gpr152
|
UTSW |
19 |
4,192,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Gpr152
|
UTSW |
19 |
4,193,790 (GRCm39) |
missense |
probably benign |
0.00 |
R5014:Gpr152
|
UTSW |
19 |
4,193,506 (GRCm39) |
missense |
probably benign |
0.00 |
R5381:Gpr152
|
UTSW |
19 |
4,192,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R5431:Gpr152
|
UTSW |
19 |
4,193,746 (GRCm39) |
missense |
probably benign |
0.21 |
R5470:Gpr152
|
UTSW |
19 |
4,193,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R7331:Gpr152
|
UTSW |
19 |
4,192,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R7350:Gpr152
|
UTSW |
19 |
4,192,963 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7806:Gpr152
|
UTSW |
19 |
4,193,487 (GRCm39) |
missense |
probably benign |
|
R8315:Gpr152
|
UTSW |
19 |
4,193,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8889:Gpr152
|
UTSW |
19 |
4,192,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9455:Gpr152
|
UTSW |
19 |
4,193,844 (GRCm39) |
missense |
probably benign |
0.01 |
R9651:Gpr152
|
UTSW |
19 |
4,192,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Gpr152
|
UTSW |
19 |
4,192,640 (GRCm39) |
missense |
probably benign |
0.00 |
R9761:Gpr152
|
UTSW |
19 |
4,193,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|