Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars2 |
G |
A |
17: 45,818,550 (GRCm39) |
D112N |
probably damaging |
Het |
Abca7 |
T |
A |
10: 79,845,778 (GRCm39) |
I1580K |
probably damaging |
Het |
Aebp1 |
A |
G |
11: 5,815,059 (GRCm39) |
D234G |
probably damaging |
Het |
Agap1 |
T |
A |
1: 89,383,153 (GRCm39) |
M1K |
probably null |
Het |
Agrn |
A |
T |
4: 156,263,389 (GRCm39) |
L345H |
probably damaging |
Het |
Amfr |
A |
G |
8: 94,725,754 (GRCm39) |
M209T |
possibly damaging |
Het |
Angel2 |
G |
A |
1: 190,673,371 (GRCm39) |
R338H |
possibly damaging |
Het |
Ankrd27 |
C |
T |
7: 35,330,674 (GRCm39) |
A866V |
probably damaging |
Het |
Apc |
G |
A |
18: 34,448,324 (GRCm39) |
R1740Q |
probably damaging |
Het |
Arhgap32 |
A |
T |
9: 32,168,233 (GRCm39) |
S739C |
possibly damaging |
Het |
Arhgap32 |
G |
C |
9: 32,168,234 (GRCm39) |
S739T |
probably benign |
Het |
Arhgef2 |
C |
T |
3: 88,543,192 (GRCm39) |
S418L |
probably benign |
Het |
Arhgef25 |
T |
C |
10: 127,019,641 (GRCm39) |
T472A |
possibly damaging |
Het |
Atrnl1 |
C |
T |
19: 57,638,846 (GRCm39) |
S328F |
probably benign |
Het |
Bahcc1 |
C |
T |
11: 120,171,000 (GRCm39) |
A1514V |
probably benign |
Het |
Calcoco2 |
C |
T |
11: 95,990,823 (GRCm39) |
E305K |
unknown |
Het |
Ccn1 |
C |
T |
3: 145,354,428 (GRCm39) |
W161* |
probably null |
Het |
Cdc42bpa |
A |
T |
1: 179,889,362 (GRCm39) |
K203* |
probably null |
Het |
Cmc1 |
A |
T |
9: 117,904,250 (GRCm39) |
I47N |
possibly damaging |
Het |
Cntln |
A |
G |
4: 84,964,540 (GRCm39) |
E656G |
possibly damaging |
Het |
Dcun1d3 |
T |
C |
7: 119,458,864 (GRCm39) |
K57R |
possibly damaging |
Het |
Ddx23 |
T |
C |
15: 98,546,492 (GRCm39) |
E559G |
probably damaging |
Het |
Dennd6a |
G |
A |
14: 26,333,193 (GRCm39) |
R367Q |
probably damaging |
Het |
Desi2 |
A |
T |
1: 178,083,702 (GRCm39) |
|
probably benign |
Het |
Dido1 |
T |
C |
2: 180,301,424 (GRCm39) |
D2160G |
unknown |
Het |
Efcab3 |
T |
C |
11: 104,929,184 (GRCm39) |
M4838T |
probably benign |
Het |
Epb41 |
A |
G |
4: 131,718,520 (GRCm39) |
|
probably null |
Het |
Esrrb |
T |
A |
12: 86,517,331 (GRCm39) |
|
probably null |
Het |
Fabp1 |
C |
A |
6: 71,180,111 (GRCm39) |
T94N |
probably benign |
Het |
Fam120a |
A |
T |
13: 49,045,482 (GRCm39) |
C785S |
probably damaging |
Het |
Fam243 |
T |
C |
16: 92,117,710 (GRCm39) |
I193V |
probably damaging |
Het |
Foxc1 |
A |
G |
13: 31,991,243 (GRCm39) |
Y18C |
probably damaging |
Het |
Fshr |
T |
C |
17: 89,293,272 (GRCm39) |
T469A |
probably benign |
Het |
Gm14399 |
T |
A |
2: 174,972,204 (GRCm39) |
H517L |
unknown |
Het |
Gm39115 |
G |
T |
7: 141,689,297 (GRCm39) |
Q159K |
unknown |
Het |
Gm7347 |
T |
A |
5: 26,262,306 (GRCm39) |
I72F |
possibly damaging |
Het |
Hmcn1 |
A |
G |
1: 150,559,466 (GRCm39) |
V2395A |
possibly damaging |
Het |
Ighv5-17 |
T |
G |
12: 113,822,858 (GRCm39) |
T88P |
probably damaging |
Het |
Insm2 |
T |
A |
12: 55,647,329 (GRCm39) |
Y358N |
probably damaging |
Het |
Kazn |
A |
T |
4: 141,844,486 (GRCm39) |
L409Q |
|
Het |
Kcnj5 |
A |
C |
9: 32,234,045 (GRCm39) |
L90R |
probably damaging |
Het |
Kcnv2 |
A |
T |
19: 27,311,084 (GRCm39) |
T484S |
probably damaging |
Het |
Kdm3b |
T |
C |
18: 34,927,557 (GRCm39) |
Y140H |
probably benign |
Het |
Kifbp |
A |
C |
10: 62,401,895 (GRCm39) |
C261W |
probably damaging |
Het |
Krt25 |
C |
T |
11: 99,212,098 (GRCm39) |
A180T |
probably benign |
Het |
Mmp1a |
A |
G |
9: 7,467,294 (GRCm39) |
E290G |
probably damaging |
Het |
Muc21 |
G |
A |
17: 35,929,761 (GRCm39) |
A1475V |
unknown |
Het |
Nr3c1 |
T |
C |
18: 39,547,654 (GRCm39) |
T755A |
probably benign |
Het |
Nr3c1 |
A |
T |
18: 39,555,786 (GRCm39) |
I517N |
probably benign |
Het |
Nxpe2 |
A |
G |
9: 48,234,339 (GRCm39) |
|
probably null |
Het |
Oaz1 |
C |
A |
10: 80,662,673 (GRCm39) |
T27K |
possibly damaging |
Het |
Or4p7 |
A |
T |
2: 88,222,050 (GRCm39) |
H153L |
probably damaging |
Het |
Or51f5 |
T |
C |
7: 102,424,634 (GRCm39) |
I301T |
probably damaging |
Het |
Or5t5 |
G |
T |
2: 86,617,034 (GRCm39) |
C320F |
probably benign |
Het |
Or6z3 |
T |
A |
7: 6,463,777 (GRCm39) |
W90R |
probably benign |
Het |
Or8k21 |
A |
G |
2: 86,145,369 (GRCm39) |
M87T |
probably benign |
Het |
Or8s5 |
A |
G |
15: 98,237,943 (GRCm39) |
V309A |
probably damaging |
Het |
Pafah2 |
A |
T |
4: 134,147,308 (GRCm39) |
K319M |
probably damaging |
Het |
Pask |
A |
T |
1: 93,259,309 (GRCm39) |
V236E |
probably damaging |
Het |
Pcdh1 |
T |
C |
18: 38,322,966 (GRCm39) |
T956A |
probably damaging |
Het |
Pcdhb18 |
C |
A |
18: 37,623,700 (GRCm39) |
N343K |
probably damaging |
Het |
Pcsk2 |
A |
T |
2: 143,532,343 (GRCm39) |
I164F |
probably damaging |
Het |
Phf1 |
T |
C |
17: 27,154,289 (GRCm39) |
Y169H |
probably damaging |
Het |
Pkdrej |
T |
A |
15: 85,705,301 (GRCm39) |
I212F |
probably benign |
Het |
Pnkp |
T |
A |
7: 44,508,114 (GRCm39) |
W146R |
probably damaging |
Het |
Prkcb |
A |
T |
7: 122,143,910 (GRCm39) |
I325F |
probably benign |
Het |
Ptpn21 |
C |
T |
12: 98,670,450 (GRCm39) |
D239N |
probably benign |
Het |
Ptprb |
A |
G |
10: 116,164,070 (GRCm39) |
T626A |
probably damaging |
Het |
Pttg1 |
T |
C |
11: 43,311,916 (GRCm39) |
N180D |
probably benign |
Het |
Raly |
G |
A |
2: 154,703,774 (GRCm39) |
R115Q |
probably damaging |
Het |
Rims2 |
A |
T |
15: 39,301,114 (GRCm39) |
M474L |
probably benign |
Het |
Sash1 |
A |
T |
10: 8,605,960 (GRCm39) |
I810N |
probably damaging |
Het |
Scnn1g |
T |
A |
7: 121,337,304 (GRCm39) |
L55* |
probably null |
Het |
Sema6b |
A |
T |
17: 56,432,573 (GRCm39) |
D543E |
possibly damaging |
Het |
Serpina11 |
C |
T |
12: 103,952,761 (GRCm39) |
G5E |
unknown |
Het |
Sesn3 |
A |
T |
9: 14,187,848 (GRCm39) |
M1L |
probably benign |
Het |
Sez6 |
T |
A |
11: 77,865,149 (GRCm39) |
I632N |
possibly damaging |
Het |
Sgo2b |
A |
T |
8: 64,394,192 (GRCm39) |
I49N |
probably damaging |
Het |
Slc30a2 |
A |
T |
4: 134,071,524 (GRCm39) |
I86F |
possibly damaging |
Het |
Slc38a6 |
T |
A |
12: 73,333,786 (GRCm39) |
W30R |
probably benign |
Het |
Spata31g1 |
A |
T |
4: 42,972,379 (GRCm39) |
T571S |
probably benign |
Het |
Spata31g1 |
A |
T |
4: 42,973,252 (GRCm39) |
I862F |
possibly damaging |
Het |
Stk31 |
T |
G |
6: 49,415,393 (GRCm39) |
V576G |
probably benign |
Het |
Szt2 |
G |
A |
4: 118,233,075 (GRCm39) |
T2297I |
unknown |
Het |
Tmem208 |
T |
C |
8: 106,061,418 (GRCm39) |
F148S |
possibly damaging |
Het |
Tprg1l |
A |
G |
4: 154,245,031 (GRCm39) |
L19P |
possibly damaging |
Het |
Tubg2 |
C |
A |
11: 101,050,897 (GRCm39) |
N207K |
probably damaging |
Het |
Ube2n |
G |
T |
10: 95,377,612 (GRCm39) |
K130N |
probably benign |
Het |
Vcan |
A |
T |
13: 89,840,852 (GRCm39) |
L1564* |
probably null |
Het |
Xkr6 |
A |
T |
14: 64,035,748 (GRCm39) |
D283V |
unknown |
Het |
Zfp654 |
T |
C |
16: 64,605,523 (GRCm39) |
H352R |
probably benign |
Het |
Zfp819 |
T |
A |
7: 43,266,506 (GRCm39) |
C330S |
probably damaging |
Het |
Zfp970 |
G |
T |
2: 177,167,086 (GRCm39) |
C220F |
probably damaging |
Het |
|
Other mutations in Usp36 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00572:Usp36
|
APN |
11 |
118,155,646 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01115:Usp36
|
APN |
11 |
118,176,786 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01720:Usp36
|
APN |
11 |
118,165,828 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02410:Usp36
|
APN |
11 |
118,167,011 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02700:Usp36
|
APN |
11 |
118,166,983 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02926:Usp36
|
APN |
11 |
118,155,609 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03145:Usp36
|
APN |
11 |
118,170,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03203:Usp36
|
APN |
11 |
118,176,636 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03265:Usp36
|
APN |
11 |
118,155,635 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0482:Usp36
|
UTSW |
11 |
118,156,020 (GRCm39) |
missense |
probably benign |
0.21 |
R0499:Usp36
|
UTSW |
11 |
118,164,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R0606:Usp36
|
UTSW |
11 |
118,153,854 (GRCm39) |
splice site |
probably benign |
|
R0646:Usp36
|
UTSW |
11 |
118,163,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Usp36
|
UTSW |
11 |
118,175,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R1646:Usp36
|
UTSW |
11 |
118,164,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Usp36
|
UTSW |
11 |
118,162,957 (GRCm39) |
critical splice donor site |
probably null |
|
R1886:Usp36
|
UTSW |
11 |
118,163,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Usp36
|
UTSW |
11 |
118,153,334 (GRCm39) |
splice site |
probably benign |
|
R2068:Usp36
|
UTSW |
11 |
118,165,844 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2146:Usp36
|
UTSW |
11 |
118,159,491 (GRCm39) |
missense |
probably benign |
0.02 |
R2191:Usp36
|
UTSW |
11 |
118,175,849 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2899:Usp36
|
UTSW |
11 |
118,167,582 (GRCm39) |
splice site |
probably benign |
|
R3176:Usp36
|
UTSW |
11 |
118,167,585 (GRCm39) |
critical splice donor site |
probably null |
|
R3177:Usp36
|
UTSW |
11 |
118,167,585 (GRCm39) |
critical splice donor site |
probably null |
|
R3276:Usp36
|
UTSW |
11 |
118,167,585 (GRCm39) |
critical splice donor site |
probably null |
|
R3277:Usp36
|
UTSW |
11 |
118,167,585 (GRCm39) |
critical splice donor site |
probably null |
|
R3615:Usp36
|
UTSW |
11 |
118,167,585 (GRCm39) |
critical splice donor site |
probably null |
|
R3616:Usp36
|
UTSW |
11 |
118,167,585 (GRCm39) |
critical splice donor site |
probably null |
|
R3768:Usp36
|
UTSW |
11 |
118,153,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Usp36
|
UTSW |
11 |
118,170,650 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3900:Usp36
|
UTSW |
11 |
118,170,650 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4484:Usp36
|
UTSW |
11 |
118,176,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R4809:Usp36
|
UTSW |
11 |
118,153,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Usp36
|
UTSW |
11 |
118,155,731 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5323:Usp36
|
UTSW |
11 |
118,156,020 (GRCm39) |
missense |
probably benign |
0.21 |
R6226:Usp36
|
UTSW |
11 |
118,168,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6266:Usp36
|
UTSW |
11 |
118,159,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R7191:Usp36
|
UTSW |
11 |
118,159,660 (GRCm39) |
missense |
probably benign |
0.39 |
R7215:Usp36
|
UTSW |
11 |
118,155,980 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7535:Usp36
|
UTSW |
11 |
118,152,872 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7675:Usp36
|
UTSW |
11 |
118,154,522 (GRCm39) |
missense |
probably benign |
0.11 |
R7843:Usp36
|
UTSW |
11 |
118,176,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R8228:Usp36
|
UTSW |
11 |
118,155,716 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8902:Usp36
|
UTSW |
11 |
118,165,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Usp36
|
UTSW |
11 |
118,167,657 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8995:Usp36
|
UTSW |
11 |
118,175,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R9024:Usp36
|
UTSW |
11 |
118,166,983 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9325:Usp36
|
UTSW |
11 |
118,160,031 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9529:Usp36
|
UTSW |
11 |
118,159,461 (GRCm39) |
nonsense |
probably null |
|
R9774:Usp36
|
UTSW |
11 |
118,153,875 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Usp36
|
UTSW |
11 |
118,164,439 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Usp36
|
UTSW |
11 |
118,167,026 (GRCm39) |
missense |
probably damaging |
1.00 |
|