Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
C |
A |
5: 144,981,627 (GRCm39) |
A154E |
probably benign |
Het |
Adamts1 |
C |
A |
16: 85,596,060 (GRCm39) |
A419S |
probably benign |
Het |
Arap2 |
C |
G |
5: 62,761,621 (GRCm39) |
V1702L |
probably benign |
Het |
Arpc1a |
C |
T |
5: 145,034,087 (GRCm39) |
P152S |
probably benign |
Het |
Bbs10 |
T |
A |
10: 111,136,628 (GRCm39) |
C580* |
probably null |
Het |
Bcam |
A |
G |
7: 19,499,376 (GRCm39) |
Y216H |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,081,405 (GRCm39) |
S1016P |
|
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cd86 |
CA |
CAA |
16: 36,426,917 (GRCm39) |
|
probably null |
Het |
Ceacam5 |
T |
A |
7: 17,491,839 (GRCm39) |
|
probably null |
Het |
Cfap57 |
A |
G |
4: 118,446,264 (GRCm39) |
V666A |
probably benign |
Het |
Cntn3 |
A |
G |
6: 102,142,305 (GRCm39) |
F1021L |
probably benign |
Het |
Cr1l |
C |
T |
1: 194,811,497 (GRCm39) |
G119D |
probably benign |
Het |
Fgf10 |
A |
T |
13: 118,851,942 (GRCm39) |
H8L |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,903,436 (GRCm39) |
|
probably null |
Het |
Frem1 |
G |
T |
4: 82,840,493 (GRCm39) |
T1811N |
probably benign |
Het |
Fsd1 |
A |
T |
17: 56,298,356 (GRCm39) |
Q227L |
probably benign |
Het |
Galk2 |
A |
G |
2: 125,738,621 (GRCm39) |
I138M |
probably damaging |
Het |
Igkv8-30 |
A |
G |
6: 70,094,582 (GRCm39) |
V7A |
possibly damaging |
Het |
Katnb1 |
G |
A |
8: 95,824,069 (GRCm39) |
A450T |
probably benign |
Het |
Kif14 |
A |
T |
1: 136,448,995 (GRCm39) |
E1465V |
possibly damaging |
Het |
Klra3 |
A |
T |
6: 130,312,941 (GRCm39) |
|
probably null |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lepr |
A |
G |
4: 101,607,535 (GRCm39) |
N251S |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,263,416 (GRCm39) |
M4379V |
probably benign |
Het |
Lrriq1 |
T |
C |
10: 103,060,826 (GRCm39) |
N92S |
probably benign |
Het |
Map3k13 |
A |
G |
16: 21,745,006 (GRCm39) |
N855S |
probably damaging |
Het |
Marf1 |
T |
A |
16: 13,954,817 (GRCm39) |
D900V |
probably damaging |
Het |
Nckap5l |
A |
T |
15: 99,321,884 (GRCm39) |
M1087K |
probably benign |
Het |
Nlrp9c |
T |
C |
7: 26,084,722 (GRCm39) |
N286D |
probably benign |
Het |
Or12j4 |
T |
C |
7: 140,047,076 (GRCm39) |
*321Q |
probably null |
Het |
Or13c7d |
C |
T |
4: 43,770,691 (GRCm39) |
A107T |
not run |
Het |
Or4k2 |
T |
C |
14: 50,424,153 (GRCm39) |
I175V |
probably benign |
Het |
Or51ah3 |
A |
T |
7: 103,210,598 (GRCm39) |
R305* |
probably null |
Het |
Or5g9 |
C |
T |
2: 85,552,297 (GRCm39) |
P183S |
possibly damaging |
Het |
Or5p72 |
T |
A |
7: 108,022,367 (GRCm39) |
S196R |
probably benign |
Het |
Pcdhga3 |
A |
G |
18: 37,808,980 (GRCm39) |
T478A |
probably benign |
Het |
Pdgfrb |
T |
C |
18: 61,199,587 (GRCm39) |
I385T |
probably benign |
Het |
Poteg |
C |
T |
8: 27,943,305 (GRCm39) |
R192W |
probably benign |
Het |
Prmt2 |
G |
T |
10: 76,061,173 (GRCm39) |
D104E |
probably benign |
Het |
Rgl2 |
T |
C |
17: 34,153,964 (GRCm39) |
F457L |
possibly damaging |
Het |
Rlbp1 |
T |
C |
7: 79,027,090 (GRCm39) |
N190S |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,816,063 (GRCm39) |
D641G |
possibly damaging |
Het |
Sh3gl1 |
A |
T |
17: 56,324,846 (GRCm39) |
M303K |
probably benign |
Het |
Slc26a5 |
A |
G |
5: 22,018,892 (GRCm39) |
V649A |
probably damaging |
Het |
Slco4c1 |
T |
C |
1: 96,765,323 (GRCm39) |
N376D |
possibly damaging |
Het |
Socs3 |
A |
T |
11: 117,858,553 (GRCm39) |
Y168* |
probably null |
Het |
Spata31d1d |
A |
T |
13: 59,876,394 (GRCm39) |
N380K |
possibly damaging |
Het |
Speer1c |
T |
C |
5: 10,295,237 (GRCm39) |
K56E |
probably damaging |
Het |
Ssbp3 |
A |
G |
4: 106,894,843 (GRCm39) |
N254S |
probably benign |
Het |
Stard10 |
C |
T |
7: 100,995,226 (GRCm39) |
S326L |
probably damaging |
Het |
Taf2 |
T |
C |
15: 54,912,135 (GRCm39) |
D524G |
possibly damaging |
Het |
Taf7 |
A |
T |
18: 37,776,053 (GRCm39) |
S171R |
probably damaging |
Het |
Tchh |
C |
T |
3: 93,353,478 (GRCm39) |
R973C |
unknown |
Het |
Tmem67 |
T |
C |
4: 12,077,337 (GRCm39) |
R172G |
possibly damaging |
Het |
Top2a |
C |
A |
11: 98,914,922 (GRCm39) |
|
probably benign |
Het |
Ttc8 |
T |
A |
12: 98,940,960 (GRCm39) |
N323K |
possibly damaging |
Het |
Txnl1 |
T |
C |
18: 63,804,667 (GRCm39) |
N276D |
probably benign |
Het |
Vmn1r18 |
A |
C |
6: 57,366,609 (GRCm39) |
|
probably null |
Het |
Vmn2r53 |
A |
T |
7: 12,315,628 (GRCm39) |
H730Q |
probably benign |
Het |
Wnk1 |
A |
C |
6: 119,947,939 (GRCm39) |
I500M |
probably damaging |
Het |
Zfp335 |
A |
T |
2: 164,744,423 (GRCm39) |
Y451N |
probably damaging |
Het |
Zfp683 |
T |
A |
4: 133,783,064 (GRCm39) |
I176N |
probably damaging |
Het |
|
Other mutations in Usp24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Usp24
|
APN |
4 |
106,216,288 (GRCm39) |
missense |
probably benign |
|
IGL00340:Usp24
|
APN |
4 |
106,258,336 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00480:Usp24
|
APN |
4 |
106,225,303 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00548:Usp24
|
APN |
4 |
106,198,495 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00655:Usp24
|
APN |
4 |
106,247,515 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00674:Usp24
|
APN |
4 |
106,229,876 (GRCm39) |
splice site |
probably benign |
|
IGL00718:Usp24
|
APN |
4 |
106,266,901 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00803:Usp24
|
APN |
4 |
106,242,723 (GRCm39) |
splice site |
probably benign |
|
IGL01161:Usp24
|
APN |
4 |
106,294,041 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01344:Usp24
|
APN |
4 |
106,236,582 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01374:Usp24
|
APN |
4 |
106,237,296 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01485:Usp24
|
APN |
4 |
106,219,429 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01736:Usp24
|
APN |
4 |
106,280,658 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01737:Usp24
|
APN |
4 |
106,244,931 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01862:Usp24
|
APN |
4 |
106,266,095 (GRCm39) |
splice site |
probably benign |
|
IGL01981:Usp24
|
APN |
4 |
106,232,965 (GRCm39) |
splice site |
probably benign |
|
IGL02090:Usp24
|
APN |
4 |
106,268,623 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02275:Usp24
|
APN |
4 |
106,244,690 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02352:Usp24
|
APN |
4 |
106,261,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02359:Usp24
|
APN |
4 |
106,261,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02391:Usp24
|
APN |
4 |
106,264,326 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02418:Usp24
|
APN |
4 |
106,293,557 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02537:Usp24
|
APN |
4 |
106,249,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02638:Usp24
|
APN |
4 |
106,295,969 (GRCm39) |
splice site |
probably benign |
|
IGL02638:Usp24
|
APN |
4 |
106,295,967 (GRCm39) |
splice site |
probably benign |
|
IGL02830:Usp24
|
APN |
4 |
106,204,584 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03125:Usp24
|
APN |
4 |
106,249,599 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03280:Usp24
|
APN |
4 |
106,237,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03350:Usp24
|
APN |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
BB010:Usp24
|
UTSW |
4 |
106,285,686 (GRCm39) |
missense |
probably benign |
|
BB020:Usp24
|
UTSW |
4 |
106,285,686 (GRCm39) |
missense |
probably benign |
|
IGL03098:Usp24
|
UTSW |
4 |
106,228,230 (GRCm39) |
missense |
probably benign |
0.11 |
R0035:Usp24
|
UTSW |
4 |
106,225,224 (GRCm39) |
missense |
probably benign |
0.18 |
R0044:Usp24
|
UTSW |
4 |
106,269,281 (GRCm39) |
splice site |
probably benign |
|
R0086:Usp24
|
UTSW |
4 |
106,249,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0125:Usp24
|
UTSW |
4 |
106,254,496 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0197:Usp24
|
UTSW |
4 |
106,264,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Usp24
|
UTSW |
4 |
106,271,601 (GRCm39) |
nonsense |
probably null |
|
R0240:Usp24
|
UTSW |
4 |
106,271,601 (GRCm39) |
nonsense |
probably null |
|
R0491:Usp24
|
UTSW |
4 |
106,259,302 (GRCm39) |
missense |
probably benign |
0.41 |
R0687:Usp24
|
UTSW |
4 |
106,277,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Usp24
|
UTSW |
4 |
106,270,875 (GRCm39) |
splice site |
probably null |
|
R0973:Usp24
|
UTSW |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
R0973:Usp24
|
UTSW |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
R0974:Usp24
|
UTSW |
4 |
106,270,875 (GRCm39) |
splice site |
probably null |
|
R0974:Usp24
|
UTSW |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
R1163:Usp24
|
UTSW |
4 |
106,278,157 (GRCm39) |
missense |
probably benign |
|
R1293:Usp24
|
UTSW |
4 |
106,280,750 (GRCm39) |
missense |
probably benign |
0.19 |
R1333:Usp24
|
UTSW |
4 |
106,199,550 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1476:Usp24
|
UTSW |
4 |
106,219,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Usp24
|
UTSW |
4 |
106,296,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R1728:Usp24
|
UTSW |
4 |
106,217,618 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1729:Usp24
|
UTSW |
4 |
106,217,618 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1753:Usp24
|
UTSW |
4 |
106,234,756 (GRCm39) |
missense |
probably benign |
0.04 |
R1917:Usp24
|
UTSW |
4 |
106,267,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Usp24
|
UTSW |
4 |
106,258,177 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2424:Usp24
|
UTSW |
4 |
106,256,310 (GRCm39) |
critical splice donor site |
probably null |
|
R2436:Usp24
|
UTSW |
4 |
106,266,842 (GRCm39) |
nonsense |
probably null |
|
R2513:Usp24
|
UTSW |
4 |
106,236,602 (GRCm39) |
splice site |
probably null |
|
R3824:Usp24
|
UTSW |
4 |
106,236,263 (GRCm39) |
missense |
probably benign |
|
R3831:Usp24
|
UTSW |
4 |
106,219,209 (GRCm39) |
critical splice donor site |
probably null |
|
R3833:Usp24
|
UTSW |
4 |
106,219,209 (GRCm39) |
critical splice donor site |
probably null |
|
R3982:Usp24
|
UTSW |
4 |
106,245,080 (GRCm39) |
missense |
probably benign |
0.38 |
R4022:Usp24
|
UTSW |
4 |
106,236,421 (GRCm39) |
splice site |
probably benign |
|
R4067:Usp24
|
UTSW |
4 |
106,216,286 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4175:Usp24
|
UTSW |
4 |
106,173,970 (GRCm39) |
missense |
probably benign |
0.00 |
R4766:Usp24
|
UTSW |
4 |
106,273,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Usp24
|
UTSW |
4 |
106,219,377 (GRCm39) |
splice site |
probably null |
|
R4798:Usp24
|
UTSW |
4 |
106,217,359 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4809:Usp24
|
UTSW |
4 |
106,270,873 (GRCm39) |
critical splice donor site |
probably null |
|
R4822:Usp24
|
UTSW |
4 |
106,273,244 (GRCm39) |
missense |
probably damaging |
0.98 |
R4906:Usp24
|
UTSW |
4 |
106,245,834 (GRCm39) |
missense |
probably benign |
0.20 |
R4934:Usp24
|
UTSW |
4 |
106,283,743 (GRCm39) |
missense |
probably benign |
0.29 |
R5074:Usp24
|
UTSW |
4 |
106,277,644 (GRCm39) |
missense |
probably benign |
0.12 |
R5151:Usp24
|
UTSW |
4 |
106,256,309 (GRCm39) |
critical splice donor site |
probably null |
|
R5220:Usp24
|
UTSW |
4 |
106,239,500 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5279:Usp24
|
UTSW |
4 |
106,242,621 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5280:Usp24
|
UTSW |
4 |
106,198,411 (GRCm39) |
missense |
probably benign |
0.18 |
R5285:Usp24
|
UTSW |
4 |
106,264,230 (GRCm39) |
missense |
probably benign |
0.00 |
R5292:Usp24
|
UTSW |
4 |
106,275,460 (GRCm39) |
missense |
probably benign |
0.06 |
R5294:Usp24
|
UTSW |
4 |
106,219,554 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5394:Usp24
|
UTSW |
4 |
106,265,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Usp24
|
UTSW |
4 |
106,232,871 (GRCm39) |
missense |
probably benign |
0.02 |
R5522:Usp24
|
UTSW |
4 |
106,229,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Usp24
|
UTSW |
4 |
106,273,244 (GRCm39) |
missense |
probably damaging |
0.98 |
R5756:Usp24
|
UTSW |
4 |
106,219,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Usp24
|
UTSW |
4 |
106,237,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R5972:Usp24
|
UTSW |
4 |
106,225,264 (GRCm39) |
missense |
probably damaging |
0.98 |
R6285:Usp24
|
UTSW |
4 |
106,231,297 (GRCm39) |
splice site |
probably null |
|
R6370:Usp24
|
UTSW |
4 |
106,237,718 (GRCm39) |
missense |
probably null |
0.20 |
R6630:Usp24
|
UTSW |
4 |
106,245,032 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6754:Usp24
|
UTSW |
4 |
106,217,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Usp24
|
UTSW |
4 |
106,219,441 (GRCm39) |
missense |
probably benign |
0.21 |
R7088:Usp24
|
UTSW |
4 |
106,244,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R7129:Usp24
|
UTSW |
4 |
106,219,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Usp24
|
UTSW |
4 |
106,239,500 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7156:Usp24
|
UTSW |
4 |
106,245,116 (GRCm39) |
critical splice donor site |
probably null |
|
R7236:Usp24
|
UTSW |
4 |
106,263,502 (GRCm39) |
splice site |
probably null |
|
R7403:Usp24
|
UTSW |
4 |
106,264,232 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7424:Usp24
|
UTSW |
4 |
106,236,304 (GRCm39) |
missense |
probably benign |
0.00 |
R7475:Usp24
|
UTSW |
4 |
106,199,550 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7505:Usp24
|
UTSW |
4 |
106,236,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Usp24
|
UTSW |
4 |
106,173,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Usp24
|
UTSW |
4 |
106,266,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Usp24
|
UTSW |
4 |
106,285,686 (GRCm39) |
missense |
probably benign |
|
R7940:Usp24
|
UTSW |
4 |
106,287,741 (GRCm39) |
missense |
probably damaging |
0.98 |
R8271:Usp24
|
UTSW |
4 |
106,285,711 (GRCm39) |
missense |
probably damaging |
0.98 |
R8348:Usp24
|
UTSW |
4 |
106,225,933 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8448:Usp24
|
UTSW |
4 |
106,225,933 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8483:Usp24
|
UTSW |
4 |
106,230,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8546:Usp24
|
UTSW |
4 |
106,259,326 (GRCm39) |
missense |
probably benign |
0.01 |
R8798:Usp24
|
UTSW |
4 |
106,236,436 (GRCm39) |
missense |
probably benign |
0.00 |
R8822:Usp24
|
UTSW |
4 |
106,269,410 (GRCm39) |
missense |
probably benign |
0.17 |
R8992:Usp24
|
UTSW |
4 |
106,234,762 (GRCm39) |
missense |
probably benign |
0.36 |
R9002:Usp24
|
UTSW |
4 |
106,275,412 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9037:Usp24
|
UTSW |
4 |
106,236,251 (GRCm39) |
missense |
probably damaging |
0.99 |
R9068:Usp24
|
UTSW |
4 |
106,232,875 (GRCm39) |
missense |
probably benign |
0.09 |
R9096:Usp24
|
UTSW |
4 |
106,254,508 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Usp24
|
UTSW |
4 |
106,216,247 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9199:Usp24
|
UTSW |
4 |
106,244,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Usp24
|
UTSW |
4 |
106,277,727 (GRCm39) |
missense |
probably benign |
0.36 |
R9251:Usp24
|
UTSW |
4 |
106,217,715 (GRCm39) |
missense |
probably benign |
0.19 |
R9423:Usp24
|
UTSW |
4 |
106,288,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9459:Usp24
|
UTSW |
4 |
106,199,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Usp24
|
UTSW |
4 |
106,261,128 (GRCm39) |
missense |
probably benign |
0.00 |
R9483:Usp24
|
UTSW |
4 |
106,219,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R9534:Usp24
|
UTSW |
4 |
106,264,312 (GRCm39) |
missense |
probably damaging |
0.97 |
R9653:Usp24
|
UTSW |
4 |
106,204,564 (GRCm39) |
missense |
probably benign |
0.03 |
R9712:Usp24
|
UTSW |
4 |
106,204,564 (GRCm39) |
missense |
probably benign |
0.03 |
X0024:Usp24
|
UTSW |
4 |
106,217,643 (GRCm39) |
missense |
probably benign |
0.09 |
X0028:Usp24
|
UTSW |
4 |
106,225,252 (GRCm39) |
missense |
probably benign |
0.01 |
X0066:Usp24
|
UTSW |
4 |
106,212,928 (GRCm39) |
missense |
possibly damaging |
0.82 |
|