Incidental Mutation 'R4747:Usp9y'
| ID |
357246 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp9y
|
| Ensembl Gene |
ENSMUSG00000069044 |
| Gene Name |
ubiquitin specific peptidase 9, Y chromosome |
| Synonyms |
Fafl2, Dffry |
| MMRRC Submission |
042029-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.064)
|
| Stock # |
R4747 (G1)
|
| Quality Score |
222 |
|
Status
|
Not validated
|
| Chromosome |
Y |
| Chromosomal Location |
1298961-1459782 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 1391284 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Asparagine
at position 629
(Y629N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000088727
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000091188]
|
| AlphaFold |
F8VPU6 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000091188
AA Change: Y629N
PolyPhen 2
Score 0.638 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000088727
Gene: ENSMUSG00000069044
AA Change: Y629N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
34 |
48 |
N/A |
INTRINSIC |
|
low complexity region
|
286 |
301 |
N/A |
INTRINSIC |
|
low complexity region
|
973 |
983 |
N/A |
INTRINSIC |
|
low complexity region
|
1089 |
1100 |
N/A |
INTRINSIC |
|
low complexity region
|
1352 |
1363 |
N/A |
INTRINSIC |
|
Pfam:UCH
|
1558 |
1955 |
9.2e-53 |
PFAM |
|
Pfam:UCH_1
|
1559 |
1909 |
4e-22 |
PFAM |
|
low complexity region
|
1959 |
1971 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.4%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the peptidase C19 family. It encodes a protein that is similar to ubiquitin-specific proteases, which cleave the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. [provided by RefSeq, Mar 2009]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 95 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933402D24Rik |
A |
G |
1: 63,795,568 (GRCm39) |
|
probably benign |
Het |
| Acadvl |
G |
T |
11: 69,903,334 (GRCm39) |
N340K |
probably damaging |
Het |
| Adgrl4 |
T |
A |
3: 151,213,077 (GRCm39) |
N372K |
probably benign |
Het |
| Adh1 |
G |
A |
3: 137,994,642 (GRCm39) |
G321S |
probably damaging |
Het |
| Ankrd26 |
G |
T |
6: 118,504,718 (GRCm39) |
N730K |
probably benign |
Het |
| Aoc2 |
A |
T |
11: 101,219,646 (GRCm39) |
|
probably null |
Het |
| Arhgef4 |
A |
G |
1: 34,762,355 (GRCm39) |
E537G |
unknown |
Het |
| Ccdc7b |
T |
C |
8: 129,904,716 (GRCm39) |
V118A |
probably benign |
Het |
| Ccdc88b |
T |
A |
19: 6,833,509 (GRCm39) |
R219W |
probably damaging |
Het |
| Ccdc97 |
T |
C |
7: 25,418,348 (GRCm39) |
|
probably null |
Het |
| Cfhr4 |
A |
T |
1: 139,625,922 (GRCm39) |
C792S |
probably damaging |
Het |
| Ciao3 |
A |
T |
17: 25,999,327 (GRCm39) |
Y247F |
probably benign |
Het |
| Cnot1 |
T |
C |
8: 96,501,310 (GRCm39) |
N86S |
probably benign |
Het |
| Comp |
T |
C |
8: 70,829,352 (GRCm39) |
C310R |
probably damaging |
Het |
| Crtc2 |
A |
T |
3: 90,167,518 (GRCm39) |
N281Y |
probably damaging |
Het |
| Cryl1 |
T |
C |
14: 57,550,559 (GRCm39) |
K102E |
probably damaging |
Het |
| Csf2ra |
G |
A |
19: 61,214,491 (GRCm39) |
R225* |
probably null |
Het |
| Dao |
A |
T |
5: 114,150,693 (GRCm39) |
D99V |
probably benign |
Het |
| Dgkd |
A |
G |
1: 87,861,889 (GRCm39) |
T815A |
probably damaging |
Het |
| Dhrs7 |
T |
C |
12: 72,699,892 (GRCm39) |
T247A |
probably benign |
Het |
| Dnah7c |
G |
C |
1: 46,572,328 (GRCm39) |
D934H |
probably damaging |
Het |
| Dnajc15 |
T |
C |
14: 78,081,896 (GRCm39) |
Y82C |
probably benign |
Het |
| Dnajc4 |
T |
C |
19: 6,966,872 (GRCm39) |
Q152R |
probably damaging |
Het |
| Dsc1 |
T |
C |
18: 20,227,615 (GRCm39) |
K541R |
probably damaging |
Het |
| Elp4 |
G |
A |
2: 105,624,952 (GRCm39) |
R196C |
probably damaging |
Het |
| Epha8 |
GC |
G |
4: 136,666,006 (GRCm39) |
|
probably null |
Het |
| Ercc6 |
T |
C |
14: 32,291,864 (GRCm39) |
V1076A |
probably benign |
Het |
| Fgd4 |
T |
C |
16: 16,241,793 (GRCm39) |
Y677C |
probably damaging |
Het |
| Fndc3b |
C |
A |
3: 27,483,114 (GRCm39) |
C1028F |
probably damaging |
Het |
| Folr1 |
T |
A |
7: 101,513,184 (GRCm39) |
D37V |
probably damaging |
Het |
| Gabrr3 |
T |
A |
16: 59,268,277 (GRCm39) |
|
probably null |
Het |
| Garem1 |
C |
A |
18: 21,263,000 (GRCm39) |
V605L |
probably benign |
Het |
| Gbp7 |
A |
T |
3: 142,248,778 (GRCm39) |
D347V |
probably damaging |
Het |
| Gdpd4 |
A |
G |
7: 97,610,840 (GRCm39) |
T87A |
possibly damaging |
Het |
| Gm12258 |
C |
A |
11: 58,750,422 (GRCm39) |
H532Q |
probably damaging |
Het |
| Herc2 |
A |
G |
7: 55,756,141 (GRCm39) |
E727G |
possibly damaging |
Het |
| Hfm1 |
G |
A |
5: 107,065,389 (GRCm39) |
H97Y |
probably benign |
Het |
| Idua |
G |
T |
5: 108,828,902 (GRCm39) |
R335L |
probably damaging |
Het |
| Ifi207 |
A |
G |
1: 173,556,633 (GRCm39) |
S702P |
probably benign |
Het |
| Kif16b |
A |
T |
2: 142,699,346 (GRCm39) |
V78D |
probably damaging |
Het |
| Klra17 |
T |
A |
6: 129,849,232 (GRCm39) |
D114V |
probably damaging |
Het |
| Krt76 |
A |
G |
15: 101,794,180 (GRCm39) |
S481P |
probably damaging |
Het |
| Lhfpl5 |
A |
G |
17: 28,798,950 (GRCm39) |
D153G |
probably damaging |
Het |
| Med21 |
T |
A |
6: 146,550,700 (GRCm39) |
D70E |
possibly damaging |
Het |
| Mroh3 |
A |
T |
1: 136,113,237 (GRCm39) |
M739K |
probably benign |
Het |
| Myo1a |
A |
G |
10: 127,550,307 (GRCm39) |
E549G |
probably damaging |
Het |
| Neu1 |
A |
G |
17: 35,153,359 (GRCm39) |
D294G |
possibly damaging |
Het |
| Nmur2 |
A |
T |
11: 55,931,105 (GRCm39) |
I202K |
probably benign |
Het |
| Nop2 |
T |
A |
6: 125,114,057 (GRCm39) |
D174E |
probably benign |
Het |
| Ogfr |
A |
T |
2: 180,236,216 (GRCm39) |
H267L |
probably damaging |
Het |
| Or10p1 |
G |
T |
10: 129,444,053 (GRCm39) |
A99E |
possibly damaging |
Het |
| Or5m8 |
A |
G |
2: 85,822,271 (GRCm39) |
T37A |
probably damaging |
Het |
| P2ry13 |
T |
A |
3: 59,117,308 (GRCm39) |
I157F |
probably benign |
Het |
| Pank4 |
T |
C |
4: 155,063,989 (GRCm39) |
V660A |
probably damaging |
Het |
| Pax6 |
C |
A |
2: 105,526,847 (GRCm39) |
P251Q |
probably benign |
Het |
| Pcdhb13 |
T |
C |
18: 37,577,868 (GRCm39) |
Y749H |
probably damaging |
Het |
| Pcdhga3 |
C |
A |
18: 37,809,799 (GRCm39) |
Q751K |
probably benign |
Het |
| Pcnt |
C |
T |
10: 76,272,299 (GRCm39) |
E186K |
possibly damaging |
Het |
| Pecam1 |
A |
T |
11: 106,575,072 (GRCm39) |
F613I |
probably benign |
Het |
| Pias2 |
T |
C |
18: 77,240,488 (GRCm39) |
*615Q |
probably null |
Het |
| Plb1 |
A |
T |
5: 32,507,003 (GRCm39) |
M1193L |
probably benign |
Het |
| Pomgnt1 |
T |
C |
4: 116,013,396 (GRCm39) |
L506P |
probably damaging |
Het |
| Qrfp |
T |
C |
2: 31,698,852 (GRCm39) |
T27A |
probably damaging |
Het |
| Relb |
C |
A |
7: 19,361,847 (GRCm39) |
|
probably null |
Het |
| Resf1 |
A |
T |
6: 149,228,392 (GRCm39) |
E479D |
probably damaging |
Het |
| Rgl1 |
G |
T |
1: 152,400,450 (GRCm39) |
C685* |
probably null |
Het |
| Ric8b |
A |
G |
10: 84,753,628 (GRCm39) |
Y8C |
probably benign |
Het |
| Rrp36 |
G |
A |
17: 46,980,893 (GRCm39) |
A161V |
possibly damaging |
Het |
| Samd9l |
G |
A |
6: 3,375,504 (GRCm39) |
Q586* |
probably null |
Het |
| Sbf1 |
C |
T |
15: 89,186,916 (GRCm39) |
D821N |
probably damaging |
Het |
| Septin8 |
G |
C |
11: 53,427,545 (GRCm39) |
A255P |
probably damaging |
Het |
| Skp2 |
T |
C |
15: 9,113,927 (GRCm39) |
T329A |
possibly damaging |
Het |
| Slc15a2 |
C |
T |
16: 36,592,498 (GRCm39) |
V220M |
probably damaging |
Het |
| Slc25a11 |
T |
A |
11: 70,536,782 (GRCm39) |
T63S |
possibly damaging |
Het |
| Sowahc |
T |
C |
10: 59,058,983 (GRCm39) |
I373T |
probably benign |
Het |
| Sptbn2 |
T |
A |
19: 4,798,182 (GRCm39) |
M1969K |
probably benign |
Het |
| St14 |
G |
A |
9: 31,015,053 (GRCm39) |
T315M |
possibly damaging |
Het |
| Tagap |
G |
A |
17: 8,151,030 (GRCm39) |
R284H |
probably benign |
Het |
| Tdpoz3 |
T |
A |
3: 93,733,476 (GRCm39) |
S50R |
possibly damaging |
Het |
| Thoc5 |
A |
G |
11: 4,854,187 (GRCm39) |
D182G |
probably damaging |
Het |
| Tinag |
A |
G |
9: 76,904,238 (GRCm39) |
V395A |
probably benign |
Het |
| Tmc8 |
A |
G |
11: 117,683,550 (GRCm39) |
S702G |
probably benign |
Het |
| Tmem202 |
A |
G |
9: 59,426,477 (GRCm39) |
S230P |
possibly damaging |
Het |
| Tmem203 |
T |
C |
2: 25,145,764 (GRCm39) |
V28A |
probably benign |
Het |
| Traf3ip1 |
A |
T |
1: 91,455,479 (GRCm39) |
S647C |
probably damaging |
Het |
| Tram1 |
A |
T |
1: 13,659,870 (GRCm39) |
I26N |
probably damaging |
Het |
| Ttc6 |
A |
T |
12: 57,721,478 (GRCm39) |
D989V |
possibly damaging |
Het |
| Ttll6 |
A |
G |
11: 96,036,372 (GRCm39) |
T334A |
possibly damaging |
Het |
| Ttn |
A |
T |
2: 76,750,086 (GRCm39) |
D3654E |
probably damaging |
Het |
| Ufd1 |
T |
G |
16: 18,639,832 (GRCm39) |
V112G |
probably damaging |
Het |
| Vmn2r1 |
A |
G |
3: 63,989,267 (GRCm39) |
I69V |
probably benign |
Het |
| Zfp180 |
A |
T |
7: 23,805,246 (GRCm39) |
Y555F |
probably damaging |
Het |
| Zfp438 |
T |
C |
18: 5,214,403 (GRCm39) |
N185S |
probably benign |
Het |
| Zfp445 |
C |
T |
9: 122,686,215 (GRCm39) |
V15I |
possibly damaging |
Het |
| Zfp462 |
A |
G |
4: 55,013,476 (GRCm39) |
E1814G |
probably benign |
Het |
|
| Other mutations in Usp9y |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
PIT4466001:Usp9y
|
UTSW |
Y |
1,432,197 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0288:Usp9y
|
UTSW |
Y |
1,333,606 (GRCm39) |
splice site |
probably benign |
|
|
R0365:Usp9y
|
UTSW |
Y |
1,364,732 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0386:Usp9y
|
UTSW |
Y |
1,316,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0395:Usp9y
|
UTSW |
Y |
1,340,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0518:Usp9y
|
UTSW |
Y |
1,307,880 (GRCm39) |
missense |
probably benign |
|
|
R0521:Usp9y
|
UTSW |
Y |
1,307,880 (GRCm39) |
missense |
probably benign |
|
|
R0530:Usp9y
|
UTSW |
Y |
1,333,600 (GRCm39) |
splice site |
probably benign |
|
|
R0759:Usp9y
|
UTSW |
Y |
1,299,097 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0849:Usp9y
|
UTSW |
Y |
1,394,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0932:Usp9y
|
UTSW |
Y |
1,315,930 (GRCm39) |
missense |
probably benign |
0.37 |
|
R1018:Usp9y
|
UTSW |
Y |
1,341,414 (GRCm39) |
splice site |
probably benign |
|
|
R1208:Usp9y
|
UTSW |
Y |
1,356,282 (GRCm39) |
missense |
probably benign |
|
|
R1208:Usp9y
|
UTSW |
Y |
1,356,282 (GRCm39) |
missense |
probably benign |
|
|
R1470:Usp9y
|
UTSW |
Y |
1,332,471 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1470:Usp9y
|
UTSW |
Y |
1,332,471 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1730:Usp9y
|
UTSW |
Y |
1,367,093 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1743:Usp9y
|
UTSW |
Y |
1,316,727 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1765:Usp9y
|
UTSW |
Y |
1,384,454 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1775:Usp9y
|
UTSW |
Y |
1,368,089 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1783:Usp9y
|
UTSW |
Y |
1,367,093 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1889:Usp9y
|
UTSW |
Y |
1,448,829 (GRCm39) |
splice site |
probably null |
|
|
R1901:Usp9y
|
UTSW |
Y |
1,303,371 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2081:Usp9y
|
UTSW |
Y |
1,381,277 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R2119:Usp9y
|
UTSW |
Y |
1,303,451 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2357:Usp9y
|
UTSW |
Y |
1,394,050 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R2873:Usp9y
|
UTSW |
Y |
1,310,502 (GRCm39) |
splice site |
probably benign |
|
|
R3938:Usp9y
|
UTSW |
Y |
1,313,741 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4323:Usp9y
|
UTSW |
Y |
1,434,407 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4385:Usp9y
|
UTSW |
Y |
1,304,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4407:Usp9y
|
UTSW |
Y |
1,336,375 (GRCm39) |
missense |
probably benign |
0.16 |
|
R4457:Usp9y
|
UTSW |
Y |
1,394,078 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4823:Usp9y
|
UTSW |
Y |
1,444,559 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4834:Usp9y
|
UTSW |
Y |
1,317,002 (GRCm39) |
missense |
probably benign |
0.32 |
|
R4872:Usp9y
|
UTSW |
Y |
1,307,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4911:Usp9y
|
UTSW |
Y |
1,308,041 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4915:Usp9y
|
UTSW |
Y |
1,316,735 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4962:Usp9y
|
UTSW |
Y |
1,384,336 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5378:Usp9y
|
UTSW |
Y |
1,315,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5422:Usp9y
|
UTSW |
Y |
1,314,676 (GRCm39) |
missense |
probably benign |
|
|
R5432:Usp9y
|
UTSW |
Y |
1,368,022 (GRCm39) |
splice site |
probably null |
|
|
R5442:Usp9y
|
UTSW |
Y |
1,336,467 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5469:Usp9y
|
UTSW |
Y |
1,364,714 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5500:Usp9y
|
UTSW |
Y |
1,341,875 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5729:Usp9y
|
UTSW |
Y |
1,381,339 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5891:Usp9y
|
UTSW |
Y |
1,341,535 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5920:Usp9y
|
UTSW |
Y |
1,316,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5948:Usp9y
|
UTSW |
Y |
1,324,996 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6062:Usp9y
|
UTSW |
Y |
1,454,199 (GRCm39) |
missense |
probably benign |
0.28 |
|
R6265:Usp9y
|
UTSW |
Y |
1,446,843 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6274:Usp9y
|
UTSW |
Y |
1,316,735 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6313:Usp9y
|
UTSW |
Y |
1,385,355 (GRCm39) |
missense |
probably benign |
|
|
R6330:Usp9y
|
UTSW |
Y |
1,340,123 (GRCm39) |
missense |
probably benign |
0.20 |
|
R6471:Usp9y
|
UTSW |
Y |
1,384,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6547:Usp9y
|
UTSW |
Y |
1,444,612 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6791:Usp9y
|
UTSW |
Y |
1,325,042 (GRCm39) |
splice site |
probably null |
|
|
R7194:Usp9y
|
UTSW |
Y |
1,304,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7341:Usp9y
|
UTSW |
Y |
1,315,759 (GRCm39) |
splice site |
probably null |
|
|
R7357:Usp9y
|
UTSW |
Y |
1,333,656 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R7374:Usp9y
|
UTSW |
Y |
1,381,305 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7404:Usp9y
|
UTSW |
Y |
1,341,780 (GRCm39) |
missense |
probably benign |
0.35 |
|
R7481:Usp9y
|
UTSW |
Y |
1,432,180 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7584:Usp9y
|
UTSW |
Y |
1,384,451 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7697:Usp9y
|
UTSW |
Y |
1,316,990 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R7713:Usp9y
|
UTSW |
Y |
1,304,411 (GRCm39) |
nonsense |
probably null |
|
|
R7790:Usp9y
|
UTSW |
Y |
1,444,573 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7900:Usp9y
|
UTSW |
Y |
1,384,354 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R7964:Usp9y
|
UTSW |
Y |
1,316,914 (GRCm39) |
missense |
probably benign |
0.19 |
|
R8396:Usp9y
|
UTSW |
Y |
1,308,034 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R8703:Usp9y
|
UTSW |
Y |
1,356,317 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8776:Usp9y
|
UTSW |
Y |
1,356,320 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8776-TAIL:Usp9y
|
UTSW |
Y |
1,356,320 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8855:Usp9y
|
UTSW |
Y |
1,395,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8866:Usp9y
|
UTSW |
Y |
1,395,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8952:Usp9y
|
UTSW |
Y |
1,332,662 (GRCm39) |
intron |
probably benign |
|
|
R9008:Usp9y
|
UTSW |
Y |
1,434,993 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9011:Usp9y
|
UTSW |
Y |
1,316,978 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9076:Usp9y
|
UTSW |
Y |
1,383,354 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9256:Usp9y
|
UTSW |
Y |
1,356,235 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9332:Usp9y
|
UTSW |
Y |
1,341,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9367:Usp9y
|
UTSW |
Y |
1,324,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9382:Usp9y
|
UTSW |
Y |
1,364,776 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9503:Usp9y
|
UTSW |
Y |
1,316,045 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9515:Usp9y
|
UTSW |
Y |
1,432,188 (GRCm39) |
missense |
probably benign |
0.28 |
|
R9792:Usp9y
|
UTSW |
Y |
1,364,679 (GRCm39) |
missense |
probably benign |
0.16 |
|
R9793:Usp9y
|
UTSW |
Y |
1,364,679 (GRCm39) |
missense |
probably benign |
0.16 |
|
R9795:Usp9y
|
UTSW |
Y |
1,364,679 (GRCm39) |
missense |
probably benign |
0.16 |
|
RF005:Usp9y
|
UTSW |
Y |
1,435,046 (GRCm39) |
missense |
probably benign |
0.43 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAGATGCTACTGTCATTTAACATGC -3'
(R):5'- ACTTATGGTTAGGAGAATACTGGTC -3'
Sequencing Primer
(F):5'- CTATGAAGGCTTGACAGATGCTCC -3'
(R):5'- GGAGAATACTGGTCATATTTTTCTCG -3'
|
| Posted On |
2015-11-11 |
Incidental Mutation