Incidental Mutation 'R4018:Usp34'
ID |
312021 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Usp34
|
Ensembl Gene |
ENSMUSG00000056342 |
Gene Name |
ubiquitin specific peptidase 34 |
Synonyms |
Murr2, A530081C03Rik |
MMRRC Submission |
040848-MU
|
Accession Numbers |
|
Is this an essential gene? |
Possibly essential
(E-score: 0.671)
|
Stock # |
R4018 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
23306895-23490560 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 23489033 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Serine
at position 3532
(P3532S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000137430
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020529]
[ENSMUST00000109539]
[ENSMUST00000128559]
[ENSMUST00000129368]
[ENSMUST00000147157]
[ENSMUST00000180046]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000020529
|
SMART Domains |
Protein: ENSMUSP00000020529 Gene: ENSMUSG00000020288
Domain | Start | End | E-Value | Type |
Aha1_N
|
29 |
163 |
2.52e-57 |
SMART |
Pfam:AHSA1
|
209 |
325 |
1.4e-23 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000109539
|
SMART Domains |
Protein: ENSMUSP00000105166 Gene: ENSMUSG00000020288
Domain | Start | End | E-Value | Type |
Aha1_N
|
2 |
115 |
2.33e-38 |
SMART |
Pfam:AHSA1
|
161 |
277 |
4.3e-22 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000122864
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124801
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125701
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000128372
|
SMART Domains |
Protein: ENSMUSP00000121255 Gene: ENSMUSG00000020288
Domain | Start | End | E-Value | Type |
Aha1_N
|
15 |
149 |
2.52e-57 |
SMART |
Pfam:AHSA1
|
195 |
311 |
7.5e-23 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000128559
|
SMART Domains |
Protein: ENSMUSP00000115134 Gene: ENSMUSG00000020288
Domain | Start | End | E-Value | Type |
Aha1_N
|
29 |
159 |
1.59e-54 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000129368
|
SMART Domains |
Protein: ENSMUSP00000121426 Gene: ENSMUSG00000056342
Domain | Start | End | E-Value | Type |
Blast:Drf_GBD
|
2 |
86 |
1e-19 |
BLAST |
low complexity region
|
231 |
244 |
N/A |
INTRINSIC |
coiled coil region
|
259 |
281 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000137823
AA Change: P3551S
|
SMART Domains |
Protein: ENSMUSP00000120747 Gene: ENSMUSG00000056342 AA Change: P3551S
Domain | Start | End | E-Value | Type |
low complexity region
|
489 |
500 |
N/A |
INTRINSIC |
low complexity region
|
530 |
544 |
N/A |
INTRINSIC |
low complexity region
|
591 |
610 |
N/A |
INTRINSIC |
coiled coil region
|
626 |
671 |
N/A |
INTRINSIC |
low complexity region
|
827 |
842 |
N/A |
INTRINSIC |
low complexity region
|
1207 |
1218 |
N/A |
INTRINSIC |
low complexity region
|
1399 |
1410 |
N/A |
INTRINSIC |
low complexity region
|
1518 |
1532 |
N/A |
INTRINSIC |
low complexity region
|
1751 |
1764 |
N/A |
INTRINSIC |
low complexity region
|
1812 |
1824 |
N/A |
INTRINSIC |
Pfam:UCH
|
1950 |
2293 |
7.6e-44 |
PFAM |
Pfam:UCH_1
|
1951 |
2249 |
3.6e-22 |
PFAM |
low complexity region
|
2542 |
2564 |
N/A |
INTRINSIC |
low complexity region
|
2672 |
2679 |
N/A |
INTRINSIC |
Blast:Drf_GBD
|
2943 |
3116 |
3e-53 |
BLAST |
low complexity region
|
3344 |
3357 |
N/A |
INTRINSIC |
coiled coil region
|
3371 |
3393 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000147157
|
SMART Domains |
Protein: ENSMUSP00000121920 Gene: ENSMUSG00000020288
Domain | Start | End | E-Value | Type |
Aha1_N
|
29 |
138 |
4.15e-26 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153409
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000180046
AA Change: P3532S
PolyPhen 2
Score 0.852 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000137430 Gene: ENSMUSG00000056342 AA Change: P3532S
Domain | Start | End | E-Value | Type |
low complexity region
|
469 |
480 |
N/A |
INTRINSIC |
low complexity region
|
510 |
524 |
N/A |
INTRINSIC |
low complexity region
|
571 |
590 |
N/A |
INTRINSIC |
coiled coil region
|
607 |
652 |
N/A |
INTRINSIC |
low complexity region
|
807 |
822 |
N/A |
INTRINSIC |
low complexity region
|
1187 |
1198 |
N/A |
INTRINSIC |
low complexity region
|
1379 |
1390 |
N/A |
INTRINSIC |
low complexity region
|
1498 |
1512 |
N/A |
INTRINSIC |
low complexity region
|
1731 |
1744 |
N/A |
INTRINSIC |
low complexity region
|
1792 |
1804 |
N/A |
INTRINSIC |
Pfam:UCH
|
1930 |
2273 |
2.3e-44 |
PFAM |
Pfam:UCH_1
|
1931 |
2229 |
1.1e-22 |
PFAM |
low complexity region
|
2522 |
2544 |
N/A |
INTRINSIC |
low complexity region
|
2652 |
2659 |
N/A |
INTRINSIC |
Blast:Drf_GBD
|
2923 |
3096 |
2e-53 |
BLAST |
low complexity region
|
3324 |
3337 |
N/A |
INTRINSIC |
coiled coil region
|
3352 |
3374 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0845  |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 92.4%
|
Validation Efficiency |
100% (33/33) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aga |
A |
G |
8: 53,523,191 |
K319R |
probably benign |
Het |
Brip1 |
G |
T |
11: 86,138,851 |
T619K |
possibly damaging |
Het |
Cd300ld2 |
G |
T |
11: 115,012,504 |
|
probably benign |
Het |
Cd300lg |
A |
G |
11: 102,041,594 |
R2G |
probably damaging |
Het |
Celsr2 |
C |
T |
3: 108,394,965 |
V2616I |
possibly damaging |
Het |
Edem3 |
C |
T |
1: 151,804,826 |
|
probably benign |
Het |
Endou |
T |
A |
15: 97,718,937 |
K235M |
probably damaging |
Het |
Gm5431 |
T |
A |
11: 48,889,168 |
N309I |
probably damaging |
Het |
Il4 |
T |
A |
11: 53,613,979 |
|
probably benign |
Het |
Iws1 |
C |
A |
18: 32,070,152 |
S27* |
probably null |
Het |
Kdm5d |
T |
C |
Y: 910,441 |
|
probably benign |
Het |
Ldb3 |
T |
C |
14: 34,552,171 |
|
probably benign |
Het |
Llgl2 |
A |
G |
11: 115,847,612 |
T284A |
probably benign |
Het |
Maml1 |
A |
T |
11: 50,265,784 |
N521K |
probably damaging |
Het |
Mlxipl |
T |
C |
5: 135,132,672 |
Y482H |
probably damaging |
Het |
Notch2 |
G |
T |
3: 98,104,565 |
C633F |
probably damaging |
Het |
Oc90 |
T |
C |
15: 65,887,608 |
D232G |
probably benign |
Het |
Olfr1453 |
T |
C |
19: 13,027,825 |
E168G |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,735,059 |
Y1717C |
unknown |
Het |
Prkca |
T |
A |
11: 107,939,602 |
I221F |
probably damaging |
Het |
Rab3c |
T |
A |
13: 110,084,194 |
K144N |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,918,414 |
N57I |
probably damaging |
Het |
Scyl3 |
A |
G |
1: 163,936,499 |
T145A |
possibly damaging |
Het |
Sept4 |
G |
A |
11: 87,585,121 |
R162Q |
probably damaging |
Het |
Slc25a39 |
A |
T |
11: 102,405,024 |
L127H |
probably damaging |
Het |
Slc9a9 |
T |
C |
9: 94,685,163 |
V95A |
probably benign |
Het |
Tsc2 |
T |
C |
17: 24,625,281 |
I279V |
probably damaging |
Het |
Vmn2r6 |
T |
C |
3: 64,556,472 |
I314V |
probably benign |
Het |
Wdr66 |
A |
G |
5: 123,322,454 |
I1160V |
probably benign |
Het |
|
Other mutations in Usp34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Usp34
|
APN |
11 |
23436020 |
missense |
probably damaging |
0.98 |
IGL00477:Usp34
|
APN |
11 |
23468879 |
missense |
probably damaging |
0.99 |
IGL01307:Usp34
|
APN |
11 |
23417676 |
missense |
probably damaging |
0.99 |
IGL01313:Usp34
|
APN |
11 |
23473206 |
missense |
probably damaging |
1.00 |
IGL01794:Usp34
|
APN |
11 |
23436020 |
missense |
probably damaging |
0.98 |
IGL01826:Usp34
|
APN |
11 |
23436020 |
missense |
probably damaging |
0.98 |
IGL01827:Usp34
|
APN |
11 |
23436020 |
missense |
probably damaging |
0.98 |
IGL01830:Usp34
|
APN |
11 |
23436020 |
missense |
probably damaging |
0.98 |
IGL01867:Usp34
|
APN |
11 |
23384411 |
missense |
possibly damaging |
0.77 |
IGL01939:Usp34
|
APN |
11 |
23345141 |
splice site |
probably benign |
|
IGL01977:Usp34
|
APN |
11 |
23452661 |
missense |
probably damaging |
1.00 |
IGL01985:Usp34
|
APN |
11 |
23452565 |
missense |
probably damaging |
1.00 |
IGL02011:Usp34
|
APN |
11 |
23471554 |
missense |
probably damaging |
0.99 |
IGL02302:Usp34
|
APN |
11 |
23467243 |
missense |
possibly damaging |
0.91 |
IGL02423:Usp34
|
APN |
11 |
23354900 |
missense |
probably benign |
0.11 |
IGL02491:Usp34
|
APN |
11 |
23432630 |
missense |
probably damaging |
0.98 |
IGL02532:Usp34
|
APN |
11 |
23370291 |
missense |
probably damaging |
0.99 |
IGL02561:Usp34
|
APN |
11 |
23351652 |
missense |
probably benign |
0.09 |
IGL02706:Usp34
|
APN |
11 |
23388659 |
splice site |
probably benign |
|
IGL02891:Usp34
|
APN |
11 |
23487166 |
missense |
probably benign |
0.09 |
IGL03079:Usp34
|
APN |
11 |
23432247 |
missense |
possibly damaging |
0.48 |
IGL03089:Usp34
|
APN |
11 |
23446958 |
missense |
possibly damaging |
0.84 |
IGL03175:Usp34
|
APN |
11 |
23488686 |
missense |
probably benign |
|
IGL03256:Usp34
|
APN |
11 |
23420090 |
nonsense |
probably null |
|
IGL03280:Usp34
|
APN |
11 |
23354897 |
missense |
probably damaging |
1.00 |
IGL03289:Usp34
|
APN |
11 |
23393818 |
missense |
possibly damaging |
0.94 |
IGL03408:Usp34
|
APN |
11 |
23446957 |
missense |
possibly damaging |
0.92 |
Chub
|
UTSW |
11 |
23464686 |
missense |
probably damaging |
0.99 |
Cicione
|
UTSW |
11 |
23489033 |
missense |
possibly damaging |
0.85 |
R5571_Usp34_680
|
UTSW |
11 |
23457975 |
missense |
probably damaging |
0.99 |
R5713_Usp34_003
|
UTSW |
11 |
23343515 |
missense |
possibly damaging |
0.94 |
Roebuck
|
UTSW |
11 |
23486810 |
splice site |
probably benign |
|
stoat
|
UTSW |
11 |
23487203 |
missense |
|
|
tunnelvision
|
UTSW |
11 |
23446968 |
missense |
|
|
I2288:Usp34
|
UTSW |
11 |
23432473 |
splice site |
probably benign |
|
R0047:Usp34
|
UTSW |
11 |
23464403 |
missense |
probably benign |
0.34 |
R0047:Usp34
|
UTSW |
11 |
23464403 |
missense |
probably benign |
0.34 |
R0099:Usp34
|
UTSW |
11 |
23363111 |
missense |
probably damaging |
1.00 |
R0240:Usp34
|
UTSW |
11 |
23433206 |
missense |
probably damaging |
0.99 |
R0240:Usp34
|
UTSW |
11 |
23433206 |
missense |
probably damaging |
0.99 |
R0403:Usp34
|
UTSW |
11 |
23333838 |
missense |
possibly damaging |
0.82 |
R0432:Usp34
|
UTSW |
11 |
23401505 |
missense |
probably damaging |
0.99 |
R0446:Usp34
|
UTSW |
11 |
23467207 |
missense |
probably damaging |
0.97 |
R0455:Usp34
|
UTSW |
11 |
23446741 |
splice site |
probably benign |
|
R0470:Usp34
|
UTSW |
11 |
23436001 |
missense |
possibly damaging |
0.94 |
R0472:Usp34
|
UTSW |
11 |
23384509 |
splice site |
probably benign |
|
R0512:Usp34
|
UTSW |
11 |
23451997 |
missense |
probably benign |
0.04 |
R0557:Usp34
|
UTSW |
11 |
23403848 |
missense |
probably damaging |
0.98 |
R0562:Usp34
|
UTSW |
11 |
23432406 |
splice site |
probably benign |
|
R0656:Usp34
|
UTSW |
11 |
23472967 |
missense |
probably damaging |
0.99 |
R0693:Usp34
|
UTSW |
11 |
23452637 |
missense |
probably damaging |
0.97 |
R0739:Usp34
|
UTSW |
11 |
23467243 |
missense |
possibly damaging |
0.91 |
R1061:Usp34
|
UTSW |
11 |
23384420 |
missense |
possibly damaging |
0.51 |
R1078:Usp34
|
UTSW |
11 |
23433175 |
splice site |
probably benign |
|
R1223:Usp34
|
UTSW |
11 |
23446464 |
splice site |
probably null |
|
R1295:Usp34
|
UTSW |
11 |
23384477 |
missense |
probably damaging |
1.00 |
R1430:Usp34
|
UTSW |
11 |
23459151 |
missense |
probably damaging |
0.97 |
R1445:Usp34
|
UTSW |
11 |
23351629 |
missense |
probably damaging |
0.99 |
R1468:Usp34
|
UTSW |
11 |
23441171 |
missense |
probably damaging |
1.00 |
R1468:Usp34
|
UTSW |
11 |
23441171 |
missense |
probably damaging |
1.00 |
R1471:Usp34
|
UTSW |
11 |
23488862 |
missense |
probably benign |
0.20 |
R1475:Usp34
|
UTSW |
11 |
23473253 |
missense |
probably damaging |
0.99 |
R1628:Usp34
|
UTSW |
11 |
23488725 |
missense |
probably damaging |
1.00 |
R1631:Usp34
|
UTSW |
11 |
23460651 |
missense |
probably damaging |
0.99 |
R1655:Usp34
|
UTSW |
11 |
23375051 |
missense |
probably benign |
0.05 |
R1741:Usp34
|
UTSW |
11 |
23364103 |
missense |
probably benign |
0.00 |
R1854:Usp34
|
UTSW |
11 |
23426153 |
missense |
probably benign |
0.24 |
R1867:Usp34
|
UTSW |
11 |
23361593 |
missense |
possibly damaging |
0.82 |
R1869:Usp34
|
UTSW |
11 |
23364479 |
missense |
probably benign |
0.37 |
R1870:Usp34
|
UTSW |
11 |
23364479 |
missense |
probably benign |
0.37 |
R1871:Usp34
|
UTSW |
11 |
23364479 |
missense |
probably benign |
0.37 |
R1967:Usp34
|
UTSW |
11 |
23364503 |
missense |
probably benign |
0.01 |
R2051:Usp34
|
UTSW |
11 |
23464468 |
missense |
probably damaging |
0.97 |
R2132:Usp34
|
UTSW |
11 |
23464556 |
missense |
possibly damaging |
0.95 |
R2156:Usp34
|
UTSW |
11 |
23382602 |
missense |
probably damaging |
0.98 |
R2205:Usp34
|
UTSW |
11 |
23385147 |
missense |
probably damaging |
0.97 |
R2342:Usp34
|
UTSW |
11 |
23403599 |
missense |
possibly damaging |
0.46 |
R3431:Usp34
|
UTSW |
11 |
23370466 |
missense |
possibly damaging |
0.95 |
R3812:Usp34
|
UTSW |
11 |
23464517 |
missense |
possibly damaging |
0.94 |
R3872:Usp34
|
UTSW |
11 |
23489033 |
missense |
possibly damaging |
0.85 |
R3873:Usp34
|
UTSW |
11 |
23489033 |
missense |
possibly damaging |
0.85 |
R3874:Usp34
|
UTSW |
11 |
23489033 |
missense |
possibly damaging |
0.85 |
R3875:Usp34
|
UTSW |
11 |
23489033 |
missense |
possibly damaging |
0.85 |
R3925:Usp34
|
UTSW |
11 |
23343640 |
missense |
probably benign |
0.28 |
R3972:Usp34
|
UTSW |
11 |
23457803 |
missense |
probably damaging |
1.00 |
R4042:Usp34
|
UTSW |
11 |
23489033 |
missense |
possibly damaging |
0.85 |
R4155:Usp34
|
UTSW |
11 |
23417676 |
missense |
probably damaging |
0.99 |
R4197:Usp34
|
UTSW |
11 |
23444189 |
missense |
probably damaging |
0.98 |
R4352:Usp34
|
UTSW |
11 |
23320727 |
missense |
possibly damaging |
0.73 |
R4379:Usp34
|
UTSW |
11 |
23384499 |
missense |
possibly damaging |
0.52 |
R4444:Usp34
|
UTSW |
11 |
23435998 |
missense |
probably damaging |
0.98 |
R4475:Usp34
|
UTSW |
11 |
23457975 |
missense |
possibly damaging |
0.95 |
R4501:Usp34
|
UTSW |
11 |
23401529 |
missense |
probably damaging |
1.00 |
R4527:Usp34
|
UTSW |
11 |
23421257 |
missense |
possibly damaging |
0.57 |
R4603:Usp34
|
UTSW |
11 |
23464633 |
missense |
probably damaging |
0.97 |
R4612:Usp34
|
UTSW |
11 |
23432268 |
missense |
probably damaging |
0.99 |
R4673:Usp34
|
UTSW |
11 |
23364480 |
small deletion |
probably benign |
|
R4707:Usp34
|
UTSW |
11 |
23487215 |
missense |
probably damaging |
1.00 |
R4736:Usp34
|
UTSW |
11 |
23393749 |
splice site |
probably null |
|
R4867:Usp34
|
UTSW |
11 |
23451999 |
missense |
probably benign |
0.28 |
R4879:Usp34
|
UTSW |
11 |
23373410 |
missense |
possibly damaging |
0.94 |
R4977:Usp34
|
UTSW |
11 |
23488982 |
missense |
probably damaging |
1.00 |
R5004:Usp34
|
UTSW |
11 |
23464586 |
missense |
probably damaging |
1.00 |
R5057:Usp34
|
UTSW |
11 |
23458086 |
intron |
probably benign |
|
R5068:Usp34
|
UTSW |
11 |
23460665 |
missense |
possibly damaging |
0.94 |
R5304:Usp34
|
UTSW |
11 |
23343616 |
missense |
probably damaging |
1.00 |
R5320:Usp34
|
UTSW |
11 |
23333739 |
missense |
probably benign |
|
R5327:Usp34
|
UTSW |
11 |
23468846 |
missense |
probably damaging |
1.00 |
R5328:Usp34
|
UTSW |
11 |
23464616 |
missense |
probably benign |
0.01 |
R5328:Usp34
|
UTSW |
11 |
23488659 |
missense |
probably benign |
0.04 |
R5390:Usp34
|
UTSW |
11 |
23444202 |
critical splice donor site |
probably null |
|
R5434:Usp34
|
UTSW |
11 |
23412271 |
missense |
probably damaging |
0.99 |
R5523:Usp34
|
UTSW |
11 |
23349198 |
missense |
probably benign |
0.39 |
R5567:Usp34
|
UTSW |
11 |
23488336 |
missense |
probably damaging |
0.97 |
R5571:Usp34
|
UTSW |
11 |
23457975 |
missense |
probably damaging |
0.99 |
R5645:Usp34
|
UTSW |
11 |
23375024 |
missense |
possibly damaging |
0.86 |
R5713:Usp34
|
UTSW |
11 |
23343515 |
missense |
possibly damaging |
0.94 |
R5719:Usp34
|
UTSW |
11 |
23354846 |
missense |
probably benign |
0.00 |
R5813:Usp34
|
UTSW |
11 |
23421340 |
missense |
probably benign |
0.38 |
R5921:Usp34
|
UTSW |
11 |
23464686 |
missense |
probably damaging |
0.99 |
R5928:Usp34
|
UTSW |
11 |
23436040 |
missense |
probably damaging |
0.98 |
R5944:Usp34
|
UTSW |
11 |
23363089 |
missense |
probably damaging |
1.00 |
R6198:Usp34
|
UTSW |
11 |
23484127 |
missense |
probably damaging |
1.00 |
R6229:Usp34
|
UTSW |
11 |
23446778 |
missense |
probably damaging |
0.99 |
R6306:Usp34
|
UTSW |
11 |
23412260 |
missense |
possibly damaging |
0.94 |
R6320:Usp34
|
UTSW |
11 |
23452520 |
missense |
probably damaging |
0.98 |
R6341:Usp34
|
UTSW |
11 |
23381353 |
missense |
probably damaging |
0.97 |
R6374:Usp34
|
UTSW |
11 |
23438914 |
missense |
probably damaging |
1.00 |
R6398:Usp34
|
UTSW |
11 |
23488666 |
missense |
probably benign |
|
R6438:Usp34
|
UTSW |
11 |
23364266 |
missense |
probably benign |
0.02 |
R6668:Usp34
|
UTSW |
11 |
23460659 |
missense |
probably damaging |
0.97 |
R6700:Usp34
|
UTSW |
11 |
23439011 |
missense |
probably damaging |
1.00 |
R6783:Usp34
|
UTSW |
11 |
23412318 |
missense |
probably damaging |
1.00 |
R6821:Usp34
|
UTSW |
11 |
23367491 |
missense |
possibly damaging |
0.79 |
R6855:Usp34
|
UTSW |
11 |
23452569 |
missense |
possibly damaging |
0.94 |
R6916:Usp34
|
UTSW |
11 |
23458023 |
missense |
probably damaging |
0.98 |
R7020:Usp34
|
UTSW |
11 |
23393954 |
missense |
probably benign |
0.05 |
R7026:Usp34
|
UTSW |
11 |
23361622 |
missense |
probably damaging |
1.00 |
R7085:Usp34
|
UTSW |
11 |
23363097 |
missense |
|
|
R7101:Usp34
|
UTSW |
11 |
23426183 |
missense |
|
|
R7168:Usp34
|
UTSW |
11 |
23464585 |
missense |
|
|
R7192:Usp34
|
UTSW |
11 |
23460571 |
missense |
|
|
R7264:Usp34
|
UTSW |
11 |
23333566 |
missense |
probably benign |
0.00 |
R7325:Usp34
|
UTSW |
11 |
23419052 |
missense |
|
|
R7343:Usp34
|
UTSW |
11 |
23488868 |
missense |
|
|
R7358:Usp34
|
UTSW |
11 |
23361683 |
missense |
probably damaging |
0.99 |
R7369:Usp34
|
UTSW |
11 |
23432361 |
missense |
|
|
R7389:Usp34
|
UTSW |
11 |
23345200 |
missense |
|
|
R7459:Usp34
|
UTSW |
11 |
23364458 |
missense |
possibly damaging |
0.53 |
R7517:Usp34
|
UTSW |
11 |
23446968 |
missense |
|
|
R7729:Usp34
|
UTSW |
11 |
23449268 |
missense |
|
|
R7777:Usp34
|
UTSW |
11 |
23382638 |
missense |
|
|
R7810:Usp34
|
UTSW |
11 |
23412314 |
missense |
|
|
R7836:Usp34
|
UTSW |
11 |
23446614 |
missense |
|
|
R7862:Usp34
|
UTSW |
11 |
23464718 |
missense |
|
|
R7993:Usp34
|
UTSW |
11 |
23377622 |
missense |
|
|
R8050:Usp34
|
UTSW |
11 |
23446787 |
missense |
|
|
R8054:Usp34
|
UTSW |
11 |
23361295 |
missense |
|
|
R8239:Usp34
|
UTSW |
11 |
23446750 |
missense |
|
|
R8266:Usp34
|
UTSW |
11 |
23486810 |
splice site |
probably benign |
|
R8347:Usp34
|
UTSW |
11 |
23412345 |
missense |
|
|
R8409:Usp34
|
UTSW |
11 |
23457811 |
missense |
|
|
R8692:Usp34
|
UTSW |
11 |
23429325 |
missense |
|
|
R8694:Usp34
|
UTSW |
11 |
23484161 |
missense |
|
|
R8734:Usp34
|
UTSW |
11 |
23444184 |
missense |
|
|
R8806:Usp34
|
UTSW |
11 |
23484143 |
missense |
|
|
R8914:Usp34
|
UTSW |
11 |
23343604 |
missense |
|
|
R8987:Usp34
|
UTSW |
11 |
23464267 |
missense |
|
|
R9013:Usp34
|
UTSW |
11 |
23370302 |
missense |
|
|
R9108:Usp34
|
UTSW |
11 |
23370528 |
missense |
|
|
R9264:Usp34
|
UTSW |
11 |
23489064 |
missense |
|
|
R9301:Usp34
|
UTSW |
11 |
23472951 |
missense |
|
|
R9375:Usp34
|
UTSW |
11 |
23487203 |
missense |
|
|
R9385:Usp34
|
UTSW |
11 |
23449223 |
missense |
|
|
R9500:Usp34
|
UTSW |
11 |
23381337 |
missense |
probably damaging |
0.99 |
R9566:Usp34
|
UTSW |
11 |
23367529 |
missense |
|
|
R9629:Usp34
|
UTSW |
11 |
23364364 |
missense |
|
|
R9679:Usp34
|
UTSW |
11 |
23444369 |
missense |
|
|
R9680:Usp34
|
UTSW |
11 |
23367385 |
missense |
possibly damaging |
0.94 |
R9686:Usp34
|
UTSW |
11 |
23474351 |
missense |
|
|
R9752:Usp34
|
UTSW |
11 |
23459182 |
missense |
probably benign |
0.11 |
X0023:Usp34
|
UTSW |
11 |
23375028 |
missense |
possibly damaging |
0.73 |
X0057:Usp34
|
UTSW |
11 |
23457824 |
missense |
possibly damaging |
0.86 |
Z1176:Usp34
|
UTSW |
11 |
23473221 |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGAAGGCCCATCTTCATTTTCAG -3'
(R):5'- CGTGAGAATAGACATGCCACG -3'
Sequencing Primer
(F):5'- GATGGTTCACATATCCGGTCACAG -3'
(R):5'- CACGTCTAATGTCAAGAAGCAGCTTG -3'
|
Posted On |
2015-04-29 |