Mutagenetix > Incidental Mutation

Incidental Mutation 'R1741:Usp34'

200368

Institutional Source

Beutler Lab

Gene Symbol

Usp34

Ensembl Gene

ENSMUSG00000056342

Gene Name

ubiquitin specific peptidase 34

Synonyms

Murr2, A530081C03Rik

MMRRC Submission

039773-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.732) question?

Stock #

R1741 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

23306895-23490560 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 23364103 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 663 (T663A)

Ref Sequence

ENSEMBL: ENSMUSP00000137430 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000180046]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000137823
AA Change: T682A

SMART Domains

Protein: ENSMUSP00000120747
Gene: ENSMUSG00000056342
AA Change: T682A

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: ENSMUST00000180046
AA Change: T663A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000137430
Gene: ENSMUSG00000056342
AA Change: T663A

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

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.5%
20x: 92.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700034E13Rik	A	G	18: 52,660,506 (GRCm38)	N37S	probably damaging	Het
Acad10	T	C	5: 121,647,836 (GRCm38)	K230R	probably damaging	Het
Actl7a	A	G	4: 56,744,252 (GRCm38)	N260D	probably benign	Het
Adam24	T	C	8: 40,679,603 (GRCm38)	Y37H	probably benign	Het
Ahcy	G	A	2: 155,064,234 (GRCm38)	A229V	probably benign	Het
Ap3b2	A	G	7: 81,467,599 (GRCm38)	V563A	possibly damaging	Het
Bcl9l	T	A	9: 44,509,689 (GRCm38)	M1427K	probably damaging	Het
Btf3	C	T	13: 98,316,296 (GRCm38)	M1I	probably null	Het
Btg4	A	T	9: 51,116,610 (GRCm38)	I27L	probably benign	Het
Ccdc171	A	G	4: 83,620,839 (GRCm38)	Y366C	probably damaging	Het
Chd3	A	G	11: 69,355,654 (GRCm38)	Y1085H	probably damaging	Het
Cnot10	T	C	9: 114,597,824 (GRCm38)	D616G	possibly damaging	Het
Crlf1	C	A	8: 70,500,906 (GRCm38)	D243E	probably damaging	Het
Cyp2b23	A	G	7: 26,673,077 (GRCm38)	V371A	possibly damaging	Het
Dennd2a	A	G	6: 39,493,157 (GRCm38)	S534P	probably damaging	Het
Eln	A	G	5: 134,729,184 (GRCm38)	V185A	unknown	Het
Epor	C	T	9: 21,959,771 (GRCm38)	G301D	probably damaging	Het
Fam83f	T	G	15: 80,692,267 (GRCm38)	V373G	possibly damaging	Het
Fbxl21	A	T	13: 56,537,102 (GRCm38)	T340S	probably benign	Het
Fcgbpl1	G	T	7: 28,157,854 (GRCm38)	C2209F	probably damaging	Het
Fez1	T	A	9: 36,843,733 (GRCm38)	D9E	probably damaging	Het
Fsip2	T	C	2: 82,989,912 (GRCm38)	F5330L	probably benign	Het
Glis1	G	A	4: 107,568,347 (GRCm38)	R197Q	probably damaging	Het
Gm10277	TC	T	11: 77,786,002 (GRCm38)		probably null	Het
Gpr158	A	G	2: 21,827,548 (GRCm38)	N1153S	probably benign	Het
Gramd4	T	C	15: 86,091,529 (GRCm38)		probably null	Het
Hhatl	T	A	9: 121,789,059 (GRCm38)	Y210F	possibly damaging	Het
Hltf	T	C	3: 20,086,188 (GRCm38)	W422R	probably damaging	Het
Hspa5	T	C	2: 34,772,692 (GRCm38)	S87P	possibly damaging	Het
Il21	T	C	3: 37,227,662 (GRCm38)	H111R	probably benign	Het
Ip6k1	G	A	9: 108,040,984 (GRCm38)	G73S	probably benign	Het
Kdm5b	A	G	1: 134,618,017 (GRCm38)	D972G	possibly damaging	Het
Kif21b	C	T	1: 136,156,142 (GRCm38)	A709V	probably damaging	Het
Kmt2d	T	C	15: 98,845,234 (GRCm38)		probably benign	Het
Lrrc14b	A	G	13: 74,363,586 (GRCm38)	L125P	probably damaging	Het
Mapk8ip3	A	G	17: 24,899,854 (GRCm38)	S1169P	probably damaging	Het
Me3	A	T	7: 89,851,833 (GRCm38)	Y584F	probably damaging	Het
Mxra7	T	G	11: 116,816,244 (GRCm38)		probably null	Het
Nf1	T	C	11: 79,443,931 (GRCm38)	S870P	probably benign	Het
Npr2	G	A	4: 43,643,350 (GRCm38)	G525S	probably damaging	Het
Nyap1	A	T	5: 137,733,125 (GRCm38)	S726T	probably damaging	Het
Padi4	A	G	4: 140,746,170 (GRCm38)	V652A	probably damaging	Het
Pclo	A	G	5: 14,676,510 (GRCm38)		probably benign	Het
Pgm2	G	A	4: 99,964,865 (GRCm38)		probably null	Het
Piezo2	A	G	18: 63,021,173 (GRCm38)	S2512P	probably damaging	Het
Ptbp3	A	T	4: 59,482,624 (GRCm38)	D386E	probably damaging	Het
Ptk2	A	G	15: 73,242,406 (GRCm38)	V701A	possibly damaging	Het
Ptpn3	A	G	4: 57,254,922 (GRCm38)	V154A	probably damaging	Het
Rassf4	T	C	6: 116,639,489 (GRCm38)	E287G	probably damaging	Het
Rnh1	C	T	7: 141,164,023 (GRCm38)	R174H	probably benign	Het
Scn9a	T	A	2: 66,487,594 (GRCm38)	I1517F	probably damaging	Het
Sftpb	C	A	6: 72,305,813 (GRCm38)	A90E	probably benign	Het
Slc39a14	T	C	14: 70,318,744 (GRCm38)	K61R	probably damaging	Het
Tmem132d	A	C	5: 127,784,858 (GRCm38)	M733R	probably benign	Het
Tmem248	A	G	5: 130,236,823 (GRCm38)	I156V	probably benign	Het
Traf2	T	C	2: 25,524,483 (GRCm38)	D339G	probably damaging	Het
Trappc11	A	G	8: 47,529,327 (GRCm38)		probably null	Het
Tuba8	T	A	6: 121,222,768 (GRCm38)	I137N	possibly damaging	Het
Txlnb	A	G	10: 17,838,947 (GRCm38)	T376A	probably damaging	Het
Vmn2r26	T	A	6: 124,061,472 (GRCm38)	F669I	probably damaging	Het
Wdr95	G	A	5: 149,595,396 (GRCm38)		probably null	Het
Wfdc8	T	G	2: 164,608,869 (GRCm38)		probably benign	Het
Zfp64	A	C	2: 168,926,318 (GRCm38)	V458G	probably benign	Het
Zfp868	C	T	8: 69,611,868 (GRCm38)	G272D	probably damaging	Het

Other mutations in Usp34

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00092:Usp34	APN	11	23,436,020 (GRCm38)	missense	probably damaging	0.98
IGL00477:Usp34	APN	11	23,468,879 (GRCm38)	missense	probably damaging	0.99
IGL01307:Usp34	APN	11	23,417,676 (GRCm38)	missense	probably damaging	0.99
IGL01313:Usp34	APN	11	23,473,206 (GRCm38)	missense	probably damaging	1.00
IGL01794:Usp34	APN	11	23,436,020 (GRCm38)	missense	probably damaging	0.98
IGL01826:Usp34	APN	11	23,436,020 (GRCm38)	missense	probably damaging	0.98
IGL01827:Usp34	APN	11	23,436,020 (GRCm38)	missense	probably damaging	0.98
IGL01830:Usp34	APN	11	23,436,020 (GRCm38)	missense	probably damaging	0.98
IGL01867:Usp34	APN	11	23,384,411 (GRCm38)	missense	possibly damaging	0.77
IGL01939:Usp34	APN	11	23,345,141 (GRCm38)	splice site	probably benign
IGL01977:Usp34	APN	11	23,452,661 (GRCm38)	missense	probably damaging	1.00
IGL01985:Usp34	APN	11	23,452,565 (GRCm38)	missense	probably damaging	1.00
IGL02011:Usp34	APN	11	23,471,554 (GRCm38)	missense	probably damaging	0.99
IGL02302:Usp34	APN	11	23,467,243 (GRCm38)	missense	possibly damaging	0.91
IGL02423:Usp34	APN	11	23,354,900 (GRCm38)	missense	probably benign	0.11
IGL02491:Usp34	APN	11	23,432,630 (GRCm38)	missense	probably damaging	0.98
IGL02532:Usp34	APN	11	23,370,291 (GRCm38)	missense	probably damaging	0.99
IGL02561:Usp34	APN	11	23,351,652 (GRCm38)	missense	probably benign	0.09
IGL02706:Usp34	APN	11	23,388,659 (GRCm38)	splice site	probably benign
IGL02891:Usp34	APN	11	23,487,166 (GRCm38)	missense	probably benign	0.09
IGL03079:Usp34	APN	11	23,432,247 (GRCm38)	missense	possibly damaging	0.48
IGL03089:Usp34	APN	11	23,446,958 (GRCm38)	missense	possibly damaging	0.84
IGL03175:Usp34	APN	11	23,488,686 (GRCm38)	missense	probably benign
IGL03256:Usp34	APN	11	23,420,090 (GRCm38)	nonsense	probably null
IGL03280:Usp34	APN	11	23,354,897 (GRCm38)	missense	probably damaging	1.00
IGL03289:Usp34	APN	11	23,393,818 (GRCm38)	missense	possibly damaging	0.94
IGL03408:Usp34	APN	11	23,446,957 (GRCm38)	missense	possibly damaging	0.92
Chub	UTSW	11	23,464,686 (GRCm38)	missense	probably damaging	0.99
Cicione	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R5571_Usp34_680	UTSW	11	23,457,975 (GRCm38)	missense	probably damaging	0.99
R5713_Usp34_003	UTSW	11	23,343,515 (GRCm38)	missense	possibly damaging	0.94
Roebuck	UTSW	11	23,486,810 (GRCm38)	splice site	probably benign
stoat	UTSW	11	23,487,203 (GRCm38)	missense
tunnelvision	UTSW	11	23,446,968 (GRCm38)	missense
I2288:Usp34	UTSW	11	23,432,473 (GRCm38)	splice site	probably benign
R0047:Usp34	UTSW	11	23,464,403 (GRCm38)	missense	probably benign	0.34
R0047:Usp34	UTSW	11	23,464,403 (GRCm38)	missense	probably benign	0.34
R0099:Usp34	UTSW	11	23,363,111 (GRCm38)	missense	probably damaging	1.00
R0240:Usp34	UTSW	11	23,433,206 (GRCm38)	missense	probably damaging	0.99
R0240:Usp34	UTSW	11	23,433,206 (GRCm38)	missense	probably damaging	0.99
R0403:Usp34	UTSW	11	23,333,838 (GRCm38)	missense	possibly damaging	0.82
R0432:Usp34	UTSW	11	23,401,505 (GRCm38)	missense	probably damaging	0.99
R0446:Usp34	UTSW	11	23,467,207 (GRCm38)	missense	probably damaging	0.97
R0455:Usp34	UTSW	11	23,446,741 (GRCm38)	splice site	probably benign
R0470:Usp34	UTSW	11	23,436,001 (GRCm38)	missense	possibly damaging	0.94
R0472:Usp34	UTSW	11	23,384,509 (GRCm38)	splice site	probably benign
R0512:Usp34	UTSW	11	23,451,997 (GRCm38)	missense	probably benign	0.04
R0557:Usp34	UTSW	11	23,403,848 (GRCm38)	missense	probably damaging	0.98
R0562:Usp34	UTSW	11	23,432,406 (GRCm38)	splice site	probably benign
R0656:Usp34	UTSW	11	23,472,967 (GRCm38)	missense	probably damaging	0.99
R0693:Usp34	UTSW	11	23,452,637 (GRCm38)	missense	probably damaging	0.97
R0739:Usp34	UTSW	11	23,467,243 (GRCm38)	missense	possibly damaging	0.91
R1061:Usp34	UTSW	11	23,384,420 (GRCm38)	missense	possibly damaging	0.51
R1078:Usp34	UTSW	11	23,433,175 (GRCm38)	splice site	probably benign
R1223:Usp34	UTSW	11	23,446,464 (GRCm38)	splice site	probably null
R1295:Usp34	UTSW	11	23,384,477 (GRCm38)	missense	probably damaging	1.00
R1430:Usp34	UTSW	11	23,459,151 (GRCm38)	missense	probably damaging	0.97
R1445:Usp34	UTSW	11	23,351,629 (GRCm38)	missense	probably damaging	0.99
R1468:Usp34	UTSW	11	23,441,171 (GRCm38)	missense	probably damaging	1.00
R1468:Usp34	UTSW	11	23,441,171 (GRCm38)	missense	probably damaging	1.00
R1471:Usp34	UTSW	11	23,488,862 (GRCm38)	missense	probably benign	0.20
R1475:Usp34	UTSW	11	23,473,253 (GRCm38)	missense	probably damaging	0.99
R1628:Usp34	UTSW	11	23,488,725 (GRCm38)	missense	probably damaging	1.00
R1631:Usp34	UTSW	11	23,460,651 (GRCm38)	missense	probably damaging	0.99
R1655:Usp34	UTSW	11	23,375,051 (GRCm38)	missense	probably benign	0.05
R1854:Usp34	UTSW	11	23,426,153 (GRCm38)	missense	probably benign	0.24
R1867:Usp34	UTSW	11	23,361,593 (GRCm38)	missense	possibly damaging	0.82
R1869:Usp34	UTSW	11	23,364,479 (GRCm38)	missense	probably benign	0.37
R1870:Usp34	UTSW	11	23,364,479 (GRCm38)	missense	probably benign	0.37
R1871:Usp34	UTSW	11	23,364,479 (GRCm38)	missense	probably benign	0.37
R1967:Usp34	UTSW	11	23,364,503 (GRCm38)	missense	probably benign	0.01
R2051:Usp34	UTSW	11	23,464,468 (GRCm38)	missense	probably damaging	0.97
R2132:Usp34	UTSW	11	23,464,556 (GRCm38)	missense	possibly damaging	0.95
R2156:Usp34	UTSW	11	23,382,602 (GRCm38)	missense	probably damaging	0.98
R2205:Usp34	UTSW	11	23,385,147 (GRCm38)	missense	probably damaging	0.97
R2342:Usp34	UTSW	11	23,403,599 (GRCm38)	missense	possibly damaging	0.46
R3431:Usp34	UTSW	11	23,370,466 (GRCm38)	missense	possibly damaging	0.95
R3812:Usp34	UTSW	11	23,464,517 (GRCm38)	missense	possibly damaging	0.94
R3872:Usp34	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R3873:Usp34	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R3874:Usp34	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R3875:Usp34	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R3925:Usp34	UTSW	11	23,343,640 (GRCm38)	missense	probably benign	0.28
R3972:Usp34	UTSW	11	23,457,803 (GRCm38)	missense	probably damaging	1.00
R4018:Usp34	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R4042:Usp34	UTSW	11	23,489,033 (GRCm38)	missense	possibly damaging	0.85
R4155:Usp34	UTSW	11	23,417,676 (GRCm38)	missense	probably damaging	0.99
R4197:Usp34	UTSW	11	23,444,189 (GRCm38)	missense	probably damaging	0.98
R4352:Usp34	UTSW	11	23,320,727 (GRCm38)	missense	possibly damaging	0.73
R4379:Usp34	UTSW	11	23,384,499 (GRCm38)	missense	possibly damaging	0.52
R4444:Usp34	UTSW	11	23,435,998 (GRCm38)	missense	probably damaging	0.98
R4475:Usp34	UTSW	11	23,457,975 (GRCm38)	missense	possibly damaging	0.95
R4501:Usp34	UTSW	11	23,401,529 (GRCm38)	missense	probably damaging	1.00
R4527:Usp34	UTSW	11	23,421,257 (GRCm38)	missense	possibly damaging	0.57
R4603:Usp34	UTSW	11	23,464,633 (GRCm38)	missense	probably damaging	0.97
R4612:Usp34	UTSW	11	23,432,268 (GRCm38)	missense	probably damaging	0.99
R4673:Usp34	UTSW	11	23,364,480 (GRCm38)	small deletion	probably benign
R4707:Usp34	UTSW	11	23,487,215 (GRCm38)	missense	probably damaging	1.00
R4736:Usp34	UTSW	11	23,393,749 (GRCm38)	splice site	probably null
R4867:Usp34	UTSW	11	23,451,999 (GRCm38)	missense	probably benign	0.28
R4879:Usp34	UTSW	11	23,373,410 (GRCm38)	missense	possibly damaging	0.94
R4977:Usp34	UTSW	11	23,488,982 (GRCm38)	missense	probably damaging	1.00
R5004:Usp34	UTSW	11	23,464,586 (GRCm38)	missense	probably damaging	1.00
R5057:Usp34	UTSW	11	23,458,086 (GRCm38)	intron	probably benign
R5068:Usp34	UTSW	11	23,460,665 (GRCm38)	missense	possibly damaging	0.94
R5304:Usp34	UTSW	11	23,343,616 (GRCm38)	missense	probably damaging	1.00
R5320:Usp34	UTSW	11	23,333,739 (GRCm38)	missense	probably benign
R5327:Usp34	UTSW	11	23,468,846 (GRCm38)	missense	probably damaging	1.00
R5328:Usp34	UTSW	11	23,488,659 (GRCm38)	missense	probably benign	0.04
R5328:Usp34	UTSW	11	23,464,616 (GRCm38)	missense	probably benign	0.01
R5390:Usp34	UTSW	11	23,444,202 (GRCm38)	critical splice donor site	probably null
R5434:Usp34	UTSW	11	23,412,271 (GRCm38)	missense	probably damaging	0.99
R5523:Usp34	UTSW	11	23,349,198 (GRCm38)	missense	probably benign	0.39
R5567:Usp34	UTSW	11	23,488,336 (GRCm38)	missense	probably damaging	0.97
R5571:Usp34	UTSW	11	23,457,975 (GRCm38)	missense	probably damaging	0.99
R5645:Usp34	UTSW	11	23,375,024 (GRCm38)	missense	possibly damaging	0.86
R5713:Usp34	UTSW	11	23,343,515 (GRCm38)	missense	possibly damaging	0.94
R5719:Usp34	UTSW	11	23,354,846 (GRCm38)	missense	probably benign	0.00
R5813:Usp34	UTSW	11	23,421,340 (GRCm38)	missense	probably benign	0.38
R5921:Usp34	UTSW	11	23,464,686 (GRCm38)	missense	probably damaging	0.99
R5928:Usp34	UTSW	11	23,436,040 (GRCm38)	missense	probably damaging	0.98
R5944:Usp34	UTSW	11	23,363,089 (GRCm38)	missense	probably damaging	1.00
R6198:Usp34	UTSW	11	23,484,127 (GRCm38)	missense	probably damaging	1.00
R6229:Usp34	UTSW	11	23,446,778 (GRCm38)	missense	probably damaging	0.99
R6306:Usp34	UTSW	11	23,412,260 (GRCm38)	missense	possibly damaging	0.94
R6320:Usp34	UTSW	11	23,452,520 (GRCm38)	missense	probably damaging	0.98
R6341:Usp34	UTSW	11	23,381,353 (GRCm38)	missense	probably damaging	0.97
R6374:Usp34	UTSW	11	23,438,914 (GRCm38)	missense	probably damaging	1.00
R6398:Usp34	UTSW	11	23,488,666 (GRCm38)	missense	probably benign
R6438:Usp34	UTSW	11	23,364,266 (GRCm38)	missense	probably benign	0.02
R6668:Usp34	UTSW	11	23,460,659 (GRCm38)	missense	probably damaging	0.97
R6700:Usp34	UTSW	11	23,439,011 (GRCm38)	missense	probably damaging	1.00
R6783:Usp34	UTSW	11	23,412,318 (GRCm38)	missense	probably damaging	1.00
R6821:Usp34	UTSW	11	23,367,491 (GRCm38)	missense	possibly damaging	0.79
R6855:Usp34	UTSW	11	23,452,569 (GRCm38)	missense	possibly damaging	0.94
R6916:Usp34	UTSW	11	23,458,023 (GRCm38)	missense	probably damaging	0.98
R7020:Usp34	UTSW	11	23,393,954 (GRCm38)	missense	probably benign	0.05
R7026:Usp34	UTSW	11	23,361,622 (GRCm38)	missense	probably damaging	1.00
R7085:Usp34	UTSW	11	23,363,097 (GRCm38)	missense
R7101:Usp34	UTSW	11	23,426,183 (GRCm38)	missense
R7168:Usp34	UTSW	11	23,464,585 (GRCm38)	missense
R7192:Usp34	UTSW	11	23,460,571 (GRCm38)	missense
R7264:Usp34	UTSW	11	23,333,566 (GRCm38)	missense	probably benign	0.00
R7325:Usp34	UTSW	11	23,419,052 (GRCm38)	missense
R7343:Usp34	UTSW	11	23,488,868 (GRCm38)	missense
R7358:Usp34	UTSW	11	23,361,683 (GRCm38)	missense	probably damaging	0.99
R7369:Usp34	UTSW	11	23,432,361 (GRCm38)	missense
R7389:Usp34	UTSW	11	23,345,200 (GRCm38)	missense
R7459:Usp34	UTSW	11	23,364,458 (GRCm38)	missense	possibly damaging	0.53
R7517:Usp34	UTSW	11	23,446,968 (GRCm38)	missense
R7729:Usp34	UTSW	11	23,449,268 (GRCm38)	missense
R7777:Usp34	UTSW	11	23,382,638 (GRCm38)	missense
R7810:Usp34	UTSW	11	23,412,314 (GRCm38)	missense
R7836:Usp34	UTSW	11	23,446,614 (GRCm38)	missense
R7862:Usp34	UTSW	11	23,464,718 (GRCm38)	missense
R7993:Usp34	UTSW	11	23,377,622 (GRCm38)	missense
R8050:Usp34	UTSW	11	23,446,787 (GRCm38)	missense
R8054:Usp34	UTSW	11	23,361,295 (GRCm38)	missense
R8239:Usp34	UTSW	11	23,446,750 (GRCm38)	missense
R8266:Usp34	UTSW	11	23,486,810 (GRCm38)	splice site	probably benign
R8347:Usp34	UTSW	11	23,412,345 (GRCm38)	missense
R8409:Usp34	UTSW	11	23,457,811 (GRCm38)	missense
R8692:Usp34	UTSW	11	23,429,325 (GRCm38)	missense
R8694:Usp34	UTSW	11	23,484,161 (GRCm38)	missense
R8734:Usp34	UTSW	11	23,444,184 (GRCm38)	missense
R8806:Usp34	UTSW	11	23,484,143 (GRCm38)	missense
R8914:Usp34	UTSW	11	23,343,604 (GRCm38)	missense
R8987:Usp34	UTSW	11	23,464,267 (GRCm38)	missense
R9013:Usp34	UTSW	11	23,370,302 (GRCm38)	missense
R9108:Usp34	UTSW	11	23,370,528 (GRCm38)	missense
R9264:Usp34	UTSW	11	23,489,064 (GRCm38)	missense
R9301:Usp34	UTSW	11	23,472,951 (GRCm38)	missense
R9375:Usp34	UTSW	11	23,487,203 (GRCm38)	missense
R9385:Usp34	UTSW	11	23,449,223 (GRCm38)	missense
R9500:Usp34	UTSW	11	23,381,337 (GRCm38)	missense	probably damaging	0.99
R9566:Usp34	UTSW	11	23,367,529 (GRCm38)	missense
R9629:Usp34	UTSW	11	23,364,364 (GRCm38)	missense
R9679:Usp34	UTSW	11	23,444,369 (GRCm38)	missense
R9680:Usp34	UTSW	11	23,367,385 (GRCm38)	missense	possibly damaging	0.94
R9686:Usp34	UTSW	11	23,474,351 (GRCm38)	missense
R9752:Usp34	UTSW	11	23,459,182 (GRCm38)	missense	probably benign	0.11
X0023:Usp34	UTSW	11	23,375,028 (GRCm38)	missense	possibly damaging	0.73
X0057:Usp34	UTSW	11	23,457,824 (GRCm38)	missense	possibly damaging	0.86
Z1176:Usp34	UTSW	11	23,473,221 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTGCAGACATCGAGGCCCTTAAAG -3'
(R):5'- GTGTGATACAAGCCTCCTGAGAACC -3'

Sequencing Primer
(F):5'- agaagaagaggaagaggaggag -3'
(R):5'- CTTGTGCTAAGTGAGCAGAACTC -3'

Posted On

2014-05-23