Mutagenetix > Incidental Mutation

Incidental Mutation 'R0464:Usp33'

71407

Institutional Source

Beutler Lab

Gene Symbol

Usp33

Ensembl Gene

ENSMUSG00000025437

Gene Name

ubiquitin specific peptidase 33

Synonyms

Vdu1, 9830169D19Rik

MMRRC Submission

038664-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.920) question?

Stock #

R0464 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

152052115-152099254 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 152081872 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000142708 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000026507] [ENSMUST00000117492] [ENSMUST00000123237] [ENSMUST00000197748]

AlphaFold

Q8R5K2

Predicted Effect

probably benign
Transcript: ENSMUST00000026507

SMART Domains

Protein: ENSMUSP00000026507
Gene: ENSMUSG00000025437

Domain	Start	End	E-Value	Type
Pfam:zf-UBP	30	95	1.7e-18	PFAM
low complexity region	136	148	N/A	INTRINSIC
Pfam:UCH	153	671	2.2e-71	PFAM
Pfam:UCH_1	154	387	1.4e-9	PFAM
Pfam:UCH_1	371	653	6.8e-25	PFAM
DUSP	691	774	4.4e-17	SMART
DUSP	799	883	2.44e-33	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000117492

SMART Domains

Protein: ENSMUSP00000113265
Gene: ENSMUSG00000025437

Domain	Start	End	E-Value	Type
Pfam:zf-UBP	30	95	1e-18	PFAM
low complexity region	136	148	N/A	INTRINSIC
Pfam:UCH	153	679	1.6e-64	PFAM
Pfam:UCH_1	154	387	1.2e-8	PFAM
Pfam:UCH_1	366	661	1.3e-23	PFAM
DUSP	699	782	4.4e-17	SMART
DUSP	807	891	2.44e-33	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000123237

SMART Domains

Protein: ENSMUSP00000117590
Gene: ENSMUSG00000025437

Domain	Start	End	E-Value	Type
PDB:2UZG\|A	5	45	2e-23	PDB

Predicted Effect

probably benign
Transcript: ENSMUST00000197600

Predicted Effect

probably benign
Transcript: ENSMUST00000197748

SMART Domains

Protein: ENSMUSP00000142708
Gene: ENSMUSG00000025437

Domain	Start	End	E-Value	Type
Pfam:zf-UBP	30	95	1.7e-18	PFAM
low complexity region	136	148	N/A	INTRINSIC
Pfam:UCH	153	679	2.3e-71	PFAM
Pfam:UCH_1	154	383	1.2e-9	PFAM
Pfam:UCH_1	368	661	1e-24	PFAM
DUSP	699	782	4.4e-17	SMART
DUSP	807	891	2.44e-33	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198647

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198950

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.3%
20x: 94.7%

Validation Efficiency

100% (80/80)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a deubiquinating enzyme important in a variety of processes, including Slit-dependent cell migration and beta-2 adrenergic receptor signaling. The protein is negatively regulated through ubiquitination by von Hippel-Lindau tumor protein (VHL). Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jun 2012]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ada	G	T	2: 163,574,884 (GRCm39)	Y84*	probably null	Het
Adar	T	A	3: 89,642,889 (GRCm39)	C257S	possibly damaging	Het
Adgrd1	G	T	5: 129,239,714 (GRCm39)	C507F	probably damaging	Het
Atp5f1a	T	C	18: 77,867,622 (GRCm39)	Y299H	probably benign	Het
Bok	G	T	1: 93,621,935 (GRCm39)	R77L	probably damaging	Het
Cdx2	C	A	5: 147,243,283 (GRCm39)	K170N	possibly damaging	Het
Ceacam1	A	G	7: 25,171,442 (GRCm39)	S341P	possibly damaging	Het
Cfhr3	A	T	1: 139,521,683 (GRCm39)		noncoding transcript	Het
Ckap5	A	G	2: 91,409,858 (GRCm39)	I947V	probably benign	Het
Clec2i	T	C	6: 128,872,386 (GRCm39)	Y173H	probably damaging	Het
Cttnbp2	T	C	6: 18,408,690 (GRCm39)	D977G	possibly damaging	Het
Cyp2f2	C	A	7: 26,831,962 (GRCm39)	Q406K	probably benign	Het
Ddx28	A	G	8: 106,736,685 (GRCm39)	S458P	probably damaging	Het
Dppa3	T	A	6: 122,605,492 (GRCm39)		probably null	Het
Dusp10	C	A	1: 183,801,273 (GRCm39)	L347I	probably benign	Het
Fads1	C	T	19: 10,160,429 (GRCm39)	P5L	probably benign	Het
Fbxl15	A	T	19: 46,316,951 (GRCm39)	E13D	probably benign	Het
Fhit	T	A	14: 10,991,567 (GRCm38)		probably benign	Het
Fras1	G	T	5: 96,784,662 (GRCm39)	V882F	probably damaging	Het
G3bp1	T	C	11: 55,389,452 (GRCm39)	F383L	probably damaging	Het
Gabbr1	C	T	17: 37,361,726 (GRCm39)		probably benign	Het
Ganc	T	A	2: 120,267,175 (GRCm39)	V497D	probably benign	Het
Glt8d2	T	G	10: 82,490,564 (GRCm39)	H242P	possibly damaging	Het
Gna15	T	C	10: 81,348,338 (GRCm39)	Y131C	probably benign	Het
Gpatch8	T	C	11: 102,371,712 (GRCm39)	K609E	unknown	Het
Gprc5a	A	T	6: 135,056,413 (GRCm39)	K287*	probably null	Het
Iqub	T	A	6: 24,479,262 (GRCm39)	K427*	probably null	Het
Itpr2	C	G	6: 146,277,387 (GRCm39)	D666H	probably damaging	Het
Kcnj5	T	C	9: 32,234,269 (GRCm39)	I15M	possibly damaging	Het
Kcnn2	A	G	18: 45,693,426 (GRCm39)	E334G	probably damaging	Het
Lypd6	T	A	2: 50,080,690 (GRCm39)	I126N	probably damaging	Het
Ms4a20	A	G	19: 11,089,801 (GRCm39)	L28P	probably damaging	Het
Mtus1	T	C	8: 41,455,511 (GRCm39)	D56G	probably damaging	Het
Myo1h	A	G	5: 114,498,571 (GRCm39)	D889G	probably damaging	Het
Myrf	G	C	19: 10,195,526 (GRCm39)	T428S	probably benign	Het
Nab1	T	C	1: 52,529,174 (GRCm39)	D241G	possibly damaging	Het
Naip2	A	C	13: 100,298,290 (GRCm39)	I582S	probably benign	Het
Ncbp3	C	T	11: 72,960,647 (GRCm39)		probably benign	Het
Nek1	T	A	8: 61,525,307 (GRCm39)		probably benign	Het
Nf1	T	C	11: 79,447,615 (GRCm39)	V2452A	probably benign	Het
Nlrp1b	A	C	11: 71,109,070 (GRCm39)	S144A	probably damaging	Het
Npr2	A	T	4: 43,640,597 (GRCm39)		probably null	Het
Pak3	TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	"TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC"	X: 142,526,889 (GRCm39)		probably benign	Het
Paox	T	A	7: 139,709,195 (GRCm39)		probably benign	Het
Pcdh15	T	A	10: 74,462,676 (GRCm39)		probably null	Het
Pde8b	G	A	13: 95,241,206 (GRCm39)	T202M	probably damaging	Het
Pigo	A	T	4: 43,019,814 (GRCm39)	V905D	probably benign	Het
Pik3cb	A	G	9: 98,926,796 (GRCm39)		probably null	Het
Rassf5	T	C	1: 131,139,998 (GRCm39)	N87S	probably benign	Het
Rbl1	C	A	2: 156,989,465 (GRCm39)	K1051N	probably damaging	Het
Rfx7	T	C	9: 72,525,486 (GRCm39)	V892A	probably damaging	Het
Ripply1	TTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCT	TTCCTCCTCCTCCTCCTCCTCCTCCTCCT	X: 138,680,599 (GRCm39)		probably benign	Het
Rnf144b	T	A	13: 47,396,363 (GRCm39)	Y233*	probably null	Het
Safb	C	T	17: 56,913,025 (GRCm39)	R914C	probably damaging	Het
Sbf2	T	C	7: 110,063,783 (GRCm39)		probably benign	Het
Sgo2a	A	T	1: 58,039,253 (GRCm39)	K85N	probably damaging	Het
Siglec1	A	T	2: 130,921,279 (GRCm39)	C631S	probably damaging	Het
Simc1	C	T	13: 54,684,913 (GRCm39)	R50*	probably null	Het
Skint5	T	A	4: 113,392,928 (GRCm39)	M1235L	unknown	Het
Slc22a19	A	T	19: 7,660,278 (GRCm39)	N377K	probably benign	Het
Spata31d1a	A	G	13: 59,849,573 (GRCm39)	F852L	possibly damaging	Het
Spata31e3	A	G	13: 50,402,311 (GRCm39)		probably benign	Het
Srbd1	G	A	17: 86,427,430 (GRCm39)	S401F	probably damaging	Het
Stk36	C	A	1: 74,650,331 (GRCm39)	Q288K	probably damaging	Het
Styx	T	C	14: 45,609,908 (GRCm39)	S191P	probably benign	Het
Supt6	T	A	11: 78,107,164 (GRCm39)	N1214I	probably benign	Het
Tcim	T	A	8: 24,928,644 (GRCm39)	D90V	probably damaging	Het
Tdpoz1	T	A	3: 93,578,782 (GRCm39)	M1L	probably damaging	Het
Tep1	T	A	14: 51,085,141 (GRCm39)	T881S	probably benign	Het
Tlr5	C	T	1: 182,801,275 (GRCm39)	A193V	probably benign	Het
Tmem117	T	A	15: 94,612,800 (GRCm39)	F112Y	probably damaging	Het
Tnrc6c	C	T	11: 117,651,375 (GRCm39)	R1633W	probably damaging	Het
Trh	T	C	6: 92,220,649 (GRCm39)		probably null	Het
Triobp	A	G	15: 78,851,186 (GRCm39)	R447G	possibly damaging	Het
Trip6	A	G	5: 137,311,943 (GRCm39)	F46S	probably damaging	Het
Ubxn4	G	A	1: 128,190,641 (GRCm39)	E256K	probably benign	Het
Vmn2r60	A	T	7: 41,785,255 (GRCm39)	I156F	probably damaging	Het
Wdr17	T	C	8: 55,123,427 (GRCm39)		probably benign	Het
Wdr35	G	T	12: 9,077,472 (GRCm39)		probably benign	Het
Wwp1	C	T	4: 19,638,763 (GRCm39)		probably benign	Het
Zfp652	T	C	11: 95,654,475 (GRCm39)	C293R	probably damaging	Het

Other mutations in Usp33

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00433:Usp33	APN	3	152,079,046 (GRCm39)	missense	probably benign	0.00
IGL01085:Usp33	APN	3	152,074,206 (GRCm39)	missense	possibly damaging	0.89
IGL01335:Usp33	APN	3	152,097,854 (GRCm39)	missense	probably damaging	0.99
IGL02095:Usp33	APN	3	152,087,431 (GRCm39)	missense	possibly damaging	0.94
IGL02323:Usp33	APN	3	152,076,024 (GRCm39)	missense	probably benign
IGL03010:Usp33	APN	3	152,074,233 (GRCm39)	missense	probably benign	0.04
R0576:Usp33	UTSW	3	152,089,756 (GRCm39)	nonsense	probably null
R0583:Usp33	UTSW	3	152,073,891 (GRCm39)	missense	probably damaging	1.00
R0715:Usp33	UTSW	3	152,086,211 (GRCm39)	missense	probably damaging	1.00
R1445:Usp33	UTSW	3	152,074,271 (GRCm39)	missense	probably damaging	0.99
R1507:Usp33	UTSW	3	152,080,400 (GRCm39)	missense	possibly damaging	0.84
R1600:Usp33	UTSW	3	152,085,247 (GRCm39)	missense	probably damaging	0.98
R1673:Usp33	UTSW	3	152,073,919 (GRCm39)	missense	probably damaging	1.00
R1945:Usp33	UTSW	3	152,085,223 (GRCm39)	missense	probably benign	0.07
R1961:Usp33	UTSW	3	152,086,265 (GRCm39)	missense	probably damaging	1.00
R1973:Usp33	UTSW	3	152,065,923 (GRCm39)	missense	possibly damaging	0.64
R2231:Usp33	UTSW	3	152,079,023 (GRCm39)	missense	probably benign	0.00
R2299:Usp33	UTSW	3	152,080,258 (GRCm39)	missense	probably damaging	0.99
R3001:Usp33	UTSW	3	152,063,579 (GRCm39)	missense	probably damaging	0.99
R3002:Usp33	UTSW	3	152,063,579 (GRCm39)	missense	probably damaging	0.99
R3923:Usp33	UTSW	3	152,080,428 (GRCm39)	critical splice donor site	probably null
R4366:Usp33	UTSW	3	152,074,149 (GRCm39)	missense	probably benign	0.44
R4821:Usp33	UTSW	3	152,064,310 (GRCm39)	missense	probably benign	0.00
R5256:Usp33	UTSW	3	152,097,333 (GRCm39)	nonsense	probably null
R5396:Usp33	UTSW	3	152,089,824 (GRCm39)	missense	possibly damaging	0.77
R5445:Usp33	UTSW	3	152,080,260 (GRCm39)	missense	probably damaging	1.00
R5877:Usp33	UTSW	3	152,085,233 (GRCm39)	missense	probably damaging	1.00
R5877:Usp33	UTSW	3	152,085,113 (GRCm39)	missense	possibly damaging	0.91
R5884:Usp33	UTSW	3	152,073,967 (GRCm39)	missense	probably benign
R5913:Usp33	UTSW	3	152,086,229 (GRCm39)	missense	probably damaging	1.00
R5920:Usp33	UTSW	3	152,080,320 (GRCm39)	missense	probably damaging	1.00
R6331:Usp33	UTSW	3	152,081,887 (GRCm39)	missense	probably damaging	1.00
R6516:Usp33	UTSW	3	152,079,053 (GRCm39)	missense	probably benign	0.01
R6624:Usp33	UTSW	3	152,087,435 (GRCm39)	missense	probably damaging	1.00
R6679:Usp33	UTSW	3	152,074,124 (GRCm39)	missense	possibly damaging	0.46
R7196:Usp33	UTSW	3	152,089,828 (GRCm39)	missense	possibly damaging	0.87
R7250:Usp33	UTSW	3	152,097,999 (GRCm39)	nonsense	probably null
R7310:Usp33	UTSW	3	152,066,026 (GRCm39)	nonsense	probably null
R7569:Usp33	UTSW	3	152,097,302 (GRCm39)	missense	probably damaging	1.00
R7644:Usp33	UTSW	3	152,063,589 (GRCm39)	missense	possibly damaging	0.47
R8118:Usp33	UTSW	3	152,065,996 (GRCm39)	missense	probably damaging	1.00
R8229:Usp33	UTSW	3	152,075,929 (GRCm39)	missense	probably benign
R8333:Usp33	UTSW	3	152,080,297 (GRCm39)	missense	probably damaging	1.00
R8774:Usp33	UTSW	3	152,085,213 (GRCm39)	nonsense	probably null
R8774-TAIL:Usp33	UTSW	3	152,085,213 (GRCm39)	nonsense	probably null
R8854:Usp33	UTSW	3	152,073,967 (GRCm39)	missense	probably benign	0.10
R8953:Usp33	UTSW	3	152,080,420 (GRCm39)	missense	possibly damaging	0.92
R9480:Usp33	UTSW	3	152,079,086 (GRCm39)	missense	possibly damaging	0.90
X0025:Usp33	UTSW	3	152,072,395 (GRCm39)	missense	probably damaging	1.00
X0058:Usp33	UTSW	3	152,065,983 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCATGTGCCCACACCATGCTTG -3'
(R):5'- GCCTCTCTGAAAGGTCCACACATC -3'

Sequencing Primer
(F):5'- GCATGTGGCAGGTATAGTAAATTC -3'
(R):5'- GGTGCTACTGTTACCATAGTAATCC -3'

Posted On

2013-09-30