Mutagenetix > Incidental Mutation

Incidental Mutation 'R4959:Usp16'

382206

Institutional Source

Beutler Lab

Gene Symbol

Usp16

Ensembl Gene

ENSMUSG00000025616

Gene Name

ubiquitin specific peptidase 16

Synonyms

2810483I07Rik, 6330514E22Rik, UBP-M, 1200004E02Rik

MMRRC Submission

042556-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4959 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

87251833-87280403 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 87277802 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 684 (M684K)

Ref Sequence

ENSEMBL: ENSMUSP00000114058 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000026704] [ENSMUST00000026710] [ENSMUST00000119504] [ENSMUST00000144759] [ENSMUST00000175977] [ENSMUST00000177376]

AlphaFold

Q99LG0

Predicted Effect

probably benign
Transcript: ENSMUST00000026704

SMART Domains

Protein: ENSMUSP00000026704
Gene: ENSMUSG00000025613

Domain	Start	End	E-Value	Type
Pfam:Cpn60_TCP1	39	529	6.7e-156	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000026710
AA Change: M685K

PolyPhen 2 Score 0.787 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000026710
Gene: ENSMUSG00000025616
AA Change: M685K

Domain	Start	End	E-Value	Type
Pfam:zf-UBP	48	127	2.5e-23	PFAM
coiled coil region	149	182	N/A	INTRINSIC
Pfam:UCH	194	821	2e-54	PFAM
Pfam:UCH_1	195	800	3.8e-15	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000119504
AA Change: M684K

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000114058
Gene: ENSMUSG00000025616
AA Change: M684K

Domain	Start	End	E-Value	Type
Pfam:zf-UBP	48	127	6.9e-24	PFAM
coiled coil region	149	181	N/A	INTRINSIC
Pfam:UCH	193	732	1.2e-36	PFAM
Pfam:UCH_1	194	737	2.5e-12	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135399

Predicted Effect

probably benign
Transcript: ENSMUST00000144759

SMART Domains

Protein: ENSMUSP00000116323
Gene: ENSMUSG00000025616

Domain	Start	End	E-Value	Type
Pfam:zf-UBP	48	127	2e-24	PFAM
coiled coil region	149	181	N/A	INTRINSIC
Pfam:UCH	193	330	2.4e-23	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146386

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149656

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176241

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000177485

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000177275

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176589

Predicted Effect

probably benign
Transcript: ENSMUST00000175977

SMART Domains

Protein: ENSMUSP00000135651
Gene: ENSMUSG00000025613

Domain	Start	End	E-Value	Type
Pfam:Cpn60_TCP1	39	132	4.5e-32	PFAM
Pfam:Cpn60_TCP1	120	470	1.9e-94	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000177376

SMART Domains

Protein: ENSMUSP00000135498
Gene: ENSMUSG00000025613

Domain	Start	End	E-Value	Type
PDB:4B2T\|Q	1	51	1e-29	PDB
SCOP:d1oela1	26	51	8e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000175750

SMART Domains

Protein: ENSMUSP00000134920
Gene: ENSMUSG00000025613

Domain	Start	End	E-Value	Type
Pfam:Cpn60_TCP1	1	238	1.2e-69	PFAM

Meta Mutation Damage Score

0.8964

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.6%
20x: 89.7%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a deubiquitinating enzyme that is phosphorylated at the onset of mitosis and then dephosphorylated at the metaphase/anaphase transition. It can deubiquitinate H2A, one of two major ubiquitinated proteins of chromatin, in vitro and a mutant form of the protein was shown to block cell division. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit embryonic lethality at E6. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	A	T	12: 71,211,321 (GRCm39)	E685V	possibly damaging	Het
2700049A03Rik	G	T	12: 71,211,320 (GRCm39)	E685*	probably null	Het
6820408C15Rik	T	A	2: 152,282,808 (GRCm39)	I221K	possibly damaging	Het
Aadacl3	A	T	4: 144,183,656 (GRCm39)	C136S	probably benign	Het
Abhd16a	T	A	17: 35,321,318 (GRCm39)	S498T	probably benign	Het
Acrv1	G	A	9: 36,605,996 (GRCm39)		probably null	Het
Adamts18	G	A	8: 114,463,357 (GRCm39)	R830*	probably null	Het
Art3	A	G	5: 92,551,478 (GRCm39)	Y279C	probably damaging	Het
Atm	A	T	9: 53,426,601 (GRCm39)	D552E	probably benign	Het
Ccdc154	T	C	17: 25,389,888 (GRCm39)	L508P	probably damaging	Het
Ccser2	A	T	14: 36,662,753 (GRCm39)	S144T	probably benign	Het
Cgn	C	T	3: 94,685,564 (GRCm39)	A320T	probably benign	Het
Cklf	A	G	8: 104,988,184 (GRCm39)	K106E	probably benign	Het
Clec12a	C	A	6: 129,330,628 (GRCm39)	T70K	probably benign	Het
CN725425	G	A	15: 91,129,904 (GRCm39)	A256T	possibly damaging	Het
Crb2	G	T	2: 37,680,482 (GRCm39)	R470L	probably damaging	Het
Csn1s1	T	G	5: 87,821,120 (GRCm39)	S33A	probably benign	Het
D630045J12Rik	C	T	6: 38,125,302 (GRCm39)	V1571M	possibly damaging	Het
Deup1	G	A	9: 15,523,310 (GRCm39)	Q58*	probably null	Het
Dph2	T	A	4: 117,748,527 (GRCm39)	D82V	probably damaging	Het
Dsp	C	T	13: 38,375,686 (GRCm39)	A1157V	probably benign	Het
Evi5l	G	T	8: 4,255,406 (GRCm39)	V477L	probably benign	Het
Fam187b	T	A	7: 30,681,687 (GRCm39)	H131Q	probably damaging	Het
Fam193b	A	G	13: 55,691,097 (GRCm39)	I259T	probably damaging	Het
Fam91a1	A	G	15: 58,303,059 (GRCm39)	T323A	probably benign	Het
Fat4	T	G	3: 39,037,195 (GRCm39)	S3616A	probably benign	Het
Fbxo38	A	T	18: 62,655,578 (GRCm39)	N369K	probably benign	Het
Fitm1	T	A	14: 55,813,831 (GRCm39)		probably null	Het
Fkbp5	T	C	17: 28,647,343 (GRCm39)	E164G	probably damaging	Het
Fpr-rs3	T	C	17: 20,844,211 (GRCm39)	Y310C	possibly damaging	Het
Fryl	A	T	5: 73,192,401 (GRCm39)	M2678K	probably benign	Het
Fsip2	T	C	2: 82,815,169 (GRCm39)	I3634T	probably benign	Het
Gm3233	T	C	10: 77,595,399 (GRCm39)		probably benign	Het
Gzmd	T	G	14: 56,369,955 (GRCm39)	T9P	unknown	Het
Htr2b	A	T	1: 86,027,813 (GRCm39)	I231N	probably damaging	Het
Il2ra	A	G	2: 11,681,664 (GRCm39)	T90A	possibly damaging	Het
Kbtbd2	A	G	6: 56,758,943 (GRCm39)	F60S	probably benign	Het
Kif21b	G	A	1: 136,076,108 (GRCm39)	C299Y	possibly damaging	Het
Lsm5	A	T	6: 56,680,309 (GRCm39)	D44E	probably damaging	Het
Mapk1	T	A	16: 16,836,170 (GRCm39)	M106K	probably damaging	Het
Mpp2	A	G	11: 101,954,117 (GRCm39)	V193A	probably damaging	Het
Muc4	T	C	16: 32,575,437 (GRCm39)	S1398P	possibly damaging	Het
Ndufs2	A	G	1: 171,065,578 (GRCm39)	Y282H	probably damaging	Het
Nes	T	A	3: 87,882,983 (GRCm39)	L414Q	probably damaging	Het
Neurl2	T	A	2: 164,675,122 (GRCm39)		probably null	Het
Ngef	A	G	1: 87,431,070 (GRCm39)	F159S	possibly damaging	Het
Nlrx1	T	C	9: 44,165,448 (GRCm39)	H816R	possibly damaging	Het
Or10v5	A	G	19: 11,806,300 (GRCm39)	L30P	probably benign	Het
Or1e22	A	T	11: 73,376,893 (GRCm39)	Y252*	probably null	Het
Or2f1	T	C	6: 42,721,621 (GRCm39)	S217P	probably damaging	Het
Or4c106	T	C	2: 88,682,516 (GRCm39)	V74A	possibly damaging	Het
Or4f17-ps1	T	A	2: 111,357,969 (GRCm39)	F103L	probably damaging	Het
Or4p7	T	A	2: 88,221,674 (GRCm39)	L28I	probably benign	Het
Or7g35	A	G	9: 19,496,504 (GRCm39)	T224A	probably benign	Het
Pcgf2	A	T	11: 97,582,515 (GRCm39)	Y7N	possibly damaging	Het
Pdlim5	G	A	3: 142,017,740 (GRCm39)		probably benign	Het
Pdzd2	A	G	15: 12,375,734 (GRCm39)	V1467A	probably damaging	Het
Pigp	C	A	16: 94,160,006 (GRCm39)	G134V	probably benign	Het
Pik3c2g	T	C	6: 139,789,657 (GRCm39)	Y385H	possibly damaging	Het
Pnliprp2	G	A	19: 58,754,750 (GRCm39)	E265K	probably benign	Het
Prl3c1	G	T	13: 27,386,471 (GRCm39)		probably null	Het
Ptpn4	A	T	1: 119,692,826 (GRCm39)	Y110*	probably null	Het
Ptprq	C	T	10: 107,522,416 (GRCm39)	V546I	probably damaging	Het
Rd3l	C	T	12: 111,946,578 (GRCm39)		probably null	Het
Rpl37	G	A	15: 5,147,128 (GRCm39)	R56Q	possibly damaging	Het
Rttn	A	T	18: 89,060,292 (GRCm39)	H998L	probably damaging	Het
Rufy1	A	T	11: 50,292,315 (GRCm39)	F491L	probably benign	Het
Simc1	T	G	13: 54,673,131 (GRCm39)	V493G	possibly damaging	Het
Slc22a14	CTTTCCTGAA	C	9: 119,003,101 (GRCm39)		probably benign	Het
Slc25a46	A	T	18: 31,735,807 (GRCm39)	I144N	possibly damaging	Het
Smtn	A	T	11: 3,477,825 (GRCm39)	M1K	probably null	Het
Snd1	C	A	6: 28,884,250 (GRCm39)	Y766*	probably null	Het
Spata31d1d	C	T	13: 59,875,102 (GRCm39)	G811D	probably damaging	Het
Spta1	A	C	1: 174,074,174 (GRCm39)	D2371A	probably damaging	Het
Stard6	A	C	18: 70,631,631 (GRCm39)	D74A	possibly damaging	Het
Stim2	G	T	5: 54,262,712 (GRCm39)	R318L	probably benign	Het
Sufu	C	T	19: 46,463,991 (GRCm39)	T401I	possibly damaging	Het
Suz12	G	A	11: 79,920,057 (GRCm39)	G539D	probably damaging	Het
Sytl2	C	G	7: 90,025,245 (GRCm39)	S411C	probably damaging	Het
Taf6	G	A	5: 138,181,465 (GRCm39)	Q156*	probably null	Het
Tead4	T	C	6: 128,247,950 (GRCm39)	D29G	probably damaging	Het
Thada	T	C	17: 84,751,611 (GRCm39)	Y455C	probably damaging	Het
Tlr6	G	C	5: 65,111,002 (GRCm39)	T635S	possibly damaging	Het
Tlr9	A	G	9: 106,101,876 (GRCm39)	D389G	probably benign	Het
Tmem54	A	T	4: 129,002,073 (GRCm39)	H40L	probably damaging	Het
Trappc9	G	T	15: 72,808,905 (GRCm39)	N540K	probably damaging	Het
Trbv28	C	T	6: 41,248,788 (GRCm39)	S106F	probably damaging	Het
Trrap	A	T	5: 144,793,770 (GRCm39)	H3384L	probably damaging	Het
Vat1	G	A	11: 101,351,426 (GRCm39)	T305M	probably damaging	Het
Vmn2r85	A	G	10: 130,257,302 (GRCm39)	S544P	probably damaging	Het
Vps8	T	C	16: 21,278,536 (GRCm39)	S267P	probably damaging	Het
Ylpm1	T	A	12: 85,096,719 (GRCm39)	V1242E	probably damaging	Het
Zfp267	C	T	3: 36,218,285 (GRCm39)	R102C	possibly damaging	Het
Zfp322a	T	C	13: 23,541,052 (GRCm39)	Y230C	probably damaging	Het
Zfp352	T	A	4: 90,112,376 (GRCm39)	V172E	probably benign	Het
Zfp936	A	T	7: 42,839,034 (GRCm39)	H167L	probably damaging	Het
Zkscan14	A	G	5: 145,132,302 (GRCm39)	Y410H	probably benign	Het
Zkscan17	A	G	11: 59,394,538 (GRCm39)	M21T	probably damaging	Het
Zswim4	G	T	8: 84,938,852 (GRCm39)	A1010D	probably benign	Het

Other mutations in Usp16

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01322:Usp16	APN	16	87,263,164 (GRCm39)	missense	possibly damaging	0.95
IGL01589:Usp16	APN	16	87,276,071 (GRCm39)	missense	probably benign	0.00
IGL02570:Usp16	APN	16	87,277,781 (GRCm39)	missense	probably damaging	1.00
IGL02736:Usp16	APN	16	87,261,723 (GRCm39)	missense	possibly damaging	0.75
IGL02973:Usp16	APN	16	87,276,627 (GRCm39)	missense	probably damaging	1.00
IGL03066:Usp16	APN	16	87,268,721 (GRCm39)	missense	probably damaging	1.00
PIT1430001:Usp16	UTSW	16	87,270,020 (GRCm39)	missense	probably damaging	0.99
R0395:Usp16	UTSW	16	87,272,334 (GRCm39)	missense	probably damaging	1.00
R0619:Usp16	UTSW	16	87,269,052 (GRCm39)	missense	probably benign	0.02
R1146:Usp16	UTSW	16	87,271,536 (GRCm39)	missense	possibly damaging	0.93
R1146:Usp16	UTSW	16	87,271,536 (GRCm39)	missense	possibly damaging	0.93
R1549:Usp16	UTSW	16	87,261,722 (GRCm39)	missense	probably damaging	1.00
R1557:Usp16	UTSW	16	87,259,030 (GRCm39)	critical splice donor site	probably null
R1776:Usp16	UTSW	16	87,276,204 (GRCm39)	missense	probably damaging	0.97
R1818:Usp16	UTSW	16	87,276,020 (GRCm39)	nonsense	probably null
R1835:Usp16	UTSW	16	87,277,795 (GRCm39)	missense	probably damaging	1.00
R2022:Usp16	UTSW	16	87,270,014 (GRCm39)	missense	probably damaging	1.00
R2146:Usp16	UTSW	16	87,270,075 (GRCm39)	critical splice donor site	probably null
R2432:Usp16	UTSW	16	87,263,246 (GRCm39)	critical splice donor site	probably null
R3110:Usp16	UTSW	16	87,268,736 (GRCm39)	splice site	probably null
R3112:Usp16	UTSW	16	87,268,736 (GRCm39)	splice site	probably null
R3771:Usp16	UTSW	16	87,255,571 (GRCm39)	start codon destroyed	probably null	1.00
R4353:Usp16	UTSW	16	87,267,242 (GRCm39)	missense	probably damaging	1.00
R4973:Usp16	UTSW	16	87,277,802 (GRCm39)	missense	probably damaging	0.99
R5276:Usp16	UTSW	16	87,267,339 (GRCm39)	critical splice donor site	probably null
R5753:Usp16	UTSW	16	87,279,787 (GRCm39)	missense	probably damaging	0.98
R6230:Usp16	UTSW	16	87,261,686 (GRCm39)	missense	possibly damaging	0.48
R6267:Usp16	UTSW	16	87,280,079 (GRCm39)	missense	probably benign	0.00
R6473:Usp16	UTSW	16	87,280,023 (GRCm39)	missense	probably benign	0.00
R6736:Usp16	UTSW	16	87,267,285 (GRCm39)	missense	probably damaging	1.00
R7006:Usp16	UTSW	16	87,268,724 (GRCm39)	missense	probably damaging	1.00
R7012:Usp16	UTSW	16	87,255,632 (GRCm39)	critical splice donor site	probably null
R7040:Usp16	UTSW	16	87,277,817 (GRCm39)	missense	probably damaging	1.00
R7136:Usp16	UTSW	16	87,280,059 (GRCm39)	missense	probably benign
R7295:Usp16	UTSW	16	87,268,977 (GRCm39)	missense	probably benign	0.44
R7434:Usp16	UTSW	16	87,276,207 (GRCm39)	nonsense	probably null
R7497:Usp16	UTSW	16	87,263,174 (GRCm39)	nonsense	probably null
R7571:Usp16	UTSW	16	87,261,723 (GRCm39)	missense	possibly damaging	0.75
R7576:Usp16	UTSW	16	87,276,188 (GRCm39)	missense	probably benign	0.34
R7624:Usp16	UTSW	16	87,273,693 (GRCm39)	missense	probably benign	0.23
R7889:Usp16	UTSW	16	87,271,472 (GRCm39)	missense	probably benign	0.44
R8499:Usp16	UTSW	16	87,271,536 (GRCm39)	missense	possibly damaging	0.93
R8779:Usp16	UTSW	16	87,276,297 (GRCm39)	missense	probably benign	0.00
R9182:Usp16	UTSW	16	87,276,542 (GRCm39)	missense	probably benign	0.00
R9251:Usp16	UTSW	16	87,266,640 (GRCm39)	missense	probably benign	0.08
R9367:Usp16	UTSW	16	87,261,669 (GRCm39)	missense	probably benign	0.01
R9707:Usp16	UTSW	16	87,263,235 (GRCm39)	missense	probably benign
R9746:Usp16	UTSW	16	87,276,120 (GRCm39)	missense	probably benign	0.00
X0061:Usp16	UTSW	16	87,276,345 (GRCm39)	missense	probably benign	0.01
X0064:Usp16	UTSW	16	87,268,613 (GRCm39)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- AAATGTGCTGCTGCTTACATTCTTC -3'
(R):5'- AGCTCTAGAAACCAGGACTGTC -3'

Sequencing Primer
(F):5'- GCTTACATTCTTCATGTGTTATGGAC -3'
(R):5'- ACCAGGACTGTCTAAATTTCTTCAC -3'

Posted On

2016-04-27