Mutagenetix > Incidental Mutation

Incidental Mutation 'R7535:Usp29'

583511

Institutional Source

Beutler Lab

Gene Symbol

Usp29

Ensembl Gene

ENSMUSG00000051527

Gene Name

ubiquitin specific peptidase 29

Synonyms

Ocat

MMRRC Submission

045607-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7535 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

6730578-6967219 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 6961220 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Proline at position 21 (T21P)

Ref Sequence

ENSEMBL: ENSMUSP00000143283 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054055] [ENSMUST00000197117] [ENSMUST00000198068] [ENSMUST00000200535]

AlphaFold

Q9ES63

Predicted Effect

possibly damaging
Transcript: ENSMUST00000054055
AA Change: T21P

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000062349
Gene: ENSMUSG00000051527
AA Change: T21P

Domain	Start	End	E-Value	Type
Pfam:UCH_N	1	107	6.1e-37	PFAM
low complexity region	162	179	N/A	INTRINSIC
low complexity region	200	214	N/A	INTRINSIC
Pfam:UCH	288	823	6.1e-53	PFAM
Pfam:UCH_1	289	615	2.3e-16	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000197117
AA Change: T21P

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000143283
Gene: ENSMUSG00000051527
AA Change: T21P

Domain	Start	End	E-Value	Type
PDB:3U12\|B	11	73	3e-7	PDB
low complexity region	82	95	N/A	INTRINSIC
low complexity region	169	186	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000198068
AA Change: T21P

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000143267
Gene: ENSMUSG00000051527
AA Change: T21P

Domain	Start	End	E-Value	Type
PDB:3U12\|B	11	123	3e-6	PDB
low complexity region	169	186	N/A	INTRINSIC
low complexity region	207	221	N/A	INTRINSIC
Pfam:UCH	295	830	7.9e-52	PFAM
Pfam:UCH_1	296	626	9.6e-16	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000200535
AA Change: T21P

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000143769
Gene: ENSMUSG00000051527
AA Change: T21P

Domain	Start	End	E-Value	Type
Pfam:UCH_N	8	114	8.3e-34	PFAM
low complexity region	169	186	N/A	INTRINSIC
low complexity region	207	221	N/A	INTRINSIC
Pfam:UCH	295	830	2.8e-51	PFAM
Pfam:UCH_1	296	622	1.1e-14	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (82/82)

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610037L13Rik	T	G	4: 107,894,900	S159A	probably benign	Het
Abca7	T	A	10: 80,001,629	L449Q	probably benign	Het
Agtpbp1	T	C	13: 59,504,253	T415A	probably benign	Het
Akt3	A	T	1: 177,097,034	V165D	probably damaging	Het
Cbr2	T	A	11: 120,729,802	I219F	probably damaging	Het
Cdh20	T	A	1: 104,975,043	D486E	probably damaging	Het
Cenpe	A	G	3: 135,243,762	S103G	possibly damaging	Het
Chd4	T	A	6: 125,128,873	S1818T	probably benign	Het
Chst5	T	C	8: 111,890,163	D275G	probably damaging	Het
Clca1	A	G	3: 145,018,567	I244T	probably damaging	Het
Cyp2c54	A	G	19: 40,070,272	Y239H	probably benign	Het
Ddx25	A	G	9: 35,543,655	F446L	possibly damaging	Het
Dgkb	T	C	12: 38,136,647	L265P	probably damaging	Het
Dis3	A	G	14: 99,089,979	S363P	probably benign	Het
Disp3	T	C	4: 148,242,866	E1187G	probably damaging	Het
Dopey2	G	A	16: 93,806,361	G2061R	probably damaging	Het
Dsp	T	C	13: 38,192,789	S1517P	probably benign	Het
Epg5	T	A	18: 78,032,926	V2513E	probably benign	Het
Fryl	T	A	5: 73,098,196	T831S	probably benign	Het
Gm6309	A	T	5: 146,168,290	V271D	probably damaging	Het
H2-M2	G	T	17: 37,482,637	S159R	probably benign	Het
Helq	A	G	5: 100,790,133		probably null	Het
Herc1	G	C	9: 66,474,853	D3621H	probably damaging	Het
Hsd11b2	A	T	8: 105,519,123	I87F	probably damaging	Het
Ice2	A	G	9: 69,432,078	N959S	probably damaging	Het
Ifi47	T	A	11: 49,096,625	D406E	probably damaging	Het
Ifit3	T	G	19: 34,587,880	S275R	probably damaging	Het
Insl5	C	A	4: 103,018,198	K118N	probably damaging	Het
Irf7	A	T	7: 141,264,637	F158I	probably benign	Het
Kat2b	T	C	17: 53,624,403	L143P	probably damaging	Het
Klk1b1	A	T	7: 43,970,322	N102Y	probably damaging	Het
Krt13	C	T	11: 100,117,998	G410S	unknown	Het
Larp6	A	T	9: 60,724,154	T70S	probably benign	Het
Lrrc37a	T	C	11: 103,501,857	E914G	possibly damaging	Het
Mindy4	T	C	6: 55,297,753		probably null	Het
Myl10	G	C	5: 136,697,971	V70L	probably benign	Het
Myom2	A	G	8: 15,117,679	Y1088C	probably damaging	Het
Mysm1	T	C	4: 94,952,215	N655D	probably benign	Het
Nbas	T	A	12: 13,279,389	S112T	probably damaging	Het
Neb	A	G	2: 52,165,103		probably null	Het
Noxred1	G	A	12: 87,233,432	A42V	probably benign	Het
Olfm5	G	A	7: 104,154,237	P340S	possibly damaging	Het
Olfr1031	T	A	2: 85,991,901	V28E	probably benign	Het
Olfr1039	A	G	2: 86,131,264	V133A	probably benign	Het
Olfr1505	A	G	19: 13,919,085	K22E	probably benign	Het
Olfr167	T	C	16: 19,514,794	T281A	probably damaging	Het
Olfr749	G	A	14: 50,736,665	P166S	probably benign	Het
Pccb	A	T	9: 100,994,562		probably null	Het
Pnn	T	A	12: 59,072,137	V502E	probably benign	Het
Pole2	A	T	12: 69,222,429	I98K	probably benign	Het
Ptpn18	G	A	1: 34,473,364	D417N	possibly damaging	Het
Rasgrp4	A	G	7: 29,139,059	K111E	probably benign	Het
Rbbp6	G	A	7: 122,990,143	M351I	probably benign	Het
Rgs19	T	G	2: 181,691,308	H53P	probably damaging	Het
Rin1	A	T	19: 5,052,536	T369S	probably benign	Het
Rnaset2b	G	A	17: 6,991,739	E135K	possibly damaging	Het
Rprd2	G	A	3: 95,776,587	P379S	probably damaging	Het
Sbno1	A	G	5: 124,413,279	L47P	possibly damaging	Het
Slamf6	T	A	1: 171,919,758	L29Q	unknown	Het
Slc16a14	T	C	1: 84,913,122	Y154C	probably damaging	Het
Slc22a29	A	G	19: 8,169,978	F340S	probably damaging	Het
Slc6a4	T	G	11: 77,015,150	I259S	possibly damaging	Het
Smarca4	G	A	9: 21,647,625	V651I	possibly damaging	Het
Susd5	C	T	9: 114,064,040	A62V	possibly damaging	Het
Syt1	T	A	10: 108,627,422		probably null	Het
Taf10	T	C	7: 105,740,910	I218T	probably benign	Het
Tas1r1	C	A	4: 152,028,362	V745F	probably benign	Het
Tas2r125	C	A	6: 132,910,324	T225K	probably damaging	Het
Tcp11l2	G	T	10: 84,594,659	R216L	possibly damaging	Het
Tnks1bp1	C	T	2: 85,063,280	Q1184*	probably null	Het
Treml2	T	A	17: 48,302,819	V93D	probably damaging	Het
Trim11	G	A	11: 58,982,065	E192K	probably damaging	Het
Trim43a	A	G	9: 88,588,148	K336E	probably damaging	Het
Tspan33	T	A	6: 29,717,589	I268N	possibly damaging	Het
Tstd2	C	T	4: 46,116,960	C458Y	probably damaging	Het
Ttc6	A	G	12: 57,576,519	S235G	probably benign	Het
Usp36	A	T	11: 118,262,046	S1084T	possibly damaging	Het
Vps39	T	A	2: 120,324,695	N550I	probably damaging	Het
Wdr47	A	G	3: 108,629,711	I572V	probably benign	Het
Zfp112	A	T	7: 24,126,710	Y705F	probably damaging	Het
Zfp282	A	G	6: 47,904,944	T522A	probably benign	Het
Zfp292	T	C	4: 34,811,487	D524G	probably benign	Het
Zfp90	A	T	8: 106,424,268	K204N	possibly damaging	Het
Zmym2	T	C	14: 56,957,079	S1265P	probably damaging	Het

Other mutations in Usp29

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00659:Usp29	APN	7	6962282	missense	probably benign	0.06
IGL01588:Usp29	APN	7	6962611	missense	probably benign	0.33
IGL02032:Usp29	APN	7	6962018	missense	probably benign	0.41
IGL02052:Usp29	APN	7	6962526	missense	probably benign	0.06
IGL02331:Usp29	APN	7	6962156	missense	probably benign	0.16
IGL02551:Usp29	APN	7	6963353	splice site	probably null
IGL02573:Usp29	APN	7	6962618	splice site	probably null
IGL02894:Usp29	APN	7	6961634	missense	probably benign	0.00
R0029:Usp29	UTSW	7	6961581	missense	probably damaging	0.99
R0142:Usp29	UTSW	7	6962335	missense	probably benign	0.12
R0452:Usp29	UTSW	7	6963182	missense	possibly damaging	0.82
R0680:Usp29	UTSW	7	6962885	missense	possibly damaging	0.92
R1161:Usp29	UTSW	7	6961530	missense	probably damaging	1.00
R2391:Usp29	UTSW	7	6963771	splice site	probably null
R3104:Usp29	UTSW	7	6962053	nonsense	probably null
R4119:Usp29	UTSW	7	6962806	missense	probably benign	0.03
R4490:Usp29	UTSW	7	6961950	missense	possibly damaging	0.68
R4598:Usp29	UTSW	7	6962480	missense	probably benign	0.06
R4606:Usp29	UTSW	7	6963357	splice site	probably null
R4670:Usp29	UTSW	7	6962915	missense	possibly damaging	0.91
R4777:Usp29	UTSW	7	6962748	missense	probably benign	0.07
R4783:Usp29	UTSW	7	6961391	missense	probably damaging	1.00
R4785:Usp29	UTSW	7	6961391	missense	probably damaging	1.00
R4896:Usp29	UTSW	7	6962159	missense	probably benign	0.29
R4915:Usp29	UTSW	7	6961505	missense	probably benign
R4944:Usp29	UTSW	7	6961928	missense	possibly damaging	0.92
R5004:Usp29	UTSW	7	6962159	missense	probably benign	0.29
R5171:Usp29	UTSW	7	6962075	missense	probably damaging	0.99
R5268:Usp29	UTSW	7	6961584	missense	probably damaging	0.98
R5572:Usp29	UTSW	7	6962192	missense	probably benign	0.12
R5933:Usp29	UTSW	7	6961745	missense	probably benign
R6694:Usp29	UTSW	7	6962277	missense	probably benign	0.03
R7389:Usp29	UTSW	7	6963458	missense	possibly damaging	0.82
R7446:Usp29	UTSW	7	6961220	missense	possibly damaging	0.93
R7447:Usp29	UTSW	7	6961220	missense	possibly damaging	0.93
R7537:Usp29	UTSW	7	6961220	missense	possibly damaging	0.93
R8081:Usp29	UTSW	7	6963630	missense	probably benign	0.02
R8233:Usp29	UTSW	7	6962407	missense	probably benign	0.12
R8703:Usp29	UTSW	7	6961322	missense	probably benign	0.32
R8725:Usp29	UTSW	7	6962918	missense	probably damaging	0.98
R8727:Usp29	UTSW	7	6962918	missense	probably damaging	0.98
R8844:Usp29	UTSW	7	6961892	missense	probably benign	0.02
R9173:Usp29	UTSW	7	6961637	missense	possibly damaging	0.92
R9616:Usp29	UTSW	7	6963180	missense	possibly damaging	0.91
R9623:Usp29	UTSW	7	6961397	missense	possibly damaging	0.60

Predicted Primers

PCR Primer
(F):5'- AAGCTGATGGTGGTCAGTTAAG -3'
(R):5'- CGATGAGTAAGGATGTGTCGTCTC -3'

Sequencing Primer
(F):5'- GGTCAGTTAAGAGTTTAACCAGCCC -3'
(R):5'- AAGGATGTGTCGTCTCTCAAAG -3'

Posted On

2019-10-17