Mutagenetix > Incidental Mutations

Incidental Mutation 'R4878:Otud7b'

375042

Institutional Source

Beutler Lab

Gene Symbol

Otud7b

Ensembl Gene

ENSMUSG00000038495

Gene Name

OTU domain containing 7B

Synonyms

4930463P07Rik, 2900060B22Rik, Za20d1

MMRRC Submission

042487-MU

Accession Numbers

Is this an essential gene?

Essential (E-score: 1.000) question?

Stock #

R4878 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

96104527-96161129 bp(+) (GRCm38)

Type of Mutation

utr 5 prime

DNA Base Change (assembly)

T to A at 96136510 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000121847 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035519] [ENSMUST00000090785] [ENSMUST00000098849] [ENSMUST00000132980] [ENSMUST00000138206]

Predicted Effect

probably benign
Transcript: ENSMUST00000035519

SMART Domains

Protein: ENSMUSP00000046413
Gene: ENSMUSG00000038495

Domain	Start	End	E-Value	Type
PDB:2L2D\|A	1	59	1e-25	PDB
low complexity region	112	124	N/A	INTRINSIC
Pfam:OTU	189	359	4.9e-30	PFAM
low complexity region	482	498	N/A	INTRINSIC
low complexity region	527	558	N/A	INTRINSIC
low complexity region	821	836	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000090785

SMART Domains

Protein: ENSMUSP00000088291
Gene: ENSMUSG00000038495

Domain	Start	End	E-Value	Type
PDB:2L2D\|A	1	59	1e-25	PDB
low complexity region	112	124	N/A	INTRINSIC
Pfam:OTU	189	359	4.9e-30	PFAM
low complexity region	482	498	N/A	INTRINSIC
low complexity region	527	558	N/A	INTRINSIC
low complexity region	821	836	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000098849

SMART Domains

Protein: ENSMUSP00000096449
Gene: ENSMUSG00000038495

Domain	Start	End	E-Value	Type
PDB:2L2D\|A	1	59	1e-25	PDB
low complexity region	112	124	N/A	INTRINSIC
Pfam:OTU	189	359	4.7e-27	PFAM
low complexity region	482	498	N/A	INTRINSIC
low complexity region	527	558	N/A	INTRINSIC
Pfam:zf-A20	797	821	6.3e-10	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000132980

SMART Domains

Protein: ENSMUSP00000115699
Gene: ENSMUSG00000038495

Domain	Start	End	E-Value	Type
Pfam:UBA_4	6	44	8.1e-8	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000138206

SMART Domains

Protein: ENSMUSP00000121847
Gene: ENSMUSG00000038495

Domain	Start	End	E-Value	Type
Pfam:UBA_4	6	44	2.7e-7	PFAM
low complexity region	112	124	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146660

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.8%
20x: 93.8%

Validation Efficiency

96% (70/73)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased body weight, tertiary lymphoid hyperplasia, increased stimulated B cell proliferation and survival and decreased susceptibility to C. rodentium infection. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4	C	A	4: 144,613,845	H47N	possibly damaging	Het
Adgrg3	A	T	8: 95,035,086	N159I	possibly damaging	Het
Agrn	A	T	4: 156,170,845	L1449Q	probably damaging	Het
Anks6	C	T	4: 47,030,795	G601S	probably damaging	Het
Atg2a	A	T	19: 6,250,244	E694V	probably damaging	Het
Ccndbp1	T	A	2: 121,014,691	L363*	probably null	Het
Cdh16	A	T	8: 104,618,064	D478E	probably damaging	Het
Cep295	A	T	9: 15,334,956	W735R	probably benign	Het
Cnnm2	C	T	19: 46,859,083	P682S	probably benign	Het
Daam2	C	A	17: 49,460,710	R951L	probably damaging	Het
Dmxl1	T	A	18: 49,851,476	F180I	probably damaging	Het
Dnajc6	T	C	4: 101,599,034		probably benign	Het
Efemp2	A	T	19: 5,480,761		probably benign	Het
Emilin1	A	G	5: 30,917,066	D217G	probably benign	Het
Enpep	A	T	3: 129,276,771	M829K	probably benign	Het
Epb41l4a	A	G	18: 33,798,572	V623A	probably damaging	Het
Erlin2	T	A	8: 27,027,166		probably null	Het
Fbln2	T	C	6: 91,256,995		probably null	Het
Gga3	A	T	11: 115,591,321	I157N	probably damaging	Het
Gm884	A	G	11: 103,617,891		probably benign	Het
Gtpbp6	C	T	5: 110,107,311		probably benign	Het
Hps4	T	C	5: 112,375,368	V584A	probably benign	Het
Ighv1-50	T	C	12: 115,119,947	Y51C	probably benign	Het
Kif13b	T	C	14: 64,806,154	L1801P	probably benign	Het
Kif16b	T	C	2: 142,848,003	I330V	probably damaging	Het
Klb	A	T	5: 65,348,490	R27W	probably damaging	Het
Lrif1	A	T	3: 106,735,640	K169M	probably damaging	Het
Met	A	G	6: 17,549,059	D970G	probably damaging	Het
Mical3	A	T	6: 120,969,387	M1051K	possibly damaging	Het
Mios	A	G	6: 8,215,094	N97D	probably benign	Het
Msh5	G	A	17: 35,038,456	R321C	probably damaging	Het
Mybpc1	T	C	10: 88,551,430	Q473R	possibly damaging	Het
Ncoa1	C	T	12: 4,275,004	G970D	probably damaging	Het
Neb	T	C	2: 52,219,394	Y232C	probably damaging	Het
Nefh	A	G	11: 4,941,333	S429P	probably damaging	Het
Notch3	C	T	17: 32,147,085	G1014D	probably damaging	Het
Nup107	A	T	10: 117,751,418	C859S	probably benign	Het
Olfr1033	A	G	2: 86,041,455	I47V	probably benign	Het
Olfr136	T	G	17: 38,335,627	F157V	probably benign	Het
Olfr412	T	C	11: 74,364,848	Y60H	probably damaging	Het
Pde1a	A	T	2: 79,878,139	S312T	probably benign	Het
Piwil1	G	T	5: 128,740,981	R94L	probably damaging	Het
Pnma2	G	A	14: 66,917,054	W309*	probably null	Het
Ppef2	A	C	5: 92,228,740		probably null	Het
Rabac1	T	A	7: 24,969,967	Q212L	possibly damaging	Het
Rad51	T	C	2: 119,120,492		probably benign	Het
Rbm48	A	T	5: 3,591,853		probably benign	Het
Rft1	C	T	14: 30,677,804	S315L	probably benign	Het
Rgs13	C	T	1: 144,171,479	M1I	probably null	Het
Rhbg	A	C	3: 88,247,453	S215A	probably benign	Het
Rufy2	A	T	10: 63,002,211	N379I	probably damaging	Het
Slc17a1	T	C	13: 23,880,654	L367P	probably damaging	Het
Slc25a39	G	A	11: 102,403,675	R308C	probably benign	Het
Smo	A	G	6: 29,753,571	T149A	probably benign	Het
Sqle	A	G	15: 59,316,085	K81E	probably benign	Het
Tfpi	A	G	2: 84,452,555		probably null	Het
Tnk2	A	G	16: 32,679,630	D572G	probably damaging	Het
Ubr5	A	T	15: 38,006,564	M1149K	probably benign	Het
Utrn	T	A	10: 12,727,758	Q626L	probably damaging	Het
Virma	T	A	4: 11,544,971	H1643Q	probably damaging	Het
Wnt3	G	T	11: 103,808,205	G46C	possibly damaging	Het
Zkscan7	G	T	9: 122,890,800	G184*	probably null	Het

Other mutations in Otud7b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01344:Otud7b	APN	3	96150980	splice site	probably benign
IGL01651:Otud7b	APN	3	96153490	nonsense	probably null
IGL01941:Otud7b	APN	3	96155459	missense	probably benign	0.00
IGL02376:Otud7b	APN	3	96155037	missense	possibly damaging	0.48
IGL03047:Otud7b	APN	3	96150984	splice site	probably benign
IGL03189:Otud7b	APN	3	96155478	missense	probably benign
PIT4434001:Otud7b	UTSW	3	96140465	missense	probably damaging	1.00
R0605:Otud7b	UTSW	3	96144959	unclassified	probably benign
R1364:Otud7b	UTSW	3	96151451	missense	probably damaging	1.00
R1570:Otud7b	UTSW	3	96155891	missense	probably damaging	1.00
R2172:Otud7b	UTSW	3	96153520	intron	probably null
R2199:Otud7b	UTSW	3	96155772	missense	probably damaging	1.00
R2842:Otud7b	UTSW	3	96136594	missense	probably damaging	1.00
R2914:Otud7b	UTSW	3	96155955	missense	probably benign	0.01
R4716:Otud7b	UTSW	3	96150910	missense	probably damaging	0.96
R4810:Otud7b	UTSW	3	96136607	missense	probably damaging	1.00
R5327:Otud7b	UTSW	3	96155738	missense	probably benign
R5376:Otud7b	UTSW	3	96153524	intron	probably null
R5530:Otud7b	UTSW	3	96141488	missense	probably damaging	1.00
R5741:Otud7b	UTSW	3	96144304	missense	probably damaging	1.00
R5877:Otud7b	UTSW	3	96151960	nonsense	probably null
R6365:Otud7b	UTSW	3	96155250	missense	probably benign	0.03
R7095:Otud7b	UTSW	3	96155237	missense	probably benign	0.01
R7404:Otud7b	UTSW	3	96136625	critical splice donor site	probably null
R7793:Otud7b	UTSW	3	96155211	missense	probably benign	0.01
R7840:Otud7b	UTSW	3	96155373	missense	probably damaging	1.00
R7923:Otud7b	UTSW	3	96155373	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCAATCCCTGGGCTACATC -3'
(R):5'- GAGGGTTTACAGCACTCAAAAC -3'

Sequencing Primer
(F):5'- TGGGCTACATCCTCAGTGC -3'
(R):5'- CAGCACTCAAAACATTTTTCTGATCC -3'

Posted On

2016-03-17