Mutagenetix > Incidental Mutations

Incidental Mutation 'R0390:Larp4b'

98815

Institutional Source

Beutler Lab

Gene Symbol

Larp4b

Ensembl Gene

ENSMUSG00000033499

Gene Name

La ribonucleoprotein domain family, member 4B

Synonyms

Larp5, D13Wsu64e

MMRRC Submission

038596-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.424) question?

Stock #

R0390 (G1)

Quality Score

185

Status

Validated

Chromosome

Chromosomal Location

9093881-9174451 bp(+) (GRCm38)

Type of Mutation

intron

DNA Base Change (assembly)

T to A at 9158107 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000139578 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000091829] [ENSMUST00000091829] [ENSMUST00000188211] [ENSMUST00000188211] [ENSMUST00000188939] [ENSMUST00000188939]

Predicted Effect

probably null
Transcript: ENSMUST00000091829

SMART Domains

Protein: ENSMUSP00000089437
Gene: ENSMUSG00000033499

Domain	Start	End	E-Value	Type
LA	156	234	3.25e-36	SMART
RRM	239	309	6.25e-2	SMART
low complexity region	510	529	N/A	INTRINSIC
low complexity region	586	597	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000091829

SMART Domains

Protein: ENSMUSP00000089437
Gene: ENSMUSG00000033499

Domain	Start	End	E-Value	Type
LA	156	234	3.25e-36	SMART
RRM	239	309	6.25e-2	SMART
low complexity region	510	529	N/A	INTRINSIC
low complexity region	586	597	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000188211

SMART Domains

Protein: ENSMUSP00000140993
Gene: ENSMUSG00000033499

Domain	Start	End	E-Value	Type
LA	156	234	3.25e-36	SMART
RRM	239	309	6.25e-2	SMART
low complexity region	510	529	N/A	INTRINSIC
low complexity region	586	597	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000188211

SMART Domains

Protein: ENSMUSP00000140993
Gene: ENSMUSG00000033499

Domain	Start	End	E-Value	Type
LA	156	234	3.25e-36	SMART
RRM	239	309	6.25e-2	SMART
low complexity region	510	529	N/A	INTRINSIC
low complexity region	586	597	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000188939

SMART Domains

Protein: ENSMUSP00000139578
Gene: ENSMUSG00000033499

Domain	Start	End	E-Value	Type
LA	156	234	3.25e-36	SMART
RRM	239	309	6.25e-2	SMART
low complexity region	510	529	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000188939

SMART Domains

Protein: ENSMUSP00000139578
Gene: ENSMUSG00000033499

Domain	Start	End	E-Value	Type
LA	156	234	3.25e-36	SMART
RRM	239	309	6.25e-2	SMART
low complexity region	510	529	N/A	INTRINSIC

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.1%
3x: 98.1%
10x: 95.9%
20x: 92.0%

Validation Efficiency

98% (110/112)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of an evolutionarily conserved protein family implicated in RNA metabolism and translation. Members of this family are characterized by the presence of an La motif, which is often located adjacent to one or more RNA recognition motifs (RRM). Together, the two motifs constitute the functional region of the protein and enable its interaction with the RNA substrate. This protein family is divided into five sub-families: the genuine La proteins and four La-related protein (LARP) sub-families. The protein encoded by this gene belongs to LARP sub-family 4. It is a cytoplasmic protein that may play a stimulatory role in translation. [provided by RefSeq, Oct 2012]

Allele List at MGI

Other mutations in this stock

Total: 110 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A730017C20Rik	T	A	18: 59,075,688	V136E	probably damaging	Het
Adam18	C	T	8: 24,674,054	G38R	probably benign	Het
Ap2m1	T	C	16: 20,541,099	M183T	probably damaging	Het
Apob	A	T	12: 7,988,678	I364F	probably damaging	Het
Arl6	A	T	16: 59,622,421		probably benign	Het
Cand2	A	G	6: 115,774,653	M15V	possibly damaging	Het
Cbl	A	G	9: 44,201,005	F131S	probably damaging	Het
Ccdc151	T	A	9: 21,991,708	H442L	probably benign	Het
Ccdc74a	A	G	16: 17,650,476	S321G	probably benign	Het
Cdc14b	T	C	13: 64,210,192		probably benign	Het
Cep152	T	C	2: 125,576,869		probably benign	Het
Cep290	A	G	10: 100,508,758	E479G	probably benign	Het
Chrm2	T	G	6: 36,524,111	I301R	probably benign	Het
Clec2e	A	G	6: 129,093,468	W197R	probably damaging	Het
Cnot10	G	T	9: 114,629,150	S96*	probably null	Het
Col19a1	A	G	1: 24,289,655		probably benign	Het
Csmd2	T	C	4: 128,133,673		probably benign	Het
Cthrc1	A	T	15: 39,086,764	*172L	probably null	Het
Cul9	A	T	17: 46,528,589	I821N	probably benign	Het
Daam1	G	C	12: 71,975,304		probably benign	Het
Dhx58	A	T	11: 100,699,264	I398N	probably damaging	Het
Dip2b	T	A	15: 100,193,913	H844Q	probably damaging	Het
Dmac2	A	G	7: 25,621,029	D50G	probably damaging	Het
Dmxl1	C	A	18: 49,879,362	Q1529K	probably benign	Het
Dtna	C	T	18: 23,597,501	P315L	probably damaging	Het
Ep300	T	C	15: 81,640,116	S1382P	unknown	Het
Fat2	A	T	11: 55,310,777	N490K	probably damaging	Het
Flg2	T	A	3: 93,200,355		probably benign	Het
Gm13084	T	A	4: 143,811,699	D234V	probably benign	Het
Gpatch1	T	C	7: 35,281,381		probably benign	Het
Grin2a	C	A	16: 9,579,585	K879N	possibly damaging	Het
Hacd3	A	C	9: 65,001,022	I164S	possibly damaging	Het
Hinfp	A	C	9: 44,298,948	C197G	probably damaging	Het
Hsd17b12	T	C	2: 94,114,990		probably benign	Het
Hsd3b1	A	T	3: 98,853,039	L212Q	probably damaging	Het
Ifrd1	C	T	12: 40,214,094		probably null	Het
Igf2bp2	A	G	16: 22,081,801	F129L	possibly damaging	Het
Kirrel3	T	A	9: 35,020,163	I409N	probably damaging	Het
Klhdc10	T	C	6: 30,447,412	I204T	probably damaging	Het
Kpna6	A	T	4: 129,657,804	S65R	possibly damaging	Het
Lama3	A	T	18: 12,407,563	D308V	probably benign	Het
Lgr6	C	T	1: 134,994,010	A199T	probably damaging	Het
Lyzl1	A	T	18: 4,169,175	T11S	probably benign	Het
Man1c1	A	G	4: 134,578,315	L366P	probably damaging	Het
Mef2a	A	G	7: 67,251,724	M100T	probably damaging	Het
Mettl13	G	A	1: 162,538,889	H474Y	possibly damaging	Het
Mmp3	A	G	9: 7,451,320	D352G	probably benign	Het
Mns1	T	C	9: 72,452,804	I412T	probably damaging	Het
Mon2	T	C	10: 123,007,021	D1501G	probably null	Het
Mylk	G	T	16: 34,875,620	G242W	probably damaging	Het
Nav1	T	C	1: 135,449,966	D1715G	possibly damaging	Het
Nckap1l	T	C	15: 103,453,883	S2P	probably damaging	Het
Nek3	A	T	8: 22,128,729		probably benign	Het
Nfrkb	A	G	9: 31,388,897		probably benign	Het
Nlrp4d	T	C	7: 10,388,778	D53G	probably benign	Het
Nol8	T	C	13: 49,662,152	S561P	probably damaging	Het
Nuf2	A	C	1: 169,525,297		probably benign	Het
Ofcc1	T	A	13: 40,015,313	D866V	possibly damaging	Het
Olfr195	A	G	16: 59,149,299	I150V	probably benign	Het
Optn	A	G	2: 5,046,195	L125P	probably benign	Het
Otoa	T	A	7: 121,131,341	F588Y	probably benign	Het
Pappa	T	A	4: 65,351,613		probably null	Het
Pde5a	T	G	3: 122,835,583	C635W	probably damaging	Het
Pdgfb	A	T	15: 80,003,419		probably null	Het
Pih1d2	T	A	9: 50,621,046	C135S	probably damaging	Het
Plcg1	G	T	2: 160,752,366	C361F	probably damaging	Het
Ppp4r4	T	C	12: 103,601,360		probably benign	Het
Prdm10	G	A	9: 31,349,268		probably null	Het
Prex2	T	A	1: 11,089,706		probably null	Het
Prss56	T	G	1: 87,184,730		probably null	Het
Prtg	A	G	9: 72,844,958	K209E	probably benign	Het
Ptprc	G	A	1: 138,122,575	T36I	possibly damaging	Het
Rasgrp4	A	G	7: 29,145,860	Y302C	probably damaging	Het
Rb1cc1	T	A	1: 6,248,634	M759K	probably damaging	Het
Rbm15b	T	A	9: 106,885,998	M324L	probably benign	Het
Rcbtb2	T	C	14: 73,178,547	V500A	probably damaging	Het
Rgs6	A	G	12: 83,133,677	K434R	probably damaging	Het
Rims1	C	T	1: 22,596,526	A125T	possibly damaging	Het
Robo3	A	G	9: 37,422,177	V746A	probably benign	Het
Rtl1	C	T	12: 109,591,386	E1340K	unknown	Het
Sacs	G	A	14: 61,205,640	D1712N	possibly damaging	Het
Samd4b	G	A	7: 28,403,977	P19S	probably benign	Het
Samhd1	T	C	2: 157,114,231	Y347C	probably damaging	Het
Sema6d	T	A	2: 124,658,490	I393N	probably damaging	Het
Sigmar1	C	T	4: 41,741,243	A4T	probably benign	Het
Skint9	C	A	4: 112,389,179	L245F	probably benign	Het
Slc35f5	T	C	1: 125,585,095	L372P	probably damaging	Het
Smc1b	A	T	15: 85,066,277	I1182N	probably damaging	Het
Smyd3	A	G	1: 178,957,573		probably benign	Het
Sptlc1	T	C	13: 53,337,612	D417G	probably benign	Het
Sv2c	T	C	13: 96,088,708	N31S	probably benign	Het
Tjp1	T	C	7: 65,314,990	D811G	probably damaging	Het
Top2b	A	G	14: 16,418,442	T1221A	probably benign	Het
Tph2	T	C	10: 115,174,109	D182G	probably damaging	Het
Traf6	C	T	2: 101,688,588	Q141*	probably null	Het
Ttn	T	C	2: 76,756,931	D21574G	probably damaging	Het
Uba2	T	A	7: 34,151,021	N367I	probably benign	Het
Ube2b	T	C	11: 51,988,602		probably benign	Het
Ubr5	G	T	15: 38,030,672	L426I	probably benign	Het
Ugt2a2	T	A	5: 87,464,148	H301L	probably benign	Het
Upf2	T	A	2: 6,018,894		probably benign	Het
Utrn	T	C	10: 12,710,060	D991G	probably benign	Het
Vmn2r25	T	C	6: 123,823,181	D734G	probably damaging	Het
Vmn2r68	T	A	7: 85,233,249		probably benign	Het
Vmn2r68	C	G	7: 85,233,258		probably null	Het
Vwf	T	A	6: 125,626,361	Y891*	probably null	Het
Wwox	C	T	8: 114,706,278	T228I	probably benign	Het
Zer1	C	T	2: 30,108,213		probably benign	Het
Zfp180	C	T	7: 24,104,707	H184Y	possibly damaging	Het
Zfp68	A	T	5: 138,607,225	Y279N	probably benign	Het

Other mutations in Larp4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01746:Larp4b	APN	13	9158124	missense	probably damaging	0.99
IGL02519:Larp4b	APN	13	9158580	missense	probably benign	0.04
IGL02609:Larp4b	APN	13	9170680	missense	probably damaging	1.00
R0116:Larp4b	UTSW	13	9170688	missense	probably damaging	1.00
R0585:Larp4b	UTSW	13	9147493	missense	probably damaging	1.00
R0585:Larp4b	UTSW	13	9170701	missense	probably benign	0.08
R0751:Larp4b	UTSW	13	9166309	splice site	probably benign
R1184:Larp4b	UTSW	13	9166309	splice site	probably benign
R1202:Larp4b	UTSW	13	9166326	missense	possibly damaging	0.84
R1525:Larp4b	UTSW	13	9145450	missense	probably damaging	1.00
R1599:Larp4b	UTSW	13	9122150	missense	probably damaging	1.00
R1637:Larp4b	UTSW	13	9151097	missense	probably benign	0.12
R1833:Larp4b	UTSW	13	9151199	missense	possibly damaging	0.89
R1852:Larp4b	UTSW	13	9137303	critical splice donor site	probably null
R1962:Larp4b	UTSW	13	9136842	missense	probably benign
R2359:Larp4b	UTSW	13	9158163	missense	probably damaging	0.97
R2973:Larp4b	UTSW	13	9166311	splice site	probably benign
R3803:Larp4b	UTSW	13	9158554	missense	probably benign	0.03
R4810:Larp4b	UTSW	13	9158591	missense	probably benign
R4828:Larp4b	UTSW	13	9170898	missense	probably damaging	1.00
R5135:Larp4b	UTSW	13	9170737	missense	probably damaging	1.00
R5250:Larp4b	UTSW	13	9170977	utr 3 prime	probably benign
R5259:Larp4b	UTSW	13	9158184	missense	probably damaging	0.98
R5379:Larp4b	UTSW	13	9136909	missense	probably benign	0.17
R5436:Larp4b	UTSW	13	9168900	missense	possibly damaging	0.93
R5616:Larp4b	UTSW	13	9158659	missense	probably damaging	0.98
R5774:Larp4b	UTSW	13	9170643	splice site	probably null
R5818:Larp4b	UTSW	13	9158560	missense	probably benign
R6007:Larp4b	UTSW	13	9168757	missense	probably benign	0.13
R6248:Larp4b	UTSW	13	9158702	missense	probably benign	0.01
R6452:Larp4b	UTSW	13	9147467	missense	probably damaging	0.98
R6501:Larp4b	UTSW	13	9168793	missense	probably damaging	1.00
R7324:Larp4b	UTSW	13	9158580	missense	probably benign	0.04
R7689:Larp4b	UTSW	13	9136798	missense	probably damaging	1.00

Predicted Primers

Posted On

2014-01-10