Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02367:Rpl15-ps6'

290776

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rpl15-ps6

Ensembl Gene

ENSMUSG00000057262

Gene Name

ribosomal protein L15, pseudogene 6

Synonyms

Gm10020

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02367

Quality Score

Status

Chromosome

Chromosomal Location

52341013-52341624 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 52341368 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000130678 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081993]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000081993

SMART Domains

Protein: ENSMUSP00000130678
Gene: ENSMUSG00000057262

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_L15e	2	193	4e-101	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930407I10Rik	T	C	15: 81,949,748 (GRCm39)	L1215P	probably benign	Het
Angptl7	T	C	4: 148,584,601 (GRCm39)	N49S	possibly damaging	Het
Asns	A	G	6: 7,685,411 (GRCm39)		probably benign	Het
Atr	T	A	9: 95,781,194 (GRCm39)	Y1419*	probably null	Het
Bptf	A	T	11: 106,964,178 (GRCm39)	I1672N	probably benign	Het
Cgas	G	A	9: 78,341,667 (GRCm39)	T370I	probably benign	Het
Chd1	A	G	17: 17,610,315 (GRCm39)	T490A	probably damaging	Het
Cyfip2	A	T	11: 46,167,732 (GRCm39)	C223*	probably null	Het
Ddr1	G	A	17: 35,994,372 (GRCm39)	A801V	probably damaging	Het
Dnah12	T	C	14: 26,430,316 (GRCm39)	V308A	probably benign	Het
Dync2h1	A	G	9: 7,158,926 (GRCm39)	V703A	probably damaging	Het
Fgd3	A	G	13: 49,440,802 (GRCm39)	F210L	probably damaging	Het
Gm6526	T	G	14: 43,988,262 (GRCm39)	V171G	probably damaging	Het
Grin3a	A	G	4: 49,702,805 (GRCm39)	Y894H	probably damaging	Het
Grm3	C	A	5: 9,561,660 (GRCm39)	C730F	probably damaging	Het
Habp4	C	A	13: 64,321,905 (GRCm39)	P181T	probably damaging	Het
Hdac4	A	G	1: 91,886,171 (GRCm39)		probably benign	Het
Ints5	A	G	19: 8,872,959 (GRCm39)	D306G	probably benign	Het
Mid2	T	A	X: 139,637,245 (GRCm39)	I273N	probably damaging	Het
Ndufs2	A	T	1: 171,066,934 (GRCm39)	Y114*	probably null	Het
Neu4	G	T	1: 93,952,213 (GRCm39)	R194L	probably damaging	Het
Ntng1	A	T	3: 110,042,829 (GRCm39)		probably null	Het
Nub1	A	G	5: 24,894,392 (GRCm39)	M1V	probably null	Het
Olfml2a	A	G	2: 38,844,680 (GRCm39)	T379A	probably benign	Het
Or9e1	A	T	11: 58,732,338 (GRCm39)	I133F	probably benign	Het
Pex3	G	T	10: 13,400,643 (GRCm39)	Q303K	probably benign	Het
Pmp2	A	T	3: 10,247,560 (GRCm39)	I43N	probably damaging	Het
Pnliprp1	T	A	19: 58,726,601 (GRCm39)	D319E	probably benign	Het
Rap1gap2	A	T	11: 74,288,181 (GRCm39)		probably null	Het
Rwdd3	A	G	3: 120,952,679 (GRCm39)	V104A	probably damaging	Het
Sbf1	A	T	15: 89,191,775 (GRCm39)	V157E	probably damaging	Het
Slc4a11	T	A	2: 130,526,879 (GRCm39)	I750F	probably damaging	Het
Tcea1	G	A	1: 4,948,356 (GRCm39)		probably null	Het
Ush2a	A	T	1: 188,516,943 (GRCm39)	M3218L	probably benign	Het
Utp20	G	A	10: 88,607,715 (GRCm39)		probably benign	Het
Zfp493	T	A	13: 67,935,089 (GRCm39)	Y347*	probably null	Het
Zswim6	T	C	13: 107,880,637 (GRCm39)		noncoding transcript	Het

Other mutations in Rpl15-ps6

Allele	Source	Chr	Coord	Type	Predicted Effect
R5080:Rpl15-ps6	UTSW	15	52,341,446 (GRCm39)	exon	noncoding transcript
R5231:Rpl15-ps6	UTSW	15	52,341,440 (GRCm39)	exon	noncoding transcript
R5569:Rpl15-ps6	UTSW	15	52,341,624 (GRCm39)	exon	noncoding transcript
R6516:Rpl15-ps6	UTSW	15	52,341,200 (GRCm39)	exon	noncoding transcript
R6640:Rpl15-ps6	UTSW	15	52,341,016 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16