Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02454:Rps4l-ps'

293754

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rps4l-ps

Ensembl Gene

ENSMUSG00000046411

Gene Name

ribosomal protein S4-like, pseudogene

Synonyms

Gm6816

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.385) question?

Stock #

IGL02454

Quality Score

Status

Chromosome

Chromosomal Location

114526194-114526961 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 114526499 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000059737

SMART Domains

Protein: ENSMUSP00000049881
Gene: ENSMUSG00000046411

Domain	Start	End	E-Value	Type
Pfam:RS4NT	3	32	4.5e-16	PFAM
S4	35	99	2.74e-3	SMART
Blast:ACTIN	171	239	1e-27	BLAST

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Amz2	T	G	11: 109,324,887 (GRCm39)		probably benign	Het
Atp13a5	A	G	16: 29,051,560 (GRCm39)	F1104S	probably benign	Het
Cacna1c	T	C	6: 118,579,141 (GRCm39)	N1610S	probably damaging	Het
Ccnl1	A	T	3: 65,864,318 (GRCm39)	D122E	probably damaging	Het
Crtc2	G	A	3: 90,166,474 (GRCm39)	G65S	probably benign	Het
Dnah17	T	C	11: 117,971,593 (GRCm39)	T2160A	probably damaging	Het
Fads3	T	G	19: 10,032,483 (GRCm39)	L278R	probably damaging	Het
Foxp4	A	T	17: 48,186,507 (GRCm39)	L424*	probably null	Het
Gm10392	A	T	11: 77,409,216 (GRCm39)	E310V	probably damaging	Het
Gm11554	T	A	11: 99,694,815 (GRCm39)	S133C	unknown	Het
Hacd2	T	A	16: 34,926,761 (GRCm39)	F253L	probably benign	Het
Il3ra	T	C	14: 14,351,113 (GRCm38)	S212P	probably benign	Het
Mdn1	T	C	4: 32,694,674 (GRCm39)		probably null	Het
Mtfr1l	A	T	4: 134,257,696 (GRCm39)	L111H	probably damaging	Het
Mysm1	A	G	4: 94,858,741 (GRCm39)		probably benign	Het
Or10j2	C	A	1: 173,098,507 (GRCm39)	S255Y	probably damaging	Het
Or52d1	T	C	7: 103,755,819 (GRCm39)	V111A	probably damaging	Het
Plec	A	T	15: 76,075,231 (GRCm39)	F357I	probably damaging	Het
Polr3a	C	A	14: 24,525,891 (GRCm39)	V450L	possibly damaging	Het
Prkd1	T	C	12: 50,411,456 (GRCm39)	K764R	probably benign	Het
Pxn	C	T	5: 115,690,325 (GRCm39)	P256S	probably damaging	Het
Rbm25	T	A	12: 83,707,096 (GRCm39)	F247L	probably benign	Het
Rfx4	C	T	10: 84,675,970 (GRCm39)	T62M	possibly damaging	Het
Scn11a	A	G	9: 119,587,610 (GRCm39)	I1378T	probably benign	Het
Siglecg	T	C	7: 43,058,319 (GRCm39)	S69P	probably benign	Het
Stox1	T	C	10: 62,503,605 (GRCm39)	Y61C	probably damaging	Het
Tex55	T	A	16: 38,648,309 (GRCm39)	T267S	probably benign	Het
Tnks	C	T	8: 35,298,882 (GRCm39)		probably benign	Het
Tpr	A	G	1: 150,306,943 (GRCm39)	S1587G	probably benign	Het
Trappc6b	A	G	12: 59,090,433 (GRCm39)	*97Q	probably null	Het
Usf3	T	C	16: 44,037,545 (GRCm39)	V675A	probably damaging	Het
Wdr7	C	T	18: 63,929,299 (GRCm39)	T1045M	probably benign	Het
Zc3h11a	A	T	1: 133,552,254 (GRCm39)	C618S	probably benign	Het
Zfp398	T	C	6: 47,817,301 (GRCm39)	V47A	possibly damaging	Het
Zzz3	A	G	3: 152,134,211 (GRCm39)	N423S	probably benign	Het

Other mutations in Rps4l-ps

Allele	Source	Chr	Coord	Type	Predicted Effect
R4527:Rps4l-ps	UTSW	7	114,526,403 (GRCm39)	exon	noncoding transcript
R4719:Rps4l-ps	UTSW	7	114,526,537 (GRCm39)	exon	noncoding transcript
R5345:Rps4l-ps	UTSW	7	114,526,433 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16