Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01015:Rps2-ps10'

54076

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rps2-ps10

Ensembl Gene

ENSMUSG00000091957

Gene Name

ribosomal protein S2, pseudogene 10

Synonyms

Gm8553

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01015

Quality Score

Status

Chromosome

Chromosomal Location

61392110-61393058 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

C to T at 61392896 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000025468 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025468]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000025468

SMART Domains

Protein: ENSMUSP00000025468
Gene: ENSMUSG00000024575

Domain	Start	End	E-Value	Type
GAF	73	232	1.36e-21	SMART
GAF	254	441	3.21e-23	SMART
low complexity region	478	495	N/A	INTRINSIC
Blast:HDc	496	540	3e-11	BLAST
HDc	556	734	6.95e-8	SMART
Blast:HDc	759	786	1e-8	BLAST
low complexity region	817	837	N/A	INTRINSIC
low complexity region	839	853	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000076842

SMART Domains

Protein: ENSMUSP00000100598
Gene: ENSMUSG00000057244

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_S5	29	95	3.9e-30	PFAM
Pfam:Ribosomal_S5_C	112	185	1.9e-24	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000170335

SMART Domains

Protein: ENSMUSP00000133092
Gene: ENSMUSG00000091957

Domain	Start	End	E-Value	Type
low complexity region	6	53	N/A	INTRINSIC
Pfam:Ribosomal_S5	102	166	5.7e-34	PFAM
Pfam:Ribosomal_S5_C	185	256	2.4e-30	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 30 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ano4	A	G	10: 88,870,961 (GRCm39)	Y238H	probably damaging	Het
Apol7a	T	C	15: 77,274,055 (GRCm39)		probably benign	Het
Cacna1d	A	T	14: 29,773,699 (GRCm39)		probably benign	Het
Col12a1	A	G	9: 79,541,023 (GRCm39)	V2368A	probably damaging	Het
Creb3l4	A	G	3: 90,150,138 (GRCm39)	M1T	probably null	Het
Dpys	T	C	15: 39,710,045 (GRCm39)	D128G	probably damaging	Het
Ero1b	A	G	13: 12,616,623 (GRCm39)		probably null	Het
Fcgbpl1	T	C	7: 27,854,743 (GRCm39)	C1790R	probably damaging	Het
Fcgr4	A	G	1: 170,853,358 (GRCm39)	S188G	possibly damaging	Het
Fry	A	G	5: 150,346,252 (GRCm39)	D1587G	probably benign	Het
Gm43638	T	A	5: 87,634,473 (GRCm39)	R45*	probably null	Het
Gm7647	T	A	5: 95,111,746 (GRCm39)	C152S	probably benign	Het
Golga3	T	G	5: 110,335,583 (GRCm39)	M299R	probably benign	Het
Iqub	A	T	6: 24,501,005 (GRCm39)		probably benign	Het
Irak3	A	T	10: 119,978,695 (GRCm39)	Y493*	probably null	Het
Jakmip1	G	T	5: 37,242,750 (GRCm39)	E13*	probably null	Het
Morc3	G	A	16: 93,659,534 (GRCm39)	C446Y	probably damaging	Het
Mroh2b	G	A	15: 4,971,024 (GRCm39)	D1010N	probably damaging	Het
Or14c44	A	G	7: 86,061,998 (GRCm39)	T184A	probably damaging	Het
Or2y16	T	A	11: 49,335,201 (GRCm39)	N174K	probably damaging	Het
Or5m9	A	T	2: 85,876,996 (GRCm39)	M57L	possibly damaging	Het
Pkhd1	G	A	1: 20,593,482 (GRCm39)	H1544Y	possibly damaging	Het
Smco1	T	C	16: 32,092,887 (GRCm39)	V186A	probably damaging	Het
Snx1	C	T	9: 66,001,713 (GRCm39)	E314K	possibly damaging	Het
Timd2	T	C	11: 46,567,170 (GRCm39)	Y255C	probably benign	Het
Tnc	A	T	4: 63,935,571 (GRCm39)	I455K	probably benign	Het
Tsc22d1	A	G	14: 76,656,181 (GRCm39)	I31V	possibly damaging	Het
Tyk2	A	G	9: 21,031,996 (GRCm39)	S360P	probably benign	Het
Uroc1	G	T	6: 90,335,883 (GRCm39)		probably benign	Het
Vmn1r122	A	T	7: 20,867,761 (GRCm39)	V98E	probably damaging	Het

Posted On

2013-06-28