Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01467:Psma5-ps'

88131

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Psma5-ps

Ensembl Gene

ENSMUSG00000050490

Gene Name

proteasome subunit alpha 5, pseudogene

Synonyms

Gm8394

Accession Numbers

Essential gene?

Probably essential (E-score: 0.913) question?

Stock #

IGL01467

Quality Score

Status

Chromosome

Chromosomal Location

85149352-85150303 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 85149986 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: ENSMUST00000079684

SMART Domains

Protein: ENSMUSP00000078625
Gene: ENSMUSG00000050490

Domain	Start	End	E-Value	Type
Proteasome_A_N	8	30	6.32e-8	SMART
Pfam:Proteasome	31	220	5.6e-57	PFAM

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
Adam1a	A	G	5: 121,657,791 (GRCm39)	C501R	probably damaging	Het
Atxn1	C	T	13: 45,720,669 (GRCm39)	V409I	probably damaging	Het
Cdkn2aip	T	C	8: 48,164,247 (GRCm39)	R489G	probably damaging	Het
Cgn	A	G	3: 94,686,898 (GRCm39)	S135P	probably damaging	Het
Cpne3	C	A	4: 19,553,737 (GRCm39)	C98F	probably benign	Het
Cyp2c23	T	C	19: 44,003,512 (GRCm39)	N221S	possibly damaging	Het
Dnah8	A	G	17: 30,998,890 (GRCm39)	N3525S	probably damaging	Het
Efr3b	T	C	12: 4,019,597 (GRCm39)	E560G	probably damaging	Het
Eif2b5	C	A	16: 20,327,714 (GRCm39)	C154*	probably null	Het
Eps8l2	A	G	7: 140,941,514 (GRCm39)	E595G	probably damaging	Het
Gm9839	A	T	1: 32,559,032 (GRCm39)	I350N	probably damaging	Het
Hdlbp	A	T	1: 93,345,420 (GRCm39)		probably benign	Het
Il18rap	A	T	1: 40,587,799 (GRCm39)	I466F	probably damaging	Het
Itpr1	T	A	6: 108,465,457 (GRCm39)	I2123N	probably damaging	Het
Jakmip2	A	G	18: 43,715,352 (GRCm39)	I58T	probably benign	Het
Kdm2a	A	G	19: 4,374,435 (GRCm39)	S899P	probably damaging	Het
Mmp15	T	A	8: 96,092,959 (GRCm39)	F113I	probably benign	Het
Neb	T	C	2: 52,049,499 (GRCm39)	H6448R	possibly damaging	Het
Or1j12	C	T	2: 36,342,656 (GRCm39)	R20*	probably null	Het
Or2m13	T	C	16: 19,226,539 (GRCm39)	T77A	probably benign	Het
Pdgfc	A	G	3: 81,116,398 (GRCm39)	T251A	probably damaging	Het
Pdgfra	T	C	5: 75,346,292 (GRCm39)		probably null	Het
Pdpk1	A	G	17: 24,307,144 (GRCm39)	S269P	probably damaging	Het
Pip4k2c	A	T	10: 127,035,498 (GRCm39)	F347L	probably benign	Het
Platr26	T	C	2: 71,553,656 (GRCm39)		noncoding transcript	Het
Pnisr	C	T	4: 21,874,650 (GRCm39)		probably benign	Het
Rab3gap1	T	A	1: 127,858,121 (GRCm39)		probably null	Het
Scn10a	C	T	9: 119,487,478 (GRCm39)	V619I	probably benign	Het
Slc38a11	T	A	2: 65,147,200 (GRCm39)	T426S	probably benign	Het
Son	T	C	16: 91,454,165 (GRCm39)	S971P	possibly damaging	Het
Stk33	T	A	7: 108,928,796 (GRCm39)	I239L	probably damaging	Het
Tiparp	G	T	3: 65,460,030 (GRCm39)	G442*	probably null	Het
Tmem270	G	T	5: 134,930,815 (GRCm39)		probably benign	Het
Vmn2r4	A	T	3: 64,313,816 (GRCm39)	N388K	probably damaging	Het
Zfp750	A	T	11: 121,403,767 (GRCm39)	C369*	probably null	Het

Other mutations in Psma5-ps

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01336:Psma5-ps	APN	10	85,150,028 (GRCm39)	exon	noncoding transcript
IGL02638:Psma5-ps	APN	10	85,149,698 (GRCm39)	exon	noncoding transcript
IGL03253:Psma5-ps	APN	10	85,149,556 (GRCm39)	exon	noncoding transcript
R1929:Psma5-ps	UTSW	10	85,149,595 (GRCm39)	exon	noncoding transcript
R2271:Psma5-ps	UTSW	10	85,149,595 (GRCm39)	exon	noncoding transcript
R2893:Psma5-ps	UTSW	10	85,149,848 (GRCm39)	exon	noncoding transcript
R4689:Psma5-ps	UTSW	10	85,150,065 (GRCm39)	exon	noncoding transcript
R4711:Psma5-ps	UTSW	10	85,149,667 (GRCm39)	exon	noncoding transcript
R5537:Psma5-ps	UTSW	10	85,149,913 (GRCm39)	exon	noncoding transcript
R5934:Psma5-ps	UTSW	10	85,150,145 (GRCm39)	exon	noncoding transcript
T0722:Psma5-ps	UTSW	10	85,149,457 (GRCm39)	exon	noncoding transcript

Posted On

2013-11-18