Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03253:Psma5-ps'

414587

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: 0.905) question?

Stock #

IGL03253

Quality Score

Status

Chromosome

Chromosomal Location

85149352-85150303 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 85149556 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: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	G	A	12: 71,187,657 (GRCm39)	V98I	probably benign	Het
Aadacl4	G	T	4: 144,349,858 (GRCm39)	V372L	probably benign	Het
Acp5	A	T	9: 22,039,083 (GRCm39)	I210N	probably damaging	Het
Ash1l	G	A	3: 88,891,981 (GRCm39)	A1287T	probably damaging	Het
AU018091	A	T	7: 3,214,002 (GRCm39)	C72S	probably damaging	Het
Ccdc178	G	A	18: 21,978,068 (GRCm39)	Q800*	probably null	Het
Cd47	A	T	16: 49,714,561 (GRCm39)	H190L	probably benign	Het
Clca3a2	T	A	3: 144,777,324 (GRCm39)	H849L	probably benign	Het
Cmya5	G	A	13: 93,227,778 (GRCm39)	Q2437*	probably null	Het
Depdc5	T	C	5: 33,026,157 (GRCm39)		probably benign	Het
Erp44	T	A	4: 48,208,750 (GRCm39)	I237F	probably benign	Het
Gramd1a	C	T	7: 30,839,271 (GRCm39)	W8*	probably null	Het
Gucy2d	C	T	7: 98,100,871 (GRCm39)	A398V	probably benign	Het
Hecw2	T	C	1: 53,871,875 (GRCm39)	E1357G	possibly damaging	Het
Ighv1-11	T	C	12: 114,579,468 (GRCm39)		probably benign	Het
Itih3	A	C	14: 30,633,880 (GRCm39)		probably null	Het
Kcnk5	A	G	14: 20,192,405 (GRCm39)	V252A	probably benign	Het
Kif14	A	G	1: 136,415,198 (GRCm39)	E771G	probably damaging	Het
Klc1	T	C	12: 111,748,078 (GRCm39)		probably benign	Het
Myom3	A	G	4: 135,510,408 (GRCm39)	E567G	possibly damaging	Het
Or4a70	A	G	2: 89,324,143 (GRCm39)	V171A	possibly damaging	Het
Pfpl	A	G	19: 12,407,393 (GRCm39)	D548G	probably damaging	Het
Rad54l2	A	G	9: 106,581,422 (GRCm39)	V833A	probably damaging	Het
Scnn1g	A	T	7: 121,337,156 (GRCm39)	K6*	probably null	Het
Sun1	T	C	5: 139,209,341 (GRCm39)		probably benign	Het
Synj2	A	G	17: 6,053,434 (GRCm39)		probably null	Het
Ttc1	T	A	11: 43,629,650 (GRCm39)	E172V	probably benign	Het
Ttn	A	G	2: 76,599,364 (GRCm39)	V19215A	probably damaging	Het
Vwa3a	A	G	7: 120,378,092 (GRCm39)	I461V	probably benign	Het
Wdr73	A	G	7: 80,547,694 (GRCm39)	M110T	probably benign	Het
Zfand4	A	T	6: 116,261,770 (GRCm39)	D111V	probably damaging	Het
Zscan4f	T	A	7: 11,135,270 (GRCm39)	N225K	probably benign	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
IGL01467:Psma5-ps	APN	10	85,149,986 (GRCm39)	exon	noncoding transcript
IGL02638:Psma5-ps	APN	10	85,149,698 (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

2016-08-02