Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02275:Vdac3-ps1'

287319

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vdac3-ps1

Ensembl Gene

Gene Name

voltage-dependent anion channel 3, pseudogene 1

Synonyms

ENSMUSG00000075053

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.558) question?

Stock #

IGL02275

Quality Score

Status

Chromosome

Chromosomal Location

18030324-18031629 bp(-) (GRCm38)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 18030794 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000099736

SMART Domains

Protein: ENSMUSP00000137236
Gene: ENSMUSG00000075053

Domain	Start	End	E-Value	Type
Pfam:Porin_3	3	276	4.8e-85	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700037C18Rik	T	A	16: 3,906,282 (GRCm38)	D130V	probably damaging	Het
4930596D02Rik	T	C	14: 35,811,923 (GRCm38)	T9A	probably benign	Het
Anapc1	C	A	2: 128,659,852 (GRCm38)	A757S	probably benign	Het
Bpifa6	A	T	2: 153,992,272 (GRCm38)	D328V	probably benign	Het
Casc1	T	C	6: 145,177,364 (GRCm38)	Y592C	probably damaging	Het
Cdh19	T	A	1: 110,925,886 (GRCm38)	K275I	probably benign	Het
Col18a1	A	G	10: 77,059,383 (GRCm38)	I1148T	possibly damaging	Het
Commd1	A	T	11: 22,900,017 (GRCm38)	V222D	probably damaging	Het
Crim1	T	A	17: 78,369,998 (GRCm38)	M876K	possibly damaging	Het
Dennd1b	C	A	1: 139,081,254 (GRCm38)	H232N	probably damaging	Het
Dhx57	T	C	17: 80,274,839 (GRCm38)	T393A	probably benign	Het
Gabrb2	G	T	11: 42,591,894 (GRCm38)	R193L	probably benign	Het
Gm5828	T	A	1: 16,769,118 (GRCm38)		noncoding transcript	Het
Gm6483	C	T	8: 19,691,613 (GRCm38)	P55S	probably damaging	Het
Hsp90ab1	T	C	17: 45,568,438 (GRCm38)	Y619C	possibly damaging	Het
Kctd19	A	G	8: 105,396,374 (GRCm38)	I136T	probably damaging	Het
Olfr134	G	T	17: 38,175,686 (GRCm38)	V201L	probably benign	Het
Olfr1361	A	C	13: 21,659,000 (GRCm38)	F108V	probably benign	Het
Sel1l	T	C	12: 91,815,015 (GRCm38)	Y532C	probably damaging	Het
Sirpb1a	A	G	3: 15,410,409 (GRCm38)		probably null	Het
Ush2a	C	T	1: 188,263,269 (GRCm38)	T79M	possibly damaging	Het
Usp24	T	C	4: 106,387,493 (GRCm38)	V1215A	probably damaging	Het
Vmn2r75	T	C	7: 86,165,140 (GRCm38)	T382A	probably benign	Het
Vps53	T	C	11: 76,047,123 (GRCm38)	Y728C	probably benign	Het

Other mutations in Vdac3-ps1

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01133:Vdac3-ps1	APN	13	18,031,449 (GRCm38)	exon	noncoding transcript
IGL01530:Vdac3-ps1	APN	13	18,031,506 (GRCm38)	exon	noncoding transcript
IGL02001:Vdac3-ps1	APN	13	18,031,388 (GRCm38)	exon	noncoding transcript
IGL02028:Vdac3-ps1	APN	13	18,030,884 (GRCm38)	exon	noncoding transcript
IGL02965:Vdac3-ps1	APN	13	18,030,846 (GRCm38)	exon	noncoding transcript
R1292:Vdac3-ps1	UTSW	13	18,031,295 (GRCm38)	exon	noncoding transcript
R4582:Vdac3-ps1	UTSW	13	18,031,592 (GRCm38)	exon	noncoding transcript
R5941:Vdac3-ps1	UTSW	13	18,031,202 (GRCm38)	exon	noncoding transcript

Posted On

2015-04-16