Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03324:Stxbp3-ps'

416582

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Stxbp3-ps

Ensembl Gene

ENSMUSG00000071640

Gene Name

syntaxin-binding protein 3, pseudogene

Synonyms

Stxbp3b, Munc18c(L)

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.301) question?

Stock #

IGL03324

Quality Score

Status

Chromosome

Chromosomal Location

9535156-9536547 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 9535714 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: ENSMUST00000090527

SMART Domains

Protein: ENSMUSP00000088014
Gene: ENSMUSG00000071640

Domain	Start	End	E-Value	Type
Pfam:Sec1	33	253	1.2e-48	PFAM

Meta Mutation Damage Score

0.2588

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
1700018F24Rik	A	G	5: 144,982,261 (GRCm39)	E282G	probably benign	Het
Abca12	T	A	1: 71,353,167 (GRCm39)	K758N	probably benign	Het
Acacb	A	T	5: 114,363,915 (GRCm39)	R1459*	probably null	Het
Aco1	A	G	4: 40,186,363 (GRCm39)	T592A	probably benign	Het
Aldh2	C	T	5: 121,713,188 (GRCm39)	G256D	probably benign	Het
Apbb2	A	T	5: 66,469,500 (GRCm39)		probably null	Het
Apoe	A	T	7: 19,430,462 (GRCm39)	I260K	probably benign	Het
Cep89	G	A	7: 35,124,078 (GRCm39)		probably benign	Het
Coq3	A	G	4: 21,900,361 (GRCm39)	D196G	probably benign	Het
Crispld2	C	T	8: 120,742,110 (GRCm39)	R153W	probably damaging	Het
Enox1	A	G	14: 77,852,925 (GRCm39)	E397G	probably damaging	Het
Gpatch1	A	G	7: 34,998,705 (GRCm39)	Y342H	probably damaging	Het
Gpatch1	T	A	7: 34,993,120 (GRCm39)	E575V	possibly damaging	Het
Grid2	T	C	6: 64,406,806 (GRCm39)	V722A	possibly damaging	Het
Hsh2d	T	C	8: 72,947,356 (GRCm39)	F18L	probably damaging	Het
Htra2	C	T	6: 83,030,737 (GRCm39)	D190N	probably damaging	Het
Lrfn2	A	G	17: 49,377,915 (GRCm39)	N332S	probably damaging	Het
Naa10	C	T	X: 72,963,568 (GRCm39)		probably null	Het
Nlrp4f	T	C	13: 65,343,042 (GRCm39)	E179G	possibly damaging	Het
Or13p10	T	A	4: 118,523,069 (GRCm39)	F118L	probably benign	Het
Or14j1	G	A	17: 38,146,165 (GRCm39)	G92S	probably benign	Het
Or4c111	A	T	2: 88,843,903 (GRCm39)	C168*	probably null	Het
Prss46	T	A	9: 110,678,747 (GRCm39)	N46K	probably benign	Het
Rep15	A	C	6: 146,934,163 (GRCm39)	M1L	possibly damaging	Het
Slc10a4	G	T	5: 73,169,286 (GRCm39)	A105S	probably damaging	Het
Slc26a9	A	T	1: 131,691,748 (GRCm39)	T664S	probably damaging	Het
Tmf1	C	A	6: 97,140,614 (GRCm39)	R754L	probably damaging	Het
Xcr1	T	A	9: 123,685,549 (GRCm39)	Y71F	probably benign	Het
Yars1	C	T	4: 129,104,328 (GRCm39)	T324I	probably benign	Het
Zfp106	A	G	2: 120,365,868 (GRCm39)	S180P	probably benign	Het

Other mutations in Stxbp3-ps

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00569:Stxbp3-ps	APN	19	9,535,186 (GRCm39)	exon	noncoding transcript
IGL01296:Stxbp3-ps	APN	19	9,535,256 (GRCm39)	exon	noncoding transcript
IGL01455:Stxbp3-ps	APN	19	9,535,371 (GRCm39)	exon	noncoding transcript
IGL02698:Stxbp3-ps	APN	19	9,535,688 (GRCm39)	exon	noncoding transcript
IGL02756:Stxbp3-ps	APN	19	9,535,193 (GRCm39)	exon	noncoding transcript
R0217:Stxbp3-ps	UTSW	19	9,536,496 (GRCm39)	exon	noncoding transcript
R4522:Stxbp3-ps	UTSW	19	9,536,474 (GRCm39)	critical splice donor site	noncoding transcript
R5030:Stxbp3-ps	UTSW	19	9,535,714 (GRCm39)	exon	noncoding transcript
R5541:Stxbp3-ps	UTSW	19	9,535,334 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02