Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00569:Stxbp3-ps'

332647

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 #

IGL00569

Quality Score

Status

Chromosome

Chromosomal Location

9535156-9536547 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 9535186 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

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
Abca6	T	G	11: 110,077,875 (GRCm39)	N1311H	possibly damaging	Het
Adrm1b	T	C	3: 92,335,707 (GRCm39)	T332A	probably benign	Het
Apol8	C	T	15: 77,634,255 (GRCm39)	R107H	probably benign	Het
Cacna1a	T	A	8: 85,189,343 (GRCm39)	I98N	probably damaging	Het
Clps	T	A	17: 28,779,636 (GRCm39)		probably benign	Het
Dcc	T	A	18: 71,517,296 (GRCm39)		probably null	Het
Dock10	A	G	1: 80,562,729 (GRCm39)	F544L	probably damaging	Het
Eif2ak2	A	T	17: 79,176,912 (GRCm39)	S218T	probably benign	Het
Faf1	T	C	4: 109,819,077 (GRCm39)	*650Q	probably null	Het
Fxn	A	T	19: 24,244,714 (GRCm39)	I142N	probably damaging	Het
Gm10610	A	T	7: 83,198,778 (GRCm39)		noncoding transcript	Het
Hspa1l	C	T	17: 35,196,441 (GRCm39)	T160I	probably damaging	Het
Kcng4	A	G	8: 120,353,070 (GRCm39)	V280A	probably benign	Het
Khsrp	T	C	17: 57,330,092 (GRCm39)	T646A	possibly damaging	Het
Lilra6	A	G	7: 3,917,588 (GRCm39)	S136P	probably damaging	Het
Lmo7	T	G	14: 102,124,487 (GRCm39)	N315K	probably damaging	Het
Map3k5	A	G	10: 19,810,790 (GRCm39)	T147A	possibly damaging	Het
Mical3	T	C	6: 120,938,585 (GRCm39)	E1134G	possibly damaging	Het
Nek3	A	G	8: 22,648,722 (GRCm39)	L103P	probably damaging	Het
Nudt17	G	T	3: 96,614,343 (GRCm39)	P222Q	probably damaging	Het
Pla2r1	G	T	2: 60,250,769 (GRCm39)	T1386K	probably benign	Het
Ptpn13	A	G	5: 103,738,872 (GRCm39)		probably benign	Het
Rgl1	A	C	1: 152,447,368 (GRCm39)	S134A	probably benign	Het
Rnls	T	A	19: 33,145,888 (GRCm39)	E195V	probably benign	Het
Sall4	T	C	2: 168,597,232 (GRCm39)	N536S	probably benign	Het
Serinc3	G	T	2: 163,469,921 (GRCm39)	P309Q	probably damaging	Het
Smc5	G	A	19: 23,213,329 (GRCm39)	R528C	probably damaging	Het
Tmem67	T	A	4: 12,061,826 (GRCm39)	I549L	probably damaging	Het
Trank1	C	A	9: 111,174,579 (GRCm39)	H269N	possibly damaging	Het
Wdr87-ps	A	T	7: 29,233,565 (GRCm39)		noncoding transcript	Het

Other mutations in Stxbp3-ps

Allele	Source	Chr	Coord	Type	Predicted Effect
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
IGL03324:Stxbp3-ps	APN	19	9,535,714 (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

2015-08-05