Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00232:Gm6576'

306819

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm6576

Ensembl Gene

ENSMUSG00000090544

Gene Name

predicted gene 6576

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL00232

Quality Score

Status

Chromosome

Chromosomal Location

27025414-27026296 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 27025884 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000126334 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000169678]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000169678

SMART Domains

Protein: ENSMUSP00000126334
Gene: ENSMUSG00000090544

Domain	Start	End	E-Value	Type
low complexity region	1	12	N/A	INTRINSIC
low complexity region	14	35	N/A	INTRINSIC
Pfam:Ribosomal_S5	84	148	1.4e-30	PFAM
Pfam:Ribosomal_S5_C	167	238	3.6e-28	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
4930407I10Rik	C	A	15: 81,950,581 (GRCm39)	Q1493K	probably benign	Het
Anapc1	A	T	2: 128,487,050 (GRCm39)		probably benign	Het
Armc8	T	C	9: 99,387,787 (GRCm39)		probably null	Het
Asz1	T	G	6: 18,055,541 (GRCm39)		probably null	Het
Atp6v0a4	G	A	6: 38,069,725 (GRCm39)	R56*	probably null	Het
Bend6	T	C	1: 33,922,619 (GRCm39)	D8G	possibly damaging	Het
Ccdc171	T	A	4: 83,600,561 (GRCm39)	C870*	probably null	Het
Cd163	A	G	6: 124,306,060 (GRCm39)		probably benign	Het
Chd2	A	G	7: 73,118,325 (GRCm39)	S1098P	probably damaging	Het
Col6a5	T	G	9: 105,759,882 (GRCm39)	D1946A	probably damaging	Het
Gypa	T	G	8: 81,231,408 (GRCm39)		probably benign	Het
Ighv9-3	T	C	12: 114,104,691 (GRCm39)		probably benign	Het
Itgb1	T	G	8: 129,440,399 (GRCm39)		probably benign	Het
Kctd15	A	T	7: 34,350,170 (GRCm39)		probably null	Het
Krtap13	A	C	16: 88,548,423 (GRCm39)	S22A	possibly damaging	Het
Masp1	C	T	16: 23,276,841 (GRCm39)	E555K	possibly damaging	Het
Med13l	T	A	5: 118,862,136 (GRCm39)	S360T	probably damaging	Het
Men1	G	A	19: 6,387,237 (GRCm39)		probably null	Het
Mfsd13a	A	G	19: 46,354,958 (GRCm39)	Y45C	probably damaging	Het
Neb	T	C	2: 52,125,568 (GRCm39)	D3662G	possibly damaging	Het
Nkx6-1	T	C	5: 101,807,371 (GRCm39)	D337G	possibly damaging	Het
Nlrc5	T	C	8: 95,211,251 (GRCm39)		probably null	Het
Palb2	T	C	7: 121,720,287 (GRCm39)	H468R	probably damaging	Het
Plscr1l1	C	T	9: 92,233,005 (GRCm39)	R43*	probably null	Het
Rai1	T	G	11: 60,076,217 (GRCm39)	Y94D	probably damaging	Het
Slc27a3	A	T	3: 90,292,748 (GRCm39)	Y605*	probably null	Het
Sox4	C	A	13: 29,136,956 (GRCm39)	G17W	probably damaging	Het
Trpm7	T	C	2: 126,670,951 (GRCm39)	E677G	possibly damaging	Het
Tstd2	A	T	4: 46,120,002 (GRCm39)		probably benign	Het
Unc5c	T	C	3: 141,494,701 (GRCm39)	I412T	probably damaging	Het

Other mutations in Gm6576

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01325:Gm6576	APN	15	27,025,970 (GRCm39)	exon	noncoding transcript
IGL02027:Gm6576	APN	15	27,025,952 (GRCm39)	exon	noncoding transcript
IGL02416:Gm6576	APN	15	27,026,073 (GRCm39)	exon	noncoding transcript
IGL02670:Gm6576	APN	15	27,025,598 (GRCm39)	exon	noncoding transcript
R0128:Gm6576	UTSW	15	27,026,086 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16