Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02670:Gm6576'

302891

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 #

IGL02670

Quality Score

Status

Chromosome

Chromosomal Location

27025386-27026207 bp(+) (GRCm38)

Type of Mutation

exon

DNA Base Change (assembly)

A to C at 27025512 bp (GRCm38)

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: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438A13Rik	C	T	3: 36,967,305 (GRCm38)	Q2193*	probably null	Het
Asb1	T	C	1: 91,546,918 (GRCm38)		probably benign	Het
Cnot6	G	A	11: 49,685,114 (GRCm38)	Q178*	probably null	Het
Col5a1	C	T	2: 27,974,715 (GRCm38)	A737V	unknown	Het
Cyp27b1	T	C	10: 127,050,358 (GRCm38)	S303P	probably benign	Het
Dnah5	T	C	15: 28,409,296 (GRCm38)	L3620P	probably damaging	Het
Dock7	A	T	4: 98,966,286 (GRCm38)		probably null	Het
Fam161b	T	C	12: 84,357,594 (GRCm38)	D104G	probably benign	Het
Fam8a1	A	G	13: 46,673,604 (GRCm38)	M284V	possibly damaging	Het
Fkbp3	T	A	12: 65,069,103 (GRCm38)	K65*	probably null	Het
Gatb	A	G	3: 85,613,551 (GRCm38)		probably null	Het
Gm572	A	T	4: 148,651,228 (GRCm38)	H38L	probably benign	Het
L2hgdh	G	A	12: 69,692,480 (GRCm38)	R406W	possibly damaging	Het
Lmo7	A	T	14: 101,880,980 (GRCm38)	T214S	probably damaging	Het
Map3k12	T	C	15: 102,503,546 (GRCm38)	H361R	probably benign	Het
Mios	T	C	6: 8,235,378 (GRCm38)		probably benign	Het
Mta1	T	C	12: 113,130,121 (GRCm38)	L315P	probably damaging	Het
Pask	A	C	1: 93,310,818 (GRCm38)	V1315G	probably damaging	Het
Pias4	A	T	10: 81,164,070 (GRCm38)	C50S	probably damaging	Het
Rgs11	G	A	17: 26,207,631 (GRCm38)	V279I	probably benign	Het
Sgk1	T	A	10: 21,928,546 (GRCm38)	C92S	probably benign	Het
Slc2a13	C	T	15: 91,497,509 (GRCm38)	G259E	probably damaging	Het
Slc5a4b	A	G	10: 76,075,100 (GRCm38)	C301R	probably damaging	Het
Sstr4	G	T	2: 148,396,533 (GRCm38)	G355*	probably null	Het
Tnrc6a	T	A	7: 123,171,312 (GRCm38)	L775Q	possibly damaging	Het
Vmn1r218	A	G	13: 23,137,004 (GRCm38)	I94V	probably benign	Het
Xpa	A	G	4: 46,185,682 (GRCm38)	F99L	probably benign	Het

Other mutations in Gm6576

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00232:Gm6576	APN	15	27,025,798 (GRCm38)	exon	noncoding transcript
IGL01325:Gm6576	APN	15	27,025,884 (GRCm38)	exon	noncoding transcript
IGL02027:Gm6576	APN	15	27,025,866 (GRCm38)	exon	noncoding transcript
IGL02416:Gm6576	APN	15	27,025,987 (GRCm38)	exon	noncoding transcript
R0128:Gm6576	UTSW	15	27,026,000 (GRCm38)	exon	noncoding transcript

Posted On

2015-04-16