Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00598:Gm5464'

5867

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5464

Ensembl Gene

ENSMUSG00000075553

Gene Name

predicted gene 5464

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL00598

Quality Score

Status

Chromosome

Chromosomal Location

67106299-67108454 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

C to T at 67106836 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000022629 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022629] [ENSMUST00000100453]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000022629

SMART Domains

Protein: ENSMUSP00000022629
Gene: ENSMUSG00000022048

Domain	Start	End	E-Value	Type
Pfam:Amidohydro_1	64	453	4.3e-54	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000100453
AA Change: L158F

SMART Domains

Protein: ENSMUSP00000098020
Gene: ENSMUSG00000075553
AA Change: L158F

Domain	Start	End	E-Value	Type
low complexity region	11	22	N/A	INTRINSIC
low complexity region	142	161	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225817

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 11 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Cdh11	T	C	8: 103,377,281 (GRCm39)	N455S	probably damaging	Het
Cimip4	C	T	15: 78,270,438 (GRCm39)	G110D	probably damaging	Het
Clock	T	C	5: 76,377,311 (GRCm39)	I663V	probably benign	Het
Farp2	A	T	1: 93,531,103 (GRCm39)	M534L	probably benign	Het
Ncoa1	T	A	12: 4,328,218 (GRCm39)	R873S	probably benign	Het
Neb	G	A	2: 52,098,313 (GRCm39)	T4616I	possibly damaging	Het
Pbrm1	A	G	14: 30,752,884 (GRCm39)	D107G	probably damaging	Het
Pdcd7	A	T	9: 65,263,700 (GRCm39)	K223*	probably null	Het
Ppp2r5b	A	G	19: 6,280,998 (GRCm39)	F277S	probably damaging	Het
Ripor1	G	A	8: 106,348,065 (GRCm39)		probably benign	Het
Serpina12	G	A	12: 103,997,373 (GRCm39)	H383Y	probably benign	Het

Other mutations in Gm5464

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01782:Gm5464	APN	14	67,106,837 (GRCm39)	unclassified	probably benign
R0369:Gm5464	UTSW	14	67,106,774 (GRCm39)	unclassified	probably benign
R7221:Gm5464	UTSW	14	67,106,681 (GRCm39)	missense	unknown
R8411:Gm5464	UTSW	14	67,106,555 (GRCm39)	missense	unknown
R9592:Gm5464	UTSW	14	67,106,366 (GRCm39)	start codon destroyed	probably null

Posted On

2012-04-20