Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01808:Gm5885'

155727

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5885

Ensembl Gene

Gene Name

predicted gene 5885

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.067) question?

Stock #

IGL01808

Quality Score

Status

Chromosome

Chromosomal Location

133506185-133508453 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 133508181 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000178578

SMART Domains

Protein: ENSMUSP00000136262
Gene: ENSMUSG00000095412

Domain	Start	End	E-Value	Type
Pfam:Pro-rich	1	166	2.5e-13	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203357

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ager	A	T	17: 34,818,431 (GRCm39)	Q266L	probably damaging	Het
Amz1	A	G	5: 140,727,034 (GRCm39)		probably benign	Het
Ebf2	C	T	14: 67,651,932 (GRCm39)	A488V	probably benign	Het
Gnas	T	C	2: 174,140,490 (GRCm39)	S220P	probably damaging	Het
Gpr171	G	A	3: 59,005,572 (GRCm39)	P68S	probably damaging	Het
H2ax	T	C	9: 44,246,246 (GRCm39)	I63T	possibly damaging	Het
H2-M9	A	T	17: 36,952,711 (GRCm39)		probably null	Het
Igsf9	T	C	1: 172,312,370 (GRCm39)	V27A	probably benign	Het
Kcnh6	G	T	11: 105,914,753 (GRCm39)		probably benign	Het
Mapkbp1	A	G	2: 119,853,650 (GRCm39)		probably null	Het
Mllt6	C	A	11: 97,563,310 (GRCm39)	H298N	possibly damaging	Het
Mtmr3	A	G	11: 4,447,404 (GRCm39)	I352T	probably damaging	Het
Mtrr	T	C	13: 68,714,212 (GRCm39)	D509G	probably benign	Het
Ncan	C	T	8: 70,560,090 (GRCm39)		probably null	Het
Or51aa2	T	A	7: 103,187,781 (GRCm39)	Y220F	probably damaging	Het
Pcdhb4	T	C	18: 37,442,067 (GRCm39)	V459A	probably damaging	Het
Phrf1	C	A	7: 140,840,879 (GRCm39)	P1274Q	probably damaging	Het
Slc4a2	T	C	5: 24,645,205 (GRCm39)	L1125P	probably damaging	Het
Synpo	T	C	18: 60,735,280 (GRCm39)	I650V	probably benign	Het
Tsc1	G	A	2: 28,552,519 (GRCm39)	R86H	probably damaging	Het
Ugt2a3	A	G	5: 87,473,414 (GRCm39)	V501A	probably benign	Het
Vmn1r203	T	C	13: 22,708,717 (GRCm39)	I166T	probably benign	Het
Vps13a	A	G	19: 16,687,650 (GRCm39)	C933R	probably damaging	Het
Zfp142	A	T	1: 74,615,184 (GRCm39)	F342Y	probably damaging	Het

Other mutations in Gm5885

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02026:Gm5885	APN	6	133,508,291 (GRCm39)	exon	noncoding transcript
IGL02364:Gm5885	APN	6	133,507,092 (GRCm39)	splice site	noncoding transcript
R1613:Gm5885	UTSW	6	133,508,205 (GRCm39)	exon	noncoding transcript
R2141:Gm5885	UTSW	6	133,506,238 (GRCm39)	exon	noncoding transcript
R4352:Gm5885	UTSW	6	133,508,152 (GRCm39)	exon	noncoding transcript

Posted On

2014-02-04