Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01771:Or10aa4-ps1'

153854

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Or10aa4-ps1

Ensembl Gene

ENSMUSG00000102603

Gene Name

olfactory receptor family 10 subfamily AA member 4, pseudogene 1

Synonyms

Olfr431-ps1, Gm5033, GA_x6K02T2P20D-21123424-21122522

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01771

Quality Score

Status

Chromosome

Chromosomal Location

173879564-173880107 bp(+) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

T to C at 173878887 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000150596 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062665] [ENSMUST00000213211] [ENSMUST00000213381]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000062665

SMART Domains

Protein: ENSMUSP00000060341
Gene: ENSMUSG00000047048

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	306	3.7e-47	PFAM
Pfam:7TM_GPCR_Srsx	35	307	1.2e-7	PFAM
Pfam:7tm_1	41	289	6.5e-21	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000192435

Predicted Effect

probably benign
Transcript: ENSMUST00000213211

Predicted Effect

probably benign
Transcript: ENSMUST00000213381

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 20 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Capn10	T	A	1: 92,868,087 (GRCm39)	W185R	probably damaging	Het
Frmd8	A	G	19: 5,919,603 (GRCm39)	L148P	probably damaging	Het
Gk5	T	C	9: 96,059,488 (GRCm39)	C447R	probably damaging	Het
Hip1r	T	A	5: 124,137,606 (GRCm39)	V704D	possibly damaging	Het
Kcnj10	C	A	1: 172,197,150 (GRCm39)	H221Q	probably benign	Het
Klk1b8	A	T	7: 43,604,290 (GRCm39)	I253L	probably damaging	Het
Or1ad8	A	G	11: 50,898,593 (GRCm39)	T265A	probably benign	Het
Or1e29	A	T	11: 73,667,490 (GRCm39)	I221N	probably damaging	Het
Or5ac22	T	C	16: 59,134,891 (GRCm39)	N293S	probably damaging	Het
Or8k40	C	T	2: 86,584,626 (GRCm39)	C152Y	probably benign	Het
Pdp2	A	T	8: 105,320,754 (GRCm39)	Y201F	probably benign	Het
Ppfia1	A	T	7: 144,036,094 (GRCm39)	I1112K	probably benign	Het
Ppwd1	A	G	13: 104,353,624 (GRCm39)	I378T	probably damaging	Het
Rhbdd1	T	A	1: 82,355,313 (GRCm39)	D248E	probably benign	Het
Sec14l5	T	C	16: 4,996,494 (GRCm39)		probably null	Het
Sel1l3	T	G	5: 53,279,183 (GRCm39)	D960A	probably damaging	Het
Slc35f3	T	C	8: 127,115,951 (GRCm39)	Y293H	probably benign	Het
Wwc1	A	G	11: 35,744,185 (GRCm39)		probably null	Het
Zan	T	C	5: 137,391,330 (GRCm39)	N4718S	unknown	Het
Zfyve16	T	C	13: 92,658,680 (GRCm39)	I410M	probably benign	Het

Posted On

2014-02-04