OR4M2-OT1

OR4M2 overlapping transcript 1, the group of Overlapping transcripts

Basic information

Region (hg38): 15:22015232-22095857

Links

ENSG00000285472 ∙ NCBI:101927079 ∙ ∙ HGNC:56199 ∙ ∙ ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR4M2-OT1 gene.

• Inborn genetic diseases (19 variants)
• not provided (6 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR4M2-OT1 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type	Pathogenic	Likely pathogenic	VUS	Likely benign	Benign	Sum
synonymous				2		2
missense			11	1	3	15
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding			7	1		8
Total	0	0	18	4	3

Variants in OR4M2-OT1

This is a list of pathogenic ClinVar variants found in the OR4M2-OT1 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position	Type	Phenotype	Significance	ClinVar
15-22080671-G-A		not specified	Uncertain significance (May 28, 2024)
15-22080683-C-T		not specified	Uncertain significance (Jan 09, 2024)
15-22080755-T-G		not specified	Uncertain significance (Jan 25, 2023)
15-22080794-C-T		not specified	Uncertain significance (Dec 07, 2023)
15-22080799-A-G		not specified	Uncertain significance (Jan 24, 2024)
15-22080896-T-C		not specified	Uncertain significance (Sep 13, 2023)
15-22081040-G-A		not specified	Uncertain significance (Oct 10, 2023)
15-22081074-G-T			Likely benign (Apr 01, 2022)
15-22081081-T-C		not specified	Uncertain significance (Dec 01, 2022)
15-22081093-A-G		not specified	Uncertain significance (Feb 12, 2024)
15-22081180-C-T		not specified	Uncertain significance (May 24, 2024)
15-22081193-C-A		not specified	Uncertain significance (Jan 30, 2024)
15-22081205-C-T		not specified	Uncertain significance (Aug 19, 2023)
15-22081283-T-G		not specified	Uncertain significance (Nov 23, 2022)
15-22081292-C-T		not specified	Uncertain significance (May 03, 2023)
15-22081303-A-G		not specified	Uncertain significance (Oct 05, 2022)
15-22081332-C-A		not specified	Uncertain significance (Oct 05, 2023)
15-22081406-C-T		not specified	Uncertain significance (Dec 18, 2023)
15-22081502-A-G		not specified	Uncertain significance (May 12, 2024)
15-22094529-T-C		not specified	Uncertain significance (Jan 04, 2024)
15-22094533-A-G			Likely benign (Mar 01, 2023)
15-22094536-C-A		not specified	Uncertain significance (May 03, 2023)
15-22094574-C-A		not specified	Uncertain significance (Apr 08, 2022)
15-22094582-C-A		not specified	Uncertain significance (Dec 27, 2022)
15-22094643-G-A		not specified	Uncertain significance (Sep 16, 2021)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP