OR11H1

olfactory receptor family 11 subfamily H member 1, the group of Olfactory receptors, family 11

Basic information

Region (hg38): 22:15528192-15529139

Links

ENSG00000130538 ∙ NCBI:81061 ∙ ∙ HGNC:15404 ∙ Uniprot:Q8NG94 ∙ AlphaFold ∙ 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 OR11H1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR11H1 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				1		1
missense			56	1		57
nonsense						0
start loss			1			1
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	57	2	0

Variants in OR11H1

This is a list of pathogenic ClinVar variants found in the OR11H1 region.

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

Position	Type	Phenotype	Significance	ClinVar
22-15528194-G-T		not specified	Uncertain significance (Feb 06, 2024)
22-15528195-A-G		not specified	Uncertain significance (Nov 26, 2024)
22-15528207-C-A		not specified	Uncertain significance (Jan 15, 2025)
22-15528219-T-C		not specified	Uncertain significance (Feb 25, 2025)
22-15528221-T-C			Likely benign (Mar 01, 2023)
22-15528243-C-T		not specified	Uncertain significance (Jan 18, 2023)
22-15528248-A-T		not specified	Uncertain significance (Apr 07, 2023)
22-15528266-G-T		not specified	Uncertain significance (Jun 04, 2024)
22-15528279-T-A		not specified	Uncertain significance (Oct 05, 2022)
22-15528336-A-C		not specified	Uncertain significance (Oct 06, 2022)
22-15528360-C-T		not specified	Uncertain significance (Jun 10, 2024)
22-15528364-G-C		not specified	Uncertain significance (Aug 08, 2023)
22-15528366-C-T		not specified	Uncertain significance (Dec 24, 2024)
22-15528419-G-T		not specified	Uncertain significance (Jun 21, 2023)
22-15528423-G-A		not specified	Uncertain significance (Nov 10, 2022)
22-15528459-C-T		not specified	Uncertain significance (Jan 08, 2025)
22-15528471-A-G		not specified	Uncertain significance (Dec 17, 2023)
22-15528519-T-C		not specified	Uncertain significance (Sep 20, 2023)
22-15528537-T-A		not specified	Likely benign (Aug 09, 2021)
22-15528543-C-T		not specified	Uncertain significance (Oct 03, 2022)
22-15528559-C-A		not specified	Uncertain significance (Jun 05, 2023)
22-15528569-G-T		not specified	Uncertain significance (Oct 25, 2024)
22-15528579-A-G		not specified	Uncertain significance (Oct 13, 2023)
22-15528584-C-G		not specified	Uncertain significance (Jul 05, 2023)
22-15528586-G-A		not specified	Uncertain significance (Apr 07, 2022)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
OR11H1	protein_coding	protein_coding	ENST00000252835	1	982

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p
0.0000103	0.110	0	0	0	0	0.00

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	-3.32	131	59.1	2.22	0.00000270	1995
Missense in Polyphen		39	16.832	2.317		598
Synonymous	-4.52	48	21.4	2.24	9.25e-7	611
Loss of Function	-1.46	6	3.18	1.88	2.28e-7	83

LoF frequencies by population

Ethnicity	Sum of pLOFs	p
African & African-American	0.00	0.00
Ashkenazi Jewish	0.00	0.00
East Asian	0.00	0.00
Finnish	0.00	0.00
European (Non-Finnish)	0.00	0.00
Middle Eastern	0.00	0.00
South Asian	0.00	0.00
Other	0.00	0.00

dbNSFP

Source: dbNSFP

• Function: FUNCTION: Odorant receptor. {ECO:0000305}.
• Pathway: Olfactory transduction - Homo sapiens (human);Olfactory receptor activity;Signaling by GPCR;Signal Transduction;Olfactory Signaling Pathway;G alpha (s) signalling events;GPCR downstream signalling (Consensus)

Haploinsufficiency Scores

• pHI: 0.155
• hipred: N
• hipred_score: 0.255

Essentials

• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 4.76e-7

Gene Damage Prediction

	All	Recessive	Dominant
Mendelian	Medium	Medium	Medium
Primary Immunodeficiency	Medium	Medium	Medium
Cancer	Medium	Medium	Medium

Gene ontology

• Biological process: G protein-coupled receptor signaling pathway;detection of chemical stimulus involved in sensory perception of smell
• Cellular component: plasma membrane;integral component of membrane
• Molecular function: G protein-coupled receptor activity;olfactory receptor activity