OR4D11

olfactory receptor family 4 subfamily D member 11, the group of Olfactory receptors, family 4

Basic information

Region (hg38): 11:59503576-59504511

Previous symbols: [ "OR4D11P" ]

Links

ENSG00000176200 ∙ NCBI:219986 ∙ ∙ HGNC:15174 ∙ Uniprot:Q8NGI4 ∙ 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 OR4D11 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR4D11 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						0
missense			17	1		18
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	17	1	0

Variants in OR4D11

This is a list of pathogenic ClinVar variants found in the OR4D11 region.

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

Position	Type	Phenotype	Significance	ClinVar
11-59503720-G-A		not specified	Uncertain significance (Dec 21, 2022)
11-59503747-C-T		not specified	Uncertain significance (Jun 22, 2024)
11-59503758-C-A		not specified	Uncertain significance (Apr 17, 2023)
11-59503777-A-G		not specified	Likely benign (May 01, 2022)
11-59503813-A-G		not specified	Uncertain significance (Feb 23, 2024)
11-59503867-A-G		not specified	Uncertain significance (Nov 08, 2022)
11-59503931-C-A		not specified	Uncertain significance (May 20, 2024)
11-59503931-C-T		not specified	Uncertain significance (Jul 09, 2021)
11-59503946-T-G		not specified	Uncertain significance (Oct 05, 2023)
11-59503985-G-C		not specified	Uncertain significance (Mar 17, 2023)
11-59504003-C-T		not specified	Uncertain significance (Feb 12, 2024)
11-59504124-G-C		not specified	Uncertain significance (Jun 03, 2022)
11-59504125-G-C		not specified	Uncertain significance (Oct 12, 2022)
11-59504135-T-C		not specified	Uncertain significance (Aug 03, 2022)
11-59504150-C-A			Uncertain significance (-)
11-59504207-T-G		not specified	Uncertain significance (May 04, 2022)
11-59504212-T-C		not specified	Uncertain significance (Sep 14, 2021)
11-59504221-G-C		not specified	Uncertain significance (Sep 20, 2023)
11-59504297-C-A		not specified	Uncertain significance (Jan 16, 2024)
11-59504329-G-A		not specified	Uncertain significance (Sep 16, 2021)
11-59504460-G-C		not specified	Uncertain significance (May 03, 2023)
11-59504469-G-A		not specified	Uncertain significance (Mar 29, 2024)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
OR4D11	protein_coding	protein_coding	ENST00000313253	1	936

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p
0.00000456	0.131	0	0	0	0	0.00

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	-0.904	195	163	1.20	0.00000819	2010
Missense in Polyphen		73	53.492	1.3647		731
Synonymous	-0.774	75	66.9	1.12	0.00000353	673
Loss of Function	-0.841	7	4.98	1.41	2.12e-7	72

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)

Recessive Scores

• pRec: 0.0806

Intolerance Scores

• loftool: 0.758
• rvis_EVS: -0.05
• rvis_percentile_EVS: 50.22

Haploinsufficiency Scores

• pHI: 0.115
• hipred: N
• hipred_score: 0.170
• ghis: 0.390

Essentials

• essential_gene_CRISPR2: S
• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 0.0140

Gene Damage Prediction

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

Mouse Genome Informatics

• Gene name: Olfr1423

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