ZNF491

zinc finger protein 491, the group of Zinc fingers C2H2-type

Basic information

Region (hg38): 19:11797667-11809622

Links

ENSG00000177599 ∙ NCBI:126069 ∙ ∙ HGNC:23706 ∙ Uniprot:Q8N8L2 ∙ 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 ZNF491 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZNF491 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			35	1		36
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	35	1	0

Variants in ZNF491

This is a list of pathogenic ClinVar variants found in the ZNF491 region.

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

Position	Type	Phenotype	Significance	ClinVar
19-11806006-T-C		not specified	Uncertain significance (Jul 09, 2024)
19-11806013-G-C		not specified	Uncertain significance (Mar 07, 2024)
19-11806018-C-T		not specified	Uncertain significance (Sep 17, 2021)
19-11806102-C-T		not specified	Uncertain significance (May 09, 2023)
19-11806177-A-G		not specified	Uncertain significance (Feb 12, 2025)
19-11806245-A-C		not specified	Uncertain significance (Dec 28, 2022)
19-11806294-C-A		not specified	Uncertain significance (Jun 22, 2024)
19-11806294-C-T		not specified	Uncertain significance (Jan 19, 2025)
19-11806453-C-A		not specified	Uncertain significance (Sep 08, 2024)
19-11806460-T-A		not specified	Uncertain significance (Jan 01, 2025)
19-11806468-G-A		not specified	Uncertain significance (May 09, 2024)
19-11806473-G-C		not specified	Uncertain significance (Mar 06, 2023)
19-11806477-G-A		not specified	Uncertain significance (Jun 06, 2023)
19-11806477-G-C		not specified	Uncertain significance (Sep 11, 2024)
19-11806484-T-A		not specified	Uncertain significance (Nov 18, 2023)
19-11806523-G-C		not specified	Uncertain significance (Apr 26, 2023)
19-11806543-A-T		not specified	Uncertain significance (Oct 08, 2024)
19-11806561-G-A		not specified	Uncertain significance (Oct 17, 2024)
19-11806621-C-T		not specified	Uncertain significance (Jul 20, 2022)
19-11806710-T-C		not specified	Uncertain significance (Dec 14, 2024)
19-11806713-C-T		not specified	Uncertain significance (Feb 08, 2025)
19-11806714-G-T		not specified	Uncertain significance (Oct 24, 2024)
19-11806729-G-A		not specified	Likely benign (Feb 20, 2025)
19-11806778-A-G		not specified	Uncertain significance (May 20, 2024)
19-11806789-C-G		not specified	Uncertain significance (May 16, 2023)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
ZNF491	protein_coding	protein_coding	ENST00000323169	1	11956

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	-0.392	253	236	1.07	0.0000118	2910
Missense in Polyphen		75	74.198	1.0108		967
Synonymous	1.76	59	78.9	0.748	0.00000390	759
Loss of Function

LoF frequencies by population

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

dbNSFP

Source: dbNSFP

• Function: FUNCTION: May be involved in transcriptional regulation.

Intolerance Scores

• loftool: 0.664
• rvis_EVS: 0.89
• rvis_percentile_EVS: 89.24

Haploinsufficiency Scores

• pHI: 0.200
• hipred: N
• hipred_score: 0.112
• ghis: 0.486

Essentials

• essential_gene_CRISPR: N
• essential_gene_CRISPR2: N
• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 0.00000250

Gene Damage Prediction

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

Gene ontology

• Biological process: regulation of transcription by RNA polymerase II
• Cellular component: nucleus
• Molecular function: DNA-binding transcription factor activity, RNA polymerase II-specific;DNA binding;metal ion binding