ZBTB44-DT

ZBTB44 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 11:130314106-130446210

Links

ENSG00000175773 ∙ NCBI:646383 ∙ ∙ HGNC:54265 ∙ ∙ ∙ 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 ZBTB44-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZBTB44-DT 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						0
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	0	0	0

Variants in ZBTB44-DT

This is a list of pathogenic ClinVar variants found in the ZBTB44-DT region.

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

Position	Type	Phenotype	Significance	ClinVar
11-130405610-G-A		not specified	Uncertain significance (Apr 17, 2025)
11-130405656-C-T		not specified	Uncertain significance (Oct 19, 2024)
11-130405659-C-G		not specified	Uncertain significance (Jan 29, 2024)
11-130405664-C-T		not specified	Uncertain significance (Sep 14, 2023)
11-130405677-C-T		not specified	Uncertain significance (Jan 11, 2023)
11-130405683-C-T		not specified	Uncertain significance (Jun 28, 2022)
11-130405705-C-G		not specified	Uncertain significance (Jan 08, 2024)
11-130405776-T-C		not specified	Uncertain significance (Jan 04, 2025)
11-130405829-G-T		not specified	Uncertain significance (Aug 16, 2022)
11-130405830-G-C		not specified	Uncertain significance (May 07, 2025)
11-130405868-G-A		not specified	Uncertain significance (Feb 22, 2025)
11-130405889-C-T		not specified	Uncertain significance (May 07, 2025)
11-130405890-G-A		not specified	Uncertain significance (Apr 27, 2023)
11-130405904-C-T		not specified	Uncertain significance (Sep 29, 2023)
11-130405926-C-T		not specified	Uncertain significance (Oct 20, 2021)
11-130405931-T-C		not specified	Uncertain significance (May 31, 2023)
11-130406037-T-A		not specified	Uncertain significance (Apr 24, 2025)
11-130406058-G-C		not specified	Uncertain significance (Nov 13, 2024)
11-130406066-C-T		not specified	Uncertain significance (Jan 31, 2022)
11-130406067-G-C		not specified	Uncertain significance (Apr 09, 2025)
11-130406076-C-T		not specified	Uncertain significance (May 25, 2025)
11-130406119-G-T		Oromandibular-limb hypogenesis spectrum	Uncertain significance (Aug 12, 2016)
11-130408516-C-T		not specified	Uncertain significance (Feb 16, 2023)
11-130408543-G-A		not specified	Uncertain significance (Apr 07, 2025)
11-130408548-G-A		not specified	Uncertain significance (Mar 27, 2025)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP