DDX11L8

DEAD/H-box helicase 11 like 8 (pseudogene)

Basic information

Region (hg38): 12:12310-13501

Links

ENSG00000256263

∙ NCBI:100302090 ∙ ∙ HGNC:37101 ∙ Uniprot:A8MPP1 ∙ 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 DDX11L8 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the DDX11L8 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

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP

Function: FUNCTION: Putative DNA helicase. {ECO:0000250}.;

Gene ontology

Biological process: nucleobase-containing compound metabolic process;DNA duplex unwinding;establishment of sister chromatid cohesion
Cellular component: nucleus;nucleolus
Molecular function: DNA binding;RNA binding;ATP-dependent DNA helicase activity;protein binding;ATP binding