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Gene: DCAF8L2 (DDB1 and CUL4 associated factor 8 like 2) Homo sapiens
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Symbol: DCAF8L2
Name: DDB1 and CUL4 associated factor 8 like 2
Description: ASSOCIATED WITH autistic disorder; Neurodevelopmental Disorders; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH aflatoxin B1; arsane; arsenic atom
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: DDB1 and CUL4 associated factor 8-like 2; DDB1- and CUL4-associated factor 8-like protein 2; WD repeat domain 42C; WD repeat-containing protein 42C; WDR42C
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X27,468,941 - 27,749,942 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X27,734,205 - 27,768,050 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X27,662,480 - 27,677,442 (+)NCBINCBI36hg18NCBI36
CeleraX31,893,400 - 31,895,412 (+)NCBI
Cytogenetic MapXp21.3NCBI
HuRefX25,504,432 - 25,506,739 (+)NCBIHuRef
CHM1_1X27,795,652 - 27,797,664 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on DCAF8L2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1342776
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.