Developmental Brain Disorder Gene Database

Missense Gene

Gene

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Missense

CSDE1

HGNC:29905 (protein-coding gene)

cold shock domain containing E1

Unique Cases:: 3

Disorders:: ID, ASD

Last Updated:: November 4, 2024

Gene Summary:

Gene Function: RNA-binding protein involved in translationally coupled mRNA turnover (PubMed:11051545, PubMed:15314026). Implicated with other RNA- binding proteins in the cytoplasmic deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of instability (mCRD) domain (PubMed:11051545, PubMed:15314026). Required for efficient formation of stress granules (PubMed:29395067). {ECO:0000269|PubMed:11051545, ECO:0000269|PubMed:15314026, ECO:0000269|PubMed:29395... (Source: Uniprot)

Previous symbols: No previous symbols

Alias symbols: D1S155E, UNR

Chromosomal Location: 1p13.2

Genomic Coordinates: GRCh37:chr1:115259534-115300671; GRCh38:chr1:114716916-114757984

Associated Disorders: Intellectual Disability, Autism

Predictive Scores:

HI Score (Decipher): 7.61

pLI (gnomAD): 1.00

LOEUF (gnomAD): 0.14

Classifications from External Sources:

SFARI Score (SFARI): 1

DDG2P Classification (DDG2P): Limited

ClinGen Classification (ClinGen): Definitive1

GenCC Classification (GenCC): Definitive1

Cases:

Publications:

External References:

NCBI: Gene

Integrates information from a wide range of species. A record may include nomenclature, Reference Sequences (RefSeqs), maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific resources worldwide.

NCBI: Gene

Gene Reviews

An international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families.

Gene Reviews

DECIPHER

DECIPHER (DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources) is an interactive web-based database which incorporates a suite of tools designed to aid the interpretation of genomic variants. DECIPHER enhances clinical diagnosis by retrieving information from a variety of bioinformatics resources relevant to the variant found in the patient.

DECIPHER

SFARI

SFARI Gene is an evolving online database designed to permit quick entrée into the genetics of autism, and to help researchers track the ever-expanding genetic risk factors that emerge in the literature.

SFARI

ClinGen

ClinGen is a National Institutes of Health (NIH)-funded resource dedicated to building an authoritative central resource that defines the clinical relevance of genes and variants for use in precision medicine and research.

ClinGen

GenCC

The GenCC DB provides information pertaining to the validity of gene-disease relationships, with a current focus on Mendelian diseases.

GenCC

gnomAD

The Genome Aggregation Database (gnomAD) is a resource developed by an international coalition of investigators, with the goal of aggregating and harmonizing both exome and genome sequencing data from a wide variety of large-scale sequencing projects, and making summary data available for the wider scientific community.