SYCE2 synaptonemal complex central element protein 2

Gene ID: 256126, updated on 19-Sep-2024
Gene type: protein coding
Also known as: CESC1

Summary

The protein encoded by this gene is part of the synaptonemal complex formed between homologous chromosomes during meiotic prophase. The encoded protein associates with SYCP1 and SYCE1 and is found only where chromosome cores are synapsed. [provided by RefSeq, Dec 2012]

Associated conditions

See all available tests in GTR for this gene

Description	Tests
An atlas of genetic influences on human blood metabolites. GeneReviews: Not available
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. GeneReviews: Not available
Seventy-five genetic loci influencing the human red blood cell. GeneReviews: Not available

Genomic context

Location:: 19p13.13

Sequence:: Chromosome: 19; NC_000019.10 (12898786..12919293, complement)

Total number of exons:: 6

Genomic Sequence

Go to nucleotideGraphics FASTA GenBank

Variation

Resource	Links for this gene
ClinVar	Variants reported to ClinVar
dbVar	Studies and variants
SNP	Variation Viewer for SYCE2 variants
Genome viewer	Explore NCBI-annotated and select non-NCBI annotated genome assemblies

Links

ClinVar
Related medical variations
dbVar
Link from Gene to dbVar
OMIM
Link to related OMIM entry
PubMed (OMIM)
Gene links to PubMed derived from omim_pubmed_cited links
RefSeq RNAs
Link to Nucleotide RefSeq RNAs
RefSeqGene
Link to Nucleotide RefSeqGenes
Variation Viewer
Related Variants

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