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SPTY2D1 SPT2 chromatin protein domain containing 1 [ Homo sapiens (human) ]

Gene ID: 144108, updated on 2-Nov-2024

Summary

Official Symbol
SPTY2D1provided by HGNC
Official Full Name
SPT2 chromatin protein domain containing 1provided by HGNC
Primary source
HGNC:HGNC:26818
See related
Ensembl:ENSG00000179119 AllianceGenome:HGNC:26818
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
Spt2
Summary
Enables DNA binding activity; histone binding activity; and histone chaperone activity. Involved in heterochromatin formation; nucleosome assembly; and regulation of DNA-templated transcription. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Nov 2024]
Expression
Ubiquitous expression in bone marrow (RPKM 18.4), gall bladder (RPKM 8.3) and 25 other tissues See more
Orthologs
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Genomic context

See SPTY2D1 in Genome Data Viewer
Location:
11p15.1
Exon count:
6
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (18606403..18634342, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (18704496..18732445, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (18627950..18655889, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene UEV and lactate/malate dehyrogenase domains Neighboring gene ReSE screen-validated silencer GRCh37_chr11:18600575-18600756 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4503 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4504 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4505 Neighboring gene Sharpr-MPRA regulatory region 13786 Neighboring gene uncharacterized LOC112268073 Neighboring gene MTCH1 pseudogene 2 Neighboring gene Sharpr-MPRA regulatory region 7651 Neighboring gene mitochondrial sheath formation associated Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr11:18637160-18638359 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3192 Neighboring gene uncharacterized LOC105376578 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4507 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:18670593-18671313 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:18671314-18672033 Neighboring gene SRSF3 pseudogene 1

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

Phenotypes

EBI GWAS Catalog

Description
Biological, clinical and population relevance of 95 loci for blood lipids.
EBI GWAS Catalog
Discovery and refinement of loci associated with lipid levels.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Clone Names

  • FLJ39441, DKFZp686I068, DKFZp686F1942

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables DNA binding IBA
Inferred from Biological aspect of Ancestor
more info
 
enables DNA binding IDA
Inferred from Direct Assay
more info
PubMed 
enables RNA polymerase I core binding ISS
Inferred from Sequence or Structural Similarity
more info
 
enables histone binding IBA
Inferred from Biological aspect of Ancestor
more info
 
enables histone binding IDA
Inferred from Direct Assay
more info
PubMed 
enables histone chaperone activity IMP
Inferred from Mutant Phenotype
more info
PubMed 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Process Evidence Code Pubs
involved_in heterochromatin formation IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in nucleosome assembly IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in nucleosome assembly IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of DNA-templated transcription IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in transcription by RNA polymerase I IBA
Inferred from Biological aspect of Ancestor
more info
 
Component Evidence Code Pubs
is_active_in nucleolus IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nucleolus IDA
Inferred from Direct Assay
more info
 
located_in nucleolus ISS
Inferred from Sequence or Structural Similarity
more info
 
located_in nucleoplasm IDA
Inferred from Direct Assay
more info
 

General protein information

Preferred Names
protein SPT2 homolog
Names
SPT2 domain-containing protein 1
SPT2, Suppressor of Ty, domain containing 1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_194285.3NP_919261.2  protein SPT2 homolog

    See identical proteins and their annotated locations for NP_919261.2

    Status: VALIDATED

    Source sequence(s)
    AF086471, AF452716, AK096760, AL834393, BC036844, BC056261, BX538046, BX641102, BX647798, BX648114, BX648478
    Consensus CDS
    CCDS31441.1
    UniProtKB/Swiss-Prot
    Q68D10, Q6AWA5, Q6MZI5, Q7Z390, Q7Z470, Q86VG8, Q8N3E7, Q8N417, Q8N8I3
    UniProtKB/TrEMBL
    B4E223
    Related
    ENSP00000337991.5, ENST00000336349.6
    Conserved Domains (1) summary
    pfam08243
    Location:604667
    SPT2; SPT2 chromatin protein

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    18606403..18634342 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    18704496..18732445 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)