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    SP8 Sp8 transcription factor [ Homo sapiens (human) ]

    Gene ID: 221833, updated on 2-Nov-2024

    Summary

    Official Symbol
    SP8provided by HGNC
    Official Full Name
    Sp8 transcription factorprovided by HGNC
    Primary source
    HGNC:HGNC:19196
    See related
    Ensembl:ENSG00000164651 MIM:608306; AllianceGenome:HGNC:19196
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    BTD
    Summary
    The protein encoded by this gene is an SP family transcription factor that in mouse has been shown to be essential for proper limb development. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]
    Expression
    Biased expression in prostate (RPKM 3.9) and skin (RPKM 0.2) See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See SP8 in Genome Data Viewer
    Location:
    7p21.1
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (20782279..20786886, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (20918318..20922938, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (20821899..20826505, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene RAS like proto-oncogene A pseudogene Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:20681108-20682307 Neighboring gene NANOG hESC enhancer GRCh37_chr7:20693236-20693793 Neighboring gene ATP binding cassette subfamily B member 5 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr7:20815756-20816338 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr7:20816339-20816919 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:20822883-20823543 Neighboring gene VISTA enhancer hs844 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:20835446-20836154 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17992 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17994 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17993 Neighboring gene VISTA enhancer hs1019 Neighboring gene NANOG hESC enhancer GRCh37_chr7:20855921-20856533 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr7:20866537-20867736 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:20874484-20874984 Neighboring gene long intergenic non-protein coding RNA 1162 Neighboring gene ribosomal protein L23 pseudogene 8 Neighboring gene ribosomal protein S26 pseudogene 30

    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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide association of lipid-lowering response to statins in combined study populations.
    EBI GWAS Catalog
    Genome-wide association study of bipolar I disorder in the Han Chinese population.
    EBI GWAS Catalog
    Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General protein information

    Preferred Names
    transcription factor Sp8
    Names
    specificity protein 8

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    Genomic

    1. NG_029244.2 RefSeqGene

      Range
      5004..9611
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_182700.6NP_874359.2  transcription factor Sp8 isoform 1

      See identical proteins and their annotated locations for NP_874359.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the shorter transcript but encodes the longer isoform (1).
      Source sequence(s)
      AC005060, AI632278, AY167047, KF511006
      Consensus CDS
      CCDS43555.1
      UniProtKB/TrEMBL
      A8K350
      Related
      ENSP00000408792.2, ENST00000418710.3
      Conserved Domains (4) summary
      COG5048
      Location:389456
      COG5048; FOG: Zn-finger [General function prediction only]
      sd00017
      Location:379398
      ZF_C2H2; C2H2 Zn finger [structural motif]
      pfam00096
      Location:434456
      zf-C2H2; Zinc finger, C2H2 type
      pfam13465
      Location:420443
      zf-H2C2_2; Zinc-finger double domain
    2. NM_198956.4NP_945194.1  transcription factor Sp8 isoform 2

      See identical proteins and their annotated locations for NP_945194.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) includes an alternate internal exon and initiates translation from a downstream start codon, compared to variant 1. The resulting isoform (2) is shorter at the N-terminus, compared to isoform 1.
      Source sequence(s)
      AC005060, AI632278, AK290465, DA497089, KF511006
      Consensus CDS
      CCDS5372.1
      UniProtKB/Swiss-Prot
      Q7Z615, Q7Z616, Q8IXZ3, Q96MJ1
      UniProtKB/TrEMBL
      A8K350
      Related
      ENSP00000354482.4, ENST00000361443.4
      Conserved Domains (4) summary
      COG5048
      Location:371438
      COG5048; FOG: Zn-finger [General function prediction only]
      sd00017
      Location:361380
      ZF_C2H2; C2H2 Zn finger [structural motif]
      pfam00096
      Location:416438
      zf-C2H2; Zinc finger, C2H2 type
      pfam13465
      Location:402425
      zf-H2C2_2; Zinc-finger double domain

    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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      20782279..20786886 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      20918318..20922938 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)