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    SFTA3 surfactant associated 3 [ Homo sapiens (human) ]

    Gene ID: 253970, updated on 10-Dec-2024

    Summary

    Official Symbol
    SFTA3provided by HGNC
    Official Full Name
    surfactant associated 3provided by HGNC
    Primary source
    HGNC:HGNC:18387
    See related
    Ensembl:ENSG00000257520 MIM:617860; AllianceGenome:HGNC:18387
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SPH; SP-H; NANCI; PAHRF; SFTPH
    Summary
    Involved in wound healing. Located in cytoplasm and extracellular space. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Restricted expression toward lung (RPKM 71.4) See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See SFTA3 in Genome Data Viewer
    Location:
    14q13.3
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (36473288..36519556, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (30662595..30708840, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (36942493..36988761, complement)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene DPPA3 pseudogene 2 Neighboring gene RNA, U7 small nuclear 93 pseudogene Neighboring gene VISTA enhancer hs1538 Neighboring gene VISTA enhancer hs704 Neighboring gene VISTA enhancer hs1166 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36974689-36975264 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr14:36977998-36978653 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36983846-36984473 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:36986696-36987694 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36988853-36989852 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36989853-36990852 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36990853-36991852 Neighboring gene uncharacterized LOC105370453 Neighboring gene NKX2-1 antisense RNA 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36994071-36995009 Neighboring gene NK2 homeobox 1 Neighboring gene phosphorylase kinase regulatory subunit beta pseudogene 2 Neighboring gene ReSE screen-validated silencer GRCh37_chr14:37025714-37025870 Neighboring gene ribosomal protein L29 pseudogene 3

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    General gene information

    Markers

    Other Names

    • NKX2.1 associated non-coding intergenic RNA
    • Nkx2.1-associated noncoding intergenic RNA
    • pulmonary arterial hypertension related factor
    • putative protein SFTA3
    • surfactant-associated protein 3
    • surfactant-associated protein H

    Clone Names

    • FLJ23494

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    involved_in wound healing IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in clathrin-coated endocytic vesicle TAS
    Traceable Author Statement
    more info
     
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in endoplasmic reticulum membrane TAS
    Traceable Author Statement
    more info
     
    located_in extracellular region TAS
    Traceable Author Statement
    more info
     
    located_in extracellular space IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in lamellar body TAS
    Traceable Author Statement
    more info
     

    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.

    RNA

    1. NR_138597.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    2. NR_138598.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    3. NR_138599.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    4. NR_138600.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    5. NR_138601.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    6. NR_161362.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    7. NR_161363.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    8. NR_161364.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
    9. NR_161365.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL132857
      Related
      ENST00000521945.1

    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_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      36473288..36519556 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      30662595..30708840 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001101341.1: Suppressed sequence

      Description
      NM_001101341.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    2. NM_001331217.1: Suppressed sequence

      Description
      NM_001331217.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    3. NM_001352986.1: Suppressed sequence

      Description
      NM_001352986.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    4. NM_001352987.1: Suppressed sequence

      Description
      NM_001352987.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.