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ZSWIM5P1 zinc finger SWIM-type containing 5 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100130110, updated on 10-Oct-2023

Summary

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Official Symbol
ZSWIM5P1provided by HGNC
Official Full Name
zinc finger SWIM-type containing 5 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:43768
See related
Ensembl:ENSG00000235430 AllianceGenome:HGNC:43768
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See ZSWIM5P1 in Genome Data Viewer
Location:
17p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (15768520..15771426, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (15674868..15677774, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (15671834..15674740, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene ZNF286A-TBC1D26 readthrough (NMD candidate) Neighboring gene TBC1 domain family member 26 Neighboring gene uncharacterized LOC105371559 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:15672089-15672589 Neighboring gene CDRT15 pseudogene 2 Neighboring gene RNA, 5S ribosomal pseudogene 436 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:15689807-15690306 Neighboring gene interleukin 6 signal transducer pseudogene 1 Neighboring gene Meis homeobox 3 pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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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.

Genomic

  1. NG_022443.2 

    Range
    101..3007
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    15768520..15771426 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    15674868..15677774 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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