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HYDIN2 HYDIN axonemal central pair apparatus protein 2 (pseudogene) [ Homo sapiens (human) ]

Gene ID: 100288805, updated on 23-Nov-2021


Official Symbol
HYDIN2provided by HGNC
Official Full Name
HYDIN axonemal central pair apparatus protein 2 (pseudogene)provided by HGNC
Primary source
See related
Gene type
RefSeq status
Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
Biased expression in testis (RPKM 2.1), brain (RPKM 0.8) and 12 other tissues See more
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Genomic context

See HYDIN2 in Genome Data Viewer
Exon count:
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (146486332..146822034)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 Unlocalized Scaffold NT_167207.1 (132569..468683, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371233 Neighboring gene uncharacterized LOC107985591 Neighboring gene RNA, 5S ribosomal pseudogene 536 Neighboring gene NBPF member 12 Neighboring gene profilin 1 pseudogene 8 Neighboring gene phosphodiesterase 4D interacting protein pseudogene

Genomic regions, transcripts, and products


  • Project title: 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


Products Interactant Other Gene Complex Source Pubs Description

General gene information


Other Names

  • HYDIN, axonemal central pair apparatus protein pseudogene 1
  • HYDIN2, axonemal central pair apparatus protein (pseudogene)
  • hydrocephalus inducing homolog 2

Clone Names

  • FLJ14665, KIAA1864, DKFZp761B238, DKFZp761M1613

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables triplet codon-amino acid adaptor activity IEA
Inferred from Electronic Annotation
more info
Process Evidence Code Pubs
involved_in translation IEA
Inferred from Electronic Annotation
more info

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.


  1. NR_103556.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AB058767, AC241929, AC245407, AK027571, AL833826, AL834340, BG292092, DA303757, DR000174, H53415

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly


  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_049745.1: Suppressed sequence

    NR_049745.1: This RefSeq was suppressed because it was not a good representation of the HYDIN2 locus.
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