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

Gene ID: 100288805, updated on 8-Jun-2016
Official Symbol
HYDIN2provided by HGNC
Official Full Name
HYDIN2, axonemal central pair apparatus protein (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:33129
See related
MIM:610813
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HYDINP1
Annotation information
Note: This locus is part of a 360-kb interchromosomal duplication at chromosome band 16q22. Compared to GeneID:54768, this locus is missing several exons and contains a 1-bp deletion, both of which result in frameshifts. Consequently, this locus does not appear capable of expressing a protein and is annotated as a pseudogene. [13 Feb 2013]
Location:
1q21.1
Exon count:
46
Annotation release Status Assembly Chr Location
108 current GRCh38.p7 (GCF_000001405.33) 1 NC_000001.11 (146547489..146822034)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NT_167207.1 (132569..407510, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985591 Neighboring gene uncharacterized LOC102724558 Neighboring gene uncharacterized LOC107985569 Neighboring gene neuroblastoma breakpoint family member 12 Neighboring gene profilin 1 pseudogene 8

Products Interactant Other Gene Complex Source Pubs Description

Markers

Other Names

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

Clone Names

  • FLJ14665, KIAA1864, DKFZp761B238, DKFZp761M1613

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_103556.1 RNA Sequence

    Status: INFERRED

    Source sequence(s)
    AB058767, AC241929, AK027571, AL833826, AL834340

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 108 details...

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

Reference GRCh38.p7 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p7 Primary Assembly

    Range
    146547489..146822034
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018912.2 Alternate CHM1_1.1

    Range
    147915615..148190160
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_049745.1: Suppressed sequence

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