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SLC9B1P2 solute carrier family 9 member B1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 389000, updated on 23-Nov-2021

Summary

Official Symbol
SLC9B1P2provided by HGNC
Official Full Name
solute carrier family 9 member B1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:37493
See related
Ensembl:ENSG00000214329
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
NHEDC1P2
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Genomic context

See SLC9B1P2 in Genome Data Viewer
Location:
2p11.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (91882906..91931714, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (92070932..92119740, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ATP binding cassette subfamily D member 1 pseudogene 5 Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 6 Neighboring gene ACTR3B pseudogene 2 Neighboring gene CHEK2 pseudogene 3

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • Na+/H+ exchanger domain containing 1 pseudogene 2
  • solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 pseudogene 2
  • solute carrier family 9, subfamily B (cation proton antiporter 2), member 1 pseudogene 2

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_009550.2 

    Range
    101..48909
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    GenBank, FASTA, Sequence Viewer (Graphics)

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

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    91882906..91931714 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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