U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

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

Gene ID: 389000, updated on 10-Oct-2023

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 AllianceGenome:HGNC:37493
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
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Location:
2p11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (91882906..91931714, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (92110703..92159510)
105.20220307 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 H3K27ac hESC enhancer GRCh37_chr2:92039806-92040306 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:92040307-92040807 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)

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.

Genomic

  1. NG_009550.2 

    Range
    101..48909
    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_000002.12 Reference GRCh38.p14 Primary Assembly

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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    92110703..92159510
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)