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SLC9B1P1 solute carrier family 9 member B1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100128190, updated on 22-Sep-2022

Summary

Official Symbol
SLC9B1P1provided by HGNC
Official Full Name
solute carrier family 9 member B1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:37492
See related
Ensembl:ENSG00000183704 AllianceGenome:HGNC:37492
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
NHEDC1P1
Summary
Predicted to enable solute:proton antiporter activity. Predicted to be involved in proton transmembrane transport and sodium ion transport. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See SLC9B1P1 in Genome Data Viewer
Location:
Yq11.21
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (11340390..11385695, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (11561740..11607031, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (13496066..13541371, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene double homeobox 4 like 19 (pseudogene) Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 5 Neighboring gene ACTR3B pseudogene 1 Neighboring gene CHEK2 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • Na+/H+ exchanger domain containing 1 pseudogene 1
  • Putative protein SLC9B1-like 1
  • solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 pseudogene 1
  • solute carrier family 9, subfamily B (cation proton antiporter 2), member 1 pseudogene 1

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables solute:proton antiporter activity IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
involved_in proton transmembrane transport IEA
Inferred from Electronic Annotation
more info
 
involved_in sodium ion transport IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in membrane 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.

Genomic

  1. NG_023008.2 

    Range
    101..45406
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    11340390..11385695 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    11561740..11607031 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)