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SLC9B1P4 solute carrier family 9 member B1 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 644768, updated on 13-May-2022

Summary

Official Symbol
SLC9B1P4provided by HGNC
Official Full Name
solute carrier family 9 member B1 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:43583
See related
AllianceGenome:HGNC:43583
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See SLC9B1P4 in Genome Data Viewer
Location:
22q11.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (16428755..16476875, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (17104605..17152726, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (16909498..16957618, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene ATP binding cassette subfamily D member 1 pseudogene 4 Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 9 Neighboring gene ACTR3B pseudogene 6 Neighboring gene CHEK2 pseudogene 4

Genomic regions, transcripts, and products

General gene information

Other Names

  • Na+/H+ exchanger domain containing 1 pseudogene
  • solute carrier family 9, subfamily B (NHA1, cation proton antiporter 1), member 1 pseudogene 4
  • solute carrier family 9, subfamily B (cation proton antiporter 2), member 1 pseudogene 4

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_022866.3 

    Range
    101..48221
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    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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    16428755..16476875 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160024.1 Reference GRCh38.p14 PATCHES

    Range
    400761..448881 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    17104605..17152726 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)