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SPATA31B1P SPATA31 subfamily B member 1, pseudogene [ Homo sapiens (human) ]

Gene ID: 404770, updated on 17-Sep-2024

Summary

Official Symbol
SPATA31B1Pprovided by HGNC
Official Full Name
SPATA31 subfamily B member 1, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:31411
See related
Ensembl:ENSG00000231649 AllianceGenome:HGNC:31411
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
FAM75B; C9orf36B; SPATA31B1
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Genomic context

See SPATA31B1P in Genome Data Viewer
Location:
9q21.32
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (82057397..82063844, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (94207031..94213479, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (84672312..84678759, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376105 Neighboring gene uncharacterized LOC105376107 Neighboring gene SPATA31 subfamily D member 2, pseudogene Neighboring gene SPATA31 subfamily D member 1 Neighboring gene DEAD-box helicase 10 pseudogene 2 Neighboring gene ribosomal protein S2 pseudogene 34

Genomic regions, transcripts, and products

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_046749.1 

    Range
    101..6548
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    82057397..82063844 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    94207031..94213479 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001098807.1: Suppressed sequence

    Description
    NM_001098807.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
  2. NM_001164339.1: Suppressed sequence

    Description
    NM_001164339.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.