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SPATA31E3P SPATA31 subfamily E member 3, pseudogene [ Homo sapiens (human) ]

Gene ID: 646507, updated on 10-Oct-2023

Summary

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Official Symbol
SPATA31E3Pprovided by HGNC
Official Full Name
SPATA31 subfamily E member 3, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:43828
See related
AllianceGenome:HGNC:43828
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
FAM75E3P
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Genomic context

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Location:
15q11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (22403038..22407023)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (20075134..20079119)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (23466073..23470058, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene arginine-glutamic acid dipeptide repeats pseudogene 3 Neighboring gene RING finger protein 145-like Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:23454295-23455138 Neighboring gene golgin A8 family member E, pseudogene Neighboring gene RNA, 7SL, cytoplasmic 545, pseudogene Neighboring gene uncharacterized LOC124900355 Neighboring gene MPHOSPH10 pseudogene 9

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • family with sequence similarity 75, member E3, pseudogene

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_022101.3 

    Range
    101..4086
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    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_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    22403038..22407023
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160017.1 Reference GRCh38.p14 PATCHES

    Range
    3297527..3301512
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    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187604.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    47507..51492
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    20075134..20079119
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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