XKRYP6 XK related, Y-linked pseudogene 6 [Homo sapiens (human)] - Gene

Summary

Official Symbol: XKRYP6provided by HGNC
Official Full Name: XK related, Y-linked pseudogene 6provided by HGNC
Primary source: HGNC:HGNC:23913
See related: AllianceGenome:HGNC:23913
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

Location:: Yq11.23

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	Y	NC_000024.10 (25952590..25954387)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	Y	NC_060948.1 (26765036..26766834)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	Y	NC_000024.9 (28098737..28100534)

Chromosome Y - NC_000024.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

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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Markers

sY2835 (e-PCR)
- UniSTS:514878

sY2858 (e-PCR)
- UniSTS:514901

sY1740 (e-PCR)
- UniSTS:514672

sY1742 (e-PCR)
- UniSTS:514674

Other Names

X Kell blood group precursor-related, Y-linked pseudogene 6
X-linked Kx blood group related, Y-linked pseudogene 6
XK, Kell blood group complex subunit-related family, member 3 pseudogene
XK, Kell blood group complex subunit-related, Y-linked pseudogene 6

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.