LOC728688 ubiquitin like with PHD and ring finger domains 1 pseudogene [Homo sapiens (human)] - Gene

Summary

Gene symbol: LOC728688
Gene description: ubiquitin like with PHD and ring finger domains 1 pseudogene
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information: Note: This gene is designated as a pseudogene for ubiquitin-like with PHD and ring finger domains 1 (UHRF1, GeneID 29128) because it has a single-exon alignment and the predicted protein is shorter by approximately 40% (489 aa vs. UHRF1 isoforms of 793 aa and 806 aa). On the alternate Celera assembly, this locus was designated as a protein-coding gene, however, the NCBI RefSeq Project treats this as a pseudogene. [13 Feb 2013]
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Genomic context

Location:: 12p12.2

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	12	NC_000012.12 (20551569..20554360)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	12	NC_060936.1 (20430031..20432823)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	12	NC_000012.11 (20704503..20707294)

Chromosome 12 - NC_000012.12 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?

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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

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General gene information

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Markers

RH26361 (e-PCR)
- UniSTS:90369

G22294 (e-PCR)
- UniSTS:67554

PMC128323P1 (e-PCR)
- UniSTS:270576

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.