ALG1L15P ALG1 like 15, pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: ALG1L15Pprovided by HGNC
Official Full Name: ALG1 like 15, pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:44384
See related: AllianceGenome:HGNC:44384
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:: 3q25.31

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	3	NC_000003.12 (156044129..156044950, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	3	NC_060927.1 (158818752..158819573, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	3	NC_000003.11 (155761918..155762739, complement)

Chromosome 3 - NC_000003.12 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

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

SHGC-146410 (e-PCR)
- UniSTS:172604

SHGC-149644 (e-PCR)
- UniSTS:183684

Other Names

asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog pseudogene
asparagine-linked glycosylation 1-like 15, pseudogene
asparagine-linked glycosylation 1-like 2 pseudogene
beta-1,4-mannosyltransferase 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.