ALG1L8P ALG1 like 8, pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: ALG1L8Pprovided by HGNC
Official Full Name: ALG1 like 8, pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:44377
See related: Ensembl:ENSG00000227620 AllianceGenome:HGNC:44377
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:: 11q13.2

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	11	NC_000011.10 (67785270..67793345)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	11	NC_060935.1 (67780462..67788541)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	11	NC_000011.9 (67552741..67560816)

Chromosome 11 - NC_000011.10 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?

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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

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

REN80967 (e-PCR)
- UniSTS:405765

REN80968 (e-PCR)
- UniSTS:405766

REN80977 (e-PCR)
- UniSTS:405775

REN80988 (e-PCR)
- UniSTS:405786

REN80994 (e-PCR)
- UniSTS:405792

SHGC-77297 (e-PCR)
- UniSTS:8694

Other Names

asparagine-linked glycosylation 1 homolog pseudogene
asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog pseudogene
asparagine-linked glycosylation 1-like 8, 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.