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IGLL4P immunoglobulin lambda like polypeptide 4, pseudogene [ Homo sapiens (human) ]

Gene ID: 100287528, updated on 10-Oct-2023

Summary

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Official Symbol
IGLL4Pprovided by HGNC
Official Full Name
immunoglobulin lambda like polypeptide 4, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:38475
See related
AllianceGenome:HGNC:38475
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
IGLL4
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Genomic context

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Location:
22q11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (20632590..20632826)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (21041290..21041526)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (20986877..20987113)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene coiled-coil domain containing 74B pseudogene 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr22:20954774-20954964 Neighboring gene sphingomyelin phosphodiesterase 4 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:20964690-20965288 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:20986473-20986998 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:20988186-20988928 Neighboring gene small G protein signaling modulator 1 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr22:20998359-20998915 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:21003243-21003749 Neighboring gene MPRA-validated peak4458 silencer Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:21008422-21009052 Neighboring gene solute carrier family 9 member 3 pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Identification of three new Ig lambda-like genes in man. Chang H, et al. J Exp Med, 1986 Feb 1. PMID 3003227, Free PMC Article

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)

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_021207.2 

    Range
    101..337
    Download
    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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    20632590..20632826
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    21041290..21041526
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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