U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

DYNLL1P5 dynein light chain LC8-type 1 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 106480681, updated on 17-Sep-2024

Summary

Go to the top of the page Help
Official Symbol
DYNLL1P5provided by HGNC
Official Full Name
dynein light chain LC8-type 1 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:49656
See related
AllianceGenome:HGNC:49656
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
See DYNLL1P5 in Genome Data Viewer
Location:
3q25.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (154657256..154657763)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (157431213..157431720)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (154375045..154375552)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_65446 Neighboring gene G protein-coupled receptor 149 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_65451 Neighboring gene DEAD-box helicase 50 pseudogene 2 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_65484 Neighboring gene synaptophysin like 1 pseudogene 1 Neighboring gene ribosomal protein L9 pseudogene 15 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:154484051-154484552 Neighboring gene uncharacterized LOC105374170

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See Variation Viewer (GRCh37.p13)

General gene information

Go to the top of the page Help

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_043252.2 

    Range
    101..608
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    154657256..154657763
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    157431213..157431720
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials