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LIN37 lin-37 DREAM MuvB core complex component [ Homo sapiens (human) ]

Gene ID: 55957, updated on 4-Jan-2025

Summary

Official Symbol
LIN37provided by HGNC
Official Full Name
lin-37 DREAM MuvB core complex componentprovided by HGNC
Primary source
HGNC:HGNC:33234
See related
Ensembl:ENSG00000267796 AllianceGenome:HGNC:33234
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
F25965; lin-37; ZK418.4
Summary
This gene encodes a protein expressed in the eye. [provided by RefSeq, Jul 2008]
Expression
Ubiquitous expression in testis (RPKM 7.7), placenta (RPKM 6.8) and 25 other tissues See more
Orthologs
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Genomic context

See LIN37 in Genome Data Viewer
Location:
19q13.12
Exon count:
10
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (35748576..35754519)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (38293885..38299832)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (36239477..36245420)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14497 Neighboring gene ReSE screen-validated silencer GRCh37_chr19:36234871-36235031 Neighboring gene U2 small nuclear RNA auxiliary factor 1 like 4 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:36238731-36239245 Neighboring gene presenilin enhancer, gamma-secretase subunit Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:36239246-36239760 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:36248182-36248753 Neighboring gene heat shock protein family B (small) member 6 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14500 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 14501 Neighboring gene proline and serine rich 3 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:36257953-36258804

Genomic regions, transcripts, and products

Expression

  • Project title: Tissue-specific circular RNA induction during human fetal development
  • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
  • BioProject: PRJNA270632
  • Publication: PMID 26076956
  • Analysis date: Mon Apr 2 22:54:59 2018

Pathways from PubChem

Interactions

General gene information

Potential readthrough

Included gene: PSENEN

Clone Names

  • MGC9505

Gene Ontology Provided by GOA

Component Evidence Code Pubs
part_of Myb complex  
located_in nucleoplasm  
part_of transcription repressor complex  

General protein information

Preferred Names
protein lin-37 homolog
Names
antolefinin
lin-37 homolog
protein F25965

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.

mRNA and Protein(s)

  1. NM_001369780.1NP_001356709.1  protein lin-37 homolog isoform 2

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) differs in the 5' UTR and coding sequence compared to variant 1. The resulting isoform (2) is shorter at the N-terminus compared to isoform 1.
    Source sequence(s)
    AC002398, AD000671, KC877720, KC877725
    Conserved Domains (1) summary
    pfam15306
    Location:70226
    LIN37
  2. NM_019104.3NP_061977.1  protein lin-37 homolog isoform 1

    See identical proteins and their annotated locations for NP_061977.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) encodes the longer isoform (1).
    Source sequence(s)
    BC009071, CB152701, DC396639
    Consensus CDS
    CCDS62642.1
    UniProtKB/Swiss-Prot
    A8KAQ1, O14557, Q7Z2T9, Q96GY3
    Related
    ENSP00000301159.7, ENST00000301159.14
    Conserved Domains (1) summary
    pfam15306
    Location:84240
    LIN37

RNA

  1. NR_163146.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC002398, AD000671, KC877720, KC877725

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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    35748576..35754519
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    38293885..38299832
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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