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FOXD4L4 forkhead box D4 like 4 [ Homo sapiens (human) ]

Gene ID: 349334, updated on 23-Nov-2023

Summary

Official Symbol
FOXD4L4provided by HGNC
Official Full Name
forkhead box D4 like 4provided by HGNC
Primary source
HGNC:HGNC:23762
See related
Ensembl:ENSG00000184659 MIM:611085; AllianceGenome:HGNC:23762
Gene type
protein coding
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FOXD4b; FOXD4L2; bA460E7.2
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in anatomical structure morphogenesis; cell differentiation; and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be part of chromatin. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

Location:
9q21.11
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (65737146..65738396)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (80057244..80058494, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (70427649..70428899, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379447 Neighboring gene Sharpr-MPRA regulatory region 13873 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:70489243-70489833 Neighboring gene Zn regulated GTPase metalloprotein activator 1E Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:70450935-70451544 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:70427620-70428156 Neighboring gene immunoglobulin kappa variable 1/OR-3 (pseudogene) Neighboring gene uncharacterized LOC101928381

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in anatomical structure morphogenesis IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in cell differentiation IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
 
Component Evidence Code Pubs
part_of chromatin ISA
Inferred from Sequence Alignment
more info
 
located_in nucleus IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
forkhead box protein D4-like 4
Names
FOXD4-like 4
forkhead box D4-like 2
forkhead box protein D4-like 2
forkhead box protein D4b
myeloid factor-gamma
winged helix factor-1
winged helix transcription factor beta

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_199244.3NP_954714.2  forkhead box protein D4-like 4

    See identical proteins and their annotated locations for NP_954714.2

    Status: INFERRED

    Source sequence(s)
    BX284632
    Consensus CDS
    CCDS75845.1
    UniProtKB/Swiss-Prot
    Q5RIB4, Q6VB85, Q8WXT5
    UniProtKB/TrEMBL
    Q3MI95
    Related
    ENSP00000366630.1, ENST00000377413.3
    Conserved Domains (1) summary
    pfam00250
    Location:108194
    Forkhead; Forkhead domain

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    65737146..65738396
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    80057244..80058494 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001099279.1: Suppressed sequence

    Description
    NM_001099279.1: This RefSeq was permanently suppressed because it is a redundant RefSeq for this FOXD4-like family member.