Human Gene FOXJ1 (ENST00000322957.7_7) from GENCODE V47lift37
  Description: forkhead box J1 (from RefSeq NM_001454.4)
Gencode Transcript: ENST00000322957.7_7
Gencode Gene: ENSG00000129654.8_9
Transcript (Including UTRs)
   Position: hg19 chr17:74,132,414-74,137,326 Size: 4,913 Total Exon Count: 3 Strand: -
Coding Region
   Position: hg19 chr17:74,133,434-74,136,476 Size: 3,043 Coding Exon Count: 2 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr17:74,132,414-74,137,326)mRNA (may differ from genome)Protein (421 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: FOXJ1_HUMAN
DESCRIPTION: RecName: Full=Forkhead box protein J1; AltName: Full=Forkhead-related protein FKHL13; AltName: Full=Hepatocyte nuclear factor 3 forkhead homolog 4; Short=HFH-4;
FUNCTION: May play an important role in cell fate determination during lung development and in spermatogenesis (By similarity).
SUBCELLULAR LOCATION: Nucleus.
TISSUE SPECIFICITY: Testis, oviduct, lung and brain cortex.
DEVELOPMENTAL STAGE: Expressed in developing lung, kidney and central nervous system.
DISEASE: Genetic variations in FOXJ1 may be associated with susceptibility to allergic rhinitis (ALRH) [MIM:607154]. Allergic rhinitis is a common disease of complex inheritance and is characterized by mucosal inflammation caused by allergen exposure.
SIMILARITY: Contains 1 fork-head DNA-binding domain.

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: FOXJ1
Diseases sorted by gene-association score: rhinitis (9), allergic rhinitis (8), primary ciliary dyskinesia (2), pulmonary immaturity (1), autosomal dominant nonsyndromic deafness 20 (1), kartagener syndrome (1), visceral heterotaxy (1)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 18.81 RPKM in Testis
Total median expression: 49.16 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -144.90301-0.481 Picture PostScript Text
3' UTR -462.101020-0.453 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR001766 - TF_fork_head
IPR018122 - TF_fork_head_CS
IPR011991 - WHTH_trsnscrt_rep_DNA-bd

Pfam Domains:
PF00250 - Forkhead domain

SCOP Domains:
46785 - "Winged helix" DNA-binding domain

ModBase Predicted Comparative 3D Structure on Q92949
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologGenome Browser
Gene Details    Gene Details
Gene Sorter    Gene Sorter
  Ensembl  SGD
     Protein Sequence
     Alignment

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000976 transcription regulatory region sequence-specific DNA binding
GO:0000978 RNA polymerase II core promoter proximal region sequence-specific DNA binding
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
GO:0001077 transcriptional activator activity, RNA polymerase II core promoter proximal region sequence-specific binding
GO:0003677 DNA binding
GO:0003700 transcription factor activity, sequence-specific DNA binding
GO:0005515 protein binding
GO:0043565 sequence-specific DNA binding

Biological Process:
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0002508 central tolerance induction
GO:0002635 negative regulation of germinal center formation
GO:0002897 positive regulation of central B cell tolerance induction
GO:0002924 negative regulation of humoral immune response mediated by circulating immunoglobulin
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006366 transcription from RNA polymerase II promoter
GO:0006959 humoral immune response
GO:0007283 spermatogenesis
GO:0007368 determination of left/right symmetry
GO:0007389 pattern specification process
GO:0007420 brain development
GO:0007507 heart development
GO:0030030 cell projection organization
GO:0030036 actin cytoskeleton organization
GO:0030856 regulation of epithelial cell differentiation
GO:0032088 negative regulation of NF-kappaB transcription factor activity
GO:0033085 negative regulation of T cell differentiation in thymus
GO:0035089 establishment of apical/basal cell polarity
GO:0035502 metanephric part of ureteric bud development
GO:0042130 negative regulation of T cell proliferation
GO:0044458 motile cilium assembly
GO:0045409 negative regulation of interleukin-6 biosynthetic process
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0050869 negative regulation of B cell activation
GO:0050900 leukocyte migration
GO:0060271 cilium assembly
GO:0060428 lung epithelium development
GO:0060429 epithelium development
GO:0060972 left/right pattern formation
GO:0072016 glomerular parietal epithelial cell development
GO:0090630 activation of GTPase activity
GO:1901248 positive regulation of lung ciliated cell differentiation

Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  BC046460 - Homo sapiens forkhead box J1, mRNA (cDNA clone MGC:35202 IMAGE:5171637), complete cds.
X99349 - H.sapiens mRNA for fork head homologue 4.
JD498680 - Sequence 479704 from Patent EP1572962.
JD229935 - Sequence 210959 from Patent EP1572962.
JD053417 - Sequence 34441 from Patent EP1572962.
JD141571 - Sequence 122595 from Patent EP1572962.
JD475130 - Sequence 456154 from Patent EP1572962.
JD125970 - Sequence 106994 from Patent EP1572962.
JD178225 - Sequence 159249 from Patent EP1572962.
JD477419 - Sequence 458443 from Patent EP1572962.
JD383444 - Sequence 364468 from Patent EP1572962.
JD180177 - Sequence 161201 from Patent EP1572962.
JD310151 - Sequence 291175 from Patent EP1572962.
JD479340 - Sequence 460364 from Patent EP1572962.
JD115544 - Sequence 96568 from Patent EP1572962.
U69537 - Human forkhead transcription factor HFH-4 (HFH-4) mRNA, complete cds.
JD075474 - Sequence 56498 from Patent EP1572962.
KJ891181 - Synthetic construct Homo sapiens clone ccsbBroadEn_00575 FOXJ1 gene, encodes complete protein.
AB463648 - Synthetic construct DNA, clone: pF1KB7711, Homo sapiens FOXJ1 gene for forkhead box J1, without stop codon, in Flexi system.
AB464532 - Synthetic construct DNA, clone: pF1KB8393, Homo sapiens FOXJ1 gene for forkhead box J1, without stop codon, in Flexi system.
DQ577598 - Homo sapiens piRNA piR-45710, complete sequence.
JD483870 - Sequence 464894 from Patent EP1572962.
JD227097 - Sequence 208121 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: ENST00000322957.1, ENST00000322957.2, ENST00000322957.3, ENST00000322957.4, ENST00000322957.5, ENST00000322957.6, FKHL13 , FOXJ1 , FOXJ1_HUMAN, HFH4 , NM_001454, O00630, Q92949, uc317rji.1, uc317rji.2
UCSC ID: ENST00000322957.7_7
RefSeq Accession: NM_001454.4
Protein: Q92949 (aka FOXJ1_HUMAN or FXJ1_HUMAN)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.