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NKX2-1
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  • NKX2-1
PROTEIN STRUCTURE
ANTIBODIES
AND
VALIDATION
Protein structures
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

NKX2-1
Synonyms BCH, NKX2A, TITF1, TTF-1, TTF1
Gene descriptioni

Full gene name according to HGNC.

NK2 homeobox 1
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Read more
Cancer-related genes
Disease related genes
Human disease related genes
Transcription factors
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Read more
Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 14
Cytoband q13.3
Chromosome location (bp) 36516392 - 36521149
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

3
Ensembl ENSG00000136352 (version 103.38)
Entrez gene 7080
HGNC HGNC:11825
UniProt P43699 (UniProt - Evidence at protein level)
neXtProt NX_P43699
Antibodypedia NKX2-1 antibodies


PROTEIN STRUCTUREi

The Structure section provides predicted structures from the Alphafold protein structure database and available experimental structures from Protein Data Bank (PDB).

In the Structure drop-down menu all experimental structures from PDB are available for selection and display. The structures are displayed using the NGL Viewer and can be zoomed-in and rotated either manually or by checking the Autorotate box. The Color scheme can be selected to show the residue index, chain name or confidence score (as B-factors and pLDDT score for experimental and predicted structures, respectively). The positions for available antigen sequences in the structure are shown if Antigens is turned to ON, and the Variants slider can be used to show the positions of clinical and population variants.https://github.com/nglviewer/ngl

Read more

Predicted


Description: Structure prediction from Alphafold project. Structure version 2

# Chains: 1      # Clinical variants: 7      # Population variants: 193

Antigens:

Off
On

Variants:

Off
Clinical
Population

Color scheme:

Confidence
Residue index
Chain name

Autorotate:

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On



PROTEIN BROWSERi

The protein browser displays the antigen location on the target protein(s) and the features of the target protein. The tabs at the top of the protein view section can be used to switch between the different splice variants to which an antigen has been mapped.

At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target.

Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more).

The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more).

If a signal peptide is predicted by a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius (turquoise) and/or transmembrane regions (orange) are predicted by MDM, these are displayed.

Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.
NKX2-1-201
NKX2-1-202
NKX2-1-203


PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The ENSP identifier links to the Ensembl website protein summary, while the ENST identifier links to the Ensembl website transcript summary for the selected splice variant. The data in the UniProt column can be expanded to show links to all matching UniProt identifiers for this protein.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The Gene Ontology terms assigned to this protein are listed if expanding the Gene ontology column. The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide (according to a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius) and the number of predicted transmembrane region(s) (according to MDM) are also reported.
Splice variant UniProt Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
NKX2-1-201
ENSP00000346879
ENST00000354822
P43699 [Direct mapping]
Homeobox protein Nkx-2.1
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Transcription factors
   Helix-turn-helix domains
Cancer-related genes
   COSMIC somatic mutations in cancer genes
   COSMIC Amplifications
   COSMIC Somatic Mutations
Disease related genes
Human disease related genes
   Endocrine and metabolic diseases
   Thyroid gland diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Show all
GO:0000122 [negative regulation of transcription by RNA polymerase II]
GO:0000785 [chromatin]
GO:0000976 [transcription regulatory region sequence-specific DNA binding]
GO:0000977 [RNA polymerase II transcription regulatory region sequence-specific DNA binding]
GO:0000978 [RNA polymerase II cis-regulatory region sequence-specific DNA binding]
GO:0000981 [DNA-binding transcription factor activity, RNA polymerase II-specific]
GO:0001161 [intronic transcription regulatory region sequence-specific DNA binding]
GO:0001764 [neuron migration]
GO:0003677 [DNA binding]
GO:0003700 [DNA-binding transcription factor activity]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0005667 [transcription regulator complex]
GO:0006355 [regulation of transcription, DNA-templated]
GO:0006357 [regulation of transcription by RNA polymerase II]
GO:0006644 [phospholipid metabolic process]
GO:0007389 [pattern specification process]
GO:0007411 [axon guidance]
GO:0007420 [brain development]
GO:0007492 [endoderm development]
GO:0007626 [locomotory behavior]
GO:0008134 [transcription factor binding]
GO:0009725 [response to hormone]
GO:0009887 [animal organ morphogenesis]
GO:0010628 [positive regulation of gene expression]
GO:0010719 [negative regulation of epithelial to mesenchymal transition]
GO:0019899 [enzyme binding]
GO:0021537 [telencephalon development]
GO:0021759 [globus pallidus development]
GO:0021766 [hippocampus development]
GO:0021795 [cerebral cortex cell migration]
GO:0021798 [forebrain dorsal/ventral pattern formation]
GO:0021877 [forebrain neuron fate commitment]
GO:0021879 [forebrain neuron differentiation]
GO:0021892 [cerebral cortex GABAergic interneuron differentiation]
GO:0021895 [cerebral cortex neuron differentiation]
GO:0021983 [pituitary gland development]
GO:0022029 [telencephalon cell migration]
GO:0030154 [cell differentiation]
GO:0030324 [lung development]
GO:0030336 [negative regulation of cell migration]
GO:0030512 [negative regulation of transforming growth factor beta receptor signaling pathway]
GO:0030878 [thyroid gland development]
GO:0030900 [forebrain development]
GO:0031128 [developmental induction]
GO:0033327 [Leydig cell differentiation]
GO:0042753 [positive regulation of circadian rhythm]
GO:0043565 [sequence-specific DNA binding]
GO:0045892 [negative regulation of transcription, DNA-templated]
GO:0045893 [positive regulation of transcription, DNA-templated]
GO:0045944 [positive regulation of transcription by RNA polymerase II]
GO:0048511 [rhythmic process]
GO:0048646 [anatomical structure formation involved in morphogenesis]
GO:0048663 [neuron fate commitment]
GO:0048709 [oligodendrocyte differentiation]
GO:0060430 [lung saccule development]
GO:0060441 [epithelial tube branching involved in lung morphogenesis]
GO:0060486 [club cell differentiation]
GO:0060510 [type II pneumocyte differentiation]
Show all
401 aa
41.7 kDa
No 0
NKX2-1-202
ENSP00000429607
ENST00000498187
P43699 [Direct mapping]
Homeobox protein Nkx-2.1
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Transcription factors
   Helix-turn-helix domains
Cancer-related genes
   COSMIC somatic mutations in cancer genes
   COSMIC Amplifications
   COSMIC Somatic Mutations
Disease related genes
Human disease related genes
   Endocrine and metabolic diseases
   Thyroid gland diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Show all
GO:0000122 [negative regulation of transcription by RNA polymerase II]
GO:0000785 [chromatin]
GO:0000976 [transcription regulatory region sequence-specific DNA binding]
GO:0000977 [RNA polymerase II transcription regulatory region sequence-specific DNA binding]
GO:0000978 [RNA polymerase II cis-regulatory region sequence-specific DNA binding]
GO:0000981 [DNA-binding transcription factor activity, RNA polymerase II-specific]
GO:0001161 [intronic transcription regulatory region sequence-specific DNA binding]
GO:0003677 [DNA binding]
GO:0003700 [DNA-binding transcription factor activity]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0006355 [regulation of transcription, DNA-templated]
GO:0006357 [regulation of transcription by RNA polymerase II]
GO:0007420 [brain development]
GO:0008134 [transcription factor binding]
GO:0009725 [response to hormone]
GO:0010628 [positive regulation of gene expression]
GO:0010719 [negative regulation of epithelial to mesenchymal transition]
GO:0019899 [enzyme binding]
GO:0021759 [globus pallidus development]
GO:0030154 [cell differentiation]
GO:0030324 [lung development]
GO:0030336 [negative regulation of cell migration]
GO:0030512 [negative regulation of transforming growth factor beta receptor signaling pathway]
GO:0030878 [thyroid gland development]
GO:0030900 [forebrain development]
GO:0042753 [positive regulation of circadian rhythm]
GO:0045892 [negative regulation of transcription, DNA-templated]
GO:0045893 [positive regulation of transcription, DNA-templated]
GO:0045944 [positive regulation of transcription by RNA polymerase II]
GO:0048511 [rhythmic process]
GO:0060441 [epithelial tube branching involved in lung morphogenesis]
Show all
371 aa
38.6 kDa
No 0
NKX2-1-203
ENSP00000428341
ENST00000518149
P43699 [Direct mapping]
Homeobox protein Nkx-2.1
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Transcription factors
   Helix-turn-helix domains
Cancer-related genes
   COSMIC somatic mutations in cancer genes
   COSMIC Amplifications
   COSMIC Somatic Mutations
Disease related genes
Human disease related genes
   Endocrine and metabolic diseases
   Thyroid gland diseases
Mapped to neXtProt
   neXtProt - Evidence at protein level
Show all
GO:0000122 [negative regulation of transcription by RNA polymerase II]
GO:0000785 [chromatin]
GO:0000976 [transcription regulatory region sequence-specific DNA binding]
GO:0000977 [RNA polymerase II transcription regulatory region sequence-specific DNA binding]
GO:0000978 [RNA polymerase II cis-regulatory region sequence-specific DNA binding]
GO:0000981 [DNA-binding transcription factor activity, RNA polymerase II-specific]
GO:0001161 [intronic transcription regulatory region sequence-specific DNA binding]
GO:0003677 [DNA binding]
GO:0003700 [DNA-binding transcription factor activity]
GO:0005515 [protein binding]
GO:0005634 [nucleus]
GO:0005654 [nucleoplasm]
GO:0006355 [regulation of transcription, DNA-templated]
GO:0006357 [regulation of transcription by RNA polymerase II]
GO:0007420 [brain development]
GO:0008134 [transcription factor binding]
GO:0009725 [response to hormone]
GO:0010628 [positive regulation of gene expression]
GO:0010719 [negative regulation of epithelial to mesenchymal transition]
GO:0019899 [enzyme binding]
GO:0021759 [globus pallidus development]
GO:0030154 [cell differentiation]
GO:0030324 [lung development]
GO:0030336 [negative regulation of cell migration]
GO:0030512 [negative regulation of transforming growth factor beta receptor signaling pathway]
GO:0030878 [thyroid gland development]
GO:0030900 [forebrain development]
GO:0042753 [positive regulation of circadian rhythm]
GO:0045892 [negative regulation of transcription, DNA-templated]
GO:0045893 [positive regulation of transcription, DNA-templated]
GO:0045944 [positive regulation of transcription by RNA polymerase II]
GO:0048511 [rhythmic process]
GO:0060441 [epithelial tube branching involved in lung morphogenesis]
Show all
371 aa
38.6 kDa
No 0

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The Human Protein Atlas project is funded
by the Knut & Alice Wallenberg Foundation.