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FANCL
HPA
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  • SUMMARY

  • TISSUE

  • BRAIN

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  • SUBCELL

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  • FANCL
STRUCTURE STRUCTURE
Protein structures
Structure methods
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.

FANCL
Synonyms FAAP43, FLJ10335, PHF9, Pog
Gene descriptioni

Full gene name according to HGNC.

FA complementation group L
Protein classi

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

Read more
Disease related genes
Enzymes
Human disease related genes
Metabolic proteins
Potential drug targets
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.

Intracellular
Protein evidence Evidence at protein level (all genes)

HUMAN PROTEIN ATLAS INFORMATIONi

Summary of RNA expression analysis and annotation data generated within the Human Protein Atlas project.

Single cell type
expression clusteri

The RNA data was used to cluster genes according to their expression across single cell types. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Pituitary endocrine cells - Neuroendocrine signaling (mainly)
Single cell type specificityi

The RNA specificity category is based on mRNA expression levels in the analyzed cell types based on scRNA-seq data from normal tissues. The categories include: cell type enriched, group enriched, cell type enhanced, low cell type specificity and not detected.

Cell type enhanced (Lactotrophs, Oligodendrocytes, Somatotrophs, Thyrotrophs)
Tissue expression
cluster (RNA)i

The RNA data was used to cluster genes according to their expression across tissues. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Non-specific - Basic cellular processes (mainly)
Tissue specificity (RNA)i

The RNA specificity category is based on mRNA expression levels in the consensus dataset which is calculated from the RNA expression levels in samples from HPA and GTEX. The categories include: tissue enriched, group enriched, tissue enhanced, low tissue specificity and not detected.

Low tissue specificity
Subcellular locationi

Main subcellular location based on data generated in the subcellular section of the Human Protein Atlas.

Localized to the Nuclear bodies In addition localized to the Vesicles
Secretome annotationi

All genes with at least one predicted secreted isoform have been annotated and classified with the aim to determine if the corresponding protein(s) are:

  • secreted into blood
  • locally secreted
  • or actually being attached to membrane or retained in intracellular locations like mitochondria, endoplasmatic reticulum (ER), Golgi apparatus or lysosomes.
Not available
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 2
Cytoband p16.1
Chromosome location (bp) 58159243 - 58241410
Number of transcriptsi

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

33
Ensembl ENSG00000115392 (version 109)
Entrez gene 55120
HGNC HGNC:20748
UniProt Q9NW38
GeneCards FANCL
PROTEIN BROWSERi

The Structure section provides in-house generated structures, predicted using the Alphafold source code, for the majority of the proteins and their related isoforms.

Displaying protein features on the AlphaFold structures

Individual splice variants can be selected in the top part of the Protein Browser (see below) and different transcript-related features such as transmembrane regions, InterPro domains and antigen sequences for antibodies can be displayed in the structure by clicking on the respective features in the Protein Browser.

Clinical and population-based amino acid variants based on data from the Ensembl variation database and AlphaMissense (AM) predictions can be highlighted using the sliders to the right of the structure. These can also be used to colour the entire structure by residue index or make the structure autorotate.The structures are displayed using the NGL Viewer and can also be zoomed-in and rotated manually.

The Protein Browser

The ProteinBrowser displays the antigen location on the target protein(s) and the features of the target protein. Transcript names and schematic transcript structures including exons, introns and UTRs for the different isoforms are shown on top, and can be used to switch between the structures for the different splice variants.

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).

Signal peptides (turquoise) and membrane regions (orange) based on predictions using the majority decision methods MDM and MDSEC are also 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.

«
FANCL-201
FANCL-202
FANCL-203
FANCL-206
FANCL-207
FANCL-208
FANCL-210
FANCL-211
FANCL-213
FANCL-214
FANCL-217
FANCL-220
FANCL-222
FANCL-225
FANCL-243
FANCL-262
FANCL-273
FANCL-277
FANCL-291
FANCL-301
FANCL-303
FANCL-314
FANCL-319
FANCL-327
FANCL-329
FANCL-330
FANCL-335
FANCL-339
FANCL-340
FANCL-343
FANCL-345
FANCL-349
FANCL-352
»

Description:

Color scheme:
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Alphamissense variants:
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Autorotate:
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PROTEIN INFORMATIONi

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

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

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 length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.

Splice variant SwissProt TrEMBL Protein class Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
FANCL-201 Q9NW38
Enzymes
Metabolic proteins
Predicted intracellular proteins
Disease related genes
Potential drug targets
Human disease related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
375 aa
42.9 kDa
No 0
FANCL-202 Q9NW38
Enzymes
Metabolic proteins
Predicted intracellular proteins
Disease related genes
Potential drug targets
Human disease related genes
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
Show all
380 aa
43.4 kDa
No 0
FANCL-203 B5MC31
Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
347 aa
39.8 kDa
No 0
FANCL-206 H7C1M0
Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
390 aa
44.5 kDa
No 0
FANCL-207 C9J512
Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
227 aa
25.7 kDa
No 0
FANCL-208 C9JZA9
Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
316 aa
35.8 kDa
No 0
FANCL-210 A0A087X0C0
Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
142 aa
16.4 kDa
No 0
FANCL-211 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
356 aa
40.6 kDa
No 0
FANCL-213 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
370 aa
42.3 kDa
No 0
FANCL-214 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
156 aa
18.1 kDa
No 0
FANCL-217 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
336 aa
38.5 kDa
No 0
FANCL-220 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
361 aa
41.1 kDa
No 0
FANCL-222 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
164 aa
18.1 kDa
No 0
FANCL-225 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
395 aa
45 kDa
No 0
FANCL-243 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
372 aa
42.5 kDa
No 0
FANCL-262 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
123 aa
14.1 kDa
No 0
FANCL-273 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
146 aa
17.2 kDa
No 0
FANCL-277 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
321 aa
36.3 kDa
No 0
FANCL-291 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
207 aa
23.8 kDa
No 0
FANCL-301 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
228 aa
25.8 kDa
No 0
FANCL-303 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
83 aa
9.6 kDa
No 0
FANCL-314 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
199 aa
22.6 kDa
No 0
FANCL-319 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
307 aa
34.8 kDa
No 0
FANCL-327 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
371 aa
42.2 kDa
No 0
FANCL-329 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
212 aa
24.3 kDa
No 0
FANCL-330 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
218 aa
25.1 kDa
No 0
FANCL-335 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
340 aa
38.9 kDa
No 0
FANCL-339 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
242 aa
27.8 kDa
No 0
FANCL-340 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
223 aa
25.5 kDa
No 0
FANCL-343 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
223 aa
25.2 kDa
No 0
FANCL-345 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
239 aa
27.4 kDa
No 0
FANCL-349 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
352 aa
40.3 kDa
No 0
FANCL-352 Metabolic proteins
Predicted intracellular proteins
Human disease related genes
Protein evidence (Ezkurdia et al 2014)
367 aa
42.1 kDa
No 0
Show allShow less

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