FIP1L1

GENERAL INFORMATION

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Gene name

FIP1L1

Gene description

Factor interacting with PAPOLA and CPSF1

Protein class

Cancer-related genes
Disease related genes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous nuclear expression.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Supportive based on 1 antibody.
HPA037475
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

FIP1L1 (HGNC Symbol)

Synonyms

DKFZp586K0717, FIP1

Description

Factor interacting with PAPOLA and CPSF1 (HGNC Symbol)

Entrez gene summary

This gene encodes a subunit of the CPSF (cleavage and polyadenylation specificity factor) complex that polyadenylates the 3' end of mRNA precursors. This gene, the homolog of yeast Fip1 (factor interacting with PAP), binds to U-rich sequences of pre-mRNA and stimulates poly(A) polymerase activity. Its N-terminus contains a PAP-binding site and its C-terminus an RNA-binding domain. An interstitial chromosomal deletion on 4q12 creates an in-frame fusion of human genes FIP1L1 and PDGFRA (platelet-derived growth factor receptor, alpha). The FIP1L1-PDGFRA fusion gene encodes a constitutively activated tyrosine kinase that joins the first 233 amino acids of FIP1L1 to the last 523 amino acids of PDGFRA. This gene fusion and chromosomal deletion is the cause of some forms of idiopathic hypereosinophilic syndrome (HES). This syndrome, recently reclassified as chronic eosinophilic leukemia (CEL), is responsive to treatment with tyrosine kinase inhibitors. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

Chromosome

4

Cytoband

q12

Chromosome location (bp)

53377643 - 54295272

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000145216 (version 78.38)

Entrez gene

81608

UniProt

Q6UN15 (UniProt - Evidence at protein level)

neXtProt

NX_Q6UN15

Antibodypedia

FIP1L1 antibodies


PROTEIN BROWSER

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ENST00000306932
 
ENST00000337488
 
ENST00000358575
 
ENST00000504094
 
ENST00000507166
 
ENST00000507922
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

FIP1L1-001 ENSP00000336752
ENST00000337488
Q6UN15
Show all »
Show » Show » 594 66.5 No 0
FIP1L1-002 ENSP00000351383
ENST00000358575
Q6UN15
Show all »
Show » Show » 588 65.7 No 0
FIP1L1-003 ENSP00000302993
ENST00000306932
Q6UN15
Show all »
Show » Show » 520 58.4 No 0
FIP1L1-005 ENSP00000423325
ENST00000507166
Q6UN15
Show all »
Show » Show » 849 94.7 No 0
FIP1L1-009 ENSP00000425456
ENST00000507922
Q6UN15
Show all »
Show » Show » 378 40.8 No 0
FIP1L1-010 ENSP00000421691
ENST00000504094
H0Y8P7
Show all »
Show » 254 29.5 No 0