DYRK1A

GENERAL INFORMATION

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Gene name

DYRK1A

Gene description

Dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A

Protein class

Disease related genes
Enzymes
Potential drug targets
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

Cytoplasmic expression in essentially all cells types.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA015323 , HPA015810
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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

DYRK1A (HGNC Symbol)

Synonyms

DYRK, DYRK1, MNBH

Description

Dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome. Alternative splicing of this gene generates several transcript variants differing from each other either in the 5' UTR or in the 3' coding region. These variants encode at least five different isoforms. [provided by RefSeq, Jul 2008]

Chromosome

21

Cytoband

q22.13

Chromosome location (bp)

37365790 - 37517450

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000157540 (version 78.38)

Entrez gene

1859

UniProt

Q13627 (UniProt - Evidence at protein level)

neXtProt

NX_Q13627

Antibodypedia

DYRK1A antibodies


PROTEIN BROWSER

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ENST00000338785
 
ENST00000339659
 
ENST00000398956
 
ENST00000398960
 
ENST00000426672
 
ENST00000455097
 
 
 
 


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)

DYRK1A-001 ENSP00000342690
ENST00000338785
Q13627
Show all »
Show » Show » 584 66.1 No 0
DYRK1A-003 ENSP00000340373
ENST00000339659
Q13627
Show all »
Show » Show » 754 84.6 No 0
DYRK1A-004 ENSP00000398483
ENST00000455097
Q76N25
Show all »
Show » Show » 46 5 No 0
DYRK1A-005 ENSP00000412269
ENST00000426672
E7EMI5
Show all »
Show » Show » 131 14.9 No 0
DYRK1A-006 ENSP00000381932
ENST00000398960
Q13627
Show all »
Show » Show » 763 85.6 No 0
DYRK1A-008 ENSP00000381929
ENST00000398956
Q13627
Show all »
Show » Show » 529 60.3 No 0