AK1

GENERAL INFORMATION

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Gene name

AK1

Gene description

Adenylate kinase 1

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (fallopian tube, heart muscle, lung, skeletal muscle)
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression at variable levels in several different cell types, most abundant in fallopian tube, Leydig cells and skeletal muscle.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA006456 , CAB009893
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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

Thyroid gland

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:  Group enriched (fallopian tube, heart muscle, lung, skeletal muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

AK1

Synonyms

Description

Adenylate kinase 1 (HGNC Symbol)

Entrez gene summary

Adenylate kinase is an enzyme involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate group among adinine nucleotides. Three isozymes of adenylate kinase have been identified in vertebrates, adenylate isozyme 1 (AK1), 2 (AK2) and 3 (AK3). AK1 is found in the cytosol of skeletal muscle, brain and erythrocytes, whereas AK2 and AK3 are found in the mitochondria of other tissues including liver and heart. AK1 was identified because of its association with a rare genetic disorder causing nonspherocytic hemolytic anemia where a mutation in the AK1 gene was found to reduce the catalytic activity of the enzyme. [provided by RefSeq, Jul 2008]

Chromosome

9

Cytoband

q34.11

Chromosome location (bp)

127866480 - 127877743

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000106992 (version 78.38)

Entrez gene

203

UniProt

P00568 (UniProt - Evidence at protein level)

neXtProt

NX_P00568

Antibodypedia

AK1 antibodies


PROTEIN BROWSER

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ENST00000223836
 
ENST00000373156
 
ENST00000373176
 
ENST00000413016
 
 
 
 


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)

AK1-008 ENSP00000362271
ENST00000373176
P00568
Show all »
Show » Show » 194 21.6 No 0
AK1-009 ENSP00000223836
ENST00000223836
Q5T9B7
Show all »
Show » Show » 210 23.4 No 0
AK1-010 ENSP00000362249
ENST00000373156
P00568
Show all »
Show » Show » 194 21.6 No 0
AK1-011 ENSP00000392314
ENST00000413016
Show » 135 15.4 No 0