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JCAD junctional cadherin 5 associated [ Homo sapiens (human) ]

Gene ID: 57608, updated on 7-Aug-2022

Summary

Official Symbol
JCADprovided by HGNC
Official Full Name
junctional cadherin 5 associatedprovided by HGNC
Primary source
HGNC:HGNC:29283
See related
Ensembl:ENSG00000165757 MIM:614398; AllianceGenome:HGNC:29283
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
KIAA1462
Summary
This gene encodes an endothelial cell-to-cell junction protein. Naturally occurring mutations in this gene are associated with coronary artery disease, late onset alzheimer disease, and emphysema distribution. [provided by RefSeq, Mar 2017]
Expression
Broad expression in fat (RPKM 28.1), lung (RPKM 20.0) and 17 other tissues See more
Orthologs
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Genomic context

See JCAD in Genome Data Viewer
Location:
10p11.23
Exon count:
7
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (30012803..30115494, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (30043840..30146523, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (30301732..30404423, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902403 Neighboring gene uncharacterized LOC107984218 Neighboring gene uncharacterized LOC101929256 Neighboring gene Sharpr-MPRA regulatory region 14462 Neighboring gene uncharacterized LOC105376477 Neighboring gene uncharacterized LOC101929279

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

EBI GWAS Catalog

Description
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.
EBI GWAS Catalog
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.
EBI GWAS Catalog

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

General protein information

Preferred Names
junctional cadherin 5-associated protein
Names
junctional protein associated with coronary artery disease

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_053080.1 RefSeqGene

    Range
    60909..107692
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001350001.2NP_001336930.1  junctional cadherin 5-associated protein isoform 2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) differs in the 5' UTR, contains an alternate exon in the 5' region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (2) has a shorter N-terminus, compared to isoform 1. Both variants 2 and 3 encode the same isoform (2).
    Source sequence(s)
    AL158036
    Conserved Domains (1) summary
    pfam15351
    Location:11210
    JCAD; Junctional protein associated with coronary artery disease
  2. NM_001350021.2NP_001336950.1  junctional cadherin 5-associated protein isoform 2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) differs in the 5' UTR, contains an alternate exon in the 5' region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (2) has a shorter N-terminus, compared to isoform 1. Both variants 2 and 3 encode the same isoform (2).
    Source sequence(s)
    AL158036, AL360172, BX648192
    Conserved Domains (1) summary
    pfam15351
    Location:11210
    JCAD; Junctional protein associated with coronary artery disease
  3. NM_001350022.2NP_001336951.1  junctional cadherin 5-associated protein isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) differs in the 5' UTR compared to variant 1. Both variants 1 and 4 encode the same isoform (1).
    Source sequence(s)
    AL158036, AL360172
    Consensus CDS
    CCDS41500.1
    UniProtKB/Swiss-Prot
    Q9BYJ2
    Conserved Domains (1) summary
    pfam15351
    Location:11348
    JCAD; Junctional protein associated with coronary artery disease
  4. NM_020848.4NP_065899.1  junctional cadherin 5-associated protein isoform 1

    See identical proteins and their annotated locations for NP_065899.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes the longer isoform (1).
    Source sequence(s)
    AL158036, CB988996
    Consensus CDS
    CCDS41500.1
    UniProtKB/Swiss-Prot
    Q9BYJ2, Q9P266
    Related
    ENSP00000364526.1, ENST00000375377.2
    Conserved Domains (1) summary
    pfam15351
    Location:11348
    JCAD; Junctional protein associated with coronary artery disease

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    30012803..30115494 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    30043840..30146523 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)