CLMP CXADR like membrane protein

Gene ID: 79827, updated on 18-Sep-2024
Gene type: protein coding
Also known as: ACAM; ASAM; CSBM; CSBS

Summary

This gene encodes a type I transmembrane protein that is localized to junctional complexes between endothelial and epithelial cells and may have a role in cell-cell adhesion. Expression of this gene in white adipose tissue is implicated in adipocyte maturation and development of obesity. This gene is also essential for normal intestinal development and mutations in the gene are associated with congenital short bowel syndrome. [provided by RefSeq, Aug 2015]

Associated conditions

See all available tests in GTR for this gene

Description	Tests
Congenital short bowel syndrome, autosomal recessive MedGen: CN296805OMIM: 615237GeneReviews: Not available	See labs

Genomic context

Location:: 11q24.1

Sequence:: Chromosome: 11; NC_000011.10 (123069872..123195248, complement)

Total number of exons:: 7

Genomic Sequence

Go to nucleotideGraphics FASTA GenBank

Variation

Resource	Links for this gene
ClinVar	Variants reported to ClinVar
dbVar	Studies and variants
SNP	Variation Viewer for CLMP variants
Genome viewer	Explore NCBI-annotated and select non-NCBI annotated genome assemblies

Links

ClinVar
Related medical variations
dbVar
Link from Gene to dbVar
MedGen
Related information in MedGen
OMIM
Link to related OMIM entry
PubMed (OMIM)
Gene links to PubMed derived from omim_pubmed_cited links
RefSeq RNAs
Link to Nucleotide RefSeq RNAs
RefSeqGene
Link to Nucleotide RefSeqGenes
Variation Viewer
Related Variants

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