Gene Gene information from NCBI Gene database.
Entrez ID 2862
Gene name Motilin receptor
Gene symbol MLNR
Synonyms (NCBI Gene)
GPR38MTLR1
Chromosome 13
Chromosome location 13q14.2
Summary Motilin is a 22 amino acid peptide hormone expressed throughout the gastrointestinal (GI) tract. The protein encoded by this gene is a motilin receptor which is a member of the G-protein coupled receptor 1 family. This member is a multi-pass transmembrane
miRNA miRNA information provided by mirtarbase database.
2
miRTarBase ID miRNA Experiments Reference
MIRT029591 hsa-miR-26b-5p Microarray 19088304
MIRT047537 hsa-miR-10a-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005829 Component Cytosol IDA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602885 4495 ENSG00000102539
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O43193
Protein name Motilin receptor (G-protein coupled receptor 38)
Protein function Receptor for motilin.
PDB 8IBU , 8IBV
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 55 187 7 transmembrane receptor (rhodopsin family) Family
PF00001 7tm_1 219 355 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed only in thyroid, stomach, and bone marrow.
Sequence
Sequence length 412
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Neuroactive ligand-receptor interaction
Hormone signaling
  Peptide ligand-binding receptors
G alpha (q) signalling events
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Deafness Deafness Pubtator 21505449 Associate
★☆☆☆☆
Found in Text Mining only
Gastroparesis Gastroparesis Pubtator 35297797 Associate
★☆☆☆☆
Found in Text Mining only
Microcephaly Microcephaly BEFREE 21505449
★☆☆☆☆
Found in Text Mining only
Microcephaly Microcephaly Pubtator 21505449 Associate
★☆☆☆☆
Found in Text Mining only
Polycystic Ovary Syndrome Polycystic ovary syndrome Pubtator 31278444 Associate
★☆☆☆☆
Found in Text Mining only