Gene Gene information from NCBI Gene database.
Entrez ID 57408
Gene name Leucine rich repeat transmembrane protein 1
Gene symbol LRTM1
Synonyms (NCBI Gene)
HT017
Chromosome 3
Chromosome location 3p14.3
miRNA miRNA information provided by mirtarbase database.
12
miRTarBase ID miRNA Experiments Reference
MIRT649154 hsa-miR-642a-3p HITS-CLIP 23824327
MIRT649153 hsa-miR-642b-3p HITS-CLIP 23824327
MIRT649152 hsa-miR-2681-5p HITS-CLIP 23824327
MIRT649154 hsa-miR-642a-3p HITS-CLIP 23824327
MIRT649153 hsa-miR-642b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HBL6
Protein name Leucine-rich repeat and transmembrane domain-containing protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 50 110 Leucine rich repeat Repeat
PF13855 LRR_8 74 134 Leucine rich repeat Repeat
PF13855 LRR_8 98 144 Leucine rich repeat Repeat
PF13855 LRR_8 122 181 Leucine rich repeat Repeat
Sequence
MKGELLLFSSVIVLLQVVCSCPDKCYCQSSTNFVDCSQQGLAEIPSHLPPQTRTLHLQDN
QIHHLPAFAFRSV
PWLMTLNLSNNSLSNLAPGAFHGLQHLQVLNLTQNSLLSLESRLFHS
LPQLRELDLSSNNISHLPTSLGET
WENLTILAVQQNQLQQLDRALLESMPSVRLLLLKDN
L
WKCNCHLLGLKLWLEKFVYKGGLTDGIICESPDTWKGKDLLRIPHELYQPCPLPAPDPV
SSQAQWPGSAHGVVLRPPENHNAGERELLECELKPKPRPANLRHAIATVIITGVVCGIVC
LMMLAAAIYGCTYAAITAQYHGGPLAQTNDPGKVEEKERFDSSPA
Sequence length 345
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOBLASTOMA MULTIFORME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOMA 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
Zimmerman Laband syndrome Zimmerman Laband Syndrome BEFREE 17163523
★☆☆☆☆
Found in Text Mining only