Gene Gene information from NCBI Gene database.
Entrez ID 157638
Gene name LRAT domain containing 2
Gene symbol LRATD2
Synonyms (NCBI Gene)
BCMP101FAM84BNSE2
Chromosome 8
Chromosome location 8q24.21
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 12477722, 25416956, 25640309, 28514442, 31515488, 32296183, 33961781
GO:0005737 Component Cytoplasm IDA 12477722, 25468996
GO:0005886 Component Plasma membrane IDA 12477722
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609483 24166 ENSG00000168672
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96KN1
Protein name Protein LRATD2 (Breast cancer membrane protein 101) (LRAT domain-containing 2) (Protein FAM84B) (Protein NSE2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04970 LRAT 114 160 Lecithin retinol acyltransferase Domain
PF04970 LRAT 146 214 Lecithin retinol acyltransferase Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in esophageal squamous cell carcinomas. {ECO:0000269|PubMed:16490593}.
Sequence
MGNQVEKLTHLSYKEVPTADPTGVDRDDGPRIGVSYIFSNDDEDVEPQPPPQGPDGGGLP
DGGDGPPPPQPQPYDPRLHEVECSVFYRDECIYQKSFAPGSAALSTYTPENLLNKCKPGD
LVEFVSQAQYPHWAVYVGNFQVVHL
HRLEVINSFLTDASQGRRGRVVNDLYRYKPLSSSA
VVRNALAHVGAKERELSWRNSESFAAWCRYGKRE
FKIGGELRIGKQPYRLQIQLSAQRSH
TLEFQSLEDLIMEKRRNDQIGRAAVLQELATHLHPAEPEEGDSNVARTTPPPGRPPAPSS
EEEDGEAVAH
Sequence length 310
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA 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
Breast Carcinoma Breast Carcinoma BEFREE 30526553
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 37651838 Associate
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Carcinogenesis Pubtator 37651838 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Carcinoma BEFREE 16490593, 28186973
★☆☆☆☆
Found in Text Mining only
Esophageal carcinoma Esophageal Carcinoma BEFREE 16490593
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Esophagus Neoplasm BEFREE 16490593
★☆☆☆☆
Found in Text Mining only
Esophageal Squamous Cell Carcinoma Esophageal squamous cell carcinoma Pubtator 26759717 Associate
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 36419094 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer BEFREE 30526553
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of esophagus Esophagus Neoplasm BEFREE 16490593
★☆☆☆☆
Found in Text Mining only