Gene Gene information from NCBI Gene database.
Entrez ID 340745
Gene name Leucine rich repeat, Ig-like and transmembrane domains 2
Gene symbol LRIT2
Synonyms (NCBI Gene)
LRRC22
Chromosome 10
Chromosome location 10q23.1
miRNA miRNA information provided by mirtarbase database.
33
miRTarBase ID miRNA Experiments Reference
MIRT1117745 hsa-miR-1236 CLIP-seq
MIRT1117746 hsa-miR-1237 CLIP-seq
MIRT1117747 hsa-miR-1248 CLIP-seq
MIRT1117748 hsa-miR-1291 CLIP-seq
MIRT1117749 hsa-miR-3125 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
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.
A6NDA9
Protein name Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 (Leucine-rich repeat-containing protein 22)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 56 115 Leucine rich repeat Repeat
PF13855 LRR_8 113 163 Leucine rich repeat Repeat
PF13927 Ig_3 252 331 Domain
Sequence
MASVFHYFLLVLVFLDTHAAQPFCLPGCTCSEESFGRTLQCTSVSLGKIPGNLSEEFKQV
RIENSPLFEMPQGSFINMSTLEYLWLNFNNISVIHLGALEHLPELRELRLEG
NKLCSVPW
TAFRATPLLRVLDLKRNKIDALPELALQFLVSLTYLDLSSNRL
TVVSKSVFLNWPAYQKC
RQPDCGAEILSSLVVALHDNPWVCDCRLRGLVQFVKSITLPVILVNSYLICQGPLSKAGQ
LFHETELSACMKPQISTPSANITIRAGQNVTLRCLAQASPSPSIAWTYPLSMWREFDVLT
SSTGEDTALSELAIPAAHLVDSGNYTCMASN
SIGKSNLVISLHVQPAQALHAPDSLSIPS
EGNAYIDLRVVKQTVHGILLEWLAVADTSKEEWFTLYIASDEAFRKEVVHIGPGINTYAV
DDLLPGTKYEACLSLEGQPPHQGQCVAFVTGRDAGGLEAREHLLHVTVVLCVVLLAVPVG
AYAWAAQGPCSCSKWVLRGCLHRRKAPSCTPAAPQSKDGSFREHPAVCDDGEGHIDTEGD
KEKGGTEDNS
Sequence length 550
Interactions View interactions
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
SYSTEMIC LUPUS ERYTHEMATOSUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations