Log in to bookmark this gene

Bookmark This Gene

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 Show/Hide all (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 Reference Evidence Score
SYSTEMIC LUPUS ERYTHEMATOSUS — GWAS catalog 36750564
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations