Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
137994
Gene name Gene Name - the full gene name approved by the HGNC.
Leucine zipper and EF-hand containing transmembrane protein 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
LETM2
Synonyms (NCBI Gene) Gene synonyms aliases
SLC55A2
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p11.23
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT716072 hsa-miR-4438 HITS-CLIP 19536157
MIRT716071 hsa-miR-455-5p HITS-CLIP 19536157
MIRT716070 hsa-miR-6504-3p HITS-CLIP 19536157
MIRT716069 hsa-miR-619-5p HITS-CLIP 19536157
MIRT716068 hsa-miR-6506-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005743 Component Mitochondrial inner membrane IEA
GO:0006875 Process Cellular metal ion homeostasis IBA 21873635
GO:0016021 Component Integral component of membrane IEA
GO:0043022 Function Ribosome binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620380 14648 ENSG00000165046
Protein
UniProt ID Q2VYF4
Protein name LETM1 domain-containing protein LETM2, mitochondrial (LETM1 and EF-hand domain-containing protein 2) (Leucine zipper-EF-hand-containing transmembrane protein 1-like)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07766 LETM1 122 386 LETM1-like protein Family
Sequence
MAFYSYNSVLAIARTRFPSHFVHPTCSSYSPSCAFLHLPDSHLNKTCMKNYESKKYSDPS
QPGNTVLHPGTRLIQKLHTSTCWLQEVPGKPQLEQATKHPQVTSPQATKETGMEIKEGKQ
SYRQKIMDELKYYYNGFYLLWIDAKVAARMVWRLLHGQVLTRRERRRLLRTCVDFFRLVP
FMVFLIVPFMEFLLPVFLKLFPEMLPSTFESESKKEEKQKKKMAVKLELAKFLQETMTEM
ARRNRAKMGDASTQLSSYVKQVQTGHKPSTKEIVRFSKLFEDQLALEHLDRPQLVALCKL
LELQTFGTNNLLRFQLLMKLKSIKADDEIIAKEGVTALSVSELQAACRARGMRSLGLTEE
QLRQQLTEWQDLHLKENVPPSLLLLS
RTFYLIDVKPKPIEIPLSGEAPKTDILVELPTFT
ESKENMVDLAPQLKGTKDEDFIQPPPVTSSPITPSTPISLPKGPITSSEEPTLQAKSQMT
AQNSKASSKGA
Sequence length 491
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
30285260, 28991256, 26198764
Unknown
Disease term Disease name Evidence References Source
Bipolar Disorder Bipolar Disorder GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 21666749
Carcinoma Squamous Cell Associate 21666749
Tuberculosis Associate 36476775