SFTA2 (surfactant associated 2)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
389376
Gene name Gene Name - the full gene name approved by the HGNC.
Surfactant associated 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SFTA2
Synonyms (NCBI Gene) Gene synonyms aliases
GSGL541, SFTPG, SP-G, UNQ541
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.33
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(5)
miRTarBase ID miRNA Experiments Reference
MIRT1342109 hsa-miR-1976 CLIP-seq
MIRT1342110 hsa-miR-2861 CLIP-seq
MIRT1342111 hsa-miR-324-5p CLIP-seq
MIRT1342112 hsa-miR-4707-5p CLIP-seq
MIRT1342113 hsa-miR-4763-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(4)
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005794 Component Golgi apparatus IEA
GO:0030133 Component Transport vesicle IEA
GO:0031410 Component Cytoplasmic vesicle IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q6UW10
Protein name Surfactant-associated protein 2 (Surfactant-associated protein G) (SP-G)
Protein function Putative surfactant protein.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15210 SFTA2 20 → 78 Surfactant-associated protein 2 Family
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in lung, where it is detected in type II pneumocytes in the alveolus, and in nonciliated epithelium in bronchioli (at protein level). Also detected at lower levels in cervix, esophagus, stomach, testis and kidne
Sequence
Sequence length 78
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (6)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Asthma Asthma (time to event) N/A N/A GWAS
Mental Depression Major depressive disorder N/A N/A GWAS
Psoriasis Psoriasis N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Show/Hide Text Mining Associations (8)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 30914778
Cerebral Palsy Associate 38163449
Colorectal Neoplasms Associate 32351322, 35587572
Dry Eye Syndromes Stimulate 35628592
Fatigue Syndrome Chronic Associate 34403736
Lung Neoplasms Associate 37471639
Pancreatic Neoplasms Associate 36817451
Pneumonia Associate 31487037