Log in to bookmark this gene

Bookmark This Gene

Gene Gene information from NCBI Gene database.
Entrez ID 155038
Gene name GTPase, IMAP family member 8
Gene symbol GIMAP8
Synonyms (NCBI Gene)
IAN-9IAN6IAN9IANT
Chromosome 7
Chromosome location 7q36.1
Summary This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 20
miRNA miRNA information provided by mirtarbase database.
28 Show/Hide all (28)
miRTarBase ID miRNA Experiments Reference
MIRT036429 hsa-miR-1226-3p CLASH 23622248
MIRT1019017 hsa-miR-1302 CLIP-seq
MIRT1019018 hsa-miR-148a CLIP-seq
MIRT1019019 hsa-miR-148b CLIP-seq
MIRT1019020 hsa-miR-152 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10 Show/Hide all (10)
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003924 Function GTPase activity IBA
GO:0005525 Function GTP binding IEA
GO:0005737 Component Cytoplasm IEA
GO:0005739 Component Mitochondrion IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616962 21792 ENSG00000171115
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8ND71
Protein name GTPase IMAP family member 8 (Immune-associated nucleotide-binding protein 9) (IAN-9) (Protein IanT)
Protein function Exerts an anti-apoptotic effect in the immune system and is involved in responses to infections.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04548 AIG1 439 → 655 AIG1 family Domain
PF04548 AIG1 11 → 220 AIG1 family Domain
PF04548 AIG1 248 → 437 AIG1 family Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the spleen, intestine, liver, and colon, as well as in lung, placenta, kidney, muscle, and heart. Extremely low expression, if any, in brain, in thymus, bone marrow, and blood leukocytes (PubMed:15474311). Detected in T-ce
Sequence
Sequence length 665
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
Thyroid cancer, nonmedullary, 1 Uncertain significance ClinVar —
★★★★★
★★☆☆☆
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 Neoplasms Breast neoplasm Pubtator 32523132 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Down Syndrome Down syndrome Pubtator 32523132 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only
Hypertension Hypertension Pubtator 32410228 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 18462827
★★★★★
★☆☆☆☆
Found in Text Mining only