Gene Gene information from NCBI Gene database.
Entrez ID 23080
Gene name AVL9 cell migration associated
Gene symbol AVL9
Synonyms (NCBI Gene)
KIAA0241
Chromosome 7
Chromosome location 7p14.3
miRNA miRNA information provided by mirtarbase database.
529
miRTarBase ID miRNA Experiments Reference
MIRT027030 hsa-miR-103a-3p Sequencing 20371350
MIRT031518 hsa-miR-16-5p Sequencing 20371350
MIRT036418 hsa-miR-1226-3p CLASH 23622248
MIRT723583 hsa-miR-3613-3p HITS-CLIP 19536157
MIRT723582 hsa-miR-4668-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IBA
GO:0005768 Component Endosome IEA
GO:0016020 Component Membrane IEA
GO:0016477 Process Cell migration IDA 22595670
GO:0055037 Component Recycling endosome IDA 22595670
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612927 28994 ENSG00000105778
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NBF6
Protein name Late secretory pathway protein AVL9 homolog
Protein function Functions in cell migration.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09794 Avl9 16 520 Transport protein Avl9 Family
Sequence
Sequence length 648
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ARTHRITIS, JUVENILE CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
JUVENILE CHRONIC POLYARTHRITIS Disgenet
★★☆☆☆
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
Conventional (Clear Cell) Renal Cell Carcinoma Renal Carcinoma BEFREE 30122945
★☆☆☆☆
Found in Text Mining only
Degenerative polyarthritis Arthritis GWASDB_DG 22763110
★☆☆☆☆
Found in Text Mining only
Juvenile arthritis Arthritis CTD_human_DG 19565504
★☆☆☆☆
Found in Text Mining only
Juvenile psoriatic arthritis Juvenile arthritis CTD_human_DG 19565504
★☆☆☆☆
Found in Text Mining only
Juvenile-Onset Still Disease Still Disease CTD_human_DG 19565504
★☆☆☆☆
Found in Text Mining only
Myopia Myopia Pubtator 34241624 Associate
★☆☆☆☆
Found in Text Mining only
Polyarthritis, Juvenile, Rheumatoid Factor Negative Seronegative polyarthritis CTD_human_DG 19565504
★☆☆☆☆
Found in Text Mining only
Polyarthritis, Juvenile, Rheumatoid Factor Positive Polyarthritis, Rheumatoid Factor Positive CTD_human_DG 19565504
★☆☆☆☆
Found in Text Mining only
Renal Cell Carcinoma Renal Carcinoma BEFREE 30122945
★☆☆☆☆
Found in Text Mining only