IGFL4 (IGF like family member 4)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 444882
Gene name IGF like family member 4
Gene symbol IGFL4
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.32
miRNA miRNA information provided by mirtarbase database.
34
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (34)
miRTarBase ID miRNA Experiments Reference
MIRT1062349 hsa-miR-1275 CLIP-seq
MIRT1062350 hsa-miR-3065-5p CLIP-seq
MIRT1062351 hsa-miR-3664-5p CLIP-seq
MIRT1062352 hsa-miR-4325 CLIP-seq
MIRT1062353 hsa-miR-4525 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (3)
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding IBA
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
610547 32931 ENSG00000204869
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6B9Z1
Protein name Insulin growth factor-like family member 4
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14653 IGFL 26 → 108 Insulin growth factor-like family Family
Tissue specificity TISSUE SPECIFICITY: Detected in the cerebellum. {ECO:0000269|PubMed:16890402}.
Sequence
Sequence length 124
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (1)
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
SCOLIOSIS — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations