Log in to bookmark this gene

Bookmark This Gene

Gene Gene information from NCBI Gene database.
Entrez ID 145407
Gene name Armadillo like helical domain containing 4
Gene symbol ARMH4
Synonyms (NCBI Gene)
C14orf37UT2c14_5376
Chromosome 14
Chromosome location 14q23.1
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8 Show/Hide all (8)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 33961781
GO:0016020 Component Membrane IDA 36649229
GO:0016020 Component Membrane IEA
GO:0050727 Process Regulation of inflammatory response IDA 36649229
GO:1903939 Process Regulation of TORC2 signaling IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86TY3
Protein name Armadillo-like helical domain-containing protein 4 (Upstream of mTORC2 protein)
Protein function May modulate immune response and may play a role in inflammation (PubMed:36649229). Down-modulates STAT3 signaling throught direct interaction with IL6ST, resulting in the inhibition of phosphorylation of STAT3 at 'Tyr-705' (PubMed:26927669). Ma
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15767 DUF4696 28 → 610 Domain of unknown function (DUF4696) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in podocytes. {ECO:0000269|PubMed:36649229}.
Sequence
Sequence length 774
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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.
Show/Hide Unknown Diseases (9)
Phenotype Name Clinical Significance Source Reference Evidence Score
ALZHEIMER'S DISEASE NEUROPATHOLOGIC CHANGE — GWAS catalog 25188341
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA — GWAS catalog 25188341
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LUPUS NEPHRITIS — GWAS catalog 24925725
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MIGRAINE DISORDER — GWAS catalog 34294844, 35115687
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MYOCARDIAL INFARCTION — GWAS catalog 33532862, 38072966
★★★★★
★★☆☆☆
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
Multiple Myeloma Multiple myeloma BEFREE 26927669
★★★★★
★☆☆☆☆
Found in Text Mining only
PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1, DIGENIC Proteasome-associated autoinflammatory syndrome, digenic CLINVAR_DG
★★★★★
★☆☆☆☆
Found in Text Mining only