Gene Gene information from NCBI Gene database.
Entrez ID 118812
Gene name MORN repeat containing 4
Gene symbol MORN4
Synonyms (NCBI Gene)
C10orf83UTAbA548K23.4rtp
Chromosome 10
Chromosome location 10q24.2
miRNA miRNA information provided by mirtarbase database.
455
miRTarBase ID miRNA Experiments Reference
MIRT635004 hsa-miR-383-3p HITS-CLIP 23824327
MIRT635003 hsa-miR-4786-5p HITS-CLIP 23824327
MIRT635002 hsa-miR-6878-5p HITS-CLIP 23824327
MIRT635001 hsa-miR-6731-5p HITS-CLIP 23824327
MIRT635000 hsa-miR-8085 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 25822849, 31515488, 32296183, 32814053, 33961781
GO:0005737 Component Cytoplasm IDA 25822849
GO:0005737 Component Cytoplasm IEA
GO:0032420 Component Stereocilium IEA
GO:0032426 Component Stereocilium tip IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617736 24001 ENSG00000171160
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NDC4
Protein name MORN repeat-containing protein 4 (Protein 44050) (Retinophilin)
Protein function Plays a role in promoting axonal degeneration following neuronal injury by toxic insult or trauma.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02493 MORN 16 38 MORN repeat Repeat
PF02493 MORN 39 61 MORN repeat Repeat
PF02493 MORN 62 84 MORN repeat Repeat
PF02493 MORN 85 107 MORN repeat Repeat
Sequence
Sequence length 146
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 Evidence Score
BELL'S PALSY GWAS catalog
★★☆☆☆
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
Prostatic Neoplasms Prostatic Neoplasms BEFREE 10428464
★☆☆☆☆
Found in Text Mining only