MORN2 (MORN repeat containing 2)

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Gene Gene information from NCBI Gene database.
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Entrez ID 729967
Gene name MORN repeat containing 2
Gene symbol MORN2
Synonyms (NCBI Gene)
BLOCK27MOPT
Chromosome 2
Chromosome location 2p22.1
miRNA miRNA information provided by mirtarbase database.
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miRTarBase ID miRNA Experiments Reference
MIRT048107 hsa-miR-197-3p CLASH 23622248
MIRT1155632 hsa-miR-142-3p CLIP-seq
MIRT1155633 hsa-miR-3124-3p CLIP-seq
MIRT1155634 hsa-miR-3160-5p CLIP-seq
MIRT1155635 hsa-miR-3671 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0001669 Component Acrosomal vesicle IEA
GO:0005515 Function Protein binding IPI 25416956
GO:0005634 Component Nucleus IEA
GO:0007283 Process Spermatogenesis IEA
GO:0030154 Process Cell differentiation IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
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UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q502X0
Protein name MORN repeat-containing protein 2 (MORN motif protein in testis)
Protein function Might have a role in spermatogenesis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02493 MORN 15 → 37 MORN repeat Repeat
PF02493 MORN 38 → 59 MORN repeat Repeat
Sequence 
MNGFGRLEHFSGAVYEGQFKDNMFHGLGTYTFPNGAKYTGNFNENRVEGEGEYTDIQGLE
WSGNFHFTAAPDLKLKLHM
Sequence length 79
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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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
AMYOTROPHIC LATERAL SCLEROSIS — GWAS catalog 19451621
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations

No strongly related genes found yet for MORN2.

No additional diseases found yet through genes similar to MORN2.