Gene Gene information from NCBI Gene database.
Entrez ID 83607
Gene name AMMECR1 like
Gene symbol AMMECR1L
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2q14.3
miRNA miRNA information provided by mirtarbase database.
757
miRTarBase ID miRNA Experiments Reference
MIRT027316 hsa-miR-101-3p Sequencing 20371350
MIRT047569 hsa-miR-10a-5p CLASH 23622248
MIRT046855 hsa-miR-221-3p CLASH 23622248
MIRT046528 hsa-miR-15b-5p CLASH 23622248
MIRT042613 hsa-miR-423-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IBA
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.
Q6DCA0
Protein name AMMECR1-like protein
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01871 AMMECR1 109 280 AMMECR1 Family
Sequence
MGKRRCVPPLEPKLAAGCCGVKKPKLSGSGTHSHGNQSTTVPGSSSGPLQNHQHVDSSSG
RENVSDLTLGPGNSPITRMNPASGALSPLPRPNGTANTTKNLVVTAEMCCYCFDVLYCHL
YGFPQPRLPRFTNDPYPLFVTWKTGRDKRLRGCIGTFSAMNLHSGLREYTLTSALKDSRF
PPLTREELPKLFCSVSLLTNFEDASDYLDWEVGVHGIRIEFINEKGVKRTATYLPEVAKE
QDWDQIQTIDSLLRKGGFKAPITSEFRKTIKLTRYRSEKV
TISYAEYIASRQHCFQNGTL
HAPPLYNHYS
Sequence length 310
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations