Gene Gene information from NCBI Gene database.
Entrez ID 91368
Gene name CDKN2A interacting protein N-terminal like
Gene symbol CDKN2AIPNL
Synonyms (NCBI Gene)
C2AIL
Chromosome 5
Chromosome location 5q31.1
miRNA miRNA information provided by mirtarbase database.
319
miRTarBase ID miRNA Experiments Reference
MIRT049773 hsa-miR-92a-3p CLASH 23622248
MIRT704786 hsa-miR-106a-5p HITS-CLIP 23313552
MIRT704785 hsa-miR-106b-5p HITS-CLIP 23313552
MIRT704784 hsa-miR-17-5p HITS-CLIP 23313552
MIRT704783 hsa-miR-20a-5p HITS-CLIP 23313552
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:0005515 Function Protein binding IPI 26496610, 26779609, 32296183, 33961781, 34591612
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.
Q96HQ2
Protein name CDKN2AIP N-terminal-like protein (CDKN2A-interacting protein N-terminal-like protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11952 XTBD 24 113 XRN-Two Binding Domain, XTBD Family
Sequence
Sequence length 116
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
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations