C2orf72 (chromosome 2 open reading frame 72)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Protein Associated diseases
Entrez ID 257407
Gene name Chromosome 2 open reading frame 72
Gene symbol C2orf72
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2q37.1
miRNA miRNA information provided by mirtarbase database.
657
Gene miRNA Other IDs Protein Associated diseases
Show/Hide all (657)
miRTarBase ID miRNA Experiments Reference
MIRT045871 hsa-miR-128-3p CLASH 23622248
MIRT613266 hsa-miR-8485 HITS-CLIP 19536157
MIRT613265 hsa-miR-329-3p HITS-CLIP 19536157
MIRT613264 hsa-miR-362-3p HITS-CLIP 19536157
MIRT613263 hsa-miR-574-3p HITS-CLIP 19536157
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A6NCS6
Protein name Uncharacterized protein C2orf72
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15443 DUF4630 139 → 293 Domain of unknown function (DUF4630) Family
Sequence 
MERELEALAARLARPAEPPFQALVEAAGGRGQVLLVGELWEREQSRALLRDFARAVFPPE
PGAAKPGGAAAEGAGPGAARGAQRAARAAGAAGAAAAAARAIRSPLVFVLCRASSLAARE
PRRRLREMLRDVRGRRRAGAALVGVLVAEAGPEDAVAPGLRLLEALLRAVFGRQAGGPVQ
AAAYCPGLPASCLAVQAAACRALQAAGAGQPVEGAWERPGLPGLLACFSWGPWSRRKNQD
VAACRSSAQEDFQEPEEELPLTAIFPNGDCDDLGRGSKACDGVVHTPAEPTGDSR
Sequence length 295
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Gene miRNA Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (2)
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
COLORECTAL CANCER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLORECTAL CARCINOMA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations