Gene Gene information from NCBI Gene database.
Entrez ID 646457
Gene name Chromosome 19 open reading frame 67
Gene symbol C19orf67
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19p13.12
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.
A6NJJ6
Protein name UPF0575 protein C19orf67
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11771 DUF3314 179 335 Protein of unknown function (DUF3314) Family
Sequence
MATEQWFEGSLPLDPGETPPPDALEPGTPPCGDPSRSTPPGRPGNPSEPDPEDAEGRLAE
ARASTSSPKPLVPRPGPAPPRLSLDTLFSPITQQLRYLLKKADDFQSYLLYSRDQVQKEQ
LAKAMPTFLQMCEPYFLYLEAAARSIPPIYGPLQELVRKGLLEISQQLTLRLEQLVLMYA
SFGFVDLEEMNPLSISCFFCGRFSISLSHEVSIFRYCAPTAYTASRFPRYLYKKMRWHLE
ATPEAPGRGQDSLVDYYFLCYRDTWEDTGQSPANSCPQIQKLWSIGRWVPLGPAEDDLYS
WILCPQPLGDYQQLLTIGFEEPTPTLATDLLVQIL
TGQAGQARPPSAAGPAGWAAQGS
Sequence length 358
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
BRONCHIOLITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BRONCHITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations