CIROZ (ciliated left-right organizer protein containing ZP-N domains)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
148345
Gene name Gene Name - the full gene name approved by the HGNC.
Ciliated left-right organizer protein containing ZP-N domains
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CIROZ
Synonyms (NCBI Gene) Gene synonyms aliases
C1orf127, HTX14
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.22
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(16)
miRTarBase ID miRNA Experiments Reference
MIRT1948905 hsa-miR-1207-3p CLIP-seq
MIRT1948906 hsa-miR-3144-5p CLIP-seq
MIRT1948907 hsa-miR-3180-5p CLIP-seq
MIRT1948908 hsa-miR-3191 CLIP-seq
MIRT1948909 hsa-miR-4652-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(3)
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IDA 39753129
GO:0005576 Component Extracellular region IEA
GO:0061966 Process Establishment of left/right asymmetry IMP 39753129
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
619700 26730 ENSG00000175262
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q8N9H9
Protein name Ciliated left-right organizer ZP-N domains-containing protein (Ciliated left-right organizer protein containing ZP-N domains)
Protein function Plays a role in left-right patterning process.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15094 DUF4556 2 → 198 Family
Sequence 
MKCPMLRSRLGQESVHCGPMFIQVSRPLPLWRDNRQTPWLLSLRGELVASLEDASLMGLY
VDMNATTVTVQSPRQGLLQRWEVSGGQQALPGVSFQPESEVLVHIPKQRLGLVKRGSYIE
ETLSLRFLRVHQSNIFMVTENKDFVVVSIPAAGVLQVQRCQEVGGTPGTQAFYRVDLSLE
FAEMAAPVLWTVESFFQCVGSGTESPASTAALRTTPSPPSPGPETPPAGVPPAASSQVWA
AGPAAQEWLSRDLLHRPSDALAKKGLGPFLQTAKPARRGQTSASILPRVVQAQRGPQPPP
GEAGIPGHPTPPATLPSEPVEGVQASPWRPRPVLPTHPALTLPVSSDASSPSPPAPRPER
PESLLVSGPSVTLTEGLGTVRPEQDPAKSPGSPLLLRGLSSGDVAAPEPIMGEPGQASEE
FQPLARPWRATLAAEELVSHRSPGEPQETCSGTEVERPRQTGPGLPREGARGHMDLSSSE
PSQDIEGPGLSILPARDATFSTPSVRQPDPSAWLSSGPELTGMPRVRLAAPLAVLPMEPL
PPEPVRPAALLTPEASSVGGPDQARYLESAPGWPVGQEEWGVAHTSSPPSTQTLSLWAPT
GVLLPSLVELEYPFQAGRGASLQQELTEPTLALSAESHRPPELQDSVEGLSERPSR
Sequence length 656
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Heterotaxy, Visceral visceral heterotaxy N/A N/A GenCC