CCDC177

Gene

coiled-coil domain containing 177

Gene summary

No gene description available in the current model. Review primary literature for detailed gene function and characteristics.

Previous symbols:
  • C14orf162

MANE transcript

NM_001271507.2

Inheritance

—

ClinVar variants

U:1

Top phenotype

—

Max pathogenic AF

—

Genomic locus

chr14:69,569,799-69,574,871

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~5.1 kb
Loading mutation effect viewer...

GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to CCDC177 variants in ClinVar

1 Conditions Cataloged
not providedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001271507.2. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
1
clinvar
1
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total001001
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 3 of 3 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001271507.2RefSeqNP_001258436.11MANE Select
ENST00000599174.3EnsemblENSP00000469474.11MANE Select
ENST00001136424.1EnsemblENSP00000814424.11Standard

dbNSFP Gene Annotations

Source: dbNSFP

Essentials

Essential (CRISPR)
N
Essential (CRISPR2)
N

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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