CCIN
calicin | BTBD20, KBTBD14

The protein encoded by this gene is a basic protein of the sperm head cytoskeleton. This protein contains kelch repeats and a BTB/POZ domain and is necessary for normal morphology during sperm differentiation. This gene is intronless. [provided by RefSeq, Jul 2008]

Biological processes 12 terms
Expression (TPM)
CCIN — as a Regulated Gene

TFs regulating CCIN 0 TFs

Transcription factors with Perturb-seq knockdown data for CCIN. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = CCIN upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to CCIN

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of CCIN, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chr9:36,163,065–36,163,901 5.5 kb Proximal (<10kb) 343
chr9:36,166,123–36,166,839 2.5 kb Proximal (<10kb) 515

Genome Browser

Genomic view of the CCIN locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chr9:36,153,065 – 36,176,839
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq