CCNYL1B

gene
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Summary

CCNYL1B (cyclin Y like 1B, HGNC:56313) is a protein-coding gene on chromosome 16p11.2, encoding Cyclin-Y-like protein 1B (A0A8V8TMC4).

Predicted to be involved in regulation of canonical Wnt signaling pathway. Predicted to be active in plasma membrane.

Source: NCBI Gene 102724485 — RefSeq curated summary.

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:56313
Approved symbolCCNYL1B
Namecyclin Y like 1B
Location16p11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000284209
Ensembl biotypeprotein_coding
Entrez102724485

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 2 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000638228, ENST00000850918, ENST00000850919

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000638228 — 10 exons

ExonStartEnd
ENSE000038025313435556734355729
ENSE000038032743437156434371664
ENSE000038068403436855134368586
ENSE000038074633436043334360599
ENSE000038091433435149934353684
ENSE000038093673436536534365416
ENSE000038101433436465934364778
ENSE000038949603438078434381110
ENSE000039704393437701534377049
ENSE000039704403437939934379458

Expression profiles

Bgee: expression breadth broad, 18 present calls, max score 79.84.

Top tissues by expression

94 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047379.84gold quality
left testisUBERON:000453369.53gold quality
testisUBERON:000047369.41gold quality
right testisUBERON:000453469.20gold quality
bone marrowUBERON:000237147.64gold quality
colonic epitheliumUBERON:000039742.24gold quality
adrenal tissueUBERON:001830341.78silver quality
hindlimb stylopod muscleUBERON:000425240.14silver quality
calcaneal tendonUBERON:000370139.77gold quality
bone marrow cellCL:000209239.13gold quality
ventricular zoneUBERON:000305336.48gold quality
body of pancreasUBERON:000115036.35silver quality
ganglionic eminenceUBERON:000402335.49gold quality
sural nerveUBERON:001548835.48gold quality
monocyteCL:000057635.38gold quality
muscle of legUBERON:000138335.32silver quality
pancreasUBERON:000126434.73silver quality
leukocyteCL:000073834.68gold quality
gastrocnemiusUBERON:000138834.19silver quality
bloodUBERON:000017832.27gold quality
islet of LangerhansUBERON:000000631.37silver quality
corpus callosumUBERON:000233631.19gold quality
olfactory segment of nasal mucosaUBERON:000538631.08silver quality
right uterine tubeUBERON:000130230.67gold quality
lymph nodeUBERON:000002930.40silver quality
cerebellumUBERON:000203730.23gold quality
prefrontal cortexUBERON:000045130.18gold quality
right hemisphere of cerebellumUBERON:001489030.18gold quality
cerebellar hemisphereUBERON:000224530.16gold quality
cerebellar cortexUBERON:000212930.10gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.08

Regulation

Is transcription factor: no

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_rerioccnyl1ENSDARG00000099692
drosophila_melanogasterCycYFBGN0032378
caenorhabditis_elegansWBGENE00022697

Paralogs (2): CCNY (ENSG00000108100), CCNYL1 (ENSG00000163249)

Protein

Protein identifiers

Cyclin-Y-like protein 1BA0A8V8TMC4 (reviewed: A0A8V8TMC4)

All UniProt accessions (1): A0A8V8TMC4

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the cyclin family. Cyclin Y subfamily.

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

IDNameType
IPR006671Cyclin_NDomain
IPR036915Cyclin-like_sfHomologous_superfamily

Pfam: PF00134

UniProt features (2 total): chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A8V8TMC4-F171.850.29

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 13 (showing top): GOBP_REGULATION_OF_WNT_SIGNALING_PATHWAY, GOMF_KINASE_ACTIVATOR_ACTIVITY, GOBP_CANONICAL_WNT_SIGNALING_PATHWAY, chr16p11, GOMF_PROTEIN_SERINE_THREONINE_KINASE_ACTIVATOR_ACTIVITY, GOMF_ENZYME_ACTIVATOR_ACTIVITY, GOMF_ENZYME_REGULATOR_ACTIVITY, GOMF_CYCLIN_DEPENDENT_PROTEIN_SERINE_THREONINE_KINASE_ACTIVATOR_ACTIVITY, GOBP_REGULATION_OF_CANONICAL_WNT_SIGNALING_PATHWAY, GOMF_MOLECULAR_FUNCTION_ACTIVATOR_ACTIVITY, GOBP_WNT_SIGNALING_PATHWAY, GOMF_CYCLIN_DEPENDENT_PROTEIN_KINASE_REGULATOR_ACTIVITY, GOMF_KINASE_REGULATOR_ACTIVITY

GO Biological Process (1): regulation of canonical Wnt signaling pathway (GO:0060828)

GO Molecular Function (0):

GO Cellular Component (1): plasma membrane (GO:0005886)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of Wnt signaling pathway1
canonical Wnt signaling pathway1
membrane1
cell periphery1

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A7H0DN99, A0A8V8TMC4, D3YUJ3, I2HAA0, O01501, O13818, O14260, O14332, O17657, O42575, O43008, P06776, P0C7X3, P17214, P25009, P30645, P34624, P36034, P38729, P52924, P53053, P53124, Q03080, Q05930, Q07788, Q08C99, Q08CI4, Q09792, Q10326, Q10PQ9, Q22695, Q28EL0, Q4R871, Q5IBH7, Q5ICL9, Q5MJ70, Q5T2Q4, Q5U5D0, Q6NRF4, Q75D04

Diamond homologs: A0A8V8TMC4, A6NIR3, D3YUJ3, P0C7X3, P34624, Q08CI4, Q28EL0, Q4R871, Q5T2Q4, Q5U5D0, Q5VUJ5, Q5VW22, Q6NRF4, Q8BGU5, Q8N7R7, Q8ND76, Q96P64, A1L520, A5PK26, O74345, O75689, O80925, O82171, O94601, O97902, P35197, P38682, P40529, Q04412, Q09531, Q0WQQ1, Q10165, Q10367, Q14161, Q15027, Q15057, Q17R07, Q1AAU6, Q1ZXH8, Q28CM8

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1156332255 (16:34352899 T>A), RS1158545589 (16:34366099 A>G), RS1159807100 (16:34375548 A>G,T), RS1159967311 (16:34365969 G>A), RS1159969578 (16:34354273 G>A), RS1160124320 (16:34352889 G>C), RS1163012912 (16:34375381 T>C), RS1163221116 (16:34353814 C>T), RS1163649042 (16:34352796 T>C), RS1163654078 (16:34365814 T>C), RS1163670031 (16:34375927 C>A), RS1166789759 (16:34375274 T>G), RS1168815628 (16:34353189 T>C), RS1169126811 (16:34375790 C>T), RS1170595694 (16:34375762 T>C)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.