CCNYL1

gene
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Also known as FLJ40432

Summary

CCNYL1 (cyclin Y like 1, HGNC:26868) is a protein-coding gene on chromosome 2q33.3, encoding Cyclin-Y-like protein 1 (Q8N7R7). Key regulator of Wnt signaling implicated in various biological processes including male fertility, embryonic neurogenesis and cortex development.

Predicted to enable protein kinase binding activity. Predicted to be involved in regulation of canonical Wnt signaling pathway. Predicted to act upstream of or within flagellated sperm motility; regulation of protein kinase activity; and spermatogenesis. Located in plasma membrane.

Source: NCBI Gene 151195 — RefSeq curated summary.

At a glance

  • GWAS associations: 4
  • Clinical variants (ClinVar): 44 total
  • MANE Select transcript: NM_001330218

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26868
Approved symbolCCNYL1
Namecyclin Y like 1
Location2q33.3
Locus typegene with protein product
StatusApproved
AliasesFLJ40432
Ensembl geneENSG00000163249
Ensembl biotypeprotein_coding
OMIM620559
Entrez151195

Gene structure

Transcript identifiers

Ensembl transcripts: 13 — 10 protein_coding, 2 nonsense_mediated_decay, 1 protein_coding_CDS_not_defined

ENST00000295414, ENST00000339882, ENST00000392209, ENST00000420321, ENST00000420822, ENST00000452312, ENST00000468768, ENST00000650811, ENST00000930497, ENST00000930498, ENST00000930499, ENST00000930500, ENST00000930501

RefSeq mRNA: 3 — MANE Select: NM_001330218 NM_001142300, NM_001330218, NM_152523

CCDS: CCDS2377, CCDS46503, CCDS82564

Canonical transcript exons

ENST00000295414 — 10 exons

ExonStartEnd
ENSE00001072745207733947207734047
ENSE00001286242207740655207740706
ENSE00001286266207726842207726876
ENSE00001286291207753588207756174
ENSE00001755884207711640207712116
ENSE00002433124207724800207724874
ENSE00003525108207742223207742342
ENSE00003578398207747047207747213
ENSE00003602165207750957207751119
ENSE00003691050207737411207737446

Expression profiles

Bgee: expression breadth ubiquitous, 218 present calls, max score 98.84.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 17.2811 / max 248.5179, expressed in 1802 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
2489615.41181796
248941.2890686
248950.5803353

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
secondary oocyteCL:000065598.84gold quality
oocyteCL:000002398.52gold quality
spermCL:000001995.92gold quality
rectumUBERON:000105289.66gold quality
right coronary arteryUBERON:000162588.36gold quality
mucosa of stomachUBERON:000119988.10gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099187.98gold quality
calcaneal tendonUBERON:000370187.60gold quality
body of pancreasUBERON:000115087.28gold quality
esophagus squamous epitheliumUBERON:000692087.03gold quality
bone marrow cellCL:000209287.02gold quality
mucosa of transverse colonUBERON:000499187.00gold quality
esophagus mucosaUBERON:000246986.63gold quality
transverse colonUBERON:000115786.53gold quality
colonic epitheliumUBERON:000039785.69gold quality
mucosa of sigmoid colonUBERON:000499385.41gold quality
lower esophagus mucosaUBERON:003583485.37gold quality
pancreasUBERON:000126485.24gold quality
right lobe of liverUBERON:000111485.03gold quality
monocyteCL:000057685.02gold quality
smooth muscle tissueUBERON:000113584.95gold quality
islet of LangerhansUBERON:000000684.80gold quality
leukocyteCL:000073884.76gold quality
colonic mucosaUBERON:000031784.51gold quality
esophagusUBERON:000104384.39gold quality
left coronary arteryUBERON:000162684.36gold quality
colonUBERON:000115584.32gold quality
omental fat padUBERON:001041484.24gold quality
peritoneumUBERON:000235884.13gold quality
large intestineUBERON:000005984.12gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes11.48
E-ENAD-17no46.16

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

131 targeting CCNYL1, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-200B-3P100.0073.312693
HSA-MIR-200C-3P100.0073.352685
HSA-MIR-429100.0073.442698
HSA-MIR-29A-3P100.0073.111835
HSA-MIR-29B-3P100.0073.181833
HSA-MIR-29C-3P100.0073.151833
HSA-MIR-3925-3P100.0069.951237
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-513B-5P99.9969.962150
HSA-MIR-33A-5P99.9968.621055
HSA-MIR-33B-5P99.9968.581062
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-118499.9968.191458
HSA-MIR-477599.9875.006394
HSA-MIR-103A-3P99.9869.141595
HSA-MIR-10799.9869.141595
HSA-MIR-480399.9871.993117
HSA-MIR-60799.9773.625593
HSA-MIR-590-3P99.9674.346478
HSA-MIR-548AJ-3P99.9673.385345
HSA-MIR-548X-3P99.9673.385345
HSA-MIR-570-3P99.9672.414910
HSA-MIR-548AA99.9670.643753
HSA-MIR-548AP-3P99.9670.643753
HSA-MIR-548T-3P99.9670.643753
HSA-MIR-767-5P99.9570.85993
HSA-MIR-548J-3P99.9472.614881
HSA-MIR-539-5P99.9370.302855
HSA-MIR-548AE-3P99.9372.664867
HSA-MIR-548AH-3P99.9372.544872

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_rerioccnyl1ENSDARG00000099692
mus_musculusCcnyl1ENSMUSG00000070871
rattus_norvegicusCcnyl1ENSRNOG00000023807
drosophila_melanogasterCycYFBGN0032378
caenorhabditis_elegansWBGENE00022697

Paralogs (2): CCNY (ENSG00000108100), CCNYL1B (ENSG00000284209)

Protein

Protein identifiers

Cyclin-Y-like protein 1Q8N7R7 (reviewed: Q8N7R7)

All UniProt accessions (5): A0A494C0K2, C9IYB8, Q8N7R7, H7BZD2, H7C0P7

UniProt curated annotations — full annotation on UniProt →

Function. Key regulator of Wnt signaling implicated in various biological processes including male fertility, embryonic neurogenesis and cortex development. Activates the cyclin-dependent kinase CDK16, and promotes sperm maturation.

Subunit / interactions. Interacts with CDK16; this interaction mutually increases the stability of CDK16 and CCNYL1 and increases the kinase activity of CDK16.

Subcellular location. Cell membrane.

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

Isoforms (3)

UniProt IDNamesCanonical?
Q8N7R7-11yes
Q8N7R7-22
Q8N7R7-33

RefSeq proteins (3): NP_001135772, NP_001317147, NP_689736 (=MANE)

Domains & families (InterPro)

IDNameType
IPR006671Cyclin_NDomain
IPR012399Cyclin_YFamily
IPR013763Cyclin-like_domDomain
IPR036915Cyclin-like_sfHomologous_superfamily

Pfam: PF00134

UniProt features (8 total): modified residue 4, splice variant 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8N7R7-F175.100.47

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (4): 67, 105, 112, 344

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 176 (showing top): TGGTGCT_MIR29A_MIR29B_MIR29C, GOBP_REGULATION_OF_WNT_SIGNALING_PATHWAY, GOBP_MALE_GAMETE_GENERATION, GGGTGGRR_PAX4_03, GOMF_KINASE_ACTIVATOR_ACTIVITY, GOBP_CANONICAL_WNT_SIGNALING_PATHWAY, GOBP_CILIUM_MOVEMENT, GOBP_CILIUM_OR_FLAGELLUM_DEPENDENT_CELL_MOTILITY, ZIC1_01, CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_5, CHARAFE_BREAST_CANCER_LUMINAL_VS_BASAL_DN, USF_02, GOBP_DEVELOPMENTAL_PROCESS_INVOLVED_IN_REPRODUCTION, MASSARWEH_TAMOXIFEN_RESISTANCE_UP, MAX_01

GO Biological Process (7): regulation of protein phosphorylation (GO:0001932), spermatogenesis (GO:0007283), nervous system development (GO:0007399), cell differentiation (GO:0030154), flagellated sperm motility (GO:0030317), regulation of canonical Wnt signaling pathway (GO:0060828), regulation of cyclin-dependent protein serine/threonine kinase activity (GO:0000079)

GO Molecular Function (2): protein kinase binding (GO:0019901), protein binding (GO:0005515)

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein phosphorylation1
regulation of protein modification process1
regulation of phosphorylation1
developmental process involved in reproduction1
male gamete generation1
system development1
cellular developmental process1
cilium-dependent cell motility1
cilium movement involved in cell motility1
sperm motility1
regulation of Wnt signaling pathway1
canonical Wnt signaling pathway1
cyclin-dependent protein serine/threonine kinase activity1
regulation of protein serine/threonine kinase activity1
kinase binding1
binding1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

596 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CCNYL1CDK16Q00536857
CCNYL1CDK14O94921573
CCNYL1METTL21AQ8WXB1565
CCNYL1ZNF614Q8N883544
CCNYL1CLRN3Q8NCR9492
CCNYL1TUBG2Q9NRH3465
CCNYL1ZNF211Q13398464
CCNYL1SPEM1Q8N4L4453
CCNYL1CD300LBA8K4G0451
CCNYL1CAMSAP1Q5T5Y3449
CCNYL1PLEKHM3Q6ZWE6441
CCNYL1CYB5R2Q6BCY4433
CCNYL1LPXNO60711426
CCNYL1SMC6Q96SB8426
CCNYL1HSF2BPO75031422

IntAct

48 interactions, top by confidence:

ABTypeScore
CDK16CCNYL1psi-mi:“MI:0914”(association)0.800
CDK16CCNYL1psi-mi:“MI:0915”(physical association)0.800
BIRC2HTRA2psi-mi:“MI:0914”(association)0.650
GYPATCAF2psi-mi:“MI:0914”(association)0.640
CDK16CDK17psi-mi:“MI:0914”(association)0.620
FYTTD1UBA6psi-mi:“MI:0914”(association)0.530
HOXB5VPS37Cpsi-mi:“MI:0914”(association)0.530
GJB7PALM3psi-mi:“MI:0914”(association)0.530
TMEM185ATSPAN6psi-mi:“MI:0914”(association)0.530
PI4K2AGABARAPpsi-mi:“MI:0914”(association)0.530
TAS2R7ATP2B4psi-mi:“MI:0914”(association)0.500
YWHABPLEKHG3psi-mi:“MI:0914”(association)0.480
GPC1SNAP23psi-mi:“MI:0915”(physical association)0.400
GPC1GANABpsi-mi:“MI:0915”(physical association)0.400
CDK16PKMpsi-mi:“MI:0914”(association)0.350
CKAP5TACC3psi-mi:“MI:0914”(association)0.350
RTEL1-TNFRSF6BFAM13Apsi-mi:“MI:0914”(association)0.350
WEE1CEP350psi-mi:“MI:0914”(association)0.350
CDK16YWHAQpsi-mi:“MI:0914”(association)0.350
CDK17ACACBpsi-mi:“MI:0914”(association)0.350
YWHAEDEPDC5psi-mi:“MI:0914”(association)0.350
HIDE1TMEM120Bpsi-mi:“MI:0914”(association)0.350
GYPAHYKKpsi-mi:“MI:0914”(association)0.350
DUSP22POTEFpsi-mi:“MI:0914”(association)0.350
CERS2VPS37Cpsi-mi:“MI:0914”(association)0.350
TACSTD2RIMOC1psi-mi:“MI:0914”(association)0.350
HORMAD2WASH3Ppsi-mi:“MI:0914”(association)0.350
FIS1QSOX1psi-mi:“MI:0914”(association)0.350
CENPMDNM1Lpsi-mi:“MI:0914”(association)0.350
CCNYL1PPLpsi-mi:“MI:0914”(association)0.350

BioGRID (97): CCNYL1 (Affinity Capture-RNA), CCNYL1 (Affinity Capture-RNA), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS), CCNY (Affinity Capture-MS), CCNYL1 (Affinity Capture-MS)

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance33
Likely benign4
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1612 predictions. Top by Δscore:

VariantEffectΔscore
2:207712113:GAAG:Gdonor_gain1.0000
2:207712114:AAG:Adonor_gain1.0000
2:207712115:AG:Adonor_gain1.0000
2:207712115:AGG:Adonor_loss1.0000
2:207712116:GG:Gdonor_gain1.0000
2:207712117:G:GAdonor_loss1.0000
2:207712117:G:GGdonor_gain1.0000
2:207712118:T:Gdonor_loss1.0000
2:207724795:TATA:Tacceptor_loss1.0000
2:207724796:ATAG:Aacceptor_loss1.0000
2:207724798:A:AGacceptor_gain1.0000
2:207724798:A:Cacceptor_loss1.0000
2:207724799:G:GAacceptor_gain1.0000
2:207724799:GATTT:Gacceptor_gain1.0000
2:207726840:A:AGacceptor_gain1.0000
2:207726841:G:GGacceptor_gain1.0000
2:207726841:GT:Gacceptor_gain1.0000
2:207726875:AT:Adonor_gain1.0000
2:207726877:G:GAdonor_loss1.0000
2:207726877:G:GGdonor_gain1.0000
2:207726878:T:Gdonor_loss1.0000
2:207740707:G:GGdonor_gain1.0000
2:207742217:TTTCA:Tacceptor_loss1.0000
2:207742218:TTCA:Tacceptor_loss1.0000
2:207742219:TCA:Tacceptor_loss1.0000
2:207742220:CA:Cacceptor_loss1.0000
2:207742221:A:AGacceptor_gain1.0000
2:207742221:A:ATacceptor_loss1.0000
2:207742221:AGC:Aacceptor_gain1.0000
2:207742222:G:GCacceptor_gain1.0000

AlphaMissense

2380 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:207724850:T:CF91L1.000
2:207724851:T:CF91S1.000
2:207724851:T:GF91C1.000
2:207724852:C:AF91L1.000
2:207724852:C:GF91L1.000
2:207733977:A:CS121R1.000
2:207733979:C:AS121R1.000
2:207733979:C:GS121R1.000
2:207733993:T:AI126K1.000
2:207733993:T:GI126R1.000
2:207734014:T:AV133D1.000
2:207734023:C:AP136H1.000
2:207737421:G:CA148P1.000
2:207737422:C:AA148E1.000
2:207737425:T:AI149K1.000
2:207737425:T:GI149R1.000
2:207737446:G:TR156I1.000
2:207742283:T:CF194L1.000
2:207742284:T:CF194S1.000
2:207742285:T:AF194L1.000
2:207742285:T:GF194L1.000
2:207742298:T:CF199L1.000
2:207742300:T:AF199L1.000
2:207742300:T:GF199L1.000
2:207742304:G:CA201P1.000
2:207742307:G:CA202P1.000
2:207742314:T:AL204Q1.000
2:207742314:T:CL204P1.000
2:207742317:C:TT205I1.000
2:207742322:G:AE207K1.000

dbSNP variants (sampled 300 via entrez): RS1000154338 (2:207724064 T>C,G), RS1000179612 (2:207740983 C>A,T), RS1000196925 (2:207710564 G>A,C), RS1000259394 (2:207753044 AAAAT>A), RS1000296213 (2:207751398 C>T), RS1000296587 (2:207736843 C>A), RS1000355485 (2:207722422 T>C), RS1000407081 (2:207735394 C>A,G), RS1000469069 (2:207717966 T>A), RS1000592763 (2:207754481 A>C,G), RS1000652874 (2:207711786 G>T), RS1000708786 (2:207717507 A>C), RS1000730875 (2:207724061 A>G), RS1000862179 (2:207744221 G>A), RS1000936248 (2:207741274 G>A,C,T)

Disease associations

OMIM: gene MIM:620559 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

4 associations (top):

StudyTraitp-value
GCST004776_34Systolic blood pressure9.000000e-11
GCST004776_84Systolic blood pressure1.000000e-07
GCST006103_20Interleukin-6 levels4.000000e-06
GCST008157_64Body fat mass5.000000e-06

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0006335systolic blood pressure
EFO:0004810interleukin-6 measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

36 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, increases expression7
trichostatin Aaffects cotreatment, decreases expression, affects expression4
(+)-JQ1 compoundincreases expression3
Acetaminophenincreases expression2
Nickelincreases expression2
Phenylmercuric Acetateaffects cotreatment, decreases expression2
Tobacco Smoke Pollutionaffects expression, increases expression2
Cyclosporineincreases expression, decreases expression2
FR900359affects phosphorylation1
alpha-pineneaffects cotreatment, increases oxidation, increases abundance1
methylparabendecreases expression1
methacrylaldehydeaffects cotreatment, increases oxidation, increases abundance1
di-n-butylphosphoric acidaffects expression1
K 7174increases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphinaffects cotreatment, decreases expression1
2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidinedecreases expression, increases response to substance1
Acroleinaffects cotreatment, increases oxidation, increases abundance1
Air Pollutantsaffects cotreatment, increases abundance, increases oxidation1
Arbutinincreases expression1
Cadmiumincreases expression1
Caffeineaffects phosphorylation1
Drugs, Chinese Herbaldecreases expression1
Estradiolincreases expression1
Folic Aciddecreases expression1
Hydrogen Peroxideaffects expression1
Ozoneaffects cotreatment, increases oxidation, increases abundance1
Phenobarbitalaffects expression1
Rotenonedecreases expression1
Smokedecreases expression1

Cellosaurus cell lines

1 cell lines: 1 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_SH54HAP1 CCNYL1 (-)Cancer cell lineMale

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.