CCDC87

gene
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Also known as FLJ10786

Summary

CCDC87 (coiled-coil domain containing 87, HGNC:25579) is a protein-coding gene on chromosome 11q13.2, encoding Coiled-coil domain-containing protein 87 (Q9NVE4). Plays a role in spermatogenesis, where it is important for normal sperm head morphology.

Predicted to be involved in positive regulation of acrosome reaction and positive regulation of fertilization.

Source: NCBI Gene 55231 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 141 total
  • MANE Select transcript: NM_018219

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25579
Approved symbolCCDC87
Namecoiled-coil domain containing 87
Location11q13.2
Locus typegene with protein product
StatusApproved
AliasesFLJ10786
Ensembl geneENSG00000182791
Ensembl biotypeprotein_coding
Entrez55231

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000333861

RefSeq mRNA: 1 — MANE Select: NM_018219 NM_018219

CCDS: CCDS8145

Canonical transcript exons

ENST00000333861 — 1 exons

ExonStartEnd
ENSE000013151176659017666593063

Expression profiles

Bgee: expression breadth ubiquitous, 107 present calls, max score 84.14.

FANTOM5 (CAGE): breadth broad, TPM avg 0.8894 / max 61.3476, expressed in 449 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1208170.7778395
1208180.111647

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047384.14gold quality
left testisUBERON:000453378.29gold quality
right testisUBERON:000453477.80gold quality
testisUBERON:000047376.23gold quality
triceps brachiiUBERON:000150965.06gold quality
adult organismUBERON:000702364.93gold quality
gluteal muscleUBERON:000200064.88gold quality
male germ cellCL:000001562.49gold quality
spermCL:000001962.02gold quality
tongue squamous epitheliumUBERON:000691961.67gold quality
secondary oocyteCL:000065561.60gold quality
olfactory bulbUBERON:000226461.46gold quality
type B pancreatic cellCL:000016961.33gold quality
islet of LangerhansUBERON:000000660.91gold quality
quadriceps femorisUBERON:000137760.41gold quality
vastus lateralisUBERON:000137959.88gold quality
nasal cavity epitheliumUBERON:000538457.40gold quality
pancreatic ductal cellCL:000207956.16silver quality
prefrontal cortexUBERON:000045156.02gold quality
cortical plateUBERON:000534354.74silver quality
myocardiumUBERON:000234954.55gold quality
muscle tissueUBERON:000238554.11silver quality
oocyteCL:000002353.29gold quality
smooth muscle tissueUBERON:000113553.18gold quality
deltoidUBERON:000147652.69gold quality
epithelial cell of pancreasCL:000008352.31gold quality
Brodmann (1909) area 46UBERON:000648351.90gold quality
left ventricle myocardiumUBERON:000656651.86gold quality
hindlimb stylopod muscleUBERON:000425250.09silver quality
thymusUBERON:000237049.94gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.13

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

17 targeting CCDC87, 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-570-3P99.9672.414910
HSA-MIR-4778-3P99.9370.401818
HSA-MIR-6857-5P99.8765.32985
HSA-MIR-607999.8468.541170
HSA-MIR-4659A-3P99.8072.624248
HSA-MIR-4659B-3P99.8072.624248
HSA-MIR-4708-3P99.5167.99870
HSA-MIR-361299.4566.021333
HSA-MIR-65099.4565.771309
HSA-MIR-6828-5P99.3169.211433
HSA-MIR-3190-5P98.8764.891345
HSA-MIR-445098.2668.35725
HSA-MIR-1226-5P96.5065.28643
HSA-MIR-6782-5P96.4564.42612
HSA-MIR-60195.9867.59421
HSA-MIR-6888-5P95.8963.78831
HSA-MIR-4474-5P94.2367.95568

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_rerioccdc87ENSDARG00000045683
mus_musculusCcdc87ENSMUSG00000067872
rattus_norvegicusCcdc87ENSRNOG00000071751

Protein

Protein identifiers

Coiled-coil domain-containing protein 87Q9NVE4 (reviewed: Q9NVE4)

All UniProt accessions (1): Q9NVE4

UniProt curated annotations — full annotation on UniProt →

Function. Plays a role in spermatogenesis, where it is important for normal sperm head morphology. Also required for the acrosome reaction and thus normal male fertility.

Similarity. Belongs to the CCDC87 family.

RefSeq proteins (1): NP_060689* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR037383CCDC87Family

Pfam: PF03999

UniProt features (6 total): sequence variant 2, sequence conflict 2, chain 1, coiled-coil region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9NVE4-F162.530.09

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 58 (showing top): GOBP_SINGLE_FERTILIZATION, GOBP_POSITIVE_REGULATION_OF_REPRODUCTIVE_PROCESS, GOBP_MALE_GAMETE_GENERATION, chr11q13, GOBP_REGULATION_OF_REPRODUCTIVE_PROCESS, GOBP_REGULATION_OF_ACROSOME_REACTION, GOBP_ACROSOME_REACTION, GOBP_DEVELOPMENTAL_PROCESS_INVOLVED_IN_REPRODUCTION, NIKOLSKY_BREAST_CANCER_11Q12_Q14_AMPLICON, GOBP_FERTILIZATION, YGCGYRCGC_UNKNOWN, HATADA_METHYLATED_IN_LUNG_CANCER_UP, WAKABAYASHI_ADIPOGENESIS_PPARG_RXRA_BOUND_36HR, WAKABAYASHI_ADIPOGENESIS_PPARG_RXRA_BOUND_8D, GOBP_REGULATION_OF_FERTILIZATION

GO Biological Process (5): spermatogenesis (GO:0007283), single fertilization (GO:0007338), cell differentiation (GO:0030154), positive regulation of fertilization (GO:1905516), positive regulation of acrosome reaction (GO:2000344)

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (0):

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
fertilization2
positive regulation of reproductive process2
developmental process involved in reproduction1
male gamete generation1
cellular developmental process1
regulation of fertilization1
acrosome reaction1
regulation of acrosome reaction1
binding1

Protein interactions and networks

STRING

182 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CCDC87DCDC2BA2VCK2561
CCDC87MIX23Q4VC31513
CCDC87CCDC97Q96F63479
CCDC87PRR14LQ5THK1477
CCDC87FAM184BQ9ULE4451
CCDC87ARHGAP6O43182365
CCDC87UBR4Q5T4S7361
CCDC87MIPEPQ99797344
CCDC87ZNF451Q9Y4E5337
CCDC87ANO5Q75V66324
CCDC87ZNF329Q86UD4305
CCDC87MTCL1Q9Y4B5301
CCDC87PDE1CQ14123282
CCDC87ZNF592Q92610262
CCDC87SUN2Q9UH99251

IntAct

30 interactions, top by confidence:

ABTypeScore
GOLGA2CCDC87psi-mi:“MI:0915”(physical association)0.720
SUN2LMNApsi-mi:“MI:0914”(association)0.720
TRIM27CCDC87psi-mi:“MI:0915”(physical association)0.560
CCDC87KRT15psi-mi:“MI:0915”(physical association)0.560
USHBP1CCDC87psi-mi:“MI:0915”(physical association)0.560
TRIM54CCDC87psi-mi:“MI:0915”(physical association)0.560
CCDC87USHBP1psi-mi:“MI:0915”(physical association)0.560
CCDC87TRIM27psi-mi:“MI:0915”(physical association)0.560
CCDC87TRIM54psi-mi:“MI:0915”(physical association)0.560
CDR2CCDC87psi-mi:“MI:0915”(physical association)0.560
CCDC87STAT3psi-mi:“MI:0915”(physical association)0.490
STAT3CCDC87psi-mi:“MI:0915”(physical association)0.490
YAP1CCDC87psi-mi:“MI:0407”(direct interaction)0.440
CCDC87KASH5psi-mi:“MI:0915”(physical association)0.370
SUN2MYO1Cpsi-mi:“MI:0914”(association)0.350
MKI67ARHGAP10psi-mi:“MI:0914”(association)0.350
ESR2PSMD11psi-mi:“MI:0914”(association)0.350
CCDC87GOLGA2psi-mi:“MI:0915”(physical association)0.000
CCDC87CDR2psi-mi:“MI:0915”(physical association)0.000

BioGRID (23): CCDC87 (Two-hybrid), CCDC87 (Two-hybrid), CCDC87 (Two-hybrid), TRIM54 (Two-hybrid), USHBP1 (Two-hybrid), CCDC155 (Two-hybrid), CCDC87 (Two-hybrid), CCDC87 (Affinity Capture-MS), CCDC87 (Affinity Capture-MS), CCDC87 (Affinity Capture-RNA), CCDC87 (Two-hybrid), CCDC87 (Two-hybrid), CCDC87 (Affinity Capture-MS), CCDC87 (Affinity Capture-MS), CCDC87 (Protein-peptide)

ESM2 similar proteins: A0JNF3, A1L253, A2AHC3, A3KP40, A5PLN7, A5WUN7, A6H5Y1, B1AXH1, B2GUZ2, D3Z8E6, E9PV87, E9Q309, H6D7E6, O14513, O60303, P0CAX8, P28290, Q14B48, Q1G7G9, Q2KHM9, Q32LN6, Q49A88, Q566N9, Q5HYW2, Q5PQL8, Q5REU9, Q5T5Y3, Q5VT06, Q60664, Q66H35, Q66MI6, Q6A000, Q6AYP4, Q6NSV7, Q6NXP0, Q6ZRS4, Q6ZVD7, Q80VP2, Q8BJS7, Q8CB14

Diamond homologs: Q8CDL9, Q9NVE4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance131
Likely benign10
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

97 predictions. Top by Δscore:

VariantEffectΔscore
11:66592872:G:Tdonor_gain0.9900
11:66593041:G:GTdonor_gain0.9900
11:66592872:G:GTdonor_gain0.9700
11:66593042:A:Tdonor_gain0.9700
11:66593058:GTTAC:Gdonor_gain0.9700
11:66593059:TTACT:Tdonor_gain0.9700
11:66593056:GGGT:Gdonor_gain0.9300
11:66592941:G:GTdonor_gain0.9100
11:66593047:A:Tdonor_gain0.8900
11:66592941:G:Tdonor_gain0.8800
11:66592924:G:Tdonor_gain0.8700
11:66592969:T:TAdonor_gain0.8700
11:66592970:G:GAdonor_gain0.8700
11:66592876:G:GTdonor_gain0.8600
11:66592971:G:GGdonor_gain0.8600
11:66593062:C:Gdonor_gain0.8500
11:66592968:G:GTdonor_gain0.8100
11:66592924:G:GTdonor_gain0.8000
11:66592992:C:Tdonor_gain0.8000
11:66592968:GTG:Gdonor_gain0.7900
11:66592986:C:Gdonor_gain0.7400
11:66592967:GGTG:Gdonor_gain0.7300
11:66592955:G:GTdonor_gain0.7100
11:66592964:GCCG:Gdonor_gain0.7000
11:66592873:A:Tdonor_gain0.6600
11:66592966:C:Adonor_gain0.6600
11:66592963:AGCC:Adonor_gain0.5700
11:66593062:C:CGdonor_gain0.5600
11:66592991:GC:Gdonor_gain0.5200
11:66592966:CGGTG:Cdonor_loss0.5100

AlphaMissense

5512 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:66592644:G:CS124R0.987
11:66592644:G:TS124R0.987
11:66592646:T:GS124R0.987
11:66592733:A:GW95R0.986
11:66592733:A:TW95R0.986
11:66592530:G:CC162W0.985
11:66592314:G:CS234R0.984
11:66592314:G:TS234R0.984
11:66592316:T:GS234R0.984
11:66592744:A:GL91P0.984
11:66592636:A:GL127P0.981
11:66592647:G:CS123R0.981
11:66592647:G:TS123R0.981
11:66592649:T:GS123R0.981
11:66592681:A:GL112P0.980
11:66592672:C:GR115P0.979
11:66592543:A:GL158P0.977
11:66592532:A:GC162R0.975
11:66592492:A:GL175P0.971
11:66592731:C:AW95C0.969
11:66592731:C:GW95C0.969
11:66592519:A:GL166P0.967
11:66592531:C:TC162Y0.967
11:66592678:C:GR113P0.966
11:66592669:A:GL116P0.964
11:66591177:A:CF613L0.963
11:66591177:A:TF613L0.963
11:66591179:A:GF613L0.963
11:66591192:G:CF608L0.962
11:66591192:G:TF608L0.962

dbSNP variants (sampled 300 via entrez): RS1000727023 (11:66594179 A>G), RS1001942552 (11:66594791 A>C,T), RS1002857887 (11:66592715 C>A,G,T), RS1003140973 (11:66592929 C>A), RS1003191553 (11:66593926 T>C), RS1003473448 (11:66594225 G>C), RS1003701432 (11:66589861 G>C), RS1003732738 (11:66589681 C>A,T), RS1005670519 (11:66589711 C>A), RS1005707688 (11:66594299 C>T), RS1006371587 (11:66594803 C>T), RS1007572179 (11:66594965 A>C), RS1007614575 (11:66590396 T>A), RS1008372278 (11:66591962 T>A,C), RS1010244995 (11:66594220 G>A)

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

2 associations (top):

StudyTraitp-value
GCST001241_12Bipolar disorder2.000000e-07
GCST007576_250Chronotype5.000000e-13

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0008328chronotype measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

13 total (human), top 13 by PubMed support.

ChemicalActions (top 5)PubMed papers
(+)-JQ1 compoundincreases expression2
Benzo(a)pyreneincreases methylation, affects methylation, increases expression2
sotorasibaffects cotreatment, increases expression1
sodium arseniteincreases expression1
ferrous chloridedecreases expression1
trametinibincreases expression, affects cotreatment1
NVP-BKM120increases expression, affects cotreatment1
Sunitinibdecreases expression1
Smokedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Urethanedecreases expression1
Okadaic Acidincreases expression1
S-Nitrosoglutathioneincreases expression1

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.