FAM9A

gene
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Also known as TEX39A

Summary

FAM9A (family with sequence similarity 9 member A, HGNC:18403) is a protein-coding gene on chromosome Xp22.31, encoding Protein FAM9A (Q8IZU1).

This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be a nuclear protein that is localized to the nucleolus, and has some similarity to a synaptonemal complex protein. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Source: NCBI Gene 171482 — RefSeq curated summary.

At a glance

  • GWAS associations: 7
  • Clinical variants (ClinVar): 55 total
  • MANE Select transcript: NM_174951

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:18403
Approved symbolFAM9A
Namefamily with sequence similarity 9 member A
LocationXp22.31
Locus typegene with protein product
StatusApproved
AliasesTEX39A
Ensembl geneENSG00000183304
Ensembl biotypeprotein_coding
OMIM300477
Entrez171482

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000381003, ENST00000543214

RefSeq mRNA: 2 — MANE Select: NM_174951 NM_001171186, NM_174951

CCDS: CCDS14131

Canonical transcript exons

ENST00000381003 — 10 exons

ExonStartEnd
ENSE0000129721287962688796382
ENSE0000130892287936588793756
ENSE0000131831487981508798181
ENSE0000131968687950788795420
ENSE0000132574987912808791379
ENSE0000135318987907958791172
ENSE0000136478588013118801383
ENSE0000148719788000818800209
ENSE0000167837087989668799094
ENSE0000170188487983598798479

Expression profiles

Bgee: expression breadth broad, 20 present calls, max score 82.18.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.18gold quality
right testisUBERON:000453467.06gold quality
left testisUBERON:000453365.89gold quality
testisUBERON:000047365.06gold quality
sural nerveUBERON:001548864.58gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099155.22gold quality
lower lobe of lungUBERON:000894952.08silver quality
buccal mucosa cellCL:000233650.45gold quality
upper leg skinUBERON:000426247.86silver quality
right lobe of liverUBERON:000111446.29gold quality
substantia nigra pars reticulataUBERON:000196643.39gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451143.37gold quality
liverUBERON:000210742.76gold quality
secondary oocyteCL:000065542.57gold quality
heart right ventricleUBERON:000208042.51gold quality
vastus lateralisUBERON:000137941.41gold quality
quadriceps femorisUBERON:000137741.37gold quality
superficial temporal arteryUBERON:000161441.33gold quality
palpebral conjunctivaUBERON:000181241.10gold quality
mucosa of paranasal sinusUBERON:000503040.98gold quality
amniotic fluidUBERON:000017340.69gold quality
jejunal mucosaUBERON:000039940.59gold quality
biceps brachiiUBERON:000150740.57gold quality
epithelium of nasopharynxUBERON:000195140.45gold quality
myocardiumUBERON:000234940.45gold quality
gingival epitheliumUBERON:000194940.43gold quality
germinal epithelium of ovaryUBERON:000130440.33gold quality
esophagus squamous epitheliumUBERON:000692040.29gold quality
skeletal muscle tissue of biceps brachiiUBERON:000450240.27gold quality
jejunumUBERON:000211540.18gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes2.63

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

30 targeting FAM9A, 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-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-428299.9975.366408
HSA-MIR-493-5P99.9672.472382
HSA-MIR-1236-3P99.9468.041695
HSA-MIR-3529-3P99.9073.553045
HSA-MIR-5003-3P99.8569.292517
HSA-MIR-6752-3P99.7266.711587
HSA-MIR-377-5P99.7065.28712
HSA-MIR-608699.7065.38699
HSA-MIR-130399.6569.771662
HSA-MIR-510-3P99.5470.062965
HSA-MIR-3160-5P99.2869.071938
HSA-MIR-7854-3P99.0866.261117
HSA-MIR-4738-3P98.9867.981846
HSA-MIR-42198.9067.041883
HSA-MIR-4709-3P98.8868.041594
HSA-MIR-1288-5P98.8567.01734
HSA-MIR-118398.7567.101116
HSA-MIR-807898.3265.73361
HSA-MIR-425797.8668.051190
HSA-MIR-203B-3P97.8266.27979
HSA-MIR-4799-3P97.7865.97893
HSA-MIR-4720-5P97.4665.67893
HSA-MIR-5588-5P97.4665.70913
HSA-MIR-6760-3P96.3568.311001
HSA-MIR-59196.2968.16611
HSA-MIR-6506-3P96.0168.4980

Literature-anchored findings (GeneRIF, showing 1)

  • Expressed exclusively in testis; protein is located in the nucleus, and localizes to the nucleolus. (PMID:12213195)

Cross-species orthologs

21 orthologs

OrganismSymbolGene ID
danio_reriosycp3ENSDARG00000013438
mus_musculusXlr4cENSMUSG00000031362
mus_musculusXlr3aENSMUSG00000057836
mus_musculusXlr3cENSMUSG00000058147
mus_musculusXlr5aENSMUSG00000058328
mus_musculusXlr5cENSMUSG00000067764
mus_musculusXlr4bENSMUSG00000067768
mus_musculusXlr5bENSMUSG00000072479
mus_musculusXlr3bENSMUSG00000073125
mus_musculusGm14692ENSMUSG00000079577
mus_musculusGm1140ENSMUSG00000079578
mus_musculusXlr4aENSMUSG00000079845
rattus_norvegicusXlr5cENSRNOG00000050177
rattus_norvegicusXlr4aENSRNOG00000055822
rattus_norvegicusFam9cl1ENSRNOG00000062315
rattus_norvegicusLOC100911047ENSRNOG00000064693
rattus_norvegicusLOC100911047ENSRNOG00000068104
rattus_norvegicusFam9cENSRNOG00000069253
rattus_norvegicusENSRNOG00000075733
rattus_norvegicusENSRNOG00000087898
rattus_norvegicusENSRNOG00000088563

Paralogs (3): SYCP3 (ENSG00000139351), FAM9B (ENSG00000177138), FAM9C (ENSG00000187268)

Protein

Protein identifiers

Protein FAM9AQ8IZU1 (reviewed: Q8IZU1)

All UniProt accessions (1): Q8IZU1

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Nucleus. Nucleolus.

Tissue specificity. Expressed exclusively in testis.

Similarity. Belongs to the XLR/SYCP3 family.

RefSeq proteins (2): NP_001164657, NP_777611* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR051443XLR/SYCP3Family

UniProt features (9 total): compositionally biased region 6, region of interest 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8IZU1-F166.590.21

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 34 (showing top): GSE45365_NK_CELL_VS_CD8A_DC_MCMV_INFECTION_UP, GOBP_MALE_GAMETE_GENERATION, ACEVEDO_LIVER_CANCER_WITH_H3K27ME3_UP, GOBP_CELLULAR_PROCESS_INVOLVED_IN_REPRODUCTION_IN_MULTICELLULAR_ORGANISM, GOBP_DEVELOPMENTAL_PROCESS_INVOLVED_IN_REPRODUCTION, GOBP_MEIOTIC_CELL_CYCLE, GOCC_NUCLEOLUS, GOCC_NUCLEAR_CHROMOSOME, GOCC_CONDENSED_NUCLEAR_CHROMOSOME, chrXp22, GOCC_SYNAPTONEMAL_STRUCTURE, MIR3529_3P, MIR1303, MIR1236_3P, MIR421

GO Biological Process (2): spermatid development (GO:0007286), meiotic cell cycle (GO:0051321)

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

GO Cellular Component (3): synaptonemal complex (GO:0000795), nucleolus (GO:0005730), nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
germ cell development1
spermatid differentiation1
cell cycle1
sexual reproduction1
reproductive process1
meiotic nuclear division1
binding1
synaptonemal structure1
nuclear lumen1
intracellular membraneless organelle1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

616 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
FAM9ASYCP3Q8IZU3905
FAM9AARSFP54793574
FAM9AANOS1P23352571
FAM9ASHROOM2Q13796448
FAM9ACPXCR1Q8N123445
FAM9AAMMECR1Q9Y4X0391
FAM9AAKAP17AQ02040388
FAM9ANXF5Q9H1B4379
FAM9AVCX3AQ9NNX9358
FAM9ASYAP1Q96A49357
FAM9APAGE2BQ5JRK9349
FAM9APUDPQ08623345
FAM9AASMTLO95671340
FAM9APNPLA4P41247322
FAM9AFBXO43Q4G163313

IntAct

207 interactions, top by confidence:

ABTypeScore
MLLT3FAM9Apsi-mi:“MI:0915”(physical association)0.740
FAM9BFAM9Apsi-mi:“MI:0915”(physical association)0.560
NAB2FAM9Apsi-mi:“MI:0915”(physical association)0.560
RUNX1T1FAM9Apsi-mi:“MI:0915”(physical association)0.560
SDCBPFAM9Apsi-mi:“MI:0915”(physical association)0.560
PRR20DFAM9Apsi-mi:“MI:0915”(physical association)0.560
ESRRAFAM9Apsi-mi:“MI:0915”(physical association)0.560
FAM9ANXF1psi-mi:“MI:0915”(physical association)0.560
TXLNAFAM9Apsi-mi:“MI:0915”(physical association)0.560
ZBTB6FAM9Apsi-mi:“MI:0915”(physical association)0.560
ZFP91FAM9Apsi-mi:“MI:0915”(physical association)0.560
TRAF5FAM9Apsi-mi:“MI:0915”(physical association)0.560
ESRRGFAM9Apsi-mi:“MI:0915”(physical association)0.560
LCE1EFAM9Apsi-mi:“MI:0915”(physical association)0.560
PHC1FAM9Apsi-mi:“MI:0915”(physical association)0.560
FAM9AH2BC15psi-mi:“MI:0915”(physical association)0.560
FAM9ATHAP1psi-mi:“MI:0915”(physical association)0.560
FAM9ATRIM41psi-mi:“MI:0915”(physical association)0.560
FAM9AZNF775psi-mi:“MI:0915”(physical association)0.560
TRAF2FAM9Apsi-mi:“MI:0915”(physical association)0.560
FAM9APICK1psi-mi:“MI:0915”(physical association)0.560
RNF151FAM9Apsi-mi:“MI:0915”(physical association)0.560
FAM9AINTS12psi-mi:“MI:0915”(physical association)0.560
HOMER1FAM9Apsi-mi:“MI:0915”(physical association)0.560
ARPC3FAM9Apsi-mi:“MI:0915”(physical association)0.560
FAM9ACTNNA3psi-mi:“MI:0915”(physical association)0.560
FAM9AMCRS1psi-mi:“MI:0915”(physical association)0.560
FAM9Apsi-mi:“MI:0915”(physical association)0.560
FAM9ASTAC3psi-mi:“MI:0915”(physical association)0.560
RNF4FAM9Apsi-mi:“MI:0915”(physical association)0.560

BioGRID (87): FAM9A (Two-hybrid), ACAD11 (Affinity Capture-MS), NOLC1 (Affinity Capture-MS), GOPC (Affinity Capture-MS), PTRF (Affinity Capture-MS), MLLT3 (Affinity Capture-MS), PNN (Affinity Capture-MS), NAF1 (Affinity Capture-MS), RNPS1 (Affinity Capture-MS), SRRM2 (Affinity Capture-MS), AP3B1 (Affinity Capture-MS), AP3M1 (Affinity Capture-MS), CWC22 (Affinity Capture-MS), JMJD6 (Affinity Capture-MS), NAP1L3 (Affinity Capture-MS)

ESM2 similar proteins: A0A1D9BZF0, A6QL64, B4DH59, B5DUH6, D3YZV8, E9Q6E9, O43493, O46383, O77733, P06916, P08116, P0C758, P0DKJ7, P0DKJ8, P0DPF3, P31568, P62521, Q01033, Q01042, Q1HVF7, Q2W8Q7, Q3BBV2, Q42626, Q42627, Q4ZJZ1, Q4ZJZ3, Q5JPF3, Q5MJ10, Q6AXX0, Q6GX35, Q6IC83, Q6P3W6, Q6PGQ1, Q7M4S9, Q7M732, Q86T75, Q8BP27, Q8IZU1, Q8N2N9, Q96QF7

Diamond homologs: Q8IZT9, Q8IZU0, Q8IZU1, Q4R764, Q8IZU3

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance49
Likely benign4
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

1697 predictions. Top by Δscore:

VariantEffectΔscore
X:8791279:CAGTT:Cdonor_gain1.0000
X:8793164:T:TAdonor_gain1.0000
X:8793753:CTTT:Cacceptor_gain1.0000
X:8795076:A:ACdonor_gain1.0000
X:8795077:C:CCdonor_gain1.0000
X:8795088:T:TAdonor_gain1.0000
X:8795094:T:TAdonor_gain1.0000
X:8795417:CTGC:Cacceptor_gain1.0000
X:8795418:TGC:Tacceptor_gain1.0000
X:8795419:GC:Gacceptor_gain1.0000
X:8795420:CC:Cacceptor_gain1.0000
X:8795421:C:CCacceptor_gain1.0000
X:8795427:C:CTacceptor_gain1.0000
X:8796212:A:Tacceptor_gain1.0000
X:8796379:TCAG:Tacceptor_gain1.0000
X:8796380:CAG:Cacceptor_gain1.0000
X:8796380:CAGC:Cacceptor_gain1.0000
X:8796381:AG:Aacceptor_gain1.0000
X:8796383:C:CCacceptor_gain1.0000
X:8798347:TAA:Tdonor_gain1.0000
X:8798347:TAAAC:Tdonor_gain1.0000
X:8798348:AAA:Adonor_gain1.0000
X:8798348:AAACA:Adonor_gain1.0000
X:8798354:TTTA:Tdonor_loss1.0000
X:8798355:TTA:Tdonor_loss1.0000
X:8798356:TAC:Tdonor_loss1.0000
X:8798357:A:ACdonor_gain1.0000
X:8798357:AC:Adonor_gain1.0000
X:8798357:ACC:Adonor_gain1.0000
X:8798358:C:CCdonor_gain1.0000

AlphaMissense

2199 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:8795388:A:GL174S0.961
X:8793748:A:CF280L0.960
X:8793748:A:TF280L0.960
X:8793750:A:GF280L0.960
X:8795376:A:GL178P0.960
X:8795412:C:GR166P0.959
X:8795376:A:TL178H0.942
X:8799072:G:CF38L0.937
X:8799072:G:TF38L0.937
X:8799074:A:GF38L0.937
X:8795414:T:AK165N0.925
X:8795414:T:GK165N0.925
X:8795367:T:GY181S0.921
X:8795394:C:GR172P0.921
X:8798436:A:CF88L0.919
X:8798436:A:TF88L0.919
X:8798438:A:GF88L0.919
X:8793736:C:AQ284H0.914
X:8793736:C:GQ284H0.914
X:8796293:C:GA155P0.914
X:8796270:T:AK162N0.911
X:8796270:T:GK162N0.911
X:8795420:C:AR163S0.910
X:8795420:C:GR163S0.910
X:8795385:A:GL175P0.909
X:8796274:A:GL161P0.909
X:8793729:A:GW287R0.908
X:8793729:A:TW287R0.908
X:8796295:C:GR154P0.906
X:8795413:G:TR166S0.900

dbSNP variants (sampled 300 via entrez): RS1000934069 (X:8801572 C>G,T), RS1001386431 (X:8801958 G>C,T), RS1001433596 (X:8796673 A>G), RS1001607164 (X:8797241 A>G), RS1003060175 (X:8791942 G>A,C,T), RS1003106966 (X:8802612 C>T), RS1003417611 (X:8792321 G>A), RS1003498337 (X:8799910 G>A), RS1003896853 (X:8800273 C>A,T), RS1005353334 (X:8790503 G>C), RS1005403987 (X:8795169 T>C), RS1005941633 (X:8797261 G>A), RS1006861232 (X:8791715 G>C), RS1006915138 (X:8791179 CA>C,CAA,CAAA), RS1007066582 (X:8801276 C>A,G,T)

Disease associations

OMIM: gene MIM:300477 | disease phenotypes:

GenCC curated gene-disease

Mondo (1): male infertility (MONDO:0005372)

Orphanet (0):

HPO phenotypes

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

GWAS associations

7 associations (top):

StudyTraitp-value
GCST003983_43Male-pattern baldness4.000000e-08
GCST003994_14Age at voice drop3.000000e-09
GCST005984_21Glomerular filtration rate5.000000e-09
GCST005985_11Creatinine levels5.000000e-09
GCST005994_15Hematocrit3.000000e-08
GCST005995_5Hemoglobin4.000000e-08
GCST90020091_13Estradiol levels7.000000e-30

EFO canonical traits (4, from GWAS)

EFO IDTrait name
EFO:0007888age at voice drop
EFO:0004348hematocrit
EFO:0004509hemoglobin measurement
EFO:0004697estradiol measurement

MeSH disease descriptors (1)

DescriptorNameTree numbers
D007248Infertility, MaleC12.100.500.430; C12.100.750.700; C12.200.294.430

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

6 total (human), top 6 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, decreases expression, increases methylation2
benzo(e)pyreneincreases methylation1
Acetaminophendecreases expression1
Arsenicaffects methylation1
Methapyrileneincreases methylation1
Aflatoxin B1increases expression1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT02202382PHASE4COMPLETEDEffects of Korean Red Ginseng on Male Infertility
NCT02204826PHASE4COMPLETEDEffects of Korean Red Ginseng on Semen Parameters in Male Infertility Patients: a Randomized, Placebo-controlled, Double-blind Clinical Study
NCT03802864PHASE4COMPLETEDPost-operative Pain Control of Testicular Sperm Extraction Using Liposomal Bupivacaine
NCT06100432PHASE4ACTIVE_NOT_RECRUITINGEffect of Eurycoma Longifolia (DLBS5055) and Multivitamins (Vitamin C+Vitamin E+ β-carotene) for Infertile Males
NCT07523022PHASE4ENROLLING_BY_INVITATIONComparison of the Effect of Gonadotropin and Clomiphene Citrate Treatment on Sperm Parameters and the Outcome of Assisted Reproductive Procedures in Subfertile Men Based on the APHRODITE Groups
NCT00975117PHASE3COMPLETEDSpermotrend in the Treatment of Male Infertility
NCT01407432PHASE3COMPLETEDImpact of Folates in the Care of the Male Infertility
NCT01895816PHASE3COMPLETEDHerbal Tonic Fertile Supplement(ZO2C5)
NCT02605070PHASE3TERMINATEDPilot Study on the Effects of FSH Treatment on the Epigenetic Characteristics of Spermatozoa in Infertile Patients With Severe Oligozoospermia
NCT07402759PHASE3ACTIVE_NOT_RECRUITINGImpact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men
NCT01880086PHASE2COMPLETEDClomiphene Citrate for the Treatment of Low Testosterone Associated With Chronic Opioid Pain Medication Administration
NCT02061384PHASE2COMPLETEDRA-2 13-cis Retinoic Acid (Isotretinoin)
NCT02421887PHASE2COMPLETEDMales, Antioxidants, and Infertility Trial
NCT05200663PHASE2UNKNOWNEfficacy Comparison of Tamoxifen and Tamoxifen With Antioxidants on Semen Quality of Male With Idiopathic Infertility
NCT05290558PHASE2ACTIVE_NOT_RECRUITINGThe Therapeutic Effects of Bu Shen Yi Jing Pill on Semen Quality in Sub Fertile Males: a Randomized Controlled Trial
NCT06091969PHASE2NOT_YET_RECRUITINGSupplementation for Male Subfertility
NCT01595308PHASE1COMPLETEDA Pilot Study to Evaluate the Effect of Pomegranate Juice on Semen Parameters in Healthy Male Volunteers
NCT02122211PHASE1COMPLETEDCholine Dehydrogenase and Sperm Function: Effects of Betaine
NCT02575924PHASE1UNKNOWNInfluence of Culture Media on Clinical Outcomes in Poor Responders or Severe Male Infertility
NCT01304927PHASE2/PHASE3COMPLETEDVitamin D Supplementation and Male Infertility: The CBG-study a Randomized Clinical Trial
NCT02349945PHASE2/PHASE3COMPLETEDFSH Receptor Polymorphism p.N680S and Efficacy of FSH Therapy
NCT05222841PHASE2/PHASE3COMPLETEDThe Effectiveness of Spermotrend Food Supplement in the Treatment of Male Infertility
NCT05616598PHASE2/PHASE3COMPLETEDEffect of New Oral Treatment for Hepatitis C Virus on Seminal Parameters
NCT02025270PHASE1/PHASE2COMPLETEDMSCs For Treatment of Azoospermic Patients
NCT04541459EARLY_PHASE1UNKNOWNValidation of New Devices Against Ambient Electromagnetic Radiation
NCT05792813EARLY_PHASE1UNKNOWNEfficacy and Safety of Linggui Yangyuan Paste in Patients With Male Infertility
NCT06188936EARLY_PHASE1COMPLETEDHome Semen Analysis Tests As a Screening Tool for Fertility Patients
NCT00012480Not specifiedCOMPLETEDEffect of Environmental Exposures on the Egg Fertilizing Ability of Human Sperm
NCT00044369Not specifiedCOMPLETEDRole of the Toxic Metal Cadmium in the Mechanism Producing Infertility With a Varicocele
NCT00119925Not specifiedUNKNOWN‘SPRING’-Study: Subfertility Guidelines: Patient Related Implementation in the Netherlands Among Gynaecologists
NCT00178516Not specifiedCOMPLETEDVitamin E and Male Infertility
NCT00315029Not specifiedCOMPLETEDPatient-Centered Implementation Trial for Single Embryo Transfer
NCT00341120Not specifiedCOMPLETEDGenetic Causes of Male Infertility
NCT00481403Not specifiedCOMPLETEDStudy of Sperm Molecular Factors Implicated in Male Fertility
NCT00548977Not specifiedCOMPLETEDGenetic Studies Spermatogenic Failure
NCT00596739Not specifiedCOMPLETEDA Study of the Pre- and Post-operative Semen Analyses and Reproductive Hormone Levels of Men Undergoing Weight-reduction Surgery
NCT00756561Not specifiedCOMPLETEDHOP-2A - Intratesticular Hormone Levels
NCT00961558Not specifiedTERMINATEDCanadian Varicocelectomy Initiative (CVI): Effects on Male Fertility and Testicular Function of Varicocelectomy
NCT01075334Not specifiedUNKNOWNIs a Carnitine Based Food Supplement (PorimoreTM) for Infertile Men Superior to Folate and Zinc With Regard to Pregnancy Rates in Intrauterine Insemination Cycles?
NCT01178463Not specifiedUNKNOWNSpermatogonial Stem Cells in Azoospermic Patients: a Comparison Between Obstructive and Non-obstructive Azoospermia
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): androgenetic alopecia, male infertility