SYCE1 - synaptonemal complex central element protein 1 Gene

Also Known as CT76; POF12; SPGF15; C10orf94

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 93426

About SYCE1

Cytogenetic location: 10q26.3 Genomic coordinates (GRCh38): 10:133,553,899-133,568,291 (from NCBI)

This gene has 5 transcripts (splice variants), 117 orthologues, 1 paralogue and is associated with 4 phenotypes. Biased expression in testis (RPKM 31.6), placenta (RPKM 4.3) and 1 other tissue.

Summary

This gene encodes a member of the synaptonemal complex, which links homologous chromosomes during prophase I of meiosis. The tripartite structure of the complex is highly conserved amongst metazoans. It consists of two lateral elements and a central region formed by transverse elements and a central element. The protein encoded by this gene localizes to the central element and is required for initiation and elongation of the synapsis. Allelic variants of this gene have been associated with premature ovarian failure and spermatogenic failure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]

SYCE1 Products (3)

mRNA Protein Name
NM_001143763.2 NP_001137235.1 synaptonemal complex central element protein 1 isoform 3
NM_001143764.3 NP_001137236.1 synaptonemal complex central element protein 1 isoform 4
NM_130784.4 NP_570140.1 synaptonemal complex central element protein 1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SYCE1 Protein Structure

SYCE1

SYCE1: Synaptonemal complex central element protein 1 (47 - 198)

  • 0
  • 100
  • 200
  • 300
  • 351 a.a.
Protein Preferred Names Protein Names

synaptonemal complex central element protein 1

  • cancer/testis antigen 76

SYCE1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SYCE1 Q8N0S2 CCDC102B Homo sapiens Q68D86 25416956
Intra
SYCE1 Q8N0S2 CCDC102B Homo sapiens Q68D86 25416956
Intra
SYCE1 Q8N0S2 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
SYCE1 Q8N0S2 TPM3 Homo sapiens Q5VU62 25416956
Intra
SYCE1 Q8N0S2 TPM1 Homo sapiens P09493-5 25416956
Intra
SYCE1 Q8N0S2 IQUB Homo sapiens Q8NA54 25416956
Intra
SYCE1 Q8N0S2 BFSP2 Homo sapiens Q13515 25416956
Intra
SYCE1 Q8N0S2 BFSP2 Homo sapiens Q13515 25416956
Intra
SYCE1 Q8N0S2 EDRF1 Homo sapiens Q3B7T1-5 25416956
Intra
SYCE1 Q8N0S2 CBY2 Homo sapiens Q8NA61-2 27107012
Intra
SYCE1 Q8N0S2 CBY2 Homo sapiens Q8NA61-2 32296183
Intra
SYCE1 Q8N0S2 SPATC1L Homo sapiens Q9H0A9-2 32296183
Intra
SYCE1 Q8N0S2 KIFC3 Homo sapiens Q9BVG8 25416956
Intra
SYCE1 Q8N0S2 KIFC3 Homo sapiens Q9BVG8 25416956
Intra
SYCE1 Q8N0S2 SSX2 Homo sapiens Q16385 25416956
Intra
SYCE1 Q8N0S2 SSX2 Homo sapiens Q16385 25416956
Intra
SYCE1 Q8N0S2 RBCK1 Homo sapiens Q9BYM8 25416956
Intra
SYCE1 Q8N0S2 HAUS1 Homo sapiens Q96CS2 25416956
Intra
SYCE1 Q8N0S2 ZNF124 Homo sapiens Q15973 25416956
Intra
SYCE1 Q8N0S2 TXN2 Homo sapiens Q99757 32296183
Intra
SYCE1 Q8N0S2 TSG101 Homo sapiens Q99816 25416956
Intra
SYCE1 Q8N0S2 TSG101 Homo sapiens Q99816 25416956
Intra
SYCE1 Q8N0S2 TSG101 Homo sapiens Q99816 32296183
Intra
SYCE1 Q8N0S2 TSG101 Homo sapiens Q99816 25416956
Intra
SYCE1 Q8N0S2 TPM1 Homo sapiens P09493 25416956
Intra
SYCE1 Q8N0S2 TPM1 Homo sapiens P09493 33961781
Intra
SYCE1 Q8N0S2 TPM3 Homo sapiens P06753 25416956
Intra
SYCE1 Q8N0S2 TPM3 Homo sapiens P06753 25416956
Intra
SYCE1 Q8N0S2 TRAF1 Homo sapiens Q13077 25416956
Intra
SYCE1 Q8N0S2 TRAF1 Homo sapiens Q13077 25416956
Intra
SYCE1 Q8N0S2 KAT5 Homo sapiens Q92993 32296183
Intra
SYCE1 Q8N0S2 SMARCE1 Homo sapiens Q969G3 25416956
Intra
SYCE1 Q8N0S2 SMARCE1 Homo sapiens Q969G3 25416956
Intra
SYCE1 Q8N0S2 SMARCE1 Homo sapiens Q969G3 25416956
Intra
SYCE1 Q8N0S2 WASHC3 Homo sapiens Q9Y3C0 31515488
Intra
SYCE1 Q8N0S2 WASHC3 Homo sapiens Q9Y3C0 25416956
Intra
SYCE1 Q8N0S2 HMG20B Homo sapiens Q9P0W2 25416956
Intra
SYCE1 Q8N0S2 FAM161A Homo sapiens Q3B820 25416956
Intra
SYCE1 Q8N0S2 FAM161B Homo sapiens Q96MY7 32296183
Intra
SYCE1 Q8N0S2 FAM161B Homo sapiens Q96MY7 32296183
Intra
SYCE1 Q8N0S2 TRIM41 Homo sapiens Q8WV44 32296183
Intra
SYCE1 Q8N0S2 HSPB7 Homo sapiens Q9UBY9 25416956
Intra
SYCE1 Q8N0S2 HSPB7 Homo sapiens Q9UBY9 25416956
Intra
SYCE1 Q8N0S2 CINP Homo sapiens Q9BW66 25416956
Intra
SYCE1 Q8N0S2 CINP Homo sapiens Q9BW66 25416956
Intra
SYCE1 Q8N0S2 CINP Homo sapiens Q9BW66 25416956
Intra
SYCE1 Q8N0S2 CYTH3 Homo sapiens O43739 25416956
Intra
SYCE1 Q8N0S2 CYTH3 Homo sapiens O43739 33961781
Intra
SYCE1 Q8N0S2 CYTH3 Homo sapiens O43739 25416956
Intra
SYCE1 Q8N0S2 CBY2 Homo sapiens Q8NA61 25416956
Intra
SYCE1 Q8N0S2 SKA1 Homo sapiens Q96BD8 25416956
Intra
SYCE1 Q8N0S2 SKA1 Homo sapiens Q96BD8 25416956
Intra
SYCE1 Q8N0S2 VPS25 Homo sapiens Q9BRG1 32296183
Intra
SYCE1 Q8N0S2 EXOC8 Homo sapiens Q8IYI6 32296183
Intra
SYCE1 Q8N0S2 NME7 Homo sapiens Q9Y5B8 32296183
Intra
SYCE1 Q8N0S2 BEX2 Homo sapiens Q9BXY8 32296183
Intra
SYCE1 Q8N0S2 HOOK1 Homo sapiens Q9UJC3 25416956
Intra
SYCE1 Q8N0S2 HOOK1 Homo sapiens Q9UJC3 33961781
Intra
SYCE1 Q8N0S2 HOOK1 Homo sapiens Q9UJC3 25416956
Intra
SYCE1 Q8N0S2 MRFAP1L1 Homo sapiens Q96HT8 25416956
Intra
SYCE1 Q8N0S2 MRFAP1L1 Homo sapiens Q96HT8 25416956
Intra
SYCE1 Q8N0S2 ALOX5 Homo sapiens P09917 25416956
Intra
SYCE1 Q8N0S2 STX19 Homo sapiens Q8N4C7 25416956
Intra
SYCE1 Q8N0S2 STX19 Homo sapiens Q8N4C7 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Spermatogenic Failure 15
  • SPGF15

  • Spermatogenic Failure, 15

Premature Ovarian Failure 12
  • POF12

Male Infertility With Azoospermia Or Oligozoospermia Due To Single Gene Mutation
Spermatogenic Failure
  • Azoospermia

  • Spgf

  • Spermatogenic Failure, Susceptibility To

  • Absent Sperm

  • Aspermatogenesis

  • Infertility Due To Azoospermia

  • Hypospermatogenesis

  • Azoospermatism

46 Xx Gonadal Dysgenesis
  • Ovarian Dysgenesis

  • Gonadal Dysgenesis, 46,Xx

  • Dysgenesis, Ovarian

Spermatogenic Failure 10
  • SPGF10

  • Spermatogenic Failure With Defective Sperm Annulus

Premature Menopause
  • Primary Ovarian Insufficiency

  • Premature Ovarian Failure

  • Hypergonadotropic Hypogonadism

  • Premature Ovarian Insufficiency

  • Menopause - Premature

  • Menopause Praecox

  • Menopause Premature

  • Menopause, Premature

  • Female Hypergonadotropic Hypogonadism

  • Hypergonadotrophic Ovarian Failure

  • Primary Female Hypogonadism

  • Pof - [Premature Ovarian Failure]

  • Ovarian Failure

  • Ovarian Secretion Suppression

  • Ovary Hyposecretion

  • Ovary Secretion Deficiency

  • Premature Menopause Nos

Spermatogenic Failure 5
  • Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa

  • Infertility Associated With Multi-Tailed Spermatozoa And Excessive Dna

  • SPGF5

  • Macrocephalic Sperm Head Syndrome

  • Male Infertility Due To Macrozoospermia

  • Infertility Associated With Multitailed Spermatozoa And Excessive Dna

  • Macrozoospermia

  • Male Infertility Due To Large-Headed Multiflagellar Polyploid Spermatozoa

  • Infertility Associated With Multi-Tailed Spermatozoa And Excessive Deoxyribonucleic Acid

  • Large-Headed Multiflagellar Polyploid Spermatozoa

  • Male Infertility With Large-Headed Multiflagellar Polyploid Spermatozoa

Spermatogenic Failure, X-Linked, 1
  • Sertoli Cell-Only Syndrome

  • Germinal Cell Aplasia

  • Del Castillo Syndrome

  • SPGFX1

  • X-Linked Spermatogenic Failure 1

  • Congenital Absence Of Germinal Epithelium Of Testes

Multiple Synostoses Syndrome
  • Symphalangism-Brachydactyly Syndrome

  • Deafness-Hermann Type Symphalangism Syndrome

  • Facio-Audio-Symphalangism

  • Hearing Loss-Hermann Type Symphalangism Syndrome

  • Wl Syndrome

  • Multiple Synostosis Syndrome

Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome
  • Icf Syndrome

  • Immunodeficiency Syndrome, Variable

  • Ciid

  • Centromeric Instability, Immunodeficiency Syndrome

  • Immune Deficiency, Variable, With Centromeric Instability Of Chromosomes 1, 9, And 16

  • Icf

Spermatogenic Failure, Y-Linked, 2
  • SPGFY2

  • Spermatogenic Failure, Nonobstructive, Y-Linked

  • Y-Linked Spermatogenic Failure 2

  • Azoospermia, Nonobstructive, Y-Linked

  • Oligozoospermia, Nonobstructive, Y-Linked

  • Oligospermia, Nonobstructive, Y-Linked

  • Spermatogenic Arrest, Y-Linked

  • Nonobstructive Y-Linked Spermatogenic Failure

  • Spermatogenic Failure Y-Linked 2

  • Azoospermia Non-Obstructive Y-Linked

  • Non-Obstructive Azoospermia And Infertility

  • Oligospermia Non-Obstructive Y-Linked

  • Oligozoospermia Non-Obstructive Y-Linked

  • Spermatogenic Arrest Y-Linked

  • Spermatogenic Failure Nonobstructive Y-Linked

Perrault Syndrome
  • Gonadal Dysgenesis, Xx Type, With Deafness

  • Ovarian Dysgenesis With Sensorineural Deafness

  • Gonadal Dysgenesis, Xx Type

  • Gonadal Dysgenesis With Auditory Dysfunction, Autosomal Recessive Inheritance

  • Gonadal Dysgenesis With Sensorineural Deafness, Autosomal Recessive Inheritance

  • Xx Gonodal Dysgenesis-Deafness Syndrome

  • Xx Gonodal Dysgenesis-Hearing Loss Syndrome

  • Gonadal Dysgenesis Xx Type Deafness

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus SYCE1 VGNC VGNC:35504
Rattus norvegicus SYCE1 RGD RGD:1559853
Felis catus SYCE1 VGNC VGNC:97651
Canis familiaris SYCE1 VGNC VGNC:47014
Mus musculus SYCE1 MGD MGI:1921325
Others SYCE1 NCBI