STPG2 - sperm tail PG-rich repeat containing 2 Gene

Also Known as C4orf37

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 285555

About STPG2

This gene has 3 transcripts (splice variants), 144 orthologues and 5 paralogues. Low expression observed in reference dataset.

STPG2 Products (1)

mRNA Protein Name
NM_174952.3 NP_777612.1 sperm-tail PG-rich repeat-containing protein 2

STPG2 Protein Structure

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (21 - 30)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (63 - 73)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (119 - 148)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (157 - 203)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (213 - 243)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (257 - 268)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (351 - 377)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (400 - 410)

SHIPPO-rpt

SHIPPO-rpt: Sperm-tail PG-rich repeat (433 - 443)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 459 a.a.
Protein Preferred Names Protein Names

sperm-tail PG-rich repeat-containing protein 2

Related Diseases

Diseases Alias
Floating-Harbor Syndrome

  • FLHS

  • Fhs

  • Pelletier-Leisti Syndrome

  • Short Stature With Delayed Bone Age, Expressive Language Delay, A Triangular Face With A Prominent Nose And Deep-Set Eyes

  • Leisti-Hollander-Rimoin Syndrome
Sotos Syndrome 2

  • Sotos2

  • Sotos Syndrome, Type 2
Marshall-Smith Syndrome

  • MRSHSS

  • Accelerated Skeletal Maturation-Facial Dysmorphism-Failure To Thrive Syndrome

  • Mss
Helsmoortel-Van Der Aa Syndrome

  • HVDAS

  • Mrd28

  • Adnp Syndrome

  • Adnp-Related Syndromic Intellectual Disability-Autism Spectrum Disorder

  • Mental Retardation, Autosomal Dominant 28

  • Adnp-Related Multiple Congenital Anomalies - Intellectual Disability - Autism Spectrum Disorder

  • Mental Retardation, Autosomal Dominant 28, Formerly

  • Mrd28, Formerly

  • Autosomal Dominant Mental Retardation 28

  • Adnp-Related Intellectual Disability And Autism Spectrum Disorder

  • Adnp-Related Multiple Congenital Anomalies-Intellectual Disability-Autism Spectrum Disorder
Hypotonia-Cystinuria Syndrome

  • Cystinuria With Mitochondrial Disease

  • 2p21 Microdeletion Syndrome

  • HCS

  • Homozygous 2p16 Deletion Syndrome, Formerly

  • 2p21 Deletion Syndrome

  • Del(2)(P21)

  • Monosomy 2p21

  • Atypical Hypotonia-Cystinuria Syndrome

  • Atypical Hcs
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13956 STPG2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus STPG2 MGD MGI:2685863
Rattus norvegicus STPG2 RGD RGD:1591946
Macaca mulatta STPG2 VGNC VGNC:78231
Bos taurus STPG2 VGNC VGNC:106957
Canis familiaris STPG2 VGNC VGNC:46936
Others STPG2 NCBI