1. Gene
  2. STPG2 - sperm tail PG-rich repeat containing 2 Gene

STPG2 - sperm tail PG-rich repeat containing 2 Gene

Homo sapiens

Also known as C4orf37

Gene ID: 285555 | Gene type: protein coding

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

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