1. Gene
  2. SYPL1 - synaptophysin like 1 Gene

SYPL1 - synaptophysin like 1 Gene

Homo sapiens

Also known as SYPL; H-SP1

Gene ID: 6856 | Gene type: protein coding

About SYPL1

Cytogenetic location: 7q22.3 Genomic coordinates (GRCh38): 7:106,090,505-106,112,576 (from NCBI)

This gene has 10 transcripts (splice variants), 236 orthologues and 3 paralogues. Ubiquitous expression in thyroid (RPKM 63.3), esophagus (RPKM 56.9) and 25 other tissues.

Summary

Predicted to be involved in chemical synaptic transmission. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

SYPL1 Products(13)

mRNA Protein Name
NM_001381910.1 NP_001368839.1 synaptophysin-like protein 1 isoform c
NM_001381911.1 NP_001368840.1 synaptophysin-like protein 1 isoform d
NM_001381912.1 NP_001368841.1 synaptophysin-like protein 1 isoform e
NM_001381913.1 NP_001368842.1 synaptophysin-like protein 1 isoform f
NM_001381915.1 NP_001368844.1 synaptophysin-like protein 1 isoform g
NM_001381916.1 NP_001368845.1 synaptophysin-like protein 1 isoform h
NM_001381917.1 NP_001368846.1 synaptophysin-like protein 1 isoform i precursor
NM_001381918.1 NP_001368847.1 synaptophysin-like protein 1 isoform j
NM_001381919.1 NP_001368848.1 synaptophysin-like protein 1 isoform j
NM_001381920.1 NP_001368849.1 synaptophysin-like protein 1 isoform k
NM_001381921.1 NP_001368850.1 synaptophysin-like protein 1 isoform k
NM_006754.5 NP_006745.1 synaptophysin-like protein 1 isoform a
NM_182715.4 NP_874384.1 synaptophysin-like protein 1 isoform b

SYPL1 Protein Structure

MARVEL

MARVEL: Membrane-associating domain (29 - 231)

  • 0
  • 100
  • 200
  • 259 a.a.
Protein Preferred Names Protein Names

synaptophysin-like protein 1

pantophysin

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Dominant 35

MRD35

Intellectual Disability-Macrocephaly-Hypotonia-Behavioral Abnormalities Syndrome

Autosomal Dominant Non-Syndromic Intellectual Disability 35

Mental Retardation, Autosomal Dominant 35

Autosomal Dominant Intellectual Developmental Disorder 35

Autosomal Dominant Mental Retardation 35

Mental Retardation, Autosomal Dominant, Type 35

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 SYPL1 VGNC VGNC:53679
Mus musculus SYPL1 MGD MGI:108081
Canis familiaris SYPL1 VGNC VGNC:47039
Macaca mulatta SYPL1 VGNC VGNC:78073
Rattus norvegicus SYPL1 RGD RGD:1359569