1. Gene
  2. SRPRA - SRP receptor subunit alpha Gene

SRPRA - SRP receptor subunit alpha Gene

Homo sapiens

Also known as DP; SRPR; Sralpha

Gene ID: 6734 | Gene type: protein coding

About SRPRA

Cytogenetic location: 11q24.2 Genomic coordinates (GRCh38): 11:126,235,930-126,268,895 (from NCBI)

This gene has 7 transcripts (splice variants), 211 orthologues and 1 paralogue. Ubiquitous expression in thyroid (RPKM 41.3), salivary gland (RPKM 33.7) and 25 other tissues.

Summary

The gene encodes a subunit of the endoplasmic reticulum signal recognition particle receptor that, in conjunction with the signal recognition particle, is involved in the targeting and translocation of signal sequence tagged secretory and membrane proteins across the endoplasmic reticulum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]

SRPRA Products(2)

mRNA Protein Name
NM_001177842.2 NP_001171313.1 signal recognition particle receptor subunit alpha isoform 2
NM_003139.4 NP_003130.2 signal recognition particle receptor subunit alpha isoform 1

SRPRA Protein Structure

SRP-alpha_N

SRP-alpha_N: Signal recognition particle, alpha subunit, N-terminal (27 - 301)

SRP54_N

SRP54_N: SRP54-type protein, helical bundle domain (321 - 393)

SRP54

SRP54: SRP54-type protein, GTPase domain (419 - 636)

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  • 638 a.a.
Protein Preferred Names Protein Names

signal recognition particle receptor subunit alpha

DP-alpha

Related Diseases

Diseases Alias
Shwachman-Diamond Syndrome 1

Shwachman-Diamond Syndrome

Shwachman Syndrome

Shwachman-Bodian-Diamond Syndrome

Sds

Pancreatic Insufficiency And Bone Marrow Dysfunction

Shwachman-Bodian Syndrome

SDS1

Lipomatosis Of Pancreas, Congenital

Congenital Lipomatosis Of Pancreas

Shwachman-Diamond Type Metaphyseal Dysplasia

Metaphyseal Chondrodysplasia, Shwachman Type

Shwachman-Diamond-Oski Syndrome

Severe Congenital Neutropenia

Congenital Neutropenia

Neutropenia, Severe Congenital

Congenital Agranulocytosis

Infantile Genetic Agranulocytosis

Kostmann Disease

Kostmann'S Agranulocytosis

Kostmann'S Syndrome

Severe Infantile Genetic Neutropenia

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
Macaca mulatta SRPRA VGNC VGNC:77885
Canis familiaris SRPRA VGNC VGNC:53450
Rattus norvegicus SRPRA RGD RGD:1311504
Mus musculus SRPRA MGD MGI:1914648
Bos taurus SRPRA VGNC VGNC:56282
Felis catus SRPRA VGNC VGNC:104332