SEC61A1 - SEC61 translocon subunit alpha 1 Gene

Also Known as HNFJ4; SEC61; ADTKD5; HSEC61; SEC61A

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 29927

About SEC61A1

Cytogenetic location: 3q21.3 Genomic coordinates (GRCh38): 3:128,051,641-128,071,683 (from NCBI)

This gene has 22 transcripts (splice variants), 283 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in thyroid (RPKM 81.0), placenta (RPKM 70.7) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the SECY/SEC61- alpha family. It appears to play a crucial role in the insertion of secretory and membrane polypeptides into the endoplasmic reticulum. This protein found to be tightly associated with membrane-bound ribosomes, either directly or through adaptor proteins. This gene encodes an alpha subunit of the heteromeric Sec61 complex, which also contains beta and gamma subunits. [provided by RefSeq, Jul 2008]

SEC61A1 Products (3)

mRNA Protein Name
NM_001400328.1 NP_001387257.1 protein transport protein Sec61 subunit alpha isoform 1 isoform 2
NM_001400329.1 NP_001387258.1 protein transport protein Sec61 subunit alpha isoform 1 isoform 3
NM_013336.4 NP_037468.1 protein transport protein Sec61 subunit alpha isoform 1 isoform 1

SEC61A1 Protein Structure

Plug_translocon

Plug_translocon: Plug domain of Sec61p (40 - 74)

SecY

SecY: SecY translocase (75 - 459)

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

protein transport protein Sec61 subunit alpha isoform 1

  • SEC61 translocon alpha 1 subunit

SEC61A1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SEC61A1 P61619 HSPA5 Homo sapiens P11021 22796945
Intra
SEC61A1 P61619 CANX Homo sapiens P27824 22314232
Intra
SEC61A1 P61619 CANX Homo sapiens P27824 22314232
Cross: Cross-species interaction Intra: Intraspecies interaction

SEC61A1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82080 SEC61A Antibody (YA1825) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat
HY-P87069 SEC61A Antibody (YA6762) WB, IHC-P Human, Mouse, Rat

Related Diseases

Diseases Alias
Tubulointerstitial Kidney Disease, Autosomal Dominant, 5
  • Hyperuricemic Nephropathy, Familial Juvenile, 4

  • ADTKD5

  • Hnfj4

  • Hyperuricemic Nephropathy, Familial Juvenile Type 4

  • Familial Juvenile Hyperuricemic Nephropathy 4

Polycystic Liver Disease
  • Autosomal Dominant Polycystic Liver Disease

  • Isolated Polycystic Liver Disease

  • Pcld

  • Congenital Cystic Liver Disease

  • Congenital Hepatic Cyst

  • Fibrocystic Liver Disease

  • Isolated Autosomal Dominant Polycystic Liver Disease

  • Adpcld

  • Liver Disease, Polycystic

  • Multiple Cysts Of Liver

  • Pld - [Polycystic Liver Disease]

  • Polycystic Liver Disorder

  • Polycystic Liver

  • Congenital Polycystic Disease Of Liver

  • Congenital Polycystic Liver Disease

Buruli Ulcer
  • Buruli Ulcer, Susceptibility To

  • Buruli Ulcer Disease

  • Mycobacterium Ulcerans

  • Mycobacterium Ulcerans, Susceptibility To

  • Bairnsdale Ulcer

  • Daintree Ulcer

  • Mossman Ulcer

  • Searl Ulcer

  • Searle'S Ulcer

  • Bud

Kidney Disease
  • Renal Failure

  • Kidney Failure

  • Kidney Diseases

  • Nephropathy

  • Abnormality Of The Kidney

  • Impaired Renal Function Disease

  • Renal Anomaly

  • Kidney Dysfunction

  • Renal Disease

  • Nephropathies

  • Renal Failure Adverse Event

  • Abnormal Renal Function

Autosomal Dominant Severe Congenital Neutropenia
  • Severe Congenital Neutropenia Autosomal Dominant

  • Neutropenia, Congenital, Severe, Autosomal Dominant

Tubulointerstitial Kidney Disease, Autosomal Dominant, 1
  • Familial Juvenile Hyperuricemic Nephropathy

  • Mckd2

  • Familial Juvenile Hyperuricemic Nephropathy Type 1

  • Fjhn

  • Medullary Cystic Kidney Disease 2

  • Uromodulin-Associated Kidney Disease

  • Medullary Cystic Kidney Disease Type 2

  • ADTKD1

  • Hnfj1

  • Glomerulocystic Kidney Disease With Hyperuricemia And Isosthenuria

  • Adtkd-Umod

  • Familial Juvenile Hyperuricemic Nephropathy 1

  • Umod-Related Adtkd

  • Umod-Related Autosomal Dominant Tubulointerstitial Kidney Disease

  • Hyperuricemic Nephropathy, Familial Juvenile, 1

  • Gouty Nephropathy, Familial Juvenile

  • Medullary Cystic Kidney Disease 2, Autosomal Dominant

  • Admckd2

  • Autosomal Dominant Tubulointerstitial Kidney Disease Due To Umod Mutations

  • Adtkd Due To Umod Mutations

  • Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related

  • Autosomal Dominant Medullary Cystic Kidney Disease Type 2

  • Umod-Associated Kidney Disease

  • Uromodulin Kidney Disease

  • Familial Gout-Kidney Disease

  • Familial Gouty Nephropathy

  • Umak

  • Umod-Related Kidney Disease

  • Uromodulin Storage Disease

  • Fjhn1

  • Gouty Nephropathy Familial Juvenile

  • Nephropathy Familial With Gout

  • Hyperuricemic Nephropathy, Familial Juvenile 1

  • Hyperuricemic Nephropathy, Familial Juvenile

  • Kidney Disease, Glomerulocystic, With Hyperuricemia And Isosthenuria

  • Nephropathy, Hyperuricemic, Juvenile, Familial, Type 1

  • Kidney Disease, Cystic, Medullary, Type 2

  • Medullary Cystic Kidney Disease Type Ii

  • Familial Juvenile Gout

Uterine Corpus Sarcoma
  • Sarcoma Of Corpus Uteri

  • Sarcoma Of Uterus

  • Sarcoma Of The Corpus Uteri

  • Uterine Sarcoma

  • Sarcoma, Nos Of Uterus

Retinitis Pigmentosa 61
  • RP61

  • Retinitis Pigmentosa, Type 61

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Zellweger Syndrome
  • Cerebrohepatorenal Syndrome

  • Zellweger Leukodystrophy

  • Zs

  • Congenital Iron Overload

  • Chr

  • Zws

  • Severe Pbd-Zsd

  • Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

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 SEC61A1 VGNC VGNC:49153
Canis familiaris SEC61A1 VGNC VGNC:49614
Mus musculus SEC61A1 MGD MGI:1858417
Rattus norvegicus SEC61A1 RGD RGD:68321
Felis catus SEC61A1 VGNC VGNC:64973
Macaca mulatta SEC61A1 VGNC VGNC:77265
Others SEC61A1 NCBI