ASGR1 - asialoglycoprotein receptor 1 Gene

Also Known as HL-1; ASGPR; ASGPR1; CLEC4H1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 432

About ASGR1

Cytogenetic location: 17p13.1 Genomic coordinates (GRCh38): 17:7,173,431-7,179,370 (from NCBI)

This gene has 9 transcripts (splice variants), 155 orthologues and 14 paralogues. Biased expression in liver (RPKM 145.0) and testis (RPKM 4.7).

Summary

This gene encodes a subunit of the asialoglycoprotein receptor. This receptor is a transmembrane protein that plays a critical role in serum glycoprotein homeostasis by mediating the endocytosis and lysosomal degradation of glycoproteins with exposed terminal galactose or N-acetylgalactosamine residues. The asialoglycoprotein receptor may facilitate hepatic Infection by multiple viruses including hepatitis B, and is also a target for liver-specific drug delivery. The asialoglycoprotein receptor is a hetero-oligomeric protein composed of major and minor subunits, which are encoded by different genes. The protein encoded by this gene is the more abundant major subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]

ASGR1 Products (2)

mRNA Protein Name
NM_001197216.3 NP_001184145.1 asialoglycoprotein receptor 1 isoform b
NM_001671.5 NP_001662.1 asialoglycoprotein receptor 1 isoform a
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
21988832 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ASGR1 Protein Structure

Lectin_N

Lectin_N: Hepatic lectin, N-terminal domain (6 - 144)

Lectin_C

Lectin_C: Lectin C-type domain (172 - 279)

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

asialoglycoprotein receptor 1

  • C-type lectin domain family 4 member H1

ASGR1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ASGR1 P07306 CYB5R3 Homo sapiens P00387 32296183
Intra
ASGR1 P07306 CYB5R3 Homo sapiens P00387 32296183
Intra
ASGR1 P07306 CERS2 Homo sapiens Q96G23
Y2H
21988832
Intra
ASGR1 P07306 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
ASGR1 P07306 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
ASGR1 P07306 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
ASGR1 P07306 NEMP1 Homo sapiens O14524-2 32296183
Intra
ASGR1 P07306 NEMP1 Homo sapiens O14524-2 32296183
Intra
ASGR1 P07306 HIBADH Homo sapiens P31937 32296183
Intra
ASGR1 P07306 HIBADH Homo sapiens P31937 32296183
Intra
ASGR1 P07306 HIBADH Homo sapiens P31937 32296183
Intra
ASGR1 P07306 GPX8 Homo sapiens Q8TED1 32296183
Intra
ASGR1 P07306 GPX8 Homo sapiens Q8TED1 32296183
Intra
ASGR1 P07306 GPX8 Homo sapiens Q8TED1 32296183
Intra
ASGR1 P07306 AHNAK2 Homo sapiens Q8IVF2-3 32296183
Intra
ASGR1 P07306 AHNAK2 Homo sapiens Q8IVF2-3 32296183
Intra
ASGR1 P07306 AHNAK2 Homo sapiens Q8IVF2-3 32296183
Intra
ASGR1 P07306 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
ASGR1 P07306 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
ASGR1 P07306 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
ASGR1 P07306 ATP1B4 Homo sapiens Q9UN42 32296183
Intra
ASGR1 P07306 ATP1B4 Homo sapiens Q9UN42 32296183
Intra
ASGR1 P07306 ATP1B4 Homo sapiens Q9UN42 32296183
Intra
ASGR1 P07306 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
ASGR1 P07306 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
ASGR1 P07306 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
ASGR1 P07306 LEUTX Homo sapiens A8MZ59 32296183
Intra
ASGR1 P07306 LEUTX Homo sapiens A8MZ59 32296183
Intra
ASGR1 P07306 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
ASGR1 P07306 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
ASGR1 P07306 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
ASGR1 P07306 SUSD3 Homo sapiens Q96L08 32296183
Intra
ASGR1 P07306 SUSD3 Homo sapiens Q96L08 32296183
Intra
ASGR1 P07306 SUSD3 Homo sapiens Q96L08 32296183
Intra
ASGR1 P07306 FAM209A Homo sapiens Q5JX71 32296183
Intra
ASGR1 P07306 FAM209A Homo sapiens Q5JX71 32296183
Intra
ASGR1 P07306 FAM209A Homo sapiens Q5JX71 32296183
Intra
ASGR1 P07306 AMIGO1 Homo sapiens Q86WK6 32296183
Intra
ASGR1 P07306 AMIGO1 Homo sapiens Q86WK6 32296183
Intra
ASGR1 P07306 AMIGO1 Homo sapiens Q86WK6 32296183
Intra
ASGR1 P07306 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
ASGR1 P07306 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
ASGR1 P07306 RNF19B Homo sapiens Q6ZMZ0 32296183
Intra
ASGR1 P07306 APH1A Homo sapiens Q96BI3 32296183
Intra
ASGR1 P07306 APH1A Homo sapiens Q96BI3 32296183
Intra
ASGR1 P07306 APH1A Homo sapiens Q96BI3 32296183
Intra
ASGR1 P07306 MCEMP1 Homo sapiens Q8IX19 32296183
Intra
ASGR1 P07306 MCEMP1 Homo sapiens Q8IX19 32296183
Intra
ASGR1 P07306 MCEMP1 Homo sapiens Q8IX19 32296183
Intra
ASGR1 P07306 FCGR1A Homo sapiens P12314 32296183
Intra
ASGR1 P07306 FCGR1A Homo sapiens P12314 32296183
Intra
ASGR1 P07306 FCGR1A Homo sapiens P12314 32296183
Intra
ASGR1 P07306 BLCAP Homo sapiens P62952 32296183
Intra
ASGR1 P07306 BLCAP Homo sapiens P62952 32296183
Intra
ASGR1 P07306 BLCAP Homo sapiens P62952 32296183
Intra
ASGR1 P07306 SAR1A Homo sapiens Q9NR31 32296183
Intra
ASGR1 P07306 SAR1A Homo sapiens Q9NR31 32296183
Intra
ASGR1 P07306 SAR1A Homo sapiens Q9NR31 32296183
Intra
ASGR1 P07306 SLC10A1 Homo sapiens Q14973 32296183
Intra
ASGR1 P07306 SLC10A1 Homo sapiens Q14973 32296183
Intra
ASGR1 P07306 SLC10A1 Homo sapiens Q14973 32296183
Intra
ASGR1 P07306 TMX2 Homo sapiens Q9Y320 32296183
Intra
ASGR1 P07306 TMX2 Homo sapiens Q9Y320 32296183
Intra
ASGR1 P07306 TMX2 Homo sapiens Q9Y320 32296183
Intra
ASGR1 P07306 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
ASGR1 P07306 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
ASGR1 P07306 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
ASGR1 P07306 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
ASGR1 P07306 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
ASGR1 P07306 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
ASGR1 P07306 IGFBP5 Homo sapiens P24593 32296183
Intra
ASGR1 P07306 CLDN7 Homo sapiens O95471 32296183
Intra
ASGR1 P07306 CLDN7 Homo sapiens O95471 32296183
Intra
ASGR1 P07306 VSIR Homo sapiens Q9H7M9 32296183
Intra
ASGR1 P07306 VSIR Homo sapiens Q9H7M9 32296183
Intra
ASGR1 P07306 VSIR Homo sapiens Q9H7M9 32296183
Intra
ASGR1 P07306 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
ASGR1 P07306 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
ASGR1 P07306 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
ASGR1 P07306 KIR2DL3 Homo sapiens P43628 32296183
Intra
ASGR1 P07306 KIR2DL3 Homo sapiens P43628 32296183
Intra
ASGR1 P07306 KIR2DL3 Homo sapiens P43628 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ASGR1 Proteins

Cat. No. Product Name Accession Purity
HY-P7610 ASGR1/ASGPR1 Protein, Human (HEK293, His) P07306-1 (Q62-L291) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P78931 ASGR1/ASGPR1 Protein, Human (Biotinylated, HEK293, His-Avi) P07306-1 (Q62-L291) ≥ 95%, as determined by reducing SDS-PAGE.

ASGR1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81553 ASGPR1 Antibody (YA1298) WB, IHC-P, ICC/IF, IP, FC, IF-Tissue Human, Rat

Related Diseases

Diseases Alias
Hepatitis
  • Chronic Hepatitis

  • Chronic Persistent Hepatitis

  • Acute Hepatitis

  • Hepatitis, Chronic

  • Acute And Subacute Liver Necrosis

  • Acute/Subac. Necrosis Of Liver

  • Animal Hepatitis

  • Hepatitis Chronic

  • Hepatitis A

  • Hepatitis, Animal

  • Hepatitis Due To Toxoplasmosis

  • Hepatitis In Toxoplasmosis

  • Toxoplasmal Hepatitis

  • Chronic Hepatitis, Unspecified

  • Chronic Active Hepatitis Nec

  • Other Specified Chronic Hepatitis

  • Chronic Persistent Hepatitis Nec

  • Chronic Lobular Hepatitis Nec

Hepatitis B
  • Chronic Hepatitis B

  • Hepatitis B Infection

  • Serum Hepatitis

  • HBV

  • Hepatitis B Chronic

  • Hbv, Susceptibility To

  • Hepatitis B, Chronic

  • Chronic Hepatitis B Without Delta Agent

  • Chronic Hbv - [Hepatitis B Virus] Infection

  • Hepatitis B Nos

  • Chronic Type B Viral Hepatitis

  • Hep B Nos

Hepatitis E
Autoimmune Hepatitis
  • Aih

  • Hepatitis, Autoimmune

  • Autoimmune Chronic Active Hepatitis

  • Autoimmune Hepatitis With Centrilobular Necrosis

  • Autoimmune Chronic Hepatitis

  • Hepatitis Autoimmune

Acute Gonococcal Cervicitis
  • Gonococcal Cervicitis

  • Acute Gonorrhea Of Cervix

Amelogenesis Imperfecta, Type Ib
  • AI1B

  • Aih2

  • Amelogenesis Imperfecta Type 1b

  • Amelogenesis Imperfecta Type Ib

  • Hereditary Localized Enamel Hypoplasia

  • Amelogenesis Imperfecta - Hypoplastic Autosomal Dominant - Local

  • Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant

  • Enamel Hypoplasia, Hereditary Localized

  • Autosomal Dominant Hypoplastic Local Amelogenesis Imperfecta

  • Amelogenesis Imperfecta 1b

  • Amelogenesis Imperfecta Hypoplastic 2

  • Amelogenesis Imperfecta Hypoplastic Local Autosomal Dominant

Amelogenesis Imperfecta, Type Ie
  • Aih1

  • Amelogenesis Imperfecta Type 1e

  • AI1E

  • Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 1

  • Amelogenesis Imperfecta, Hypomaturation Type, With Snow-Capped Teeth

  • Enamel Hypoplasia, X-Linked

  • Amelogenesis Imperfecta Type Ie

  • Amelogenesis Imperfecta Hypoplastic/Hypomaturation X-Linked 1

  • Enamel Hypoplasia X-Linked

  • Amelogenesis Imperfecta, X-Linked 1

  • Amelogenesis Imperfecta, Type 1e

  • Amelogenesis Imperfecta Hypomaturationtype With Snow-Capped Teeth

  • X-Linked Amelogenesis Imperfecta 1

  • X-Linked Amelogenesis Imperfecta Hypoplastic/Hypomaturation 1

  • X-Linked Enamel Hypoplasia

  • Amelogenesis Imperfecta X-Linked 1

  • Amelogenesis Imperfecta 1e

  • Amelogenesis Imperfecta, Hypoplastic/Hypomaturation Type 1e

  • Amelogenesis Imperfecta Hypomaturation Type With Snow-Capped Teeth

  • Xai

  • X-Linked Amelogenesis Imperfecta

  • Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 2

Acute Cervicitis
Amyloidosis, Hereditary, Transthyretin-Related
  • Transthyretin Amyloidosis

  • Familial Amyloid Polyneuropathy

  • Ttr Amyloid Neuropathy

  • Transthyretin Amyloid Neuropathy

  • Transthyretin Amyloid Polyneuropathy

  • Fap

  • Familial Transthyretin Amyloidosis

  • Amyloidosis Transthyretin Related

  • Type I Familial Amyloid Polyneuropathy

  • Familial Amyloid Polyneuropathy Type I

  • Attrv122i Amyloidosis

  • Hereditary Amyloidosis, Transthyretin-Related

  • Amyloid Polyneuropathy, Familial

  • Attr Amyloidosis

  • Attrm Amyloidosis

  • Corino De Andrade'S Disease

  • Paramyloidosis

  • Transthyretin-Related Hereditary Amyloidosis

  • Ttr Amyloidosis

  • Hereditary Attr Amyloidosis

  • Portuguese Polyneuritic Amyloidosis

  • Portuguese Type Familial Amyloid Neuropathy

  • Swiss Type Amyloid Polyneuropathy

  • Type Ii Familial Amyloid Polyneuropathy

  • Attrv30m Amyloidosis

  • Attrv30m-Related Amyloidosis

  • Familial Amyloid Polyneuropathy, Portuguese-Swedish-Japanese Type

  • Attr Cardiomyopathy

  • Attrv122i-Related Amyloidosis

  • Ttr-Related Amyloid Cardiomyopathy

  • Ttr-Related Cardiac Amyloidosis

  • Transthyretin Amyloid Cardiopathy

  • Transthyretin-Related Familial Amyloid Cardiomyopathy

  • Amyloidosis, Transthyretin-Related

  • AMYL-TTR

  • Amyloidosis I

  • Amyloidosis Ohio Type

  • Amyloidosis Type 7

  • Amyloidosis Vii

  • Amyloid Polyneuropathy

  • Attr

  • Familial Amyloid Polyneuropathy Type Ii

  • Hereditary Amyloidosis Transthyretin-Related

  • Leptomeningeal Amyloidosis

  • Meningocerebrovascular Amyloidosis

  • Oculoleptomeningeal Amyloidosis

  • Familial Amyloid Polyneuropathies

  • Amyloidosis, Leptomeningeal

  • Senile Cardiac Amyloidosis

  • Amyloid Neuropathies, Familial

  • Danish Type Familial Amyloid Cardiomyopathy

  • Familial Amyloid Neuropathy, Portuguese Type

  • Amyloid Polyneuropathy, Swiss Type

  • Hereditary Oculoleptomeningeal Amyloid Angiopathy

  • Amyloid Neuropathies

Crigler-Najjar Syndrome, Type I
  • Crigler-Najjar Syndrome

  • Crigler-Najjar Syndrome Type 1

  • Bilirubin Udp Glucuronyl Transferase Deficiency

  • Crigler Najjar Syndrome

  • Crigler Najjar Syndrome, Type 1

  • Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency

  • Bilirubin-Ugt Deficiency

  • Hyperbilirubinemia, Crigler-Najjar Type I

  • Hblrcn1

  • Familial Nonhemolytic Unconjugated Hyperbilirubinemia

  • Hereditary Unconjugated Hyperbilirubinemia

  • Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency Type 1

  • Bilirubin-Ugt Deficiency Type 1

  • Crigler-Najjar Syndrome 1

  • CN1

  • Cn-I

  • Crigler-Najjar Syndrome Type I

  • Hereditary Unconjugated Hyperbilirubinaemia

  • Ugt Deficiency

  • Bilirubin Glucuronosyltransferase Deficiency

  • Crigler-Najjar Disease Or Syndrome

  • Deficiency Of Glucuronosyltransferase

  • Glucuronyl Transferase Deficiency

  • Glucuronyltransferase Deficiency

  • Udp Glucuronyl Transferase Deficiency

  • Cns - [Crigler-Najjar Syndrome]

  • Congenital Familial Nonhemolytic Jaundice

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
Rattus norvegicus ASGR1 RGD RGD:2160
Mus musculus ASGR1 MGD MGI:88081
Bos taurus ASGR1 VGNC VGNC:26209
Macaca mulatta ASGR1 VGNC VGNC:99120
Others ASGR1 NCBI