ZNRF3 - zinc and ring finger 3 Gene

Also Known as RNF203; BK747E2.3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84133

About ZNRF3

Cytogenetic location: 22q12.1 Genomic coordinates (GRCh38): 22:28,883,572-29,057,488 (from NCBI)

This gene has 3 transcripts (splice variants), 202 orthologues, 1 paralogue and is associated with 81 phenotypes. Ubiquitous expression in kidney (RPKM 4.8), brain (RPKM 4.7) and 24 other tissues.

Summary

Enables Frizzled binding activity and ubiquitin-protein transferase activity. Involved in cellular protein metabolic process and negative regulation of Wnt signaling pathway. Is integral component of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ZNRF3 Products (2)

mRNA Protein Name
NM_001206998.2 NP_001193927.1 E3 ubiquitin-protein ligase ZNRF3 isoform 1 precursor
NM_032173.4 NP_115549.2 E3 ubiquitin-protein ligase ZNRF3 isoform 2
Molecular Function GO Annotation Evidence References Source
enables frizzled binding IPI
IPI: Inferred from physical interaction
22575959 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
22575959 GOA
enables ubiquitin-protein transferase activity IDA
IDA: Inferred from direct assay
22575959 GOA
Biological Process GO Annotation Evidence References Source
involved in Wnt receptor catabolic process IMP
IMP: Inferred from mutant phenotype
22575959 GOA
involved in negative regulation of canonical Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
22575959 GOA
involved in negative regulation of non-canonical Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
22575959 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
22575959 GOA
involved in ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
22575959 GOA
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
22575959 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

ZNRF3 Protein Structure

zf-RING_2

zf-RING_2: Ring finger domain (292 - 334)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 936 a.a.
Protein Preferred Names Protein Names

E3 ubiquitin-protein ligase ZNRF3

  • CTA-292E10.6

ZNRF3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ZNRF3 Q9ULT6 RSPO1 Homo sapiens Q2MKA7
SPR
24165923
Intra
ZNRF3 Q9ULT6 RSPO1 Homo sapiens Q2MKA7 22575959
Intra
ZNRF3 Q9ULT6 RSPO1 Homo sapiens Q2MKA7 22575959
Intra
ZNRF3 Q9ULT6 LGR4 Homo sapiens Q9BXB1 22575959
Intra
ZNRF3 Q9ULT6 FZD6 Homo sapiens O60353 22575959
Intra
ZNRF3 Q9ULT6 LRP6 Homo sapiens O75581 22575959
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ZNRF3 Proteins

Cat. No. Product Name Accession Purity
HY-P78750 ZNRF3 Protein, Human (HEK293, His) Q9ULT6-1 (K56-M219) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Adrenal Carcinoma
  • Adrenal Cancer

  • Adrenal Gland Cancer

  • Malignant Neoplasm Of Adrenal Gland

  • Adrenal Gland Neoplasms

  • Carcinoma Of The Adrenal Gland

  • Adrenal Neoplasm

  • Malignant Adrenal Tumor

  • Neoplasm Of Adrenal Gland

  • Tumor Of The Adrenal Gland

  • Adrenal Gland Neoplasm

  • Adrenocortical Carcinoma

  • Adrenal Gland Malignancy

  • Suprarenal Cancer

  • Malignant Neoplasm Of Suprarenal Gland

  • Malignant Neoplasm Of Adrenal Gland, Unspecified

  • Malignant Tumour Of Adrenal Gland

  • Suprarenal Gland Cancer

  • Primary Malignant Neoplasm Of Adrenal Gland

Tetraamelia Syndrome
  • Tetra-Amelia Syndrome

  • Tetraamelia-Multiple Malformations Syndrome

  • Tetra-Amelia

  • Tetra-Amelia, Autosomal Recessive

  • Tetraamelia, Autosomal Recessive

  • Total Amelia

  • Zimmer Phocomelia

  • Tetams

  • Zimmer Taub Sova Syndrome

Uterine Corpus Endometrial Carcinoma
Osteoblastoma
Adrenal Cortex Disease
  • Adrenal Cortex Diseases

Skin Melanoma
  • Cutaneous Melanoma

  • Malignant Ear Melanoma

  • Malignant Lip Melanoma

  • Malignant Lower Limb Melanoma

  • Malignant Melanoma Of Ear And/Or External Auricular Canal

  • Malignant Melanoma Of Skin Of Lower Limb

  • Malignant Melanoma Of Skin Of Trunk Except Scrotum

  • Malignant Melanoma Of Skin Of Upper Limb

  • Malignant Neck Melanoma

  • Malignant Scalp Melanoma

  • Malignant Trunk Melanoma

  • Malignant Upper Limb Melanoma

  • Melanoma, Cutaneous Malignant

  • Melanoma

  • Malignant Melanoma Of Skin

  • Melanoma Nos

  • Malignant Mole, Meaning Melanoma Of Unspecified Site

  • Melanoma Of Unspecified Site

  • Cutaneous Malignant Melanoma

  • Mm - [Malignant Melanoma]

Adrenal Cortical Carcinoma
  • Adrenocortical Carcinoma

  • Adrenal Cortex Carcinoma

  • Carcinoma Of The Adrenal Cortex

  • Acc

  • Adrenocortical Cancer

  • Carcinoma Adrenocortical

Carney Complex Variant
  • Carney Complex

  • Carney Syndrome

  • Carney Complex, Type 1

  • Lamb Syndrome

  • Name Syndrome

  • Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome

  • Carney Complex - Trismus - Pseudocamptodactyly Syndrome

  • Carney Complex, Type 2

  • Car

  • Cnc1

  • Carney Myxoma-Endocrine Complex

  • Myxoma - Spotty Pigmentation - Endocrine Overactivity

  • Myxoma, Spotty Pigmentation, And Endocrine Overactivity

  • Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome

  • Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome

  • Carney Complex-Trismus-Pseudocamptodactyly Syndrome

  • CACOV

Li-Fraumeni Syndrome
  • Sarcoma Family Syndrome Of Li And Fraumeni

  • Sbla Syndrome

  • LFS

  • Li-Fraumeni Familiar Cancer Susceptibility Syndrome

  • Sarcoma, Breast, Leukaemia And Adrenal Gland Syndrome

  • Lfs1

  • Li Fraumeni Syndrome

  • Sarcoma, Breast, Leukemia, And Adrenal Gland Syndrome

  • Lfl

  • Sbla Syndrome Li-Fraumeni-Like Syndrome

  • Li-Fraumeni Syndrome 1

Beckwith-Wiedemann Syndrome
  • Wiedemann-Beckwith Syndrome

  • BWS

  • Exomphalos-Macroglossia-Gigantism Syndrome

  • Emg Syndrome

  • Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation

  • Emg Abnormality

  • Wbs

  • Exomphalos Macroglossia Gigantism Syndrome

  • Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation

  • Macroglossia Exomphalos Gigantism

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
Felis catus ZNRF3 VGNC VGNC:67372
Macaca mulatta ZNRF3 VGNC VGNC:79114
Canis familiaris ZNRF3 VGNC VGNC:48840
Mus musculus ZNRF3 MGD MGI:3039616
Rattus norvegicus ZNRF3 RGD RGD:1593771
Bos taurus ZNRF3 VGNC VGNC:55766
Others ZNRF3 NCBI