1. Gene
  2. ZNRF3 - zinc and ring finger 3 Gene

ZNRF3 - zinc and ring finger 3 Gene

Homo sapiens

Also known as RNF203; BK747E2.3

Gene ID: 84133 | Gene type: protein coding

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
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference 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 Reference 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 Reference 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 Reference
Intra
ZNRF3 Q9ULT6 RSPO1 Homo sapiens Q2MKA7
SPR
24165923
Intra
ZNRF3 Q9ULT6 RSPO1 Homo sapiens Q2MKA7
Pull Down
22575959
Intra
ZNRF3 Q9ULT6 RSPO1 Homo sapiens Q2MKA7
Anti Tag CoIP
22575959
Intra
ZNRF3 Q9ULT6 LGR4 Homo sapiens Q9BXB1
Anti Tag CoIP
22575959
Intra
ZNRF3 Q9ULT6 FZD6 Homo sapiens O60353
Anti Bait CoIP
22575959
Intra
ZNRF3 Q9ULT6 LRP6 Homo sapiens O75581
Anti Bait CoIP
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%

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