1. Gene
  2. LNX2 - ligand of numb-protein X 2 Gene

LNX2 - ligand of numb-protein X 2 Gene

Homo sapiens

Also known as PDZRN1

Gene ID: 222484 | Gene type: protein coding

About LNX2

Cytogenetic location: 13q12.2 Genomic coordinates (GRCh38): 13:27,545,913-27,621,107 (from NCBI)

This gene has 2 transcripts (splice variants), 206 orthologues and 5 paralogues. Ubiquitous expression in testis (RPKM 9.5), small intestine (RPKM 7.4) and 25 other tissues.

Summary

Predicted to enable ubiquitin-protein transferase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Apr 2022]

LNX2 Products(1)

mRNA Protein Name
NM_153371.4 NP_699202.1 ligand of Numb protein X 2

LNX2 Protein Structure

zf-C3HC4

zf-C3HC4: Zinc finger, C3HC4 type (RING finger) (50 - 86)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (235 - 315)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (339 - 418)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (469 - 544)

PDZ

PDZ: PDZ domain (Also known as DHR or GLGF) (603 - 682)

  • 0
  • 200
  • 400
  • 600
  • 690 a.a.
Protein Preferred Names Protein Names

ligand of Numb protein X 2

PDZ domain containing ring finger 1

Related Diseases

Diseases Alias
Q Fever

Infection Due To Coxiella Burnetii

Quadrilateral Fever

Query Fever

Nine Mile Fever

Coxiella Burnetii Fever

Q Fever Pneumonia

Coxiellosis

Pneumonia In Q Fever

Australian Q Fever

Balkan Grippe

Neutropenia, Severe Congenital, X-Linked

X-Linked Severe Congenital Neutropenia

XLN

SCNX

Severe Congenital Neutropenia X-Linked

Neutropenia, Congenital, Severe, X-Linked

Hyperekplexia

Hereditary Hyperekplexia

Kok Disease

Congenital Stiff Man Syndrome

Familial Startle Disease

Sthe

Stiff-Baby Syndrome

Hereditary Hyperexplexia

Startle Disease

Exaggerated Startle Reaction

Hyperexplexia Hereditary

Startle Disease, Familial

Startle Reaction, Exaggerated

Stiff-Man Syndrome, Congenital

Stiff-Person Syndrome, Congenital

Congenital Stiff-Man Syndrome

Congenital Stiff-Person Syndrome

Familial Hyperekplexia

Startle Syndrome

Stiff Baby Syndrome

Hyperekplexia, Hereditary

Stiff-Person Syndrome

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 LNX2 RGD RGD:1308222
Macaca mulatta LNX2 VGNC VGNC:106268
Felis catus LNX2 VGNC VGNC:63254
Bos taurus LNX2 VGNC VGNC:30946
Canis familiaris LNX2 VGNC VGNC:42732
Mus musculus LNX2 MGD MGI:2155959