LINGO2 - leucine rich repeat and Ig domain containing 2 Gene

Also Known as LERN3; LRRN6C

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 158038

About LINGO2

Cytogenetic location: 9p21.2-p21.1 Genomic coordinates (GRCh38): 9:27,937,617-29,213,601 (from NCBI)

This gene has 9 transcripts (splice variants), 274 orthologues and 25 paralogues. Low expression observed in reference dataset.

Summary

Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be integral component of membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

LINGO2 Products (4)

mRNA Protein Name
NM_001258282.3 NP_001245211.1 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2 precursor
NM_001354574.2 NP_001341503.1 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2 precursor
NM_001354575.2 NP_001341504.1 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2 precursor
NM_152570.4 NP_689783.1 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2 precursor

LINGO2 Protein Structure

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (27 - 56)

LRR_8

LRR_8: Leucine rich repeat (106 - 165)

LRR_1

LRR_1: Leucine Rich Repeat (275 - 296)

LRR_8

LRR_8: Leucine rich repeat (298 - 357)

I-set

I-set: Immunoglobulin I-set domain (415 - 500)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 606 a.a.
Protein Preferred Names Protein Names

leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2

  • leucine rich repeat neuronal 6C

Related Diseases

Diseases Alias
Essential Tremor
  • Benign Essential Tremor

  • Familial Tremor

  • Hereditary Essential Tremor

  • Essential Hereditary Tremor

  • Shaky Hand Syndrome

  • Benign Essential Tremor Syndrome

  • Tremor Hereditary Essential

  • Essential Tremor, Susceptibility To

  • Tremor, Hereditary Essential

Tremor, Hereditary Essential, 5
  • ETM5

  • Essential Tremor 5

  • Essential Tremor, Hereditary, 5

  • Hereditary Essential Tremor 5

  • Tremor, Hereditary Essential 5

  • Tremor, Essential Hereditary, Type 5

Tremor, Hereditary Essential, 4
  • ETM4

  • Essential Tremor 4

  • Essential Tremor, Hereditary, 4

  • Hereditary Essential Tremor 4

  • Tremor, Hereditary Essential 4

  • Tremor, Hereditary Essential, Type 4

Tremor, Hereditary Essential, 1
  • ETM1

  • Fet1

  • Essential Tremor 1

  • Tremor, Familial Essential, 1

  • Essential Tremor, Hereditary, 1

  • Hereditary Essential Tremor 1

  • Tremor Hereditary Essential, 1

  • Tremor Familial Essential, 1

  • Tremor, Hereditary Essential 1

  • Tremor, Essential Hereditary, Type 1

Ectodermal Dysplasia 14, Hair/Tooth Type With Or Without Hypohidrosis
  • ECTD14

  • Ectodermal Dysplasia 14

  • Ectn14

Motion Sickness
  • Airsickness

  • Carsickness

  • Seasickness

  • Travel Sickness

  • Riders' Vertigo

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 LINGO2 VGNC VGNC:63237
Canis familiaris LINGO2 VGNC VGNC:42689
Rattus norvegicus LINGO2 RGD RGD:1310773
Bos taurus LINGO2 VGNC VGNC:30900
Mus musculus LINGO2 MGD MGI:2442298
Macaca mulatta LINGO2 VGNC VGNC:74095
Others LINGO2 NCBI