1. Gene
  2. LRIG3 - leucine rich repeats and immunoglobulin like domains 3 Gene

LRIG3 - leucine rich repeats and immunoglobulin like domains 3 Gene

Homo sapiens

Also known as LIG3

Gene ID: 121227 | Gene type: protein coding

About LRIG3

Cytogenetic location: 12q14.1 Genomic coordinates (GRCh38): 12:58,872,155-58,920,504 (from NCBI)

This gene has 9 transcripts (splice variants), 209 orthologues, 22 paralogues and is associated with 69 phenotypes. Broad expression in thyroid (RPKM 16.5), skin (RPKM 7.2) and 24 other tissues.

Summary

Predicted to act upstream of or within otolith morphogenesis. Located in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

LRIG3 Products(2)

mRNA Protein Name
NM_001136051.3 NP_001129523.1 leucine-rich repeats and immunoglobulin-like domains protein 3 isoform 1 precursor
NM_153377.5 NP_700356.2 leucine-rich repeats and immunoglobulin-like domains protein 3 isoform 2 precursor

LRIG3 Protein Structure

LRR_4

LRR_4: Leucine Rich repeats (2 copies) (122 - 161)

LRR_8

LRR_8: Leucine rich repeat (168 - 227)

LRR_8

LRR_8: Leucine rich repeat (312 - 371)

LRR_8

LRR_8: Leucine rich repeat (387 - 442)

I-set

I-set: Immunoglobulin I-set domain (499 - 599)

I-set

I-set: Immunoglobulin I-set domain (603 - 693)

I-set

I-set: Immunoglobulin I-set domain (697 - 784)

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  • 1119 a.a.
Protein Preferred Names Protein Names

leucine-rich repeats and immunoglobulin-like domains protein 3

LIG-3

Related Diseases

Diseases Alias
Urofacial Syndrome 1

Urofacial Syndrome

Ochoa Syndrome

Hydronephrosis With Peculiar Facial Expression

Ufs

Inverted Smile And Occult Neuropathic Bladder

Partial Facial Palsy With Urinary Abnormalities

UFS1

Urofacial Ochoa'S Syndrome

Urofacial Syndrome Type 1

Facial Palsy, Partial, With Urinary Abnormalities

Hydronephrosis-Inverted Smile

Inverted Smile-Neurogenic Bladder

Hydronephrosis-Inverted Smile Syndrome

Inverted Smile-Neurogenic Bladder Syndrome

Partial Facial Palsy Partial With Urinary Abnormalities

Urologic Diseases

Charcot-Marie-Tooth Disease

Cmt

Hmsn

Hereditary Motor And Sensory Neuropathy

Pma

Cmt - Charcot-Marie-Tooth Disease

Charcot Marie Tooth Disease

Charcot-Marie-Tooth Hereditary Neuropathy

Charcot-Marie-Tooth Syndrome

Peroneal Muscular Atrophy

Hereditary Motor And Sensory Neuropathies

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 LRIG3 VGNC VGNC:63282
Bos taurus LRIG3 VGNC VGNC:30984
Macaca mulatta LRIG3 VGNC VGNC:100073
Mus musculus LRIG3 MGD MGI:2443955
Rattus norvegicus LRIG3 RGD RGD:1561255
Canis familiaris LRIG3 VGNC VGNC:42769