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

LRIG3 - leucine rich repeats and immunoglobulin like domains 3 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：富亮氨酸的重复序列和免疫球蛋白样结构域 3

种属: Homo sapiens

同用名: LIG3

基因 ID: 121227 | 基因类型: protein coding

关于 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.

功能概要

预测作用于耳石形态发生的上游或内部。位于细胞外空间。 [由基因组资源联盟提供，2022 年 4 月]

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

LRIG3 基因产物(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 蛋白结构

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)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1119 a.a.
蛋白主名 其他名称

leucine-rich repeats and immunoglobulin-like domains protein 3

LIG-3

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (3)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS07789 LRIG3 Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS22616 Lrig3 Mouse Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS29131 Lrig3 Rat Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 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
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