1. Gene
  2. FGF22 - fibroblast growth factor 22 Gene

FGF22 - fibroblast growth factor 22 Gene

中文名称:成纤维细胞生长因子 22

种属: Homo sapiens

基因 ID: 27006 | 基因类型: protein coding

关于 FGF22

Cytogenetic location: 19p13.3 Genomic coordinates (GRCh38): 19:639,879-644,373 (from NCBI)

This gene has 3 transcripts (splice variants), 182 orthologues and 21 paralogues. Biased expression in skin (RPKM 1.5), brain (RPKM 0.4) and 7 other tissues.

功能概要

该基因编码的蛋白质是成纤维细胞生长因子 (FGF) 家族的成员。 FGF 家族成员具有广泛的促有丝分裂和细胞存活活性,并参与多种生物过程,包括胚胎发育、细胞生长、形态发生、组织修复、肿瘤生长和侵袭。该基因的小鼠同系物被发现优先在毛囊的内根鞘中表达,这表明它在毛发发育中发挥作用。可变剪接导致多个转录本变体。[RefSeq 提供,2014 年 7 月]

The protein encoded by this gene is a member of the Fibroblast Growth Factor (FGF) family. FGF Family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The mouse homolog of this gene was found to be preferentially expressed in the inner root sheath of the hair follicle, which suggested a role in hair development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

FGF22 基因产物(2)

mRNA Protein Name
NM_001300812.3 NP_001287741.1 fibroblast growth factor 22 isoform 2 precursor
NM_020637.2 NP_065688.1 fibroblast growth factor 22 isoform 1 precursor

FGF22 蛋白结构

FGF

FGF: Fibroblast growth factor (41 - 165)

  • 0
  • 100
  • 170 a.a.
蛋白主名 其他名称

fibroblast growth factor 22

FGF-22

重组 FGF22 蛋白

目录号 产品名 蛋白编号 纯度
HY-P79140 FGF-22 Protein, Human (His) Q9HCT0 (T23-S170) ≥95%
HY-P700063AF Animal-Free FGF-22 Protein, Human (His) Q9HCT0 (T23-S170) ≥95%
HY-P700494 FGF-22 Protein, Human (His-SUMO) Q9HCT0 (T23-S170) ≥95%

关联疾病

疾病名称 别名
Breast Giant Fibroadenoma

Giant Fibroadenoma

Giant Fibroadenoma Of Breast

Lacrimoauriculodentodigital Syndrome

Ladd Syndrome

Levy-Hollister Syndrome

Lacrimo-Auriculo-Dento-Digital Syndrome

LADD

Lacrimoauriculodento-Digital Syndrome

Levy Hollister Syndrome

Lard Syndrome

Lacrimoauriculoradiodental Syndrome

LADDS

Congenital Duodenal Obstruction Due To Malrotation Of Intestine

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

直系同源

种属 基因名 来源 基因 ID
Mus musculus FGF22 MGD MGI:1914362
Canis familiaris FGF22 VGNC VGNC:40849
Macaca mulatta FGF22 VGNC VGNC:72648
Bos taurus FGF22 VGNC VGNC:52233
Felis catus FGF22 VGNC VGNC:102584
Rattus norvegicus FGF22 RGD RGD:620177
Others FGF22 NCBI