1. Gene
  2. FGF16 - fibroblast growth factor 16 Gene

FGF16 - fibroblast growth factor 16 Gene

中文名称:成纤维细胞生长因子 16

种属: Homo sapiens

同用名: MF4; FGF-16

基因 ID: 8823 | 基因类型: protein coding

关于 FGF16

Cytogenetic location: Xq21.1 Genomic coordinates (GRCh38): X:77,447,389-77,457,278 (from NCBI)

This gene has 1 transcript (splice variant), 196 orthologues, 21 paralogues and is associated with 2 phenotypes. Low expression observed in reference dataset.

功能概要

该基因编码的蛋白质家族成员参与多种生物过程,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。该基因在心脏细胞中表达,是心脏正常发育所必需的。在具有掌骨 4-5 融合的个体中也观察到该基因的突变。[RefSeq 提供,2014 年 3 月]

This gene encodes a member of a family of proteins that are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene is expressed in cardiac cells and is required for proper heart development. Mutation in this gene was also observed in individuals with metacarpal 4-5 fusion. [provided by RefSeq, Mar 2014]

FGF16 基因产物(1)

mRNA Protein Name
NM_003868.3 NP_003859.1 fibroblast growth factor 16

FGF16 蛋白结构

FGF

FGF: Fibroblast growth factor (2 - 96)

  • 0
  • 100
  • 116 a.a.
蛋白主名 其他名称

fibroblast growth factor 16

metacarpal 4-5 fusion

重组 FGF16 蛋白

目录号 产品名 蛋白编号 纯度
HY-P7344 FGF-16 Protein, Human (CHO) O43320 (A2-R207) ≥95%
HY-P700059AF Animal-Free FGF-16 Protein, Human (His) O43320 (A1-R207) ≥95%

关联疾病

疾病名称 别名
Metacarpal 4-5 Fusion

Syndactyly Type 8

MF4

Fusion Of Metacarpals 4 And 5

Metacarpals 4 And 5 Fusion

Metacarpal 4 5 Fusion

Syndactyly, Type Iii

Syndactyly Type 3

SDTY3

Ring And Little Finger Syndactyly

Syndactyly Of Fingers Iv And V

Syndactyly Of Fingers 4 And 5

Ringand Little Finger Syndactyly

Syndactyly Of Fingers Four And Five

Syndactyly Of The Ring And Little Finger

Sd3

Syndactyly 3

Syndactyly Type Iii

4-5 Finger Syndactyly

Syndactyly, Type 3

Zygodactyly 1

Zd1

Zygodactyly Type 1

Sd1, Weidenreich Type

Sd1a

Syndactyly Type 1, Weidenreich Type

Syndactyly Type 1a

Zygodactyly, Weidenreich Type

Chromosome 2q35 Duplication Syndrome

Syndactyly

Syndactyly Type 1

Sdty1

Zygodactyly

Syndactyly, Type I

Sd1

Syndactyly, Type 1, With Or Without Craniosynostosis

Symphalangism

Non-Syndromic Syndactyly

Symphalangy

Webbing Of Digits

Syndactyly, Type 1

Syndactyly, Type Iv

Syndactyly Type 4

Polysyndactyly, Haas Type

SDTY4

Haas Type Syndactyly

Sd4

Polysyndactyly Type Haas

Syndactyly 4

Polysyndactyly Haas Type

Syndactyly Type Iv

Beare-Stevenson Cutis Gyrata Syndrome

Cutis Gyrata Syndrome Of Beare And Stevenson

Beare-Stevenson Syndrome

BSTVS

Cutis Gyrata-Acanthosis Nigricans-Craniosynostosis Syndrome

Beare Stevenson Syndrome

Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis

Cutis Gyrata Syndrome Of Beare-Stevenson

Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans

SADDAN

Saddan Dysplasia

Severe Achondroplasia With Developmental Delay And Acanthosis Nigricans

Severe Achondroplasia-Developmental Delay-Acanthosis Nigricans Syndrome

Ssb Syndrome

Skeleton Skin Brain Syndrome

Skeleton-Skin-Brain Syndrome

Achondroplasia

Poland Syndrome

Poland Anomaly

Poland Sequence

Poland Syndactyly

Poland'S Syndrome

Poland'S Anomaly

Poland'S Syndactyly

Acro-Pectoro-Renal Field Defect

Brachydactyly, Absent Pectoral Muscles And Agenesis/Hypoplasia Of Kidneys

Unilateral Defect Of Pectoralis Muscle And Syndactyly Of The Hand

Unilateral Defect Of Pectoralis Major And Syndactyly Of The Hand

Multiple Synostoses Syndrome

Symphalangism-Brachydactyly Syndrome

Deafness-Hermann Type Symphalangism Syndrome

Facio-Audio-Symphalangism

Hearing Loss-Hermann Type Symphalangism Syndrome

Wl Syndrome

Multiple Synostosis Syndrome

Crouzon Syndrome

Crouzon Craniofacial Dysostosis

Craniofacial Dysostosis

Cfd1

Craniofacial Dysostosis Type 1

Crouzon Disease

Crouzon'S Disease

Craniofacial Dysostosis, Type I

Craniofacial Dysarthrosis

Craniofacial Dysostosis Syndrome

CS

Craniofacial Dysostosis Type I

Vogt Cephalosyndactyly

Cardiomyopathy, Familial Hypertrophic, 1

Asymmetric Septal Hypertrophy

Familial Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy 1

CMH1

Hypertrophic Cardiomyopathy 19

CMH

Ventricular Hypertrophy, Hereditary

Ash

Hypertrophic Subaortic Stenosis, Idiopathic

Cardiomyopathy, Familial Hypertrophic

Cardiomyopathy, Hypertrophic, 1, Digenic

Cardiomyopathy, Familial Hypertrophic 1

Hcm

Hereditary Ventricular Hypertrophy

Idiopathic Hypertrophic Subaortic Stenosis

Hypertrophic Cardiomyopathy

Cardiomyopathy, Hypertrophic, Familial

Cardiomyopathy, Hypertrophic, 1

Familial Asymmetric Septal Hypertrophy

Heritable Hypertrophic Cardiomyopathy

Fhc

Cardiomyopathy, Hypertrophic, Familial, Type 1

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
Felis catus FGF16 VGNC VGNC:62248
Macaca mulatta FGF16 VGNC VGNC:72646
Rattus norvegicus FGF16 RGD RGD:71052
Bos taurus FGF16 VGNC VGNC:28973
Mus musculus FGF16 MGD MGI:1931627
Canis familiaris FGF16 VGNC VGNC:40843