1. Gene
  2. FGF17 - fibroblast growth factor 17 Gene

FGF17 - fibroblast growth factor 17 Gene

中文名称:成纤维细胞生长因子 17

种属: Homo sapiens

同用名: HH20; FGF-13; FGF-17

基因 ID: 8822 | 基因类型: protein coding

关于 FGF17

Cytogenetic location: 8p21.3 Genomic coordinates (GRCh38): 8:22,039,672-22,048,809 (from NCBI)

This gene has 4 transcripts (splice variants), 100 orthologues, 21 paralogues and is associated with 4 phenotypes. Low expression observed in reference dataset.

功能概要

该基因编码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,并参与多种生物学过程,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。这种蛋白质在胚胎发生过程中以及在成人小脑和皮质中表达,可能对血管生长和正常大脑发育至关重要。该基因的突变是低促性腺激素性性腺功能减退症 20 伴或不伴嗅觉缺失的原因。交替剪接导致多个转录本变体。[RefSeq 提供,2015 年 1 月]

This gene encodes a member of the Fibroblast Growth Factor (FGF) family. Member of the FGF Family 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. This protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

FGF17 基因产物(2)

mRNA Protein Name
NM_001304478.1 NP_001291407.1 fibroblast growth factor 17 isoform 2 precursor
NM_003867.4 NP_003858.1 fibroblast growth factor 17 isoform 1 precursor

FGF17 蛋白结构

FGF

FGF: Fibroblast growth factor (53 - 175)

  • 0
  • 100
  • 200
  • 216 a.a.
蛋白主名 其他名称

fibroblast growth factor 17

重组 FGF17 蛋白

目录号 产品名 蛋白编号 纯度
HY-P72652 FGF-17 Protein, Human (HEK293, His) O60258 (T23-T216) ≥95%
HY-P72653 FGF-17 Protein, Mouse (His) P63075 (T23-T216) ≥95%
HY-P700060AF Animal-Free FGF-17 Protein, Human (His) O60258 (T23-T216) ≥95%
HY-P71905A FGF-17 Protein, Human (His) O60258 (T23-T216) ≥95%
HY-P700287 FGF-17 Protein, Human O60258 (T23-T216) ≥95%

关联疾病

疾病名称 别名
Hypogonadotropic Hypogonadism 20 With Or Without Anosmia

HH20

Hypogonadotropic Hypogonadism 20 Without Anosmia

Hypogonadism, Hypogonadotropic, Type 20 With/Without Anosmia

Normosmic Congenital Hypogonadotropic Hypogonadism

Normosmic Idiopathic Hypogonadotropic Hypogonadism

Nihh

Kallmann Syndrome

Hypogonadism With Anosmia

Kallman'S Syndrome

Anosmic Hypogonadism

Anosmic Idiopathic Hypogonadotropic Hypogonadism

Hypogonadotropic Hypogonadism And Anosmia

Hypogonadotropic Hypogonadism-Anosmia Syndrome

Olfacto-Genital Pathological Sequence

Familial Hypogonadism With Anosmia

Kallman Syndrome

Dysplasia Olfactogenitalis Of De Morsier

Kallmann'S Syndrome

Congenital Hypogonadotropic Hypogonadism With Anosmia

Hypogonadotropic Hypogonadism 7 With Or Without Anosmia

Idiopathic Hypogonadotropic Hypogonadism

HH7

Hypogonadism, Isolated Hypogonadotropic

Ihh

Hypogonadism, Isolated, Hypogonadotropic

Hypogonadotropic Hypogonadism

Isolated Hypogonadotropic Hypogonadism

Hypogonadotropic Hypogonadism 7 Without Anosmia

Congenital Hypogonadotropic Hypogonadism Normosmic

Hh

Klinefelter Syndrome

Isolated Gonadotropin Deficiency

Hypogonadotropic Hypogonadism

Klinefelter Syndrome

Klinefelter'S Syndrome

Xxy Syndrome

Xxy Trisomy

Hypogonadotropism

47, Xxy

Congenital Idiopathic Hypogonadotropic Hypogonadism

Isolated Congenital Gonadotropin Deficiency

47,Xxy Syndrome

47, Xxy Syndrome

Klinefelters Syndrome

Hypogonadism

Klinefelter Syndrome In Males

Klinefelter Syndrome, Unspecified

Klinefelter Syndrome Karyotype 47, Xxy

Hypogonadism
Generalized Epilepsy With Febrile Seizures Plus, Type 8

GEFSP8

Gefs+8

Generalized Epilepsy With Febrile Seizures Plus 8

Gefs+, Type 8

Generalised Epilepsy With Febrile Seizures Plus 8

Generalised Epilepsy With Febrile Seizures Plus Type 8

Generalized Epilepsy With Febrile Seizures Plus Type 8

Spinocerebellar Ataxia, X-Linked 5

SCAX5

X-Linked Spinocerebellar Ataxia 5

X-Linked Non Progressive Cerebellar Ataxia

Generalized Epilepsy With Febrile Seizures Plus, Type 4

GEFSP4

Gefs+4

Generalized Epilepsy With Febrile Seizures Plus 4

Gefs+, Type 4

Generalised Epilepsy With Febrile Seizures Plus 4

Generalised Epilepsy With Febrile Seizures Plus Type 4

Generalized Epilepsy With Febrile Seizures Plus Type 4

Febrile Seizures, Familial, 7

FEB7

Febrile Convulsions, Familial, 7

Familial Febrile Seizures 7

Familial Febrile Convulsions 7

Febrile Seizures, Familial, 9

FEB9

Febrile Convulsions, Familial, 9

Familial Febrile Seizures 9

Familial Febrile Convulsions 9

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

Intracranial Cavernous Angioma

Intracranial Cavernoma

Intracranial Cavernous Hemangioma

Intracranial Structure Hemangioma

Angioma Of Intracranial Structure

Hemangioma Of Intracranial Structure

Hemangioma Of Intracranial Structures

Hypotrichosis
Hypertrichosis Universalis Congenita, Ambras Type

Ambras Syndrome

Hypertrichosis, Congenital Generalized

HTC1

HTC2

Chromosome Xq27.1 Interchromosomal Insertion Syndrome

Cgh

Hcg

Ambras Type Hypertrichosis Universalis Congenita

X-Linked Congenital Generalized Hypertrichosis

Congenital Generalized Hypertrichosis, Macias-Flores Type

Macias Flores-Garcia Cruz-Rivera Syndrome

Htc 1

Hypertrichosis Universalis Congenita Ambras Type

Hypertrichosis Congenital Generalized X-Linked

Macias-Flores Garcia-Cruz Rivera Syndrome

Congenital Generalized Hypertrichosis, Ambras Type

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

Familial Febrile Seizures

Familial Febrile Convulsions

Feb

Febrile Seizures, Familial

Sensorineural Hearing Loss

Sensory Hearing Loss

Sensorineural Deafness

Sensorineural Hearing Loss Disorder

Hearing Loss, Sensorineural

Central Hearing Loss

High Frequency Deafness

High Frequency Hearing Loss

High-Frequency Hearing Loss

Perceptive Deafness

Perceptive Hearing Loss

Perceptive Hearing Loss Or Deafness

Hearing Loss Sensorineural

Deafness Sensorineural

Hearing Loss High-Frequency

Hearing Loss, Central

Hearing Loss, High-Frequency

Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

Septooptic Dysplasia

Septo-Optic Dysplasia

De Morsier Syndrome

Growth Hormone Deficiency With Pituitary Anomalies

SOD

Pituitary Hormone Deficiency, Combined, 5

Septo-Optic Dysplasia Spectrum

Septo-Optic Dysplasia With Growth Hormone Deficiency

Pituitary Hormone Deficiency, Combined 5

Hypopituitarism And Septooptic 'Dysplasia'

GHDPA

CPHD5

Dysplasia, Septo-Optic

Kallmann Syndrome

Orofacial Cleft

Cleft, Orofacial

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
Rattus norvegicus FGF17 RGD RGD:2607
Mus musculus FGF17 MGD MGI:1202401
Bos taurus FGF17 VGNC VGNC:56967
Canis familiaris FGF17 VGNC VGNC:40844
Felis catus FGF17 VGNC VGNC:62249
Others FGF17 NCBI