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  2. FEZF2 - FEZ family zinc finger 2 Gene

FEZF2 - FEZ family zinc finger 2 Gene

中文名称:FEZ 系列锌指 2

种属: Homo sapiens

同用名: FEZ; TOF; FEZL; FKSG36; ZFP312; ZNF312

基因 ID: 55079 | 基因类型: protein coding

关于 FEZF2

Cytogenetic location: 3p14.2 Genomic coordinates (GRCh38): 3:62,369,681-62,373,550 (from NCBI)

This gene has 3 transcripts (splice variants), 193 orthologues and 28 paralogues. Restricted expression toward brain (RPKM 4.1).

功能概要

预测启用转录顺式调节区结合活性。预测参与转录的正调控,DNA 模板化。预计在几个过程的上游或内部起作用,包括 RNA 聚合酶 II 对转录的负调节;神经系统发育;和神经元分化的调节。预计活跃于核心。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable transcription cis-regulatory region binding activity. Predicted to be involved in positive regulation of transcription, DNA-templated. Predicted to act upstream of or within several processes, including negative regulation of transcription by RNA polymerase II; nervous system development; and regulation of neuron differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

FEZF2 基因产物(1)

mRNA Protein Name
NM_018008.4 NP_060478.3 fez family zinc finger protein 2

FEZF2 蛋白结构

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (291 - 315)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (333 - 355)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (375 - 399)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (417 - 440)

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  • 459 a.a.
蛋白主名 其他名称

fez family zinc finger protein 2

forebrain embryonic zinc finger-like protein 2

关联疾病

疾病名称 别名
Uterine Inversion

Inversion Of Uterus During Delivery

Myopathy, Myosin Storage, Autosomal Dominant

MSMA

Myopathy, Hyaline Body, Autosomal Dominant

Myopathy With Lysis Of Type I Myofibrils

Autosomal Dominant Hyaline Body Myopathy

Hyaline Body Myopathy Autosomal Dominant

Thymic Dysplasia
Partial Fetal Alcohol Syndrome
Autoimmune Polyendocrine Syndrome Type 1

Whitaker Syndrome

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy

Autoimmune Polyglandular Syndrome I

Polyglandular Type I Autoimmune Syndrome

Autoimmune Polyendocrine Syndrome

Autoimmune Polyendocrinopathy

Autoimmune Polyglandular Failure

Autoimmune Polyglandular Syndrome

Polyendocrinopathies, Autoimmune

Lloyd'S Syndrome

Aps

Polyendocrinopathies Autoimmune

Polyendocrine Autoimmunity Syndrome

Lloyd Syndrome

Polyglandular Autoimmune Deficiency

Progressive Pluriglandular Insufficiency

Pluriglandular Autoimmune Atrophy

Pluriglandular Autoimmune Syndrome

Thyroid-Adrenocortical Insufficiency Syndrome

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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
Bos taurus FEZF2 VGNC VGNC:28960
Mus musculus FEZF2 MGD MGI:1859823
Felis catus FEZF2 VGNC VGNC:62235
Canis familiaris FEZF2 VGNC VGNC:40829
Rattus norvegicus FEZF2 RGD RGD:1311068
Macaca mulatta FEZF2 VGNC VGNC:72485