1. Gene
  2. PHF21B - PHD finger protein 21B Gene

PHF21B - PHD finger protein 21B Gene

中文名称:PHD 指蛋白 21B

种属: Homo sapiens

同用名: PHF4; BHC80L

基因 ID: 112885 | 基因类型: protein coding

关于 PHF21B

Cytogenetic location: 22q13.31 Genomic coordinates (GRCh38): 22:44,881,162-45,010,005 (from NCBI)

This gene has 12 transcripts (splice variants), 173 orthologues and 5 paralogues. Biased expression in testis (RPKM 1.4), brain (RPKM 1.4) and 8 other tissues.

功能概要

预测可启用金属离子结合活性。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Apr 2022]

PHF21B 基因产物(5)

mRNA Protein Name
NM_001135862.3 NP_001129334.1 PHD finger protein 21B isoform 2
NM_001242450.2 NP_001229379.1 PHD finger protein 21B isoform 3
NM_001284296.2 NP_001271225.1 PHD finger protein 21B isoform 4
NM_001413063.1 NP_001399992.1 PHD finger protein 21B isoform 2
NM_138415.5 NP_612424.1 PHD finger protein 21B isoform 1
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
26871637 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

PHF21B 蛋白结构

PHD

PHD: PHD-finger (355 - 398)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 531 a.a.
蛋白主名 其他名称

PHD finger protein 21B

PHD finger protein 4

关联疾病

疾病名称 别名
Mitochondrial Dna Depletion Syndrome 1

MTDPS1

Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Tymp-Related

Myoneurogastrointestinal Encephalopathy Syndrome

Polip Syndrome

Mitochondrial Dna Depletion Syndrome, Type 1

Mngie, Tymp-Related

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, And Intestinal Pseudoobstruction

Mitochondrial Dna Depletion Syndrome 1, Mngie Type

Mitochondrial Neurogastrointestinal Encephalomyopathy

Mitochondrial Neurogastrointestinal Encephalopathy Syndrome Tymp-Related

Myoneurogastrointestinal Encephalomyopathy

Polyneuropathy Ophthalmoplegia Leukoencephalopathy And Intestinal Pseudoobstruction

Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

Chromosome 22q11.2 Deletion Syndrome, Distal

22q11.2 Deletion Syndrome

Autosomal Dominant Opitz G/Bbb Syndrome

Catch22

Cayler Cardiofacial Syndrome

Conotruncal Anomaly Face Syndrome

Digeorge Syndrome

Sedlackova Syndrome

Shprintzen Syndrome

Velocardiofacial Syndrome

22q11.2 Distal Deletion Syndrome

Distal 22q11.2 Microdeletion Syndrome

22q11.2ds

Vcfs

Velo-Cardio-Facial Syndrome

Distal Chromosome 22q11.2 Deletion Syndrome

Chromosome 22q11.2 Deletion Syndrome Distal

Chromosome 22q11.2 Deletion Syndrome

Deletion 22q11.2 Syndrome

22q11ds

Catch 22

Digeorge Sequence

Microdeletion 22q11.2

Monosomy 22q11

Takao Syndrome

Distal Del(22)(Q11.2)

Distal Monosomy 22q11.2

Catch 22 Syndrome

Chromosome Deletion Syndrome 22q11.2, Distal

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
Macaca mulatta PHF21B VGNC VGNC:75861
Rattus norvegicus PHF21B RGD RGD:1308739
Bos taurus PHF21B VGNC VGNC:32822
Canis familiaris PHF21B VGNC VGNC:108212
Mus musculus PHF21B MGD MGI:2443812
Felis catus PHF21B VGNC VGNC:64143