2. Gene
  3. ZDBF2 - zinc finger DBF-type containing 2 Gene

ZDBF2 - zinc finger DBF-type containing 2 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：含 DBF 型锌指 2

种属: Homo sapiens

同用名: Slx9

基因 ID: 57683 | 基因类型: protein coding

关于 ZDBF2

Cytogenetic location: 2q33.3 Genomic coordinates (GRCh38): 2:206,274,663-206,314,427 (from NCBI)

This gene has 10 transcripts (splice variants), 1 gene allele and 93 orthologues. Ubiquitous expression in adrenal (RPKM 4.6), brain (RPKM 4.3) and 25 other tissues.

功能概要

该基因编码一种含有 DBF4 型锌指结构域的蛋白质。该基因在淋巴细胞中有印记和父本表达，但在胎盘中更随机地表达。可变剪接导致多个转录本变体。[RefSeq 提供，2015 年 11 月]

This gene encodes a protein containing DBF4-type zinc finger domains. This gene is imprinted and paternally expressed in lymphocytes but is more stochastically expressed in the placenta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]

ZDBF2 基因产物(3)

mRNA Protein Name
NM_001285549.2 NP_001272478.1 DBF4-type zinc finger-containing protein 2 isoform 2
NM_001369654.1 NP_001356583.1 DBF4-type zinc finger-containing protein 2 isoform 1
NM_020923.3 NP_065974.1 DBF4-type zinc finger-containing protein 2 isoform 1

ZDBF2 蛋白结构

zf-DBF

zf-DBF: DBF zinc finger (2 - 32)

  • 0
  • 400
  • 800
  • 1200
  • 1600
  • 2000
  • 2354 a.a.
蛋白主名 其他名称

DBF4-type zinc finger-containing protein 2

关联疾病

疾病名称 别名
Nasopalpebral Lipoma-Coloboma Syndrome

Nasopalpebral Lipoma Coloboma Syndrome

NPLCS

Palpebral Coloboma-Lipoma Syndrome

Palpebral Coloboma Lipoma Syndrome
Achromatopsia 7

ACHM7

Achromatopsia, Type 7
Temple Syndrome

Uniparental Disomy, Maternal, Chromosome 14

Temple Syndrome Due To Paternal 14q32.2 Microdeletion

Paternal Del(14)(Q32.2)

Temple Syndrome Due To Paternal 14q32.2 Hypomethylation

Temple Syndrome Due To Maternal Uniparental Disomy Of Chromosome 14

Upd(14)Mat
Chromosome 2q37 Deletion Syndrome

Albright Hereditary Osteodystrophy-Like Syndrome

2q37 Microdeletion Syndrome

Brachydactyly-Intellectual Disability Syndrome

Deletion 2q37

2q37 Deletion Syndrome

Brachydactyly-Mental Retardation Syndrome

Bdmr

Albright Hereditary Osteodystrophy Type 3

Del(2)(Q37)

Monosomy 2q37qter

Albright'S Hereditary Osteodystrophy-Like Syndrome

Monosomy 2q37

Chromosome Deletion Syndrome 2q37
Pseudohypoparathyroidism, Type Ib

Pseudohypoparathyroidism Type 1b

PHP1B

Pseudohypoparathyroidism Ib

Pseudohypoparathyroidism Type Ib

Php Ib

Pseudohypoparathyroidism 1b
Silver-Russell Syndrome 1

Silver-Russell Syndrome

Russell-Silver Syndrome

Silver-Russell Dwarfism

Rss

SRS1

Srs

Silver Russell Dwarfism

Russell Silver Syndrome

Silver Russell Syndrome
Transient Neonatal Diabetes Mellitus

Diabetes Mellitus, Transient Neonatal

Tndm

Chromosome 6-Associated Transient Diabetes Mellitus

Dmtn

Diabetes Mellitus, 6q24-Related Transient Neonatal

Tndm1

Neonatal Diabetes Mellitus, Transient

Tndm -[Transient Neonatal Diabetes Mellitus]
Kagami-Ogata Syndrome

Paternal Uniparental Disomy Of Chromosome 14

Uniparental Disomy, Paternal, Chromosome 14

Kos

Mca Due To 14q32.2 Maternally Expressed Gene Defect

Paternal Uniparental Disomy 14

Kagami-Ogata Syndrome Due To Maternal 14q32.2 Microdeletion

Maternal Del(14)(Q32.2)

Maternal Monosomy 14q32.2

Kagami-Ogata Syndrome Due To Maternal 14q32.2 Hypermethylation

Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14

Upd(14)Pat
Beckwith-Wiedemann Syndrome

Wiedemann-Beckwith Syndrome

BWS

Exomphalos-Macroglossia-Gigantism Syndrome

Emg Syndrome

Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation

Emg Abnormality

Wbs

Exomphalos Macroglossia Gigantism Syndrome

Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation

Macroglossia Exomphalos Gigantism
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS16010 ZDBF2 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta ZDBF2 VGNC VGNC:99423
Bos taurus ZDBF2 VGNC VGNC:56156
Mus musculus ZDBF2 MGD MGI:1921134
Felis catus ZDBF2 VGNC VGNC:107692
Canis familiaris ZDBF2 VGNC VGNC:48576
Rattus norvegicus ZDBF2 RGD RGD:1560005
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