2. Gene
  3. OOEP - oocyte expressed protein Gene

OOEP - oocyte expressed protein Gene

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

中文名称：卵母细胞表达蛋白

种属: Homo sapiens

同用名: KHDC2; FLOPED; HOEP19; C6orf156

基因 ID: 441161 | 基因类型: protein coding

关于 OOEP

Cytogenetic location: 6q13 Genomic coordinates (GRCh38): 6:73,368,555-73,369,897 (from NCBI)

This gene has 3 transcripts (splice variants), 98 orthologues and 1 paralogue. Biased expression in testis (RPKM 5.4), placenta (RPKM 0.5) and 1 other tissue.

功能概要

预测启用 RNA 结合活性。预计参与多个过程，包括细胞骨架组织；通过同源重组正调控双链断裂修复；和减数分裂核分裂的正调控。预计在几个过程的上游或内部起作用，包括胚胎植入；子宫内胚胎发育；和蛋白质磷酸化。位于细胞质和细胞核中。皮质下母体复合体的一部分。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable RNA binding activity. Predicted to be involved in several processes, including Cytoskeleton organization; positive regulation of double-strand break repair via homologous recombination; and positive regulation of meiotic nuclear division. Predicted to act upstream of or within several processes, including embryo implantation; in utero embryonic development; and protein phosphorylation. Located in cytoplasm and nucleus. Part of subcortical maternal complex. [provided by Alliance of Genome Resources, Apr 2022]

OOEP 基因产物(1)

mRNA Protein Name
NM_001080507.3 NP_001073976.1 oocyte-expressed protein homolog
基因本体论
  • 分子功能
  • 细胞组分
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
25542835 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
25542835 GOA
located in nucleus IDA
IDA: 通过直接分析推断
25542835 GOA
part of protein-containing complex IDA
IDA: 通过直接分析推断
26537248 GOA
part of subcortical maternal complex IDA
IDA: 通过直接分析推断
25542835 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
蛋白主名 其他名称

oocyte-expressed protein homolog

KH homology domain containing 2

OOEP 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
OOEP A6NGQ2 ABI2 Homo sapiens Q9NYB9-2
Validated Y2H
32296183
种属内
OOEP A6NGQ2 TCEANC Homo sapiens Q8N8B7-2
Validated Y2H
32296183
种属内
OOEP A6NGQ2 KHDC3L Homo sapiens Q587J8
Anti Tag CoIP
25542835
种属内
OOEP A6NGQ2 LONRF1 Homo sapiens Q17RB8
Validated Y2H
32296183
种属内
OOEP A6NGQ2 TLE6 Homo sapiens Q9H808-1
Anti Tag CoIP
25542835
种属内
OOEP A6NGQ2 SNRPB Homo sapiens P14678-2
Validated Y2H
32296183
种属内
OOEP A6NGQ2 NTAQ1 Homo sapiens Q96HA8
Validated Y2H
32296183
种属内
OOEP A6NGQ2 ENKD1 Homo sapiens Q9H0I2
Validated Y2H
32296183
种属内
OOEP A6NGQ2 ALOX5 Homo sapiens P09917
Validated Y2H
32296183
种属内
OOEP A6NGQ2 KIF9 Homo sapiens Q9HAQ2
Validated Y2H
32296183
种属内
OOEP A6NGQ2 AIRIM Homo sapiens Q9NX04
Validated Y2H
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Gestational Trophoblastic Neoplasm

Hydatidiform Mole

Molar Pregnancy

Gestational Trophoblastic Neoplasia

Gestational Trophoblastic Tumor

Gtn

Gestational Trophoblastic Disease

Gestational Trophoblastic Neoplasms

Hydatidiform Mole, Recurrent, 1

Hydatidiform Mole Benign

Trophoblastic Disease

Trophoblastic Disease Nos

Trophoblastic Disorder

Vesicular Mole Nos

Vesicular Mole

Hydatidiform Mole Nos
Trophoblastic Neoplasm

Trophoblastic Tumor

Trophoblastic Neoplasms
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
Pseudohypoparathyroidism, Type Ib

Pseudohypoparathyroidism Type 1b

PHP1B

Pseudohypoparathyroidism Ib

Pseudohypoparathyroidism Type Ib

Php Ib

Pseudohypoparathyroidism 1b
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
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
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-RS09788 OOEP Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Canis familiaris OOEP VGNC VGNC:44125
Rattus norvegicus OOEP RGD RGD:1311103
Macaca mulatta OOEP VGNC VGNC:82201
Bos taurus OOEP VGNC VGNC:32431
Felis catus OOEP VGNC VGNC:97545
Mus musculus OOEP MGD MGI:1915218
Others OOEP NCBI
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