2. Gene
  3. KRTCAP3 - keratinocyte associated protein 3 Gene

KRTCAP3 - keratinocyte associated protein 3 Gene

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

中文名称：角化细胞相关蛋白 3

种属: Homo sapiens

同用名: KCP3

基因 ID: 200634 | 基因类型: protein coding

关于 KRTCAP3

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:27,442,381-27,446,481 (from NCBI)

This gene has 7 transcripts (splice variants), 180 orthologues and 1 paralogue. Broad expression in colon (RPKM 15.6), small intestine (RPKM 13.3) and 22 other tissues.

功能概要

预计是膜的组成部分。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

KRTCAP3 基因产物(3)

mRNA Protein Name
NM_001168364.2 NP_001161836.1 keratinocyte-associated protein 3
NM_001321325.2 NP_001308254.1 keratinocyte-associated protein 3
NM_173853.4 NP_776252.2 keratinocyte-associated protein 3
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
32296183 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

KRTCAP3 蛋白结构

BCLP

BCLP: Beta-casein like protein (19 - 211)

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

keratinocyte-associated protein 3

keratinocytes associated protein 3

KRTCAP3 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
KRTCAP3 Q53RY4 FNDC9 Homo sapiens Q8TBE3
Y2H Array
32296183
种属内
KRTCAP3 Q53RY4 FNDC9 Homo sapiens Q8TBE3
Validated Y2H
32296183
种属内
KRTCAP3 Q53RY4 FNDC9 Homo sapiens Q8TBE3
Y2H Prey Pooling
32296183
种属内
KRTCAP3 Q53RY4 MEOX2 Homo sapiens Q6FHY5
Validated Y2H
32296183
种属内
KRTCAP3 Q53RY4 MEOX2 Homo sapiens Q6FHY5
Y2H Array
32296183
种属内
KRTCAP3 Q53RY4 MEOX2 Homo sapiens Q6FHY5
Y2H Prey Pooling
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
Short-Rib Thoracic Dysplasia 10 With Or Without Polydactyly

SRTD10

Short-Rib Thoracic Dysplasia 10 Without Polydactyly

Short Rib-Polydactyly Syndrome
Retinitis Pigmentosa 71

RP71

Retinitis Pigmentosa, Type 71
Bardet-Biedl Syndrome 22

BBS22

Bardet-Biedl Syndrome 20, Formerly

Bbs20, Formerly
Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy
Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1
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-RS07473 KRTCAP3 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus KRTCAP3 RGD RGD:1596516
Macaca mulatta KRTCAP3 VGNC VGNC:74152
Canis familiaris KRTCAP3 VGNC VGNC:42545
Bos taurus KRTCAP3 VGNC VGNC:30752
Mus musculus KRTCAP3 MGD MGI:1917065
Felis catus KRTCAP3 VGNC VGNC:63176
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z