1. Gene
  2. IQCE - IQ motif containing E Gene

IQCE - IQ motif containing E Gene

中文名称:含 E 的 IQ 基序

种属: Homo sapiens

同用名: PAPA7; 1700028P05Rik

基因 ID: 23288 | 基因类型: protein coding

关于 IQCE

Cytogenetic location: 7p22.3 Genomic coordinates (GRCh38): 7:2,558,979-2,614,728 (from NCBI)

This gene has 17 transcripts (splice variants), 69 orthologues, 1 paralogue and is associated with 2 phenotypes. Broad expression in testis (RPKM 11.3), brain (RPKM 6.8) and 24 other tissues.

功能概要

参与肢体形态发生。预测为膜的外在成分。预计是质膜蛋白复合物的一部分。 [由基因组资源联盟提供,2022 年 4 月]

Involved in limb morphogenesis. Predicted to be extrinsic component of membrane. Predicted to be part of plasma membrane protein complex. [provided by Alliance of Genome Resources, Apr 2022]

IQCE 基因产物(6)

mRNA Protein Name
NM_001287499.2 NP_001274428.1 IQ domain-containing protein E isoform 3
NM_001287500.2 NP_001274429.1 IQ domain-containing protein E isoform 4
NM_001287501.2 NP_001274430.1 IQ domain-containing protein E isoform 5
NM_001287502.2 NP_001274431.1 IQ domain-containing protein E isoform 6
NM_001410865.1 NP_001397794.1 IQ domain-containing protein E isoform 7
NM_152558.5 NP_689771.3 IQ domain-containing protein E isoform 1

IQCE 蛋白结构

IQ

IQ: IQ calmodulin-binding motif (544 - 561)

IQ

IQ: IQ calmodulin-binding motif (603 - 620)

  • 0
  • 200
  • 400
  • 600
  • 695 a.a.
蛋白主名 其他名称

IQ domain-containing protein E

IQCE 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
IQCE Q6IPM2 HEL-S-72 Homo sapiens B4DJ51
Y2H Array
25416956
种属内
IQCE Q6IPM2 HEL-S-72 Homo sapiens B4DJ51
Validated Y2H
25416956
种属内
IQCE Q6IPM2 q9brl5_human Homo sapiens Q9BRL5
Validated Y2H
25416956
种属内
IQCE Q6IPM2 q9brl5_human Homo sapiens Q9BRL5
Y2H Prey Pooling
25416956
种属内
IQCE Q6IPM2 q9brl5_human Homo sapiens Q9BRL5
Y2H Array
25416956
种属内
IQCE Q6IPM2 GPSM3 Homo sapiens Q9Y4H4
Validated Y2H
32296183
种属内
IQCE Q6IPM2 PSMA3 Homo sapiens P25788
Validated Y2H
25416956
种属内
IQCE Q6IPM2 PSMA3 Homo sapiens P25788
Y2H Array
25416956
种属内
IQCE Q6IPM2 PSMA3 Homo sapiens P25788
Y2H Prey Pooling
25416956
种属内
IQCE Q6IPM2 PSMA3 Homo sapiens P25788
Y2H Array
24722188
种属内
IQCE Q6IPM2 TTC23L Homo sapiens Q6PF05
Y2H Array
24722188
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
Polydactyly, Postaxial, Type A7

PAPA7

Polydactyly, Postaxial, A7

Polydactyly, Postaxial, Type A1

Postaxial Polydactyly Type A

Polydactyly, Postaxial

Postaxial Polydactyly

PAPA1

Postaxial Polydactyly, Type A

Papa

Polydactyly, Postaxial, Types A1 And B

Postaxial Polydactyly Type B

Polydactyly Postaxial

Polydactyly, Postaxial A1

Polydactyly, Postaxial B

PAPB

Postaxial Polydactyly, Type A1/B

Polydactyly, Postaxial, Type A

Pyogenic Arthritis, Pyoderma Gangrenosum And Acne

Postaxial Polydactyly, Type B

Chromosome 2q35 Duplication Syndrome

Syndactyly

Syndactyly Type 1

Sdty1

Zygodactyly

Syndactyly, Type I

Sd1

Syndactyly, Type 1, With Or Without Craniosynostosis

Symphalangism

Non-Syndromic Syndactyly

Symphalangy

Webbing Of Digits

Syndactyly, Type 1

Retinal Degeneration

Degeneration Of Retina

Brachydactyly
Polydactyly

Non-Syndromic Polydactyly

Polydactyly, Postaxial

Postaxial Polydactyly

Supernumerary Digit

Extra Digits

Hyperdactyly

Polydactylia

Polydactylism

Supernumerary Digits

Weyers Acrofacial Dysostosis

Curry-Hall Syndrome

Weyers Acrodental Dysostosis

WAD

Acrodental Dysostosis Of Weyers

Acrofacial Dysostosis, Weyers Type

Acrofacial Dysostosis Of Weyers

Curry Hall Syndrome

Short-Rib Thoracic Dysplasia 14 With Polydactyly

SRTD14

Basal Cell Carcinoma, Infundibulocystic

Basal Cell Carcinoma With Follicular Differentiation

Infundibulocystic Basal Cell Carcinoma

Skin Infundibulocystic Basal Cell Carcinoma

Skin Tag

Fibroepithelial Polyp

Fibroepithelial Polyp Of Skin

Soft Fibroma

Skin Tags

Cutaneous Tag

Gardner Fibroma

Acrochordon

Fibroma Molle

Laurin-Sandrow Syndrome

Sandrow Syndrome

Tetramelic Mirror-Image Polydactyly

Mirror-Image Polydactyly

Mirror Hands And Feet With Nasal Defects

Tmip

LSS

Mip

Mirror Hands And Feets-Nasal Defects Syndrome

Fibula And Ulna, Duplication Of, With Absence Of Tibia And Radius

Miccor Hands And Feet With Nasal Defects

Mipduplication Of Fibuland Ulna With Absence Of Tibia And Radius

Fibula Ulna Duplication Tibia Radius Absence

Laurin Sandrow Syndrome

Duplication Of Fibula And Ulna With Absence Of Tibia And Radius

Segmental Laurin-Sandrow Syndrome

Laurin-Sandrow Syndrome, Segmental

Greig Cephalopolysyndactyly Syndrome

GCPS

Polysyndactyly With Peculiar Skull Shape

Polysyndactyly With Peculiars Skull Shape

Greig Syndrome

Cephalopolysyndactyly Syndrome

Greig Cephalo-Poly-Syndactyly Syndrome

Cephalopolysyndactyly, Greig Syndrome

Aarskog Syndrome

Acrofacial Dysostosis
Ellis-Van Creveld Syndrome

Chondroectodermal Dysplasia

Mesoectodermal Dysplasia

EVC

Ellis Van Creveld Syndrome

Mesodermic Dysplasia

Ellis-Van Creveld Dysplasia

Pallister-Hall Syndrome

PHS

Hypothalamic Hamartomas

Hypothalamic Hamartoblastoma, Hypopituitarism, Imperforate Anus, And Postaxial Polydactyly

Hypothalamic Hamartoblastoma Syndrome

Hamartoma Of The Hypothalamus

Pallister Hall Syndrome

Hall-Pallister Syndrome

Hypothalamic Hamartoblastoma Hypopituitarism Imperforate Anus And Postaxial Polydactyly

Hamartoma, Hypothalamic

Bardet-Biedl Syndrome

Bbs

Biedl-Bardet Syndrome

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
Mus musculus IQCE MGD MGI:1921489
Canis familiaris IQCE VGNC VGNC:42076
Macaca mulatta IQCE VGNC VGNC:73678
Rattus norvegicus IQCE RGD RGD:1311349
Felis catus IQCE VGNC VGNC:62962
Bos taurus IQCE VGNC VGNC:30253