1. Gene
  2. MEOX1 - mesenchyme homeobox 1 Gene

MEOX1 - mesenchyme homeobox 1 Gene

中文名称:间充质同源盒 1

种属: Homo sapiens

同用名: KFS2; MOX1

基因 ID: 4222 | 基因类型: protein coding

关于 MEOX1

Cytogenetic location: 17q21.31 Genomic coordinates (GRCh38): 17:43,640,389-43,661,922 (from NCBI)

This gene has 3 transcripts (splice variants), 199 orthologues, 1 paralogue and is associated with 3 phenotypes. Biased expression in fat (RPKM 15.6), heart (RPKM 8.2) and 11 other tissues.

功能概要

该基因编码非成簇、发散、类似触角足的同源盒基因亚家族的成员。编码的蛋白质可能在调节体节发育的分子信号网络中发挥作用。已经描述了编码不同亚型的选择性剪接转录物变体。[RefSeq 提供,2008 年 7 月]

This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

MEOX1 基因产物(3)

mRNA Protein Name
NM_001040002.2 NP_001035091.1 homeobox protein MOX-1 isoform 3
NM_004527.4 NP_004518.1 homeobox protein MOX-1 isoform 1
NM_013999.4 NP_054705.1 homeobox protein MOX-1 isoform 2
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
23275563 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: 通过直接分析推断
28473536 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

MEOX1 蛋白结构

Homeobox

Homeobox: Homeobox domain (172 - 228)

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

homeobox protein MOX-1

MEOX1 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
Intra MEOX1 P50221 CCDC102B Homo sapiens Q68D86
Validated Y2H
32296183
Intra MEOX1 P50221 MID2 Homo sapiens Q9UJV3-2
Validated Y2H
32296183
Intra MEOX1 P50221 a0a384me25_human Homo sapiens A0A384ME25
Y2H Array
25416956
Intra MEOX1 P50221 a0a384me25_human Homo sapiens A0A384ME25
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 a0a384me25_human Homo sapiens A0A384ME25
Validated Y2H
25416956
Intra MEOX1 P50221 INPP5J Homo sapiens Q15735
Validated Y2H
32296183
Intra MEOX1 P50221 PAGE3 Homo sapiens Q5JUK9
Y2H Array
25416956
Intra MEOX1 P50221 NDOR1 Homo sapiens Q9UHB4
Validated Y2H
32296183
Intra MEOX1 P50221 CCDC103 Homo sapiens Q8IW40
Validated Y2H
32296183
Intra MEOX1 P50221 NEIL2 Homo sapiens Q969S2
Validated Y2H
32296183
Intra MEOX1 P50221 NEIL2 Homo sapiens Q969S2
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 CIB3 Homo sapiens Q96Q77
Validated Y2H
25416956
Intra MEOX1 P50221 CIB3 Homo sapiens Q96Q77
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 TXNL4B Homo sapiens Q9NX01
Validated Y2H
32296183
Intra MEOX1 P50221 SEC14L4 Homo sapiens Q9UDX3
Validated Y2H
32296183
Intra MEOX1 P50221 UNC45A Homo sapiens Q9H3U1
Validated Y2H
32296183
Intra MEOX1 P50221 DUSP3 Homo sapiens P51452
Validated Y2H
32296183
Intra MEOX1 P50221 DMWD Homo sapiens G5E9A7
Validated Y2H
32814053
Intra MEOX1 P50221 DMWD Homo sapiens G5E9A7
Y2H Array
32814053
Intra MEOX1 P50221 DMWD Homo sapiens G5E9A7
Y2H Pooling
32814053
Intra MEOX1 P50221 TRIML2 Homo sapiens Q8N7C3
Validated Y2H
32296183
Intra MEOX1 P50221 TRAPPC2L Homo sapiens Q9UL33-2
Validated Y2H
32296183
Intra MEOX1 P50221 PM20D2 Homo sapiens Q8IYS1
Validated Y2H
32296183
Intra MEOX1 P50221 ZNF410 Homo sapiens Q86VK4-3
Validated Y2H
32296183
Intra MEOX1 P50221 PRKAG1 Homo sapiens P54619
Validated Y2H
32296183
Intra MEOX1 P50221 CACNB3 Homo sapiens P54284
Validated Y2H
32296183
Intra MEOX1 P50221 KCTD7 Homo sapiens Q96MP8-2
Validated Y2H
32296183
Intra MEOX1 P50221 ACOT12 Homo sapiens Q8WYK0
Validated Y2H
32296183
Intra MEOX1 P50221 SPAG8 Homo sapiens Q99932-2
Validated Y2H
32296183
Intra MEOX1 P50221 PPM1F Homo sapiens Q6IPC0
Validated Y2H
32296183
Intra MEOX1 P50221 ATG9A Homo sapiens Q7Z3C6-3
Validated Y2H
32296183
Intra MEOX1 P50221 PDE4C Homo sapiens Q08493-2
Validated Y2H
32296183
Intra MEOX1 P50221 PCP2 Homo sapiens Q8IVA1
Validated Y2H
32296183
Intra MEOX1 P50221 SPIC Homo sapiens Q8N5J4
Validated Y2H
32296183
Intra MEOX1 P50221 UBXN2B Homo sapiens Q14CS0
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 UBXN2B Homo sapiens Q14CS0
Validated Y2H
25416956
Intra MEOX1 P50221 APBB2 Homo sapiens Q92870-2
Validated Y2H
32814053
Intra MEOX1 P50221 APBB2 Homo sapiens Q92870-2
Y2H Pooling
32814053
Intra MEOX1 P50221 APBB2 Homo sapiens Q92870-2
Y2H Array
32814053
Intra MEOX1 P50221 MKRN3 Homo sapiens Q13064
Validated Y2H
32296183
Intra MEOX1 P50221 MID1 Homo sapiens O15344
Y2H Array
31515488
Intra MEOX1 P50221 MID1 Homo sapiens O15344
Validated Y2H
25416956
Intra MEOX1 P50221 MID1 Homo sapiens O15344
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 MID1 Homo sapiens O15344
Y2H Array
25416956
Intra MEOX1 P50221 UBE2R2 Homo sapiens Q712K3
Validated Y2H
32296183
Intra MEOX1 P50221 UBE2R2 Homo sapiens Q712K3
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 HMBOX1 Homo sapiens Q6NT76
Validated Y2H
32296183
Intra MEOX1 P50221 TCP11L1 Homo sapiens Q9NUJ3
Validated Y2H
32296183
Intra MEOX1 P50221 KANK2 Homo sapiens Q63ZY3
Validated Y2H
32296183
Intra MEOX1 P50221 CNOT11 Homo sapiens Q9UKZ1
Validated Y2H
32296183
Intra MEOX1 P50221 QRICH1 Homo sapiens Q2TAL8
Validated Y2H
25416956
Intra MEOX1 P50221 QRICH1 Homo sapiens Q2TAL8
Y2H Array
25416956
Intra MEOX1 P50221 POLR3GL Homo sapiens Q9BT43
Validated Y2H
32296183
Intra MEOX1 P50221 C1orf50 Homo sapiens Q9BV19
Validated Y2H
32296183
Intra MEOX1 P50221 CSNK2A1 Homo sapiens P68400
Validated Y2H
32296183
Intra MEOX1 P50221 MCRS1 Homo sapiens Q96EZ8
Validated Y2H
32296183
Intra MEOX1 P50221 BYSL Homo sapiens Q13895
Validated Y2H
32296183
Intra MEOX1 P50221 TXLNA Homo sapiens P40222
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 TXLNA Homo sapiens P40222
Validated Y2H
25416956
Intra MEOX1 P50221 NAGK Homo sapiens Q9UJ70
Validated Y2H
25416956
Intra MEOX1 P50221 PARVG Homo sapiens Q9HBI0
Validated Y2H
32296183
Intra MEOX1 P50221 ANAPC2 Homo sapiens Q9UJX6
Validated Y2H
32296183
Intra MEOX1 P50221 MORF4L1 Homo sapiens Q9UBU8
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 MORF4L1 Homo sapiens Q9UBU8
Y2H Array
25416956
Intra MEOX1 P50221 PELI2 Homo sapiens Q9HAT8
Validated Y2H
32296183
Intra MEOX1 P50221 CKS1B Homo sapiens P61024
Validated Y2H
25416956
Intra MEOX1 P50221 CKS1B Homo sapiens P61024
Validated Y2H
32296183
Intra MEOX1 P50221 HTT Homo sapiens P42858
Y2H Array
32814053
Intra MEOX1 P50221 EMD Homo sapiens P50402
Validated Y2H
32296183
Intra MEOX1 P50221 SPRED1 Homo sapiens Q7Z699
Validated Y2H
32814053
Intra MEOX1 P50221 SPRED1 Homo sapiens Q7Z699
Y2H Array
32814053
Intra MEOX1 P50221 SPRED1 Homo sapiens Q7Z699
Y2H Pooling
32814053
Intra MEOX1 P50221 CWF19L2 Homo sapiens Q2TBE0
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 CWF19L2 Homo sapiens Q2TBE0
Validated Y2H
32296183
Intra MEOX1 P50221 ZCCHC10 Homo sapiens Q8TBK6
Validated Y2H
32296183
Intra MEOX1 P50221 TRIP10 Homo sapiens Q15642-2
Validated Y2H
32296183
Intra MEOX1 P50221 MAPK9 Homo sapiens P45984
Y2H Array
31515488
Intra MEOX1 P50221 MAPK9 Homo sapiens P45984
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 MAPK9 Homo sapiens P45984
Y2H Array
25416956
Intra MEOX1 P50221 PIN1 Homo sapiens Q13526
Validated Y2H
32296183
Intra MEOX1 P50221 CIAO1 Homo sapiens O76071
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 CIAO1 Homo sapiens O76071
Validated Y2H
25416956
Intra MEOX1 P50221 C14orf119 Homo sapiens Q9NWQ9
Validated Y2H
32296183
Intra MEOX1 P50221 TRIM41 Homo sapiens Q8WV44
Validated Y2H
32296183
Intra MEOX1 P50221 C2CD6 Homo sapiens Q53TS8
Validated Y2H
32296183
Intra MEOX1 P50221 L3MBTL2 Homo sapiens Q969R5
Validated Y2H
32296183
Intra MEOX1 P50221 RBM41 Homo sapiens Q96IZ5
Validated Y2H
32296183
Intra MEOX1 P50221 EIF4EBP1 Homo sapiens Q13541
Validated Y2H
32296183
Intra MEOX1 P50221 APPL1 Homo sapiens Q9UKG1
Y2H Array
25416956
Intra MEOX1 P50221 APPL1 Homo sapiens Q9UKG1
Validated Y2H
25416956
Intra MEOX1 P50221 SYT17 Homo sapiens Q9BSW7
Validated Y2H
25416956
Intra MEOX1 P50221 SYT17 Homo sapiens Q9BSW7
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 GCC1 Homo sapiens Q96CN9
Validated Y2H
32296183
Intra MEOX1 P50221 HOMER3 Homo sapiens Q9NSC5
Validated Y2H
32296183
Intra MEOX1 P50221 PLCD4 Homo sapiens Q9BRC7
Validated Y2H
32296183
Intra MEOX1 P50221 BNIP2 Homo sapiens Q12982
Validated Y2H
32296183
Intra MEOX1 P50221 ALOX5 Homo sapiens P09917
Validated Y2H
25416956
Intra MEOX1 P50221 AIRIM Homo sapiens Q9NX04
Validated Y2H
32296183
Intra MEOX1 P50221 DCX Homo sapiens O43602
Validated Y2H
25416956
Intra MEOX1 P50221 DCX Homo sapiens O43602
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 HYCC2 Homo sapiens Q8IXS8
Validated Y2H
32296183
Intra MEOX1 P50221 MLX Homo sapiens Q9UH92-3
Validated Y2H
32296183
Intra MEOX1 P50221 OSGIN1 Homo sapiens Q9UJX0
Validated Y2H
32296183
Intra MEOX1 P50221 TCEANC Homo sapiens Q8N8B7
Y2H Prey Pooling
25416956
Intra MEOX1 P50221 TCEANC Homo sapiens Q8N8B7
Validated Y2H
25416956
Intra MEOX1 P50221 TCEANC Homo sapiens Q8N8B7
Y2H Array
25416956
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
Klippel-Feil Syndrome 2, Autosomal Recessive

Klippel-Feil Syndrome 2

KFS2

Cervical Vertebral Fusion Autosomal Recessive

Kfs, Autosomal Recessive

Cervical Vertebral Fusion, Autosomal Recessive

Kfs Autosomal Recessive

Klippel-Feil Syndrome, Type 2, Autosomal Recessive

Klippel Feil Syndrome Recessive Type

Isolated Klippel-Feil Syndrome

Congenital Cervical Vertebral Fusion

Congenital Fused Cervical Segments

Klippel-Feil Malformation

Klippel-Feil Sequence

Klippel-Feil Syndrome

Cervical Vertebral Fusion

Congenital Dystrophia Brevicollis

Cervical Fusion Syndrome

Klippel-Feil Deformity

Autosomal Dominant Klippel-Feil Syndrome

Congenital Synostosis Of Cervical Vertebrae

Klippel-Feil And Turner Syndrome

Klippel-Feil Deformity, Deafness And Facial Asymmetry

Klippel Feil Syndrome

Cervical Vertebral Fusion Syndrome

Dystrophia Brevicollis Congenita

Fusion Of Cervical Vertebrae

Kfs

Klippel-Feil Sequence

Vertebral Cervical Fusion Syndrome

Klippel-Feil Syndrome, Autosomal Dominant

Klippel-Feil Malformation

Isolated Klippel-Feil Syndrome

Diaphanospondylodysostosis

Vertebral Ossification, Defect In, With Nephrogenic Rests

DSD

Defect In Vertebral Ossification With Nephrogenic Rests

Marginal Corneal Ulcer
Van Buchem Disease

Hyperostosis Corticalis Generalisata

Hyperphosphatasemia Tarda

VBCH

Sost-Related Sclerosing Bone Dysplasia

Endosteal Hyperostosis Autosomal Recessive

Sclerosteosis

Endosteal Hyperostosis, Autosomal Recessive

Hyperotosis Corticalis Generalisata Familiaris

Sost Sclerosing Bone Dysplasia

Smith-Lemli-Opitz Syndrome

Spondyloepiphyseal Dysplasia Congenita

SEDC

Sed Congenita

Spondyloepiphyseal Dysplasia, Congenital Type

Late Spondyloepiphyseal Dysplasia

Sed, Congenital Type

Congenital Spondyloepiphyseal Dysplasia

Spranger-Wiedemann Disease

Spondyloepiphyseal Dysplasia Congenital Type

Dysplasia, Spondyloepiphyseal, Congenita

Spondyloepiphyseal Dysplasia, Congenita

Spondyloepiphyseal Dysplasia Tarda, X-Linked

Jervell And Lange-Nielsen Syndrome 1

Jervell And Lange-Nielsen Syndrome

Jervell-Lange Nielsen Syndrome

Prolonged Qt Interval In Ekg And Sudden Death

Cardioauditory Syndrome Of Jervell And Lange-Nielsen

Surdo-Cardiac Syndrome

JLNS1

Deafness, Congenital, And Functional Heart Disease

Jlns

Long Qt Interval-Deafness Syndrome

Jervell And Lange-Nielson Syndrome

Jervell Lange-Nielsen Syndrome

Autosomal Recessive Long Qt Syndrome

Cardio-Auditory-Syncope Syndrome

Long Qt Interval-Hearing Loss Syndrome

Congenital Deafness And Functional Heart Disease

Long Qt Interval-Deafness

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 MEOX1 MGD MGI:103220
Canis familiaris MEOX1 VGNC VGNC:43157
Felis catus MEOX1 VGNC VGNC:68234
Macaca mulatta MEOX1 VGNC VGNC:82183
Rattus norvegicus MEOX1 RGD RGD:1308911
Bos taurus MEOX1 VGNC VGNC:31386