KEGG ORTHOLOGY: K24403

ORTHOLOGY: K24403

Entry

K24403                      KO

Symbol

KIAA0319, AAVR

Name

dyslexia-associated protein KIAA0319

Disease

H01899

Dyslexia

Brite

KEGG Orthology (KO) [BR:ko00001]
09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking
    K24403  KIAA0319, AAVR; dyslexia-associated protein KIAA0319
Membrane trafficking [BR:ko04131]
Endocytosis
  Clathrin-mediated endocytosis
   Others
    K24403  KIAA0319, AAVR; dyslexia-associated protein KIAA0319

Genes

HSA:	9856(DYLX2)

PTR:

PPS:

GGO:

PON:

NLE:

HMH:

MCC:

MCF:

MTHB:

MNI:

CSAB:

CATY:

PANU:

TGE:

MLEU:

RRO:

RBB:

TFN:

PTEH:

CANG:

CJC:

SBQ:

CIMI:

CSYR:

MMUR:

LCAT:

PCOQ:

OGA:

MMU:	210108(D130043K22Rik)

MCAL:

110308163

MPAH:

110334012(Kiaa0319)

RNO:

MCOC:

ANU:

MUN:

CGE:

MAUA:

PROB:

PLEU:

MORG:

AAMP:

HGL:

CPOC:

DORD:

DSP:

PLOP:

NCAR:

MMMA:

OCU:

OPI:

GVR:

CFA:

CLUD:

VVP:

VLG:

NPO:

AML:

UMR:

UAH:

UAR:

ELK:

LLV:

MPUF:

MNP:

MLK:

NVS:

ORO:

EJU:

ZCA:

MLX:

NSU:

FCA:

PYU:

PCOO:

PBG:

PVIV:

LRUF:

PTG:

PPAD:

PUC:

AJU:

BTA:

BOM:

BIU:

BBUB:

BBIS:

CHX:

OAS:

BTAX:

ODA:

CCAD:

MBEZ:

SSC:

CFR:

CBAI:

CDK:

VPC:

BACU:

BMUS:

LVE:

OOR:

DLE:

PCAD:

PSIU:

NASI:

ECB:

EPZ:

EAI:

RFQ:

TOD:

LAV:

TMU:

MDO:

GAS:

SHR:

AFZ:

PCW:

GGA:

PCOC:

MGP:

CJO:

TPAI:

LMUT:

NMEL:

APLA:

ACYG:

CATA:

AFUL:

TGU:

LSR:

SCAN:

PMOA:

OTC:

PRUF:

GFR:

FAB:

OMA:

PHI:

PMAJ:

CCAE:

CCW:

CBRC:

ETL:

ZAB:

ACHL:

SVG:

MMEA:

HRT:

FPG:

FCH:

CLV:

EGZ:

NNI:

PLET:

PCAO:

ACUN:

TALA:

PADL:

AFOR:

ACHC:

HALD:

HLE:

AGEN:

GCL:

CCRI:

CMAC:

MUI:

BREG:

FGA:

GSTE:

LDI:

MNB:

OHA:

NNT:

SHAB:

DPUB:

CPEA:

AVIT:

CVF:

RTD:

CUCA:

TEO:

BRHI:

AAM:

AROW:

NPD:

TGT:

DNE:

SCAM:

ASN:

AMJ:

CPOO:

GGN:

PSS:

CMY:

CCAY:

DCC:

CPIC:

TST:

CABI:

MRV:

ACS:

ASAO:

PVT:

SUND:

PBI:

CTIG:

PGUT:

APRI:

PTEX:

NSS:

VKO:

PMUA:

PRAF:

ZVI:

HCG:

GJA:

STOW:

EMC:

XTR:

NPR:

RTEM:

BBUF:

BGAR:

DRE:	794624(si:ch73-215d9.1)

SRX:

SANH:

SGH:

CCAR:

CAUA:

CGIB:

PTET:

LROH:

OMC:

PPRM:

RKG:

MAMB:

CIDE:

MASI:

TROS:

TDW:

MANU:

IPU:

IFU:

PHYP:

SMEO:

TFD:

TVC:

AMEX:

CMAO:

EEE:

CHAR:

SFM:

AANG:

LOC:

PSPA:

ARUT:

LCM:

CMK:

CPLA:

HOC:

LERI:

LRJ:

Reference

PMID:16600991

Authors

Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, Loturco J, Monaco AP

Title

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.

Journal

Hum Mol Genet 15:1659-66 (2006)
DOI:10.1093/hmg/ddl089

Sequence

[hsa:9856]

LinkDB

DBGET integrated database retrieval system