Reviewed, UniProtKB/Swiss-Prot Q96QS3 (ARX_HUMAN)

Names and origin

Protein names

Recommended name:
    Homeobox protein ARX
Alternative name(s):
    Aristaless-related homeobox

Gene names

Name:

ARX

Organism

Homo sapiens (Human)

Taxonomic identifier

9606 [NCBI]

Taxonomic lineage

Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo

Protein attributes

Sequence length	562 AA.
Sequence status	Complete.
Sequence processing	The displayed sequence is not processed.
Protein existence	Evidence at protein level.

General annotation (Comments)

Function	Transcription factor required for normal brain development. May be important for maintenance of specific neuronal subtypes in the cerebral cortex and axonal guidance in the floor plate.
Subcellular location	NucleusBy similarity.
Tissue specificity	Expressed predominantly in fetal and adult brain and skeletal muscle. Expression is specific to the telencephalon and ventral thalamus. There is an absence of expression in the cerebellum throughout development and also in adult.
Involvement in disease	Defects in ARX are the cause of lissencephaly X-linked type 2 (LISX2) [MIM:300215]; also known as lissencephaly X-linked with ambiguous genitalia (XLAG). LISX2 is a classic type lissencephaly associated with abnormal genitalia. LISX2 patients have severe congenital or postnatal microcephaly, lissencephaly, agenesis of the corpus callosum, neonatal-onset intractable epilepsy, poor temperature regulation, chronic diarrhea, and ambiguous or underdeveloped genitalia. Defects in ARX are a cause of X-linked infantile spasm syndrome (ISSX) [MIM:308350]; also known as X-linked West syndrome. The disorder is characterized by infantile spasms, hypsarrhythmia on EEG, and developmental arrest leading to severe to profound mental retardation. Defects in ARX are a cause of myoclonic epilepsy X-linked with intellectual disability and spasticity (XMEIDS) [MIM:300432]. XMEIDS is characterized by myoclonic epilepsy with generalized spasticity and intellectual deficit. Defects in ARX are a cause of Partington syndrome (PRTS) [MIM:309510]; also known as X-linked syndromic mental retardation 1 (MRXS1). PRTS is characterized by mental retardation, episodic dystonic hand movements, and dysarthria. Defects in ARX are the cause of non-syndromic mental retardation X-linked type 54 (MRX54) [MIM:300419]. Mental retardation is a mental disorder characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs. Defects in ARX are the cause of agenesis of corpus callosum with abnormal genitalia (ACC with abnormal genitalia) [MIM:300004]. ACC with abnormal genitalia consists of a brain and genital malformations syndrome.
Sequence similarities	Belongs to the paired homeobox family. Bicoid subfamily. Contains 1 homeobox DNA-binding domain. Contains 1 OAR domain.

Ontologies

Keywords
Biological process	Differentiation Neurogenesis Transcription Transcription regulation
Cellular component	Nucleus
Coding sequence diversity	Triplet repeat expansion
Disease	Disease mutation Epilepsy Lissencephaly Mental retardation
Domain	Homeobox
Ligand	DNA-binding
Molecular function	Developmental protein
Gene Ontology (GO)
None. [Check GOA]

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view
Molecule processing
	Chain	1 – 562	562	Homeobox protein ARX
Regions
	DNA binding	328 – 387	60	Homeobox
	Motif	530 – 543	14	OAR
	Compositional bias	100 – 155	56	Ala-rich
	Compositional bias	224 – 253	30	Glu-rich
	Compositional bias	395 – 459	65	Pro-rich
	Compositional bias	425 – 544	120	Ala-rich
Natural variations
	Natural variant	33	1	L → P in MRX54.
	Natural variant	115	1	A → AAAAAAAA in ISSX.
	Natural variant	155	1	A → AAAAAAAAA in ISSX and PRTS; also found in non-specific mental retardation families; frequent mutation.
	Natural variant	286	1	G → S in MRX54. dbSNP rs28935479.
	Natural variant	332	1	R → H in LISX2.
	Natural variant	332	1	R → P in LISX2.
	Natural variant	333	1	T → N in ACC with abnormal genitalia.
	Natural variant	343	1	L → Q in LISX2.
	Natural variant	353	1	P → L in XMEIDS.
	Natural variant	353	1	P → R in LISX2.
	Natural variant	521	1	A → T in LISX2; severe phenotype.

Sequences

	Sequence		Length	Mass (Da)
	Q96QS3-1 [UniParc]. Last modified December 1, 2001. Version 1. Checksum: FBDF41E387C65532	FASTA	562	58,160
	10 20 30 40 50 60 MSNQYQEEGC SERPECKSKS PTLLSSYCID SILGRRSPCK MRLLGAAQSL PAPLTSRADP 70 80 90 100 110 120 EKAVQGSPKS SSAPFEAELH LPPKLRRLYG PGGGRLLQGA AAAAAAAAAA AAAAATATAG 130 140 150 160 170 180 PRGEAPPPPP PTARPGERPD GAGAAAAAAA AAAAAWDTLK ISQAPQVSIS RSKSYRENGA 190 200 210 220 230 240 PFVPPPPALD ELGGPGGVTH PEERLGVAGG PGSAPAAGGG TGTEDDEEEL LEDEEDEDEE 250 260 270 280 290 300 EELLEDDEEE LLEDDARALL KEPRRCPVAA TGAVAAAAAA AVATEGGELS PKEELLLHPE 310 320 330 340 350 360 DAEGKDGEDS VCLSAGSDSE EGLLKRKQRR YRTTFTSYQL EELERAFQKT HYPDVFTREE 370 380 390 400 410 420 LAMRLDLTEA RVQVWFQNRR AKWRKREKAG AQTHPPGLPF PGPLSATHPL SPYLDASPFP 430 440 450 460 470 480 PHHPALDSAW TAAAAAAAAA FPSLPPPPGS ASLPPSGAPL GLSTFLGAAV FRHPAFISPA 490 500 510 520 530 540 FGRLFSTMAP LTSASTAAAL LRQPTPAVEG AVASGALADP ATAAADRRAS SIAALRLKAK 550 560 EHAAQLTQLN ILPGTSTGKE VC

References

[1]	"Human ARX gene: genomic characterization and expression." Ohira R.H., Zhang Y.H., Guo W., Dipple K., Shih S., Doerr J., Huang B.-L., Fu L., Abu-Khalil A., Geschwind D., McCabe E. Mol. Genet. Metab. 77:179-179(2002) [PubMed: 12359145] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY.
[2]	"Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation." Turner G., Partington M., Kerr B., Mangelsdorf M., Gecz J. Am. J. Med. Genet. 112:405-411(2002) [PubMed: 12376946] [Abstract] Cited for: VARIANT ISSX ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-155 INS.
[3]	"ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation." Bienvenu T., Poirier K., Friocourt G., Bahi N., Beaumont D., Fauchereau F., Ben-Jeema L., Zemni R., Vinet M.-C., Francis F., Couvert P., Gomot M., Moraine C., van Bokhoven H., Kalscheuer V., Frints S., Gecz J., Ohzaki K. , Chaabouni H., Fryns J.-P., Desportes V., Beldjord C., Chelly J. Hum. Mol. Genet. 11:981-991(2002) [PubMed: 11971879] [Abstract] Cited for: VARIANTS MRX54 PRO-33 AND SER-286, TISSUE SPECIFICITY.
[4]	"Mutations in the human ortholog of aristaless cause X-linked mental retardation and epilepsy." Stroemme P., Mangelsdorf M.E., Shaw M.A., Lower K.M., Lewis S.M.E., Bruyere H., Luetcherath V., Gedeon A.K., Wallace R.H., Scheffer I.E., Turner G., Partington M., Frints S.G.M., Fryns J.-P., Sutherland G.R., Mulley J.C., Gecz J. Nat. Genet. 30:441-445(2002) [PubMed: 11889467] [Abstract] Cited for: VARIANT XMEIDS LEU-353, VARIANTS ISSX ALA-ALA-ALA-ALA-ALA-ALA-ALA-115 INS AND ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-155 INS, VARIANT PRTS ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-155 INS, TISSUE SPECIFICITY.
[5]	"Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans." Kitamura K., Yanazawa M., Sugiyama N., Miura H., Iizuka-Kogo A., Kusaka M., Omichi K., Suzuki R., Kato-Fukui Y., Kamiirisa K., Matsuo M., Kamijo S., Kasahara M., Yoshioka H., Ogata T., Fukuda T., Kondo I., Kato M. , Dobyns W.B., Yokoyama M., Morohashi K. Nat. Genet. 32:359-369(2002) [PubMed: 12379852] [Abstract] Cited for: VARIANTS LISX2 HIS-332 AND GLN-343.
[6]	"Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation." Kato M., Das S., Petras K., Kitamura K., Morohashi K., Abuelo D.N., Barr M., Bonneau D., Brady A.F., Carpenter N.J., Cipero K.L., Frisone F., Fukuda T., Guerrini R., Iida E., Itoh M., Lewanda A.F., Nanba Y. , Oka A., Proud V.K., Saugier-Veber P., Schelley S.L., Selicorni A., Shaner R., Silengo M., Stewart F., Sugiyama N., Toyama J., Toutain A., Vargas A.L., Yanazawa M., Zackai E.H., Dobyns W.B. Hum. Mutat. 23:147-159(2004) [PubMed: 14722918] [Abstract] Cited for: VARIANTS LISX2 PRO-332; HIS-332; GLN-343; ARG-353 AND THR-521, VARIANT ACC WITH ABNORMAL GENITALIA ASN-333.
+	Additional computationally mapped references.

Web resources

GeneReviews

Cross-references

Sequence databases
EMBLGenBankDDBJ	AY038071 mRNA. Translation: AAK93901.1.
RefSeq	NP_620689.1.
UniGene	Hs.300304
3D structure databases
HSSP	HSSP built from PDB template 1FJL based on UniProtKB P06601.
ModBase	Search...
Genome annotation databases
Ensembl	ENSG00000004848. Homo sapiens. [Contig view]
GeneID	170302.
KEGG	hsa:170302.
Organism-specific databases
H-InvDB	HIX0056192.
HGNC	HGNC:18060. ARX.
MIM	300004. phenotype. 300215. phenotype. 300382. gene. 300419. phenotype. 300432. phenotype. 308350. phenotype. 309510. phenotype.
Orphanet	452. Lissencephaly, X linked - agenesis of the corpus callosum - genital anomalies. 777. Mental retardation, X linked, nonspecific. 2508. Micrencephaly - corpus callosum agenesis. 94083. Partington syndrome. 3175. Spasticity - mental retardation - epilepsy, X-linked. 3451. West syndrome.
PharmGKB	PA25024.
GenAtlas	Search...
GeneCards	Search...
Phylogenomic databases
HOGENOM	Q96QS3.
HOVERGEN	Q96QS3.
Gene expression databases
ArrayExpress	Q96QS3.
CleanEx	HS_ARX.
GermOnline	ENSG00000004848. Homo sapiens.
Family and domain databases
InterPro	IPR003654. Homeo_OAR. IPR001356. Homeobox. IPR012287. Homeodomain-rel. IPR000047. HTH_lambrepressr. [Graphical view]
Gene3D	G3DSA:1.10.10.60. Homeodomain-rel. 1 hit.
Pfam	PF00046. Homeobox. 1 hit. PF03826. OAR. 1 hit. [Graphical view]
PRINTS	PR00024. HOMEOBOX. PR00031. HTHREPRESSR.
ProDom	PD000010. Homeobox. 1 hit. [Graphical view] [Entries sharing at least one domain]
SMART	SM00389. HOX. 1 hit. [Graphical view]
PROSITE	PS00027. HOMEOBOX_1. 1 hit. PS50071. HOMEOBOX_2. 1 hit. PS50803. OAR. 1 hit. [Graphical view]
BLOCKS	Search...
Other Resources
LinkHub	Q96QS3.
SOURCE	Search...
ProtoNet	Search...

Entry information

Entry name

ARX_HUMAN

Accession

Primary (citable) accession number: Q96QS3

Entry history

Integrated into UniProtKB/Swiss-Prot:	January 27, 2003
Last sequence update:	December 1, 2001
Last modified:	July 22, 2008
This is version 62 of the entry and version 1 of the sequence. [Complete history]

Entry status

Reviewed (UniProtKB/Swiss-Prot)

Annotation project

HPI (Human Proteome Initiative)