Atrx (alpha thalassemia/mental retardation syndrome X-linked)

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Keyword

Gene: Atrx (alpha thalassemia/mental retardation syndrome X-linked) Rattus norvegicus

Symbol:

Atrx

Name:

alpha thalassemia/mental retardation syndrome X-linked

Description:

ENCODES a protein that exhibits chromatin binding (ortholog); chromo shadow domain binding (ortholog); INVOLVED IN forebrain development (ortholog); ASSOCIATED WITH alpha-Thalassemia (ortholog); Alpha-Thalassemia Myelodysplasia Syndrome (ortholog); ATR-X syndrome (ortholog); FOUND IN heterochromatin (ortholog); nuclear chromosome (ortholog); nucleus (ortholog); INTERACTS WITH (+)-pilocarpine; 17beta-estradiol; 2,6-dinitrotoluene

Type:

protein-coding

RefSeq Status:

MODEL

Also known as:

alpha thalassemia/mental retardation syndrome X-linked homolog; alpha thalassemia/mental retardation syndrome X-linked homolog (human); alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae); alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S.cerevisiae); alpha thalassemia/mental retardation syndrome X-linked homolog; ATP-dependent helicase ATRX; helicase II; pABP-2; transcriptional regulator ATRX; X-linked nuclear protein; Xnp

Orthologs:

Homo sapiens : ATRX (alpha thalassemia/mental retardation syndrome X-linked) HGNC
Mus musculus : Atrx (alpha thalassemia/mental retardation syndrome X-linked homolog (human)) MGI

Latest Assembly:

RGSC Genome Assembly v3.4

NCBI Annotation Information:

Annotation category: partial on reference assembly

Position:

Map	Chr	Position	Strand	Source
Rat Cytogenetic Map	X	q31		NCBI
RGSC Genome Assembly v5.0	X	77,469,573 - 77,515,177	-	NCBI
RGSC Genome Assembly v5.0	X	55,945,344 - 56,101,032	-	NCBI
RGSC Genome Assembly v3.4	X	93,903,794 - 94,051,337	-	NCBI
Rat Celera Assembly	X	72,166,665 - 72,281,853	-	NCBI
Genome Assembly 3.1	X	94,034,366 - 94,057,029	-	NCBI