Oculocerebrorenal syndrome of Lowe, Homo sapiens

Expression Profile:

View expression levels using UniGene's EST ProfileViewer
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Highly represented (1.4 pct) in cDNA library dbEST:9106, EN0098.

Highly represented (1.4 pct) in cDNA library dbEST:9121, ET0256.

GEO profiles:

Gene expression profiles in the NCBI Gene Expression Omnibus database

cDNA Sources:

brain; uterus; testis; lung; mixed; prostate; eye; embryonic tissue; ovary; thyroid; mouth; trachea; thymus; kidney; placenta; intestine; mammary gland; pancreas; connective tissue; uncharacterized tissue; larynx; parathyroid; bladder; skin; adrenal gland; ascites; cervix; stomach; liver; muscle; pituitary gland; bone; lymph node; vascular

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Finding cDNAs

UGID:147315 UniGene Hs.126357 Homo sapiens (human) OCRL

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Oculocerebrorenal syndrome of Lowe (OCRL)

GENE EXPRESSION

Tissues and development stages from this gene's sequences survey gene expression. Links to other NCBI expression resources.

MAPPING POSITION

Genomic location specified by transcript mapping, radiation hybrid mapping, genetic mapping or cytogenetic mapping.

	Chromosome:	X
	Map position:	Xq25-q26.1

SEQUENCES

Sequences representing this gene; mRNAs, ESTs, and gene predictions supported by transcribed sequences.

mRNA sequences (10)

NM_000276.3	Homo sapiens oculocerebrorenal syndrome of Lowe (OCRL), transcript variant a, mRNA	PA
NM_001587.3	Homo sapiens oculocerebrorenal syndrome of Lowe (OCRL), transcript variant b, mRNA	PA
BC094726.1	Homo sapiens oculocerebrorenal syndrome of Lowe, mRNA (cDNA clone MGC:104549 IMAGE:30528571), complete cds	PA
AK226116.1	Homo sapiens mRNA for phosphatidylinositol polyphosphate 5-phosphatase isoform a variant, clone: hj01740
BC130612.1	Homo sapiens oculocerebrorenal syndrome of Lowe, mRNA (cDNA clone MGC:163484 IMAGE:40146643), complete cds
BC018003.1	Homo sapiens, clone IMAGE:4272671, mRNA, partial cds	A
AK293107.1	Homo sapiens cDNA FLJ75418 complete cds, highly similar to Homo sapiens oculocerebrorenal syndrome of Lowe (OCRL), transcript variant a, mRNA
U57627.2	Human fetal brain oculocerebrorenal syndrome (OCRL1) mRNA, complete cds	PA
BC025253.2	Homo sapiens oculocerebrorenal syndrome of Lowe, mRNA (cDNA clone IMAGE:4864910), partial cds	A
S62085.1	OCRL-1 [human, patient 2, mRNA Partial Mutant, 169 nt]

EST sequences (10 of 283) [Show all sequences]

AA978334.1	Clone IMAGE:1568119	lung	3' read
AA977667.1	Clone IMAGE:1558362	lung	3' read
AA996072.1	Clone IMAGE:1607157	mammary gland	3' read	A
AA904845.1	Clone IMAGE:1504670	mixed	3' read	A
AA906612.1	Clone IMAGE:1522008	lung	3' read
R18793.1	Clone IMAGE:27337	brain	5' read
AI082506.1	Clone IMAGE:1660224	embryonic tissue	3' read	A
AI150582.1	Clone IMAGE:1752144	testis	3' read
AI214412.1	Clone IMAGE:1839359	testis	3' read	A
AI219718.1	Clone IMAGE:1842226	mixed	3' read	A

Key to Symbols

P Has similarity to known Proteins (after translation)
A Contains a poly-Adenylation signal
S Sequence is a Suboptimal member of this cluster
M Clone is putatively CDS-complete by MGC criteria