Ornithine aminotransferase (gyrate atrophy), Homo sapiens

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Finding cDNAs

UGID:914079 UniGene Hs.523332 Homo sapiens (human) OAT

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Ornithine aminotransferase (gyrate atrophy) (OAT)

SELECTED PROTEIN SIMILARITIES

Comparison of sequences in UniGene with selected protein reference sequences. The alignments can suggest function of a gene.

Reference Protein		Species	Id(%)	Len(aa)
XP_001135130.1	PREDICTED: hypothetical protein isoform 3	P. troglodytes	100.0	438
NP_001021175.1	C16A3.10c	C. elegans	72.1	197
XP_956417.1	ornithine aminotransferase	N. crassa	61.5	405

GENE EXPRESSION

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

	Expression Profile:	View expression levels using UniGene's EST ProfileViewer [Show more entries with profiles like this]
	GEO profiles:	Gene expression profiles in the NCBI Gene Expression Omnibus database
	cDNA Sources:	brain; kidney; skin; testis; uncharacterized tissue; uterus; embryonic tissue; mixed; placenta; trachea; intestine; vascular; lung; liver; mammary gland; salivary gland; blood; connective tissue; prostate; esophagus; stomach; heart; adrenal gland; cervix; eye; spleen; bone marrow; pancreas; pharynx; ascites; bone; umbilical cord; bladder; mouth; lymph node; thyroid; thymus; muscle; ovary; ganglia; nerve; pituitary gland; larynx

MAPPING POSITION

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

	Chromosome:	10
	Map position:	10q26

SEQUENCES

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

mRNA sequences (13)

M23204.1	Human ornithine-oxo-acid aminotransferase mRNA, exons 3-11, complete cds	P
NM_000274.2	Homo sapiens ornithine aminotransferase (gyrate atrophy) (OAT), nuclear gene encoding mitochondrial protein, mRNA	A
CR457045.1	Homo sapiens full open reading frame cDNA clone RZPDo834H0811D for gene OAT, ornithine aminotransferase (gyrate atrophy); complete cds, incl. stopcodon	P
CR605069.1	full-length cDNA clone CS0DF029YK22 of Fetal brain of Homo sapiens (human)	P
CR604740.1	full-length cDNA clone CS0DJ012YD17 of T cells (Jurkat cell line) Cot 10-normalized of Homo sapiens (human)	P
CR749808.1	Homo sapiens mRNA; cDNA DKFZp781A11155 (from clone DKFZp781A11155)	PA
AB208817.1	Homo sapiens mRNA for ornithine aminotransferase precursor variant protein	P
M12267.1	Human ornithine aminotransferase mRNA, complete cds	P
M14963.1	Human ornithine aminotransferase mRNA, complete cds	P
BC000964.2	Homo sapiens ornithine aminotransferase (gyrate atrophy), mRNA (cDNA clone MGC:5182 IMAGE:3449883), complete cds	PA
Y07511.1	Human mRNA for kidney ornithine aminotransferase (EC 2.6.1.13)	P
BC016928.1	Homo sapiens ornithine aminotransferase (gyrate atrophy), mRNA (cDNA clone MGC:21248 IMAGE:3913352), complete cds	PA
AK312561.1	Homo sapiens cDNA, FLJ92935, Homo sapiens ornithine aminotransferase (gyrate atrophy) (OAT),nuclear gene encoding mitochondrial protein, mRNA

EST sequences (10 of 1190) [Show all sequences]

R14629.1	Clone IMAGE:35712	brain	5' read	P
R17018.1	Clone IMAGE:129855	mixed	3' read	A
R17055.1	Clone IMAGE:129855	mixed	5' read	P
AI015521.1	Clone IMAGE:1636058	kidney	3' read	A
R18242.1	Clone IMAGE:30578	brain	5' read	P
R18862.1	Clone IMAGE:27153	brain	5' read	P
AA909769.1	Clone IMAGE:1476564	uncharacterized tissue	3' read	A
AA885891.1	Clone IMAGE:1492565	kidney	3' read	A
AI146919.1	Clone IMAGE:1666746	skin	3' read	A
AI160813.1	Clone IMAGE:1715477	placenta	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