Gene neighbors for Gene (Select 6579) - Gene - NCBI

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 127823798 LOC127823798 ID: 127823798	NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:21654373-21655080 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21501429..21502146)
Select item 127823797 LOC127823797 ID: 127823797	NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:21572391-21572952 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21419457..21420018)
Select item 127823796 LOC127823796 ID: 127823796	NANOG hESC enhancer GRCh37_chr12:21569666-21570167 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21416732..21417233)
Select item 127823795 LOC127823795 ID: 127823795	OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:21547931-21548862 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21394997..21395928)
Select item 127823794 LOC127823794 ID: 127823794	H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:21546997-21547930 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21394063..21394996)
Select item 127823793 LOC127823793 ID: 127823793	NANOG hESC enhancer GRCh37_chr12:21491840-21492346 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21338906..21339412)
Select item 127823792 LOC127823792 ID: 127823792	NANOG hESC enhancer GRCh37_chr12:21477387-21477904 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21324453..21324970)
Select item 127823791 LOC127823791 ID: 127823791	H3K4me1 hESC enhancer GRCh37_chr12:21402494-21402994 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21249560..21250060)
Select item 126861479 LOC126861479 ID: 126861479	CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:21386467-21387666 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21233533..21234732)
Select item 124903123 LOC124903123 ID: 124903123	uncharacterized LOC124903123 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21231281..21231456)
Select item 124902895 LOC124902895 ID: 124902895	uncharacterized LOC124902895 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21234049..21250563, complement)
Select item 100422582 ELOCP31 ID: 100422582	elongin C pseudogene 31 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21447556..21448315, complement)	TCEB1P31
Select item 79912 PYROXD1 ID: 79912	pyridine nucleotide-disulphide oxidoreductase domain 1 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21437655..21471250)	MFM8	617220
Select item 10599 SLCO1B1 ID: 10599	solute carrier organic anion transporter family member 1B1 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21131194..21239796)	HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6	604843
Select item 6579 SLCO1A2 ID: 6579	solute carrier organic anion transporter family member 1A2 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21264600..21419634, complement)	OATP, OATP-A, OATP1A2, SLC21A3	602883
Select item 5965 RECQL ID: 5965	RecQ like helicase [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21468910..21501635, complement)	RECON1, RecQ1, RECQL	600537
Select item 3375 IAPP ID: 3375	islet amyloid polypeptide [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (21354959..21379980)	DAP, IAP	147940

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Gene neighbors for Gene (Select 6579) (17)
Gene
solute carrier organic anion transporter family member 1A2 isoform 1 [Homo sapie...
solute carrier organic anion transporter family member 1A2 isoform 1 [Homo sapiens]
gi|1904926758|ref|NP_001373808.1|

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