homo sapiens[Organism] AND A4GNT - Gene

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 51146 A4GNT ID: 51146	alpha-1,4-N-acetylglucosaminyltransferase [Homo sapiens (human)]	Chromosome 3, NC_000003.12 (138123713..138133302, complement)	alpha4GnT	616709
Select item 3383 ICAM1 ID: 3383	intercellular adhesion molecule 1 [Homo sapiens (human)]	Chromosome 19, NC_000019.10 (10271120..10286615)	BB2, CD54, P3.58	147840
Select item 3107 HLA-C ID: 3107	major histocompatibility complex, class I, C [Homo sapiens (human)]	Chromosome 6, NC_000006.12 (31268749..31272092, complement)	D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1	142840
Select item 2152 F3 ID: 2152	coagulation factor III, tissue factor [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (94529173..94541759, complement)	CD142, TF, TFA	134390
Select item 5445 PON2 ID: 5445	paraoxonase 2 [Homo sapiens (human)]	Chromosome 7, NC_000007.14 (95404862..95435028, complement)		602447
Select item 821 CANX ID: 821	calnexin [Homo sapiens (human)]	Chromosome 5, NC_000005.10 (179678656..179731641)	CNX, IP90, P90	114217
Select item 7846 TUBA1A ID: 7846	tubulin alpha 1a [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (49184795..49189080, complement)	B-ALPHA-1, LIS3, TUBA3	602529
Select item 10159 ATP6AP2 ID: 10159	ATPase H+ transporting accessory protein 2 [Homo sapiens (human)]	Chromosome X, NC_000023.11 (40580970..40606848)	APT6M8-9, ATP6IP2, ATP6M8-9, CDG2R, ELDF10, HT028, M8-9, MRXE, MRXSH, MSTP009, PRR, RENR, XMRE, XPDS	300556
Select item 291 SLC25A4 ID: 291	solute carrier family 25 member 4 [Homo sapiens (human)]	Chromosome 4, NC_000004.12 (185143266..185150382)	AAC1, ANT, ANT 1, ANT1, MTDPS12, MTDPS12A, PEO2, PEO3, PEOA2, T1	103220
Select item 3239 HOXD13 ID: 3239	homeobox D13 [Homo sapiens (human)]	Chromosome 2, NC_000002.12 (176087487..176095944)	BDE, BDSD, HOX4I, SPD, SPD1	142989
Select item 640 BLK ID: 640	BLK proto-oncogene, Src family tyrosine kinase [Homo sapiens (human)]	Chromosome 8, NC_000008.11 (11494387..11564599)	MODY11	191305
Select item 6687 SPG7 ID: 6687	SPG7 matrix AAA peptidase subunit, paraplegin [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (89508388..89557768)	CAR, CMAR, PGN, SPG5C	602783
Select item 2812 GP1BB ID: 2812	glycoprotein Ib platelet subunit beta [Homo sapiens (human)]	Chromosome 22, NC_000022.11 (19723539..19724771)	BDPLT1, BS, CD42C, GPIBB, GPIbbeta	138720
Select item 3140 MR1 ID: 3140	major histocompatibility complex, class I-related [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (181033387..181061938)	HLALS	600764
Select item 55624 POMGNT1 ID: 55624	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (46188683..46220305, complement)	GNTI.2, GnT I.2, LGMD2O, LGMDR15, MEB, MGAT1.2, RP76, gnT-I.2	606822
Select item 10585 POMT1 ID: 10585	protein O-mannosyltransferase 1 [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (131502918..131523799)	LGMD2K, LGMDR11, MDDGA1, MDDGB1, MDDGC1, RT	607423
Select item 54499 TMCO1 ID: 54499	transmembrane and coiled-coil domains 1 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (165724291..165768922, complement)	CFSMR1, HP10122, PCIA3, PNAS-136, TMCC4	614123
Select item 10447 FAM3C ID: 10447	FAM3 metabolism regulating signaling molecule C [Homo sapiens (human)]	Chromosome 7, NC_000007.14 (121348878..121396396, complement)	GS3786, ILEI	608618
Select item 7127 TNFAIP2 ID: 7127	TNF alpha induced protein 2 [Homo sapiens (human)]	Chromosome 14, NC_000014.9 (103121469..103137439)	B94, EXOC3L3	603300
Select item 3613 IMPA2 ID: 3613	inositol monophosphatase 2 [Homo sapiens (human)]	Chromosome 18, NC_000018.10 (11981507..12030877)		605922