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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NZU5	LIM and cysteine-rich domains protein 1	LMCD1	0	1
Q9NZU1	Leucine-rich repeat transmembrane protein FLRT1	FLRT1	4	1
Q9NZU0	Leucine-rich repeat transmembrane protein FLRT3	FLRT3 KIAA1469	9	8
Q9NZT2	Opioid growth factor receptor	OGFR	0	1
Q9NZT1	Calmodulin-like protein 5	CALML5 CLSP	1	2
Q9NZS9	Bifunctional apoptosis regulator	BFAR BAR RNF47	1	0
Q9NZS2	Killer cell lectin-like receptor subfamily F member 1	KLRF1 CLEC5C ML	4	0
Q9NZR4	Visual system homeobox 1	VSX1 RINX	0	1
Q9NZR2	Low-density lipoprotein receptor-related protein 1B	LRP1B LRPDIT	49	18
Q9NZR1	Tropomodulin-2	TMOD2 NTMOD	2	1
Q9NZQ7	Programmed cell death 1 ligand 1	CD274 B7H1 PDCD1L1 PDCD1LG1 PDL1	5	1
Q9NZQ3	NCK-interacting protein with SH3 domain	NCKIPSD AF3P21 SPIN90	1	1
Q9NZP8	Complement C1r subcomponent-like protein	C1RL C1RL1 C1RLP CLSPA	8	34
Q9NZP5	Olfactory receptor 5AC2	OR5AC2	1	0
Q9NZP2	Olfactory receptor 6C2	OR6C2	2	0
Q9NZP0	Olfactory receptor 6C3	OR6C3	1	0
Q9NZN8	CCR4-NOT transcription complex subunit 2	CNOT2 CDC36 NOT2	14	4
Q9NZN5	Rho guanine nucleotide exchange factor 12	ARHGEF12 KIAA0382 LARG	1	1
Q9NZN4	EH domain-containing protein 2	EHD2 PAST2	0	1
Q9NZN1	Interleukin-1 receptor accessory protein-like 1	IL1RAPL1 OPHN4	6	0	B-cell lymphoma Bell's palsy Coffin-Lowry syndrome Klinefelter syndrome Marfan syndrome Meckel's diverticulum Patau syndrome X-linked adrenal hypoplasia congenita allergic asthma asthma attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome brain cancer breast cancer breast carcinoma cancer cardiovascular system disease chromosome Xp21 deletion syndrome clubfoot diffuse large B-cell lymphoma embryoma facial nerve disease facial paralysis heart disease hepatocellular carcinoma immune system disease intellectual disability intrinsic asthma learning disability liver cancer melanoma non-syndromic X-linked intellectual disability obesity obsolete ymphosarcoma placental insufficiency pyloric stenosis rheumatoid arthritis situs inversus skin melanoma syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy vitiligo
Q9NZM6	Polycystin-2-like protein 2	PKD2L2	2	0
Q9NZM5	Ribosome biogenesis protein NOP53	NOP53 GLT GLTSCR2 PICT1	0	1
Q9NZM4	BRD4-interacting chromatin-remodeling complex-associated protein	BICRA GLTSCR1	7	2
Q9NZM3	Intersectin-2	ITSN2 KIAA1256 SH3D1B SWAP	15	3
Q9NZM1	Myoferlin	MYOF FER1L3 KIAA1207	5	2

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