Results for the protein: NP

Results for the Protein: NP_005568

116292750

4018

LPA

NCBI

apolipoprotein(a) precursor [Homo sapiens]

Known Diseases associated with this Protein:
LIPOPROTEIN(A) DEFICIENCY, CONGENITAL

1

9

1

9

0

Tips:

The Domains on the Default View are decided by the Domain's E-Value.

Clicking a check box will display or hide the correlated domain.

To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic.

Default View: KR - cd00108 KR - smart00130 Kringle - pfam00051 Tryp_SPc - smart00020 Tryp_SPc - cd00190 Trypsin - pfam00089	RefSeq Protein: NP_005568 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
KR	cd00108	2.2e-41	139	220
KR	cd00108	2.2e-41	253	334
KR	cd00108	2.2e-41	367	448
KR	cd00108	2.2e-41	481	562
KR	cd00108	2.2e-41	595	676
KR	cd00108	2.2e-41	709	790
KR	cd00108	6.5e-40	823	904
KR	cd00108	1e-39	937	1018
KR	cd00108	2.1e-41	1051	1132
KR	cd00108	1.6e-41	1165	1246
KR	cd00108	1.3e-41	1271	1352
KR	cd00108	2.8e-42	1385	1466
KR	cd00108	8.4e-42	1499	1580
KR	cd00108	6.4e-48	1613	1694
KR	cd00108	1e-39	1717	1800
Tryp_SPc	cd00190	8.8e-97	1820	2036
Kringle	pfam00051	1.3e-48	28	105
Kringle	pfam00051	4.5e-48	142	219
Kringle	pfam00051	4.5e-48	256	333
Kringle	pfam00051	4.5e-48	370	447
Kringle	pfam00051	4.5e-48	484	561
Kringle	pfam00051	4.5e-48	598	675
Kringle	pfam00051	4.5e-48	712	789
Kringle	pfam00051	5.6e-47	826	903
Kringle	pfam00051	7.7e-44	940	1017
Kringle	pfam00051	3.3e-46	1054	1131
Kringle	pfam00051	6.4e-41	1168	1245
Kringle	pfam00051	7.5e-42	1274	1351
Kringle	pfam00051	2.6e-44	1388	1465
Kringle	pfam00051	5.5e-42	1502	1579
Kringle	pfam00051	7.6e-49	1616	1693
Kringle	pfam00051	9.5e-51	1720	1799
Trypsin	pfam00089	1.3e-76	1820	2033
KR	smart00130	4e-43	26	107
KR	smart00130	5.8e-43	140	221
KR	smart00130	5.8e-43	254	335
KR	smart00130	5.8e-43	368	449
KR	smart00130	5.8e-43	482	563
KR	smart00130	5.8e-43	596	677
KR	smart00130	5.8e-43	710	791
KR	smart00130	3.4e-41	824	905
KR	smart00130	6.1e-41	938	1019
KR	smart00130	5.9e-42	1052	1133
KR	smart00130	2.4e-40	1166	1247
KR	smart00130	1.3e-40	1272	1353
KR	smart00130	8.5e-44	1386	1467
KR	smart00130	1.4e-42	1500	1581
KR	smart00130	2.3e-48	1614	1695
KR	smart00130	6.2e-42	1718	1801
Tryp_SPc	smart00020	6.8e-91	1819	2033

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
dbSNP	rs3124784	Polymorphism	p.ARG2016CYS	N/A
dbSNP	rs41272112	Polymorphism	p.ARG1421GLN	N/A
dbSNP	rs41265936	Polymorphism	p.GLY1822ALA	N/A
dbSNP	rs76062330	Polymorphism	p.GLY1823VAL	N/A
dbSNP	rs3798220	Polymorphism	p.ILE1891MET	N/A
dbSNP	rs7765803	Polymorphism	p.LEU1358VAL	N/A
dbSNP	rs7765781	Polymorphism	p.LEU1372VAL	N/A
dbSNP	rs1801693	Polymorphism	p.MET1679THR	N/A
dbSNP	rs41272110	Polymorphism	p.THR1399PRO	N/A
OMIM	152200.0004	Disease	p.ARG21TER	LIPOPROTEIN(a) DEFICIENCY, CONGENITAL

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