Results for the protein: NP

Results for the Protein: NP_001165780

288856248

91624

NEXN

NCBI

nexilin isoform 2 [Homo sapiens]

Known Diseases associated with this Protein:
CARDIOMYOPATHY, DILATED, 1CC
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20

4

1

4

1

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: Ig2_FGFRL1-like - cd05856 I-set - pfam07679 Ig2_FGFR_like - cd05729 IG_like - smart00410 IG - smart00409 Ig2_FGFR - cd05857 ig - pfam00047 Ig5_Contactin_like - cd04969 Ig_Titin_like - cd05748 Ig4_Neogenin - cd05723 Ig - cd00096	RefSeq Protein: NP_001165780 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
Ig2_FGFR_like	cd05729	1.1e-06	522	607
Ig2_FGFR	cd05857	0.00047	525	607
Ig5_Contactin_like	cd04969	0.00035	532	607
Ig4_Neogenin	cd05723	3.3e-06	534	607
Ig_Titin_like	cd05748	4.7e-05	534	607
Ig	cd00096	7.9e-07	535	604
ig	pfam00047	0.00037	532	592
I-set	pfam07679	2.1e-16	518	607
IG_like	smart00410	4.8e-13	524	608
IG	smart00409	4.8e-13	524	608

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
dbSNP	rs1166698	Polymorphism	p.GLY181ARG	N/A
OMIM	613121.0005	Disease	p.ARG215CYS	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20
OMIM	613121.0004	Disease	p.GLN67GLU	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20
OMIM	613121.0003	Disease	p.PRO547THR	CARDIOMYOPATHY, DILATED, 1CC
OMIM	613121.0002	Disease	p.TYR588CYS	CARDIOMYOPATHY, DILATED, 1CC

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