Results for the protein: NP

Results for the Protein: NP_056532

557357745

50489

CD207

NCBI

C-type lectin domain family 4 member K [Homo sapiens]

Known Diseases associated with this Protein:
BIRBECK GRANULE DEFICIENCY

1

8

1

8

0

Tips:

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

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Default View: CLECT - smart00034 CLECT_NK_receptors_l - cd03593 CLECT_DC-SIGN_like - cd03590 CLECT_CSPGs - cd03588 CLECT_CEL-1_like - cd03589 CLECT_REG-1_like - cd03594 CLECT_attractin_like - cd03597 CLECT_collectin_like - cd03591 CLECT_EMBP_like - cd03598 CLECT_VCBS - cd03603 CLECT_1 - cd03602 CLECT - cd00037 CLECT_selectins_like - cd03592 Lectin_C - pfam00059	RefSeq Protein: NP_056532 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
CLECT_DC-SIGN_like	cd03590	4.7e-64	195	321
CLECT_NK_receptors_l	cd03593	4.4e-21	195	321
CLECT_CEL-1_like	cd03589	3.4e-18	196	321
CLECT_REG-1_like	cd03594	7.3e-10	197	321
CLECT_attractin_like	cd03597	0.0003	197	321
CLECT_collectin_like	cd03591	2.8e-06	204	321
CLECT_EMBP_like	cd03598	0.00034	204	321
CLECT	cd00037	3.9e-36	205	321
CLECT_selectins_like	cd03592	2.9e-11	205	321
CLECT_1	cd03602	1.2e-07	205	321
CLECT_VCBS	cd03603	9.8e-12	205	318
Lectin_C	pfam00059	9e-34	212	321
CLECT	smart00034	1.6e-32	195	320

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
dbSNP	rs10489990	Polymorphism	p.ALA55VAL	N/A
dbSNP	rs72911708	Polymorphism	p.ARG66GLN	N/A
dbSNP	rs13383830	Polymorphism	p.ASN288ASP	N/A
dbSNP	rs17718987	Polymorphism	p.GLN136GLU	N/A
dbSNP	rs72836219	Polymorphism	p.GLU114VAL	N/A
dbSNP	rs57302492	Polymorphism	p.LYS313ILE	N/A
dbSNP	rs17006436	Polymorphism	p.PRO213SER	N/A
dbSNP	rs741326	Polymorphism	p.VAL278ALA	N/A
OMIM	604862.0001	Disease	p.TRP264ARG	BIRBECK GRANULE DEFICIENCY

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