RecName: Full=Platelet glycoprotein Ib beta chain; Short=GP-Ib beta; S - Protein

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...

GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families. [Ann Hematol. 2023]
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families.
Barozzi S, Pecci A, Marinoni M, Fontana G, Zanchetta ME, Noris P, Savoia A, Faleschini M. Ann Hematol. 2023 Mar; 102(3):677-679. Epub 2022 Dec 21.
A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly. [Int J Mol Sci. 2021]
A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly.
Barozzi S, Bozzi V, De Rocco D, Giangregorio T, Noris P, Savoia A, Pecci A. Int J Mol Sci. 2021 Sep 22; 22(19). Epub 2021 Sep 22.
A novel frameshift GP1BB mutation causes autosomal dominant macrothrombocytopenia with decreased vWF receptor expression but normal platelet aggregation. [Platelets. 2022]
A novel frameshift GP1BB mutation causes autosomal dominant macrothrombocytopenia with decreased vWF receptor expression but normal platelet aggregation.
Dunstan-Harrison C, Morison IM, Ledgerwood EC. Platelets. 2022 Feb 17; 33(2):324-327. Epub 2021 Apr 4.

RefSeq genomic sequence
See the genomic reference sequence for the GP1BB gene (NG_007974.1).
RefSeq protein
See the reference protein sequence for platelet glycoprotein Ib beta chain precursor (NP_000398.1).

PubMed
PubMed articles cited by protein sequence record
Taxonomy
Taxonomy sequences associated with protein record
BioSystems
BioSystems
CDD Search Results
Display conserved domains within a protein
Conserved Domains (Concise)
Link to a concise list of conserved domains in a protein
Conserved Domains (Full)
Link to conserved domains within a protein
Domain Relatives
Display proteins with similar conserved domain architecture
Full text in PMC
Free full text articles in PMC
Gene
Link to related Genes
Identical Structures
3D structures for identical protein sequences
OMIM
OMIM records associated with protein sequence
Protein (RefSeq)
Protein gi (UniProtKB) to protein gi (refseq)
PubMed (Weighted)
Links to pubmed
Related Structures (List)
List of related structures

P13224 [Domain Mapping of Disease Mut...]
P13224
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Platelet glycoprotein Ib beta chain; Short=GP-Ib beta; Short=GPIb-...
RecName: Full=Platelet glycoprotein Ib beta chain; Short=GP-Ib beta; Short=GPIb-beta; Short=GPIbB; AltName: Full=Antigen CD42b-beta; AltName: CD_antigen=CD42c; Flags: Precursor
gi|121532|sp|P13224.1|GP1BB_HUMAN

Protein
Mirlet7b microRNA let-7b [Rattus norvegicus]
Mirlet7b microRNA let-7b [Rattus norvegicus]
Gene ID:100313990

Gene
Lactobacillus buchneri 16S ribosomal RNA
Lactobacillus buchneri 16S ribosomal RNA
gi|175019|gb|M58811.1|LBARR16SJ

Nucleotide
Leber Congenital Amaurosis
Leber Congenital Amaurosis
A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY O...<br/>Year introduced: 2010

MeSH
HIS5 histidinol-phosphate transaminase [Saccharomyces cerevisiae S288C]
HIS5 histidinol-phosphate transaminase [Saccharomyces cerevisiae S288C]
Gene ID:854690

Gene

Your browsing activity is empty.

Activity recording is turned off.

Protein