ZFIN Gene: spegb

ZFIN ID: ZDB-GENE-081104-517

ZFIN ID: ZDB-GENE-081104-517

Gene Name:

striated muscle enriched protein kinase b

Gene Symbol:

spegb Nomenclature History

Previous Name:

si:ch211-195m20.1

Gene Type:

protein_coding_gene

Location:

Chr: 9 Mapping Details/Browsers

Description:

Predicted to have ATP binding activity and protein serine/threonine kinase activity. Predicted to be involved in protein phosphorylation. Human ortholog(s) of this gene implicated in centronuclear myopathy 5. Orthologous to human SPEG (striated muscle enriched protein kinase).

Genome Resources:

Alliance (1), Ensembl(GRCz11):ENSDARG00000009567 (2)

GENE EXPRESSION No data available

MUTATIONS AND SEQUENCE TARGETING REAGENTS

Allele	Type	Localization	Consequence	Mutagen	Suppliers
la029608Tg	Transgenic Insertion	Unknown	Unknown	DNA	Zebrafish International Resource Center (ZIRC) (order this)
sa732	Point Mutation	Unknown	Splice Site	ENU	Zebrafish International Resource Center (ZIRC) (order this)
sa10121	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa15274	Point Mutation	Unknown	Splice Site	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa15486	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa17142	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa31739	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa34720	Point Mutation	Unknown	Splice Site	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)

PHENOTYPE No data available

DISEASE ASSOCIATED WITH spegb HUMAN ORTHOLOG

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
centronuclear myopathy 5	Alliance	Centronuclear myopathy 5	615959

DISEASE ASSOCIATED WITH spegb VIA EXPERIMENTAL MODELS No data available

GENE ONTOLOGY

Ontology	GO Term
Biological Process	phosphorylation (more)
Cellular Component	M band (more)
Molecular Function	ATP binding (more)

GO Terms (all 11)

PROTEIN FAMILIES, DOMAINS AND SITES No links to external sites available

TRANSCRIPTS
Type	Name	Length (nt)	Analysis
mRNA	spegb-201 (1)	11941	Select Tool ZFIN BLAST NCBI BLAST Ensembl UCSC BLAT

Browsers: NCBI, Ensembl, ZFIN

INTERACTIONS AND PATHWAYS

ANTIBODIES No data available

PLASMIDS No data available

CONSTRUCTS WITH SEQUENCES FROM spegb No data available

MARKER RELATIONSHIPS

spegb Contained in:

[BAC] CH211-195M20 (1), CH211-247B3 (1)

SEQUENCE INFORMATION

Type	Accession #	Length (nt/aa)	Analysis
Genomic	GenBank:BX322540 (1)	156150 nt	Select Tool MegaBLAST Ensembl
Polypeptide	UniProtKB:F1R3X9 (1)	3061 aa	Select Tool ZFIN BLAST SIB BLAST Ensembl Protein Blast

Sequence Information (all 3)

ORTHOLOGY for spegb ( Chr: 9 )

CITATIONS (17)

{{control.fieldName}} Edit

Attributions

Add new Alias

Attributions for Alias: {{control.newAlias}}

Delete Alias: