SHISA7 - shisa family member 7 Gene

Homo sapiens

Also known as CKAMP59

Gene ID: 729956 | Gene type: protein coding

About SHISA7

Cytogenetic location: 19q13.42 Genomic coordinates (GRCh38): 19:55,428,740-55,443,300 (from NCBI)

This gene has 2 transcripts (splice variants), 219 orthologues and 3 paralogues. Biased expression in brain (RPKM 7.7), testis (RPKM 0.8) and 1 other tissue.

Summary

Predicted to enable GABA Receptor binding activity and ionotropic glutamate receptor binding activity. Predicted to be involved in several processes, including gamma-aminobutyric acid receptor clustering; regulation of signaling receptor activity; and regulation of synaptic plasticity. Predicted to be located in asymmetric, glutamatergic, excitatory synapse. Predicted to be part of AMPA glutamate receptor complex. Predicted to be active in glutamatergic synapse; postsynaptic density; and synaptic membrane. Predicted to be integral component of postsynaptic specialization membrane. [provided by Alliance of Genome Resources, Apr 2022]

SHISA7 Products(1)

mRNA	Protein	Name
NM_001145176.2	NP_001138648.1	protein shisa-7 precursor

SHISA7 Protein Structure

Shisa

0
100
200
300
400
500
538 a.a.

Protein Preferred Names

Protein Names

protein shisa-7

GABA(A) receptor auxiliary subunit Shisa7

Related Diseases

Diseases

Alias

Chromosome 22q11.2 Deletion Syndrome, Distal

22q11.2 Deletion Syndrome	Autosomal Dominant Opitz G/Bbb Syndrome
Catch22	Cayler Cardiofacial Syndrome
Conotruncal Anomaly Face Syndrome	Digeorge Syndrome
Sedlackova Syndrome	Shprintzen Syndrome
Velocardiofacial Syndrome	22q11.2 Distal Deletion Syndrome
Distal 22q11.2 Microdeletion Syndrome	22q11.2ds
Vcfs	Velo-Cardio-Facial Syndrome
Distal Chromosome 22q11.2 Deletion Syndrome	Chromosome 22q11.2 Deletion Syndrome Distal
Chromosome 22q11.2 Deletion Syndrome	Deletion 22q11.2 Syndrome
22q11ds	Catch 22
Digeorge Sequence	Microdeletion 22q11.2
Monosomy 22q11	Takao Syndrome
Distal Del(22)(Q11.2)	Distal Monosomy 22q11.2
Catch 22 Syndrome	Chromosome Deletion Syndrome 22q11.2, Distal

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS12870	SHISA7 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SHISA7	RGD	RGD:1583944
Bos taurus	SHISA7	VGNC	VGNC:52247
Mus musculus	SHISA7	MGD	MGI:3605641
Felis catus	SHISA7	VGNC	VGNC:65124
Canis familiaris	SHISA7	VGNC	VGNC:53978

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