SCAPER

SCAPER
Identifiers
Aliases	SCAPER, ZNF291, Zfp291, MSTP063, S-phase cyclin A associated protein in the ER, IDDRP
External IDs	OMIM: 611611 MGI: 1925976 HomoloGene: 32488 GeneCards: SCAPER
Gene location (Human)
Chr.	Chromosome 15 (human)
End	76,905,444 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	55,845,403 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; Achilles tendon; ; ganglionic eminence; ; hypothalamus; ; anterior pituitary; ; gastrocnemius muscle; ; cerebellar hemisphere; ; Brodmann area 9; ; cingulate gyrus; ; prefrontal cortex;
	Top expressed in
	arcuate nucleus; ; otolith organ; ; utricle; ; median eminence; ; secondary oocyte; ; paraventricular nucleus of hypothalamus; ; piriform cortex; ; ventromedial nucleus; ; supraoptic nucleus; ; habenula;
	More reference expression data
	n/a
Orthologs
	49855
	244891
	ENSG00000140386
	244891
	Q9BY12
	n/a
NM_001145923; NM_020843; NM_001353009; NM_001353010; NM_001353011;
	NM_001353012
	NM_001081341; NM_175536; NM_001357652; NM_001357653
NP_001139395; NP_065894; NP_001339938; NP_001339939; NP_001339940;
	NP_001339941
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

SCAPER (S-phase CyclinA Associated Protein residing in the Endoplasmic Reticulum) is a gene located on the long arm of chromosome 15 (15q24.3). It was first identified in 2007.^[5]

Gene[edit]

This gene lies on the Crick strand and has 30 exons.

Protein[edit]

The gene encodes a 1399-amino acid protein with a predicted weight of 158 kilodaltons. It has a C2H2-type zinc finger motif, a putative transmembrane domain, an ER retrieval signal at the C terminus, 4 coiled-coil domains, 6 potential RXL motifs and 6 consensus Cdk phosphorylation sites.

Biochemistry[edit]

The encoded protein is found in the nucleus and endoplasmic reticulum.

It is found in all tissues tested. It appears to have a role in the cell cycle.

Clinical significance[edit]

Mutations in this gene have been associated with intellectual disability and retinitis pigmentosa.^[6]^[7]^[8]

References[edit]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000140386 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: 244891 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Tsang WY, Wang L, Chen Z, Sánchez I, Dynlacht BD (2007) SCAPER, a novel cyclin A-interacting protein that regulates cell cycle progression. J Cell Biol 178(4):621-633
^ Tatour Y, Sanchez-Navarro I, Chervinsky E, Hakonarson H, Gawi H, Tahsin-Swafiri S, Leibu R, Lopez-Molina MI, Fernandez-Sanz G, Ayuso C, Ben-Yosef, T (2017) Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability. J Med Genet 54:698-704
^ Jauregui R, Thomas AL, Liechty B, Velez G, Mahajan VB, Clark L, Tsang SH (2019) SCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosa. Am J Med Genet A 179(2):312-316
^ Kahrizi K, Huber M, Galetzka D, Dewi S, Schröder J, Weis E, Kariminejad A, Fattahi Z, Ropers HH, Schweiger S, Najmabadi H, Winter J (2019) Homozygous variants in the gene SCAPER cause syndromic intellectual disability. Am J Med Genet A

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000140386 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: 244891 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[Tsang2007-5] Tsang WY, Wang L, Chen Z, Sánchez I, Dynlacht BD (2007) SCAPER, a novel cyclin A-interacting protein that regulates cell cycle progression. J Cell Biol 178(4):621-633

[Tatour2017-6] Tatour Y, Sanchez-Navarro I, Chervinsky E, Hakonarson H, Gawi H, Tahsin-Swafiri S, Leibu R, Lopez-Molina MI, Fernandez-Sanz G, Ayuso C, Ben-Yosef, T (2017) Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability. J Med Genet 54:698-704

[Jauregui2017-7] Jauregui R, Thomas AL, Liechty B, Velez G, Mahajan VB, Clark L, Tsang SH (2019) SCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosa. Am J Med Genet A 179(2):312-316

[Kahrizi2019-8] Kahrizi K, Huber M, Galetzka D, Dewi S, Schröder J, Weis E, Kariminejad A, Fattahi Z, Ropers HH, Schweiger S, Najmabadi H, Winter J (2019) Homozygous variants in the gene SCAPER cause syndromic intellectual disability. Am J Med Genet A

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