Manteia - Molecule gene

ENSMUSG00000030649

Mus musculus

Features

Gene ID:	ENSMUSG00000030649

Biological name :	Anapc15

Synonyms :	Anapc15 / Anaphase-promoting complex subunit 15 / P60007

Possible biological names infered from orthology :

Species:	Mus musculus

Chr. number:	7
Strand:	1
Band:	E2
Gene start:	101863715
Gene end:	101901849

Corresponding Affymetrix probe sets:	10372091 (MoGene1.0st) 10555576 (MoGene1.0st) 1424327_at (Mouse Genome 430 2.0 Array) 1424328_s_at (Mouse Genome 430 2.0 Array) 1428734_at (Mouse Genome 430 2.0 Array) 1447666_x_at (Mouse Genome 430 2.0 Array)

Cross references:	Ensembl peptide - ENSMUSP00000136164 Ensembl peptide - ENSMUSP00000120373 Ensembl peptide - ENSMUSP00000147346 Ensembl peptide - ENSMUSP00000147669 Ensembl peptide - ENSMUSP00000040286 Ensembl peptide - ENSMUSP00000095839 Ensembl peptide - ENSMUSP00000102586 Ensembl peptide - ENSMUSP00000102591 Ensembl peptide - ENSMUSP00000114771 NCBI entrez gene - 75430 See in Manteia. MGI - MGI:1922680 RefSeq - XM_017312359 RefSeq - XM_006508279 RefSeq - XM_006508280 RefSeq - XM_006508282 RefSeq - XM_006508284 RefSeq - XM_006508285 RefSeq - XM_011241930 RefSeq - XM_011241931 RefSeq - XM_011241932 RefSeq - XM_011241933 RefSeq - XM_011241935 RefSeq - XM_017312358 RefSeq - NM_001291348 RefSeq - NM_001291349 RefSeq - NM_001291352 RefSeq - NM_001291353 RefSeq - NM_027532 RefSeq Peptide - NP_001278278 RefSeq Peptide - NP_001278281 RefSeq Peptide - NP_001278282 RefSeq Peptide - NP_081808 RefSeq Peptide - NP_001278277 swissprot - A0A1B0GR24 swissprot - E9Q0Y1 swissprot - G5E8M3 swissprot - H3BIU1 swissprot - A0A1B0GRU6 swissprot - P60007 Ensembl - ENSMUSG00000030649

See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed

Ortholog prediction (from Ensembl)

Ortholog name	ID	Species
F1QY75	ENSDARG00000101285	Danio rerio
	ENSGALG00000032499	Gallus gallus

Paralog prediction (from Ensembl)

Paralog name	ID	Similarity(%)
Anapc15-ps / anaphase prompoting complex C subunit 15, pseudogene / P60006* / ANAPC15* / anaphase promoting complex subunit 15*	ENSMUSG00000074780	96

Protein motifs (from Interpro)

Interpro ID	Name
IPR026182	Anaphase-promoting complex subunit 15

Gene Ontology (GO)

Type	GO ID	Term	Ev.Code
biological_process	GO:0007049	cell cycle	IEA
biological_process	GO:0051301	cell division	IEA
biological_process	GO:0090266	regulation of mitotic cell cycle spindle assembly checkpoint	IBA
cellular_component	GO:0005680	anaphase-promoting complex	IBA
molecular_function	GO:0003674	molecular_function	ND

Pathways (from Reactome)

Pathway description

No match

Phenotype (from MGI, Zfin or HPO)

ID	Phenotype	Definition	Genetic BG
MP:0000428	abnormal craniofacial morphology	"anomalous structure or development of the face and/or cranium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0000783	abnormal forebrain morphology	"malformed or absent anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:38857]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0000841	abnormal hindbrain morphology	"malformed caudal region of the brain; includes cerebellum, pons and medulla oblongata" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:45302]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0000897	abnormal midbrain	"malformation or malfunction associated with the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions, including eye movement and coordination of auditory and visual reflexes" [J:23882, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0001293	anophthalmia	"congenital absence of all tissues of the eyes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CML, J:71979]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0001297	microphthalmia	"reduced average size of the eyes" [J:18048]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0001556	increased circulating HDL cholesterol level	"higher than average level of high density lipoprotein in the blood; this molecule transports cholesterol to the liver for excretion in bile" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:47439]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0001697	abnormal embryo size	"anomalous proportions of embryo compared to littermates" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0001711	abnormal placenta		Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0001785	edema	"an accumulation of an excessive amount of watery fluid in cells or intercellular tissues" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54065]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0002080	prenatal lethality	"death anytime between fertilization and E18.5" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0003717	pallor	"an unnatural paleness to the skin, generally attributable to anemia" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0003720	abnormal neural tube closure	"abnormal invagination and fusion of the neuroepithelial layer in early development" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:99099]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0003984	embryonic growth retardation	"slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0004258	abnormal placenta size	"anomaly in the size or shape of the organ of metabolic interchange between fetus and mother" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0005633	increased circulating sodium level	"greater than the normal concentration in the blood of this metallic element, the most plentiful extracellular ion in the body and the principal determinant of extracellular fluid volume" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, RGD:Rat Genome Database submission]	Show Allelic Composition: Adipor1^{tm1b(EUCOMM)Hmgu}/Adipor1^{tm1b(EUCOMM)Hmgu} Genetic Background: C57BL/6N-Adipor1^{tm1b(EUCOMM)Hmgu}/H
MP:0011100	complete preweaning lethality	"death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0011239	abnormal skin coloration	"a variation in an expected skin color or complexion that may be due to inflammation, pigment defects or other causes" [MGI:llw2]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J
MP:0011495	abnormal head shape	"any anomaly in the characteristic surface outline or contour of a head of an organism" [MGI:csmith]	Show Allelic Composition: Anapc15^{tm1.1(KOMP)Vlcg}/Anapc15^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Anapc15^{tm1.1(KOMP)Vlcg}/J

Interacting proteins (from Reactome)

Interactor ID

Name

Interaction type

No match

1 s.

External programs and data are copyrighted by and are the property of their respective authors. The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation
		© Olivier Tassy / Olivier Pourquie 2007-2024 contact: otassy@igbmc.fr