Manteia

ENSMUSG00000034390

Mus musculus

Features

Gene ID:	ENSMUSG00000034390

Biological name :	Cmip

Synonyms :	C-Maf-inducing protein / Cmip / Q9D486

Possible biological names infered from orthology :	Q8IY22

Species:	Mus musculus

Chr. number:	8
Strand:	1
Band:	E1
Gene start:	117257064
Gene end:	117459430

Corresponding Affymetrix probe sets:	10575775 (MoGene1.0st) 10575777 (MoGene1.0st) 1427980_at (Mouse Genome 430 2.0 Array) 1453015_at (Mouse Genome 430 2.0 Array)

Cross references:	Ensembl peptide - ENSMUSP00000092795 Ensembl peptide - ENSMUSP00000130264 NCBI entrez gene - 74440 See in Manteia. MGI - MGI:1921690 RefSeq - XM_011248527 RefSeq - NM_001163262 RefSeq - NM_028941 RefSeq - XM_006531434 RefSeq - XM_006531435 RefSeq - XM_006531436 RefSeq Peptide - NP_083217 RefSeq Peptide - NP_001156734 swissprot - Q9D486 Ensembl - ENSMUSG00000034390

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

Ortholog prediction (from Ensembl)

Ortholog name	ID	Species
cmip	ENSDARG00000062933	Danio rerio
CMIP	ENSGALG00000038494	Gallus gallus
CMIP	ENSG00000153815	Homo sapiens

Paralog prediction (from Ensembl)

Paralog name

Similarity(%)

No match

Protein motifs (from Interpro)

Interpro ID	Name
IPR011993	PH-like domain superfamily
IPR032675	Leucine-rich repeat domain superfamily

Gene Ontology (GO)

Type	GO ID	Term	Ev.Code
biological_process	GO:0008150	biological_process	ND
cellular_component	GO:0005634	nucleus	IEA
cellular_component	GO:0005654	nucleoplasm	ISO
cellular_component	GO:0005737	cytoplasm	IEA
cellular_component	GO:0005829	cytosol	ISO
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:0000480	increased number of ribs	"greater than normal numbers of the pairs of bony structures that make up the body wall" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]	Show Allelic Composition: Casq2^{tm1b(KOMP)Wtsi}/Casq2⁺ Genetic Background: C57BL/6N-Casq2^{tm1b(KOMP)Wtsi}/Ucd
MP:0000489	abnormal large intestine morphology	"structural or developmental anomalies of the intestinum crassum " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0000496	abnormal small intestine morphology	"structural or developmental anomalies of the intestinum tenue " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0001879	abnormal lymphatic vessel morphology	"malformation of the network of vessels which carries lymph around the body" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0002169	no phenotype detected	"normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0002951	small thyroid gland	"reduced size of the endocrine gland located in the front and to the sides of the upper part of the trachea, and which secretes thyroid hormone and calcitonin " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0003262	intestinal/bowel diverticulum	"a pouch or sac protruding from the intestinal or bowel wall " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0003826	abnormal Mullerian duct morphology	"malformation of the transient embryonic tubes that empty into the cloaca and in the female develop into the oviducts, uterus, and vagina" [smb:Susan M Bello, Mouse Genome Informatics Curator]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0004160	retroesophageal right subclavian artery	"the subclavian artery aberrantly originates from the aortic arch distal to the origin of the left subclavian artery, i.e., it is the last branch of the aortic arch" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0004647	decreased lumbar vertebrae number	"reduced number of the six bony segments of the spine located anterior to the sacral vertebrae and posterior to the thoracic vertebrae" [MESH:National Library of Medicine_Medical Subject Headings]	Show Allelic Composition: Casq2^{tm1b(KOMP)Wtsi}/Casq2⁺ Genetic Background: C57BL/6N-Casq2^{tm1b(KOMP)Wtsi}/Ucd
MP:0004651	increased thoracic vertebrae number	"increased number of the thirteen bony segments of the spine located anterior to the lumbar vertebrae and posterior to the cervical vertebrae" [MESH:National Library of Medicine_Medical Subject Headings]	Show Allelic Composition: Casq2^{tm1b(KOMP)Wtsi}/Casq2⁺ Genetic Background: C57BL/6N-Casq2^{tm1b(KOMP)Wtsi}/Ucd
MP:0009820	abnormal liver vasculature morphology	"any structural anomaly of the blood vessel network of the bile-secreting exocrine gland" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0010420	muscular ventricular septal defect	"abnormal communications between the two lower chambers of the heart, involving the muscular septum and often occurring as multiple communications, and includes central muscular or midmuscular, apical, or marginal communications when the defect is along the RV-septal junction; any single defect observed from the LV aspect may have several openings on the RV aspect" [http://emedicine.medscape.com]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
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: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0011683	dual inferior vena cava	"presence of two inferior vena cavae, often resulting from the persistence of both supracardinal veins during development; the two structures may be symmetric or asymmetric but typically join together at the renal vein" [MGI:csmith, PMID:10835118]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013834	thin hypoglossal nerve	"slender appearance of the motor nerve which innervates all the intrinsic and all but one of the extrinsic muscles of the tongue" [ISBN:0-683-40008-8]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013835	absent hypoglossal nerve	"absence of the motor nerve which innervates all the intrinsic and all but one of the extrinsic muscles of the tongue" [ISBN:0-683-40008-8]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013840	absent segment of posterior cerebral artery	"absence of a portion of one of a pair of blood vessels that supplies oxygenated blood to the posterior aspect of the brain" [UBERON:0001636]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013963	jugular vein stenosis		Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013968	multiple persisting craniopharyngeal ducts		Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013975	abnormal coronary sinus connection		Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013986	abnormal vitelline vein topology	"abnormal position of the paired veins that carry blood from the yolk sac back to the embryo" [MGI:csmith]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0014001	abnormal vertebral artery topology	"abnormal position of the first branch of the left and right subclavian arteries that merge to form the single midline basilar artery; branches of the vertebral arteries supply the musculature of the neck" [MGI:csmith]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0014018	embryo tumor	"presence of an unspecified tumor or aberrant growth in a prenatal orgnaism" [MGI:csmith]	Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd
MP:0014019	embryo cyst		Show Allelic Composition: Cbln3^{tm1.1(KOMP)Vlcg}/Cbln3^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Cbln3^{tm1.1(KOMP)Vlcg}/Ucd

Interacting proteins (from Reactome)

Interactor ID

Name

Interaction type

No match

0 s.

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		© Olivier Tassy / Olivier Pourquie 2007-2024 contact: otassy@igbmc.fr