Manteia

ENSMUSG00000074388

Mus musculus

Features

Gene ID:	ENSMUSG00000074388

Biological name :	Gm5544

Synonyms :	Gm5544

Possible biological names infered from orthology :

Species:	Mus musculus

Chr. number:	3
Strand:	1
Band:	F2.2
Gene start:	97930173
Gene end:	97967018

Corresponding Affymetrix probe sets:	10494592 (MoGene1.0st) 1460130_at (Mouse Genome 430 2.0 Array)

Cross references:	NCBI entrez gene - 433632 See in Manteia. MGI - MGI:3648209 Ensembl - ENSMUSG00000074388

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

Ortholog prediction (from Ensembl)

Ortholog name

Species

No match

Paralog prediction (from Ensembl)

Paralog name

Similarity(%)

No match

Protein motifs (from Interpro)

Interpro ID

Name

No match

Gene Ontology (GO)

Type

GO ID

Term

Ev.Code

No match

Pathways (from Reactome)

Pathway description

No match

Phenotype (from MGI, Zfin or HPO)

ID	Phenotype	Definition	Genetic BG
MP:0000106	abnormal basisphenoid bone morphology	"malformed base of the sphenoid bone" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
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: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1⁺ Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0000562	polydactyly	"greater than 5 digits on one or more autopods" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0000914	exencephaly	"neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0002989	small kidney	"reduced physical bulk one or both of the organs responsible for urine secretion" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0003686	abnormal eye muscle morphology	"malformation of the muscles of the eye" [smb:Susan M Bello, Mouse Genome Informatics Curator]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0004442	occipital bone foramen	"presence of a hole in the bone at the lower, posterior part of the skull" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0004463	basisphenoid bone foramen	"the presence of one or more holes in part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0004613	fusion of vertebral arches	"improper union of the dorsal part of adjacent vertebra" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0011110	partial preweaning lethality	"the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0012501	abnormal pericardial cavity morphology	"any structural anomaly of the anatomical body cavity in which the heart lies; the pericardial cavity forms in the lateral plate mesoderm above the buccopharyngeal membrane, as part of the early intraembryonic coelom, and is initially continuous with the two early pleural cavities" [MGI:anna]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013830	abnormal intrathoracic topology of vagus nerve	"abnormal position of the vagus nerve in the intrathoracic region" [MGI:csmith]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013836	abnormal hypoglossal nerve topology	"abnormal position of the hypoglossal nerve " [MGI:csmith]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{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: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013848	subcutaneous edema	"accumulation of watery or serous fluid in the subcutaneous region below the skin" [MGI:csmith]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013971	blood in lymph vessels		Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{tm1.1(KOMP)Vlcg}/Ucd
MP:0013985	abnormal umbilical vein topology	"abnormal position of the umbilical vein in relationship to other umbilical cord structures" [MGI:csmith]	Show Allelic Composition: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{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: Fgfr1^{tm1.1(KOMP)Vlcg}/Fgfr1^{tm1.1(KOMP)Vlcg} Genetic Background: C57BL/6N-Fgfr1^{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