ENSMUSG00000014686


Mus musculus

Features
Gene ID: ENSMUSG00000014686
  
Biological name :Ceacam16
  
Synonyms : Carcinoembryonic antigen-related cell adhesion molecule 16 / Ceacam16 / E9QA28
  
Possible biological names infered from orthology : Q2WEN9
  
Species: Mus musculus
  
Chr. number: 7
Strand: -1
Band: A3
Gene start: 19852097
Gene end: 19861299
  
Corresponding Affymetrix probe sets: 10560695 (MoGene1.0st)   
  
Cross references: Ensembl peptide - ENSMUSP00000014830
Ensembl peptide - ENSMUSP00000147247
NCBI entrez gene - 330483     See in Manteia.
MGI - MGI:2685615
RefSeq - XM_006540109
RefSeq - XM_011250605
RefSeq - NM_001033419
RefSeq - XM_006540110
RefSeq Peptide - NP_001028591
swissprot - E9QA28
swissprot - A0A140LJK4
Ensembl - ENSMUSG00000014686
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 si:dkey-11o1.7ENSDARG00000105324Danio rerio
 Q2WEN9ENSG00000213892Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q925P2 / Ceacam2 / Carcinoembryonic antigen-related cell adhesion molecule 2 / PSG4* / PSG5* / PSG6* / PSG7* / PSG8* / PSG9* / PSG2* / PSG1* / PSG3* / PSG11* / Q9UQ74* / Q00888* / Q00887* ...ENSMUSG0000005438528
P31809 / Ceacam1 / Carcinoembryonic antigen-related cell adhesion molecule 1 / PSG3* / PSG4* / PSG5* / PSG1* / PSG6* / PSG7* / PSG8* / PSG9* / PSG2* / PSG11* / Q9UQ74* / P11464* / P11465* ...ENSMUSG0000007427228
Ceacam3 / carcinoembryonic antigen-related cell adhesion molecule 3 / PSG3* / PSG4* / PSG5* / PSG6* / PSG7* / PSG8* / PSG9* / PSG2* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* ...ENSMUSG0000005322821
Q9D871 / Ceacam18 / Carcinoembryonic antigen-related cell adhesion molecule 18 / A8MTB9*ENSMUSG0000003047220
Psg20 / pregnancy-specific glycoprotein 20 / PSG9* / PSG6* / PSG5* / PSG4* / PSG3* / PSG8* / PSG2* / PSG7* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P4...ENSMUSG0000006330518
Psg17 / PSG8* / PSG7* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG1* / PSG9* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40198* / P40199* / Q00887* / Q00888* / ...ENSMUSG0000000454018
Q9D2Z1 / Ceacam20 / Carcinoembryonic antigen-related cell adhesion molecule 20 ENSMUSG0000007077718
Psg25 / PSG8* / PSG7* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG1* / PSG9* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40198* / P40199* / Q00887* / Q00888* / ...ENSMUSG0000007079818
Ceacam15 / A0A0B4J1L0 / Carcinoembryonic antigen-related cell adhesion molecule 15 ENSMUSG0000007879518
Psg21 / PSG8* / PSG7* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG1* / PSG9* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40198* / P40199* / Q00887* / Q00888* / ...ENSMUSG0000007079617
Q3UKK2 / Ceacam5 / Carcinoembryonic antigen-related cell adhesion molecule 5 / PSG7* / PSG6* / PSG5* / PSG1* / PSG4* / PSG3* / PSG2* / PSG9* / PSG8* / PSG11* / Q9UQ74* / P06731* / P11464* ...ENSMUSG0000000878917
Psg28 / PSG8* / PSG7* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG1* / PSG9* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40198* / P40199* / Q00887* / Q00888* / ...ENSMUSG0000003037317
Psg26 / pregnancy-specific glycoprotein 26 / PSG9* / PSG6* / PSG5* / PSG4* / PSG3* / PSG8* / PSG2* / PSG7* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40...ENSMUSG0000007079917
Psg27 / pregnancy-specific glycoprotein 27 / PSG9* / PSG6* / PSG5* / PSG4* / PSG3* / PSG8* / PSG2* / PSG7* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40...ENSMUSG0000007079717
Psg19 / pregnancy specific glycoprotein 19 / PSG9* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG8* / PSG7* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40...ENSMUSG0000000454217
Psg18 / pregnancy specific glycoprotein 18 / PSG9* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG8* / PSG7* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40...ENSMUSG0000000350517
Psg22 / Q810J1 / Pregnancy-specific glycoprotein 22 / PSG6* / PSG5* / PSG4* / PSG3* / PSG8* / PSG2* / PSG9* / PSG7* / PSG1* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31...ENSMUSG0000004490317
Psg23 / PSG8* / PSG7* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG1* / PSG9* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40198* / P40199* / Q00887* / Q00888* / ...ENSMUSG0000007435917
Ceacam9 / carcinoembryonic antigen-related cell adhesion molecule 9 / Q3KPI0* / CEACAM21* / carcinoembryonic antigen related cell adhesion molecule 21*ENSMUSG0000000720916
Psg16 / PSG8* / PSG7* / PSG6* / PSG5* / PSG4* / PSG3* / PSG2* / PSG1* / PSG9* / PSG11* / Q9UQ74* / P06731* / P11464* / P11465* / P13688* / P31997* / P40198* / P40199* / Q00887* / Q00888* / ...ENSMUSG0000006676015


Protein motifs (from Interpro)
Interpro ID Name
 IPR003598  Immunoglobulin subtype 2
 IPR003599  Immunoglobulin subtype
 IPR007110  Immunoglobulin-like domain
 IPR013783  Immunoglobulin-like fold
 IPR036179  Immunoglobulin-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007605 sensory perception of sound IEA
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005615 extracellular space IEA
 cellular_componentGO:0032426 stereocilium tip IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0042802 identical protein binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001516 abnormal motor coordination/ balance "altered ability of an animal to maintain skillful and effective interaction of movements or maintenance of equilibrium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cbln3tm1.1(KOMP)Vlcg/Cbln3tm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Cbln3tm1.1(KOMP)Vlcg/Ucd

 MP:0002702 decreased circulating free fatty acid level "lower than normal levels of unesterified fatty acids in the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Cbln3tm1.1(KOMP)Vlcg/Cbln3tm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Cbln3tm1.1(KOMP)Vlcg/Ucd

 MP:0004736 abnormal distortion product otoacoustic emission "any abnormality in the sound produced by the cochlea in response to stimulation with 2 simultaneous tones of different frequencies; this measurement is particularly useful in assessing the functional state of OHCs" [eMedicine:http://www.emedicine.com/ent/topic372.htm, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1+,Tg(Alb-E2F1)8Sst/0
Genetic Background: involves: C57BL/6 * CBA

 MP:0004749 nonsyndromic hearing loss "a form of progressive hearing loss that is not associated with visible abnormalities of the external ear or other signs and symptoms; the vast majority of hereditary hearing loss is nonsyndromic and can be associated with abnormalities of the middle ear and/or inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1+,Tg(Alb-E2F1)8Sst/0
Genetic Background: involves: C57BL/6 * CBA

 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: Cbln3tm1.1(KOMP)Vlcg/Cbln3tm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Cbln3tm1.1(KOMP)Vlcg/Ucd

 MP:0006336 abnormal otoacoustic response "anomaly in the acoustic energy produced by the cochlea in the presence or absence of sound stimulation" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Enpp3tm1Ktak/Enpp3tm1Ktak,P2rx7tm1Gab/P2rx7tm1Gab
Genetic Background: either: (involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6) or (involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6)

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
Show

Allelic Composition: Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1+,Tg(Alb-E2F1)8Sst/0
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Ceacam16tm1(KOMP)Wtsi/Ceacam16tm1(KOMP)Wtsi
Genetic Background: involves: C57BL/6J * C57BL/6JOlaHsd * C57BL/6N

 MP:0012121 sclerocornea "a congenital anomaly of the eye in which partial or complete corneal opacity is present and resembles the sclera, with no clear boundary between these structures" [MGI:csmith]
Show

Allelic Composition: Cbln3tm1.1(KOMP)Vlcg/Cbln3tm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Cbln3tm1.1(KOMP)Vlcg/Ucd

 MP:0013962 absent Hensen stripe "absence of the dark, nonstriated, V-shaped band (ridge) that is normally found on the underside of the tectorial membrane (TM) in the basal region of the cochlea, from which fine gelatinous trabeculae extend to fix the TM to the border cells, i.e. cells directly adjacent to the inner phalangeal cells" [ISBN:3662026767, PMID:25080593]
Show

Allelic Composition: Ceacam16tm1(KOMP)Wtsi/Ceacam16tm1(KOMP)Wtsi
Genetic Background: involves: C57BL/6J * C57BL/6JOlaHsd * C57BL/6N

 MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology "any structural anomaly of the laminated, striated-sheet matrix within which collagen fibrils of the TM are imbedded; the striated sheet matrix is formed by two types of fine-diameter collagen filaments, a light and a dark staining type that lie in parallel within the plane of each sheet and are extensively linked along their length by staggered cross bridges; it originates medially within the sulcal zone, extends to the marginal band and is particularly evident in apical regions of the cochlea, where it has a less compressed appearance" [PMID:18797289, PMID:24363064]
Show

Allelic Composition: Ceacam16tm1(KOMP)Wtsi/Ceacam16tm1(KOMP)Wtsi
Genetic Background: involves: C57BL/6J * C57BL/6JOlaHsd * C57BL/6N

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
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