ENSG00000140157


Homo sapiens

Features
Gene ID: ENSG00000140157
  
Biological name :NIPA2
  
Synonyms : NIPA2 / non imprinted in Prader-Willi/Angelman syndrome 2 / Q8N8Q9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 15
Strand: 1
Band: q11.2
Gene start: 22838641
Gene end: 22868384
  
Corresponding Affymetrix probe sets: 212129_at (Human Genome U133 Plus 2.0 Array)   212133_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000437746
Ensembl peptide - ENSP00000381096
Ensembl peptide - ENSP00000453700
Ensembl peptide - ENSP00000337618
Ensembl peptide - ENSP00000352762
Ensembl peptide - ENSP00000381095
NCBI entrez gene - 81614     See in Manteia.
OMIM - 608146
RefSeq - XM_017022663
RefSeq - XM_017022654
RefSeq - XM_017022655
RefSeq - XM_017022656
RefSeq - XM_017022657
RefSeq - XM_017022658
RefSeq - XM_017022659
RefSeq - XM_017022660
RefSeq - XM_017022661
RefSeq - XM_017022662
RefSeq - NM_001008860
RefSeq - NM_001008892
RefSeq - NM_001008894
RefSeq - NM_001184888
RefSeq - NM_001184889
RefSeq - NM_030922
RefSeq - XM_005272546
RefSeq - XM_005272547
RefSeq - XM_005272548
RefSeq - XM_005272550
RefSeq - XM_005272552
RefSeq - XM_005272553
RefSeq - XM_006720364
RefSeq - XM_006720365
RefSeq - XM_006720366
RefSeq - XM_006720367
RefSeq - XM_011543877
RefSeq - XM_011543878
RefSeq - XM_011543879
RefSeq - XM_011543880
RefSeq - XM_017022645
RefSeq - XM_017022646
RefSeq - XM_017022647
RefSeq - XM_017022648
RefSeq - XM_017022649
RefSeq - XM_017022650
RefSeq - XM_017022651
RefSeq - XM_017022652
RefSeq - XM_017022653
RefSeq Peptide - NP_001008892
RefSeq Peptide - NP_001008894
RefSeq Peptide - NP_001171817
RefSeq Peptide - NP_001171818
RefSeq Peptide - NP_112184
RefSeq Peptide - NP_001008860
swissprot - A0A024R372
swissprot - H0YMQ7
swissprot - Q8N8Q9
Ensembl - ENSG00000140157
  
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 nipa2ENSDARG00000055912Danio rerio
 NIPA2ENSGALG00000016737Gallus gallus
 Nipa2ENSMUSG00000030452Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
NIPAL1 / Q6NVV3 / NIPA like domain containing 1ENSG0000016329366
NIPAL4 / Q0D2K0 / NIPA like domain containing 4ENSG0000017254858
NIPA1 / Q7RTP0 / non imprinted in Prader-Willi/Angelman syndrome 1ENSG0000017011337
NIPAL2 / Q9H841 / NIPA like domain containing 2ENSG0000010436125
NIPAL3 / Q6P499 / NIPA like domain containing 3ENSG0000000146124


Protein motifs (from Interpro)
Interpro ID Name
 IPR008521  Magnesium transporter NIPA


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006811 ion transport IEA
 biological_processGO:0015693 magnesium ion transport IBA
 biological_processGO:1903830 magnesium ion transmembrane transport IEA
 cellular_componentGO:0005768 endosome IEA
 cellular_componentGO:0005769 early endosome IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IBA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0015095 magnesium ion transmembrane transporter activity IEA


Pathways (from Reactome)
Pathway description
Miscellaneous transport and binding events


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
No match
  


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






 

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