Logo
Home Search BLAST Integration Document Link Support Citation

Gene Information
Gene ID:3842
Symbol:TNPO1
Full Name:transportin 1
Alias:IPO2|KPNB2|MIP|MIP1|TRN
Organism:Homo sapiens (Human)
Chromosome:5
Genetic Location:5q13.2
Physical Location:72148173-72245970 on NC_000005.8
Gene Type:protein-coding
Orthologs:This gene has no orthologs in other dataset(s).
Gene in Ethanol Study Datasets
Gene Information
Original ID1:AL049378
Fold Change:1.3
P Value:0.044
Dataset Information
Name:12774316
Method:Microarray
Tissue:Temporal cortex
Phenotype:Alcohol dependence (AD)/Alcohol abuse/Alcoholism
Publication:Sokolov et al. J Neurosci Res. (2003) Transcription profiling reveals mitochondrial, ubiquitin and signaling systems abnormalities in postmortem brains from subjects with a history of alcohol abuse or dependence. PubMed
Summary:To identify candidate mechanisms for alcohol abuse, the expression of 12,626 genes was measured in postmortem temporal cortex from 11 subjects with a history of alcohol abuse or dependence, with or without other psychiatric diagnoses and compared pairwise with the expression in 11 nonalcoholic subjects matched for the other psychiatric diagnoses and demographics. Genes were defined to have altered expression in alcohol abuse if: 1) the gene showed decreased expression in at least 10 of 11 subjects with alcohol abuse, or showed increased expression in at least 10 of 11 subjects with this diagnosis compared to matched non-abusers (P<0.007, X2test); or 2) the difference in the mean abuser/non-abuser ratio for the gene from value of 1.0 was significant at P<0.05 (one sample t-test). In subjects with a history of alcohol abuse or dependence, 163 genes were changed significantly.
Linkage Dataset
MarkerLODP valueLocation (bp)
D5S647  66282906
Region:66282906-76193808
Phenotype:Alcoholism phenotype along with age, gender, and P300 or constraint
Name:15211641
Method:Linkage
Publication:Hill et al. Am J Med Genet B Neuropsychiatr Genet. (2004) A genome wide search for alcoholism susceptibility genes. PubMed
Summary:A total of 360 markers for 22 autosomes were spaced at an average distance of 9.4cMand genotyping performed for 330 members of these multiplex families. Extensive clinical data, personality variation, and event-related potential characteristics were available for reducing heterogeneity and detecting robust linkage signals. Multipoint linkage analysis using different analytic strategies give strong support for loci on chromosomes 1, 2, 6, 7, 10, 12, 14, 16, and 17. Thirty five markers with LOD score >2.0 at baseline using the binary alcoholism phenotype along with age, gender, and P300 or constraint (Table III). Here we listed the genes between two near markers or genes near a separate marker (within 2Mb).
Gene Refseq Sequence Annotation
mRNAProteinReference assembly Genomic
NM_002270.3NP_002261.3NC_000005.8 range: 72148173..72245970
NM_153188.2NP_694858.1NC_000005.8 range: 72148173..72245970
Gene Ontology (GO) Annotation
GO IDGO TermCategoryEvidence (PubMed)
GO:0005634nucleusCellular ComponentTAS (9144189)
GO:0005643nuclear poreCellular ComponentIEA
GO:0005737cytoplasmCellular ComponentTAS (9144189)
GO:0005515protein bindingMolecular FunctionIPI (10353245)
GO:0008139nuclear localization sequence bindingMolecular FunctionTAS (8808633)
GO:0008565protein transporter activityMolecular FunctionIEA
GO:0000059protein import into nucleus, dockingBiological ProcessIEA
GO:0000060protein import into nucleus, translocationBiological ProcessTAS (9144189)
Other Database Cross Links
NCBI Entrez Gene:3842
HGNC:6401
Ensembl:ENSG00000083312
MIM:602901
HPRD:04210
HuGE Navigator:3842
dbSNP:TNPO1
GeneCard:TNPO1
AceView:TNPO1