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Chromosome 7 - NC_000007.14
Genomic Sequence: NC_000007.14 Chromosome 7 Reference GRCh38.p14 Primary Assembly NW_017852929.1 Chromosome 7 Reference GRCh38.p14 PATCHES NG_051213.1 RefSeqGene NC_060931.1 Chromosome 7 Alternate T2T-CHM13v2.0 NC_000007.13 Chromosome 7 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
See all (19) citations in PubMed
Find tests for this gene in the NIH Genetic Testing Registry (GTR)
Review eQTL and phenotype association data in this region using PheGenI
See variants in ClinVar
See studies and variants in dbVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
NEW Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.
NG_051213.1 RefSeqGene
NM_001145715.3 → NP_001139187.1 importin subunit alpha-8
See identical proteins and their annotated locations for NP_001139187.1
Status: REVIEWED
The following sections contain reference sequences that belong to a specific genome build. Explain
This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.
NC_000007.14 Reference GRCh38.p14 Primary Assembly
XM_017012211.2 → XP_016867700.1 importin subunit alpha-8 isoform X8
XM_011516215.3 → XP_011514517.1 importin subunit alpha-8 isoform X3
XM_017012213.2 → XP_016867702.1 importin subunit alpha-8 isoform X5
XM_017012209.2 → XP_016867698.1 importin subunit alpha-8 isoform X2
XM_017012215.2 → XP_016867704.1 importin subunit alpha-8 isoform X6
XM_017012208.2 → XP_016867697.1 importin subunit alpha-8 isoform X1
XM_017012210.2 → XP_016867699.1 importin subunit alpha-8 isoform X4
XM_017012214.2 → XP_016867703.1 importin subunit alpha-8 isoform X5
XM_017012212.2 → XP_016867701.1 importin subunit alpha-8 isoform X5
XM_017012216.2 → XP_016867705.1 importin subunit alpha-8 isoform X7
NW_017852929.1 Reference GRCh38.p14 PATCHES
XM_054332121.1 → XP_054188096.1 importin subunit alpha-8 isoform X8
XM_054332119.1 → XP_054188094.1 importin subunit alpha-8 isoform X3
XM_054332124.1 → XP_054188099.1 importin subunit alpha-8 isoform X5
XM_054332123.1 → XP_054188098.1 importin subunit alpha-8 isoform X5
XM_054332118.1 → XP_054188093.1 importin subunit alpha-8 isoform X2
XM_054332126.1 → XP_054188101.1 importin subunit alpha-8 isoform X6
XM_054332117.1 → XP_054188092.1 importin subunit alpha-8 isoform X1
XM_054332120.1 → XP_054188095.1 importin subunit alpha-8 isoform X4
XM_054332125.1 → XP_054188100.1 importin subunit alpha-8 isoform X5
XM_054332122.1 → XP_054188097.1 importin subunit alpha-8 isoform X5
XM_054332127.1 → XP_054188102.1 importin subunit alpha-8 isoform X7
NC_060931.1 Alternate T2T-CHM13v2.0
XM_054358223.1 → XP_054214198.1 importin subunit alpha-8 isoform X3
XM_054358227.1 → XP_054214202.1 importin subunit alpha-8 isoform X5
XM_054358226.1 → XP_054214201.1 importin subunit alpha-8 isoform X5
XM_054358222.1 → XP_054214197.1 importin subunit alpha-8 isoform X2
XM_054358229.1 → XP_054214204.1 importin subunit alpha-8 isoform X6
XM_054358221.1 → XP_054214196.1 importin subunit alpha-8 isoform X1
XM_054358224.1 → XP_054214199.1 importin subunit alpha-8 isoform X4
XM_054358228.1 → XP_054214203.1 importin subunit alpha-8 isoform X5
XM_054358225.1 → XP_054214200.1 importin subunit alpha-8 isoform X5
XM_054358230.1 → XP_054214205.1 importin subunit alpha-8 isoform X7
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