KEGG   Homo sapiens (human): 100101267
Entry
100101267         CDS       T01001                                 
Symbol
POM121C, POM121-2
Name
(RefSeq) POM121 transmembrane nucleoporin C
  KO
K14316  nuclear pore complex protein Nup121
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
hsa05014  Amyotrophic lateral sclerosis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    100101267 (POM121C)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    100101267 (POM121C)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    100101267 (POM121C)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA surveillance and transport factors
   Transport factors
    Nuclear pore complex
     100101267 (POM121C)
SSDB
Motif
Pfam: POM121
Other DBs
NCBI-GeneID: 100101267
NCBI-ProteinID: NP_001092885
OMIM: 615754
HGNC: 34005
Ensembl: ENSG00000272391
UniProt: A8CG34 B4DET5 B4DDR5
Position
7:complement(75416786..75486299)
AA seq 987 aa
MVCSPVTVRIAPPDRRFSRSAIPEQIISSTLSSPSSNAPDPCAKETVLSALKEKKKKRTV
EEEDQIFLDGQENKRRRHDSSGSGHSAFEPLVASGVPASFVPKPGSLKRGLNSQSSDDHL
NKRSRSSSMSSLTGAYTSGIPSSSRNAITSSYSSTRGISQLWKRNGPSSSPFSSPASSRS
QTPERPAKKIREEELCHHSSSSTPLAADKESQGEKAADTTPRKKQNSNSQSTPGSSGQRK
RKVQLLPSRRGEQLTLPPPPQLGYSITAEDLDLEKKASLQWFNQALEDKSDAASNSVTET
PPTTQPSFTFTLPAAATASPPTSLLAPSTNPLLESLKKMQTPPSLPPCPESAGAATTEAL
SPPKTPSLLPPLGLSQSGPPGLLPSPSFDSKPPTTLLGLIPAPSMVPATDTKAPPTLQAE
TATKPQATSAPSPAPKQSFLFGTQNTSPSSPAAPAASSASPMFKPIFTAPPKSEKEGLTP
PGPSVSATAPSSSSLPTTTSTTAPTFQPVFSSMGPPASVPLPAPFFKQTTTPATAPTTTA
PLFTGLASATSAVAPITSASPSTDSASKPAFGFGINSVSSSSVSTTTSTATAASQPFLFG
APQASAASFTPAMGSIFQFGKPPALPTTTTVTTFSQSLPTAVPTATSSSAADFSGFGSTL
ATSAPATSSQPTLTFSNTSTPTFNIPFGSSAKSPLPSYPGANPQPAFGAAEGQPPGAAKP
ALTPSFGSSFTFGNSAAPAPATAPTPAPASTIKIVPAHVPTPIQPTFGGATHSAFGLKAT
ASAFGAPASSQPAFGGSTAVFSFGAATSSGFGATTQTASSGSSSSVFGSTTPSPFTFGGS
AAPAGSGSFGINVATPGSSATTGAFSFGAGQSGSTATSTPFTGGLGQNALGTTGQSTPFA
FNVGSTTESKPVFGGTATPTFGQNTPAPGVGTSGSSLSFGASSAPAQGFVGVGPFGSAAP
SFSIGAGSKTPGARQRLQARRQHTRKK
NT seq 2964 nt   +upstreamnt  +downstreamnt
atggtgtgtagcccagtgactgtgaggatcgcccctcctgacagaagattttcacgttct
gcgataccagagcagataatcagctcaacactgtcgtcaccatcaagtaatgccccagac
ccatgtgcaaaggagactgtactgagtgccctcaaagagaagaagaagaaaaggacagtg
gaggaagaagaccaaatattccttgatggccaggaaaataaaagaaggcgccatgatagc
agtggcagtggacattcagcatttgagcccctggtggccagtggagtccccgcttctttt
gtgcctaagcctgggtctctgaagagaggcctcaattctcagagctcagatgaccacttg
aataagagatcccgaagctcttccatgagctccttgacaggcgcttacacaagtggcatc
cctagctccagccgcaatgccattaccagttcctacagctccactcgaggcatctcacag
ctgtggaagagaaatggccccagttcatcacccttctctagcccagcctcatcccgctcc
cagacaccggagaggccagcaaagaaaataagagaagaagagctgtgtcatcattccagt
tcttcaactccattggcagcagacaaggagtcccagggagaaaaggctgcagatacaacc
ccaaggaagaaacaaaactcgaattctcagtctacacctggcagctctgggcagcgtaag
cggaaagttcagctgctgccttctcggcgaggggaacagctgaccttgcctccacctccc
cagcttggctattcgatcactgccgaggacctagacttagagaagaaggcttcattacag
tggttcaaccaggccttggaggacaagagtgatgctgcctcgaactctgtcactgagacc
ccacctaccactcagccttcatttacctttaccctgcctgctgctgcaactgcctcccca
cccacctccctcctggccccaagcaccaacccactgttagagagcttgaagaagatgcag
actcccccgagcctgccaccctgcccagaatctgctggagcagcaaccactgaggccctc
tcacctccaaagacacccagcctcctacccccgctgggtttatcacagtcagggccgcca
gggctgctccccagcccctcctttgactccaaacccccgaccactttgctggggctgatc
cctgctccatccatggtaccagccactgacaccaaggcacctccaacccttcaggcagag
acggctaccaaaccccaagccacatctgccccgtcccccgcccccaagcaaagcttcctg
tttggaacacagaacacctcaccttccagccctgccgcccctgctgcatcttcagcatct
cccatgttcaagcccattttcacggctccacccaagagtgagaaggaaggcctcacaccg
cctggcccttcagtctcagccacagcgccctccagctcctccctccccacgaccaccagc
accacagccccgaccttccagcctgtctttagcagcatggggccacctgcatctgtgccc
ttgcctgctcccttcttcaagcagacaactactcccgccactgctcccaccacaactgcc
ccgctcttcactggcctggccagcgccacctctgctgtggctcccatcacctctgccagt
ccatccacagactctgcttcgaagcctgcgtttggctttggcataaacagtgtgagcagc
agcagtgtgagtaccacgaccagcaccgccactgccgcctcacagcctttcctcttcggg
gcgccccaggcctctgctgccagcttcaccccggccatgggctccatattccagtttggc
aaacctcctgccttgcccacaaccaccacagtcaccaccttcagccagtccctgcccact
gccgtgccaacggccaccagcagcagcgctgccgactttagtggttttggcagcaccctc
gccacctccgccccggccaccagcagccagcccactctgacgttcagtaacacgagcacc
cccacgttcaacattccctttggctcaagcgccaagtccccgctcccatcatatccggga
gccaacccccagcccgcatttggggccgctgaggggcagccaccgggggccgccaagcca
gcccttacccccagctttggcagctctttcacttttggaaactctgcagccccggccccg
gctactgcacccacacctgcacctgcgtccacgatcaagatcgtgcctgcgcacgtgcct
acgcccatccagcctacctttggcggtgccacgcactcggcgtttggattgaaagccacg
gcttccgccttcggcgctcccgccagctcacagcccgcctttggcggctccactgctgtc
ttctccttcggtgcagccaccagctccggctttggagccaccacccagaccgccagcagc
gggagcagcagctcggtgtttggcagcacaacaccatcacccttcacgtttgggggttcg
gcagcccccgctggcagtgggagctttgggatcaacgtggccaccccaggctccagcgcc
accaccggagctttcagctttggagcaggacagagtgggagcacagccacctccaccccc
ttcacagggggcttaggtcagaacgccctgggcaccaccggccagagcacaccgtttgcc
ttcaacgtgggcagcacaactgagagcaaacctgtgtttggaggcaccgccacccccacc
tttggtcagaacacccctgcgcctggagtgggcacatcgggcagcagcctctcctttggg
gcatcttcagcacccgcccaaggctttgttggtgttggaccgttcggatcggcggcccct
tcattttccattggtgcgggatccaagaccccaggggctcgacagcgactgcaggcccga
aggcagcacacccgcaaaaagtag

  All links  
Disease (1)   
   OMIM (1)   
Gene (52)   
   RefGene (47)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (5)   
   UniProt (3)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (35)   
   RefSeq(nuc) (3)   
   GenBank (16)   
   EMBL (16)   
Protein domain (1)   
   Pfam (1)   
All databases (94)   

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