KEGG   Homo sapiens (human): 79882
Entry
79882             CDS       T01001                                 
Symbol
ZC3H14, MRT56, MSUT-2, NY-REN-37, SUT2, UKp68
Name
(RefSeq) zinc finger CCCH-type containing 14
  KO
K23038  zinc finger CCCH domain-containing protein 14
Organism
hsa  Homo sapiens (human)
Disease
H00768  Autosomal recessive intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    79882 (ZC3H14)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA processing factors
   Other processing factors
    79882 (ZC3H14)
SSDB
Motif
Pfam: zf-CCCH_2 PWI
Other DBs
NCBI-GeneID: 79882
NCBI-ProteinID: NP_079100
OMIM: 613279
HGNC: 20509
Ensembl: ENSG00000100722
UniProt: Q6PJT7
Position
14:88563037..88627596
AA seq 736 aa
MEIGTEISRKIRSAIKGKLQELGAYVDEELPDYIMVMVANKKSQDQMTEDLSLFLGNNTI
RFTVWLHGVLDKLRSVTTEPSSLKSSDTNIFDSNVPSNKSNFSRGDERRHEAAVPPLAIP
SARPEKRDSRVSTSSQESKTTNVRQTYDDGAATRLMSTVKPLREPAPSEDVIDIKPEPDD
LIDEDLNFVQENPLSQKKPTVTLTYGSSRPSIEIYRPPASRNADSGVHLNRLQFQQQQNS
IHAAKQLDMQSSWVYETGRLCEPEVLNSLEETYSPFFRNNSEKMSMEDENFRKRKLPVVS
SVVKVKKFNHDGEEEEEDDDYGSRTGSISSSVSVPAKPERRPSLPPSKQANKNLILKAIS
EAQESVTKTTNYSTVPQKQTLPVAPRTRTSQEELLAEVVQGQSRTPRISPPIKEEETKGD
SVEKNQGTQQRQLLSRLQIDPVMAETLQMSQDYYDMESMVHADTRSFILKKPKLSEEVVV
APNQESGMKTADSLRVLSGHLMQTRDLVQPDKPASPKFIVTLDGVPSPPGYMSDQEEDMC
FEGMKPVNQTAASNKGLRGLLHPQQLHLLSRQLEDPNGSFSNAEMSELSVAQKPEKLLER
CKYWPACKNGDECAYHHPISPCKAFPNCKFAEKCLFVHPNCKYDAKCTKPDCPFTHVSRR
IPVLSPKPAVAPPAPPSSSQLCRYFPACKKMECPFYHPKHCRFNTQCTRPDCTFYHPTIN
VPPRHALKWIRPQTSE
NT seq 2211 nt   +upstreamnt  +downstreamnt
atggagatcggcaccgagatcagccgcaagatccggagtgccattaaggggaaattacaa
gaattaggagcttatgttgatgaagaacttcctgattacattatggtgatggtggccaac
aagaaaagtcaggaccaaatgacagaggatctgtccctgtttctagggaacaacacaatt
cgattcaccgtatggcttcatggtgtattagataaacttcgctctgttacaactgaaccc
tctagtctgaagtcttctgataccaacatctttgatagtaacgtgccttcaaacaagagc
aatttcagtcggggagatgagaggaggcatgaagctgcagtgccaccacttgccattcct
agcgcgagacctgaaaaaagagattccagagtttctacaagttcgcaggagtcaaaaacc
acaaatgtcagacagacttacgatgatggagctgcaacccgactaatgtcaacagtgaaa
cctttgagggagccagcaccctctgaagatgtgattgatattaagccagaaccagatgat
ctcattgacgaagacctcaactttgtgcaggagaatcccttatctcagaaaaaacctaca
gtgacacttacatatggttcttctcgcccttctattgaaatttatcgaccacctgcaagt
agaaatgcagatagtggtgttcatttaaacaggttgcaatttcaacagcagcagaatagt
attcatgctgccaagcagcttgatatgcagagtagttgggtatatgaaacaggacgtttg
tgtgaaccagaggtgcttaacagcttagaagaaacgtatagtccgttctttagaaacaac
tcggagaaaatgagtatggaggatgaaaactttcggaagagaaagttgcctgtggtaagt
tcagttgttaaagtaaaaaaattcaatcatgatggagaagaggaggaagaagatgatgat
tacgggtctcgaacaggaagcatctccagcagtgtgtctgtgcctgcaaagcctgaaagg
agaccttctcttccaccttctaaacaagctaacaagaatctgattttgaaggctatatct
gaagctcaagaatccgtaacaaaaacaactaactactctacagttccacagaaacagaca
cttccagttgctcccagaactcgaacttctcaagaagaattgctagcagaagtggtccag
ggacaaagtaggacccccagaataagtccccccattaaagaagaggaaacaaaaggagat
tctgtagaaaaaaatcaaggaactcaacagaggcaattattatcccgactgcaaatcgac
ccagtaatggcagaaactctgcagatgagtcaagattactatgacatggaatccatggtc
catgcagacacaagatcatttattctgaagaagccaaagctgtctgaggaagtagtagtg
gcaccaaaccaagagtcggggatgaagactgcagattcccttcgggtactttcaggacac
cttatgcagacacgagatcttgtacaaccagataaacctgcaagtcccaagtttatagtg
acgctggatggtgtccccagccccccaggatacatgtcagatcaagaggaggacatgtgc
tttgaaggaatgaaacccgtaaaccaaactgcagcctcaaacaagggactcagaggtctc
ctccacccacagcagttgcacttgctgagcaggcagcttgaggacccaaatggtagcttt
tctaacgctgagatgagtgaactgagtgtggcacagaaaccagaaaaacttttggagcgc
tgcaagtactggcctgcttgtaaaaatggggatgagtgtgcctaccatcaccccatctca
ccctgcaaagccttccccaattgtaaatttgctgaaaaatgtttgtttgttcacccaaat
tgtaaatatgatgcaaagtgtactaaaccagattgtcccttcactcatgtgagtagaaga
attccagtactgtctccaaaaccagcagttgcaccaccagcaccaccttccagtagtcag
ctctgccgttacttccctgcttgtaagaagatggaatgtcccttctatcatccaaaacat
tgtaggtttaacactcaatgtacaagaccggactgcacattctaccatcccaccattaat
gtcccaccacgacatgccttgaaatggattcgacctcaaaccagcgaatag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (15)   
   KEGG ORTHOLOGY (1)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (32)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (30)   
DNA sequence (81)   
   RefSeq(nuc) (31)   
   GenBank (25)   
   EMBL (25)   
Protein domain (2)   
   Pfam (2)   
All databases (136)   

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