KEGG   Homo sapiens (human): 79772
Entry
79772             CDS       T01001                                 
Symbol
MCTP1
Name
(RefSeq) multiple C2 and transmembrane domain containing 1
Organism
hsa  Homo sapiens (human)
SSDB
Motif
Pfam: C2 PRT_C PKC_C2 Pex24p DUF639 CEP76-C2 E7
Other DBs
NCBI-GeneID: 79772
NCBI-ProteinID: NP_078993
OMIM: 616296
HGNC: 26183
Ensembl: ENSG00000175471
UniProt: Q6DN14 B7Z4G1
Position
5:complement(94703690..95285094)
AA seq 999 aa
MEPRAAAAGEPEPPAASSSFQARLWKNLQLGVGRSKGGGGGRAGGPERRTADTPSPSPPP
PVGTGNAPARGSGAGSRWSGFKKRKQVLDRVFSSSQPNLCCSSPEPLEPGGAGRAEQGST
LRRRIREHLLPAVKGPAAASGAAGGTPPGGRSPDSAPSSSSASSSLSSSPQPPPRGDRAR
DEGARRQGPGAHLCHQKSSSLPGTACLEQLLEPPPPPAEPARSPAESRAPETGEEHGSSQ
KIINTAGTSNAEVPLADPGMYQLDITLRRGQSLAARDRGGTSDPYVKFKIGGKEVFRSKI
IHKNLNPVWEEKACILVDHLREPLYIKVFDYDFGLQDDFMGSAFLDLTQLELNRPTDVTL
TLKDPHYPDHDLGIILLSVILTPKEGESRDVTMLMRKSWKRSSKELSENEVVGSYFSVKS
LFWRTCGRPALPVLGFCRAELQNPYCKNVQFQTQSLRLSDLHRKSHLWRGIVSITLIEGR
DLKAMDSNGLSDPYVKFRLGHQKYKSKIMPKTLNPQWREQFDFHLYEERGGVIDITAWDK
DAGKRDDFIGRCQVDLSALSREQTHKLELQLEEGEGHLVLLVTLTASATVSISDLSVNSL
EDQKEREEILKRYSPLRIFHNLKDVGFLQVKVIRAEGLMAADVTGKSDPFCVVELNNDRL
LTHTVYKNLNPEWNKVFTFNIKDIHSVLEVTVYDEDRDRSADFLGKVAIPLLSIQNGEQK
AYVLKNKQLTGPTKGVIYLEIDVIFNAVKASLRTLIPKEQKYIEEENRLSKQLLLRNFIR
MKRCVMVLVNAAYYVNSCFDWDSPPRSLAAFVLFLFVVWNFELYMIPLVLLLLLTWNYFL
IISGKDNRQRDTVVEDMLEDEEEEDDKDDKDSEKKGFINKIYAIQEVCVSVQNILDEVAS
FGERIKNTFNWTVPFLSWLAIVALCVFTAILYCIPLRYIVLVWGINKFTKKLRSPYAIDN
NELLDFLSRVPSDVQVVQYQELKPDPSHSPYKRKKNNLG
NT seq 3000 nt   +upstreamnt  +downstreamnt
atggagccccgggctgccgcggcgggcgagccagagccgccggcggcgtcctcctccttc
caggcccggctctggaagaacctgcagctgggggtgggcaggagcaagggcggcgggggc
gggcgcgctgggggtccagagcgccgcactgcggacaccccgtcgccctccccgccaccc
ccggtgggcacagggaatgcaccggccagggggagtggtgcaggcagcaggtggagcggc
ttcaagaagcggaagcaagtgctggaccgagtcttctcctcctcgcagcccaacctgtgc
tgctcgtcgccggagcccctggagcccggcggcgccggcagagccgagcaggggtccacg
ctacgccgccggatccgcgagcatttgctccccgccgtaaaggggcccgcggcggcctcg
ggagcagcgggagggacgcctcctggcggacgctcccccgactcagctccttcctcttcc
tccgcctcatcctccctgtcctcctcgccccagcctcccccgaggggggaccgcgcccga
gatgagggtgcacggcgtcagggccccggggcgcacttgtgccaccagaagagctcctct
ctgccgggcaccgcctgcctggagcagctgctggagccgccgcctcctcccgcagagccg
gcgcggagtcccgcggagtctcgggccccggagacgggcgaggagcacggcagcagccag
aaaataataaacactgctggaaccagtaatgcagaagtccccttggctgatcccggaatg
taccagctggacattacattaagaaggggtcaaagtttagctgctcgagatcgaggaggg
acgagtgatccatatgtgaagtttaaaatcggaggaaaagaagtttttagaagtaagata
atacacaagaacctcaaccctgtgtgggaagaaaaagcttgtattctggttgatcatctt
agggagccattgtatataaaggtatttgactatgattttggactacaggatgactttatg
ggctcagcctttctggatctgacacaattggagttaaacaggcccacagatgtgaccctt
actctgaaagatcctcattatcctgaccatgatcttggaatcattttgctctcagtcatc
cttacccctaaagaaggagagtccagggatgtgacaatgctaatgaggaagagttggaaa
agatcaagtaaggaactttcagaaaatgaagtggttggatcttatttctctgtgaagtct
ctcttttggaggacgtgcggcaggccagctcttcctgtcctgggcttctgcagagcagag
cttcagaatccttattgcaaaaatgtacaatttcagacccaaagtttacgcctatcagac
ctacacagaaaatcgcatctttggagaggaatagtcagcatcaccttgattgaagggaga
gacctcaaggccatggattccaacgggttgagcgatccctacgtgaagttccggcttggg
catcagaagtacaagagcaagattatgccaaaaacgttgaatcctcagtggagggaacaa
tttgattttcacctttatgaagaaagaggaggagtcattgatatcactgcatgggacaaa
gatgctgggaaaagggatgatttcattggcaggtgccaggtcgacctgtcagccctcagt
agggaacagacgcacaagctggagttgcagctggaagagggtgagggacacctggtgctg
ctggtcactctgacagcatcagccacagtcagcatctctgacctgtctgtcaactccctg
gaggaccagaaggaacgagaggagatattaaagagatatagcccattgaggatatttcac
aacctgaaagatgtgggatttctccaggtgaaagtcatcagagcggaagggttaatggct
gccgacgtcactggaaaaagtgacccattttgtgtggtagaactgaacaacgatagactg
ctaacacatactgtctacaaaaatctcaatcctgagtggaataaagtcttcacgttcaac
attaaagatatccattcagttcttgaagtgacagtttatgatgaagatcgggatcgaagt
gctgactttctgggcaaagttgctataccattgctgtctattcaaaatggtgaacagaaa
gcctacgtcttgaaaaacaagcagctgacagggccaacaaagggggtcatctatcttgaa
atagatgtgatttttaatgctgtgaaagccagcttacgaacattaatacccaaagaacag
aagtacattgaagaggaaaacagactctctaaacagctgctactaagaaactttatcaga
atgaaacgttgtgtcatggtgctggtaaatgctgcatactacgttaatagttgctttgat
tgggattcacccccaaggagtctcgctgcttttgtgctctttctctttgttgtctggaac
tttgagctctacatgataccactggttttgttgttactattgacatggaactacttcttg
ataatatcagggaaagataacaggcaacgtgatacagtagtggaggacatgctagaggac
gaggaagaagaagatgacaaagatgacaaggacagtgaaaaaaagggatttataaataaa
atctatgccatccaggaggtatgtgtcagtgtccagaacatcctagatgaagtggcttcc
tttggcgaaaggataaagaatactttcaactggactgtcccattcttaagctggctggcc
attgtagccctctgtgtgttcacagccatcctgtactgcattccgctgagatacattgtc
cttgtctggggcatcaataaatttacaaaaaagcttcggagtccatatgcaattgataac
aatgaactacttgacttcctttccagagtcccttcagatgtacaagtggtgcaataccaa
gaactgaaaccagatccttctcatagcccatataaaagaaagaaaaacaatcttggctag

  All links  
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (41)   
   RefGene (35)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (95)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (92)   
DNA sequence (122)   
   RefSeq(nuc) (92)   
   GenBank (15)   
   EMBL (15)   
Protein domain (7)   
   Pfam (7)   
All databases (267)   

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