KEGG   Homo sapiens (human): 11132
Entry
11132             CDS       T01001                                 
Symbol
CAPN10, CANP10, NIDDM1
Name
(RefSeq) calpain 10
  KO
K08579  calpain-10 [EC:3.4.22.-]
Organism
hsa  Homo sapiens (human)
Disease
H00409  Type 2 diabetes mellitus
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01002 Peptidases and inhibitors [BR:hsa01002]
    11132 (CAPN10)
Peptidases and inhibitors [BR:hsa01002]
 Cysteine peptidases
  Family C2: calpain family
   11132 (CAPN10)
SSDB
Motif
Pfam: Peptidase_C2 Calpain_III
Other DBs
NCBI-GeneID: 11132
NCBI-ProteinID: NP_075571
OMIM: 605286
HGNC: 1477
Ensembl: ENSG00000142330
UniProt: Q9HC96
Position
2:240586734..240599104
AA seq 672 aa
MRAGRGATPARELFRDAAFPAADSSLFCDLSTPLAQFREDITWRRPQEICATPRLFPDDP
REGQVKQGLLGDCWFLCACAALQKSRHLLDQVIPPGQPSWADQEYRGSFTCRIWQFGRWV
EVTTDDRLPCLAGRLCFSRCQREDVFWLPLLEKVYAKVHGSYEHLWAGQVADALVDLTGG
LAERWNLKGVAGSGGQQDRPGRWEHRTCRQLLHLKDQCLISCCVLSPRAGARELGEFHAF
IVSDLRELQGQAGQCILLLRIQNPWGRRCWQGLWREGGEGWSQVDAAVASELLSQLQEGE
FWVEEEEFLREFDELTVGYPVTEAGHLQSLYTERLLCHTRALPGAWVKGQSAGGCRNNSG
FPSNPKFWLRVSEPSEVYIAVLQRSRLHAADWAGRARALVGDSHTSWSPASIPGKHYQAV
GLHLWKVEKRRVNLPRVLSMPPVAGTACHAYDREVHLRCELSPGYYLAVPSTFLKDAPGE
FLLRVFSTGRVSLSAIRAVAKNTTPGAALPAGEWGTVQLRGSWRVGQTAGGSRNFASYPT
NPCFPFSVPEGPGPRCVRITLHQHCRPSDTEFHPIGFHIFQVPEGGRSQDAPPLLLQEPL
LSCVPHRYAQEVSRLCLLPAGTYKVVPSTYLPDTEGAFTVTIATRIDRPSIHSQEMLGQF
LQEVSIMAVMKT
NT seq 2019 nt   +upstreamnt  +downstreamnt
atgcgggcgggccggggcgcgacgccggcgagggagctgttccgggacgccgccttcccc
gccgcggactcctcgctcttctgcgacttgtctacgccgctggcccagttccgcgaggac
atcacgtggaggcggccccaggagatttgtgccacaccccggctgtttccagatgaccca
cgggaagggcaggtgaagcaggggctgctgggggattgctggttcctgtgtgcctgcgcc
gcgctgcagaagagcaggcacctcctggaccaggtcattcctccgggacagccgagctgg
gccgaccaggagtaccggggctccttcacctgtcgcatttggcagtttggacgctgggtg
gaggtgaccacagatgaccgcctgccgtgccttgcagggagactctgtttctcccgctgc
cagagggaggatgtgttctggctccccttactggaaaaggtctacgccaaggtccatggg
tcctacgagcacctgtgggccgggcaggtggcggatgccctggtggacctgaccggcggc
ctggcagaaagatggaacctgaagggcgtagcaggaagcggaggccagcaggacaggcca
ggccgctgggagcacaggacttgtcggcagctgctccacctgaaggaccagtgtctgatc
agctgctgcgtgctcagccccagagcaggtgcccgggagctgggggagttccatgccttc
attgtctcggacctgcgggagctccagggtcaggcgggccagtgcatcctgctgctgcgg
atccagaacccctggggccggcggtgctggcaggggctctggagagaggggggtgaaggg
tggagccaggtagatgcagcggtagcatctgagctcctgtcccagctccaggaaggggag
ttctgggtggaggaggaggagttcctcagggagtttgacgagctcaccgttggctacccg
gtcacggaggccggccacctgcagagcctctacacagagaggctgctctgccatacgcgg
gcgctgcctggggcctgggtcaagggccagtcagcaggaggctgccggaacaacagcggc
tttcccagcaaccccaaattctggctgcgggtctcagaaccgagtgaggtgtacattgcc
gtcctgcagagatccaggctgcacgcggcggactgggcaggccgggcccgggcactggtg
ggtgacagtcatacttcgtggagcccagcgagcatcccgggcaagcactaccaggctgtg
ggtctgcacctctggaaggtagagaagcggcgggtcaatctgcctagggtcctgtccatg
ccccccgtggctggcaccgcgtgccatgcatacgaccgggaggtccacctgcgttgtgag
ctctcaccgggctactacctggctgtccccagcaccttcctgaaggacgcgccaggggag
ttcctgctccgagtcttctctaccgggcgagtctcccttagcgccatcagggcagtggcc
aagaacaccacccccggggcagccctgcctgcgggggagtgggggaccgtgcagctacgg
ggttcttggagagtcggccagacggcggggggcagcaggaactttgcctcataccccacc
aacccctgcttccccttctcggtccccgagggccctggcccccgctgcgtccgcatcact
ctgcatcagcactgccggcccagtgacaccgagttccaccccatcggcttccatatcttc
caggtcccagagggtggaaggagccaggacgcacccccactgctgctgcaggagccgctg
ctgagctgcgtgccacatcgctacgcccaggaggtgagccggctctgcctcctgcctgcg
ggcacctacaaggttgtgccctccacctacctgccggacacagagggggccttcacagtg
accatcgcaaccaggattgacaggccatccattcacagccaggagatgctgggccagttc
ctccaagaggtctccatcatggcagtgatgaaaacctaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (54)   
   RefSeq(nuc) (8)   
   GenBank (23)   
   EMBL (23)   
Protein domain (2)   
   Pfam (2)   
All databases (83)   

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