KEGG   Homo sapiens (human): 283987
Entry
283987            CDS       T01001                                 
Symbol
HID1, 17orf28, C17orf28, DEE105, DMC1, HID-1
Name
(RefSeq) HID1 domain containing
Organism
hsa  Homo sapiens (human)
Disease
H00606  Early infantile epileptic encephalopathy
SSDB
Motif
Pfam: Hid1 Dymeclin
Other DBs
NCBI-GeneID: 283987
NCBI-ProteinID: NP_085133
OMIM: 605752
HGNC: 15736
Ensembl: ENSG00000167861
UniProt: Q8IV36
Position
17:complement(74950742..74972759)
AA seq 788 aa
MGSTDSKLNFRKAVIQLTTKTQPVEATDDAFWDQFWADTATSVQDVFALVPAAEIRAVRE
ESPSNLATLCYKAVEKLVQGAESGCHSEKEKQIVLNCSRLLTRVLPYIFEDPDWRGFFWS
TVPGAGRGGQGEEDDEHARPLAESLLLAIADLLFCPDFTVQSHRRSTVDSAEDVHSLDSC
EYIWEAGVGFAHSPQPNYIHDMNRMELLKLLLTCFSEAMYLPPAPESGSTNPWVQFFCST
ENRHALPLFTSLLNTVCAYDPVGYGIPYNHLLFSDYREPLVEEAAQVLIVTLDHDSASSA
SPTVDGTTTGTAMDDADPPGPENLFVNYLSRIHREEDFQFILKGIARLLSNPLLQTYLPN
STKKIQFHQELLVLFWKLCDFNKKFLFFVLKSSDVLDILVPILFFLNDARADQSRVGLMH
IGVFILLLLSGERNFGVRLNKPYSIRVPMDIPVFTGTHADLLIVVFHKIITSGHQRLQPL
FDCLLTIVVNVSPYLKSLSMVTANKLLHLLEAFSTTWFLFSAAQNHHLVFFLLEVFNNII
QYQFDGNSNLVYAIIRKRSIFHQLANLPTDPPTIHKALQRRRRTPEPLSRTGSQEGTSME
GSRPAAPAEPGTLKTSLVATPGIDKLTEKSQVSEDGTLRSLEPEPQQSLEDGSPAKGEPS
QAWREQRRPSTSSASGQWSPTPEWVLSWKSKLPLQTIMRLLQVLVPQVEKICIDKGLTDE
SEILRFLQHGTLVGLLPVPHPILIRKYQANSGTAMWFRTYMWGVIYLRNVDPPVWYDTDV
KLFEIQRV
NT seq 2367 nt   +upstreamnt  +downstreamnt
atggggtcgaccgactccaagctgaacttccggaaggcggtgatccagctcaccaccaag
acgcagcccgtggaagccaccgatgatgccttttgggaccagttctgggcagacacagcc
acctcggtgcaggatgtgtttgcactggtgccggcagcagagatccgggccgtgcgggaa
gagtcaccctccaacttggccaccctgtgctacaaggccgttgagaagctggtgcaggga
gctgagagtggctgccactcggagaaggagaagcagatcgtcctgaactgcagccggctg
ctcacccgcgtgctgccctacatctttgaggaccccgactggaggggcttcttctggtcc
acagtgcccggggcagggcgaggagggcagggagaagaggatgatgagcatgccaggccc
ctggccgagtccctgctcctggccattgctgacctgctcttctgcccggacttcacggtt
cagagccaccggaggagcactgtggactcggcagaggacgtccactccctggacagctgt
gaatacatctgggaggctggtgtgggcttcgctcactccccccagcctaactacatccac
gatatgaaccggatggagctgctgaaactgctgctgacatgcttctccgaggccatgtac
ctgcccccagctccggaaagtggcagcaccaacccatgggttcagttcttttgttccacg
gagaacagacatgccctgcccctcttcacctccctcctcaacaccgtgtgtgcctatgac
cctgtgggctacgggatcccctacaaccacctgctcttctctgactaccgggaacccctg
gtggaggaggctgcccaggtgctcattgtcactttggaccacgacagtgccagcagtgcc
agccccactgtggacggcaccaccactggcaccgccatggatgatgccgatcctccaggc
cctgagaacctgtttgtgaactacctgtcccgcatccatcgtgaggaggacttccagttc
atcctcaagggtatagcccggctgctgtccaaccccctgctccagacctacctgcctaac
tccaccaagaagatccagttccaccaggagctgctagttctcttctggaagctctgcgac
ttcaacaagaaattcctcttcttcgtgctgaagagcagcgacgtcctagacatccttgtc
cccatcctcttcttcctcaacgatgcccgggccgatcagtctcgggtgggcctgatgcac
attggtgtcttcatcttgctgcttctgagcggggagcggaacttcggggtgcggctgaac
aaaccctactcaatccgcgtgcccatggacatcccagtcttcacagggacccacgccgac
ctgctcattgtggtgttccacaagatcatcaccagcgggcaccagcggttgcagcccctc
ttcgactgcctgctcaccatcgtggtcaacgtgtccccctacctcaagagcctgtccatg
gtgactgccaacaagttgctgcacctgctggaggccttctccaccacctggttcctcttc
tctgccgcccagaaccaccacctggtcttcttcctcctggaggtcttcaacaacatcatc
cagtaccagtttgatggcaactccaacctggtctacgccatcatccgcaagcgcagcatc
ttccaccagctggccaacctgcccacggacccgcccaccattcacaaggccctgcagcgg
cgccggcggacacctgagcccttgtctcgcaccggctcccaggagggcacctccatggag
ggctcccgccccgctgcccctgcagagccaggcaccctcaagaccagtctggtggctact
ccaggcattgacaagctgaccgagaagtcccaggtgtcagaggatggcaccttgcggtcc
ctggaacctgagccccagcagagcttggaggatggcagcccggctaagggggagcccagc
caggcatggagggagcagcggcgaccgtccacctcatcagccagtgggcagtggagccca
acgccagagtgggtcctctcctggaagtcgaagctgccgctgcagaccatcatgaggctg
ctgcaggtgctggttccgcaggtggagaagatctgcattgacaagggcctgacggatgag
tctgagatcctgcggttcctgcagcatggcaccctggtggggctgctgcccgtgccccac
cccatcctcatccgcaagtaccaggccaactcgggcactgccatgtggttccgcacctac
atgtggggcgtcatctatctgaggaatgtggacccccctgtctggtacgacaccgacgtg
aagctgtttgagatacagcgggtgtga

  All links  
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (40)   
   RefGene (21)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (14)   
   OC (1)   
Protein sequence (9)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (27)   
   RefSeq(nuc) (7)   
   GenBank (10)   
   EMBL (10)   
Protein domain (2)   
   Pfam (2)   
All databases (82)   

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