KEGG   Homo sapiens (human): 93627
Entry
93627             CDS       T01001                                 
Symbol
TBCK, FERRY1, Fy-1, HSPC302, IHPRF3, TBCKL
Name
(RefSeq) TBC1 domain containing kinase
  KO
K17544  TBC domain-containing protein kinase-like protein
Organism
hsa  Homo sapiens (human)
Disease
H01922  Infantile hypotonia with psychomotor retardation and characteristic facies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01001 Protein kinases [BR:hsa01001]
    93627 (TBCK)
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    93627 (TBCK)
Protein kinases [BR:hsa01001]
 Serine/threonine kinases: Other
  TBCK family
   93627 (TBCK)
Membrane trafficking [BR:hsa04131]
 Endosome - Lysosome transport
  Rab GTPases and associated proteins
   FERRY complex
    93627 (TBCK)
SSDB
Motif
Pfam: RabGAP-TBC Pkinase PK_Tyr_Ser-Thr RabGap-TBC_2 Rhodanese Kinase-like
Other DBs
NCBI-GeneID: 93627
NCBI-ProteinID: NP_001156907
OMIM: 616899
HGNC: 28261
Ensembl: ENSG00000145348
UniProt: Q8TEA7
Position
4:complement(106041599..106316683)
AA seq 893 aa
MFPLKDAEMGAFTFFASALPHDVCGSNGLPLTPNSIKILGRFQILKTITHPRLCQYVDIS
RGKHERLVVVAEHCERSLEDLLRERKPVSCSTVLCIAFEVLQGLQYMNKHGIVHRALSPH
NILLDRKGHIKLAKFGLYHMTAHGDDVDFPIGYPSYLAPEVIAQGIFKTTDHMPSKKPLP
SGPKSDVWSLGIILFELCVGRKLFQSLDISERLKFLLTLDCVDDTLIVLAEEHGCLDIIK
ELPETVIDLLNKCLTFHPSKRPTPDQLMKDKVFSEVSPLYTPFTKPASLFSSSLRCADLT
LPEDISQLCKDINNDYLAERSIEEVYYLWCLAGGDLEKELVNKEIIRSKPPICTLPNFLF
EDGESFGQGRDRSSLLDDTTVTLSLCQLRNRLKDVGGEAFYPLLEDDQSNLPHSNSNNEL
SAAATLPLIIREKDTEYQLNRIILFDRLLKAYPYKKNQIWKEARVDIPPLMRGLTWAALL
GVEGAIHAKYDAIDKDTPIPTDRQIEVDIPRCHQYDELLSSPEGHAKFRRVLKAWVVSHP
DLVYWQGLDSLCAPFLYLNFNNEALAYACMSAFIPKYLYNFFLKDNSHVIQEYLTVFSQM
IAFHDPELSNHLNEIGFIPDLYAIPWFLTMFTHVFPLHKIFHLWDTLLLGNSSFPFCIGV
AILQQLRDRLLANGFNECILLFSDLPEIDIERCVRESINLFCWTPKSATYRQHAQPPKPS
SDSSGGRSSAPYFSAECPDPPKTDLSRESIPLNDLKSEVSPRISAEDLIDLCELTVTGHF
KTPSKKTKSSKPKLLVVDIRNSEDFIRGHISGSINIPFSAAFTAEGELTQGPYTAMLQNF
KGKVIVIVGHVAKHTAEFAAHLVKMKYPRICILDGGINKIKPTGLLTIPSPQI
NT seq 2682 nt   +upstreamnt  +downstreamnt
atgtttcccctgaaggacgctgaaatgggagcctttaccttctttgcctcggctctgcca
catgatgtttgtggaagcaatggacttcctctcacaccaaattccatcaaaattttaggg
cgctttcaaatccttaaaaccatcacccatcccagactctgccagtatgtggatatttct
aggggaaagcatgaacgactagtggtcgtggctgaacattgtgaacgtagtctggaagac
ttgcttcgagaaaggaaacctgtgagctgttcaacggttttgtgtatagcatttgaggtt
cttcagggcttgcagtatatgaacaaacatggtatagtacacagggcattgtctcctcat
aatatcctgttggaccgaaagggacatattaaattggctaaatttggactttatcacatg
acagctcatggtgatgatgttgatttcccaatagggtatccctcgtacttggcccctgag
gtaattgcacagggaattttcaaaaccactgatcacatgccaagtaaaaaaccattgcct
tctggccccaaatcagatgtatggtctcttggaatcattttatttgagctttgtgtggga
agaaaattatttcagagcttggatatttctgaaagactaaaatttttgcttactttggat
tgtgtagatgacactttaatagttctggctgaagagcatggttgtttggacattataaag
gagcttcctgaaactgtgatagatcttttgaataagtgccttaccttccatccttctaag
aggccaaccccagatcaattaatgaaggacaaagtattcagtgaggtatcacctttatat
accccctttaccaaacctgccagtctgttttcatcttctctgagatgtgctgatttaact
ctgcctgaggatatcagtcagttgtgtaaagatataaataatgattacctggcagaaaga
tctattgaagaagtgtattacctttggtgtttggctggaggtgacttggagaaagagctt
gtcaacaaggaaatcattcgatccaaaccacctatctgcacactccccaattttctcttt
gaggatggtgaaagctttggacaaggtcgagatagaagctcgcttttagatgataccact
gtgacattgtcgttatgccagctaagaaatagattgaaagatgttggtggagaagcattt
tacccattacttgaagatgaccagtctaatttacctcattcaaacagcaataatgagttg
tctgcagctgccacgctccctttaatcatcagagagaaggatacagagtaccaactaaat
agaattattctcttcgacaggctgctaaaggcttatccatataaaaaaaaccaaatctgg
aaagaagcaagagttgacattcctcctcttatgagaggtttaacctgggctgctcttctg
ggagttgagggagctattcatgccaagtacgatgcaattgataaagacactccaattcct
acagatagacaaattgaagtggatattcctcgctgtcatcagtacgatgaactgttatca
tcaccagaaggtcatgcaaaatttaggcgtgtattaaaagcctgggtagtgtctcatcct
gatcttgtgtattggcaaggtcttgactcactttgtgctccattcctatatctaaacttc
aataatgaagccttggcttatgcatgtatgtctgcttttattcccaaatacctgtataac
ttcttcttaaaagacaactcacatgtaatacaagagtatctgactgtcttctctcagatg
attgcatttcatgatccagagctgagtaatcatctcaatgagattggtttcattccagat
ctctatgccatcccttggtttcttaccatgtttactcatgtatttccactacacaaaatt
ttccacctctgggataccttactacttgggaattcctctttcccattctgtattggagta
gcaattcttcagcagctgcgggaccggcttttggctaatggctttaatgagtgtattctt
ctcttctccgatttaccagaaattgacattgaacgctgtgtgagagaatctatcaacctg
ttttgttggactcctaaaagtgctacttacagacagcatgctcaacctccaaagccatct
tctgacagcagtggaggcagaagttcggcaccttatttctctgctgagtgtccagatcct
ccaaagacagatctgtcaagagaatccatcccattaaatgacctgaagtcagaagtatca
ccacggatttcagcagaggacctgattgacttgtgtgagctcacagtgacaggccacttc
aaaacacccagcaagaaaacaaagtccagtaaaccaaagctcctggtggttgacatccgg
aatagtgaagactttattcgtggtcacatttcaggaagcatcaacattccattcagtgct
gccttcactgcagaaggggagcttacccagggcccttacactgctatgctccagaacttc
aaagggaaggtcattgtcatcgtggggcatgtggcaaaacacacagctgagtttgcagct
caccttgtgaagatgaaatatccaagaatctgtattctagatggtggcattaataaaata
aagccaacaggcctcctcaccatcccatctcctcaaatatga

  All links  
Disease (2)   
   OMIM (2)   
Gene (17)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (31)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (29)   
DNA sequence (67)   
   RefSeq(nuc) (39)   
   GenBank (14)   
   EMBL (14)   
Protein domain (6)   
   Pfam (6)   
All databases (123)   

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