KEGG   Homo sapiens (human): 90416
Entry
90416             CDS       T01001                                 
Symbol
CCDC32, C15orf57, CFNDS
Name
(RefSeq) coiled-coil domain containing 32
  KO
K27410  coiled-coil domain-containing protein 32
Organism
hsa  Homo sapiens (human)
Disease
H02535  Neurodevelopmental disorder with dysmorphic facies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    90416 (CCDC32)
Membrane trafficking [BR:hsa04131]
 Endocytosis
  Clathrin-mediated endocytosis
   Others
    90416 (CCDC32)
SSDB
Motif
Pfam: CCDC32
Other DBs
NCBI-GeneID: 90416
NCBI-ProteinID: NP_001074260
OMIM: 618941
HGNC: 28295
Ensembl: ENSG00000128891
UniProt: Q9BV29
LinkDB
Position
15:complement(40520993..40565042)
AA seq 185 aa
MKMFESADSTATRSGQDLWAEICSCLPNPEQEDGANNAFSDSFVDSCPEGEGQREVADFA
VQPAVKPWAPLQDSEVYLASLEKKLRRIKGLNQEVTSKDMLRTLAQAKKECWDRFLQEKL
ASEFFVDGLDSDESTLEHFKRWLQPDKVAVSTEEVQYLIPPESQVEKPVAEDEPAAGDKP
AAAEQ
NT seq 558 nt   +upstreamnt  +downstreamnt
atgaaaatgtttgagagcgctgactctacagccacaagatctggccaggatctctgggct
gaaatttgttcctgtctgccaaatcctgaacaagaagatggtgccaacaatgcattctca
gactcctttgtggattcttgccctgaaggtgaaggccagagggaggtggctgactttgct
gtccagccagctgtaaagccttgggctcccttgcaggattcagaagtgtatttagcatct
ctagagaagaagctaagaagaatcaaaggtttaaatcaggaagtgacttccaaggacatg
cttcgaactctggcccaagccaagaaggaatgctgggatcggttcctccaggagaagtta
gcttcagagttctttgtggatggacttgattctgatgagagcaccttggaacatttcaag
aggtggctccagccagataaagtagccgtcagcacagaggaggtccagtatctgattcct
ccagagtcacaggttgagaagccagtggccgaggacgagccagcagccggggacaagcca
gcagcagcagaacagtaa

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