Homo sapiens (human): 90416
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CCDC32
Motif
Other DBs
NCBI-GeneID:
90416
NCBI-ProteinID:
NP_001074260
OMIM:
618941
HGNC:
28295
Ensembl:
ENSG00000128891
UniProt:
Q9BV29
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All DBs
Position
15:complement(40520993..40565042)
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AA seq
185 aa
AA seq
DB search
MKMFESADSTATRSGQDLWAEICSCLPNPEQEDGANNAFSDSFVDSCPEGEGQREVADFA
VQPAVKPWAPLQDSEVYLASLEKKLRRIKGLNQEVTSKDMLRTLAQAKKECWDRFLQEKL
ASEFFVDGLDSDESTLEHFKRWLQPDKVAVSTEEVQYLIPPESQVEKPVAEDEPAAGDKP
AAAEQ
NT seq
558 nt
NT seq
+upstream
nt +downstream
nt
atgaaaatgtttgagagcgctgactctacagccacaagatctggccaggatctctgggct
gaaatttgttcctgtctgccaaatcctgaacaagaagatggtgccaacaatgcattctca
gactcctttgtggattcttgccctgaaggtgaaggccagagggaggtggctgactttgct
gtccagccagctgtaaagccttgggctcccttgcaggattcagaagtgtatttagcatct
ctagagaagaagctaagaagaatcaaaggtttaaatcaggaagtgacttccaaggacatg
cttcgaactctggcccaagccaagaaggaatgctgggatcggttcctccaggagaagtta
gcttcagagttctttgtggatggacttgattctgatgagagcaccttggaacatttcaag
aggtggctccagccagataaagtagccgtcagcacagaggaggtccagtatctgattcct
ccagagtcacaggttgagaagccagtggccgaggacgagccagcagccggggacaagcca
gcagcagcagaacagtaa
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integrated database retrieval system