Homo sapiens (human): 285600
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Entry
285600 CDS
T01001
Symbol
C5orf36, PAPA10
Name
(RefSeq) KIAA0825
KO
K24554
protein KIAA0825
Organism
hsa
Homo sapiens (human)
Disease
H01852
Postaxial polydactyly
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09194 Poorly characterized
99996 General function prediction only
285600 (C5orf36)
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Gene cluster
GFIT
Motif
Pfam:
Spc7
Spiralin
Motif
Other DBs
NCBI-GeneID:
285600
NCBI-ProteinID:
NP_001372644
OMIM:
617266
HGNC:
28532
Ensembl:
ENSG00000185261
UniProt:
Q8IV33
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Position
5:complement(94150851..94618604)
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AA seq
324 aa
AA seq
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MDWDDEYSHNSFDLHCLLNSFPGDLEFEQIFSDIDEKIEQNAASIKHCIKEIQSEINKQC
PGVQLQTTTDCFEWLTNYNYSTSESSFISHGDLIKFFKTLQDLLKNEQNQEEMTLDLLWD
LSCHSSVSFPSTLSGTSFHFLSRTSLHSVEDNSSMDVKSMWDDIRLHLRRFLVSKLQSHN
EINNSQQKILLKKQCLQQLLFLYPESEVIIKYQNIQNKLLANLLWNCFPSYNRDSNLDVI
AHGYQSTMLKLYSVIKEDFNTLCEILAPSSMVKFIKETYLDTVTEEMAKFLENFCELQFR
ENAVRVVKTSKSSSKHRGAVHALG
NT seq
975 nt
NT seq
+upstream
nt +downstream
nt
atggattgggatgatgaatattctcataattcttttgacctacattgtttgttaaactca
tttcctggagacttggagtttgagcagatcttcagtgacattgatgaaaagattgaacaa
aatgctgcaagcataaaacattgcattaaagagatacagtccgaaattaacaaacaatgt
ccaggtgtgcagctgcaaacaacaactgactgctttgaatggctaactaactataattac
agtacatctgaatcatctttcatttctcatggagacttgataaaatttttcaaaacactg
caagatttgttgaagaatgaacaaaatcaagaagaaatgacattggatttactttgggac
ctctcctgccacagcagcgtttcattcccatcaaccctaagtggaacatctttccatttc
ctctctaggacgtctcttcattctgttgaagataattcctctatggatgtcaagtctatg
tgggatgatataagactgcatcttcgacgcttcttagtgagcaaattacaaagccataat
gaaataaacaattcacagcaaaaaattttattgaaaaagcagtgcttacaacaactcttg
tttctttatccagaatcagaagttataatcaaataccaaaacatacagaataaactgttg
gctaatcttctgtggaactgctttccttcttacaacagagattcaaatttagatgtaata
gctcatggatatcaaagtacaatgcttaagttatactcagtaataaaagaggattttaac
acactatgtgaaattttagctccatcttcaatggtgaaattcattaaagaaacttacctg
gatactgttacagaagaaatggcaaaatttcttgaaaatttttgtgagctgcagttcaga
gaaaatgctgttcgtgtggttaaaacaagcaagagctccagcaagcatagaggagcagtg
catgctttgggttag
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