Homo sapiens (human): 199699
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Entry
199699 CDS
T01001
Symbol
DAND5, CER2, CERL2, CKTSF1B3, COCO, CRL2, DANTE, GREM3, HTX13, SP1
Name
(RefSeq) DAN domain BMP antagonist family member 5
KO
K25479
DAN domain family member 5
Organism
hsa
Homo sapiens (human)
Disease
H00632
Heterotaxy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
199699 (DAND5)
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GFIT
Motif
Pfam:
DAN
Cys_knot
Motif
Other DBs
NCBI-GeneID:
199699
NCBI-ProteinID:
NP_689867
OMIM:
609068
HGNC:
26780
Ensembl:
ENSG00000179284
UniProt:
Q8N907
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Position
19:12969576..12974760
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AA seq
189 aa
AA seq
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MLLGQLSTLLCLLSGALPTGSGRPEPQSPRPQSWAAANQTWALGPGALPPLVPASALGSW
KAFLGLQKARQLGMGRLQRGQDEVAAVTLPLNPQEVIQGMCKAVPFVQVFSRPGCSAIRL
RNHLCFGHCSSLYIPGSDPTPLVLCNSCMPARKRWAPVVLWCLTGSSASRRRVKISTMLI
EGCHCSPKA
NT seq
570 nt
NT seq
+upstream
nt +downstream
nt
atgctccttggccagctatccactcttctgtgcctgcttagcggggccctgcctacaggc
tcagggaggcctgaaccccagtctcctcgacctcagtcctgggctgcagccaatcagacc
tgggctctgggcccaggggccctgcccccactggtgccagcttctgcccttgggagctgg
aaggccttcttgggcctgcagaaagccaggcagctggggatgggcaggctgcagcgtggg
caagacgaggtggctgctgtgactctgccgctgaaccctcaggaagtgatccaggggatg
tgtaaggctgtgcccttcgttcaggtgttctcccggcccggctgctcagccatacgcctc
cgaaatcatctgtgctttggtcattgctcctctctctacatccctggctcggaccccacc
ccactagtcctgtgcaacagctgtatgcctgctcgcaagcgttgggcacccgtggtcctg
tggtgtctcactggcagctcagcctcccgtcgacgggtgaagatatccaccatgctgatc
gaggggtgtcactgcagcccaaaagcatga
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