Homo sapiens (human): 81575
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Entry
81575 CDS
T01001
Symbol
APOLD1, BDVAS, VERGE
Name
(RefSeq) apolipoprotein L domain containing 1
KO
K28078
apolipoprotein L domain-containing protein 1
Organism
hsa
Homo sapiens (human)
Disease
H02749
Bleeding disorder vascular-type
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
81575 (APOLD1)
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Gene cluster
GFIT
Motif
Pfam:
ApoL
Prefoldin
Motif
Other DBs
NCBI-GeneID:
81575
NCBI-ProteinID:
NP_001123887
OMIM:
612456
HGNC:
25268
Ensembl:
ENSG00000178878
UniProt:
Q96LR9
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Position
12:12725917..12791466
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AA seq
279 aa
AA seq
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MFRAPCHRLRARGTRKARAGAWRGCTFPCLGKGMERPAAREPHGPDALRRFQGLLLDRRG
RLHGQVLRLREVARRLERLRRRSLVANVAGSSLSATGALAAIVGLSLSPVTLGTSLLVSA
VGLGVATAGGAVTITSDLSLIFCNSRELRRVQEIAATCQDQMREILSCLEFFCRWQGCGD
RQLLQCGRNASIALYNSVYFIVFFGSRGFLIPRRAEGDTKVSQAVLKAKIQKLAESLESC
TGALDELSEQLESRVQLCTKSSRGHDLKISADQRAGLFF
NT seq
840 nt
NT seq
+upstream
nt +downstream
nt
atgttccgcgcgccgtgtcaccggctgcgggccaggggtactcggaaggcgcgggcagga
gcctggcgaggatgcaccttcccctgccttggaaagggaatggagaggccggcggcccgg
gagccgcatgggcccgacgcgctgcggcgcttccagggactgctgctggaccgccgaggc
cggctgcacggccaggtgctgcgcctgcgcgaggtggcccggcgcctggagcgcctgcgc
aggcgctccctcgtagccaacgtggccggcagctcgctgagcgcaacgggcgccctcgcc
gccatcgtggggctctcgctcagcccggtcaccctggggacctcgctgctggtgtcggcc
gtggggctgggggtggccacagccggaggggccgtcaccatcacgtccgatctctcgctg
atcttctgcaactcccgggagctgcggagggtgcaggagatcgcggccacctgccaggac
cagatgcgagagatcctgagctgcctcgagtttttctgccgctggcagggctgcggggac
cgccagctgctgcagtgcgggaggaacgcctccatcgccctgtacaattctgtctacttc
atcgtcttctttggctcacgtggcttcctcatccccaggcgggcggagggggacaccaag
gttagccaggccgtgctgaaggccaagattcagaaactggccgagagcctggagtcctgc
accggggctctggacgaactcagcgagcagctggagtctcgggttcagctctgcaccaag
tccagtcgtggccacgacctcaagatctctgctgaccagcgtgcagggctgtttttctga
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