Homo sapiens (human): 10159
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Entry
10159 CDS
T01001
Symbol
ATP6AP2, APT6M8-9, ATP6IP2, ATP6M8-9, CDG2R, ELDF10, HT028, M8-9, MRXE, MRXSH, MSTP009, PRR, RENR, XMRE, XPDS
Name
(RefSeq) ATPase H+ transporting accessory protein 2
KO
K19514
renin receptor
Organism
hsa
Homo sapiens (human)
Pathway
hsa04614
Renin-angiotensin system
Disease
H00119
Congenital disorders of glycosylation type II
H00658
X-linked syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04614 Renin-angiotensin system
10159 (ATP6AP2)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Renin_r
Phosphodiest
Motif
Other DBs
NCBI-GeneID:
10159
NCBI-ProteinID:
NP_005756
OMIM:
300556
HGNC:
18305
Ensembl:
ENSG00000182220
UniProt:
O75787
Structure
PDB
PDBj
LinkDB
All DBs
Position
X:40580970..40606848
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AA seq
350 aa
AA seq
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MAVFVVLLALVAGVLGNEFSILKSPGSVVFRNGNWPIPGERIPDVAALSMGFSVKEDLSW
PGLAVGNLFHRPRATVMVMVKGVNKLALPPGSVISYPLENAVPFSLDSVANSIHSLFSEE
TPVVLQLAPSEERVYMVGKANSVFEDLSVTLRQLRNRLFQENSVLSSLPLNSLSRNNEVD
LLFLSELQVLHDISSLLSRHKHLAKDHSPDLYSLELAGLDEIGKRYGEDSEQFRDASKIL
VDALQKFADDMYSLYGGNAVVELVTVKSFDTSLIRKTRTILEAKQAKNPASPYNLAYKYN
FEYSVVFNMVLWIMIALALAVIITSYNIWNMDPGYDSIIYRMTNQKIRMD
NT seq
1053 nt
NT seq
+upstream
nt +downstream
nt
atggctgtgtttgtcgtgctcctggcgttggtggcgggtgttttggggaacgagtttagt
atattaaaatcaccagggtctgttgttttccgaaatggaaattggcctataccaggagag
cggatcccagacgtggctgcattgtccatgggcttctctgtgaaagaagacctttcttgg
ccaggactcgcagtgggtaacctgtttcatcgtcctcgggctaccgtcatggtgatggtg
aagggagtgaacaaactggctctacccccaggcagtgtcatttcgtaccctttggagaat
gcagttccttttagtcttgacagtgttgcaaattccattcactccttattttctgaggaa
actcctgttgttttgcagttggctcccagtgaggaaagagtgtatatggtagggaaggca
aactcagtgtttgaagacctttcagtcaccttgcgccagctccgtaatcgcctgtttcaa
gaaaactctgttctcagttcactccccctcaattctctgagtaggaacaatgaagttgac
ctgctctttctttctgaactgcaagtgctacatgatatttcaagcttgctgtctcgtcat
aagcatctagccaaggatcattctcctgatttatattcactggagctggcaggtttggat
gaaattgggaagcgttatggggaagactctgaacaattcagagatgcttctaagatcctt
gttgacgctctgcaaaagtttgcagatgacatgtacagtctttatggtgggaatgcagtg
gtagagttagtcactgtcaagtcatttgacacctccctcattaggaagacaaggactatc
cttgaggcaaaacaagcgaagaacccagcaagtccctataaccttgcatataagtataat
tttgaatattccgtggttttcaacatggtactttggataatgatcgccttggccttggct
gtgattatcacctcttacaatatttggaacatggatcctggatatgatagcatcatttat
aggatgacaaaccagaagattcgaatggattga
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