Homo sapiens (human): 142680
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Entry
142680 CDS
T01001
Symbol
SLC34A3, HHRH, NPT2C, NPTIIc
Name
(RefSeq) solute carrier family 34 member 3
KO
K14683
solute carrier family 34 (sodium-dependent phosphate cotransporter)
Organism
hsa
Homo sapiens (human)
Pathway
hsa04928
Parathyroid hormone synthesis, secretion and action
hsa04978
Mineral absorption
Network
nt06325
Hormone/cytokine signaling
Element
N01824
SGK1-NHERF1+NPT signaling pathway
Disease
H00214
Hypophosphatemic rickets
H02138
Hereditary hypophophatemic rickets with hypercalciuria
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04928 Parathyroid hormone synthesis, secretion and action
142680 (SLC34A3)
09154 Digestive system
04978 Mineral absorption
142680 (SLC34A3)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
142680 (SLC34A3)
04147 Exosome [BR:
hsa04147
]
142680 (SLC34A3)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC34: Type II Na+-phosphate cotransporter
142680 (SLC34A3)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of breast milk
142680 (SLC34A3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Na_Pi_cotrans
Motif
Other DBs
NCBI-GeneID:
142680
NCBI-ProteinID:
NP_001170787
OMIM:
609826
HGNC:
20305
Ensembl:
ENSG00000198569
UniProt:
Q8N130
LinkDB
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Position
9:137229730..137236555
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AA seq
599 aa
AA seq
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MPSSLPGSQVPHPTLDAVDLVEKTLRNEGTSSSAPVLEEGDTDPWTLPQLKDTSQPWKEL
RVAGRLRRVAGSVLKACGLLGSLYFFICSLDVLSSAFQLLGSKVAGDIFKDNVVLSNPVA
GLVIGVLVTALVQSSSTSSSIVVSMVAAKLLTVRVSVPIIMGVNVGTSITSTLVSMAQSG
DRDEFQRAFSGSAVHGIFNWLTVLVLLPLESATALLERLSELALGAASLTPRAQAPDILK
VLTKPLTHLIVQLDSDMIMSSATGNATNSSLIKHWCGTTGQPTQENSSCGAFGPCTEKNS
TAPADRLPCRHLFAGTELTDLAVGCILLAGSLLVLCGCLVLIVKLLNSVLRGRVAQVVRT
VINADFPFPLGWLGGYLAVLAGAGLTFALQSSSVFTAAVVPLMGVGVISLDRAYPLLLGS
NIGTTTTALLAALASPADRMLSALQVALIHFFFNLAGILLWYLVPALRLPIPLARHFGVV
TARYRWVAGVYLLLGFLLLPLAAFGLSLAGGMELAAVGGPLVGLVLLVILVTVLQRRRPA
WLPVRLRSWAWLPVWLHSLEPWDRLVTRCCPCNVCSPPKATTKEAYCYENPEILASQQL
NT seq
1800 nt
NT seq
+upstream
nt +downstream
nt
atgccgagttcccttcccggcagccaggtcccccaccccactctggacgcggttgaccta
gtggaaaagactctgaggaatgaagggacctccagttctgctccagtcttggaggaaggg
gacacagacccctggaccctccctcagctgaaggacacaagccagccctggaaagagctc
cgcgtggccggcaggctgcgccgcgtggccggcagcgtcctcaaggcctgcgggctcctc
ggcagcctgtacttcttcatctgctctctggacgtcctcagctccgccttccagctgctg
ggcagcaaagtggccggagacatcttcaaggacaacgtggtgctgtccaaccctgtggct
ggactggtcattggcgtgctggtcacagccctggtgcagagttccagcacgtcctcctcc
atcgtggtcagcatggtggctgctaagctgctgactgtccgggtgtctgtgcccatcatc
atgggtgtcaacgtaggcacatccatcaccagcaccctggtctcaatggcgcagtcaggg
gaccgggatgaatttcagagggctttcagcggctcggcggtgcacgggatcttcaactgg
ctcacagtgctggtcctgctgccactggagagcgccacggccctgctggagaggctaagt
gagctagccctgggtgccgccagcctgacacccagggcgcaggcgcccgacatcctcaag
gtgctgacgaagccgctcacacacctcatcgtgcagttggactccgacatgatcatgagc
agtgccacaggcaacgccactaacagcagtctcattaagcactggtgcggcaccacgggg
cagccgacccaggagaacagcagctgtggcgccttcggcccgtgcacagagaagaacagc
acagccccggcggacaggctgccctgccgccacctgtttgcgggcacggagctcacggac
ctggccgtgggctgcatcctgctggccggctccctgctggtgctctgcggctgcctggtc
ctcatagtcaagctgctcaactctgtgctgcgcggccgcgtggcccaggtcgtgaggaca
gtcatcaatgcggacttccccttcccgctgggctggctcggcggctacctggccgtcctc
gcgggcgccggcctgaccttcgcactgcagagcagcagcgtcttcacggcggccgtcgtg
cccctcatgggggtcggggtgatcagtctggaccgggcgtaccccctcttactgggctcc
aacatcggcaccactaccacagccctgctggctgccctggccagccccgcagacaggatg
ctcagcgccctgcaggtcgccctcatccacttcttcttcaacctggccggcatcctgctg
tggtacctggtgcctgcactgcggctgcccatcccgctggccaggcacttcggggtggtg
accgcccgttaccgctgggtggctggggtctacctgctgctcggattcctgctgctgccc
ctggcggccttcgggctctccctggcagggggcatggagctggccgctgtcgggggtccc
ctggtggggctggtgctcctcgtcatcctggttactgtcctgcagcggcgccggccggcc
tggctgcctgtccgcctgcgctcctgggcctggctccccgtctggctccattctctggag
ccctgggaccgcctggtgacccgctgctgcccctgcaacgtctgcagccccccgaaggcc
accaccaaagaggcctactgctacgagaaccctgagatcttggcctcccagcagttgtga
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integrated database retrieval system
