Homo sapiens (human): 9368
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Entry
9368 CDS
T01001
Symbol
NHERF1, EBP50, NHE-RF, NHERF, NHERF-1, NPHLOP2, SLC9A3R1
Name
(RefSeq) NHERF family PDZ scaffold protein 1
KO
K13365
sodium/hydrogen exchange regulatory cofactor NHE-RF1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04530
Tight junction
hsa04928
Parathyroid hormone synthesis, secretion and action
hsa05130
Pathogenic Escherichia coli infection
hsa05165
Human papillomavirus infection
Network
nt06166
Human papillomavirus (HPV)
nt06180
Pathogenic Escherichia coli
nt06325
Hormone/cytokine signaling
Element
N00353
HPV E6 to PTEN-PIP3-AKT signaling pathway
N01095
Escherichia Map to LPA-GNA12/13-RhoA signaling pathway
N01824
SGK1 -> NHERF1+NPT signaling pathway
Disease
H00888
Nephrolithiasis/osteoporosis, hypophosphatemic
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
9368 (NHERF1)
09150 Organismal Systems
09152 Endocrine system
04928 Parathyroid hormone synthesis, secretion and action
9368 (NHERF1)
09160 Human Diseases
09172 Infectious disease: viral
05165 Human papillomavirus infection
9368 (NHERF1)
09171 Infectious disease: bacterial
05130 Pathogenic Escherichia coli infection
9368 (NHERF1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
9368 (NHERF1)
Transporters [BR:
hsa02000
]
Other transporters
Accessory factors involved in transport [TC:
8
]
9368 (NHERF1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EBP50_C
PDZ
PDZ_6
PDZ_2
GRASP55_65
DUF5994
Motif
Other DBs
NCBI-GeneID:
9368
NCBI-ProteinID:
NP_004243
OMIM:
604990
HGNC:
11075
Ensembl:
ENSG00000109062
UniProt:
O14745
Structure
PDB
LinkDB
All DBs
Position
17:74748628..74769353
Genome browser
AA seq
358 aa
AA seq
DB search
MSADAAAGAPLPRLCCLEKGPNGYGFHLHGEKGKLGQYIRLVEPGSPAEKAGLLAGDRLV
EVNGENVEKETHQQVVSRIRAALNAVRLLVVDPETDEQLQKLGVQVREELLRAQEAPGQA
EPPAAAEVQGAGNENEPREADKSHPEQRELRPRLCTMKKGPSGYGFNLHSDKSKPGQFIR
SVDPDSPAEASGLRAQDRIVEVNGVCMEGKQHGDVVSAIRAGGDETKLLVVDRETDEFFK
KCRVIPSQEHLNGPLPVPFTNGEIQKENSREALAEAALESPRPALVRSASSDTSEELNSQ
DSPPKQDSTAPSSTSSSDPILDFNISLAMAKERAHQKRSSKRAPQMDWSKKNELFSNL
NT seq
1077 nt
NT seq
+upstream
nt +downstream
nt
atgagcgcggacgcagcggccggggcgcccctgccccggctctgctgcctggagaagggt
ccgaacggctacggcttccacctgcacggggagaagggcaagttgggccagtacatccgg
ctggtggagcccggctcgccggccgagaaggcggggctgctggcgggggaccggctggtg
gaggtgaacggcgaaaacgtggagaaggagacccaccagcaggtggtgagccgcatccgc
gccgcactcaacgccgtgcgcctgctggtggtcgaccccgagacggacgagcagctgcag
aagctcggcgtccaggtccgagaggagctgctgcgcgcccaggaagcgccggggcaggcc
gagccgccggccgccgccgaggtgcagggggctggcaacgaaaatgagcctcgcgaggcc
gacaagagccacccggagcagcgcgagcttcggcctcggctctgtaccatgaagaagggc
cccagtggctatggcttcaacctgcacagcgacaagtccaagccaggccagttcatccgg
tcagtggacccagactccccggctgaggcttcagggctccgggcccaggatcgcattgtg
gaggtgaacggggtctgcatggaggggaagcagcatggggacgtggtgtccgccatcagg
gctggcggggacgagaccaagctgctggtggtggacagggaaactgacgagttcttcaag
aaatgcagagtgatcccatctcaggagcacctgaatggtcccctgcctgtgcccttcacc
aatggggagatacagaaggagaacagtcgtgaagccctggcagaggcagccttggagagc
cccaggccagccctggtgagatccgcctccagtgacaccagcgaggagctgaattcccaa
gacagccccccaaaacaggactccacagcgccctcgtctacctcctcctccgaccccatc
ctagacttcaacatctccctggccatggccaaagagagggcccaccagaaacgcagcagc
aaacgggccccgcagatggactggagcaagaaaaacgaactcttcagcaacctctga
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