Homo sapiens (human): 4799
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Entry
4799 CDS
T01001
Symbol
NFX1, NFX2, TEG-42, Tex42
Name
(RefSeq) nuclear transcription factor, X-box binding 1
KO
K12236
transcriptional repressor NF-X1
Organism
hsa
Homo sapiens (human)
Pathway
hsa05165
Human papillomavirus infection
Network
nt06166
Human papillomavirus (HPV)
nt06511
NOTCH signaling
Element
N00373
HPV E6 to NFX1-mediated transcription
N00382
HPV E6 to Notch signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09172 Infectious disease: viral
05165 Human papillomavirus infection
4799 (NFX1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
4799 (NFX1)
04121 Ubiquitin system [BR:
hsa04121
]
4799 (NFX1)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Other zinc fingers
4799 (NFX1)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
Single Ring-finger type E3
NFX1 proteins
4799 (NFX1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
R3H
zf-NF-X1
P-loop_SecA
Motif
Other DBs
NCBI-GeneID:
4799
NCBI-ProteinID:
NP_002495
OMIM:
603255
HGNC:
7803
Ensembl:
ENSG00000086102
UniProt:
Q12986
LinkDB
All DBs
Position
9:33290516..33371157
Genome browser
AA seq
1120 aa
AA seq
DB search
MAEAPPVSGTFKFNTDAAEFIPQEKKNSGLNCGTQRRLDSNRIGRRNYSSPPPCHLSRQV
PYDEISAVHQHSYHPSGSKPKSQQTSFQSSPCNKSPKSHGLQNQPWQKLRNEKHHIRVKK
AQSLAEQTSDTAGLESSTRSESGTDLREHSPSESEKEVVGADPRGAKPKKATQFVYSYGR
GPKVKGKLKCEWSNRTTPKPEDAGPESTKPVGVFHPDSSEASSRKGVLDGYGARRNEQRR
YPQKRPPWEVEGARPRPGRNPPKQEGHRHTNAGHRNNMGPIPKDDLNERPAKSTCDSENL
AVINKSSRRVDQEKCTVRRQDPQVVSPFSRGKQNHVLKNVETHTGSLIEQLTTEKYECMV
CCELVRVTAPVWSCQSCYHVFHLNCIKKWARSPASQADGQSGWRCPACQNVSAHVPNTYT
CFCGKVKNPEWSRNEIPHSCGEVCRKKQPGQDCPHSCNLLCHPGPCPPCPAFMTKTCECG
RTRHTVRCGQAVSVHCSNPCENILNCGQHQCAELCHGGQCQPCQIILNQVCYCGSTSRDV
LCGTDVGKSDGFGDFSCLKICGKDLKCGNHTCSQVCHPQPCQQCPRLPQLVRCCPCGQTP
LSQLLELGSSSRKTCMDPVPSCGKVCGKPLPCGSLDFIHTCEKLCHEGDCGPCSRTSVIS
CRCSFRTKELPCTSLKSEDATFMCDKRCNKKRLCGRHKCNEICCVDKEHKCPLICGRKLR
CGLHRCEEPCHRGNCQTCWQASFDELTCHCGASVIYPPVPCGTRPPECTQTCARVHECDH
PVYHSCHSEEKCPPCTFLTQKWCMGKHEFRSNIPCHLVDISCGLPCSATLPCGMHKCQRL
CHKGECLVDEPCKQPCTTPRADCGHPCMAPCHTSSPCPVTACKAKVELQCECGRRKEMVI
CSEASSTYQRIAAISMASKITDMQLGGSVEISKLITKKEVHQARLECDEECSALERKKRL
AEAFHISEDSDPFNIRSSGSKFSDSLKEDARKDLKFVSDVEKEMETLVEAVNKGKNSKKS
HSFPPMNRDHRRIIHDLAQVYGLESVSYDSEPKRNVVVTAIRGKSVCPPTTLTGVLEREM
QARPPPPIPHHRHQSDKNPGSSNLQKITKEPIIDYFDVQD
NT seq
3363 nt
NT seq
+upstream
nt +downstream
nt
atggcggaggcgcctcctgtctcaggtacttttaaattcaatacagatgctgctgaattc
attcctcaggagaaaaaaaattctggtctaaattgtgggactcaaaggagactagactct
aataggattggtagaagaaattacagttcaccacctccctgtcacctttccaggcaggtc
ccttatgatgaaatctctgctgttcatcagcatagttatcatccgtcaggaagcaaacct
aagagtcagcagacgtctttccagtcctctccttgtaataaatcgcccaagagccatggc
cttcagaatcaaccttggcagaaattgaggaatgagaagcaccatatcagagtcaagaaa
gcacagagtcttgctgagcagacctcagatacagctggattagagagctcgaccagatca
gagagtgggacagacctcagagagcatagtccttctgagagtgagaaggaagttgtgggt
gcagatcccaggggagcaaaacccaaaaaagcaacacagtttgtatacagctatggtaga
ggaccaaaagtcaaggggaaactcaaatgtgaatggagtaaccgaacaactccaaaaccg
gaggatgctggacccgaaagtaccaaacctgtgggggttttccaccctgactcttcagag
gcatcctctagaaaaggagtattggatgggtatggagccagacgaaatgagcagagaaga
tacccacagaaaaggcctccctgggaagtggagggggccaggccacgaccaggcagaaat
ccaccaaaacaggagggccaccgacatacaaacgcaggacacagaaacaacatgggcccc
attccaaaggatgacctcaatgaaagaccagcaaaatctacctgtgacagtgagaacttg
gcagtcatcaacaagtcttccaggagggttgaccaagagaaatgcactgtacggaggcag
gatcctcaagtagtatctcctttctcccgaggcaaacagaaccatgtgctaaagaatgtg
gaaacgcacacaggttctctaattgaacaactaacaacagaaaaatacgagtgcatggtg
tgctgtgaattggttcgtgtcacggccccagtgtggagttgtcagagctgttaccatgtg
tttcatttgaactgcataaagaaatgggcaaggtctccagcatctcaagcagatggccag
agtggttggaggtgccctgcctgtcagaatgtttctgcacatgttcctaatacctacact
tgtttctgtggcaaggtaaagaatcctgagtggagcagaaatgaaattccacatagctgt
ggtgaggtttgtagaaagaaacagcctggccaggactgcccacattcctgtaaccttctc
tgccatccaggaccctgcccaccctgccctgcctttatgacaaaaacatgtgaatgtgga
cgaaccaggcacacagttcgctgtggtcaggctgtctcagtccactgttctaacccatgt
gagaatattttgaactgtggtcagcaccagtgtgctgagctgtgccatgggggtcagtgc
cagccttgccagatcattttgaaccaggtatgctattgcggcagcacctcccgagatgtg
ttatgtggaaccgatgtaggaaagtctgatggatttggggatttcagctgtttaaagata
tgtggcaaggacttgaaatgcggtaaccatacatgttcgcaagtgtgccaccctcagccc
tgccagcaatgcccacggctcccccagctggtgcgctgttgcccctgtggccaaactcct
ctcagccaattgctagaacttggaagtagtagtcggaaaacatgcatggaccctgtgcct
tcatgtggaaaagtgtgcggcaagcctctgccttgtggttccttagatttcattcatacc
tgtgaaaagctctgccatgaaggagactgtggaccatgctctcgcacatcagttatttcc
tgcagatgctctttcagaacaaaggagcttccatgtaccagtctcaaaagtgaagatgct
acatttatgtgtgacaagcggtgtaacaagaaacggttgtgtggacggcataaatgtaat
gagatatgctgtgtggataaggagcacaagtgtcctttgatttgtgggaggaaactccgt
tgtggccttcataggtgtgaagaaccttgtcatcgtggaaactgccagacatgctggcaa
gccagttttgatgaattaacctgccattgtggtgcatcagtgatttaccctccagttccc
tgtggtactaggccccctgaatgtacccaaacctgcgctagagtccatgagtgtgaccat
ccagtatatcattcttgtcatagtgaggagaagtgtcccccttgcactttcctaactcag
aagtggtgcatgggcaagcatgagtttcggagcaacatcccctgtcacctggttgatatc
tcttgcggattaccctgcagtgccacgctaccatgtgggatgcacaaatgtcagagactc
tgtcacaaaggggagtgtcttgtggatgagccctgcaagcagccctgcaccacccccaga
gctgactgtggtcacccgtgtatggcaccctgccataccagctcaccctgccctgtgact
gcttgtaaagctaaggtagagctacagtgtgaatgtggacgaagaaaagagatggtgatt
tgctctgaagcatctagtacttatcaaagaatagctgcaatctccatggcctctaagata
acagacatgcagcttggaggttcagtggagatcagcaagttaattaccaaaaaggaagtt
catcaagccaggctggagtgtgatgaggagtgttcagccttggaaaggaaaaagagatta
gcagaggcatttcatatcagtgaggattctgatcctttcaatatacgttcttcagggtca
aaattcagtgatagtttgaaagaagatgccaggaaggacttaaagtttgtcagtgacgtt
gagaaggaaatggaaaccctcgtggaggccgtgaataagggaaagaatagtaagaaaagc
cacagcttccctcccatgaacagagaccaccgccggatcatccatgacttggcccaagtt
tatggcctggagagcgtgagctatgacagtgaaccgaagcgcaatgtggtggtcactgcc
atcagggggaagtccgtttgtcctcctaccacgctgacaggtgtgcttgaaagggaaatg
caggcacggcctccaccaccgattcctcatcacagacatcagtcagacaagaatcctggg
agcagtaatttacagaaaataaccaaggagccaataattgactattttgacgtccaggac
taa
Homo sapiens (human): 5663
Help
Entry
5663 CDS
T01001
Symbol
PSEN1, ACNINV3, AD3, FAD, PS-1, PS1, PSNL1, S182
Name
(RefSeq) presenilin 1
KO
K04505
presenilin 1 [EC:3.4.23.-]
Organism
hsa
Homo sapiens (human)
Pathway
hsa04310
Wnt signaling pathway
hsa04330
Notch signaling pathway
hsa04722
Neurotrophin signaling pathway
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
Network
nt06166
Human papillomavirus (HPV)
nt06460
Alzheimer disease
nt06466
Pathways of neurodegeneration
nt06511
NOTCH signaling
nt06534
Unfolded protein response
Element
N00382
HPV E6 to Notch signaling pathway
N01007
Mutation-caused aberrant PSEN to mGluR5-Ca2+ -apoptotic pathway
N01008
Mutation-caused aberrant PSEN1 to mGluR5-Ca2+ -apoptotic pathway
N01010
Mutation-caused aberrant PSEN1 to PERK-ATF4 signaling pathway
N01012
Mutation-caused aberrant PSEN1 to IRE1a-XBP1 signaling pathway
N01016
Mutation-caused aberrant PSEN1 to ATF6-mediated transcription
N01017
Mutation-caused aberrant PSEN1 to anterograde axonal transport
N01478
Notch proteolytic activation
Disease
H00056
Alzheimer disease
H00078
Frontotemporal lobar degeneration
H00294
Dilated cardiomyopathy
H00681
Acne inversa
Drug target
Avagacestat:
D09869
Begacestat:
D08869
Crenigacestat:
D11151
Nirogacestat (
DG03016
):
D10960
D11453
<US>
Osugacestat:
D12235
Semagacestat:
D09377
Tarenflurbil:
D09010
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
5663 (PSEN1)
04330 Notch signaling pathway
5663 (PSEN1)
09150 Organismal Systems
09156 Nervous system
04722 Neurotrophin signaling pathway
5663 (PSEN1)
09160 Human Diseases
09172 Infectious disease: viral
05165 Human papillomavirus infection
5663 (PSEN1)
09164 Neurodegenerative disease
05010 Alzheimer disease
5663 (PSEN1)
05022 Pathways of neurodegeneration - multiple diseases
5663 (PSEN1)
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hsa01002
]
5663 (PSEN1)
Peptidases and inhibitors [BR:
hsa01002
]
Aspartic peptidases
Family A22: presenilin family
5663 (PSEN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Presenilin
Motif
Other DBs
NCBI-GeneID:
5663
NCBI-ProteinID:
NP_000012
OMIM:
104311
HGNC:
9508
Ensembl:
ENSG00000080815
UniProt:
P49768
A0A024R6A3
Structure
PDB
LinkDB
All DBs
Position
14:73136417..73223691
Genome browser
AA seq
467 aa
AA seq
DB search
MTELPAPLSYFQNAQMSEDNHLSNTVRSQNDNRERQEHNDRRSLGHPEPLSNGRPQGNSR
QVVEQDEEEDEELTLKYGAKHVIMLFVPVTLCMVVVVATIKSVSFYTRKDGQLIYTPFTE
DTETVGQRALHSILNAAIMISVIVVMTILLVVLYKYRCYKVIHAWLIISSLLLLFFFSFI
YLGEVFKTYNVAVDYITVALLIWNFGVVGMISIHWKGPLRLQQAYLIMISALMALVFIKY
LPEWTAWLILAVISVYDLVAVLCPKGPLRMLVETAQERNETLFPALIYSSTMVWLVNMAE
GDPEAQRRVSKNSKYNAESTERESQDTVAENDDGGFSEEWEAQRDSHLGPHRSTPESRAA
VQELSSSILAGEDPEERGVKLGLGDFIFYSVLVGKASATASGDWNTTIACFVAILIGLCL
TLLLLAIFKKALPALPISITFGLVFYFATDYLVQPFMDQLAFHQFYI
NT seq
1404 nt
NT seq
+upstream
nt +downstream
nt
atgacagagttacctgcaccgttgtcctacttccagaatgcacagatgtctgaggacaac
cacctgagcaatactgtacgtagccagaatgacaatagagaacggcaggagcacaacgac
agacggagccttggccaccctgagccattatctaatggacgaccccagggtaactcccgg
caggtggtggagcaagatgaggaagaagatgaggagctgacattgaaatatggcgccaag
catgtgatcatgctctttgtccctgtgactctctgcatggtggtggtcgtggctaccatt
aagtcagtcagcttttatacccggaaggatgggcagctaatctataccccattcacagaa
gataccgagactgtgggccagagagccctgcactcaattctgaatgctgccatcatgatc
agtgtcattgttgtcatgactatcctcctggtggttctgtataaatacaggtgctataag
gtcatccatgcctggcttattatatcatctctattgttgctgttctttttttcattcatt
tacttgggggaagtgtttaaaacctataacgttgctgtggactacattactgttgcactc
ctgatctggaattttggtgtggtgggaatgatttccattcactggaaaggtccacttcga
ctccagcaggcatatctcattatgattagtgccctcatggccctggtgtttatcaagtac
ctccctgaatggactgcgtggctcatcttggctgtgatttcagtatatgatttagtggct
gttttgtgtccgaaaggtccacttcgtatgctggttgaaacagctcaggagagaaatgaa
acgctttttccagctctcatttactcctcaacaatggtgtggttggtgaatatggcagaa
ggagacccggaagctcaaaggagagtatccaaaaattccaagtataatgcagaaagcaca
gaaagggagtcacaagacactgttgcagagaatgatgatggcgggttcagtgaggaatgg
gaagcccagagggacagtcatctagggcctcatcgctctacacctgagtcacgagctgct
gtccaggaactttccagcagtatcctcgctggtgaagacccagaggaaaggggagtaaaa
cttggattgggagatttcattttctacagtgttctggttggtaaagcctcagcaacagcc
agtggagactggaacacaaccatagcctgtttcgtagccatattaattggtttgtgcctt
acattattactccttgccattttcaagaaagcattgccagctcttccaatctccatcacc
tttgggcttgttttctactttgccacagattatcttgtacagccttttatggaccaatta
gcattccatcaattttatatctag
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