Homo sapiens (human): 23746
Help
Entry
23746 CDS
T01001
Symbol
AIPL1, AIPL2, LCA4
Name
(RefSeq) AIP like 1 HSP90 co-chaperone
KO
K17767
AH receptor-interacting protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04934
Cushing syndrome
hsa05207
Chemical carcinogenesis - receptor activation
Disease
H00837
Leber congenital amaurosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05207 Chemical carcinogenesis - receptor activation
23746 (AIPL1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
23746 (AIPL1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
23746 (AIPL1)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Endoplasmic reticulum membrane and cytosol
Other ER-memrane and cytosol factors
23746 (AIPL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PPIase_AIP
TPR_2
TPR_8
FKBP_C
TPR_11
TPR_12
ARM_TT21_2nd
TPR_9
CDC37_N
Motif
Other DBs
NCBI-GeneID:
23746
NCBI-ProteinID:
NP_055151
OMIM:
604392
HGNC:
359
Ensembl:
ENSG00000129221
UniProt:
Q9NZN9
F1T0B6
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:complement(6423738..6435121)
Genome browser
AA seq
384 aa
AA seq
DB search
MDAALLLNVEGVKKTILHGGTGELPNFITGSRVIFHFRTMKCDEERTVIDDSRQVGQPMH
IIIGNMFKLEVWEILLTSMRVHEVAEFWCDTIHTGVYPILSRSLRQMAQGKDPTEWHVHT
CGLANMFAYHTLGYEDLDELQKEPQPLVFVIELLQVDAPSDYQRETWNLSNHEKMKAVPV
LHGEGNRLFKLGRYEEASSKYQEAIICLRNLQTKEKPWEVQWLKLEKMINTLILNYCQCL
LKKEEYYEVLEHTSDILRHHPGIVKAYYVRARAHAEVWNEAEAKADLQKVLELEPSMQKA
VRRELRLLENRMAEKQEEERLRCRNMLSQGATQPPAEPPTEPPAQSSTEPPAEPPTAPSA
ELSAGPPAEPATEPPPSPGHSLQH
NT seq
1155 nt
NT seq
+upstream
nt +downstream
nt
atggatgccgctctgctcctgaacgtggaaggggtcaagaaaaccattctgcacgggggc
acgggcgagctcccaaacttcatcaccggatcccgagtgatctttcatttccgcaccatg
aaatgtgatgaggagcggacagtcattgacgacagtcggcaggtgggccagcccatgcac
atcatcatcggaaacatgttcaagctcgaggtctgggagatcctgcttacctccatgcgg
gtgcacgaggtggccgagttctggtgcgacaccatccacacgggggtctaccccatccta
tcccggagcctgaggcagatggcccagggcaaggaccccacagagtggcacgtgcacacg
tgcgggctggccaacatgttcgcctaccacacgctgggctacgaggacctggacgagctg
cagaaggagcctcagcctctggtctttgtgatcgagctgctgcaggttgatgccccgagt
gattaccagagggagacctggaacctgagcaatcatgagaagatgaaggcggtgcccgtc
ctccacggagagggaaatcggctcttcaagctgggccgctacgaggaggcctcttccaag
taccaggaggccatcatctgcctaaggaacctgcagaccaaggagaagccatgggaggtg
cagtggctgaagctggagaagatgatcaatactctgatcctcaactactgccagtgcctg
ctgaagaaggaggagtactatgaggtgctggagcacaccagtgatattctccggcaccac
ccaggcatcgtgaaggcctactacgtgcgtgcccgggctcacgcagaggtgtggaatgag
gccgaggccaaggcggacctccagaaagtgctggagctggagccgtccatgcagaaggcg
gtgcgcagggagctgaggctgctggagaaccgcatggcggagaagcaggaggaggagcgg
ctgcgctgccggaacatgctgagccagggtgccacgcagcctcccgcagagccacccaca
gagccacccgcacagtcatccacagagccacctgcagagccacccacagcaccatctgca
gagctgtccgcagggccccctgcagagccagccacagagccacccccgtccccagggcac
tcgctgcagcactga
Homo sapiens (human): 9049
Help
Entry
9049 CDS
T01001
Symbol
AIP, ARA9, FKBP16, FKBP37, PITA1, SMTPHN, XAP-2, XAP2
Name
(RefSeq) AHR interacting HSP90 co-chaperone
KO
K17767
AH receptor-interacting protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04934
Cushing syndrome
hsa05207
Chemical carcinogenesis - receptor activation
Network
nt06360
Cushing syndrome
Element
N00315
Mutation-inactivated AIP to AhR-mediated transcription
Disease
H01102
Pituitary adenomas
H01431
Cushing syndrome
H01483
Acromegaly
H01864
Excessive secretion of growth hormone
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05207 Chemical carcinogenesis - receptor activation
9049 (AIP)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
9049 (AIP)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
9049 (AIP)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Endoplasmic reticulum membrane and cytosol
Other ER-memrane and cytosol factors
9049 (AIP)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PPIase_AIP
FKBP_C
TPR_2
TPR_8
Motif
Other DBs
NCBI-GeneID:
9049
NCBI-ProteinID:
NP_003968
OMIM:
605555
HGNC:
358
Ensembl:
ENSG00000110711
UniProt:
O00170
Structure
PDB
PDBj
LinkDB
All DBs
Position
11:67483026..67491103
Genome browser
AA seq
330 aa
AA seq
DB search
MADIIARLREDGIQKRVIQEGRGELPDFQDGTKATFHYRTLHSDDEGTVLDDSRARGKPM
ELIIGKKFKLPVWETIVCTMREGEIAQFLCDIKHVVLYPLVAKSLRNIAVGKDPLEGQRH
CCGVAQMREHSSLGHADLDALQQNPQPLIFHMEMLKVESPGTYQQDPWAMTDEEKAKAVP
LIHQEGNRLYREGHVKEAAAKYYDAIACLKNLQMKEQPGSPEWIQLDQQITPLLLNYCQC
KLVVEEYYEVLDHCSSILNKYDDNVKAYFKRGKAHAAVWNAQEAQADFAKVLELDPALAP
VVSRELRALEARIRQKDEEDKARFRGIFSH
NT seq
993 nt
NT seq
+upstream
nt +downstream
nt
atggcggatatcatcgcaagactccgggaggacgggatccaaaaacgtgtgatacaggaa
ggccgaggagagctcccggactttcaagatgggaccaaggccacgttccactaccggacg
ctgcacagtgacgacgagggcaccgtgctggacgacagccgggctcgtggcaagcccatg
gagctcatcattggcaagaagttcaagctgcctgtgtgggagaccatcgtgtgcaccatg
cgagaaggggagattgcccagttcctctgtgacatcaagcatgtggtcctgtacccgctg
gtggccaagagtctccgcaacatcgcggtgggcaaggaccccctggagggccagcggcac
tgctgcggtgttgcacagatgcgtgaacacagctccctgggccatgctgacctggacgcc
ctgcagcagaacccccagcccctcatcttccacatggagatgctgaaggtggagagccct
ggcacgtaccagcaggacccatgggccatgacagacgaagagaaggcaaaggcagtgcca
cttatccaccaggagggcaaccggttgtaccgcgaggggcatgtgaaggaggctgctgcc
aagtactacgatgccattgcctgcctcaagaacctgcagatgaaggaacagcctgggtcc
cctgaatggatccagctggaccagcagatcacgccgctgctgctcaactactgccagtgc
aagctggtggtcgaggagtactacgaggtgctggaccactgctcttccatcctcaacaag
tacgacgacaacgtcaaggcctacttcaagcggggcaaggcccacgcggccgtgtggaat
gcccaggaggcccaggctgactttgccaaagtgctggagctggacccagccctggcgcct
gtggtgagccgagagctgcgggccctggaggcacggatccggcagaaggacgaagaggac
aaagcccggttccgggggatcttctcccattga
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integrated database retrieval system
