Neogale vison (American mink): 122904599
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Entry
122904599 CDS
T08764
Symbol
ATP6V1H
Name
(RefSeq) V-type proton ATPase subunit H isoform X1
KO
K02144
V-type H+-transporting ATPase subunit H
Organism
nvs
Neogale vison (American mink)
Pathway
nvs00190
Oxidative phosphorylation
nvs01100
Metabolic pathways
nvs04142
Lysosome
nvs04145
Phagosome
nvs04150
mTOR signaling pathway
nvs04721
Synaptic vesicle cycle
nvs05152
Tuberculosis
nvs05165
Human papillomavirus infection
nvs05323
Rheumatoid arthritis
Module
nvs_M00160
V-type ATPase, eukaryotes
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
122904599 (ATP6V1H)
09130 Environmental Information Processing
09132 Signal transduction
04150 mTOR signaling pathway
122904599 (ATP6V1H)
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
122904599 (ATP6V1H)
04142 Lysosome
122904599 (ATP6V1H)
09150 Organismal Systems
09156 Nervous system
04721 Synaptic vesicle cycle
122904599 (ATP6V1H)
09160 Human Diseases
09172 Infectious disease: viral
05165 Human papillomavirus infection
122904599 (ATP6V1H)
09171 Infectious disease: bacterial
05152 Tuberculosis
122904599 (ATP6V1H)
09163 Immune disease
05323 Rheumatoid arthritis
122904599 (ATP6V1H)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
V-ATPase_H_N
V-ATPase_H_C
Arm
ARM_ARMC5
Arm_2
Adaptin_N
HEAT
DUF2326
UCH
Motif
Other DBs
NCBI-GeneID:
122904599
NCBI-ProteinID:
XP_044101530
UniProt:
A0A8C7AF01
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Position
4:80131575..80284372
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AA seq
483 aa
AA seq
DB search
MTKMDIRGAVDAAVPTNIIAAKAAEVRANKVNWQSYLQGQMISAEDCEFIQRFEMKRSPE
EKQEMLQTEGSQCAKTFINLMTHISKEQTVQYILTMVDDMLQENHQRVSIFFDYAKRSKN
TAWSYFLPMLNRQDLFTVHMAARIIAKLAAWGKELMEGSDLNYYFNWIKTQLSSQKLRGS
GVAVETGTVSSSDSSQYVQCVAGCLQLMLRVNEYRFAWVEADGVNCIMGVLSNKCGFQLQ
YQMIFSIWLLAFSPQMCEHLRRYNIIPVLSDILQESVKEKVTRIILAAFRNFLEKSTERE
TRQEYALAMIQCKVLKQLENLEQQKYDDEDISEDIKFLLEKLGESVQDLSSFDEYSSELK
SGRLEWSPVHKSEKFWRENAVRLNEKNYELLKILTKLLEVSDDPQVLAVAAHDVGEYVRH
YPRGKRVIEQLGGKQLVMNHMHHEDQQVRYNALLAVQKLMVHNWEYLGKQLQSEQPQTAA
ARS
NT seq
1452 nt
NT seq
+upstream
nt +downstream
nt
atgaccaaaatggatatccgaggtgccgtagatgctgctgttccaacaaacattattgct
gccaaggctgcagaggttcgcgcaaataaagtgaactggcagtcctatcttcaggggcag
atgatttctgctgaagattgtgaattcattcaaaggtttgaaatgaaaagaagtcctgaa
gagaagcaagagatgctccaaactgaaggtagtcagtgtgctaaaacctttataaatttg
atgacccatatctccaaagaacagacagttcagtacatattaactatggtagatgatatg
ctgcaggaaaatcaccagcgggttagtattttctttgactatgctaaacgcagcaagaac
actgcctggtcctactttctgccaatgttgaatcggcaggatctctttactgttcatatg
gcagcaagaattattgcaaagttagcagcttgggggaaggaactaatggaaggcagtgac
ttaaattactatttcaattggataaaaactcagctgagttcacagaaactgcgtggtagc
ggtgtcgctgttgaaacaggaacagtctcttcaagtgatagttctcagtatgtgcagtgt
gttgctgggtgtctgcagttgatgcttcgggtcaatgagtaccgctttgcctgggtagaa
gcagatggggtaaactgcatcatgggtgttttgagtaacaagtgtggctttcaactccag
tatcaaatgattttttcaatatggctcctggcattcagtcctcaaatgtgtgaacacctg
cggcgctataatatcattcctgtcctgtctgatattcttcaagaatctgtgaaagagaaa
gtgacaagaattattcttgcagcattccgtaactttttggaaaaatcgactgaaagagaa
actcgccaagaatatgctctggctatgattcagtgcaaagttctgaaacagttggagaac
ttggaacagcagaagtatgatgatgaagatatcagtgaagatataaaatttcttttggaa
aaacttggtgagagtgtccaagatcttagctcatttgatgaatacagttcagaacttaaa
tctggaagattggagtggagtcctgtgcacaaatctgagaaattttggagagaaaatgct
gtgaggttaaatgagaagaattatgagctcttaaaaattttgacaaaacttctggaggtg
tcggatgatccacaagtcttagctgttgctgctcatgatgttggagaatatgtgcggcat
tatccacgaggcaaacgggtcattgaacagcttggtgggaagcagctggtcatgaaccac
atgcaccacgaggaccagcaggttcgctacaatgctcttctggctgtgcagaaactcatg
gtgcacaactgggaatatcttggtaaacagctccaatctgagcagccccagactgctgct
gcccgaagctga
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