Homo sapiens (human): 128338
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Entry
128338 CDS
T01001
Symbol
DRAM2, CORD21, PRO180, TMEM77, WWFQ154
Name
(RefSeq) DNA damage regulated autophagy modulator 2
KO
K21956
DNA damage-regulated autophagy modulator protein 2
Organism
hsa
Homo sapiens (human)
Disease
H00481
Cone-rod dystrophy and cone dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
128338 (DRAM2)
Membrane trafficking [BR:
hsa04131
]
Endosome - Lysosome transport
Others
Others
128338 (DRAM2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Frag1
Bac_export_2
Motif
Other DBs
NCBI-GeneID:
128338
NCBI-ProteinID:
NP_848549
OMIM:
613360
HGNC:
28769
Ensembl:
ENSG00000156171
UniProt:
Q6UX65
LinkDB
All DBs
Position
1:complement(111117163..111140093)
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AA seq
266 aa
AA seq
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MWWFQQGLSFLPSALVIWTSAAFIFSYITAVTLHHIDPALPYISDTGTVAPEKCLFGAML
NIAAVLCIATIYVRYKQVHALSPEENVIIKLNKAGLVLGILSCLGLSIVANFQKTTLFAA
HVSGAVLTFGMGSLYMFVQTILSYQMQPKIHGKQVFWIRLLLVIWCGVSALSMLTCSSVL
HSGNFGTDLEQKLHWNPEDKGYVLHMITTAAEWSMSFSFFGFFLTYIRDFQKISLRVEAN
LHGLTLYDTAPCPINNERTRLLSRDI
NT seq
801 nt
NT seq
+upstream
nt +downstream
nt
atgtggtggtttcagcaaggcctcagtttccttccttcagcccttgtaatttggacatct
gctgctttcatattttcatacattactgcagtaacactccaccatatagacccggcttta
ccttatatcagtgacactggtacagtagctccagaaaaatgcttatttggggcaatgcta
aatattgcggcagttttatgcattgctaccatttatgttcgttataagcaagttcatgct
ctgagtcctgaagagaacgttatcatcaaattaaacaaggctggccttgtacttggaata
ctgagttgtttaggactttctattgtggcaaacttccagaaaacaaccctttttgctgca
catgtaagtggagctgtgcttacctttggtatgggctcattatatatgtttgttcagacc
atcctttcctaccaaatgcagcccaaaatccatggcaaacaagtcttctggatcagactg
ttgttggttatctggtgtggagtaagtgcacttagcatgctgacttgctcatcagttttg
cacagtggcaattttgggactgatttagaacagaaactccattggaaccccgaggacaaa
ggttatgtgcttcacatgatcactactgcagcagaatggtctatgtcattttccttcttt
ggttttttcctgacttacattcgtgattttcagaaaatttctttacgggtggaagccaat
ttacatggattaaccctctatgacactgcaccttgccctattaacaatgaacgaacacgg
ctactttccagagatatttga
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integrated database retrieval system
