Homo sapiens (human): 10342
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Entry
10342 CDS
T01001
Symbol
TFG, HMSNP, SPG57, TF6, TRKT3
Name
(RefSeq) trafficking from ER to golgi regulator
KO
K09292
protein TFG
Organism
hsa
Homo sapiens (human)
Pathway
hsa05200
Pathways in cancer
hsa05216
Thyroid cancer
Disease
H00032
Thyroid cancer
H00266
Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
10342 (TFG)
09162 Cancer: specific types
05216 Thyroid cancer
10342 (TFG)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PB1
Motif
Other DBs
NCBI-GeneID:
10342
NCBI-ProteinID:
NP_001007566
OMIM:
602498
HGNC:
11758
Ensembl:
ENSG00000114354
UniProt:
Q92734
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:100709290..100748967
Genome browser
AA seq
400 aa
AA seq
DB search
MNGQLDLSGKLIIKAQLGEDIRRIPIHNEDITYDELVLMMQRVFRGKLLSNDEVTIKYKD
EDGDLITIFDSSDLSFAIQCSRILKLTLFVNGQPRPLESSQVKYLRRELIELRNKVNRLL
DSLEPPGEPGPSTNIPENDTVDGREEKSASDSSGKQSTQVMAASMSAFDPLKNQDEINKN
VMSAFGLTDDQVSGPPSAPAEDRSGTPDSIASSSSAAHPPGVQPQQPPYTGAQTQAGQIE
GQMYQQYQQQAGYGAQQPQAPPQQPQQYGIQYSASYSQQTGPQQPQQFQGYGQQPTSQAP
APAFSGQPQQLPAQPPQQYQASNYPAQTYTAQTSQPTNYTVAPASQPGMAPSQPGAYQPR
PGFTSLPGSTMTPPPSGPNPYARNRPPFGQGYTQPGPGYR
NT seq
1203 nt
NT seq
+upstream
nt +downstream
nt
atgaacggacagttggatctaagtgggaagctaatcatcaaagctcaacttggggaggat
attcggcgaattcctattcataatgaagatattacttatgatgaattagtgctaatgatg
caacgagttttcagaggaaaacttctgagtaatgatgaagtaacaataaagtataaagat
gaagatggagatcttataacaatttttgatagttctgacctttcctttgcaattcagtgc
agtaggatactgaaactgacattatttgttaatggccagccaagaccccttgaatcaagt
caggtgaaatatctccgtcgagaactgatagaacttcgaaataaagtgaatcgtttattg
gatagcttggaaccacctggagaaccaggaccttccaccaatattcctgaaaatgatact
gtggatggtagggaagaaaagtctgcttctgattcttctggaaaacagtctactcaggtt
atggcagcaagtatgtctgcttttgatcctttaaaaaaccaagatgaaatcaataaaaat
gttatgtcagcgtttggcttaacagatgatcaggtttcagggccacccagtgctcctgca
gaagatcgttcaggaacacccgacagcattgcttcctcctcctcagcagctcacccacca
ggcgttcagccacagcagccaccatatacaggagctcagactcaagcaggtcagattgaa
ggtcagatgtaccaacagtaccagcaacaggccggctatggtgcacagcagccgcaggct
ccacctcagcagcctcaacagtatggtattcagtattcagcaagctatagtcagcagact
ggacctcaacaacctcagcagttccagggatatggccagcaaccaacttcccaggcacca
gctcctgccttttctggtcagcctcaacaactgcctgctcagccgccacagcagtaccag
gcgagcaattatcctgcacaaacttacactgcccaaacttctcagcctactaattatact
gtggctcctgcctctcaacctggaatggctccaagccaacctggggcctatcaaccaaga
ccaggttttacttcacttcctggaagtaccatgacccctcctccaagtgggcctaatcct
tatgcgcgtaaccgtcctccctttggtcagggctatacccaacctggacctggttatcga
taa
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