Homo sapiens (human): 54496
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Entry
54496 CDS
T01001
Symbol
PRMT7, SBIDDS
Name
(RefSeq) protein arginine methyltransferase 7
KO
K11438
type III protein arginine methyltransferase [EC:
2.1.1.321
]
Organism
hsa
Homo sapiens (human)
Disease
H02481
Syndromic disorder with short stature
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
54496 (PRMT7)
Enzymes [BR:
hsa01000
]
2. Transferases
2.1 Transferring one-carbon groups
2.1.1 Methyltransferases
2.1.1.321 type III protein arginine methyltransferase
54496 (PRMT7)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HMTs (histone methyltransferases)
PRMTs (protein arginine metyltransferases)
54496 (PRMT7)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PrmA
Methyltransf_25
Methyltransf_18
Methyltransf_4
Cons_hypoth95
MTS
tRNA-synt_2c
TrmK
Methyltransf_23
PCMT
Motif
Other DBs
NCBI-GeneID:
54496
NCBI-ProteinID:
NP_001276947
OMIM:
610087
HGNC:
25557
Ensembl:
ENSG00000132600
UniProt:
Q9NVM4
LinkDB
All DBs
Position
16:68311019..68360870
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AA seq
692 aa
AA seq
DB search
MKIFCSRANPTTGSVEWLEEDEHYDYHQEIARSSYADMLHDKDRNVKYYQGIRAAVSRVK
DRGQKALVLDIGTGTGLLSMMAVTAGADFCYAIEVFKPMADAAVKIVEKNGFSDKIKVIN
KHSTEVTVGPEGDMPCRANILVTELFDTELIGEGALPSYEHAHRHLVEENCEAVPHRATV
YAQLVESGRMWSWNKLFPIHVQTSLGEQVIVPPVDVESCPGAPSVCDIQLNQVSPADFTV
LSDVLPMFSIDFSKQVSSSAACHSRRFEPLTSGRAQVVLSWWDIEMDPEGKIKCTMAPFW
AHSDPEEMQWRDHWMQCVYFLPQEEPVVQGSALYLVAHHDDYCVWYSLQRTSPEKNERVR
QMRPVCDCQAHLLWNRPRFGEINDQDRTDRYVQALRTVLKPDSVCLCVSDGSLLSVLAHH
LGVEQVFTVESSAASHKLLRKIFKANHLEDKINIIEKRPELLTNEDLQGRKVSLLLGEPF
FTTSLLPWHNLYFWYVRTAVDQHLGPGAMVMPQAASLHAVVVEFRDLWRIRSPCGDCEGF
DVHIMDDMIKRALDFRESREAEPHPLWEYPCRSLSEPWQILTFDFQQPVPLQPLCAEGTV
ELRRPGQSHAAVLWMEYHLTPECTLSTGLLEPADPEGGCCWNPHCKQAVYFFSPAPDPRA
LLGGPRTVSYAVEFHPDTGDIIMEFRHADTPD
NT seq
2079 nt
NT seq
+upstream
nt +downstream
nt
atgaagatcttctgcagtcgggccaatccgaccacggggtctgtggagtggctggaggag
gatgaacactatgattaccaccaggagattgcaaggtcatcttatgcagatatgctacat
gacaaagacagaaatgtaaaatactaccaaggtatccgggctgccgtgagcagggtgaag
gacagaggacagaaggccttggttctcgacattggcactggcacgggactcttgtcaatg
atggcggtcacagcaggtgccgacttctgctatgccatcgaggttttcaagcctatggct
gatgctgctgtgaagattgtggagaaaaatggctttagtgataagattaaggttatcaac
aagcattccaccgaggtgactgtaggtccagagggtgacatgccatgccgtgccaacatc
ctggtcacagagttgtttgacacagagctgatcggggagggggcgctgccctcctatgag
cacgcacacaggcatctcgtggaggaaaattgtgaggccgtgccccacagagccaccgtc
tatgcacagctggtggagtccgggaggatgtggtcgtggaacaagctatttcccatccac
gtgcagaccagcctcggagagcaggtcatcgtccctcccgttgacgtggagagctgccct
ggcgcaccctctgtctgtgacattcagctgaaccaggtgtcaccagccgactttacagtc
ctcagcgatgtgctgcccatgttcagcatagacttcagcaagcaagtcagtagctcagca
gcctgccatagcaggcggtttgaacctctgacatctggccgagctcaggtggttctctcg
tggtgggacattgaaatggaccctgaggggaagatcaagtgcaccatggcccccttctgg
gcacactcagacccagaggagatgcagtggcgggaccactggatgcagtgtgtgtacttc
ctgccacaagaggagcctgtggtgcagggctcagcgctctatctggtagcccaccacgat
gactactgcgtatggtacagcctgcagaggaccagccctgaaaagaatgagagagtccgc
cagatgcgccccgtgtgtgactgccaggctcacctgctctggaaccggcctcggtttgga
gagatcaatgaccaggacagaactgatcgatacgtccaggctctgaggaccgtgctgaag
ccagacagcgtgtgcctgtgtgtcagcgatggcagcctgctctccgtgctggcccatcac
ctgggggtggagcaggtgtttacagtcgagagttcagcagcttctcacaaactgttgaga
aaaatcttcaaggctaaccacttggaagataaaattaacatcatagagaaacggccggaa
ttattaacaaatgaggacctacagggcagaaaggtctctctcctcctgggcgagccgttc
ttcactaccagcctgctgccgtggcacaacctctacttctggtacgtgcggaccgctgtg
gaccagcacctggggccaggtgccatggtgatgccccaggcagcctcgctgcacgctgtg
gttgtggagttcagggacctgtggcggatccggagcccctgtggtgactgcgaaggcttc
gacgtgcacatcatggacgacatgattaagcgtgccctggacttcagggagagcagggaa
gctgagccccacccgctgtgggagtacccatgccgcagcctctccgagccctggcagatc
ctgacctttgacttccagcagccggtgcccctgcagcccctgtgtgccgagggcaccgtg
gagctcagaaggcccgggcagagccacgcagcggtgctatggatggagtaccacctgacc
ccggagtgcacgctcagcactggcctcctggagcctgcagaccccgaggggggctgctgc
tggaacccccactgcaagcaggccgtctacttcttcagccctgccccagatcccagagca
ctgctgggtggcccacggactgtcagctatgcagtggagtttcaccccgacacaggcgac
atcatcatggagttcaggcatgcagataccccagactga
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