Homo sapiens (human): 10498
Help
Entry
10498 CDS
T01001
Symbol
CARM1, PRMT4
Name
(RefSeq) coactivator associated arginine methyltransferase 1
KO
K05931
type I protein arginine methyltransferase [EC:
2.1.1.319
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa01522
Endocrine resistance
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09176 Drug resistance: antineoplastic
01522 Endocrine resistance
10498 (CARM1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
10498 (CARM1)
Enzymes [BR:
hsa01000
]
2. Transferases
2.1 Transferring one-carbon groups
2.1.1 Methyltransferases
2.1.1.319 type I protein arginine methyltransferase
10498 (CARM1)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HMTs (histone methyltransferases)
PRMTs (protein arginine metyltransferases)
10498 (CARM1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CARM1
PrmA
Methyltransf_25
MTS
Methyltransf_9
Methyltransf_11
Methyltransf_31
PRMT5
Methyltransf_23
Methyltransf_18
Methyltransf_12
Met_10
FtsJ
CMAS
TehB
Cons_hypoth95
PRMT5_C
Methyltransf_32
DREV
Motif
Other DBs
NCBI-GeneID:
10498
NCBI-ProteinID:
NP_954592
OMIM:
603934
HGNC:
23393
Ensembl:
ENSG00000142453
UniProt:
Q86X55
Structure
PDB
LinkDB
All DBs
Position
19:10871553..10923075
Genome browser
AA seq
608 aa
AA seq
DB search
MAAAAAAVGPGAGGAGSAVPGGAGPCATVSVFPGARLLTIGDANGEIQRHAEQQALRLEV
RAGPDSAGIALYSHEDVCVFKCSVSRETECSRVGKQSFIITLGCNSVLIQFATPNDFCSF
YNILKTCRGHTLERSVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNH
TDFKDKIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTDRIVVIPG
KVEEVSLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSGNMFPTIGDVHLAPFTDE
QLYMEQFTKANFWYQPSFHGVDLSALRGAAVDEYFRQPVVDTFDIRILMAKSVKYTVNFL
EAKEGDLHRIEIPFKFHMLHSGLVHGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRC
LFQSPLFAKAGDTLSGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYTGTT
PSPPPGSHYTSPSENMWNTGSTYNLSSGMAVAGMPTAYDLSSVIASGSSVGHNNLIPLAN
TGIVNHTHSRMGSIMSTGIVQGSSGAQGSGGGSTSAHYAVNSQFTMGGPAISMASPMSIP
TNTMHYGS
NT seq
1827 nt
NT seq
+upstream
nt +downstream
nt
atggcagcggcggcggcggcggtggggccgggcgcgggcggcgcggggtcggcggtcccg
ggcggcgcggggccctgcgctaccgtgtcggtgttccccggcgcccgcctcctcaccatc
ggcgacgcgaacggcgagatccagcggcacgcggagcagcaggcgctgcgcctcgaggtg
cgcgccggcccggactcggcgggcatcgccctctacagccatgaagatgtgtgtgtcttt
aagtgctcagtgtcccgagagacagagtgcagccgtgtgggcaagcagtccttcatcatc
accctgggctgcaacagcgtcctcatccagttcgccacacccaacgatttctgttccttc
tacaacatcctgaaaacctgccggggccacaccctggagcggtctgtgttcagcgagcgg
acggaggagtcttctgccgtgcagtacttccagttttatggctacctgtcccagcagcag
aacatgatgcaggactacgtgcggacaggcacctaccagcgcgccatcctgcaaaaccac
accgacttcaaggacaagatcgttcttgatgttggctgtggctctgggatcctgtcgttt
tttgccgcccaagctggagcacggaaaatctacgcggtggaggccagcaccatggcccag
cacgctgaggtcttggtgaagagtaacaacctgacggaccgcatcgtggtcatcccgggc
aaggtggaggaggtgtcactccccgagcaggtggacatcatcatctcggagcccatgggc
tacatgctcttcaacgagcgcatgctggagagctacctccacgccaagaagtacctgaag
cccagcggaaacatgtttcctaccattggtgacgtccaccttgcacccttcacggatgaa
cagctctacatggagcagttcaccaaggccaacttctggtaccagccatctttccatgga
gtggacctgtcggccctccgaggtgccgcggtggatgagtatttccggcagcctgtggtg
gacacatttgacatccggatcctgatggccaagtctgtcaagtacacggtgaacttctta
gaagccaaagaaggagatttgcacaggatagaaatcccattcaaattccacatgctgcat
tcagggctggtccacggcctggctttctggtttgacgttgctttcatcggctccataatg
accgtgtggctgtccacagccccgacagagcccctgacccactggtaccaggtgcggtgc
ctgttccagtcaccactgttcgccaaggcaggggacacgctctcagggacatgtctgctt
attgccaacaaaagacagagctacgacatcagtattgtggcccaggtggaccagaccggc
tccaagtccagtaacctcctggatctgaaaaaccccttctttagatacacgggcacaacg
ccctcacccccacccggctcccactacacatctccctcggaaaacatgtggaacacgggc
agcacctacaacctcagcagcgggatggccgtggcagggatgccgaccgcctatgacttg
agcagtgttattgccagtggctccagcgtgggccacaacaacctgattcctttagccaac
acggggattgtcaatcacacccactcccggatgggctccataatgagcacggggattgtc
caagggtcctccggcgcccagggcagtggtggtggcagcacgagtgcccactatgcagtc
aacagccagttcaccatgggcggccccgccatctccatggcgtcgcccatgtccatcccg
accaacaccatgcactacgggagctag
DBGET
integrated database retrieval system