Homo sapiens (human): 59336
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Entry
59336 CDS
T01001
Symbol
PRDM13, CDIDHH, MU-MB-20.220, PCH17, PFM10
Name
(RefSeq) PR/SET domain 13
KO
K24645
PR domain zinc finger protein 13 [EC:2.1.1.-]
Organism
hsa
Homo sapiens (human)
Disease
H00897
Pontocerebellar hypoplasia
H02966
Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
59336 (PRDM13)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 PRDM
59336 (PRDM13)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-C2H2
PRDM2_PR
zf-H2C2_2
zf-C2H2_4
SET
zf-C2H2_7th_ZNF462
zf-BED
Zf-C2H2_ZNF451
C2CH-3rd_BIRD-IDD
zf-C2HE
Motif
Other DBs
NCBI-GeneID:
59336
NCBI-ProteinID:
NP_067633
OMIM:
616741
HGNC:
13998
Ensembl:
ENSG00000112238
UniProt:
Q9H4Q3
LinkDB
All DBs
Position
6:99606833..99615562
Genome browser
AA seq
707 aa
AA seq
DB search
MHGAARAPATSVSADCCIPAGLRLGPVPGTFKLGKYLSDRREPGPKKKVRMVRGELVDES
GGSPLEWIGLIRAARNSQEQTLEAIADLPGGQIFYRALRDVQPGEELTVWYSNSLAQWFD
IPTTATPTHDEKGEERYICWYCWRTFRYPNSLKAHLRFHCVFSGGGGGAFLHHEHAARQG
AVPAADGLGLSPKPPAPDFAAPSQAGTLRPHPLGPPPVQACGAREGIKREASSAPSATSP
TPGKWGQPKKGKEQLDRALDMSGAARGQGHFLGIVGGSSAGVGSLAFYPGVRSAFKPAGL
ARAAAAAHGDPYREESSSKQGAGLALGRLLGGGRACGRPGSGENSAAGGAGHHHHHHAHH
HHHPKCLLAGDPPPPPPPGLPCSGALRGFPLLSVPPEEASAFKHVERAPPAAAALPGARY
AQLPPAPGLPLERCALPPLDPGGLKAYPGGECSHLPAVMPAFTVYNGELLYGSPATTAYY
PLKLHFGGLLKYPESISYFSGPAAAALSPAELGSLASIDREIAMHNQQLSEMAAGKGRGR
LDSGTLPPAVAAAGGTGGGGSGGSGAGKPKTGHLCLYCGKLYSRKYGLKIHMRTHTGYKP
LKCKVCLRPFGDPSNLNKHIRLHAEGNTPYRCEFCGKVLVRRRDLERHVKSRHPGQSLLA
KAGDGPGAEPGYPPEPGDPKSDDSDVDVCFTDDQSDPEVGGGGERDL
NT seq
2124 nt
NT seq
+upstream
nt +downstream
nt
atgcacggagccgccagagcgccagccaccagcgtgagtgccgactgctgcatcccggcc
ggcttgcgcctcggaccggtgcctggtaccttcaagctgggcaagtacctgtcagaccgc
agggagcccgggcctaagaaaaaggtgcgcatggtgagaggggagctggtggacgagtcg
gggggctcccctctggagtggatagggttaatccgggcagccagaaactcccaggaacag
actctggaagctattgcagacttacccggaggacagatcttctaccgagcattgcgagac
gtccagccaggggaggagctgacagtgtggtattctaactccttggctcagtggttcgac
atccccaccacagcgactccgactcacgacgagaaaggggaggagcgctacatctgctgg
tactgctggaggacgtttagataccccaacagccttaaggcacacctgcgtttccactgc
gtgttcagcggcggtggaggcggcgccttcctgcaccacgaacacgcggctcgccaaggc
gccgtcccagcggctgatggcctcggtctctccccaaaacccccggcgcccgatttcgcc
gcgccttcccaggcaggaactttgcgaccccaccccctgggcccgccaccagttcaggcc
tgcggtgcgcgggagggcatcaagcgcgaggcctcttccgcgccctcggccacctcgccg
accccaggcaagtgggggcagcccaagaagggcaaggagcagctggaccgtgccctggac
atgagcggagccgcccgaggacaagggcacttcctcggcatcgtgggcggctcctcggcg
ggggtcggcagcctggctttctaccccggcgtgcgctcagctttcaagcccgccggccta
gcgagggcggcggcggccgctcacggcgacccctaccgggaggagagcagcagcaagcaa
ggagccggcctcgctttgggcaggctgctgggcgggggccgggcgtgcgggcgccccggg
agcggggagaactcggcggcgggcggcgcgggtcaccaccatcaccaccacgcgcaccac
caccaccatcccaagtgcctgctcgctggggacccgccgccgccgccgccgcctggcctg
ccctgctctggggccctgcgcggcttccctctgctctccgtccccccggaagaggcgtcc
gccttcaagcacgtggagcgcgccccgcccgcagccgccgcgctgccaggagcgcgttat
gcgcagctgccccctgcgccggggttgcccctcgagcgctgcgcgctgccgcccctcgac
ccgggcggtctcaaagcctatccgggtggtgagtgcagccacctgcccgccgtcatgccg
gcctttacagtctacaacggggagctgctctacggctcaccggccaccaccgcttattac
ccgctcaaattgcacttcggcgggctgctgaagtatccggagtccatctcctacttcagc
gggcctgcagcggccgccctaagccccgccgagctggggtcgctggccagcatcgaccga
gagatcgccatgcacaatcagcagctgtccgagatggctgccgggaagggtcgcggacgc
ctggactcggggacgttgccaccggccgtcgcggcggcgggaggcaccgggggcggcggc
agcggaggcagcggcgcaggtaagcccaagaccggccacctgtgcctctactgtggcaag
ctgtactcgcgcaagtatgggctcaagatccacatgcggacgcacacgggctacaagcca
ctcaagtgcaaagtctgtctgcggcccttcggcgaccccagcaatctcaacaagcacatc
cggctgcacgccgagggcaatacgccctaccgctgcgagttctgcggcaaggtacttgtg
cgccgccgggacctggagcgacatgtcaagtcccgccaccctggccagagtctgctcgcc
aaagcgggcgacggcccgggtgccgagcccggctatcccccggagcctggggatcccaag
agcgacgacagtgacgtggacgtctgcttcacagacgaccagagcgaccccgaggttggg
ggcggcggggagcgcgacttgtaa
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