Homo sapiens (human): 5261
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Entry
5261 CDS
T01001
Symbol
PHKG2, GSD9C
Name
(RefSeq) phosphorylase kinase catalytic subunit gamma 2
KO
K00871
phosphorylase kinase gamma subunit [EC:
2.7.11.19
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa04020
Calcium signaling pathway
hsa04910
Insulin signaling pathway
hsa04922
Glucagon signaling pathway
Network
nt06528
Calcium signaling
Element
N01648
Ca2+/CAM-CAMK signaling pathway
Disease
H00069
Glycogen storage disease
H01760
Hepatic glycogen storage disease
H01948
Glycogen storage disease type IX
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
5261 (PHKG2)
09150 Organismal Systems
09152 Endocrine system
04910 Insulin signaling pathway
5261 (PHKG2)
04922 Glucagon signaling pathway
5261 (PHKG2)
09180 Brite Hierarchies
09181 Protein families: metabolism
01001 Protein kinases [BR:
hsa01001
]
5261 (PHKG2)
Enzymes [BR:
hsa01000
]
2. Transferases
2.7 Transferring phosphorus-containing groups
2.7.11 Protein-serine/threonine kinases
2.7.11.19 phosphorylase kinase
5261 (PHKG2)
Protein kinases [BR:
hsa01001
]
Serine/threonine kinases: CAMK group
PHK family
5261 (PHKG2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Pkinase
PK_Tyr_Ser-Thr
Kinase-like
APH
Kdo
ABC1
RIO1
Choline_kinase
Haspin_kinase
Pkinase_fungal
YrbL-PhoP_reg
DUF2805
Pox_ser-thr_kin
Motif
Other DBs
NCBI-GeneID:
5261
NCBI-ProteinID:
NP_000285
OMIM:
172471
HGNC:
8931
Ensembl:
ENSG00000156873
UniProt:
P15735
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:30748425..30761176
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AA seq
406 aa
AA seq
DB search
MTLDVGPEDELPDWAAAKEFYQKYDPKDVIGRGVSSVVRRCVHRATGHEFAVKIMEVTAE
RLSPEQLEEVREATRRETHILRQVAGHPHIITLIDSYESSSFMFLVFDLMRKGELFDYLT
EKVALSEKETRSIMRSLLEAVSFLHANNIVHRDLKPENILLDDNMQIRLSDFGFSCHLEP
GEKLRELCGTPGYLAPEILKCSMDETHPGYGKEVDLWACGVILFTLLAGSPPFWHRRQIL
MLRMIMEGQYQFSSPEWDDRSSTVKDLISRLLQVDPEARLTAEQALQHPFFERCEGSQPW
NLTPRQRFRVAVWTVLAAGRVALSTHRVRPLTKNALLRDPYALRSVRHLIDNCAFRLYGH
WVKKGEQQNRAALFQHRPPGPFPIMGPEEEGDSAAITEDEAVLVLG
NT seq
1221 nt
NT seq
+upstream
nt +downstream
nt
atgacgctggacgtggggccggaggatgagctgcccgactgggccgccgccaaagagttt
taccagaagtacgaccctaaggacgtcatcggcagaggagtgagctctgtggtccgccgt
tgtgttcatcgagctactggccacgagtttgcggtgaagattatggaagtgacagctgag
cggctgagtcctgagcagctggaggaggtgcgggaagccacacggcgagagacacacatc
cttcgccaggtcgccggccacccccacatcatcaccctcatcgattcctacgagtcttct
agcttcatgttcctggtgtttgacctgatgcggaagggagagctgtttgactatctcaca
gagaaggtggccctctctgaaaaggaaaccaggtccatcatgcggtctctgctggaagca
gtgagctttctccatgccaacaacattgtgcatcgagatctgaagcccgagaatattctc
ctagatgacaatatgcagatccgactttcagatttcgggttctcctgccacttggaacct
ggcgagaagcttcgagagttgtgtgggaccccagggtatctagcgccagagatccttaaa
tgctccatggatgaaacccacccaggctatggcaaggaggtcgacctctgggcctgtggg
gtgatcttgttcacactcctggctggctcgccacccttctggcaccggcggcagatcctg
atgttacgcatgatcatggagggccagtaccagttcagttcccccgagtgggatgaccgt
tccagcactgtcaaagacctgatctccaggctgctgcaggtggatcctgaggcacgcctg
acagctgagcaggccctacagcaccccttctttgagcgttgtgaaggcagccaaccctgg
aacctcaccccccgccagcggttccgggtggcagtgtggacagtgctggctgctggacga
gtggccctaagcacccatcgtgtacggccactgaccaagaatgcactgttgagggaccct
tatgcgctgcggtcagtgcggcacctcatcgacaactgtgccttccggctctacgggcac
tgggtaaagaaaggggagcagcagaaccgggcggctctctttcagcaccggccccctggg
ccttttcccatcatgggccctgaagaggagggagactctgctgctataactgaggatgag
gccgtgcttgtgctgggctag
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