PHKG1 (phosphorylase kinase catalytic subunit gamma 1) - Rat Genome Database

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Gene: PHKG1 (phosphorylase kinase catalytic subunit gamma 1) Homo sapiens
Analyze
Symbol: PHKG1
Name: phosphorylase kinase catalytic subunit gamma 1
RGD ID: 731844
HGNC Page HGNC:8930
Description: Predicted to enable several functions, including ATP binding activity; calmodulin binding activity; and protein kinase activity. Predicted to be involved in glycogen biosynthetic process. Predicted to be located in cytosol. Predicted to be part of phosphorylase kinase complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: PHK-gamma-M; PHKG; phosphorylase b kinase gamma catalytic chain, skeletal muscle isoform; phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform; phosphorylase kinase gamma; phosphorylase kinase gamma subunit 1; phosphorylase kinase subunit gamma-1; phosphorylase kinase, gamma 1 (muscle); serine/threonine-protein kinase PHKG1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: AC118758.1   PHKG1P1   PHKG1P2   PHKG1P3   PHKG1P4  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38756,080,295 - 56,092,952 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl756,080,283 - 56,092,996 (-)EnsemblGRCh38hg38GRCh38
GRCh37756,147,988 - 56,160,645 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36756,116,169 - 56,128,183 (-)NCBINCBI36Build 36hg18NCBI36
Build 34755,922,185 - 55,934,836NCBI
Celera767,201,579 - 67,213,594 (-)NCBICelera
Cytogenetic Map7p11.2NCBI
HuRef755,961,419 - 55,974,912 (-)NCBIHuRef
CHM1_1756,150,991 - 56,163,725 (-)NCBICHM1_1
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2756,152,223 - 56,164,936 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Phosphorylase kinase: the complexity of its regulation is reflected in the complexity of its structure. Brushia RJ and Walsh DA, Front Biosci. 1999 Sep 15;4:D618-41.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
Additional References at PubMed
PMID:2297530   PMID:2365696   PMID:2507540   PMID:7706316   PMID:7874115   PMID:7929096   PMID:7935360   PMID:8530014   PMID:8672716   PMID:8999860   PMID:9362479   PMID:9735171  
PMID:9771888   PMID:9832145   PMID:10090741   PMID:10737616   PMID:12387894   PMID:12477932   PMID:12665801   PMID:12825073   PMID:12853948   PMID:15489334   PMID:16051665   PMID:16344560  
PMID:17692548   PMID:21873635   PMID:28514442   PMID:33961781   PMID:35150045  


Genomics

Comparative Map Data
PHKG1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38756,080,295 - 56,092,952 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl756,080,283 - 56,092,996 (-)EnsemblGRCh38hg38GRCh38
GRCh37756,147,988 - 56,160,645 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36756,116,169 - 56,128,183 (-)NCBINCBI36Build 36hg18NCBI36
Build 34755,922,185 - 55,934,836NCBI
Celera767,201,579 - 67,213,594 (-)NCBICelera
Cytogenetic Map7p11.2NCBI
HuRef755,961,419 - 55,974,912 (-)NCBIHuRef
CHM1_1756,150,991 - 56,163,725 (-)NCBICHM1_1
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2756,152,223 - 56,164,936 (-)NCBI
Phkg1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395129,892,272 - 129,907,953 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl5129,892,262 - 129,927,390 (-)EnsemblGRCm39 Ensembl
GRCm385129,863,431 - 129,879,134 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5129,863,421 - 129,898,549 (-)EnsemblGRCm38mm10GRCm38
MGSCv375130,339,311 - 130,354,954 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv365130,148,144 - 130,163,787 (-)NCBIMGSCv36mm8
Celera5126,861,315 - 126,876,254 (-)NCBICelera
Cytogenetic Map5G1.3NCBI
cM Map568.26NCBI
Phkg1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81232,474,926 - 32,490,657 (+)NCBIGRCr8
mRatBN7.21226,838,822 - 26,854,547 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1226,838,968 - 26,852,850 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1227,977,113 - 27,990,411 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01228,587,651 - 28,600,949 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01227,649,136 - 27,662,434 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01230,450,431 - 30,464,314 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1230,450,316 - 30,464,352 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01232,392,860 - 32,406,743 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41228,029,616 - 28,043,499 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11227,893,003 - 27,906,887 (-)NCBI
Celera1228,545,079 - 28,558,910 (+)NCBICelera
RH 3.4 Map12452.5RGD
Cytogenetic Map12q13NCBI
Phkg1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554568,251,130 - 8,259,205 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554568,251,789 - 8,259,205 (-)NCBIChiLan1.0ChiLan1.0
PHKG1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2660,932,031 - 60,952,314 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan17109,257,096 - 109,278,312 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0756,693,252 - 56,706,474 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1757,115,573 - 57,128,900 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl757,115,921 - 57,139,516 (-)Ensemblpanpan1.1panPan2
PHKG1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.16565,560 - 577,754 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl6565,711 - 577,739 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha62,265,027 - 2,277,221 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.06369,389 - 381,583 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl6369,396 - 381,568 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.16313,135 - 325,329 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.06307,240 - 319,434 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.06478,422 - 490,616 (-)NCBIUU_Cfam_GSD_1.0
Phkg1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344126,160,534 - 126,166,510 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365437,866,141 - 7,876,033 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365437,870,081 - 7,876,033 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PHKG1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl316,822,043 - 16,834,329 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1316,822,042 - 16,831,054 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2317,074,784 - 17,082,851 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PHKG1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1212,687,561 - 2,701,145 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl212,688,054 - 2,704,036 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666041179,889,801 - 179,903,371 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Phkg1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247408,270,279 - 8,279,003 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247408,270,709 - 8,279,021 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PHKG1
31 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7p12.1-11.2(chr7:52114454-57434735)x1 copy number loss See cases [RCV000052656] Chr7:52114454..57434735 [GRCh38]
Chr7:52182150..57493216 [GRCh37]
Chr7:52149644..57498383 [NCBI36]
Chr7:7p12.1-11.2		 uncertain significance
GRCh38/hg38 7p12.1-11.2(chr7:52192528-57823293)x3 copy number gain See cases [RCV000053439] Chr7:52192528..57823293 [GRCh38]
Chr7:52260224..57882999 [GRCh37]
Chr7:52227718..57886941 [NCBI36]
Chr7:7p12.1-11.2		 uncertain significance
GRCh38/hg38 7p12.1-11.2(chr7:53450330-56107195)x3 copy number gain See cases [RCV000053440] Chr7:53450330..56107195 [GRCh38]
Chr7:53518023..56174888 [GRCh37]
Chr7:53485517..56142382 [NCBI36]
Chr7:7p12.1-11.2		 uncertain significance
GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3 copy number gain See cases [RCV000053532] Chr7:33328312..62377476 [GRCh38]
Chr7:33367924..61831899 [GRCh37]
Chr7:33334449..61469334 [NCBI36]
Chr7:7p14.3-q11.21		 pathogenic
GRCh38/hg38 7p12.1-q11.22(chr7:53274059-68576213)x3 copy number gain See cases [RCV000053534] Chr7:53274059..68576213 [GRCh38]
Chr7:53341752..68041200 [GRCh37]
Chr7:53309246..67679136 [NCBI36]
Chr7:7p12.1-q11.22		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7p11.2(chr7:55805157-56107195)x1 copy number loss See cases [RCV000134962] Chr7:55805157..56107195 [GRCh38]
Chr7:55872850..56174888 [GRCh37]
Chr7:55840344..56142382 [NCBI36]
Chr7:7p11.2		 uncertain significance
GRCh38/hg38 7p14.1-11.2(chr7:40534157-56107122)x1 copy number loss See cases [RCV000136092] Chr7:40534157..56107122 [GRCh38]
Chr7:40573756..56174815 [GRCh37]
Chr7:40540281..56142309 [NCBI36]
Chr7:7p14.1-11.2		 pathogenic
GRCh38/hg38 7p11.2(chr7:55538414-56107195)x3 copy number gain See cases [RCV000141605] Chr7:55538414..56107195 [GRCh38]
Chr7:55606107..56174888 [GRCh37]
Chr7:55573601..56142382 [NCBI36]
Chr7:7p11.2		 uncertain significance
GRCh38/hg38 7p11.2(chr7:55733060-56107195)x1 copy number loss See cases [RCV000142545] Chr7:55733060..56107195 [GRCh38]
Chr7:55800753..56174888 [GRCh37]
Chr7:55768247..56142382 [NCBI36]
Chr7:7p11.2		 benign
GRCh37/hg19 7p11.2(chr7:55874737-56172217)x1 copy number loss See cases [RCV000239822] Chr7:55874737..56172217 [GRCh37]
Chr7:7p11.2		 uncertain significance
GRCh37/hg19 7p11.2(chr7:55848150-56344705)x3 copy number gain See cases [RCV000598887] Chr7:55848150..56344705 [GRCh37]
Chr7:7p11.2		 uncertain significance
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34		 pathogenic
GRCh37/hg19 7p11.2(chr7:55874737-56172165)x3 copy number gain See cases [RCV000447572] Chr7:55874737..56172165 [GRCh37]
Chr7:7p11.2		 benign
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p11.2(chr7:54972516-56172165)x1 copy number loss See cases [RCV000445658] Chr7:54972516..56172165 [GRCh37]
Chr7:7p11.2		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_006213.5(PHKG1):c.733G>A (p.Gly245Ser) single nucleotide variant Inborn genetic diseases [RCV003302507] Chr7:56081952 [GRCh38]
Chr7:56149645 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.996C>G (p.Ile332Met) single nucleotide variant Inborn genetic diseases [RCV003270149] Chr7:56081222 [GRCh38]
Chr7:56148915 [GRCh37]
Chr7:7p11.2		 uncertain significance
GRCh37/hg19 7p11.2(chr7:55550741-56945077)x1 copy number loss See cases [RCV000512175] Chr7:55550741..56945077 [GRCh37]
Chr7:7p11.2		 likely benign
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
Single allele duplication Autism [RCV000754332] Chr7:52551984..56315037 [GRCh38]
Chr7:7p12.1-11.2		 likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_006213.5(PHKG1):c.968G>A (p.Arg323His) single nucleotide variant Inborn genetic diseases [RCV003246316] Chr7:56081250 [GRCh38]
Chr7:56148943 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.163G>A (p.Gly55Ser) single nucleotide variant Inborn genetic diseases [RCV003246323] Chr7:56087697 [GRCh38]
Chr7:56155390 [GRCh37]
Chr7:7p11.2		 uncertain significance
GRCh37/hg19 7p12.1-11.1(chr7:52809787-58025873)x1 copy number loss not provided [RCV000846150] Chr7:52809787..58025873 [GRCh37]
Chr7:7p12.1-11.1		 uncertain significance
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p11.2(chr7:55776531-56393852)x3 copy number gain not provided [RCV001834289] Chr7:55776531..56393852 [GRCh37]
Chr7:7p11.2		 likely benign
GRCh37/hg19 7p11.2(chr7:55757106-56489653)x3 copy number gain not provided [RCV001834233] Chr7:55757106..56489653 [GRCh37]
Chr7:7p11.2		 likely benign
NC_000007.13:g.(?_56079455)_(56174106_?)del deletion Deficiency of phosphoserine phosphatase [RCV001920532] Chr7:56079455..56174106 [GRCh37]
Chr7:7p11.2		 uncertain significance
NC_000007.13:g.(?_56079455)_(56174106_?)dup duplication Deficiency of phosphoserine phosphatase [RCV001993474] Chr7:56079455..56174106 [GRCh37]
Chr7:7p11.2		 uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
NM_006213.5(PHKG1):c.781G>A (p.Val261Met) single nucleotide variant Inborn genetic diseases [RCV002727609] Chr7:56081904 [GRCh38]
Chr7:56149597 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.949C>T (p.Arg317Trp) single nucleotide variant Inborn genetic diseases [RCV002727440] Chr7:56081269 [GRCh38]
Chr7:56148962 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.732C>A (p.Ser244Arg) single nucleotide variant Inborn genetic diseases [RCV002794043] Chr7:56081953 [GRCh38]
Chr7:56149646 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.889C>T (p.Arg297Trp) single nucleotide variant Inborn genetic diseases [RCV002906287] Chr7:56081659 [GRCh38]
Chr7:56149352 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.967C>T (p.Arg323Cys) single nucleotide variant Inborn genetic diseases [RCV002686971] Chr7:56081251 [GRCh38]
Chr7:56148944 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.995T>C (p.Ile332Thr) single nucleotide variant Inborn genetic diseases [RCV002777793] Chr7:56081223 [GRCh38]
Chr7:56148916 [GRCh37]
Chr7:7p11.2		 uncertain significance
GRCh37/hg19 7p12.1-11.2(chr7:53991820-56148011)x3 copy number gain not provided [RCV002475815] Chr7:53991820..56148011 [GRCh37]
Chr7:7p12.1-11.2		 uncertain significance
NM_006213.5(PHKG1):c.1114G>A (p.Glu372Lys) single nucleotide variant Inborn genetic diseases [RCV002977828] Chr7:56081104 [GRCh38]
Chr7:56148797 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.580G>A (p.Glu194Lys) single nucleotide variant Inborn genetic diseases [RCV002736971] Chr7:56082221 [GRCh38]
Chr7:56149914 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.697C>T (p.Arg233Trp) single nucleotide variant Inborn genetic diseases [RCV002822783] Chr7:56081988 [GRCh38]
Chr7:56149681 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.728T>G (p.Met243Arg) single nucleotide variant Inborn genetic diseases [RCV002798100] Chr7:56081957 [GRCh38]
Chr7:56149650 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.637A>G (p.Met213Val) single nucleotide variant Inborn genetic diseases [RCV002822367] Chr7:56082164 [GRCh38]
Chr7:56149857 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.7C>T (p.Arg3Trp) single nucleotide variant Inborn genetic diseases [RCV002759566] Chr7:56088935 [GRCh38]
Chr7:56156628 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.205G>A (p.Glu69Lys) single nucleotide variant Inborn genetic diseases [RCV002977601] Chr7:56087655 [GRCh38]
Chr7:56155348 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.203G>A (p.Arg68Gln) single nucleotide variant Inborn genetic diseases [RCV002757923] Chr7:56087657 [GRCh38]
Chr7:56155350 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.1042G>A (p.Asp348Asn) single nucleotide variant Inborn genetic diseases [RCV002804869] Chr7:56081176 [GRCh38]
Chr7:56148869 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.989G>A (p.Arg330Gln) single nucleotide variant Inborn genetic diseases [RCV002709100] Chr7:56081229 [GRCh38]
Chr7:56148922 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.1150G>A (p.Glu384Lys) single nucleotide variant Inborn genetic diseases [RCV002666509] Chr7:56081068 [GRCh38]
Chr7:56148761 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.457C>T (p.Pro153Ser) single nucleotide variant Inborn genetic diseases [RCV002803953] Chr7:56083368 [GRCh38]
Chr7:56151061 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.1063T>C (p.Tyr355His) single nucleotide variant Inborn genetic diseases [RCV002854893] Chr7:56081155 [GRCh38]
Chr7:56148848 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.789C>G (p.Asp263Glu) single nucleotide variant Inborn genetic diseases [RCV002703389] Chr7:56081896 [GRCh38]
Chr7:56149589 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.934G>A (p.Val312Met) single nucleotide variant Inborn genetic diseases [RCV002677669] Chr7:56081284 [GRCh38]
Chr7:56148977 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.845C>G (p.Ala282Gly) single nucleotide variant Inborn genetic diseases [RCV003214450] Chr7:56081703 [GRCh38]
Chr7:56149396 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.728T>C (p.Met243Thr) single nucleotide variant Inborn genetic diseases [RCV003199964] Chr7:56081957 [GRCh38]
Chr7:56149650 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.997G>A (p.Val333Ile) single nucleotide variant Inborn genetic diseases [RCV003195065] Chr7:56081221 [GRCh38]
Chr7:56148914 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.211A>C (p.Thr71Pro) single nucleotide variant Inborn genetic diseases [RCV003345968] Chr7:56087649 [GRCh38]
Chr7:56155342 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.54G>T (p.Glu18Asp) single nucleotide variant Inborn genetic diseases [RCV003373422] Chr7:56088888 [GRCh38]
Chr7:56156581 [GRCh37]
Chr7:7p11.2		 uncertain significance
NM_006213.5(PHKG1):c.905G>A (p.Arg302Gln) single nucleotide variant Inborn genetic diseases [RCV003370629] Chr7:56081643 [GRCh38]
Chr7:56149336 [GRCh37]
Chr7:7p11.2		 uncertain significance
GRCh37/hg19 7p11.2-11.1(chr7:55498635-58025873)x3 copy number gain not provided [RCV003484683] Chr7:55498635..58025873 [GRCh37]
Chr7:7p11.2-11.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2676
Count of miRNA genes:927
Interacting mature miRNAs:1141
Transcripts:ENST00000297373, ENST00000395428, ENST00000432123, ENST00000446428, ENST00000452681, ENST00000467726, ENST00000471665, ENST00000489604, ENST00000492124, ENST00000537360
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
SHGC-56973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37756,150,884 - 56,151,118UniSTSGRCh37
Build 36756,118,378 - 56,118,612RGDNCBI36
Celera767,203,788 - 67,204,022RGD
Cytogenetic Map7p11.2UniSTS
HuRef755,964,333 - 55,964,567UniSTS
CRA_TCAGchr7v2756,155,131 - 56,155,365UniSTS
PHKG1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37756,155,293 - 56,155,442UniSTSGRCh37
Celera767,208,197 - 67,208,346UniSTS
HuRef755,968,742 - 55,968,891UniSTS
CRA_TCAGchr7v2756,159,540 - 56,159,689UniSTS
RH71293  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7p11.2UniSTS
RH46930  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map7p11.2UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 263 615 23 16 18 1 1086 1022 757 6 12 13 17 101 977 1
Low 2108 2212 1572 486 1748 342 3120 1128 2971 298 1417 1561 157 1 1101 1811 4 1
Below cutoff 64 163 130 120 178 121 149 47 5 114 28 38 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001258459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001258460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_047689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005271772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC092101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH011220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069655 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC074753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB171823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X80590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000297373   ⟹   ENSP00000297373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,080,295 - 56,092,952 (-)Ensembl
RefSeq Acc Id: ENST00000395428   ⟹   ENSP00000378817
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,083,341 - 56,092,952 (-)Ensembl
RefSeq Acc Id: ENST00000432123   ⟹   ENSP00000397193
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,082,014 - 56,092,946 (-)Ensembl
RefSeq Acc Id: ENST00000446428   ⟹   ENSP00000389721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,081,717 - 56,092,932 (-)Ensembl
RefSeq Acc Id: ENST00000452681   ⟹   ENSP00000445440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,080,283 - 56,092,996 (-)Ensembl
RefSeq Acc Id: ENST00000467726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,086,875 - 56,092,977 (-)Ensembl
RefSeq Acc Id: ENST00000471665
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,083,151 - 56,087,693 (-)Ensembl
RefSeq Acc Id: ENST00000489604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,084,161 - 56,092,951 (-)Ensembl
RefSeq Acc Id: ENST00000492124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,088,554 - 56,092,996 (-)Ensembl
RefSeq Acc Id: ENST00000537360   ⟹   ENSP00000441528
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl756,080,283 - 56,092,996 (-)Ensembl
RefSeq Acc Id: NM_001258459   ⟹   NP_001245388
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
GRCh37756,147,616 - 56,160,780 (-)NCBI
HuRef755,961,419 - 55,974,912 (-)NCBI
CHM1_1756,150,991 - 56,163,725 (-)NCBI
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
CRA_TCAGchr7v2756,152,223 - 56,164,936 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001258460   ⟹   NP_001245389
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
HuRef755,961,419 - 55,974,912 (-)NCBI
CHM1_1756,150,991 - 56,163,725 (-)NCBI
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
Sequence:
RefSeq Acc Id: NM_006213   ⟹   NP_006204
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
GRCh37756,147,616 - 56,160,780 (-)NCBI
Build 36756,116,169 - 56,128,183 (-)NCBI Archive
HuRef755,961,419 - 55,974,912 (-)NCBI
CHM1_1756,150,991 - 56,163,725 (-)NCBI
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
CRA_TCAGchr7v2756,152,223 - 56,164,936 (-)NCBI
Sequence:
RefSeq Acc Id: NR_047689
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
GRCh37756,147,616 - 56,160,780 (-)NCBI
HuRef755,961,419 - 55,974,912 (-)NCBI
CHM1_1756,150,991 - 56,163,725 (-)NCBI
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
CRA_TCAGchr7v2756,152,223 - 56,164,936 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005271772   ⟹   XP_005271829
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
GRCh37756,147,616 - 56,160,780 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012324   ⟹   XP_016867813
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012326   ⟹   XP_016867815
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,092,952 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012327   ⟹   XP_016867816
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,080,295 - 56,086,419 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054358407   ⟹   XP_054214382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
RefSeq Acc Id: XM_054358408   ⟹   XP_054214383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
RefSeq Acc Id: XM_054358409   ⟹   XP_054214384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0756,240,116 - 56,252,768 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001245388 (Get FASTA)   NCBI Sequence Viewer  
  NP_001245389 (Get FASTA)   NCBI Sequence Viewer  
  NP_006204 (Get FASTA)   NCBI Sequence Viewer  
  XP_005271829 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867813 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867815 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867816 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214382 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214383 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214384 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH51327 (Get FASTA)   NCBI Sequence Viewer  
  AAH69655 (Get FASTA)   NCBI Sequence Viewer  
  AAH69679 (Get FASTA)   NCBI Sequence Viewer  
  AAH69738 (Get FASTA)   NCBI Sequence Viewer  
  AAH69754 (Get FASTA)   NCBI Sequence Viewer  
  AAH74753 (Get FASTA)   NCBI Sequence Viewer  
  AAL36972 (Get FASTA)   NCBI Sequence Viewer  
  AAS07453 (Get FASTA)   NCBI Sequence Viewer  
  BAG35704 (Get FASTA)   NCBI Sequence Viewer  
  BAH11466 (Get FASTA)   NCBI Sequence Viewer  
  BAH13029 (Get FASTA)   NCBI Sequence Viewer  
  BAH13378 (Get FASTA)   NCBI Sequence Viewer  
  CAA56681 (Get FASTA)   NCBI Sequence Viewer  
  EAX07987 (Get FASTA)   NCBI Sequence Viewer  
  EAX07989 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000297373
  ENSP00000297373.2
  ENSP00000378817.2
  ENSP00000389721.1
  ENSP00000397193.1
  ENSP00000445440
  ENSP00000445440.1
GenBank Protein Q16816 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_006204   ⟸   NM_006213
- Peptide Label: isoform 2
- UniProtKB: F5H2S1 (UniProtKB/Swiss-Prot),   B7Z1D0 (UniProtKB/Swiss-Prot),   Q75LP5 (UniProtKB/Swiss-Prot),   Q16816 (UniProtKB/Swiss-Prot),   B2R757 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001245389   ⟸   NM_001258460
- Peptide Label: isoform 3
- UniProtKB: B7Z6U2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001245388   ⟸   NM_001258459
- Peptide Label: isoform 1
- UniProtKB: B2R757 (UniProtKB/TrEMBL),   Q6NSZ4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005271829   ⟸   XM_005271772
- Peptide Label: isoform X4
- UniProtKB: B7Z6U2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867815   ⟸   XM_017012326
- Peptide Label: isoform X2
- UniProtKB: B7Z6U2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867813   ⟸   XM_017012324
- Peptide Label: isoform X1
- UniProtKB: B2R757 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867816   ⟸   XM_017012327
- Peptide Label: isoform X3
- UniProtKB: B7Z5U3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000445440   ⟸   ENST00000452681
RefSeq Acc Id: ENSP00000297373   ⟸   ENST00000297373
RefSeq Acc Id: ENSP00000441528   ⟸   ENST00000537360
RefSeq Acc Id: ENSP00000397193   ⟸   ENST00000432123
RefSeq Acc Id: ENSP00000389721   ⟸   ENST00000446428
RefSeq Acc Id: ENSP00000378817   ⟸   ENST00000395428
RefSeq Acc Id: XP_054214384   ⟸   XM_054358409
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054214383   ⟸   XM_054358408
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054214382   ⟸   XM_054358407
- Peptide Label: isoform X1
Protein Domains
Protein kinase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q16816-F1-model_v2 AlphaFold Q16816 1-387 view protein structure

Promoters
RGD ID:7210647
Promoter ID:EPDNEW_H11069
Type:initiation region
Name:PHKG1_1
Description:phosphorylase kinase catalytic subunit gamma 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11070  EPDNEW_H11071  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38756,092,952 - 56,093,012EPDNEW
RGD ID:6806004
Promoter ID:HG_KWN:57535
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:UC003TRY.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36756,118,464 - 56,118,964 (-)MPROMDB
RGD ID:6806002
Promoter ID:HG_KWN:57538
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:ENST00000297373,   ENST00000395428,   OTTHUMT00000343390,   OTTHUMT00000343391,   OTTHUMT00000343392,   OTTHUMT00000343394,   OTTHUMT00000343395,   OTTHUMT00000343397
Position:
Human AssemblyChrPosition (strand)Source
Build 36756,128,084 - 56,128,584 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8930 AgrOrtholog
COSMIC PHKG1 COSMIC
Ensembl Genes ENSG00000164776 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000297373 ENTREZGENE
  ENST00000297373.7 UniProtKB/Swiss-Prot
  ENST00000395428.3 UniProtKB/TrEMBL
  ENST00000432123.5 UniProtKB/TrEMBL
  ENST00000446428.5 UniProtKB/TrEMBL
  ENST00000452681 ENTREZGENE
  ENST00000452681.6 UniProtKB/Swiss-Prot
Gene3D-CATH Transferase(Phosphotransferase) domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000164776 GTEx
HGNC ID HGNC:8930 ENTREZGENE
Human Proteome Map PHKG1 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Phosph_kin_gamma UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:5260 UniProtKB/Swiss-Prot
NCBI Gene 5260 ENTREZGENE
OMIM 172470 OMIM
PANTHER PHOSPHORYLASE B KINASE GAMMA CATALYTIC CHAIN, SKELETAL MUSCLE/HEART ISOFORM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SERINE/THREONINE-PROTEIN KINASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Haspin_kinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33271 PharmGKB
PRINTS PHOSPHBKNASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R757 ENTREZGENE, UniProtKB/TrEMBL
  B7Z1D0 ENTREZGENE
  B7Z5U3 ENTREZGENE, UniProtKB/TrEMBL
  B7Z6U2 ENTREZGENE, UniProtKB/TrEMBL
  C9J2Q6_HUMAN UniProtKB/TrEMBL
  C9JME8_HUMAN UniProtKB/TrEMBL
  F5H2S1 ENTREZGENE
  F8WD25_HUMAN UniProtKB/TrEMBL
  PHKG1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q6NSZ4 ENTREZGENE, UniProtKB/TrEMBL
  Q75LP5 ENTREZGENE
UniProt Secondary B7Z1D0 UniProtKB/Swiss-Prot
  F5H2S1 UniProtKB/Swiss-Prot
  Q75LP5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-05-19 PHKG1  phosphorylase kinase catalytic subunit gamma 1    phosphorylase kinase gamma subunit 1  Symbol and/or name change 5135510 APPROVED
2016-03-28 PHKG1  phosphorylase kinase gamma subunit 1    phosphorylase kinase, gamma 1 (muscle)  Symbol and/or name change 5135510 APPROVED