PTAR1 (protein prenyltransferase alpha subunit repeat containing 1) - Rat Genome Database

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Gene: PTAR1 (protein prenyltransferase alpha subunit repeat containing 1) Homo sapiens
Analyze
Symbol: PTAR1
Name: protein prenyltransferase alpha subunit repeat containing 1
RGD ID: 1313649
HGNC Page HGNC:30449
Description: Predicted to enable protein prenyltransferase activity. Predicted to be active in cytoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 4930428J16Rik; FLJ45604; protein prenyltransferase alpha subunit repeat-containing protein 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38969,709,525 - 69,760,011 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl969,709,522 - 69,760,011 (-)EnsemblGRCh38hg38GRCh38
GRCh37972,324,441 - 72,374,927 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36971,514,258 - 71,564,696 (-)NCBINCBI36Build 36hg18NCBI36
Celera942,914,816 - 42,965,239 (-)NCBICelera
Cytogenetic Map9q21.12NCBI
HuRef942,163,635 - 42,214,476 (-)NCBIHuRef
CHM1_1972,470,914 - 72,521,340 (-)NCBICHM1_1
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IBA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:16341674   PMID:21873635   PMID:26186194   PMID:26472760   PMID:26496610   PMID:26638075   PMID:28514442   PMID:30021884   PMID:30194290   PMID:31209342   PMID:32128853   PMID:32694731  
PMID:32877691   PMID:33961781   PMID:34079125   PMID:35256949   PMID:35271311   PMID:35831314   PMID:36215168   PMID:36724073  


Genomics

Comparative Map Data
PTAR1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38969,709,525 - 69,760,011 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl969,709,522 - 69,760,011 (-)EnsemblGRCh38hg38GRCh38
GRCh37972,324,441 - 72,374,927 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36971,514,258 - 71,564,696 (-)NCBINCBI36Build 36hg18NCBI36
Celera942,914,816 - 42,965,239 (-)NCBICelera
Cytogenetic Map9q21.12NCBI
HuRef942,163,635 - 42,214,476 (-)NCBIHuRef
CHM1_1972,470,914 - 72,521,340 (-)NCBICHM1_1
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBIT2T-CHM13v2.0
Ptar1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391923,664,728 - 23,710,249 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1923,664,793 - 23,709,032 (+)EnsemblGRCm39 Ensembl
GRCm381923,687,361 - 23,732,885 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1923,687,429 - 23,731,668 (+)EnsemblGRCm38mm10GRCm38
MGSCv371923,761,890 - 23,795,619 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361923,754,503 - 23,787,619 (+)NCBIMGSCv36mm8
Celera1924,447,989 - 24,481,773 (+)NCBICelera
Cytogenetic Map19BNCBI
cM Map1918.45NCBI
Ptar1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81230,709,731 - 230,753,380 (+)NCBIGRCr8
mRatBN7.21221,283,306 - 221,326,861 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1221,283,415 - 221,327,073 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1229,717,742 - 229,767,783 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01236,647,804 - 236,697,839 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01229,465,840 - 229,515,871 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01241,501,679 - 241,557,651 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1241,501,679 - 241,557,651 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01248,783,205 - 248,838,996 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41227,024,689 - 227,069,914 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1549,387,260 - 49,387,780 (+)NCBI
Celera1218,495,472 - 218,538,509 (+)NCBICelera
Cytogenetic Map1q51NCBI
Ptar1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554343,309,811 - 3,348,226 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554343,309,819 - 3,356,746 (+)NCBIChiLan1.0ChiLan1.0
PTAR1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21168,914,342 - 68,964,921 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1968,920,281 - 68,972,696 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0955,037,001 - 55,087,537 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1968,471,672 - 68,522,085 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl968,480,499 - 68,522,064 (-)Ensemblpanpan1.1panPan2
PTAR1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1187,661,829 - 87,759,728 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl187,706,760 - 87,752,012 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha188,129,364 - 88,228,101 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0188,209,461 - 88,308,042 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl188,254,903 - 88,304,455 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1187,864,953 - 87,963,471 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0187,571,131 - 87,669,843 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0188,334,593 - 88,433,384 (+)NCBIUU_Cfam_GSD_1.0
Ptar1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947135,191,520 - 135,236,895 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365035,944,098 - 5,990,077 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365035,943,767 - 5,981,427 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PTAR1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1223,032,879 - 223,089,663 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11223,028,530 - 223,089,679 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21249,446,953 - 249,501,816 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PTAR1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11280,765,535 - 80,821,819 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1280,774,417 - 80,821,717 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603869,182,052 - 69,231,387 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ptar1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247363,293,697 - 3,334,014 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247363,293,695 - 3,342,492 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PTAR1
10 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q21.11-21.13(chr9:68454847-76252863)x1 copy number loss See cases [RCV000133632] Chr9:68454847..76252863 [GRCh38]
Chr9:71130848..78867779 [GRCh37]
Chr9:70259583..78057599 [NCBI36]
Chr9:9q21.11-21.13		 pathogenic
GRCh38/hg38 9p24.3-q21.12(chr9:193412-70630731)x3 copy number gain See cases [RCV000136152] Chr9:193412..70630731 [GRCh38]
Chr9:220253..73245647 [GRCh37]
Chr9:210253..72435467 [NCBI36]
Chr9:9p24.3-q21.12		 pathogenic
GRCh38/hg38 9p24.3-q21.13(chr9:193412-74615913)x3 copy number gain See cases [RCV000135954] Chr9:193412..74615913 [GRCh38]
Chr9:204193..77230829 [GRCh37]
Chr9:194193..76420649 [NCBI36]
Chr9:9p24.3-q21.13		 pathogenic
GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 copy number gain See cases [RCV000136788] Chr9:68420430..106579493 [GRCh38]
Chr9:71130848..109341774 [GRCh37]
Chr9:70225166..108381595 [NCBI36]
Chr9:9q21.11-31.2		 pathogenic
GRCh38/hg38 9q21.11-21.12(chr9:68420349-70939579)x1 copy number loss See cases [RCV000137529] Chr9:68420349..70939579 [GRCh38]
Chr9:71130848..73554495 [GRCh37]
Chr9:70225085..72744315 [NCBI36]
Chr9:9q21.11-21.12		 likely pathogenic
GRCh38/hg38 9q21.11-21.32(chr9:68499530-83670227)x1 copy number loss See cases [RCV000137963] Chr9:68499530..83670227 [GRCh38]
Chr9:71130848..86285142 [GRCh37]
Chr9:70304266..85474962 [NCBI36]
Chr9:9q21.11-21.32		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3 copy number gain See cases [RCV000139789] Chr9:69627642..111454304 [GRCh38]
Chr9:72242558..114216584 [GRCh37]
Chr9:71432378..113256405 [NCBI36]
Chr9:9q21.12-31.3		 pathogenic
GRCh38/hg38 9p24.3-q22.1(chr9:203861-88130444)x4 copy number gain See cases [RCV000141904] Chr9:203861..88130444 [GRCh38]
Chr9:203861..90745359 [GRCh37]
Chr9:193861..89935179 [NCBI36]
Chr9:9p24.3-q22.1		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q21.31(chr9:193412-79877816)x3 copy number gain See cases [RCV000143012] Chr9:193412..79877816 [GRCh38]
Chr9:204104..82492731 [GRCh37]
Chr9:194104..81682551 [NCBI36]
Chr9:9p24.3-q21.31		 pathogenic
GRCh38/hg38 9q21.11-21.13(chr9:68624483-72028837)x3 copy number gain See cases [RCV000143753] Chr9:68624483..72028837 [GRCh38]
Chr9:71239399..74643753 [GRCh37]
Chr9:70429219..73833573 [NCBI36]
Chr9:9q21.11-21.13		 likely pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain not specified [RCV003986800] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-21.13(chr9:71079379-75905808)x1 copy number loss See cases [RCV000511817] Chr9:71079379..75905808 [GRCh37]
Chr9:9q21.11-21.13		 likely pathogenic
GRCh37/hg19 9q21.11-21.31(chr9:68734571-83557267)x3 copy number gain See cases [RCV000510725] Chr9:68734571..83557267 [GRCh37]
Chr9:9q21.11-21.31		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3		 likely pathogenic
GRCh37/hg19 9q21.11-22.1(chr9:70966262-90761254)x4 copy number gain See cases [RCV000512280] Chr9:70966262..90761254 [GRCh37]
Chr9:9q21.11-22.1		 pathogenic
GRCh37/hg19 9p24.3-q21.33(chr9:203861-88189913)x3 copy number gain See cases [RCV000512431] Chr9:203861..88189913 [GRCh37]
Chr9:9p24.3-q21.33		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-21.32(chr9:68999534-84656998)x1 copy number loss not provided [RCV000683169] Chr9:68999534..84656998 [GRCh37]
Chr9:9q21.11-21.32		 pathogenic
GRCh37/hg19 9p24.3-q21.12(chr9:203861-72717793)x3 copy number gain not provided [RCV000683176] Chr9:203861..72717793 [GRCh37]
Chr9:9p24.3-q21.12		 pathogenic
GRCh37/hg19 9q21.11-21.31(chr9:68838523-83340723)x1 copy number loss not provided [RCV000748447] Chr9:68838523..83340723 [GRCh37]
Chr9:9q21.11-21.31		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
Single allele complex Glioma [RCV000754871] Chr9:23524426..87359888 [GRCh37]
Chr9:9p21.3-q21.33		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_001099666.2(PTAR1):c.26C>T (p.Ala9Val) single nucleotide variant not specified [RCV004298067] Chr9:69759913 [GRCh38]
Chr9:72374829 [GRCh37]
Chr9:9q21.12		 uncertain significance
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3		 pathogenic
GRCh37/hg19 9q21.11-21.31(chr9:70974661-81829792)x1 copy number loss not provided [RCV000846367] Chr9:70974661..81829792 [GRCh37]
Chr9:9q21.11-21.31		 pathogenic
NC_000009.11:g.12246100_101559378inv inversion Recurrent spontaneous abortion [RCV000999471] Chr9:12246100..101559378 [GRCh37]
Chr9:9p23-q22.33		 likely pathogenic
GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410) copy number gain not specified [RCV002053853] Chr9:71349994..122603410 [GRCh37]
Chr9:9q21.11-33.2		 likely pathogenic
GRCh37/hg19 9p24.3-q21.32(chr9:203861-84155399) copy number gain not specified [RCV002053820] Chr9:203861..84155399 [GRCh37]
Chr9:9p24.3-q21.32		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311) copy number loss Distal tetrasomy 15q [RCV002280776] Chr9:19356861..119513311 [GRCh37]
Chr9:9p22.1-q33.1		 uncertain significance
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 copy number gain See cases [RCV002292402] Chr9:203861..131603223 [GRCh37]
Chr9:9p24.3-q34.11		 pathogenic
GRCh37/hg19 9q21.11-21.13(chr9:70966262-76901382)x3 copy number gain not provided [RCV002475692] Chr9:70966262..76901382 [GRCh37]
Chr9:9q21.11-21.13		 uncertain significance
NM_001099666.2(PTAR1):c.35T>G (p.Val12Gly) single nucleotide variant not specified [RCV004083471] Chr9:69759904 [GRCh38]
Chr9:72374820 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.949C>T (p.Arg317Trp) single nucleotide variant not specified [RCV004211717] Chr9:69718683 [GRCh38]
Chr9:72333599 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.953A>G (p.His318Arg) single nucleotide variant not specified [RCV004143934] Chr9:69718679 [GRCh38]
Chr9:72333595 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.89A>G (p.Asp30Gly) single nucleotide variant not specified [RCV004167513] Chr9:69750948 [GRCh38]
Chr9:72365864 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.754G>A (p.Val252Met) single nucleotide variant not specified [RCV004269089] Chr9:69723519 [GRCh38]
Chr9:72338435 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.1202G>A (p.Ser401Asn) single nucleotide variant not specified [RCV004258353] Chr9:69718349 [GRCh38]
Chr9:72333265 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.877G>A (p.Glu293Lys) single nucleotide variant not specified [RCV004279863] Chr9:69723396 [GRCh38]
Chr9:72338312 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.784C>T (p.Pro262Ser) single nucleotide variant not specified [RCV004272725] Chr9:69723489 [GRCh38]
Chr9:72338405 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.812C>T (p.Pro271Leu) single nucleotide variant not specified [RCV004336184] Chr9:69723461 [GRCh38]
Chr9:72338377 [GRCh37]
Chr9:9q21.12		 likely benign
NM_001099666.2(PTAR1):c.1006A>G (p.Met336Val) single nucleotide variant not specified [RCV004515449] Chr9:69718545 [GRCh38]
Chr9:72333461 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.1003G>A (p.Ala335Thr) single nucleotide variant not specified [RCV004515448] Chr9:69718548 [GRCh38]
Chr9:72333464 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.718C>T (p.Arg240Cys) single nucleotide variant not specified [RCV004515455] Chr9:69723555 [GRCh38]
Chr9:72338471 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.828A>C (p.Glu276Asp) single nucleotide variant not specified [RCV004515456] Chr9:69723445 [GRCh38]
Chr9:72338361 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.11C>T (p.Thr4Ile) single nucleotide variant not specified [RCV004515451] Chr9:69759928 [GRCh38]
Chr9:72374844 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.109T>G (p.Cys37Gly) single nucleotide variant not specified [RCV004515450] Chr9:69750928 [GRCh38]
Chr9:72365844 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.521A>G (p.Gln174Arg) single nucleotide variant not specified [RCV004515453] Chr9:69732260 [GRCh38]
Chr9:72347176 [GRCh37]
Chr9:9q21.12		 uncertain significance
NM_001099666.2(PTAR1):c.667A>G (p.Thr223Ala) single nucleotide variant not specified [RCV004515454] Chr9:69723606 [GRCh38]
Chr9:72338522 [GRCh37]
Chr9:9q21.12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3843
Count of miRNA genes:1248
Interacting mature miRNAs:1606
Transcripts:ENST00000340434, ENST00000377200, ENST00000415701, ENST00000467511, ENST00000472967, ENST00000474925
Prediction methods:Miranda, Rnahybrid, Targetscan
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
D9S15  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37972,341,893 - 72,342,044UniSTSGRCh37
GRCh37972,341,852 - 72,342,051UniSTSGRCh37
Build 36971,531,713 - 71,531,864RGDNCBI36
Celera942,932,267 - 42,932,416RGD
Celera942,932,226 - 42,932,423UniSTS
Cytogenetic Map9q21.12UniSTS
HuRef942,181,086 - 42,181,235UniSTS
HuRef942,181,045 - 42,181,242UniSTS
Marshfield Genetic Map967.93RGD
deCODE Assembly Map966.45UniSTS
Stanford-G3 RH Map91973.0UniSTS
Whitehead-YAC Contig Map9 UniSTS
RH36245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37972,344,527 - 72,344,637UniSTSGRCh37
Build 36971,534,347 - 71,534,457RGDNCBI36
Celera942,934,898 - 42,935,008RGD
Cytogenetic Map9q21.12UniSTS
HuRef942,183,713 - 42,183,823UniSTS
GeneMap99-GB4 RH Map9240.14UniSTS
A004M30  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37972,324,487 - 72,324,629UniSTSGRCh37
Build 36971,514,307 - 71,514,449RGDNCBI36
Celera942,914,865 - 42,915,007RGD
Cytogenetic Map9q21.12UniSTS
HuRef942,163,684 - 42,163,826UniSTS
GeneMap99-GB4 RH Map9238.53UniSTS
PTAR1__6945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37972,332,897 - 72,333,455UniSTSGRCh37
Build 36971,522,717 - 71,523,275RGDNCBI36
Celera942,923,272 - 42,923,830RGD
HuRef942,172,091 - 42,172,649UniSTS
ATC-P10587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37972,338,014 - 72,338,118UniSTSGRCh37
Build 36971,527,834 - 71,527,938RGDNCBI36
Celera942,928,391 - 42,928,492RGD
Cytogenetic Map9q21.12UniSTS
HuRef942,177,210 - 42,177,311UniSTS
Whitehead-YAC Contig Map9 UniSTS
WI-18349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37972,327,206 - 72,327,307UniSTSGRCh37
Build 36971,517,026 - 71,517,127RGDNCBI36
Celera942,917,584 - 42,917,685RGD
Cytogenetic Map9q21.12UniSTS
HuRef942,166,403 - 42,166,504UniSTS
GeneMap99-GB4 RH Map9237.92UniSTS
Whitehead-RH Map9243.2UniSTS
D9S15  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q21.12UniSTS
Marshfield Genetic Map967.93UniSTS
deCODE Assembly Map966.45UniSTS
Stanford-G3 RH Map91973.0UniSTS
Whitehead-YAC Contig Map9 UniSTS


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 1579 1225 825 203 906 106 2804 811 1142 211 901 1390 113 1 807 1612 6 2
Low 860 1742 901 421 1023 359 1553 1384 2592 206 559 223 62 397 1176
Below cutoff 24 22 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001099666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366940 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_159515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_159516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_159517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005251980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423354 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054362926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054362927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054362928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054362929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054362930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AI937926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM785278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000340434   ⟹   ENSP00000344299
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl969,709,525 - 69,760,011 (-)Ensembl
RefSeq Acc Id: ENST00000377200   ⟹   ENSP00000366405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl969,709,522 - 69,759,941 (-)Ensembl
RefSeq Acc Id: ENST00000415701   ⟹   ENSP00000405943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl969,718,021 - 69,723,571 (-)Ensembl
RefSeq Acc Id: ENST00000467511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl969,731,932 - 69,734,258 (-)Ensembl
RefSeq Acc Id: ENST00000472967   ⟹   ENSP00000440164
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl969,757,123 - 69,759,959 (-)Ensembl
RefSeq Acc Id: ENST00000474925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl969,741,516 - 69,759,955 (-)Ensembl
RefSeq Acc Id: NM_001099666   ⟹   NP_001093136
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
GRCh37972,324,438 - 72,374,916 (-)NCBI
Build 36971,514,258 - 71,564,696 (-)NCBI Archive
Celera942,914,816 - 42,965,239 (-)RGD
HuRef942,163,635 - 42,214,476 (-)RGD
CHM1_1972,470,914 - 72,521,340 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001366935   ⟹   NP_001353864
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001366936   ⟹   NP_001353865
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001366937   ⟹   NP_001353866
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001366938   ⟹   NP_001353867
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001366939   ⟹   NP_001353868
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001366940   ⟹   NP_001353869
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NR_159515
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NR_159516
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: NR_159517
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005251980   ⟹   XP_005252037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
GRCh37972,324,438 - 72,374,916 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011518639   ⟹   XP_011516941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047423353   ⟹   XP_047279309
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
RefSeq Acc Id: XM_047423354   ⟹   XP_047279310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,750,829 (-)NCBI
RefSeq Acc Id: XM_047423355   ⟹   XP_047279311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,709,525 - 69,760,011 (-)NCBI
RefSeq Acc Id: XM_054362926   ⟹   XP_054218901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
RefSeq Acc Id: XM_054362927   ⟹   XP_054218902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
RefSeq Acc Id: XM_054362928   ⟹   XP_054218903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0981,876,142 - 81,917,438 (-)NCBI
RefSeq Acc Id: XM_054362929   ⟹   XP_054218904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
RefSeq Acc Id: XM_054362930   ⟹   XP_054218905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0981,876,142 - 81,926,623 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_001093136   ⟸   NM_001099666
- Peptide Label: isoform 1
- UniProtKB: Q5T7V5 (UniProtKB/Swiss-Prot),   Q5T7V6 (UniProtKB/Swiss-Prot),   Q7Z6K3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005252037   ⟸   XM_005251980
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011516941   ⟸   XM_011518639
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001353867   ⟸   NM_001366938
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001353864   ⟸   NM_001366935
- Peptide Label: isoform 2
- UniProtKB: X6R9N0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001353869   ⟸   NM_001366940
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001353868   ⟸   NM_001366939
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001353866   ⟸   NM_001366937
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001353865   ⟸   NM_001366936
- Peptide Label: isoform 3
RefSeq Acc Id: ENSP00000405943   ⟸   ENST00000415701
RefSeq Acc Id: ENSP00000366405   ⟸   ENST00000377200
RefSeq Acc Id: ENSP00000440164   ⟸   ENST00000472967
RefSeq Acc Id: ENSP00000344299   ⟸   ENST00000340434
RefSeq Acc Id: XP_047279311   ⟸   XM_047423355
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047279309   ⟸   XM_047423353
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047279310   ⟸   XM_047423354
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054218905   ⟸   XM_054362930
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054218902   ⟸   XM_054362927
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054218901   ⟸   XM_054362926
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054218904   ⟸   XM_054362929
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054218903   ⟸   XM_054362928
- Peptide Label: isoform X3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7Z6K3-F1-model_v2 AlphaFold Q7Z6K3 1-402 view protein structure

Promoters
RGD ID:7215219
Promoter ID:EPDNEW_H13356
Type:initiation region
Name:PTAR1_1
Description:protein prenyltransferase alpha subunit repeat containing 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38969,759,953 - 69,760,013EPDNEW
RGD ID:6807995
Promoter ID:HG_KWN:63610
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001099666,   OTTHUMT00000052581,   OTTHUMT00000052582,   OTTHUMT00000052584,   OTTHUMT00000052586
Position:
Human AssemblyChrPosition (strand)Source
Build 36971,564,376 - 71,564,877 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30449 AgrOrtholog
COSMIC PTAR1 COSMIC
Ensembl Genes ENSG00000188647 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000340434 ENTREZGENE
  ENST00000340434.5 UniProtKB/Swiss-Prot
  ENST00000377200 ENTREZGENE
  ENST00000377200.9 UniProtKB/TrEMBL
  ENST00000415701.6 UniProtKB/TrEMBL
  ENST00000472967.2 UniProtKB/TrEMBL
Gene3D-CATH Protein prenylyltransferase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000188647 GTEx
HGNC ID HGNC:30449 ENTREZGENE
Human Proteome Map PTAR1 Human Proteome Map
InterPro Prenyl_trans_a UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:375743 UniProtKB/Swiss-Prot
NCBI Gene 375743 ENTREZGENE
PANTHER PROTEIN FARNESYLTRANSFERASE ALPHA SUBUNIT/RAB GERANYLGERANYL TRANSFERASE ALPHA SUBUNIT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN PRENYLTRANSFERASE ALPHA SUBUNIT REPEAT-CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PPTA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134897041 PharmGKB
PROSITE PFTA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Protein prenylyltransferase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt F5GXY1_HUMAN UniProtKB/TrEMBL
  J3KQP8_HUMAN UniProtKB/TrEMBL
  PTAR1_HUMAN UniProtKB/Swiss-Prot
  Q5T7V5 ENTREZGENE
  Q5T7V6 ENTREZGENE
  Q7Z6K3 ENTREZGENE
  X6R9N0 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary Q5T7V5 UniProtKB/Swiss-Prot
  Q5T7V6 UniProtKB/Swiss-Prot