THG1L (tRNA-histidine guanylyltransferase 1 like) - Rat Genome Database

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Gene: THG1L (tRNA-histidine guanylyltransferase 1 like) Homo sapiens
Analyze
Symbol: THG1L
Name: tRNA-histidine guanylyltransferase 1 like
RGD ID: 1603030
HGNC Page HGNC
Description: Exhibits several functions, including guanyl-nucleotide exchange factor activity; magnesium ion binding activity; and purine ribonucleoside triphosphate binding activity. Involved in several processes, including protein homotetramerization; stress-induced mitochondrial fusion; and tRNA processing. Localizes to mitochondrion and transferase complex. Implicated in autosomal recessive cerebellar ataxia.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: FLJ11601; FLJ20546; hTHG1; ICF45; IHG-1; IHG1; induced by high glucose-1; induced in high glucose-1; interphase cytoplasmic foci protein 45; probable tRNA(His) guanylyltransferase; SCAR28; THG1; tRNA-histidine guanylyltransferase 1-like
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl5157,731,420 - 157,741,449 (+)EnsemblGRCh38hg38GRCh38
GRCh385157,731,420 - 157,741,449 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh375157,158,428 - 157,168,457 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365157,090,901 - 157,099,350 (+)NCBINCBI36hg18NCBI36
Celera5153,184,922 - 153,193,373 (+)NCBI
Cytogenetic Map5q33.3NCBI
HuRef5152,246,932 - 152,255,383 (+)NCBIHuRef
CHM1_15156,591,115 - 156,601,161 (+)NCBICHM1_1
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

References

References - curated
1. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:11230166   PMID:11256614   PMID:12477932   PMID:14702039   PMID:15459185   PMID:16189514   PMID:16344560   PMID:18508967   PMID:20877624   PMID:21044950   PMID:21059936  
PMID:21078997   PMID:21516116   PMID:21784897   PMID:21873635   PMID:22136300   PMID:22863883   PMID:22939629   PMID:23314748   PMID:23844012   PMID:25008184   PMID:25416956   PMID:26186194  
PMID:27107014   PMID:27307223   PMID:27499296   PMID:28514442   PMID:28700943   PMID:29568061   PMID:32296183   PMID:32877691  


Genomics

Comparative Map Data
THG1L
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl5157,731,420 - 157,741,449 (+)EnsemblGRCh38hg38GRCh38
GRCh385157,731,420 - 157,741,449 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh375157,158,428 - 157,168,457 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365157,090,901 - 157,099,350 (+)NCBINCBI36hg18NCBI36
Celera5153,184,922 - 153,193,373 (+)NCBI
Cytogenetic Map5q33.3NCBI
HuRef5152,246,932 - 152,255,383 (+)NCBIHuRef
CHM1_15156,591,115 - 156,601,161 (+)NCBICHM1_1
Thg1l
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391145,836,132 - 45,846,330 (-)NCBIGRCm39mm39
GRCm39 Ensembl1145,837,670 - 45,846,321 (-)Ensembl
GRCm381145,945,305 - 45,955,503 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1145,946,843 - 45,955,494 (-)EnsemblGRCm38mm10GRCm38
MGSCv371145,761,656 - 45,768,996 (-)NCBIGRCm37mm9NCBIm37
MGSCv361145,790,266 - 45,798,926 (-)NCBImm8
Celera1150,536,819 - 50,544,157 (-)NCBICelera
Cytogenetic Map11B1.1NCBI
Thg1l
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21030,387,929 - 30,396,579 (-)NCBI
Rnor_6.0 Ensembl1031,043,688 - 31,052,102 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01031,043,647 - 31,052,092 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01030,866,222 - 30,873,429 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41031,087,575 - 31,094,986 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11031,088,625 - 31,096,035 (-)NCBI
Celera1029,843,158 - 29,850,569 (-)NCBICelera
Cytogenetic Map10q21NCBI
Thg1l
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540811,857,380 - 11,866,270 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540811,857,380 - 11,863,786 (+)NCBIChiLan1.0ChiLan1.0
THG1L
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.15159,737,327 - 159,747,405 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5159,737,327 - 159,749,242 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v05153,116,528 - 153,127,166 (+)NCBIMhudiblu_PPA_v0panPan3
THG1L
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1452,548,481 - 52,587,582 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl452,549,741 - 52,561,754 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha452,439,674 - 52,478,767 (-)NCBI
ROS_Cfam_1.0452,983,177 - 53,022,284 (-)NCBI
UMICH_Zoey_3.1452,810,671 - 52,849,772 (-)NCBI
UNSW_CanFamBas_1.0452,916,953 - 52,956,106 (-)NCBI
UU_Cfam_GSD_1.0453,434,716 - 53,473,821 (-)NCBI
Thg1l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213107,013,000 - 107,019,071 (-)NCBI
SpeTri2.0NW_0049365155,462,344 - 5,468,475 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
THG1L
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1665,602,641 - 65,610,592 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11665,602,637 - 65,610,619 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21671,454,638 - 71,462,777 (-)NCBISscrofa10.2Sscrofa10.2susScr3
THG1L
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12360,140,439 - 60,148,893 (+)NCBI
ChlSab1.1 Ensembl2360,140,536 - 60,150,461 (+)Ensembl
Thg1l
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473331,732,247 - 31,739,150 (-)NCBI

Position Markers
RH91252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375157,157,844 - 157,157,986UniSTSGRCh37
Build 365157,090,422 - 157,090,564RGDNCBI36
Celera5153,184,443 - 153,184,585RGD
Cytogenetic Map5q33.3UniSTS
HuRef5152,246,455 - 152,246,597UniSTS
GeneMap99-GB4 RH Map5591.45UniSTS
SHGC-58349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375157,166,516 - 157,166,699UniSTSGRCh37
Build 365157,099,094 - 157,099,277RGDNCBI36
Celera5153,193,117 - 153,193,300RGD
Cytogenetic Map5q33.3UniSTS
HuRef5152,255,127 - 152,255,310UniSTS
TNG Radiation Hybrid Map573147.0UniSTS
SHGC-57583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375157,166,550 - 157,166,699UniSTSGRCh37
Build 365157,099,128 - 157,099,277RGDNCBI36
Celera5153,193,151 - 153,193,300RGD
Cytogenetic Map5q33.3UniSTS
HuRef5152,255,161 - 152,255,310UniSTS
TNG Radiation Hybrid Map573142.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1423
Count of miRNA genes:707
Interacting mature miRNAs:820
Transcripts:ENST00000231198, ENST00000521655, ENST00000523575
Prediction methods:Microtar, 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.


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 1258 277 530 61 776 64 903 512 292 192 1046 696 11 179 425 3
Low 1181 2669 1196 563 1143 401 3454 1672 3428 227 414 917 164 1 1025 2363 3 2
Below cutoff 45 32 13 14

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001317824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001317825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001317826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_017872 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC026407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK021663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY463216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC023521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA426270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR533503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA874954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY050784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000231198   ⟹   ENSP00000231198
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5157,731,420 - 157,741,449 (+)Ensembl
RefSeq Acc Id: ENST00000521655   ⟹   ENSP00000428387
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5157,731,420 - 157,739,578 (+)Ensembl
RefSeq Acc Id: ENST00000523575   ⟹   ENSP00000431090
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5157,737,910 - 157,739,698 (+)Ensembl
RefSeq Acc Id: NM_001317824   ⟹   NP_001304753
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385157,731,420 - 157,741,449 (+)NCBI
CHM1_15156,591,115 - 156,601,161 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001317825   ⟹   NP_001304754
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385157,731,420 - 157,741,449 (+)NCBI
CHM1_15156,591,115 - 156,601,161 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001317826   ⟹   NP_001304755
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385157,731,799 - 157,741,449 (+)NCBI
CHM1_15156,591,539 - 156,601,161 (+)NCBI
Sequence:
RefSeq Acc Id: NM_017872   ⟹   NP_060342
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385157,731,420 - 157,741,449 (+)NCBI
GRCh375157,158,323 - 157,166,982 (+)NCBI
Build 365157,090,901 - 157,099,350 (+)NCBI Archive
Celera5153,184,922 - 153,193,373 (+)RGD
HuRef5152,246,932 - 152,255,383 (+)ENTREZGENE
CHM1_15156,591,115 - 156,601,161 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009603   ⟹   XP_016865092
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385157,732,438 - 157,741,448 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_060342   ⟸   NM_017872
- Peptide Label: isoform 1
- UniProtKB: Q9NWX6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001304754   ⟸   NM_001317825
- Peptide Label: isoform 3
- UniProtKB: Q9NWX6 (UniProtKB/Swiss-Prot),   Q9H8R6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001304753   ⟸   NM_001317824
- Peptide Label: isoform 2
- UniProtKB: Q9NWX6 (UniProtKB/Swiss-Prot),   B4E366 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001304755   ⟸   NM_001317826
- Peptide Label: isoform 4
- UniProtKB: Q9NWX6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016865092   ⟸   XM_017009603
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000231198   ⟸   ENST00000231198
RefSeq Acc Id: ENSP00000428387   ⟸   ENST00000521655
RefSeq Acc Id: ENSP00000431090   ⟸   ENST00000523575
Protein Domains
Thg1   Thg1C

Promoters
RGD ID:6871418
Promoter ID:EPDNEW_H8874
Type:initiation region
Name:THG1L_1
Description:tRNA-histidine guanylyltransferase 1 like
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
GRCh385157,731,425 - 157,731,485EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3 copy number gain See cases [RCV000051863] Chr5:149714592..181272151 [GRCh38]
Chr5:149094155..180699152 [GRCh37]
Chr5:149074348..180631758 [NCBI36]
Chr5:5q32-35.3
pathogenic
GRCh38/hg38 5q33.1-34(chr5:152761187-167248053)x1 copy number loss See cases [RCV000052144] Chr5:152761187..167248053 [GRCh38]
Chr5:152140747..166675058 [GRCh37]
Chr5:152120940..166607636 [NCBI36]
Chr5:5q33.1-34
pathogenic
GRCh38/hg38 5q33.1-34(chr5:153195314-164014005)x1 copy number loss See cases [RCV000052145] Chr5:153195314..164014005 [GRCh38]
Chr5:152574874..163441011 [GRCh37]
Chr5:152555067..163373589 [NCBI36]
Chr5:5q33.1-34
pathogenic
GRCh38/hg38 5q33.3-35.3(chr5:156825512-181269805)x3 copy number gain See cases [RCV000133847] Chr5:156825512..181269805 [GRCh38]
Chr5:156252523..180696806 [GRCh37]
Chr5:156185101..180629412 [NCBI36]
Chr5:5q33.3-35.3
pathogenic
GRCh38/hg38 5q33.1-34(chr5:152443869-166104392)x1 copy number loss See cases [RCV000138282] Chr5:152443869..166104392 [GRCh38]
Chr5:151823430..165531397 [GRCh37]
Chr5:151803623..165463975 [NCBI36]
Chr5:5q33.1-34
pathogenic
GRCh37/hg19 5q33.2-35.1(chr5:154886174-169757448)x1 copy number loss See cases [RCV000240059] Chr5:154886174..169757448 [GRCh37]
Chr5:5q33.2-35.1
pathogenic
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
NM_017872.5(THG1L):c.164T>C (p.Val55Ala) single nucleotide variant Spinocerebellar ataxia, autosomal recessive 28 [RCV001009629]|not provided [RCV000509418] Chr5:157731604 [GRCh38]
Chr5:157158612 [GRCh37]
Chr5:5q33.3
pathogenic|not provided
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_017872.5(THG1L):c.137C>A (p.Thr46Asn) single nucleotide variant Spinocerebellar ataxia, autosomal recessive 28 [RCV001264830]|not provided [RCV000660503] Chr5:157731577 [GRCh38]
Chr5:157158585 [GRCh37]
Chr5:5q33.3
uncertain significance
NM_017872.5(THG1L):c.313G>A (p.Asp105Asn) single nucleotide variant not provided [RCV000660504] Chr5:157732989 [GRCh38]
Chr5:157159997 [GRCh37]
Chr5:5q33.3
uncertain significance
GRCh37/hg19 5q33.3(chr5:156911673-157225044)x3 copy number gain not provided [RCV000682603] Chr5:156911673..157225044 [GRCh37]
Chr5:5q33.3
uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q33.2-35.3(chr5:155344802-180693344)x3 copy number gain not provided [RCV000745284] Chr5:155344802..180693344 [GRCh37]
Chr5:5q33.2-35.3
pathogenic
GRCh37/hg19 5q33.3-35.1(chr5:156347980-169959880)x1 copy number loss not provided [RCV001005746] Chr5:156347980..169959880 [GRCh37]
Chr5:5q33.3-35.1
pathogenic
GRCh37/hg19 5q33.3-35.1(chr5:156597181-171166353)x3 copy number gain not provided [RCV000845588] Chr5:156597181..171166353 [GRCh37]
Chr5:5q33.3-35.1
pathogenic
NM_017872.5(THG1L):c.881T>C (p.Leu294Pro) single nucleotide variant not provided [RCV001009630] Chr5:157739466 [GRCh38]
Chr5:157166474 [GRCh37]
Chr5:5q33.3
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26053 AgrOrtholog
COSMIC THG1L COSMIC
Ensembl Genes ENSG00000113272 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000231198 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000428387 UniProtKB/TrEMBL
  ENSP00000431090 UniProtKB/TrEMBL
Ensembl Transcript ENST00000231198 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000521655 UniProtKB/TrEMBL
  ENST00000523575 UniProtKB/TrEMBL
Gene3D-CATH 3.30.70.3000 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000113272 GTEx
HGNC ID HGNC:26053 ENTREZGENE
Human Proteome Map THG1L Human Proteome Map
InterPro Thg1_C_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  tRNAHis_GuaTrfase_cat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  tRNAHis_GuaTrfase_Thg1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  tRNAHis_GuaTrfase_Thg1_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:54974 UniProtKB/Swiss-Prot
NCBI Gene 54974 ENTREZGENE
OMIM 618800 OMIM
  618802 OMIM
PANTHER PTHR12729 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Thg1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thg1C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162405691 PharmGKB
PIRSF tRNAHis_guanylyltransferase UniProtKB/Swiss-Prot
UniProt B4E366 ENTREZGENE, UniProtKB/TrEMBL
  E5RIQ8_HUMAN UniProtKB/TrEMBL
  H0YC78_HUMAN UniProtKB/TrEMBL
  Q9H8R6 ENTREZGENE, UniProtKB/TrEMBL
  Q9NWX6 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary D3DQJ5 UniProtKB/Swiss-Prot
  Q53G12 UniProtKB/Swiss-Prot
  Q7L5R3 UniProtKB/Swiss-Prot
  Q9H0S2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-02 THG1L  tRNA-histidine guanylyltransferase 1 like    tRNA-histidine guanylyltransferase 1-like  Symbol and/or name change 5135510 APPROVED
2015-10-06 THG1L  tRNA-histidine guanylyltransferase 1-like    tRNA-histidine guanylyltransferase 1-like (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED