Human Gene GLCCI1 (ENST00000223145.10_5) from GENCODE V47lift37
  Description: glucocorticoid induced 1 (from RefSeq NM_138426.4)
Gencode Transcript: ENST00000223145.10_5
Gencode Gene: ENSG00000106415.13_9
Transcript (Including UTRs)
   Position: hg19 chr7:8,008,427-8,128,710 Size: 120,284 Total Exon Count: 8 Strand: +
Coding Region
   Position: hg19 chr7:8,008,982-8,126,168 Size: 117,187 Coding Exon Count: 8 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionRNA StructureProtein StructureOther SpeciesmRNA Descriptions
Other NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr7:8,008,427-8,128,710)mRNA (may differ from genome)Protein (547 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
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HGNCMalacardsMGIOMIMPubMedUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: GLCI1_HUMAN
DESCRIPTION: RecName: Full=Glucocorticoid-induced transcript 1 protein;
TISSUE SPECIFICITY: Predominantly expressed in lung, spleen, thymus and testis and, at lower levels, in brain, bone marrow, peripheral leukocytes, skin and trachea.
POLYMORPHISM: Polymorphisms dbSNP:rs37972 and dbSNP:rs37973, located in GLCCI1 promoter region, are associated with a decreased response to glucorticoid treatment [MIM:614400] in asthma patients (PubMed:21991891), as well as in chronic obstructive pulmonary disease patients (PubMed:22187997). The mean increase in forced expiratory volume in 1 second in glucorticoid treated subjects who are homozygous for the mutant (G) rs37973 allele is only about one-third of that seen in similarly treated subjects who are homozygous for the wild-type allele (A) (PubMed:21991891). These polymorphisms affect GLCCI1 transcription level.

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: GLCCI1
Diseases sorted by gene-association score: glucocorticoid therapy, response to* (575), ichthyosis, congenital, autosomal recessive 11 (7), asthma (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene
  • D013749 Tetrachlorodibenzodioxin
  • D000082 Acetaminophen
  • C006780 bisphenol A
  • C006253 pirinixic acid
  • C111118 2',3,3',4',5-pentachloro-4-hydroxybiphenyl
  • C548651 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester
  • C532162 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine
  • C009505 4,4'-diaminodiphenylmethane
  • D015123 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide
  • D000111 Acetylcysteine
          more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 22.91 RPKM in Cells - EBV-transformed lymphocytes
Total median expression: 225.06 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -308.80555-0.556 Picture PostScript Text
3' UTR -604.702542-0.238 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR026639 - Glcci1
IPR026642 - Glcci1/FAM117

Pfam Domains:
PF15388 - Protein Family FAM117

ModBase Predicted Comparative 3D Structure on Q86VQ1
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
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-  Descriptions from all associated GenBank mRNAs
  BC050291 - Homo sapiens glucocorticoid induced transcript 1, mRNA (cDNA clone MGC:43752 IMAGE:5272003), complete cds.
AL833694 - Homo sapiens mRNA; cDNA DKFZp667C029 (from clone DKFZp667C029).
AK126731 - Homo sapiens cDNA FLJ44777 fis, clone BRACE3035168, moderately similar to Mus musculus glucocorticoid induced transcript 1 (Glcci1), transcript variant 2, mRNA.
AK055741 - Homo sapiens cDNA FLJ31179 fis, clone KIDNE2000245.
BC011254 - Homo sapiens, clone IMAGE:3463399, mRNA, partial cds.
AL832860 - Homo sapiens mRNA; cDNA DKFZp667I242 (from clone DKFZp667I242).
JD565472 - Sequence 546496 from Patent EP1572962.
U00959 - Human clone KDB2.12 (CAC)n/(GTG)n repeat-containing mRNA.
JD273967 - Sequence 254991 from Patent EP1572962.
JD021278 - Sequence 2302 from Patent EP1572962.
JD250291 - Sequence 231315 from Patent EP1572962.
JD034767 - Sequence 15791 from Patent EP1572962.
JD172531 - Sequence 153555 from Patent EP1572962.
JD167096 - Sequence 148120 from Patent EP1572962.
JD260046 - Sequence 241070 from Patent EP1572962.
JD475142 - Sequence 456166 from Patent EP1572962.
JD226057 - Sequence 207081 from Patent EP1572962.
MP015472 - Sequence 675 from Patent WO2019016252.
AK093655 - Homo sapiens cDNA FLJ36336 fis, clone THYMU2006303.
JD091184 - Sequence 72208 from Patent EP1572962.
JD082951 - Sequence 63975 from Patent EP1572962.
JD339464 - Sequence 320488 from Patent EP1572962.
JD241223 - Sequence 222247 from Patent EP1572962.
JD548569 - Sequence 529593 from Patent EP1572962.
JD237104 - Sequence 218128 from Patent EP1572962.
JD177279 - Sequence 158303 from Patent EP1572962.
JD036987 - Sequence 18011 from Patent EP1572962.
JD051859 - Sequence 32883 from Patent EP1572962.
JD307670 - Sequence 288694 from Patent EP1572962.
JD490511 - Sequence 471535 from Patent EP1572962.
JD245432 - Sequence 226456 from Patent EP1572962.
JD243016 - Sequence 224040 from Patent EP1572962.
JD141162 - Sequence 122186 from Patent EP1572962.
JD112574 - Sequence 93598 from Patent EP1572962.
JD411349 - Sequence 392373 from Patent EP1572962.
JD285243 - Sequence 266267 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: A4D103, ENST00000223145.1, ENST00000223145.2, ENST00000223145.3, ENST00000223145.4, ENST00000223145.5, ENST00000223145.6, ENST00000223145.7, ENST00000223145.8, ENST00000223145.9, GLCI1_HUMAN, NM_138426, Q86VQ1, Q96FD0, uc317dgt.1, uc317dgt.2
UCSC ID: ENST00000223145.10_5
RefSeq Accession: NM_138426.4
Protein: Q86VQ1 (aka GLCI1_HUMAN)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.