Human Gene RUNX1 (uc002yuk.4) Description and Page Index
  Description: Homo sapiens runt-related transcription factor 1 (RUNX1), transcript variant 1, mRNA.
RefSeq Summary (NM_001754): Core binding factor (CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters. The protein encoded by this gene represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis. Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr21:36,160,098-36,421,641 Size: 261,544 Total Exon Count: 8 Strand: -
Coding Region
   Position: hg19 chr21:36,164,432-36,421,196 Size: 256,765 Coding Exon Count: 8 

Page IndexSequence and LinksGenetic AssociationsMalaCardsCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesmRNA Descriptions
PathwaysOther NamesModel InformationMethods
Data last updated: 2013-06-15

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr21:36,160,098-36,421,641)mRNA (may differ from genome)Protein (480 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
BioGPSCGAPEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCLynxMGIOMIM
PubMedReactomeStanford SOURCETreefamUniProtKBWikipedia

-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): RUNX1
CDC HuGE Published Literature: RUNX1
Positive Disease Associations: asthma , Bilirubin , Esophageal Neoplasms , Leukemia, Myeloid, Acute , myeloblastic leukemias , Phospholipids , Stroke , Vitamin D
Related Studies:
  1. asthma
    Chae, S. C. et al. 2006, Putative association of RUNX1 polymorphisms with IgE levels in a Korean population, Exp Mol Med 2006 38(5) 583-8. [PubMed 17079875]
  2. Bilirubin
    Emelia J Benjamin et al. BMC medical genetics 2007, Genome-wide association with select biomarker traits in the Framingham Heart Study., BMC medical genetics. [PubMed 17903293]
    The Framingham GWAS represents a resource to describe potentially novel genetic influences on systemic biomarker variability. The newly described associations will need to be replicated in other studies.
  3. Esophageal Neoplasms
    Chen Wu et al. Nature genetics 2011, Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations., Nature genetics. [PubMed 21642993]
           more ... click here to view the complete list

-  MalaCards Disease Associations
  MalaCards Gene Search: RUNX1
Diseases sorted by gene-association score: platelet disorder, familial, with associated myeloid malignancy* (1550), familial platelet disorder with propensity to acute myelogenous leukemia* (500), isolated delta-storage pool disease* (350), acute myeloid leukemia with t(8;21)(q22;q22) translocation* (350), leukemia, acute myeloid* (189), leukemia, acute lymphoblastic 3* (101), myeloid leukemia (92), leukemia (51), lymphoblastic leukemia (28), blood platelet disease (22), acute leukemia (22), leukemia, chronic myeloid, somatic* (22), b-cell childhood acute lymphoblastic leukemia (20), acute lymphoblastic leukemia, childhood (20), hematologic cancer (20), childhood leukemia (14), megakaryocytic leukemia (14), chronic myelomonocytic leukemia (14), myelodysplastic syndrome (13), refractory anemia (11), hermansky-pudlak syndrome 9 (10), tetrasomy 21 (10), atypical chronic myeloid leukemia (10), chronic myelocytic leukemia (9), acute lymphocytic leukemia (9), juvenile myelomonocytic leukemia (9), core binding factor acute myeloid leukemia (8), 8p11 myeloproliferative syndrome (8), central nervous system leukemia (7), lymphoid leukemia (7), bone marrow cancer (6), acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) (5), gastric cancer, somatic (5), leukemia, acute lymphoblastic (5), aleukemic leukemia cutis (5), down syndrome (3), autosomal dominant disease (3), leukemia, acute promyelocytic, somatic (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           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: 15.35 RPKM in Minor Salivary Gland
Total median expression: 125.74 RPKM



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

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -131.62445-0.296 Picture PostScript Text
3' UTR -1248.234334-0.288 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
  Pfam Domains:
PF00853 - Runt domain
PF08504 - Runx inhibition domain

SCOP Domains:
49417 - p53-like transcription factors

ModBase Predicted Comparative 3D Structure on Q01196-8
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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 orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
 Gene Details    
 Gene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Descriptions from all associated GenBank mRNAs
  AK123035 - Homo sapiens cDNA FLJ41039 fis, clone KIDNE2017052.
D43968 - Homo sapiens mRNA for AML1b protein, complete cds.
D43969 - Homo sapiens mRNA for AML1c protein, complete cds.
X79549 - H.sapiens AML1 mRNA.
D89788 - Homo sapiens mRNA for AML1, complete cds.
D89789 - Homo sapiens mRNA for AML1, complete cds.
D89790 - Homo sapiens mRNA for AML1, complete cds.
L34598 - Homo sapiens (clone PEBP2aB) aml1 (acute myeloid leukemia 1) oncogene (AML1) mRNA, complete cds.
BC136381 - Homo sapiens runt-related transcription factor 1, mRNA (cDNA clone MGC:167991 IMAGE:9020368), complete cds.
BC144053 - Homo sapiens runt-related transcription factor 1, mRNA (cDNA clone MGC:177590 IMAGE:9052573), complete cds.
BC136380 - Homo sapiens runt-related transcription factor 1, mRNA (cDNA clone MGC:167990 IMAGE:9020367), complete cds.
AK226159 - Homo sapiens mRNA for runt-related transcription factor 1 isoform a variant, clone: sh03053.
U19601 - Homo sapiens AML-1B (AML-1B) mRNA, complete cds.
KJ890835 - Synthetic construct Homo sapiens clone ccsbBroadEn_00229 RUNX1 gene, encodes complete protein.
AB384992 - Synthetic construct DNA, clone: pF1KB4846, Homo sapiens RUNX1 gene for runt-related transcription factor 1, complete cds, without stop codon, in Flexi system.
BC110828 - Homo sapiens runt-related transcription factor 1, mRNA (cDNA clone IMAGE:5585236), partial cds.
S76350 - AML1=AML1 {altrnatively spliced, exons 5,6,d,e and c} [human, mRNA Partial, 320 nt].
S60998 - AML1=acute myeloid leukemia {alternatively spliced} [human, mRNA Partial, 894 nt].
AK310587 - Homo sapiens cDNA, FLJ17629.
AF419247 - Homo sapiens AML1/USP25 fusion protein mRNA, complete cds.
KJ189471 - Homo sapiens isolate Seg111 RUNX1/RUNX1T1 fusion protein (RUNX1/RUNX1T1 fusion) mRNA, complete cds, alternatively spliced.
KJ189464 - Homo sapiens isolate Seg103 RUNX1/RUNX1T1 fusion protein (RUNX1/RUNX1T1 fusion) mRNA, complete cds, alternatively spliced.
KJ189476 - Homo sapiens isolate Seg116 RUNX1/RUNX1T1 fusion protein (RUNX1/RUNX1T1 fusion) mRNA, complete cds, alternatively spliced.
X90979 - H.sapiens mRNA for an acute myeloid leukaemia protein (346bp).
X90977 - H.sapiens mRNA for an acute myeloid leukaemia protein (473bp).
JD373007 - Sequence 354031 from Patent EP1572962.
JD465802 - Sequence 446826 from Patent EP1572962.
JD270439 - Sequence 251463 from Patent EP1572962.
JD255664 - Sequence 236688 from Patent EP1572962.
JD080041 - Sequence 61065 from Patent EP1572962.
JD252248 - Sequence 233272 from Patent EP1572962.
JD160674 - Sequence 141698 from Patent EP1572962.
JD190291 - Sequence 171315 from Patent EP1572962.
JD263722 - Sequence 244746 from Patent EP1572962.
X90976 - H.sapiens mRNA for an acute myeloid leukaemia protein (3917bp).
JD196219 - Sequence 177243 from Patent EP1572962.
JD063968 - Sequence 44992 from Patent EP1572962.
JD304754 - Sequence 285778 from Patent EP1572962.
JD273177 - Sequence 254201 from Patent EP1572962.
JD113800 - Sequence 94824 from Patent EP1572962.
JD546706 - Sequence 527730 from Patent EP1572962.
JD554795 - Sequence 535819 from Patent EP1572962.
JD290095 - Sequence 271119 from Patent EP1572962.
JD298358 - Sequence 279382 from Patent EP1572962.
JD381897 - Sequence 362921 from Patent EP1572962.
JD041521 - Sequence 22545 from Patent EP1572962.
JD510668 - Sequence 491692 from Patent EP1572962.
JD335074 - Sequence 316098 from Patent EP1572962.
JD045836 - Sequence 26860 from Patent EP1572962.
JD436492 - Sequence 417516 from Patent EP1572962.
JD335597 - Sequence 316621 from Patent EP1572962.
JD067664 - Sequence 48688 from Patent EP1572962.
JD309507 - Sequence 290531 from Patent EP1572962.
JD166760 - Sequence 147784 from Patent EP1572962.
JD234859 - Sequence 215883 from Patent EP1572962.
JD144364 - Sequence 125388 from Patent EP1572962.
JD089288 - Sequence 70312 from Patent EP1572962.
JD491755 - Sequence 472779 from Patent EP1572962.
JD216273 - Sequence 197297 from Patent EP1572962.
JD552743 - Sequence 533767 from Patent EP1572962.
JD115335 - Sequence 96359 from Patent EP1572962.
JD121078 - Sequence 102102 from Patent EP1572962.
JD292206 - Sequence 273230 from Patent EP1572962.
JD052540 - Sequence 33564 from Patent EP1572962.
JD366134 - Sequence 347158 from Patent EP1572962.
JD334109 - Sequence 315133 from Patent EP1572962.
JD284464 - Sequence 265488 from Patent EP1572962.
JD432008 - Sequence 413032 from Patent EP1572962.
JD547333 - Sequence 528357 from Patent EP1572962.
JD129051 - Sequence 110075 from Patent EP1572962.
GU070943 - Homo sapiens C20orf112/RUNX1 fusion protein (C20orf112/RUNX1 fusion) mRNA, partial cds.
AF312387 - Homo sapiens clone L2 AML1/AMP19 fusion protein (AML1/AMP19 fusion) mRNA, complete cds.
D10570 - Homo sapiens AML1 mRNA for hypothetical protein, complete cds.
E05037 - cDNA sequence of human AML1,which is useful for a marker of AML.
D43967 - Homo sapiens mRNA for AML1a protein, complete cds.
X90978 - H.sapiens mRNA for an acute myeloid leukaemia protein (1793bp).
GU070939 - Homo sapiens RUNX1/CBFA2T2 fusion protein type 2 (RUNX1/CBFA2T2 fusion) mRNA, partial cds.
GU070941 - Homo sapiens RUNX1/C20orf112 fusion protein type 1 (RUNX1/C20orf112 fusion) mRNA, partial cds.
L21756 - Homo sapiens acute myeloid leukemia associated protein (AML1/EAP) mRNA, complete cds.
KF305770 - Homo sapiens runt-related transcription factor 1/NDC1 transmembrane nucleoporin fusion protein (RUNX1/TMEM48 fusion) gene, complete cds.
S76346 - AML1=AML1 {alternatively spliced, exons 5 and b} [human, mRNA Partial, 284 nt].
S76345 - AML1=AML1 {alternatively spliced, exons 5 and a} [human, mRNA Partial, 265 nt].
AY004251 - Homo sapiens AML1/AMP19 fusion protein (AML1/AMP19 fusion) mRNA, complete cds.
GU070942 - Homo sapiens RUNX1/C20orf112 fusion protein type 2 (RUNX1/C20orf112 fusion) mRNA, partial cds.
MH401090 - Homo sapiens RUNX1-RUNX1T1 fusion protein mRNA, partial cds.
AF312386 - Homo sapiens clone L4 AML1/AMP19 fusion protein (AML1/AMP19 fusion) mRNA, complete cds.
D13979 - Homo sapiens mRNA for AML1-MTG8 fusion protein, complete cds.
E07332 - DNA fragment including the fusion part in AML1(acute myeloleukemia)-MTG8 fusion DNA.
EU364772 - Homo sapiens AML1 translocation breakpoint mRNA sequence.
EU093088 - Homo sapiens RUNX1/ZNF687 fusion mRNA, partial sequence.
AK310646 - Homo sapiens cDNA, FLJ17688.
KF041488 - Homo sapiens RUNX1-SV2B fusion transcript 1 mRNA, partial sequence.
JD304858 - Sequence 285882 from Patent EP1572962.
JD486712 - Sequence 467736 from Patent EP1572962.
JD369005 - Sequence 350029 from Patent EP1572962.
JD294551 - Sequence 275575 from Patent EP1572962.
JD356108 - Sequence 337132 from Patent EP1572962.
JD059168 - Sequence 40192 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa05200 - Pathways in cancer
hsa05220 - Chronic myeloid leukemia
hsa05221 - Acute myeloid leukemia

Reactome (by CSHL, EBI, and GO)

Protein Q01196 (Reactome details) participates in the following event(s):

R-HSA-8865320 CBFB binds RUNX1
R-HSA-8937682 RUNX1 binds SRC
R-HSA-8938867 CCND3,(CCND1,CCND2) binds RUNX1
R-HSA-8938887 PML binds RUNX1
R-HSA-8937767 PTPN11 dephosphorylates RUNX1
R-HSA-8937744 PTPN11 binds p-7Y-RUNX1
R-HSA-8937728 SRC phosphorylates RUNX1
R-HSA-8865482 KMT2A (MLL) binds RUNX1
R-HSA-8865547 RUNX1:CBFB binds FOXP3 gene
R-HSA-8877192 RUNX1 binds FOXP3
R-HSA-8877338 RUNX1 and NFATC2 bind the IL2 gene promoter
R-HSA-8877360 RUNX1 binds the IFNG promoter
R-HSA-8877385 RUNX1 binds intron 1 of IL2RA (CD25) gene
R-HSA-8877404 RUNX1 binds the promoter of the CTLA4 gene
R-HSA-8877485 RUNX1 binds to TNFRSF18 (GITR) gene promoter and intron 1
R-HSA-8878054 HIPK2 phosphorylates RUNX1
R-HSA-8878056 RUNX1:CBFB binds EP300
R-HSA-8931981 RUNX1 binds ESR1
R-HSA-8934688 RUNX1:CBFB binds the LIFR gene promoter
R-HSA-8934742 RUNX1 binds PRMT1
R-HSA-8935732 RUNX1 binds SIN3A,(SIN3B) co-repressor
R-HSA-8935960 RUNX1 binds the TJP1 (ZO-1) gene promoter
R-HSA-8935980 RUNX1 binds the OCLN gene promoter
R-HSA-8936000 RUNX1 binds the CLDN5 (Claudin-5) gene promoter
R-HSA-8937989 RUNX1 binds PRC1 complexes
R-HSA-8938022 RUNX1:CBFB binds the NR4A3 gene promoter
R-HSA-8938053 RUNX1:CBFB binds the SERPINB13 gene promoter
R-HSA-8938150 RUNX1:CBFB binds the PRKCQ gene promoter
R-HSA-8938176 RUNX1:CBFB binds the PF4 gene promoter
R-HSA-8938199 RUNX1:CBFB binds the MYL9 gene promoter
R-HSA-8938217 RUNX1 binds the SWI/SNF complex
R-HSA-8938231 RUNX1:CBFB binds CREBBP
R-HSA-8938328 RUNX1:CBFB binds the NFE2 gene promoter
R-HSA-8938389 RUNX1:CBFB binds the LGALS3 gene promoter
R-HSA-8938913 RUNX1 binds ELF1
R-HSA-8938930 RUNX1 binds ELF2
R-HSA-8938951 RUNX1 binds PAX5 (BSAP)
R-HSA-8939054 RUNX1 binds the PRKCB gene promoter
R-HSA-8939082 RUNX1 binds the CR1 gene promoter
R-HSA-8955748 RUNX1 binds the SOCS3 gene
R-HSA-8955822 RUNX1 binds the SOCS4 gene
R-HSA-8956568 RUNX1 binds the core TAL1 complex
R-HSA-8956639 RUNX1 binds YAP1
R-HSA-8938853 CDK6 binds RUNX1
R-HSA-8934735 PRMT1 arginine-methylates RUNX1
R-HSA-8865491 RUNX1:CBFB:KMT2A binds SPI1 (PU.1) gene
R-HSA-8877348 RUNX1, FOXP3 and NFATC2 bind the IL2 gene promoter
R-HSA-8877369 RUNX1 and FOXP3 bind the IFNG gene
R-HSA-8877391 FOXP3 in complex with RUNX1 binds intron 1 of the IL2RA (CD25) gene
R-HSA-8877414 FOXP3 in complex with RUNX1 binds the CTLA4 gene promoter
R-HSA-8877490 FOXP3 in complex with RUNX1 binds to the TNFRSF18 (GITR) gene intron 1
R-HSA-8877879 RUNX1 and FOXP3 bind the RSPO3 gene promoter
R-HSA-8878050 HIPK2 phosphorylates RUNX1 and EP300
R-HSA-8932021 RUNX1 and ESR1 bind the GPAM gene enhancer
R-HSA-8932037 RUNX1 and ESR1 bind the KCTD6 gene enhancer
R-HSA-8932084 RUNX1 and ESR1 bind the AXIN1 gene
R-HSA-8935730 RUNX1:CBFB, SIN3A(SIN3B), PRMT6 and HDAC1 bind the ITGA2B promoter
R-HSA-8936599 RUNX1:CBFB, SIN3A(SIN3B), PRMT6 and HDAC1 bind the GP1BA promoter
R-HSA-8936989 RUNX1:CBFB, SIN3A(SIN3B), PRMT6 and HDAC1 bind the THBS1 gene promoter
R-HSA-8937118 RUNX1:CBFB, SIN3A(SIN3B), PRMT6 and HDAC1 bind the MIR27A gene promoter
R-HSA-8938228 RUNX1:CBFB:CREBBP binds the CSF2 (GM-CSF) gene promoter
R-HSA-8938938 RUNX1 and ELF1 bind the IL3 gene promoter
R-HSA-8956649 The complex of RUNX1 and YAP1 binds the ITCH gene promoter
R-HSA-8935740 RUNX1 and GATA1 bind the promoter of the ITGA2B gene
R-HSA-8936616 RUNX1 and GATA1 bind the promoter of the GP1BA gene
R-HSA-8936979 RUNX1 and GATA1 bind the promoter of the THBS1 gene
R-HSA-8937037 RUNX1 and GATA1 bind the promoter of the MIR27A gene
R-HSA-8952081 RUNX proteins bind the p14-ARF promoter at the CDKN2A locus
R-NUL-8865513 RUNX1 recruits KMT2A to the Spi1 gene
R-HSA-8865498 KMT2A trimethylates nucleosomes at the SPI1 gene locus producing H3K4Me3 mark
R-HSA-8936584 PRMT6 arginine methylates H3K4me2-Nucleosome at the ITGA2B gene promoter
R-HSA-8936608 PRMT6 arginine methylates H3K4me2-Nucleosome at the GP1BA gene promoter
R-HSA-8937022 PRMT6 arginine methylates H3K4me2-Nucleosome at the THBS1 gene promoter
R-HSA-8937113 PRMT6 arginine methylates H3K4me2-Nucleosome at the MIR27A gene promoter
R-HSA-8938965 RUNX1 and ELF1, ELF2 or PAX5 bind the BLK gene promoter
R-HSA-8956586 RUNX1-containing TAL1 complex binds the MYB gene enhancer
R-NUL-8865525 KTM2A trimethylates nucleosomes at the Spi1 gene locus producing H3K4Me3 mark
R-HSA-8936481 Core MLL complex methylates H3K4Me2-Nucleosome at the ITGA2B gene promoter
R-HSA-8936621 Core MLL complex methylates H3K4Me2-Nucleosome at the GP1BA gene promoter
R-HSA-8937016 Core MLL complex methylates H3K4Me2-Nucleosome at the THBS1 gene promoter
R-HSA-8937050 Core MLL complex methylates H3K4Me2-Nucleosome at the MIR27A gene promoter
R-HSA-8934593 Regulation of RUNX1 Expression and Activity
R-HSA-8939236 RUNX1 regulates transcription of genes involved in differentiation of HSCs
R-HSA-8877330 RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs)
R-HSA-8939243 RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
R-HSA-8931987 RUNX1 regulates estrogen receptor mediated transcription
R-HSA-9018519 Estrogen-dependent gene expression
R-HSA-8939247 RUNX1 regulates transcription of genes involved in interleukin signaling
R-HSA-8936459 RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
R-HSA-8935964 RUNX1 regulates expression of components of tight junctions
R-HSA-8939242 RUNX1 regulates transcription of genes involved in differentiation of keratinocytes
R-HSA-8939246 RUNX1 regulates transcription of genes involved in differentiation of myeloid cells
R-HSA-8939245 RUNX1 regulates transcription of genes involved in BCR signaling
R-HSA-8878171 Transcriptional regulation by RUNX1
R-HSA-8939256 RUNX1 regulates transcription of genes involved in WNT signaling
R-HSA-8951936 RUNX3 regulates p14-ARF
R-HSA-8939211 ESR-mediated signaling
R-HSA-212436 Generic Transcription Pathway
R-HSA-8878159 Transcriptional regulation by RUNX3
R-HSA-9006931 Signaling by Nuclear Receptors
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-162582 Signal Transduction
R-HSA-74160 Gene expression (Transcription)

-  Other Names for This Gene
  Alternate Gene Symbols: AK226159, AML1, CBFA2, NM_001754, NP_001745, Q01196-8
UCSC ID: uc002yuk.4
RefSeq Accession: NM_001754
Protein: Q01196-8, splice isoform of Q01196 CCDS: CCDS13639.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: AK226159.1
exon count: 8CDS single in 3' UTR: no RNA size: 1709
ORF size: 1443CDS single in intron: no Alignment % ID: 99.88
txCdsPredict score: 3039.50frame shift in genome: no % Coverage: 99.30
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: yes # AT/AC introns 0
selenocysteine: no end bleed into intron: 386# strange splices: 0
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.