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The Transcript Info page presents information relevant for one transcript identified by its Genomatix TranscriptID. The data includes general information about the name, the genomic location, and the length of UTRs and coding sequence. It also provides information about the tissues the transcript is expressed in. The detailed data about the cDNA mapping used for the annotation process and the sequences of the transcript and the resulting protein are shown.
The Identification table provides you with the key features of the transcript like e.g. identifiers, length, number of exons, genomic location, and the Genomatix transcript quality. The length of the UTRs and the coding sequence (CDS) are derived from the transcript sequence by in silico methods. Conflicts with the UTR/CDS annotated for the related RefSeq/GenBank sequence are indicated.
| Identification | |
|---|---|
| Organism | Homo sapiens |
| LocusID | GXL_36015 |
| Symbol | SFRS1 |
| Description | splicing factor, arginine/serine-rich 1 (splicing factor 2, alternate splicing factor) |
| Transcript length | 2026 bp |
| Number of exons | 4 |
| Transcript quality | gold (experimentally verified 5' complete transcript) |
| Genomic location | NC_000017 (-) 53435853 - 53439584 |
| 5'UTR | 87 bp |
| CDS | 606 bp (201 aa) |
| 3'UTR | 1333 bp |
For each transcript two different types of tissue association are provided.
The numbers following the tissue names indicate how often the respective tissue was annotated for this transcript.
| Tissues | |
|---|---|
| CAGE tags | ESTs |
| liver(69) adrenal gland(38) bone marrow(31) lung(24) large intestine(23) cerebrum(18) colon(17) embryo(13) cecum(12) brain(10) thymus(10) blood(7) kidney(6) adipose(6) muscle(5) rectum(4) small intestine(4) mammary gland(3) testis(3) frontal lobe(2) parietal lobe(1) spleen(1) cerebellum(1) |
na |
Transcripts in ElDorado are annotated by mapping the sequence of a cDNA from e.g. RefSeq or GenBank to the respective genomic sequence. The cDNA sequences may differ from the genomic sequences either by point mutations or insertions/deletions. Thus the resulting transcript annotated in ElDorado is not necessarily identical to the cDNA sequence used for the mapping. Gaps either in the cDNA or the genomic sequence located in the CDS of the transcript may result in frameshifts and the loss of the coding potential of the transcript. Details about this discrepancies are given in this table. The detailed output of the mapping process can be accessed by the link 'detailed mapping' in the last line of the table.
| cDNA Mapping | |
|---|---|
| The annotation of GXT_22214872 is based on mapping of AK225711. | |
| 5' not aligned | 0 bp |
| 3' not aligned | 16 bp |
| Point mutations | 1 |
| Gaps in cDNA | 0 |
| Gaps in genomic sequence | 0 |
| detailed mapping | |
The Sequences table provides the nucleotide sequence of the transcript and the protein sequence derived from. The exons in the transcript are alternately colored black and blue. Nucleotides in lower case indicate the UTRs. The coding sequence (CDS) is given in uppercase. Nucleotides correlated with a SNP are highlighted in blue. The known alleles are shown on 'mouse over'. The nucleotide sequence can be downloaded for further analysis either to your local disk or to your personal sequence directory on our server.
| Sequences | |
|---|---|
| cDNA sequence | Protein sequence |
1 agacgtggtg ccgctgcggg ctcgctctgc cgtgcgctag gcttggtggg aaggcctgtt 61 ctcgagtccg cgcttttcgt caccgccATG TCGGGAGGTG GTGTGATTCG TGGCCCCGCA 121 GGGAACAACG ATTGCCGCAT CTACGTGGGT AACTTACCTC CAGACATCCG AACCAAGGAC 181 ATTGAGGACG TGTTCTACAA ATACGGCGCT ATCCGCGACA TCGACCTCAA GAATCGCCGC 241 GGGGGACCGC CCTTCGCCTT CGTTGAGTTC GAGGACCCGC GAGACGCGGA AGACGCGGTG 301 TATGGTCGCG ACGGCTATGA TTACGATGGG TACCGTCTGC GGGTGGAGTT TCCTCGAAGC 361 GGCCGTGGAA CAGGCCGAGG CGGCGGCGGG GGTGGAGGTG GCGGAGCTCC CCGAGGTCGC 421 TATGGCCCCC CATCCAGGCG GTCTGAAAAC AGAGTGGTTG TCTCTGGACT GCCTCCAAGT 481 GGAAGTTGGC AGGATTTAAA GGATCACATG CGTGAAGCAG GTGATGTATG TTATGCTGAT 541 GTTTACCGAG ATGGCACTGG TGTCGTGGAG TTTGTACGGA AAGAAGATAT GACCTATGCA 601 GTTCGAAAAC TGGATAACAC TAAGTTTAGA TCTCATGAGG TAGGTTATAC ACGTATTCTT 661 TTCTTTGACC AGAATTGGAT ACAGTGGTCT TAAcagtgga atttcaaggt aaggattcag 721 gcaaggttgt ccaagtaaat tgccagattt ctggttttag ttacattgta ttcattcagc 781 atgtctgaag atagatgaaa gcttagatct ttcaatggaa agttctgtct atccaatagg 841 gagaaactgc ctacatccgg gttaaagttg atgggcccag aagtccaagt tatggaagat 901 ctcgatctcg aagccgtagt cgtagcagaa gccgtagcag aagcaacagc aggagtcgca 961 gttactcccc aaggagaagc agaggatcac cacgctattc tccccgtcat agcagatctc 1021 gctctcgtac ataagatgat tggtgacact ttttgtagaa cccatgttgt atacagtttt 1081 cctttattca gtacaatctt ttcatttttt aattcaaact gttttgttca gaatgggcta 1141 aagtgttgaa ttgcattctt gtaatatccc cttgctccta acatctacat tcccttcgtg 1201 tctttgataa attgtatttt aagtgatgtc atagacagga ttgtttaaat ttagttaact 1261 ccatactctt cagactgtga tattgtgtaa atgtctatct gccctggttt gtgtgaactg 1321 ggatgttggg ggtgtttgtg gttatcttac ctggggaagt tcttatgttt atcttgcttt 1381 tcatgtgtct ttctgtagac atatctgaag agatggatta agaatgcttt ggattaagga 1441 ttgtggagca catttcaatc attttaggat tgtcaaaagg aggattgagg aggatcagat 1501 caataatgga ggcaatggtt tggattggag agggctcact ggatcccaat ccttggagct 1561 ggatcattgg attcaaatca taatgtggat aggataggga ggatgaatta ccaggattca 1621 tggagcggga tcagattacc aggaacatag gagtggattc ctgccccaac caaaccgcat 1681 tcgtgtggat ttttttattc aacttaattg gctattccaa agattttttt tttcctattt 1741 ttgacgattg gagcccttaa gatgcacgat ggaattgtgt tttgcgtttt ttggtaaaag 1801 gagcaaagcg aggacctgga gataaacgct ggagcaatct ccttggaagg attcagcacg 1861 agtagatggt aaacatttaa aggggaaagg gggggtttgt ttaaaatagt aaatcagtaa 1921 gtcacttcta aatttaaaga aaacaaaatt ggagttgaag aataagtagg tttccaattg 1981 gctattgccg ttttctttga aaaaataaac attttttaaa aaacta |
1 MSGGGVIRGP AGNNDCRIYV GNLPPDIRTK DIEDVFYKYG AIRDIDLKNR RGGPPFAFVE 61 FEDPRDAEDA VYGRDGYDYD GYRLRVEFPR SGRGTGRGGG GGGGGGAPRG RYGPPSRRSE 121 NRVVVSGLPP SGSWQDLKDH MREAGDVCYA DVYRDGTGVV EFVRKEDMTY AVRKLDNTKF 181 RSHEVGYTRI LFFDQNWIQW S |
| Legend: Exons are alternately coloured black and blue. Nucleotides in lower case indicate the UTR. The CDS is given in upper case. Nucleotides highlighted in blue indicate SNPs (mouse over shows alleles). |
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