Gene ID: | ENSG00000140105 |
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Biological name : | WARS |
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Synonyms : | P23381 / tryptophanyl-tRNA synthetase / WARS |
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Possible biological names infered from orthology : | |
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Species: | Homo sapiens |
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Chr. number: | 14 |
Strand: | -1 |
Band: | q32.2 |
Gene start: | 100333788 |
Gene end: | 100376805 |
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Corresponding Affymetrix probe sets: | 200628_s_at (Human Genome U133 Plus 2.0 Array) 200629_at (Human Genome U133 Plus 2.0 Array) |
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Cross references: | Ensembl peptide - ENSP00000450978 Ensembl peptide - ENSP00000451679 Ensembl peptide - ENSP00000451716 Ensembl peptide - ENSP00000451777 Ensembl peptide - ENSP00000451887 Ensembl peptide - ENSP00000451891 Ensembl peptide - ENSP00000451894 Ensembl peptide - ENSP00000451906 Ensembl peptide - ENSP00000451922 Ensembl peptide - ENSP00000451953 Ensembl peptide - ENSP00000452358 Ensembl peptide - ENSP00000452379 Ensembl peptide - ENSP00000452519 Ensembl peptide - ENSP00000452550 Ensembl peptide - ENSP00000487316 Ensembl peptide - ENSP00000339485 Ensembl peptide - ENSP00000347495 Ensembl peptide - ENSP00000351481 Ensembl peptide - ENSP00000376620 Ensembl peptide - ENSP00000450427 Ensembl peptide - ENSP00000450500 Ensembl peptide - ENSP00000450563 Ensembl peptide - ENSP00000450623 Ensembl peptide - ENSP00000450934 Ensembl peptide - ENSP00000451027 Ensembl peptide - ENSP00000451251 Ensembl peptide - ENSP00000451349 Ensembl peptide - ENSP00000451377 Ensembl peptide - ENSP00000451402 Ensembl peptide - ENSP00000451460 Ensembl peptide - ENSP00000451469 Ensembl peptide - ENSP00000451490 Ensembl peptide - ENSP00000451544 Ensembl peptide - ENSP00000451599 NCBI entrez gene - 7453
See in Manteia.
OMIM - 191050 RefSeq - XM_017021628 RefSeq - XM_017021627 RefSeq - XM_011537136 RefSeq - XM_011537135 RefSeq - XM_011537133 RefSeq - XM_006720249 RefSeq - XM_005268044 RefSeq - NM_213646 RefSeq - NM_004184 RefSeq - NM_213645 RefSeq - NM_173701 RefSeq - XM_017021629 RefSeq Peptide - NP_998811 RefSeq Peptide - NP_004175 RefSeq Peptide - NP_776049 RefSeq Peptide - NP_998810 swissprot - G3V4A3 swissprot - G3V4C7 swissprot - G3V4N0 swissprot - G3V4N8 swissprot - G3V4Q0 swissprot - G3V4S4 swissprot - G3V5H5 swissprot - G3V5U1 swissprot - G3V5W1 swissprot - H0YJP3 swissprot - G3V3X0 swissprot - G3V3S7 swissprot - G3V3R3 swissprot - G3V3P2 swissprot - G3V277 swissprot - G3V227 swissprot - A0A024R6K8 swissprot - G3V3H8 swissprot - P23381 swissprot - P78534 swissprot - G3V339 swissprot - G3V313 swissprot - G3V2Y7 swissprot - G3V2F2 swissprot - G3V2C0 swissprot - G3V3Y5 swissprot - G3V423 swissprot - G3V456 Ensembl - ENSG00000140105
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Related genetic diseases (OMIM): | 617721 - Neuronopathy, distal hereditary motor, type IX, 617721 |