Homo sapiens (human): 3198 Help Entry 3198              CDS       T01001                                  Symbol HOXA1, BSAS, HOX1, HOX1F Name (RefSeq) homeobox A1   KO K09301   homeobox protein HoxA/B/D1 Organism hsa  Homo sapiens (human) Pathway hsa04550   Signaling pathways regulating pluripotency of stem cells Disease H00727   Athabascan brainstem dysgenesis syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     3198 (HOXA1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     3198 (HOXA1) Transcription factors [BR:hsa03000]  Eukaryotic type   Helix-turn-helix    Homeo domain ANTP: HOXL     3198 (HOXA1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Homeodomain Homeobox_KN PHC2_SAM_assoc Motif Other DBs NCBI-GeneID:  3198 NCBI-ProteinID:  NP_005513 OMIM:  142955 HGNC:  5099 Ensembl:  ENSG00000105991 Vega:  OTTHUMG00000023207 Pharos:  P49639(Tbio) UniProt:  P49639 LinkDB All DBs Position 7:complement(27092993..27096000) Genome browser AA seq 335 aa AA seqDB search MDNARMNSFLEYPILSSGDSGTCSARAYPSDHRITTFQSCAVSANSCGGDDRFLVGRGVQ IGSPHHHHHHHHRHPQPATYQTSGNLGVSYSHSSCGPSYGSQNFSAPYSPYALNQEADVS GGYPQCAPAVYSGNLSSPMVQHHHHHQGYAGGAVGSPQYIHHSYGQEHQSLALATYNNSL SPLHASHQEACRSPASETSSPAQTFDWMKVKRNPPKTGKVGEYGYLGQPNAVRTNFTTKQ LTELEKEFHFNKYLTRARRVEIAASLQLNETQVKIWFQNRRMKQKKREKEGLLPISPATP PGNDEKAEESSEKSSSSPCVPSPGSSTSDTLTTSH NT seq 1008 nt NT seq  +upstreamnt  +downstreamnt atggacaatgcaagaatgaactccttcctggaataccccatacttagcagtggcgactcg gggacctgctcagcccgagcctacccctcggaccataggattacaactttccagtcgtgc gcggtcagcgccaacagttgcggcggcgacgaccgcttcctagtgggcaggggggtgcag atcggttcgccccaccaccaccaccaccaccaccatcgccacccccagccggctacctac cagacttccgggaacctgggggtgtcctactcccactcaagttgtggtccaagctatggc tcacagaacttcagtgcgccttacagcccctacgcgttaaatcaggaagcagacgtaagt ggtgggtacccccagtgcgctcccgctgtttactctggaaatctctcatctcccatggtc cagcatcaccaccaccaccagggttatgctgggggcgcggtgggctcgcctcaatacatt caccactcatatggacaggagcaccagagcctggccctggctacgtataataactccttg tcccctctccacgccagccaccaagaagcctgtcgctcccccgcatcggagacatcttct ccagcgcagacttttgactggatgaaagtcaaaagaaaccctcccaaaacagggaaagtt ggagagtacggctacctgggtcaacccaacgcggtgcgcaccaacttcactaccaagcag ctcacggaactggagaaggagttccacttcaacaagtacctgacgcgcgcccgcagggtg gagatcgctgcatccctgcagctcaacgagacccaagtgaagatctggttccagaaccgc cgaatgaagcaaaagaaacgtgagaaggagggtctcttgcccatctctccggccaccccg ccaggaaacgacgagaaggccgaggaatcctcagagaagtccagctcttcgccctgcgtt ccttccccggggtcttctacctcagacactctgactacctcccactga

Homo sapiens (human): 3211 Help Entry 3211              CDS       T01001                                  Symbol HOXB1, HCFP3, HOX2, HOX2I, Hox-2.9 Name (RefSeq) homeobox B1   KO K09301   homeobox protein HoxA/B/D1 Organism hsa  Homo sapiens (human) Pathway hsa04550   Signaling pathways regulating pluripotency of stem cells Disease H02151   Hereditary congenital facial paresis Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     3211 (HOXB1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     3211 (HOXB1) Transcription factors [BR:hsa03000]  Eukaryotic type   Helix-turn-helix    Homeo domain ANTP: HOXL     3211 (HOXB1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Homeodomain Homeobox_KN Motif Other DBs NCBI-GeneID:  3211 NCBI-ProteinID:  NP_002135 OMIM:  142968 HGNC:  5111 Ensembl:  ENSG00000120094 Vega:  OTTHUMG00000159929 Pharos:  P14653(Tbio) UniProt:  P14653 Structure PDB LinkDB All DBs Position 17:complement(48528526..48531011) Genome browser AA seq 301 aa AA seqDB search MDYNRMNSFLEYPLCNRGPSAYSAHSAPTSFPPSSAQAVDSYASEGRYGGGLSSPAFQQN SGYPAQQPPSTLGVPFPSSAPSGYAPAACSPSYGPSQYYPLGQSEGDGGYFHPSSYGAQL GGLSDGYGAGGAGPGPYPPQHPPYGNEQTASFAPAYADLLSEDKETPCPSEPNTPTARTF DWMKVKRNPPKTAKVSEPGLGSPSGLRTNFTTRQLTELEKEFHFNKYLSRARRVEIAATL ELNETQVKIWFQNRRMKQKKREREEGRVPPAPPGCPKEAAGDASDQSTCTSPEASPSSVT S NT seq 906 nt NT seq  +upstreamnt  +downstreamnt atggactataataggatgaactccttcttagagtacccactctgtaaccggggacccagc gcctacagcgcccacagcgccccaacctcctttcccccaagctcggctcaggcggttgac agctatgcaagcgagggccgctacggtggggggctgtccagccctgcgtttcagcagaac tccggctatcccgcccagcagccgccttcgaccctgggggtgcccttccccagctccgcg ccctcggggtatgctcctgccgcctgcagccccagctacgggccttctcagtactaccct ctgggtcaatcagaaggagacggaggctattttcatccctcgagctacggggcccagcta gggggcttgtccgatggctacggagcaggtggagccggtccggggccatatcctccgcag catcccccttatgggaacgagcagaccgcgagctttgcaccggcctatgctgatctcctc tccgaggacaaggaaacaccctgcccttcagaacctaacacccccacggcccggaccttc gactggatgaaggttaagagaaacccacccaagacagcgaaggtgtcagagccaggcctg ggctcgcccagtggcctccgcaccaacttcaccacaaggcagctgacagaactggaaaag gagttccatttcaacaagtacctgagccgggcccggagggtggagattgccgccaccctg gagctcaatgaaacacaggtcaagatttggttccagaaccgacgaatgaagcagaagaag cgcgagcgagaggaaggtcgggtccccccagccccaccaggctgccccaaggaggcagct ggagatgcctcagaccagtcgacatgcacctccccggaagcctcacccagctctgtcacc tcctga

Homo sapiens (human): 3231 Help Entry 3231              CDS       T01001                                  Symbol HOXD1, HOX4, HOX4G, Hox-4.7 Name (RefSeq) homeobox D1   KO K09301   homeobox protein HoxA/B/D1 Organism hsa  Homo sapiens (human) Pathway hsa04550   Signaling pathways regulating pluripotency of stem cells Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     3231 (HOXD1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     3231 (HOXD1) Transcription factors [BR:hsa03000]  Eukaryotic type   Helix-turn-helix    Homeo domain ANTP: HOXL     3231 (HOXD1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Homeodomain Motif Other DBs NCBI-GeneID:  3231 NCBI-ProteinID:  NP_078777 OMIM:  142987 HGNC:  5132 Ensembl:  ENSG00000128645 Vega:  OTTHUMG00000132512 Pharos:  Q9GZZ0(Tbio) UniProt:  Q9GZZ0 Q96CA4 LinkDB All DBs Position 2:176188668..176190907 Genome browser AA seq 328 aa AA seqDB search MSSYLEYVSCSSSGGVGGDVLSLAPKFCRSDARPVALQPAFPLGNGDGAFVSCLPLAAAR PSPSPPAAPARPSVPPPAAPQYAQCTLEGAYEPGAAPAAAAGGADYGFLGSGPAYDFPGV LGRAADDGGSHVHYATSAVFSGGGSFLLSGQVDYAAFGEPGPFPACLKASADGHPGAFQT ASPAPGTYPKSVSPASGLPAAFSTFEWMKVKRNASKKGKLAEYGAASPSSAIRTNFSTKQ LTELEKEFHFNKYLTRARRIEIANCLHLNDTQVKIWFQNRRMKQKKREREGLLATAIPVA PLQLPLSGTTPTKFIKNPGSPSQSQEPS NT seq 987 nt NT seq  +upstreamnt  +downstreamnt atgagctcctacctggagtacgtgtcatgcagcagcagcggcggggtcggcggcgacgtg ctcagcttggcacccaagttctgccgctccgacgcccggcccgtggctctgcagcccgcc ttccctctgggcaacggcgacggcgccttcgtcagctgtctgcccctggccgccgcccga ccctcgccttcgcccccggccgcccccgcgcggccgtccgtaccgcctccggccgcgccc cagtacgcgcagtgcaccctggagggggcctacgaacctggtgccgcacctgccgcggca gctgggggcgcggactacggcttcctggggtccgggccggcgtacgacttcccgggcgtg ctggggcgggcggccgacgacggcgggtctcacgtccactacgccacctcggccgtcttc tcgggcggcggctctttcctcctcagcggccaggtggattacgcggccttcggcgaaccc ggcccttttccggcttgtctcaaagcgtcagccgacggccaccctggtgctttccagacc gcatccccggccccaggcacctaccccaagtccgtctctcccgcctccggcctccctgcc gccttcagcacgttcgagtggatgaaagtgaagaggaatgcctctaagaaaggcaaactc gccgagtatggggccgctagcccctccagcgcgatccgcacgaatttcagcaccaagcaa ctgacagaactggaaaaagagtttcatttcaataagtacttaactcgagcccggcgcatc gagatagccaactgcttgcacctgaatgacacgcaagtcaaaatctggttccagaaccgc aggatgaaacagaagaaaagggaacgagaagggcttctggccacggccattcctgtggct cccctccaacttcccctctctggaacaacccccactaagtttatcaagaaccccggcagc ccttctcagtcccaagagccttcgtga

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