Capra hircus (goat): 102191706 Help Entry 102191706         CDS       T02910                                  Symbol ACTR10 Name (RefSeq) actin-related protein 10   KO K16576   actin-related protein 10 Organism chx  Capra hircus (goat) Pathway chx04814   Motor proteins chx05014   Amyotrophic lateral sclerosis chx05016   Huntington disease chx05022   Pathways of neurodegeneration - multiple diseases chx05132   Salmonella infection Brite KEGG Orthology (KO) [BR:chx00001]  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     102191706 (ACTR10)  09160 Human Diseases   09171 Infectious disease: bacterial    05132 Salmonella infection     102191706 (ACTR10)   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     102191706 (ACTR10)    05016 Huntington disease     102191706 (ACTR10)    05022 Pathways of neurodegeneration - multiple diseases     102191706 (ACTR10)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:chx03036]     102191706 (ACTR10)   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:chx04812]     102191706 (ACTR10) Chromosome and associated proteins [BR:chx03036]  Eukaryotic type   Centrosome formation proteins    Microtubules and associated factors     Dynactin complex      102191706 (ACTR10) Cytoskeleton proteins [BR:chx04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actins     Actin-related proteins      102191706 (ACTR10) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Actin Motif Other DBs NCBI-GeneID:  102191706 NCBI-ProteinID:  XP_005685966 UniProt:  A0A452G3E9 LinkDB All DBs Position 10:complement(32685653..32712364) Genome browser AA seq 417 aa AA seqDB search MPLYEGLGSGGEKTAVVIDLGEAFTKCGFAGETGPRCIIPSVIKKAGMPKPIKVVQYNIN TEELYSYLKEFIHILYFRHLLVNPRDRRVVVIESVLCPSHFRETLTRVLFKYFEVPSVLL APSHLMALLTLGINSAMVLDCGYRESLVLPIYEGIPVLNCWGALPLGGKALHKELETQLL EQCTVDTGAAKEQSLPSVMGSIPEGILEDIKVRTCFVSDLKRGLNIQAAKFNIDGNTERP SPPPNVDYPLDGEKILHVLGSIRDSVVEILFEQDNEEKSVATLILDSLMQCPIDTRKQLA ENLVVIGGTSMLPGFLHRLLAEIRYLVEKPKYKKTLATKTFRIHTPPAKANCVAWLGGAI FGALQDILGSRSVSKDYYNQTGRIPDWCSLNNPPLEMMFDVGKNQPPLMKRAFSTEK NT seq 1254 nt NT seq  +upstreamnt  +downstreamnt atgccgctgtacgagggcctgggaagcggcggggagaaaacggcggtcgtgatagatctg ggagaggcttttaccaaatgtggatttgctggagaaactggtccaagatgtataattccc agtgtgataaaaaaagctggcatgcctaagcctatcaaagttgtacaatataacatcaat acagaagaactatattcctacctaaaggaattcatccatatactgtatttcaggcatcta ttggtgaatcccagagaccgcagagttgtggttatcgagtctgtattatgtccttcccac ttcagagagacactcactcgtgttcttttcaagtattttgaggttccatctgtcttgctt gctccaagtcatctaatggctcttcttacacttgggataaactctgccatggtgctagat tgtggatatagggagagcctggtgttacctatatatgaagggatcccagtactgaattgt tggggagcactccccttaggaggaaaagctcttcacaaggagttggaaactcaactgttg gaacaatgtactgttgacacaggtgctgctaaagaacagagccttccctctgtgatgggt tcaattccagaaggtatcttggaggacattaaagtgcgcacttgctttgttagtgatctg aagcgtggactaaacatccaggcagcaaaatttaatattgatgggaatactgagcgtccc tcaccacccccaaatgttgactacccattagatggagagaagattttacatgtacttgga tcaatcagagattctgttgtggagatcctttttgagcaagataatgaagagaaatcagtt gccactttaatattggattcccttatgcagtgcccaatagacaccaggaagcagctagca gagaatttggtagtcataggtggcacatctatgttgccaggtttccttcacagactactt gcagaaataaggtatttggtagaaaaaccaaaatataaaaaaacgcttgctaccaagaca ttccgaattcatactccacctgcaaaggctaattgtgtagcatggctaggaggagctatt tttggagcacttcaagacatacttgggagccgttcagtctctaaggattattataaccag acaggccgtatacctgattggtgttctcttaataatccacctttagaaatgatgttcgat gttgggaagaatcagcctcctctgatgaagagagcattttccactgaaaaatga

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