Homo sapiens (human): 881 Help Entry 881               CDS       T01001                                  Symbol CCIN, BTBD20, KBTBD14, SPGF91 Name (RefSeq) calicin   KO K24809   calicin Organism hsa  Homo sapiens (human) Disease H01282   Spermatogenic failure Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]     881 (CCIN) Domain-containing proteins not elsewhere classified [BR:hsa04990]  Other domain-containing proteins   BTB-POZ domain-containing proteins    881 (CCIN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Kelch_1 BTB Kelch_6 Kelch_4 Kelch_KLHDC2_KLHL20_DRC7 Kelch_3 Beta-prop_ATRN-LZTR1 BACK Kelch_2 NANM Kelch_5 TPM_phosphatase Motif Other DBs NCBI-GeneID:  881 NCBI-ProteinID:  NP_005884 OMIM:  603960 HGNC:  1568 Ensembl:  ENSG00000185972 UniProt:  Q13939 Q8WX35 Q8WWB2 LinkDB All DBs Position 9:36169388..36171334 Genome browser AA seq 588 aa AA seqDB search MKLEFTEKNYNSFVLQNLNRQRKRKEYWDMALSVDNHVFFAHRNVLAAVSPLVRSLISSN DMKTADELFITIDTSYLSPVTVDQLLDYFYSGKVVISEQNVEELLRGAQYFNTPRLRVHC NDFLIKSICRANCLRYLFLAELFELKEVSDVAYSGIRDNFHYWASPEGSMHFMRCPPVIF GRLLRDENLHVLNEDQALSALINWVYFRKEDREKYFKKFFNYINLNAVSNKTLVFASNKL VGMENTSSHTTLIESVLMDRKQERPCSLLVYQRKGALLDSVVILGGQKAHGQFNDGVFAY IIQENLWMKLSDMPYRAAALSATSAGRYIYISGGTTEQISGLKTAWRYDMDDNSWTKLPD LPIGLVFHTMVTCGGTVYSVGGSIAPRRYVSNIYRYDERKEVWCLAGKMSIPMDGTAVIT KGDRHLYIVTGRCLVKGYISRVGVVDCFDTSTGDVVQCITFPIEFNHRPLLSFQQDNILC VHSHRQSVEINLQKVKASKTTTSVPVLPNSCPLDVSHAICSIGDSKVFVCGGVTTASDVQ TKDYTINPNAFLLDQKTGKWKTLAPPPEALDCPACCLAKLPCKILQRI NT seq 1767 nt NT seq  +upstreamnt  +downstreamnt atgaaattggaattcacggagaaaaactacaatagcttcgtgctgcagaacctgaacaga cagaggaaacgcaaagagtactgggacatggccctgagtgtggacaaccacgtcttcttt gcacatcgcaatgtgctggctgctgtctccccactggtgaggagcctcatctccagcaat gacatgaagaccgctgatgagcttttcatcaccattgacaccagttacctgagcccggtc acagtggaccagcttctggactacttctatagcggcaaggtggtgatctccgagcaaaat gtggaggagctgcttcgtggggctcagtatttcaacacaccacgccttcgagttcactgt aacgacttccttattaagtccatctgccgtgccaactgcttgcgctacctcttcttggct gagctgtttgagctcaaagaggtatcagacgtagcttactctggcattcgggacaacttc cactactgggccagtcctgagggctccatgcacttcatgcgctgtccacctgttatcttt ggccgcctgctccgtgatgaaaaccttcacgtgctcaatgaagaccaggcgctcagcgca ctcatcaattgggtgtacttccggaaggaggatcgggagaagtatttcaagaagttcttc aattacatcaatctcaatgctgtctccaataagacgctggtgtttgccagcaacaagctg gtgggcatggagaacacctcatcccatacaaccctgattgagagtgtcctgatggaccgc aagcaggagcggccatgcagcctgctggtctaccagcggaaaggggccctgcttgattcc gtggtcatcctcggtggccagaaggcccacggccagttcaatgatggagtgtttgcttat atcatccaggagaacctgtggatgaagctctcagacatgccctatcgggcagcagcactt agtgccacctctgctggtcgctacatctacatctctggtggcaccactgagcagatttca gggctgaagacagcctggcggtatgacatggatgacaactcctggaccaagttgcctgac ctgcccatcgggcttgtcttccacaccatggtgacctgtggggggacagtgtactcagtg ggcgggagcattgccccaaggcggtatgtctccaacatctatcgctatgatgagcggaag gaagtctggtgcctggcaggaaagatgagcatccccatggatggcaccgccgtgatcact aaaggagacaggcatctgtacattgtcactggacggtgcttggtgaaaggttatatctcc cgggtcggggtagtggactgctttgacaccagcactggggacgtggtccagtgtatcacc ttccccattgagttcaaccatcggcccctgctctctttccaacaggacaacatcctctgc gtgcacagccaccggcagagtgtggaaatcaatctgcagaaggtgaaggcaagcaagacg accacctcagtgcctgtcttgcccaacagctgccccttggatgtgtcccatgctatatgc tccattggagacagcaaggtgtttgtatgtgggggtgtcaccactgccagcgatgtccag acaaaggactacaccatcaatccaaatgccttcttgctggaccaaaagacaggcaagtgg aagaccctggctcctccaccagaggcactggactgtcctgcctgctgtctagccaagcta ccttgcaagattcttcaaaggatttaa

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