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Genome Displays Related Resources Gene HomoloGene MANE RefSeq
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Report for CCDS7667.2 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
7667.2 |
Public |
Homo sapiens |
10 |
PWWP2B |
24 |
110 |
108 |
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Public since: CCDS release 1, NCBI annotation release 35.1, Ensembl annotation release 23
Review status: Reviewed (by RefSeq, Havana and CCDS collaboration) Sequence IDs included in CCDS 7667.2
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
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EBI |
ENST00000305233.6 |
ENSP00000306324.5 |
MANE Select |
Accepted |
alive |
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NCBI |
NM_138499.4 |
NP_612508.3 |
MANE Select |
Accepted |
alive |
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RefSeq |
Length |
Related UniProtKB/SwissProt |
Length |
Identity |
Gaps |
Mismatches |
NP_612508.3 |
590 |
Q6NUJ5-1 |
590 |
100% |
0 |
0 |
Chromosomal Locations for CCDS 7667.2
Assembly GRCh38.p14 (GCF_000001405.40)
CCDS Sequence Data |
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Blue highlighting indicates alternating exons. | Red highlighting indicates amino acids encoded across a splice junction. | | Mouse over the nucleotide or protein sequence below and click on the highlighted codon or residue to select the pair. |
Nucleotide Sequence (1773 nt): ATGGAGCCGCGCGCCGGCTGCCGGCTGCCGGTGCGGGTGGAGCAGGTCGTCAACGGCGCGCTGGTGGTCA CGGTGAGCTGCGGCGAGCGGAGCTTCGCGGGGATCCTGCTGGACTGCACGAAAAAGTCCGGCCTCTTTGG CCTACCCCCGTTGGCTCCGCTGCCCCAGGTCGATGAGTCCCCTGTCAACGACAGCCATGGCCGGGCTCCC GAGGAGGGGGATGCAGAGGTGATGCAGCTGGGGTCCAGCTCCCCCCCTCCTGCCCGCGGGGTTCAGCCCC CCGAGACCACCCGCCCCGAGCCACCCCCGCCCCTCGTGCCGCCGCTGCCCGCCGGAAGCCTGCCCCCGTA CCCTCCCTACTTCGAAGGCGCCCCCTTCCCTCACCCGCTGTGGCTCCGGGACACGTACAAGCTGTGGGTG CCCCAGCCGCCGCCCAGGACCATCAAGCGCACGCGGCGGCGTCTGTCCCGCAACCGCGACCCGGGGCGCC TCATCCTCAGCACCATCCGCCTGCGGCCGCGCCAGGTGCTCTGTGAGAAGTGCAAGAGCACGCTGAGCCC CCCGGAGGCCAGCCCCGGACCCCCAGCCGCGCCCAGGGCCCGCAGGAGGCTGGGCAGCGGCCCGGACAGG GAGCTCCGCAAGCCGGAGGAGCCGGAGAACGGCGAGCCCACGGCTGCGGCCACCGCCAGGAGGAGCAAGA GGGAGAGGCGCGAGGAGGACAGGGCCCCGGCAGAGCAGGTCCCGCGGAGCCCGGTCATCAAGATCTCCTA CAGCACGCCCCAGGGCAAGGGAGAGGTGGTCAAGATCCCCTCCCGCGTGCACGGCTCTCTGGAGCCCTTC CGTCCCCAGCAGGCCCCGCAGGACGACGGCAGCCAGGACCCCGAGGTGCTGGACAGAGAGTCCCGGGACC GGCCGTCCTGCGCGCCCTCGGCCTCCATCCCCAAGTTGAAACTGACACGGCCTGTGCCGGCCGGCGCGGA CCTGCCGCCCCCTAAGATCCGCCTGAAGCCCCACCGTCTGGGGGACAGCGAGCACGAGCCCGTGTACCGG GCCGAGCTGGTGGGGGAGCTGAACGGGTACCTGCGGGACAGCTCGCCGGCGCCCTGTGCGGACGGCCCTG CCGGTGGGCTGGCGGACTTGTCTTCTGGAAGTTCGGGTGAGGACGATGACTTCAAGAGCTGTCCCCAGGG TCCACAGGGACGCGAGGGCTTGGCTTTTCTCGTCAGCTGCCCTGAGGGGAGAGCGGACTGTGCCAGTGAG TCGGCGTGCAGCAGCGACAGCCTGGACGAGGCCAGATCGTCCGGCTCGGAAGGGACGCCGGCAGACACGG GTGACCTCTCGCCTGGCCACGGCGCGTCAGCGCCCTCGGTGTCCAGAGAGGCTCGCCAAACGGTGCCGCC CCTGACGGTCAGGCTGCACACACAGAGCGTGTCGGAGTGCATCACGGAGGACGGCAGGACTGTGGCCGTG GGGGACATCGTCTGGGGTAAGATCCATGGTTTTCCTTGGTGGCCGGCGCGTGTTCTTGACATCAGTCTCG GCCAGAAGGAGGACGGAGAGCCGTCTTGGCGAGAAGCGAAGGTCTCGTGGTTTGGTTCTCCGACTACGTC GTTCTTGTCTATTTCAAAACTCTCCCCTTTCTCTGAATTTTTCAAACTGAGATTTAATCGTAAGAAGAAG GGGATGTATCGGAAAGCTATAACCGAGGCTGCAAATGCCGCAAGACACGTGGCCCCGGAAATCAGGGAGC TCTTAACCCAGTTTGAAACGTAA
Translation (590 aa): MEPRAGCRLPVRVEQVVNGALVVTVSCGERSFAGILLDCTKKSGLFGLPPLAPLPQVDESPVNDSHGRAP EEGDAEVMQLGSSSPPPARGVQPPETTRPEPPPPLVPPLPAGSLPPYPPYFEGAPFPHPLWLRDTYKLWV PQPPPRTIKRTRRRLSRNRDPGRLILSTIRLRPRQVLCEKCKSTLSPPEASPGPPAAPRARRRLGSGPDR ELRKPEEPENGEPTAAATARRSKRERREEDRAPAEQVPRSPVIKISYSTPQGKGEVVKIPSRVHGSLEPF RPQQAPQDDGSQDPEVLDRESRDRPSCAPSASIPKLKLTRPVPAGADLPPPKIRLKPHRLGDSEHEPVYR AELVGELNGYLRDSSPAPCADGPAGGLADLSSGSSGEDDDFKSCPQGPQGREGLAFLVSCPEGRADCASE SACSSDSLDEARSSGSEGTPADTGDLSPGHGASAPSVSREARQTVPPLTVRLHTQSVSECITEDGRTVAV GDIVWGKIHGFPWWPARVLDISLGQKEDGEPSWREAKVSWFGSPTTSFLSISKLSPFSEFFKLRFNRKKK GMYRKAITEAANAARHVAPEIRELLTQFET
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