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Genome Displays Related Resources Gene HomoloGene MANE RefSeq
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Report for CCDS43660.1 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
43660.1 |
Public |
Homo sapiens |
7 |
WEE2 |
24 |
110 |
108 |
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Public since: CCDS release 5, NCBI annotation release 36.3, Ensembl annotation release 47
Review status: Reviewed (by RefSeq and Havana) Sequence IDs included in CCDS 43660.1
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
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EBI |
ENST00000397541.6 |
ENSP00000380675.2 |
MANE Select |
Accepted |
alive |
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NCBI |
NM_001105558.1 |
NP_001099028.1 |
MANE Select |
Accepted |
alive |
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RefSeq |
Length |
Related UniProtKB/SwissProt |
Length |
Identity |
Gaps |
Mismatches |
NP_001099028.1 |
567 |
P0C1S8 |
567 |
100% |
0 |
0 |
Chromosomal Locations for CCDS 43660.1
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 (1704 nt): ATGGATGACAAAGATATTGACAAAGAACTAAGGCAGAAATTAAACTTTTCCTATTGTGAGGAGACTGAGA TTGAAGGGCAGAAGAAAGTAGAAGAAAGCAGGGAGGCTTCGAGCCAAACCCCAGAGAAGGGTGAAGTGCA GGATTCAGAGGCAAAGGGTACACCACCTTGGACTCCCCTTAGCAACGTGCATGAGCTCGACACATCTTCG GAAAAAGACAAAGAAAGTCCAGATCAGATTTTGAGGACTCCAGTGTCACACCCTCTCAAATGTCCTGAGA CACCAGCCCAACCAGACAGCAGGAGCAAGCTGCTGCCCAGTGACAGCCCCTCTACTCCCAAAACCATGCT GAGCCGGTTGGTGATTTCTCCAACAGGGAAGCTTCCTTCCAGAGGCCCTAAGCATTTGAAGCTCACACCT GCTCCCCTCAAGGATGAGATGACCTCATTGGCTCTGGTCAATATTAATCCCTTCACTCCAGAGTCCTATA AAAAATTATTTCTTCAATCTGGTGGCAAGAGGAAAATAAGAGGAGATCTTGAGGAAGCTGGTCCAGAGGA AGGCAAGGGAGGGCTGCCTGCCAAGAGATGTGTTTTACGAGAAACCAACATGGCTTCCCGCTATGAAAAA GAATTCTTGGAGGTTGAAAAAATTGGGGTTGGCGAATTTGGTACAGTCTACAAGTGCATTAAGAGGCTGG ATGGATGTGTTTATGCAATAAAGCGCTCTATGAAAACTTTTACAGAATTATCAAATGAGAATTCGGCTTT GCATGAAGTTTATGCTCACGCAGTGCTTGGGCATCACCCCCATGTGGTACGTTACTATTCCTCATGGGCA GAAGATGACCACATGATCATTCAGAATGAATACTGCAATGGTGGGAGTTTGCAAGCTGCTATATCTGAAA ACACTAAGTCTGGCAATCATTTTGAAGAGCCAAAACTCAAGGACATCCTTCTACAGATTTCCCTTGGCCT TAATTACATCCACAACTCTAGCATGGTACACCTGGACATCAAACCTAGTAATATATTCATTTGTCACAAG ATGCAAAGTGAATCCTCTGGAGTCATAGAAGAAGTTGAAAATGAAGCTGATTGGTTTCTCTCTGCCAATG TGATGTATAAAATTGGTGACCTGGGCCACGCAACATCAATAAACAAACCCAAAGTGGAAGAAGGAGATAG TCGCTTCCTGGCTAATGAGATTTTGCAAGAGGATTACCGGCACCTTCCCAAAGCAGACATATTTGCCTTG GGATTAACAATTGCAGTGGCTGCAGGAGCAGAGTCATTGCCCACCAATGGTGCTGCATGGCACCATATCC GCAAGGGTAACTTTCCGGACGTTCCTCAGGAGCTCTCAGAAAGCTTTTCCAGTCTGCTCAAGAACATGAT CCAACCTGATGCCGAACAGAGACCTTCTGCAGCAGCTCTGGCCAGAAATACAGTTCTCCGGCCTTCCCTG GGAAAAACAGAAGAGCTCCAACAGCAGCTGAATTTGGAAAAGTTCAAGACTGCCACACTGGAAAGGGAAC TGAGAGAAGCCCAGCAGGCCCAGTCACCCCAGGGATATACCCATCATGGTGACACTGGGGTCTCTGGGAC CCACACAGGATCAAGAAGCACAAAACGCCTGGTGGGAGGAAAGAGTGCAAGGTCTTCAAGCTTTACCTCA GGAGAGCGTGAGCCTCTGCATTAA
Translation (567 aa): MDDKDIDKELRQKLNFSYCEETEIEGQKKVEESREASSQTPEKGEVQDSEAKGTPPWTPLSNVHELDTSS EKDKESPDQILRTPVSHPLKCPETPAQPDSRSKLLPSDSPSTPKTMLSRLVISPTGKLPSRGPKHLKLTP APLKDEMTSLALVNINPFTPESYKKLFLQSGGKRKIRGDLEEAGPEEGKGGLPAKRCVLRETNMASRYEK EFLEVEKIGVGEFGTVYKCIKRLDGCVYAIKRSMKTFTELSNENSALHEVYAHAVLGHHPHVVRYYSSWA EDDHMIIQNEYCNGGSLQAAISENTKSGNHFEEPKLKDILLQISLGLNYIHNSSMVHLDIKPSNIFICHK MQSESSGVIEEVENEADWFLSANVMYKIGDLGHATSINKPKVEEGDSRFLANEILQEDYRHLPKADIFAL GLTIAVAAGAESLPTNGAAWHHIRKGNFPDVPQELSESFSSLLKNMIQPDAEQRPSAAALARNTVLRPSL GKTEELQQQLNLEKFKTATLERELREAQQAQSPQGYTHHGDTGVSGTHTGSRSTKRLVGGKSARSSSFTS GEREPLH
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