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Genome Displays Related Resources Gene HomoloGene MANE RefSeq
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Report for CCDS55446.1 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
55446.1 |
Public |
Homo sapiens |
X |
RTL5 |
24 |
110 |
108 |
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Public since: CCDS release 8, NCBI annotation release 37.2, Ensembl annotation release 62
Review status: Reviewed (by RefSeq and Havana)
Attributes |
Nonsense-mediated decay (NMD) candidate |
Sequence IDs included in CCDS 55446.1
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
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EBI |
ENST00000479991.1 |
ENSP00000418667.1 |
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Accepted |
alive |
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EBI |
ENST00000609883.2 |
ENSP00000476792.1 |
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Accepted |
alive |
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NCBI |
NM_001024455.4 |
NP_001019626.1 |
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Accepted |
alive |
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RefSeq |
Length |
Related UniProtKB/SwissProt |
Length |
Identity |
Gaps |
Mismatches |
NP_001019626.1 |
569 |
Q5HYW3 |
569 |
100% |
0 |
0 |
Chromosomal Locations for CCDS 55446.1
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 (1710 nt): ATGTCTGAGGCGTCAGGAAATCTCAACAGCCTCCGCATGGCGAATGTGGCCCTGCGCGAAGAATTAAATG CCCTTCGCGGGGAGAATGCCAATTTGGGCCTCCAGCTCGGGAGAGCCCTGGCCGAGGTTAATTCCTTGCG GGGCAATGTCTCCAGCTACATCCGCTGGCCAGTACCCATAGTGCCCGTCCTTGCGGAGGAGAACTTGGAG TTCGCGCTCAGTGAGATCGAAGTCATTCCCGGGGGAGAACTGCCCTTCTTGTGCCGGCCTCCCCCACGCG CGGAGCCCGACTGTATCTCGGATGATCTTTTGATTAACGTGATCCAGGATCGCAGCACCCCCGACGGGCC CGCTGACCCCCCTCTGCTGCCCATCCCGCCCCCGCCGGCGCTGCCTCCGCCCGCGTCAAAGGAACCGCCC CCGCAACCCCCTCTGGCACCGCTGGAGCGGCCTGAGATAGAGCCCTTTTCAGGAGACCCAGTCTACCTGG CTGAATTCCTGATGCAGCTAGAGACCTTCATAGCCGACCATGAGGTTCATTTCCCCGGGGGCGCCGAGCG GGTGGCCTTTCTGATCTCCTTTTTCACTGGCGAAGCCAAGGACTGGGCCATCTCGGTCACCCAGGAAGGA AGCCCCTTGCATGCCAACTTCCCGCGCTTCCTGGATGAAATCCGTAAGGAATTCTGTGGCCCCATCCCCC CACGTGTGGCTAAAAAGGCCATTCGCAAGCTCAAGCAGGGCCACTGTACCCTCGGCAGCTATGCAGATGC TTTTCAGTTCCTGGCCCAATTCTTGTCTTGGGATGACTGCCGCCTCCAAAACCAATTCCTCAAAGGCCTG TCGGAATTCTTCCGCAAAGAGCTCTTATGGTCAACAGAAATGGCCGACCTGGATGAGCTGATTCTCGAAT GTGTGGAGATAGAAAGAAAAGTGCGCGTTCCCAAGCCTATCCCGCTCCCTGGAGTTCGAAATATCATCTT CCCTTTTGCTCCGAGTCCCAATGAGGAAGAAAGTGAAGATGAAGAGTACTACAGTGAAGATGAAGACCAA GAGGCACGCAGGCACAGGCTTCACTCCAAGGACCAGAGGAAGCGCATGAGGGCTTTTCAGCAAGAGATGA AGGAGAAGGAGGAGGAGGAGATGAAGAAGGAGGAAGAAATGAAGAAGAAGGAAGAGAAGGAGGAGGAGGA GGAAGAGGAAATGAAACAGAAAGAGGAGGAGGAGGAGATAAGGAACAAGAATGAGGAGGAAGGAGAGAGT AAGGATGAAGAAGATGAAGATGAGGATGGGGGCCAGAAACCAGAAGGAGAGCCACAGCAGGATCCAGGGA CTGAGGAGACCTATGGTGAGGTGGAGGAGGAGCCACTGGATGAGGCCCAAGATGATGACCTAGATGAGCT GATGGAGATGGAGCCGACCTTTGTTCACGCGTCATCCCAGACTTCTGGCCCCACAAGTGGTTACCACGCC GAAAACTTCCTGGGTGCATCACCTCCCATAATACAGCCTAGCAGACGGAGGAACCAGAATCGAGTCCCAC TTCTGGAAGGCCTTCCAGGCACCAATTCACCATTCTACAGCTCCCCCCAACTGATTCGCCGCACAGGTCG TTTAGGACAACGCCAAGTTCGAAGACGCCCCCCTGTGCTTTTCCGCCTCACTCCGAGACAGGGGGGCCAC CGAGCTGCTCGTGGCCGAATTCGAGTTTGA
Translation (569 aa): MSEASGNLNSLRMANVALREELNALRGENANLGLQLGRALAEVNSLRGNVSSYIRWPVPIVPVLAEENLE FALSEIEVIPGGELPFLCRPPPRAEPDCISDDLLINVIQDRSTPDGPADPPLLPIPPPPALPPPASKEPP PQPPLAPLERPEIEPFSGDPVYLAEFLMQLETFIADHEVHFPGGAERVAFLISFFTGEAKDWAISVTQEG SPLHANFPRFLDEIRKEFCGPIPPRVAKKAIRKLKQGHCTLGSYADAFQFLAQFLSWDDCRLQNQFLKGL SEFFRKELLWSTEMADLDELILECVEIERKVRVPKPIPLPGVRNIIFPFAPSPNEEESEDEEYYSEDEDQ EARRHRLHSKDQRKRMRAFQQEMKEKEEEEMKKEEEMKKKEEKEEEEEEEMKQKEEEEEIRNKNEEEGES KDEEDEDEDGGQKPEGEPQQDPGTEETYGEVEEEPLDEAQDDDLDELMEMEPTFVHASSQTSGPTSGYHA ENFLGASPPIIQPSRRRNQNRVPLLEGLPGTNSPFYSSPQLIRRTGRLGQRQVRRRPPVLFRLTPRQGGH RAARGRIRV
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