ZMP
ctage5
Ensembl ID:
ZFIN ID:
Description:
CTAGE family, member 5 [Source:RefSeq peptide;Acc:NP_956605]
Human Orthologues:
CTAGE1, CTAGE4, CTAGE5, CTAGE8, CTAGE9
Human Descriptions:
CTAGE family, member 4 [Source:HGNC Symbol;Acc:24772]
CTAGE family, member 5 [Source:HGNC Symbol;Acc:7057]
CTAGE family, member 8 [Source:HGNC Symbol;Acc:37294]
CTAGE family, member 9 [Source:HGNC Symbol;Acc:37275]
cutaneous T-cell lymphoma-associated antigen 1 [Source:HGNC Symbol;Acc:24346]
CTAGE family, member 5 [Source:HGNC Symbol;Acc:7057]
CTAGE family, member 8 [Source:HGNC Symbol;Acc:37294]
CTAGE family, member 9 [Source:HGNC Symbol;Acc:37275]
cutaneous T-cell lymphoma-associated antigen 1 [Source:HGNC Symbol;Acc:24346]
Mouse Orthologue:
Ctage5
Mouse Description:
CTAGE family, member 5 Gene [Source:MGI Symbol;Acc:MGI:1346056]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23018 | Essential Splice Site | Available for shipment | Available now |
| sa23017 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23018
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028311 | Essential Splice Site | None | 691 | 1 | 25 |
Genomic Location (Zv9):
Chromosome 17 (position 12935658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz11 | 17 | 13072246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACATGTTGACCATATTCCTAACGTGATTGATTTTACGGATTTTATAGG[T/A]ACAAAAATCAAGCTGTCCTTGGTATTAGCTTTGTTTAACTGTTTATAATG
Long Flanking Sequence:
AACAGTGAGCTCTTCCGCTCAGCGCAGTGCGCACTAGCAGTCAGAGTAGAGTAGCATCCGGCACCATGGCATGACAACAGATAAATGATCAGATTACAAAATACAAAATAACTCAGTTTAAATATAATCATGGCAGACGAAATTAAAGCCGAGTCGGTTGTGACGGAAGCGACTGACATGAAAGGAGCGGCGAATATTTACTACACACTCGCGGTGGAGAAAATCAAAGATGTAGGTGCCAGTGTGTGTGTGATGAAACCGCTTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGCAACTGTCAGCAGGTGTCATGTTTATTTTTTTAAGTAAGCTGTCATAGTACGCATCATGTACTCGAGTGTACTATTTGCTGGATAAATGTTGGCTTTTAGATGTGTGAACGGTTTTATAGAAAGGCATATAGCTTGTTAGCATTGCTCCATCTGTTACATGTTGACCATATTCCTAACGTGATTGATTTTACGGATTTTATAGG[T/A]ACAAAAATCAAGCTGTCCTTGGTATTAGCTTTGTTTAACTGTTTATAATGGTCTGGCAAGTTGGAAGTATATTGTGTTGTATCTTCTTGTTTGTTTTGGTCAGTTTTTGTGGGTCAGTGTGACAAAAGGATGTCTGAAATGATCAAATATCATAAAAGAGTATGCGTTAGAAGCTTTAATATTACAATGATTATAAGTAAACTCATTATTTTGTATTATTATCAAATGACTATTTTATGGAAAAGCCATTATATGTGTTTGTTTAAACTTGCAAATGAGTACAAGTTCATGTGAACTCACTAAAAAATAATCACATTACAATATATCTGTTTAAAGTGTTGTTTAATTTGTAAGAGTGTACCAATAATAAGGGGTTTAAAAGACATGTTAAAGCTTTACATGTATTATTTATACTTCCTTTTTATTTGAGAACCCATATAACTGTTTAACTTCTGTGTTTTAGGTTGTGTCTTCACTTCCTGATGACATTCGGCCTGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23017
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028311 | Nonsense | 196 | 691 | 10 | 25 |
Genomic Location (Zv9):
Chromosome 17 (position 12930405)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz11 | 17 | 13066993 |
KASP Assay ID:
2261-0746.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTATCATATTTTTTATTCCAGTCGCTCACAGAGTGCCTTTTGAAGATG[C/T]GAGATTGGGATTCAGAGGACGAGACCAGCATCGACGGCAGCACTAATATA
Long Flanking Sequence:
AACAGTTATTAACACTTTAACTCAATTTAAAGCAGTTTTCCTGAATGAAAGTATTATAGAGTAGTGTTTGTAAAATGGGTGGCGCGGTGGCACATTGAGTAGCGCTGTCGCCTCATAGAAAGAAGGTCACTGGCAACTGGGAGTAGACATTTCTTTGTGGAGTTTTCATGTTCTCCTCGTGTTTGTGTGGGTTTTCTCCGGATGCTCCGGTTTACCCCACAAGTCCAGAGACATGCACTATAGGTGAATTGGGTAAGCTACATTGTCCATGGTGTATGTGTGTGAATGAGAGTGTATGGTTGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATATGCTGGATAAGTTGCCGGTTCATTCTGCTGTGGCTATATGTAATTCCGTCACATACAGTCTAATGCTTGACTTGCTGAAACTTCATTTCTAATAATCTGTTTATCATATTTTTTATTCCAGTCGCTCACAGAGTGCCTTTTGAAGATG[C/T]GAGATTGGGATTCAGAGGACGAGACCAGCATCGACGGCAGCACTAATATAGCTGGTGCTGCGAATGGAGACAGTTCAGGTTAAAAATGTTGTTCATATTGGAATGGTGTTTTTTATTTTTTAATCTAAAGTCGGATATTGAAGTATCAGTTGTTTTTGTGCTTACAGATTTCCATCAGAAGCAAAAAGTACAGAAACTTATAGAAGCGGCCAAGGTATTTTTACTCACATCCTGTTTGATTTAAATCCAGTTAACCTTTGGCATTGCTGACCTTGCAAAGCAGAACACTGGGTTTTTAAACACAGCCCTAACATATATTATGCAGTAAATAATGTAGTCTTCCTGTTTGTCACAGATGAGTGCAGACTTGAAGTCCTTGGAGGAGGACAAGAACAGAGTGTTCGCCAAACTTGCAGATGAAATTAAAGCCAAAGAAGATCTCCATGGTAAATCATTTGCATCCACTACAATTGAAACAGGTTTTAAGATGCATGAACCTA
Associated Phenotype:
Not determined