ZMP
zgc:114121
Ensembl ID:
ZFIN ID:
Description:
coiled-coil domain-containing protein 77 [Source:RefSeq peptide;Acc:NP_001020649]
Human Orthologue:
CCDC77
Human Description:
coiled-coil domain containing 77 [Source:HGNC Symbol;Acc:28203]
Mouse Orthologue:
Ccdc77
Mouse Description:
coiled-coil domain containing 77 Gene [Source:MGI Symbol;Acc:MGI:1914450]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24591 | Essential Splice Site | Available for shipment | Available now |
sa13133 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24591
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022021 | Essential Splice Site | 67 | 466 | None | 11 |
ENSDART00000103208 | Essential Splice Site | 67 | 427 | None | 13 |
ENSDART00000138485 | None | None | 37 | None | 3 |
ENSDART00000141767 | Essential Splice Site | 67 | 466 | None | 12 |
ENSDART00000143564 | Essential Splice Site | 67 | 249 | None | 7 |
The following transcripts of ENSDARG00000014432 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 3676509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 3426561 |
GRCz11 | 25 | 3552295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGAAGCGGGTGATTCCAGTATTTTGACATCTCTATTGTTTTGTGC[A/T]GCACAAGTTGCAGTGGGAGATTCGCCAGCGTGAGGAGGAGATCGCGGAGC
Long Flanking Sequence:
ACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTTTTACGCAACGGATGCCCTTCCAGCCACAACCCATCTCTGGGAAACATCCACACACATACACTGCGGACAATTTAGCCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCAGAGAAAACCCAGGCGAATGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCCAGCTGAGGCTCGAATTAGCCACCTTCTTGCTGTCAGGTGACAGCACTACCTACTGTGCCACTGCGTTGCCGGATCCTATTTTAACATCATGAAATAAAAAAAGAGACTTATTGTGTTTCTGTCACTCCAATATGACTGGGGACACACTATACCTGCACACCGTTCTGTCTAAAAAGCTTCCGAAAGTAGATTTTGCATCAAAGGTGCCCTTTAAGGTGTTGTTTTGAAGCGGGTGATTCCAGTATTTTGACATCTCTATTGTTTTGTGC[A/T]GCACAAGTTGCAGTGGGAGATTCGCCAGCGTGAGGAGGAGATCGCGGAGCTCCAAAACGCTCTCAGCGACATGCAGATTTACCTGTTCCAGGAGAGGGAGCAGGCGCTCAGACTCTATGCAGAGAACGACCGGCTCAAGATCAGGTCAGATATAAATATATATTTATTTATTATATTTTCTTTCTTAAGAGGAAGACTTTTAGTTTCGCTGGAATAAAAAAAAATATGAAAAAAAATGTGGATGATTTTGTAGATATATGTGTAGAGATTATTTCATATATATACGGTTGAAGTCAGAATTATTAGCCCCCCCTTCGAATTTTTTCCTTTTTTAAATATTTCCCAAATTATATTTAACAAGCAAAGAGCAAGGAAATGTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCAGCTAGAATAAAAGCAGTTCTTAATTTTTTAAAACACATTTTAAGGTCAATATTTTTAGCCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13133
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022021 | Nonsense | 418 | 466 | 10 | 11 |
ENSDART00000103208 | Nonsense | 379 | 427 | 12 | 13 |
ENSDART00000138485 | None | None | 37 | None | 3 |
ENSDART00000141767 | Nonsense | 418 | 466 | 11 | 12 |
ENSDART00000143564 | None | None | 249 | None | 7 |
The following transcripts of ENSDARG00000014432 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 3668596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 3434474 |
GRCz11 | 25 | 3560208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATCAGACTCCTGCGGCAGAAAGTCAAAGATGTGGAGAAAATTCTCTTC[A/T]AAGTSAGTCGAGTCTCCCTTTCRTCTCTTCTGAAGAAATATATTWATATW
Long Flanking Sequence:
AAGTAGGTCGCTGGTTTAAGTTACAGCTAGGCCAGTTTCGGCATTTCGGTGTGCAGTTTGCATGTTCTCCCCGTGTTGGCGTGGGTTTTCTCCTGTTTCCTCCACAGTCCAAACACATGCGCTATAGGGGAATGGAAAAAACTAAATTGGCTGTAGTGTATAAGTGTAAATGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTGCAGCTGGAAAGGCATCCACTGTGTAAAACATATGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGTGACCACAGATGAATGAAAGGACTAAGCTGAAGGAAAATGAAGGAATGAAGTTATTGAAGTGTCTTTGATTGGGTTTTCAGGAGCGCTCGGATAAGATGGCCAAACGTCTTCAGCTCATGACTCGACGTTACGAAGCTCTGGAGAAACGACGAGTGATGGAGGTCGAGGGATTCAAGACCGATATCAGACTCCTGCGGCAGAAAGTCAAAGATGTGGAGAAAATTCTCTTC[A/T]AAGTCAGTCGAGTCTCCCTTTCGTCTCTTCTGAAGAAATATATTTATATTGACTCTGATAGGAACACTTCACTAGTTAACCGATTAACAGTTGACTTTTACCATTTTTTAATTCAATTTCCAGGTCTGGCGGGAGCACTTTTAGCTTAGCTTAGCATAGATTATTGAATCACATTAGACCATTAGCATCTCACTTAAAAAGGTTAAAATAGTTTTGTTTGTTTAACGCTTGACACTTCTGTAGTTACATTGTGTACTAAGACTGATGAAGGATGTAAAGATAATTTTTTTCTACGCTGATAGGCTAGGCTAGGATTAGCTTGTCTTAGCATAGATTATTGAATCAGATTAGACCATTAGCATCTCGCTTGAAAAATGTTAAAATAGTTGGTAACACTTTACAATAAGGTTCATCAGTTAATGCATTTACTAACATGAACTAATCATGAGCAACACTTGTACAGCATTTATTAATCATAACTGAACATTTACTAATGCATT
Associated Phenotype:
Not determined