ZMP
si:dkey-30c15.5
Ensembl ID:
ZFIN ID:
Description:
Coiled-coil domain-containing protein 79 [Source:UniProtKB/Swiss-Prot;Acc:Q1LX29]
Human Orthologue:
AC044802.2
Human Description:
coiled-coil domain-containing protein 79 [Source:RefSeq peptide;Acc:NP_001129977]
Mouse Orthologue:
Ccdc79
Mouse Description:
coiled-coil domain containing 79 Gene [Source:MGI Symbol;Acc:MGI:2443187]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15008 | Essential Splice Site | Available for shipment | Available now |
sa615 | Nonsense | Available for shipment | Available now |
sa23225 | Nonsense | Available for shipment | Available now |
sa6499 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15008
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 |
---|---|---|---|---|---|
ENSDART00000081468 | Essential Splice Site | 83 | 814 | 2 | 19 |
ENSDART00000142270 | Essential Splice Site | 83 | 814 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 6922460)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 7500150 |
GRCz11 | 18 | 7459085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTAAAGAGACTGCACTATTTACACTTGCATCTTTGGCTGAACTGCATGG[T/A]ATGTGTTTGGTTACATATGGAAACAGTTAAGWGAGCACTTTCAAATAATT
Long Flanking Sequence:
AATTTGTGTTAGCAAGCAATTGGACAGGTGTACCTTATAAAGTGGCCGGTGAGTGTATATTGTATTGTATTGCACAATACTCATCAATTGTACAGATCCAGTGATGTATTTTGCTTTCTAAGCTGAATGATTTCACATTTCCAGCTACCAAGACAGATTTGCGTCTTTTGCTGGAATGTCTGAAATACCAGATGAAATGGCCTGGCTCACAGAAACAAGCTCTTCTCACTATCATCTCAATCTGCAAGCAAAATGGTTTGCTTTACAGCTCAAAATATAATCAAATCAAACAGAAATACAACTTTTCTTACACAAACATAAAATTAAATATACTATTGTGCAGTTTAGTTATTGTTTTTTTGTATTTCAGATCAGTATGTTGAGTTCCTCAGAGAGATCGGAGGCATTTCCTTCATCTATAACCTATCAAAATCCAGTACTTTCTCTCAAGTTAAAGAGACTGCACTATTTACACTTGCATCTTTGGCTGAACTGCATGG[T/A]ATGTGTTTGGTTACATATGGAAACAGTTAAGAGAGCACTTTCAAATAATTCAAATAATTTCTTATGTATTTACGCTGTGTCTGAGTGCAGCGTATTTTTGTTTTATTTTATAAGCAACAGATGATAAGTCCTCCAAATTTAAAATAAAAATGAATATTTTAATTTTTATTGCATAAAATAACAAAAAGTGCCATGTTTTCAGACACGTTTTTTAGTTTTTAGATCCATTTTTCACTTTTTAAATATTCAGAAATAGTATATATTGGAATGACTCTGGCTTTTGGCATGAAATGAAAACAAACATGTCTGATTACAAACATATTTTCTCCTGCAGAGAGCTGTAAACAGGCACTGTGTAGAGAAGAGATGTTTCGAGACTTTGTGCAGCATCTGGAACAGGAAATGCCTCTGACGGAGAAAAGAGTCGCAGTGTACATGCTGTCTGTATTGGTTGCCAACAACAGTAAGTCTCACCATAAAACTTGTGTCAAAACTCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa615
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 |
---|---|---|---|---|---|
ENSDART00000081468 | Nonsense | 208 | 814 | 6 | 19 |
ENSDART00000142270 | Nonsense | 208 | 814 | 8 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 6924733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 7502423 |
GRCz11 | 18 | 7461358 |
KASP Assay ID:
554-0525.1 (used for ordering genotyping assays)
KASP Sequence:
AGATAAAGCCCTGGCTGCAAGAAGTGGCATTACCCAGGGCAGAGCTGGCA[C/T]AACCCTTATGCTCATTTATTGGAATGACTGTGGCAAACAATCGTAAGAAC
Long Flanking Sequence:
AGCGTCTGGTTTTAGACCACAATAAGCCATTAGTTTGGTGTAGGGTCGCTTTTTGTTACCAATACAGCATCAATTCATCTTGGGAATAATACTAAGTCCTGCACAGTGGCTGGATGGATTTTGAGGCATTCTTTTTGGAGAGTTGTGGCCAGGTCACCCCAAAGTGGCTCAATAATATTTAGGTCTGGTTATTGTGCAGGCCATAGGAGATGTTCAACTTCACTTTCGTGTTTACCAAACCACTCTGTCAACAGTCTTGCTGTGTGTATTGGTGCATTATCATCTTGATACACGGCACCGCCTTATATGTATATGTATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAAATACATATTTTCACAACCTGATTGTTTTTATTTCACAGAGGAGAATCAGAACGTGTGTATGAGTGTTTTTCCTGAGATAAAGCCCTGGCTGCAAGAAGTGGCATTACCCAGGGCAGAGCTGGCA[C/T]AACCCTTATGCTCATTTATTGGAATGACTGTGGCAAACAATCGTAAGAACATCAGCAAAATAACTCCATCTTACGTGCTCATTTTCTCATCGCATGTGAATCTGTATTTTTCAGCCTGTGCTCAGGAATATTTTGTGTCAGTGGGAGGCCTGGATTCACTCTCAGACACTCTTACCCGAGTTTTATCTCAGTCTACACACAGTGCTTCTGTTTGTAAGATGGCTACGATAATCACTAAAACACTTTCTGCCTGCATCTCTAATAACGGTAAGACACATGCATGCACACCCCAATATAACCCCAAATATAATACTGGGTTGATTAGGGTTTTCAGTTTCCTTTCTCTTTCTGTCTCAGAGCTGTTGGGATCTTCTTTATCAAAGCTGAGGGTTATCCCAGGACTACTGCGTCTGTTATCTAGCCCAAACCTTGATCCACAAGATCAGCTCGCTGTGGTGTTAACGACTGGACACCTCACAGATGCCTGTGGTCAGTTTTTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa23225
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 |
---|---|---|---|---|---|
ENSDART00000081468 | Nonsense | 725 | 814 | 17 | 19 |
ENSDART00000142270 | Nonsense | 725 | 814 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 6937543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 7515233 |
GRCz11 | 18 | 7474168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTTCCTTTCCCCCTTATCCTGCATTTTCTCTTAGGCCCTGACGTGAAA[C/T]AGTGGACGGATCACAGACATCTCAAGAAAAGCTCTGAAGACGCTCGCTCC
Long Flanking Sequence:
ACTGATGTAAACATCCCAAGCTTGTGGTTTGTCACTTCCACCTAAATAGATAGATGATTTTTTTTTCACGTCATCTCATACTTTAGGCATCAAATATTGACCAGTCAACTGCTTTCTATTTCTAAAATGTAATTGTAAAATATAATTGTTAATTGTAATTTTGTAAATTGTAAAATATAATTATAGTTTACTGGCATTTCTATTTGAAGCCATCATATTGAGTAAGAATGTCATAAAAGAGCATATGTGTAGAGAAGATGGCATACTTGATTATGGTATTTATACTGTGGCATACTAGAGTACTGGGTTCTATAAAGCATATGCACTTTTACACTGCCCACTAAATCATTCTAAAGATCAATGTACCTCCTCGCTTCCCTGTGCAAGTCTAACCATTTGTATTGCTTTTGCCAGCATGGACACATTTAGTATAGTTTGGTTCATTAATTCCACTTCCTTTCCCCCTTATCCTGCATTTTCTCTTAGGCCCTGACGTGAAA[C/T]AGTGGACGGATCACAGACATCTCAAGAAAAGCTCTGAAGACGCTCGCTCCAAAAATGTATAGTACTATTCATAACTGTGATTTCACGATTACAACGATCTCATCTGAAGCGTTTTAAATTCTCTTAGTCAGTCTTGCTATTTCCAGATGTTTTTTTTTAACACAGAATCAAAGAAAATGCAAATGTCAATCCAATAACTTGCTCTTCCTCTGAAATAACTTTTATCATCTTTAATGATTTTCTTCTTTAGTCTTCAGGCAGACACAGAAAGAGGCAGAACTGGTCTGATAAAGAGCTGTGCTACCTCACCAAGGGTGTGAAGAGGTTTGGTCACTCCTGGAACACCATCCTCTGGAAGTATCCCTTCCACCCCGGGCGCACCAATGTAGACCTGGCCAAGAAGTTTTACCACATGCAGGTCTCCCGATGCTTACTTACGATTTTACCCTAAGAAGATGGGTATATTTTGCATAAACTTTATAGGCTATTAAAGGGGAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6499
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081468 | Nonsense | 804 | 814 | 19 | 19 |
ENSDART00000142270 | Nonsense | 804 | 814 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 6940654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 7518344 |
GRCz11 | 18 | 7477279 |
KASP Assay ID:
554-5398.1 (used for ordering genotyping assays)
KASP Sequence:
CTAATTCGNNTTTTTTTCTCTCTCTCTTTTACTGACAGAAAGCCAAAGCC[C/T]AGGGTGTGGATCTGTCTGTTGCARAGGCCTTATAAACATCACCGAYTCAA
Long Flanking Sequence:
ATATTAATTATATTTTTTTGTGATGTGTGACAGTTAAAATGTAAAGTGTGACTTCAACAACATATATGCATTTATTTATCTGTACTCTCCAAATACTTTCATGTTTGAAATAGTATAAAACATAAATATTAAAATAGATAAATAGATCCAGTGATAGTGGGCTCCAAACATGTGTTCATTAAAAGAAAATGCTAAAGAAACTGTGACTTCTTTGGTATGTGGCTGTCATACTATTACATAACACAATCTGTCCTTGGTGTCTTTTCAGTTCAAAATGACTAACAAGACATGGCTCAATAAAAATCTAGAAACATCGGATTTTAGCCAATTTGCAATGCCAGTACCTTCGAGACTTTGTTTGTATCTAAGCTTTATCATGGAAAGCAGAGCACATACTGTAACATATTCTTGCTTCCTGTTTCATTTCCCCAATAGTGTCCTCTCAGAATCCTAATTCGTTTTTTTTTCTCTCTCTCTTTTACTGACAGAAAGCCAAAGCC[C/T]AGGGTGTGGATCTGTCTGTTGCAAAGGCCTTATAAACATCACCGACTCAAGAAAGGACGTTATGTTATTGGATATTTTTGTTTTCAGACTGTATATTTTTGTGTATAACAAGGTTATTTGTTAGAAAAAAAAAAGAGTAATGTAAAAAAAGGAGAAAAAATATTTAGTTTCTTCTTAAATTTGGTATTTTTCCGTTGTTTATTGGAAATGGAATGCAGAACTGGTCACGCATATCTATTTGTTTTCAGTCAAATCTACTTGATTTGCATGGGAGTCTATACTGTATGTATATTTGTATAAAGCTGAGCAGTGATGCGTTCCCATTGCTCCTGTCATCTAAATTCATTCCTCTTATGGCTGAAGTACACAAAGCTCTGTTACACAAAGATAATGAGGCATGGCATTTCCTTTAGATTCCTACAAACGGAAGCAGCTTAATATTTCATCAAACTTCGCTACACATTCAGTACAATAAACACAGTGAAAAGATGTTTGTTTAC
Associated Phenotype:
Not determined