ZMP
zgc:175202
Ensembl ID:
ZFIN IDs:
Description:
Zgc:175202 protein [Source:UniProtKB/TrEMBL;Acc:B0JZN4]
Human Orthologues:
CCDC88A, CCDC88C
Human Descriptions:
coiled-coil domain containing 88A [Source:HGNC Symbol;Acc:25523]
coiled-coil domain containing 88C [Source:HGNC Symbol;Acc:19967]
coiled-coil domain containing 88C [Source:HGNC Symbol;Acc:19967]
Mouse Orthologues:
Ccdc88a, Ccdc88c
Mouse Descriptions:
coiled coil domain containing 88A Gene [Source:MGI Symbol;Acc:MGI:1925177]
coiled-coil domain containing 88C Gene [Source:MGI Symbol;Acc:MGI:1915589]
coiled-coil domain containing 88C Gene [Source:MGI Symbol;Acc:MGI:1915589]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17648 | Nonsense | Available for shipment | Available now |
sa22541 | Nonsense | Available for shipment | Available now |
sa22542 | Essential Splice Site | Available for shipment | Available now |
sa2750 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17648
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 |
---|---|---|---|---|---|
ENSDART00000110103 | None | None | 983 | 3 | 30 |
ENSDART00000112470 | Nonsense | 78 | 1603 | 3 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 48639801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 46717460 |
GRCz11 | 14 | 45704752 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TKGTTGYTTGYTTGGGTTTTTTAWYCAGTGATCCCAATCCAAAGGTAGAA[C/T]AAATCTACCACAATGTGGGCGACGACAAGATTCGCAGAGTGCAGAACTTT
Long Flanking Sequence:
TACCATAACAGATAAATTCATGTACTTTACTATAGTGTGGTTGAAAGAAAAGTGTTTACTATAAACTATAAATTACTATTGTATGTTTTCTTGTTGGAGCAACTGAAGTAAACTTAATGTAAGCATTGACAACAGAGCACAGAATCTTGATGTGAACAGAGTGTTTATGATTTAAGGTGCATCTGTTTGAGGGTATTGTCGGTGAGGAAGAGGATGGATCACTCTTTCCGGAATACATGGAAGTAAACATCAGCTCCCAGAATGCAGTAAGGCAGTACCTGACGCTCACCAATGGAGTTTACCTCAATGAGGTCATGAGGATCATGTAAGACGGACTCGTTGTAAAAATAGAAAACATTTCCTCAGTTTTGTTTTTATATAATGTTGTTAAAAAGAAAGCTATCATTGATTACAGTTCAACAGTGACTCGTCATCTAATGGCAACATTTTTTGTTGTTTGTTTGGGTTTTTTATTCAGTGATCCCAATCCAAAGGTAGAA[C/T]AAATCTACCACAATGTGGGCGACGACAAGATTCGCAGAGTGCAGAACTTTTCCATCCTCAATCGCCACTTAAGATCTTACTATCAGGTACTGAAGTAACATATCAGTCATATTATTATGTGACATTATGTCTATGTATCCAGTACATTTCACTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTTATATTATATTATATTAAATTATATTATTTTATATTAAATTATATTATATTATATTATATTATAATATTTTATATTAAATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTTATATTAAATTATATTATATTATATTATATTATTTTACTTTATATTATATTAAATTATATTATTTTATATTAAATTATATTATATTATATTACTTTATATTAAATTATTTTATATTATATTATATTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22541
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 |
---|---|---|---|---|---|
ENSDART00000110103 | None | None | 983 | 7 | 30 |
ENSDART00000112470 | Nonsense | 211 | 1603 | 7 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 48654898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 46732557 |
GRCz11 | 14 | 45719849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGACTGAACGGAGCCGAGCTGCAGATTCTTTTCTGCTCAATGGCCAAA[C/T]AGATCCAGAACCTGCTAGCCCAAAGAGACACACAGCTGGAGGTCAGAGAA
Long Flanking Sequence:
TCAACTGGTTCACTTGGGACTCGAATCAGTGACCTTCTTGCTGGAAAGCACAGGTGTCAAATGCAGCTCCTGGAGAGCTGCAGCTCTGCACAGTTTAGCTTTAACCCTAATTAAACACACCTGTTCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGGTAGGTGTGTTGAAGCAGGGTTGGAACTAAAGTGTGCTGAGCAGCAGCCACCATGCCACCCGTAATCGTTTTTACAAATTTAAGTGGATTGAACATAAAACAATTAGGTTTCCCCCCCCCAAAAAAACCTTAAGAATTGAAGTTGCTTTAACTCATTTTACATAAGTAGTTTAAACAAGCAGCAGAATAATTTTTTTCAGTGTGTATATGCCTAAATCATACCTTTTGATCATTAGGTGACCCAGGACCGAAGTGCAGTCCTTCCTCTGGAGTTTGGAGATCTGTGTGGACTGAACGGAGCCGAGCTGCAGATTCTTTTCTGCTCAATGGCCAAA[C/T]AGATCCAGAACCTGCTAGCCCAAAGAGACACACAGCTGGAGGTCAGAGAACAACTGATCTTCACAATCTGGCATTTTCATATGCAAGTAGGTGAGATCTGATTTTTGCTTTTGAATGTCGTGTCTGATATTTAGAGGATAGCAGAGCTTTGTCAGGAACAGGAGTCATCTGTAAATCATATAAACACATCGAGCGGGTTTGGAGATGGATCTCCTGAAGGACTGGCCTTTCAGCTGGCGGAGAGCAAAGCTAAACTACGGCGACTCAAGCAGGAGCTGTGAGTTTATTTTTATAATGGTTTATGTCAGTGTTTCTCAACCACGTTCCTGGAGAACCATTTTCCATGTCTCCTTAATCAAACACACCTGATTCCGATCATTAGCACAGACTGAAAGACTTGTGTGATAGATGAAAGAGACATTTAAAACAAGCAGTGTTGGTTGTCCTACAGGAACATGGTTGAAAAACACTGTTTTTTTATGAAGATATGTGTCAGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22542
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110103 | Essential Splice Site | None | 983 | 13 | 30 |
ENSDART00000112470 | Essential Splice Site | 500 | 1603 | 13 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 48667247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 46744906 |
GRCz11 | 14 | 45732198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACGCCGAGCTGAGACGGCGACTGGAGCTCCTGCAGGCTGAACAAGAG[G/A]TCAGCGGATGTTTGGCCAGATTTATCCTCAGGCTACCACCTGGCTGATGT
Long Flanking Sequence:
TGGACGGGTCAATCAGTGCTTTTGAAAACACTGTCGGTTGGGTTTAGGGAAGGAGGAAGGTGGGTCAGTCGATCGGTCAGTCGACAGCGGCCTCTGTTGGATTTTCAGAACAGCAGGCGTGAATAGCACGCGAATGGGAAATTTGAGATCTCAAAAAGCGTACACAGCGGCAACTGGTGGATTTGCGAAAACAAAAACTGCAAAAAAACGTAGCTCCTGGAACGTATTTGGCATTCTCCAAAAATGTAAATAGGGGAACAGAATGAGCTTTCAGAATGAGCTTGGATTGTTTTTTTAGAGTGTAAGTAGGTTTATGAAAAAATGCCCTTGGAAATCAATCCTGACCTTGAAGTGTGTTTGTGCGTCTCTCTTACTTTGGTTCAGATCTGAAGCCCCTGAGTGAGGAGGTAAATGAGGCTTCCTCGTTGAGGCTTCTGGGAGCTGAAAACGAGAACGCCGAGCTGAGACGGCGACTGGAGCTCCTGCAGGCTGAACAAGAG[G/A]TCAGCGGATGTTTGGCCAGATTTATCCTCAGGCTACCACCTGGCTGATGTTAATTCTCAGGTCTCCCATGTACTGTATGTCTCTCTCTCTCTCTCTCACACACACAGGCTCAGCAGGGCCCAGAGAAAACCCAAGAGCTCCAGAGACTCACAGAGCAGCTCTCACAAAAGCTTCAAAACACCCTCAAGGAGGTGAGCCACTTCTGACAGATTTAAGGAGCGTTTTTTCCTTCTTTTTTCTGTGTCTACTGTCATTTTGTCCCCGTTTCAACTTTTTGAATCGGGCCCTGTCATTTCTCTTTTAACCGTTAGCTGGAGTGTCTGAAGAATGAAAATAGCAGCCTGAAGATAAATCTGGAGGAGACAAAACGCAAACGGGAAGAAGACCTAAAGACAGACAGAACAACCTCACAGGGAAAAGAAGGGAAAAAGCCAGTAATCCCAAGAGGGGAGTGTGAGGGAAATGACACGAGGAGAGAGAAACATGATGGAAAAGAAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2750
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 |
---|---|---|---|---|---|
ENSDART00000110103 | Nonsense | 908 | 983 | 28 | 30 |
ENSDART00000112470 | Nonsense | 1528 | 1603 | 27 | 29 |
Genomic Location (Zv9):
Chromosome 14 (position 48704138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 46781797 |
GRCz11 | 14 | 45769089 |
KASP Assay ID:
554-2868.1 (used for ordering genotyping assays)
KASP Sequence:
TGGGCAAAGGCAGAGGAGRAGTTTCTCAGTCCTTCAGTCCAGGAGACCAG[C/T]GATCTCAGCCTCGCATCCGCCTGCGCTCCTCTCAGACAGGAGCCTCAGCC
Long Flanking Sequence:
AACTGCTTTTATTCAAAATACAAAATACAAAATAAAACAAATAAGACTTTCTAAATAATCTAAAGAAATAATATTATCAGACACACTGTGAAAAATTCCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAAATAATAATAATTAAAGGAGGTTAAATATGTCTTACTTCTATTTTATATAAAAGTCCATAATGATCTTTACCTCACCAGGTAGAGAAAATCAATAAATAAATAAAATGAAAAAAAAAAAAAAAATGAAATAAAAATCTTTATTTTACAACTCACTTTCCTCTATTTGACCCCTCAGTTCATGACCAGGACCCCATCAGCGCTCCAGTCTCTCCAAGCCCGCTGAGGAGAATTTCATATCAAGTTGAAGAAGAGCAACCTAAAGCTAATCTGCGGACCGGACGCCGCAAACTGGGTTCTCGGCATGGCTGGGCTCTGGGCAAAGGCAGAGGAGGAGTTTCTCAGTCCTTCAGTCCAGGAGACCAG[C/T]GATCTCAGCCTCGCATCCGCCTGCGCTCCTCTCAGACAGGAGCCTCAGCCCTCTGGGAGCACGACAGCAGCCCTACACCCAGCCAGGACAGCCCCAGTGAAGAGGGCAGAGGTAAACATGATGGTGGAGAGGGGAAATTACATGCATTTGAAAAGATGCTTTTGTGGAAAATATGTAACTGAAAAGATGAATTTGAAAACAAGCATTTGTGGAAAATAAGCATTTGAAAACATGCATTTGTGCAAATTATGCATTTAAAATATGCATTTATGGACAATATGCATTTGAAAACATGCAATTTTGAAAAATTTGTAATTAAAAATATGCATTCAAAAATATTCATTTGTTGAAAATATGCATTTGAAAATGCATTTATGGACAATATGCATTAGAAAACATGCATTTTTTGAAAAATATGCATTTGAGGAAAATATGCATTTATGGAAAATATGCATTTAAAAATATGCATTTGTGAAAATATACATTTAAAAATATGCATT
Associated Phenotype:
Not determined