ZMP
ENSDARG00000044212
Ensembl ID:
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 15 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23573 | Nonsense | Available for shipment | Available now |
sa23574 | Nonsense | Available for shipment | Available now |
sa23575 | Nonsense | Available for shipment | Available now |
sa36888 | Nonsense | Available for shipment | Available now |
sa32251 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23573
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 |
---|---|---|---|---|---|
ENSDART00000077550 | Nonsense | 1375 | 2343 | 25 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 39093145)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37957128 |
GRCz11 | 19 | 37544248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAAATAATTGAGAATCTTGAAAGCCTTCGAGAAGAGGCAACTAGAGAA[A/T]GAGCGACAGAAACAGCTCAAGCAACAAGGAGAGATTCTGAGGAATTAATG
Long Flanking Sequence:
AAAAGGCTAGCAAAATGGCTTGGAGTACAAAACATGAACCAGAAATGAGAATGCAGAGAGAGGTTAGTGTTGAAGAGGAGTCAGTGGAAAGGCAAGATATGAGTGCTAACATGCAGAGAATGATCCTGGAAATTGAGCATGCCAGAGAAACTCTTAGAGGGATGAAGGATGAAGTCCAGGCAGCCAGAAAAGAAAGGTCTGAACTGGAGAACATGAAGCTTGAATTCTTAACCATGAAAAAGAACATGGAAAAAACTTATGAGCAGCAGAATGATGAGATACAAAAAGAGAAACAGCAAATAGAGAGTAGCAAAATGTTGCTAAGTAGAGAGAGAAATGATCTTGAGCAGAACAGGGCTGATTTGGAGAGACAAAAACAAATAATGGCATTGGACAAACAAAAACTCCTTGCTGAAAATGAATTACTGGAGAGAGAAAAGGCTGACGTAATAAAAATAATTGAGAATCTTGAAAGCCTTCGAGAAGAGGCAACTAGAGAA[A/T]GAGCGACAGAAACAGCTCAAGCAACAAGGAGAGATTCTGAGGAATTAATGCAGAAAATGGAAGCACTGAGCATGGAAGACTTCCAAGAAGCAAGTAAGAATCAGATGGTCGAACTAAAGAGACAGATAGACAAACTGATAGAGTTGAAGGCTGATCTGCTACAACAGCAGACAGAACTTAAGAAAACCAAAGCAGATTTAAAACAACAGATGGATGATCTTGAAAAAACAAGGTCTGAAATATTAAAACATGAAAAGGACACAGACAGTAAAACAAGAGAATTGGAGCTGATAGAAATCCAAAGACAGAAAGACGATCTAGAAACAAGAATTCAGAAATTGACCCTTGAGAAGAGAGATCTGGAGGTCCTGAGGTCTGAGATTGTCCTAGAAAAGAAAGACCTGGATCAGAAGATGAAGCAAGTGATAAGAAAGAGGGACGAGATGGAGAAAATCAGATCTGATATAGCAAATGCCACAGAGGAGATCAACAGAGAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23574
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 |
---|---|---|---|---|---|
ENSDART00000077550 | Nonsense | 1858 | 2343 | 33 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 39103453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37967436 |
GRCz11 | 19 | 37554556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGAACAGCAAAGAAATAGTTCAGAAATTAATGGTTGAAGTGGAGGAA[C/T]AGAGAAAAGACATTCGGCTCCAGAAAGAAGAACTTGACATTGAAAGACAG
Long Flanking Sequence:
ATCATAAATGGACACAGTTACAACAGAGGATTGATGAATTTGATGCTCAAGTTAGCAAACAAAAGGAAGAAGATTTAACGAAACAGAAGAAGATGGAAGAAGAAAGAAAAAGTCTAGAAGAAACCAAAATTAAAATAATCGAGATGAAGACTAAAACTGAGCCGGAAAAGATCAAGAAAGAAAAAGAGAAAGAAGAAGAAGAAGTAATGAGAGCAAAAGTAGAGATGAAGAAAGAAGAACTTGATCAGATTAAGAGCCAACTTGAAAGAGTGAGATCTGAAATAGATCATGAGCAGAAGAAACTAAATGATGACAAGAAGATGATTGAGCAGGAAAAAGAAGACCTGGAGAAGATGAAGTCTGAAATAATGAAACAAAGACAGCAGATGGAAGAAGAGAGATCAGAACTTGACAACAAGATAAAGCAGACAGATCTAGAAAGACATGACATTGAGAACAGCAAAGAAATAGTTCAGAAATTAATGGTTGAAGTGGAGGAA[C/T]AGAGAAAAGACATTCGGCTCCAGAAAGAAGAACTTGACATTGAAAGACAGAAAATTGCAGATGAACAAGGTCTTGTGGTTCAAAACAAGGCTAAACTGCAAAATGAAAATGAACGAATCAAAGAAATGGATGAGGAAATAAAGAAAGAGAAAGAAACACTGAAGGAAATGGAAGCTCATCTACGGAAGGAGAAAGAAGAAATGAGGAGCGTCATTGAAGAAACACAAAGACGACAAAAAGAGGATCTGGAGAAGATGAGCACAGACGTAAATAAACAAAACCAAGACCTGATGAACCAAAGAGACCTTCTAAAACAAGAACGAGAAGAAATAAATCATAAATGGACACAGTTACAACAGAGGATTGATGAATTTGATGCTCAAGTTAGCAAACAAAAGGAAGAAGATTTAACGAAACAGAAGAAGATGGAAGAAGAAAGAAAAAGTCTAGAAGAAACCAAAATTAAAATAATCGAGATGAAGACTAAAACTGAGCCGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23575
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 |
---|---|---|---|---|---|
ENSDART00000077550 | Nonsense | 2066 | 2343 | 35 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 39104632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37968615 |
GRCz11 | 19 | 37555735 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAGACCTTTTAGAACAAGAAAGAGAAGAAATAAATCATAAATGGAAA[C/T]AGTTACAACAGAGGATTGATGAATTTGATGCTCAAGTCAGCAAACAAAAG
Long Flanking Sequence:
TGGAGAAGATGAAGTCTGAAATAATGAAACAAAGACAGCAGATGGAAGAAGAGAGATCAGAGCTTGAAAACAAGATAAGGCAGACATATATAGAAAAATGTGACATTGAGAACAGCAAAGAAATAGTTCAGAAGTTAATGGTTGAAGTGGAAGAACAGAAGCATGAGATTCAATTCCAGAAAGAAGAACTTGACATTGAAAGACAAAAAATTGCAGATGAACAAGATCTTCTCATTCAAAATAAGAGTGAACTGCAAAATGAAAATGAGCGAATCAAGAACATAAATGAGGTAATAAAGAAAGAGAGAGAAACACTGAAGGAAATGGAAGCTTATCTTGAAAAAGAGAAAGAAGAAATGAAGAGCATCACTGAAGAAACACGACGACAAAAAGAAGATCTGGAAAAGATGAGCACACACATAAATGAACAAAAACAAGATCTGAGGAGCCAAAGAGACCTTTTAGAACAAGAAAGAGAAGAAATAAATCATAAATGGAAA[C/T]AGTTACAACAGAGGATTGATGAATTTGATGCTCAAGTCAGCAAACAAAAGGAAGAGGATTTACCAAAAGAGAAGGAGATGAAAGAAGATAGAAAAAGTCTAGAAGAGACCAAAGCCAACATCCTCGAGATGAAGACTAAAGCTGAGCCAGAGGAGATCAAGAAAGAAAAAGAAAAAGAAGAAGAAGAACAAGAAATGAGAGTAAAAGTAGAGATGGAGAGAAAAGAAATTGAGCAGATAAAGAGCCAACTCGAAAGAGTGAGATCTGAAATGGATCATGAGCAGAAGAAACTAAATGATGACAAGAAGATGATTGAGCAGGAAAAAGAAGACCTGGAGAAGATGAAGTCTGAAATAATGAAACAAAGACAGCAGATGGAAGAAGAGAGATCAGAACTTGACAAGAAGATAAAGCAGACAGATCTAGAAAAACATGACATTGAGAACAGCAAAGAAATAGTTGAAAAATTAATGGTTGAAGTGGAAAAACAGAAGCATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36888
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 |
---|---|---|---|---|---|
ENSDART00000077550 | Nonsense | 2195 | 2343 | 37 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 39105475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37969458 |
GRCz11 | 19 | 37556578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTAAAACAAGAACGAGAAGAAATGAATCATAAATTGACACAGTTACAA[C/T]AGAGGATTGATGAATTTGAGACTACAAGTAACATTCTTGTGACAACCAAA
Long Flanking Sequence:
TGAAGTCTGAAATAATGAAACAAAGACAGCAGATGGAAGAAGAGAGATCAGAACTTGACAAGAAGATAAAGCAGACAGATCTAGAAAAACATGACATTGAGAACAGCAAAGAAATAGTTGAAAAATTAATGGTTGAAGTGGAAAAACAGAAGCATGAGATTCAATTCCAGAAAGAAGAACTTGACATTGAAAGACAAAAAATTGCAGATGAACAAGATCTTCTCATTCAAAATAAGATTGAACAGCAAAATGAAAATGAACGAATCAAAGAAATGGATGAGGAAATAAAGAAAGAGAGAGAAACACTGAAGGAAATGGAAGTTAATCTACAAAAGGAGAAAGAAGAAATAGAGAGTGTCATTGAAGAAACACAAAGACGAAAAGAAGATCTGGAGAAGATGAGCACAGACATAAATGAACAAAAGCAAGACCTGATGAACCAAAGAGACCTTCTAAAACAAGAACGAGAAGAAATGAATCATAAATTGACACAGTTACAA[C/T]AGAGGATTGATGAATTTGAGACTACAAGTAACATTCTTGTGACAACCAAAATGGAAGAAAAAACAGAAATGGATGAAAAACTTCAACAGGCTATTAAGGAATATGAAAGCATCATAGAAGAAACAAACAGGAAAAGAACTGAGCTAGAAGAAATTGAGGTTGATCAGTCACAACAAAATAAAAACGTTGAGACCATGAAAGATCTTTTGGAGAAAGAGAGAAAAGACACTGAAAAGGAAAGAGAAGAGTTACAGAAACAAGCTGATGATCTGGAGATGCAAATGATAGAGCACGGAGACAAAGAGGAGATGAGCAAAAGATCACTGGATGAAGAAAAGAAGCTTTTAGAGCAGAAGGCTAATGAAATCCTGAGACAGAGAGACGACTTAGAGAAAGAAAAAGAGGACATGATGAAGAAATGGAACGAGCTGGATGGTCTTCAGAAGGAAATACAAAACCAAAAGAATGAAATGGAAGAAATCAAATGTGAGTTAGAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32251
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077550 | Nonsense | 2235 | 2343 | 37 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 39105595)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 37969578 |
GRCz11 | 19 | 37556698 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATGAAAAACTTCAACAGGCTATTAAGGAATATGAAAGCATCATAGAA[G/T]AAACAAACAGGAAAAGAACTGAGCTAGAAGAAATTGAGGTTGATCAGTCA
Long Flanking Sequence:
AAAAATTAATGGTTGAAGTGGAAAAACAGAAGCATGAGATTCAATTCCAGAAAGAAGAACTTGACATTGAAAGACAAAAAATTGCAGATGAACAAGATCTTCTCATTCAAAATAAGATTGAACAGCAAAATGAAAATGAACGAATCAAAGAAATGGATGAGGAAATAAAGAAAGAGAGAGAAACACTGAAGGAAATGGAAGTTAATCTACAAAAGGAGAAAGAAGAAATAGAGAGTGTCATTGAAGAAACACAAAGACGAAAAGAAGATCTGGAGAAGATGAGCACAGACATAAATGAACAAAAGCAAGACCTGATGAACCAAAGAGACCTTCTAAAACAAGAACGAGAAGAAATGAATCATAAATTGACACAGTTACAACAGAGGATTGATGAATTTGAGACTACAAGTAACATTCTTGTGACAACCAAAATGGAAGAAAAAACAGAAATGGATGAAAAACTTCAACAGGCTATTAAGGAATATGAAAGCATCATAGAA[G/T]AAACAAACAGGAAAAGAACTGAGCTAGAAGAAATTGAGGTTGATCAGTCACAACAAAATAAAAACGTTGAGACCATGAAAGATCTTTTGGAGAAAGAGAGAAAAGACACTGAAAAGGAAAGAGAAGAGTTACAGAAACAAGCTGATGATCTGGAGATGCAAATGATAGAGCACGGAGACAAAGAGGAGATGAGCAAAAGATCACTGGATGAAGAAAAGAAGCTTTTAGAGCAGAAGGCTAATGAAATCCTGAGACAGAGAGACGACTTAGAGAAAGAAAAAGAGGACATGATGAAGAAATGGAACGAGCTGGATGGTCTTCAGAAGGAAATACAAAACCAAAAGAATGAAATGGAAGAAATCAAATGTGAGTTAGAAACTAAAAGGATTGAAATTATTAAAGAACAGAAACGACTAGAGGAGAGTTTAAACACTGTGAATGAGGAGAGACAATATCTGGAGATCGTGAGGGTTGACTATGAAAAACACCAGCAGCAAATA
Associated Phenotype:
Not determined