ZMP
zgc:77294
Ensembl ID:
ZFIN ID:
Description:
Coiled-coil domain-containing protein 102A [Source:UniProtKB/Swiss-Prot;Acc:Q6NZW0]
Human Orthologue:
CCDC102A
Human Description:
coiled-coil domain containing 102A [Source:HGNC Symbol;Acc:28097]
Mouse Orthologue:
Ccdc102a
Mouse Description:
coiled-coil domain containing 102A Gene [Source:MGI Symbol;Acc:MGI:2686927]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9364 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17078 | Nonsense | Available for shipment | Available now |
| sa2342 | Nonsense | F2 line generated | Not yet available |
| sa5420 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa9364
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011324 | Essential Splice Site | 443 | 581 | 6 | 9 |
| ENSDART00000135322 | Essential Splice Site | 443 | 581 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 30128872)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 28521214 |
| GRCz11 | 7 | 28792364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACACCGACCTCAAGACCATCCAGAGTGAGCTGTTTGAGAGGAACAAG[G/A]TGAGGGAAGGAGAACGCCRTCCACACAGCACAAATAATCMCAAACGTACC
Long Flanking Sequence:
TGATTTATACAACCTAGATTGTGTCAAAACAGCATTACAGAGATAAACAGGCAACAAAGGAAAGGGAGAAATGAAATTTCATCATTGTGAAACAAATTCAATACATCAGAGCACATTCAGTTCTGCAGAACACTGGTTTTGTTCCAGTTATTTCAGTGATGATTCAGTTCAGCTCAATACGAATGCCAGCGTTGATGGATGTGAATTTACTCTTTCATTGCCCTCAAACTTTTTCCTAATGTGTTCTCACATCTCTCTTCCCTCTCCTGTCCTCCTGGATGTCTGTGCAGATGGAGCGTCTGCAGGTGGAGAATGCAGCAGAGTGGGGTCGTCGGGAGCGTCTGGAGACGGAAAAGCTGGCTCTGGAGAGGGAAAACAAAAAGCTGCGCACCCAGATGGAAGACCTGGAGGAGCAGCTGGCACGCAAGCGCAGGCAGGCCGCCAGCGCCCTGGACACCGACCTCAAGACCATCCAGAGTGAGCTGTTTGAGAGGAACAAG[G/A]TGAGGGAAGGAGAACGCCGTCCACACAGCACAAATAATCCCAAACGTACCCGTAAGCATTTTTCAACATCTCAGATTCTGCTGTACAGCGCTTGAGAGGTGAATGAAGTGTGGCAGCAGTTGCAAAGTATCTAAGCCCTTTTTTGTATCCGCTATCAAGATGATTTTTGGTTGATTGGAACACAAGTAGACAAGGTTGACAGTTTGTCTCTTTTGTGCAGTATCTGTGATCTTTTAATCTAATATTGCAAAACACTTGCACAGTTCACATGCTGTACAATTAAAACAAATCATATAAACAATTTAATTGGTGAACAGTTTTACAGTTTTAGATTTTTTTGTTTGTTAACTGAGTGATACAATTACAAATATAGAATGCATTTCTTTTTATTTTGTAATGCAGCATGTACACTGCCAGACAAATACCTTGTCGTTGATCCCAGTTGTAAGAGCAACAAATAGTAACTTGATTTCTAGTTGATCATTTGGAAAAGTGGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17078
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 |
|---|---|---|---|---|---|
| ENSDART00000011324 | Nonsense | 512 | 581 | 8 | 9 |
| ENSDART00000135322 | Nonsense | 512 | 581 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 30159482)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 28551824 |
| GRCz11 | 7 | 28822974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGCATTTGTTTCAGTTGGATGAGGCCCAYAATCAGACCAGAAAGCTA[C/T]AACGATCCCTGGATGAGCAGGTGGAGYAATCCGAGAATCTACAAGTTCAG
Long Flanking Sequence:
TAATTTTGCAGATTCCTATCGAAATTCTAAACTCTGGGATTCTAAATTCTGGAACTACCTGTACGTTTCAACGAAAATTATGCACACCCTCCAGCCAATCAGAATCAAGAATTTCAAAAAACCATGGAATATTATATTATATTATACAACATTGATTTTAGATTTAAAAAATGCATCAATATTAATTATTCTATGCTAGACATAACCACCATTATTAGATAAAAGAAAAATGTCAACCCATTACTTATCTGACTGTCAGACTAAATAACACTGCGTTAGTGACATGTTTAAATTAGCAAAATTCAAAGCCAAAAATATATTCACTATGCCACAGAAAACCAAATTTACATGTAACTTTGCTGTGCATAAATGTGCGTAATTCAGATCAGTGAACATAAGCTTCACTCAAGCTCTGTCTGTCAGCGGTAATGTTAATGGCCAAACTCACTATTTTGCATTTGTTTCAGTTGGATGAGGCCCATAATCAGACCAGAAAGCTA[C/T]AACGATCCCTGGATGAGCAGGTGGAGCAATCCGAGAATCTACAAGTTCAGCTGGAACACCTACAATCCAGGTAACCAGACCGATATACTGTATATGCACACTCGACAGTCTCTCTGTAGCAGGTAAACTGTTGTGAAGTGTTTTTCAGAATGTTGTGTTCCGTTCGGCTCTCTTTTGATCGGTAATGAATGCAGGATAAGCTTCTCTGTTACACAACATCATGAATAAGATGGCAGGTTTATAGTGTAAACTGTCAGCGAGTCCCTCTCTCATTATTCTGCTTGCATTCAAGCTTGCACCTACCAGCAGCCAATCCCTGGCTGCCAGGCTGTGGGTTACCGTAGTAACAGGGAGACTGGAAGCAGTGTTGTGGGCGCAGCTGGAGAGAGCAGTGATGGGCATGTCGACACGCCACTGTTTATAAGAACTAGTCATGATACTGGATTTTCTAACGTAAATTAGGAAATAATCTAATAGCATTCATTAAAATTGCCATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2342
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000011324 | Nonsense | 521 | 581 | 8 | 9 |
| ENSDART00000135322 | Nonsense | 521 | 581 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 30159509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 28551851 |
| GRCz11 | 7 | 28823001 |
KASP Assay ID:
554-2459.1 (used for ordering genotyping assays)
KASP Sequence:
CCCATAATCAGACCAGAAAGCTACAACGATCCCTGGATGAGCAGGTGGAG[C/T]AATCCGAGAATCTACAAGTTCAGCTKGAACACCTACAATCCAGGTAACCA
Long Flanking Sequence:
TAAACTCTGGGATTCTAAATTCTGGAACTACCTGTACGTTTCAACGAAAATTATGCACACCCTCCAGCCAATCAGAATCAAGAATTTCAAAAAACCATGGAATATTATATTATATTATACAACATTGATTTTAGATTTAAAAAATGCATCAATATTAATTATTCTATGCTAGACATAACCACCATTATTAGATAAAAGAAAAATGTCAACCCATTACTTATCTGACTGTCAGACTAAATAACACTGCGTTAGTGACATGTTTAAATTAGCAAAATTCAAAGCCAAAAATATATTCACTATGCCACAGAAAACCAAATTTACATGTAACTTTGCTGTGCATAAATGTGCGTAATTCAGATCAGTGAACATAAGCTTCACTCAAGCTCTGTCTGTCAGCGGTAATGTTAATGGCCAAACTCACTATTTTGCATTTGTTTCAGTTGGATGAGGCCCATAATCAGACCAGAAAGCTACAACGATCCCTGGATGAGCAGGTGGAG[C/T]AATCCGAGAATCTACAAGTTCAGCTGGAACACCTACAATCCAGGTAACCAGACCGATATACTGTATATGCACACTCGACAGTCTCTCTGTAGCAGGTAAACTGTTGTGAAGTGTTTTTCAGAATGTTGTGTTCCGTTCGGCTCTCTTTTGATCGGTAATGAATGCAGGATAAGCTTCTCTGTTACACAACATCATGAATAAGATGGCAGGTTTATAGTGTAAACTGTCAGCGAGTCCCTCTCTCATTATTCTGCTTGCATTCAAGCTTGCACCTACCAGCAGCCAATCCCTGGCTGCCAGGCTGTGGGTTACCGTAGTAACAGGGAGACTGGAAGCAGTGTTGTGGGCGCAGCTGGAGAGAGCAGTGATGGGCATGTCGACACGCCACTGTTTATAAGAACTAGTCATGATACTGGATTTTCTAACGTAAATTAGGAAATAATCTAATAGCATTCATTAAAATTGCCATTTTTAATGCATGTCTTAATTTGTTAAAGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5420
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000011324 | Nonsense | 540 | 581 | 9 | 9 |
| ENSDART00000135322 | Nonsense | 540 | 581 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 30172501)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 28564843 |
| GRCz11 | 7 | 28835993 |
KASP Assay ID:
554-3502.1 (used for ordering genotyping assays)
KASP Sequence:
RATTATTTATAACAAAAAWTGTTTAAATTGTTTTTAGGCTAAGGCGTCAG[C/T]AGAACCCTGGYCTCTTTGGCAAAATGAGGACMTCAGCTTCATCACGTTTT
Long Flanking Sequence:
GACATGTGATGTCAATTGTAATGGCTGCAGGATCTTTATTTTTGAATAATTTTATTATCGGTGGTGCAGTGGGTAGCATTGTTGCCTTACAGCAAGAAGGTCGCTGGTTCGAGTCTCGGCTGGGTCAGTTGGTATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCGTGTGGATTTCCTTCGGGTGCTCCAGTTTCCCCCATAAGTCCAACAAAATGCGCTATAGGTGAATTGGGTAAGCTAAATTATCCATAGTGTATGTATGTGATTGAGTGTATCGATGTTTCCCAGTGATAGGTTGCAGCTGGAAGGGCATCCACTGTGTAAAAAAATATGCTGGTTAAGTTGGCGGTTCATTCCGCTGTGGTGACCTTTGATTAATAAAGGAACTAAGCCGAAAAAAATGAGTGAATGAATGAGTTTTATCATCATCCGTTTTAAAATAATCAATTATTTATAACAAAAAATGTTTAAATTGTTTTTAGGCTAAGGCGTCAG[C/T]AGAACCCTGGCCTCTTTGGCAAAATGAGGACATCAGCTTCATCACGTTTTGGCCCTGAAGATGCAGACGGCCCTCCTAGCGACCCTGATGAAGATGAGGAAGAAGAACTGCAGCTCCAAATCCCCTGAACCCTTCACTGCAGACCTGGGAATGACTGAAGACTCACCGATCTCACTCGAGCATTTCACCTTCCCCTTCATTTCATCTCTCAGCGAAATCTAGAAGAGGACTTCACGACCCTCAGCAGACAGATAAACACAATCCTTTTTCAGTAGCCTATAATAAATGTGTGCCAGGGCCAAAGTACTGTCTGAAGCCTAAGAAAAACATTGCTGGTTCTAGTCCAAGTTGGCACATAGGTTATTGATAGACAAATATCAGACCCATTTATTTGACTTTTGAGGGTCCATTTGAAGCCTAGTGATTCCTATTATTCACATAAGCAGACACATGTGCTGGCACACATTGTAAACGCATTAGAGCGTCCTCAAACTTTCAGA
Associated Phenotype:
Not determined