ZMP
zgc:158569
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC325276 [Source:RefSeq peptide;Acc:NP_001076465]
Human Orthologue:
CCDC19
Human Description:
coiled-coil domain containing 19 [Source:HGNC Symbol;Acc:17229]
Mouse Orthologue:
Ccdc19
Mouse Description:
coiled-coil domain containing 19 Gene [Source:MGI Symbol;Acc:MGI:1919120]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18014 | Nonsense | Available for shipment | Available now |
sa23333 | Nonsense | Available for shipment | Available now |
sa23334 | Nonsense | Available for shipment | Available now |
sa13539 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18014
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 |
---|---|---|---|---|---|
ENSDART00000098292 | Nonsense | 97 | 497 | 5 | 12 |
ENSDART00000127379 | Nonsense | 143 | 345 | 5 | 8 |
The following transcripts of ENSDARG00000068103 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 33525682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35206957 |
GRCz11 | 18 | 35181830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGTAAATCTAGTTMTTTTGATGTTGTAAGGWTGCTGYAGAGCAGAGG[A/T]AAGCACAAATGCGCCAGGCTGACYTRTCTCGTCAGAAGAACCAGAACCTC
Long Flanking Sequence:
TACTACGAATGTCAAATTTAATGGAATTTTTGTTTAATTGCTTGGTCTACTAGAGATATCTTGTGATTCCTGATGTGCATTATGCATATGCGTATATGTATGCATGTGCATTTTTGGGGCCTATGAAAGATGATGAGATTTATTGCCTACTGTATAAAGCAGATCTCTGGAGAGTCTGGGACGGTCCTTATAATTTACCTAACATCACCAACTTAGTGCTGCTCATGGACTCCCTCTCTGCCATTTGTCATACACTGAAAAAAATAAATGATTTCTGCAAAAAACGTATATGGATTGAAGTTAAACAACTAAAATTTAGTAAATTTGTTTGTTTAAATTCCACACAAATAAATTGTTTACAACCACTTAACTTTTTTTTTTTTTTGTTAGTCCAAGGAATCATCTTTGAATCACTTTGTCATTGTACAAACAGTAAAAACTGTTATGTCCTTCAGTAAATCTAGTTCTTTTGATGTTGTAAGGATGCTGCAGAGCAGAGG[A/T]AAGCACAAATGCGCCAGGCTGACCTATCTCGTCAGAAGAACCAGAACCTCAGTGAGCTCGAAGCTGAGGCGAGGGACCGGGCCCAGTATCTATTGGAACGGGCCAACACCCTGAGAATGGAACAAGAGGACGAAGTCAAGAAGCTCAATGAGGTAAAAAGCACCAGACTAAAATGTCAAACTGTGAGCCACAAGTTGTTGCCAACATGTTGTCTTTCTGCTTGTTCAGCTGATTCAGAAAGTGCAGTGCCATGCTGTCCGGGATGTACAGATTCAGGAGAGGAAACTAAACTCTGCAGAGTGGCTGGCCGAGGAGAAGAGACTGGACGCCATGATGGAGGTGGAGCGCCGCCAGGCTTTAGAAGCTCAGGAACAAATTGAACAGCTTCGCAAACAGCAGAGGATTCAGTAAGCATGCTCACACTCTATATTCTGAACACACTGCAACACAATGTATTGCTCTCTACAGTTAATGGGTGGGGGTAATTAAAGGGGGAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23333
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 |
---|---|---|---|---|---|
ENSDART00000098292 | Nonsense | 195 | 497 | 6 | 12 |
ENSDART00000127379 | Nonsense | 241 | 345 | 6 | 8 |
The following transcripts of ENSDARG00000068103 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 33526052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35207327 |
GRCz11 | 18 | 35182200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTGGACGCCATGATGGAGGTGGAGCGCCGCCAGGCTTTAGAAGCTCAG[G/T]AACAAATTGAACAGCTTCGCAAACAGCAGAGGATTCAGTAAGCATGCTCA
Long Flanking Sequence:
CTTTTTTTTTTTTTTGTTAGTCCAAGGAATCATCTTTGAATCACTTTGTCATTGTACAAACAGTAAAAACTGTTATGTCCTTCAGTAAATCTAGTTCTTTTGATGTTGTAAGGATGCTGCAGAGCAGAGGAAAGCACAAATGCGCCAGGCTGACCTATCTCGTCAGAAGAACCAGAACCTCAGTGAGCTCGAAGCTGAGGCGAGGGACCGGGCCCAGTATCTATTGGAACGGGCCAACACCCTGAGAATGGAACAAGAGGACGAAGTCAAGAAGCTCAATGAGGTAAAAAGCACCAGACTAAAATGTCAAACTGTGAGCCACAAGTTGTTGCCAACATGTTGTCTTTCTGCTTGTTCAGCTGATTCAGAAAGTGCAGTGCCATGCTGTCCGGGATGTACAGATTCAGGAGAGGAAACTAAACTCTGCAGAGTGGCTGGCCGAGGAGAAGAGACTGGACGCCATGATGGAGGTGGAGCGCCGCCAGGCTTTAGAAGCTCAG[G/T]AACAAATTGAACAGCTTCGCAAACAGCAGAGGATTCAGTAAGCATGCTCACACTCTATATTCTGAACACACTGCAACACAATGTATTGCTCTCTACAGTTAATGGGTGGGGGTAATTAAAGGGGGAAGATGTGCATCATAGACCAGATACAGACACGTCAGGAGGAGAAACTGCTACAGGATGAGATGAAGGAACAGGAGGGTCAGCAGTTGCTGGAAAACATGGAGAGGATGCAGATGGAGGAGCTCAAGGTTCACAACGGAATATCTAAATCACTTCAAATTTCGAGTAGCTGTTTTAAGCCGCAGTGTATTTGAGTTTATTTCTGTGTGTGATGGTACCACAGGGTATAGAAAAGAAAAAGGAGGAGCAGAAGAAATTGCTTCAGGAGATTCAAAAGATAAATGAAGAGAATCTGCTTGCTAAAGAGCAAAAGAAGGAAGAAGAAAGATTAGCAGATCTACGTGCTGTAGAGTACACACGCAATAAATTGGTAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23334
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 |
---|---|---|---|---|---|
ENSDART00000098292 | Nonsense | 236 | 497 | 7 | 12 |
ENSDART00000127379 | Nonsense | 282 | 345 | 7 | 8 |
The following transcripts of ENSDARG00000068103 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 33526259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35207534 |
GRCz11 | 18 | 35182407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGGAGGAGAAACTGCTACAGGATGAGATGAAGGAACAGGAGGGTCAG[C/T]AGTTGCTGGAAAACATGGAGAGGATGCAGATGGAGGAGCTCAAGGTTCAC
Long Flanking Sequence:
CCGGGCCCAGTATCTATTGGAACGGGCCAACACCCTGAGAATGGAACAAGAGGACGAAGTCAAGAAGCTCAATGAGGTAAAAAGCACCAGACTAAAATGTCAAACTGTGAGCCACAAGTTGTTGCCAACATGTTGTCTTTCTGCTTGTTCAGCTGATTCAGAAAGTGCAGTGCCATGCTGTCCGGGATGTACAGATTCAGGAGAGGAAACTAAACTCTGCAGAGTGGCTGGCCGAGGAGAAGAGACTGGACGCCATGATGGAGGTGGAGCGCCGCCAGGCTTTAGAAGCTCAGGAACAAATTGAACAGCTTCGCAAACAGCAGAGGATTCAGTAAGCATGCTCACACTCTATATTCTGAACACACTGCAACACAATGTATTGCTCTCTACAGTTAATGGGTGGGGGTAATTAAAGGGGGAAGATGTGCATCATAGACCAGATACAGACACGTCAGGAGGAGAAACTGCTACAGGATGAGATGAAGGAACAGGAGGGTCAG[C/T]AGTTGCTGGAAAACATGGAGAGGATGCAGATGGAGGAGCTCAAGGTTCACAACGGAATATCTAAATCACTTCAAATTTCGAGTAGCTGTTTTAAGCCGCAGTGTATTTGAGTTTATTTCTGTGTGTGATGGTACCACAGGGTATAGAAAAGAAAAAGGAGGAGCAGAAGAAATTGCTTCAGGAGATTCAAAAGATAAATGAAGAGAATCTGCTTGCTAAAGAGCAAAAGAAGGAAGAAGAAAGATTAGCAGATCTACGTGCTGTAGAGTACACACGCAATAAATTGGTAAGGAAAGTCTTTATTGCTTTTTCTCTATTTTTTTTTCAAGTGTCTTGGCAGGTCTTCTGTAGTAAGTGTTGTCTGTGTGTGAAGAAACTGCAAGCAGGGCATCGCACTTATCAACGAATGATCCCAGAATGTTCCAAATGTTGCAAAGTGAAGTAAAGACCTTTTAAAATGTTTATCAGATCTTTATACGATCTTTATATGTAGCAGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13539
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 |
---|---|---|---|---|---|
ENSDART00000098292 | Nonsense | 467 | 497 | 11 | 12 |
ENSDART00000127379 | None | None | 345 | None | 8 |
The following transcripts of ENSDARG00000068103 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 33530758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35211942 |
GRCz11 | 18 | 35186805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGAGAACGGCTGGAGGAGGAGGCACGCAATCGCAGAGCCCGACTGGAT[G/T]AGATTAAAGAAAAGAAGCTCARGGAACTCAAGTATGTTCTCAACGTAAAA
Long Flanking Sequence:
GGATCCCTCTAGTGCTAAGTGAGAAATAGCACATACGTTATATTCACGGTTATACAGGAAAGAGCCATTTCTCATTCATTCTCAGTGTGAGCTTTCAACTAGTTTCAGTTATACATATGTAAAATAATTCTCAATATTTTAAGTATTACAAAATCTACCCTTAGGTGTGTCAACCTGAAACTTATACAAGCATCTCAAAGATCCATGCAAACCAGAAAGTTTACACTAAGACAGAACATTTTATATTATAAAGTTTAAGACAGAATGGACTAAGATAAAATATTTATGCTTTGTAATCTTTTTCCAGGGCACAGCAGGAGCTCATTGAGAGAGAATATGAAAAAGAGGAGCAGCGGCAGCAGCAAATCCAAAAGCATGCAGATGCTGTTAGGCAGCAGGTTCGGGAGAGAGAGATGCAGGCCGTCACTCAGCGCCGGGAGATGTTCAGAGAGAGAGAACGGCTGGAGGAGGAGGCACGCAATCGCAGAGCCCGACTGGAT[G/T]AGATTAAAGAAAAGAAGCTCAAGGAACTCAAGTATGTTCTCAACGTAAAACATAAAAGAAAACATGGGGGGTGGGGGGGGTTCAATGTCATGTGGAAACGTCCACTATGGGGATTTCGTCAGAAATCGTAAGTCATCTATAAGACTAATAAAATGCACAGCTGGCAGCAATCACAACCATTCGTAATACCAACTGTGCATCGCAGAGATACCTATTCGCTAATAAAGCCTCACAATACTAAGAAAGTCTTCAGGTTCCTTCAAAACCTCATTCGAAAGAAGAAAAAGAGAAAGGGAACGAGAAAGCTGCCAGTGTTTGACAGACTGTTTCTCCCGGTGAAAGAGTGTGTTCCACGCAGTGGCAGACGTTTGAGCTGGGTATTCTCCCTTGCCTGGGCATTCTCTGGGTACTAAAAAAGCAACACGGTCGTGCAGCTCTTTTTCGTCGTGCGACATCTTTTTCAAGATGTCGTTCTGACTGTGCATTTCTGGATGAGATGG
Associated Phenotype:
Not determined