ZMP
zgc:55870
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein C17orf85 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q803E1]
Human Orthologue:
C17orf85
Human Description:
chromosome 17 open reading frame 85 [Source:HGNC Symbol;Acc:24612]
Mouse Orthologue:
1200014J11Rik
Mouse Description:
RIKEN cDNA 1200014J11 gene Gene [Source:MGI Symbol;Acc:MGI:1914124]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15235 | Essential Splice Site | Available for shipment | Available now |
sa16251 | Essential Splice Site | Available for shipment | Available now |
sa23978 | Nonsense | Available for shipment | Available now |
sa707 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15235
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 |
---|---|---|---|---|---|
ENSDART00000065504 | Essential Splice Site | 119 | 694 | 3 | 13 |
ENSDART00000065504 | Essential Splice Site | 119 | 694 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 29775956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30976207 |
GRCz11 | 21 | 31012902 |
KASP Assay ID:
2261-5806.1 (used for ordering genotyping assays)
KASP Sequence:
AATCTGACACAGAAGRATGTGGTTCTGGAGCGGGATTTGTTGAAGAAAAG[T/A]GAGAATTCTACACAGCTGTAGATCAACACAGGATTTACACTCAACAWGAA
Long Flanking Sequence:
CATTGGTATAATGTGTGCAGTTGGTCTGTTATTTCGGAAGATCTTATGAAAGTGTTAAAAATTCTCTGGGCCAAGTTTCCTGATACTAACAGACTTCTCATTTGGCGCACTGTTTGATTCATTATGGTGATTGTTGATCATGGTACAAAGCTGCATTTTAGGTAACACGTTCCAAGACCGACTACTGAAAATATTTAGGTGTATTTGCTGCCCTCATGGATCTCAATGAGATTATGTATGGTTCCACAGGACACCAGCCGGCGATATGAAAATAAGGCTGGCACCTTCATCACTGGCATTGATGTCACGTCTAAAGTAAGTGTCAGCTGTCTGTGTGAATTATCAGGATGTCTATTGATGGATCTGTTGTTCACCATGTTTACATGTGCACAGGAGGCCATTGAGAAGAAGGAAAAGCGAGCAAGAAGATTTCATTTTCGTGCAGAGGAAAATCTGACACAGAAGGATGTGGTTCTGGAGCGGGATTTGTTGAAGAAAAG[T/A]GAGAATTCTACACAGCTGTAGATCAACACAGGATTTACACTCAACATGAAGTGAAAACTATATCTGTTTTCTGAATGTCTGAACTTGTGTTTTAGCTCTTATTAGCATATGTATAGGATATAGTAAGACAAAGGAGTAGGTTCTGTCTACAGACTGCAAGACGGGTGTCACATGATAGGGCGTCACTTGAAGTTATGGAGACCCACATCAAAACTGTGTGGTTGGCAAGATGGTGCTGTACATCAGTTATTAACATTTTACACCTACTTCACGCCCAAAGCCAACCATCATCGTTATTAACGTCTACTCCTTCCCCAAACCTAAACCCAACCATCATAGTTATTAACATCTACTCCTTCCCCAAACTTGAACCAAACCATCATAATTATTAACGCATACACCTTCCCCATTCATCATAGTTCTTAACCAAACCAAACCACCATAATTATTAACGTATATACCTTTCCCATCCATCATCATCATTATTAACGTCTCCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16251
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 |
---|---|---|---|---|---|
ENSDART00000065504 | Essential Splice Site | 119 | 694 | 3 | 13 |
ENSDART00000065504 | Essential Splice Site | 119 | 694 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 29775956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30976207 |
GRCz11 | 21 | 31012902 |
KASP Assay ID:
2261-5806.1 (used for ordering genotyping assays)
KASP Sequence:
AATCTGACACAGAAGRATGTGGTTCTGGAGCGGGATTTGTTGAAGAAAAG[T/A]GAGAATTCTACACAGCTGTAGATCAACACAGGATTTACACTCAACAWGAA
Long Flanking Sequence:
CATTGGTATAATGTGTGCAGTTGGTCTGTTATTTCGGAAGATCTTATGAAAGTGTTAAAAATTCTCTGGGCCAAGTTTCCTGATACTAACAGACTTCTCATTTGGCGCACTGTTTGATTCATTATGGTGATTGTTGATCATGGTACAAAGCTGCATTTTAGGTAACACGTTCCAAGACCGACTACTGAAAATATTTAGGTGTATTTGCTGCCCTCATGGATCTCAATGAGATTATGTATGGTTCCACAGGACACCAGCCGGCGATATGAAAATAAGGCTGGCACCTTCATCACTGGCATTGATGTCACGTCTAAAGTAAGTGTCAGCTGTCTGTGTGAATTATCAGGATGTCTATTGATGGATCTGTTGTTCACCATGTTTACATGTGCACAGGAGGCCATTGAGAAGAAGGAAAAGCGAGCAAGAAGATTTCATTTTCGTGCAGAGGAAAATCTGACACAGAAGGATGTGGTTCTGGAGCGGGATTTGTTGAAGAAAAG[T/A]GAGAATTCTACACAGCTGTAGATCAACACAGGATTTACACTCAACATGAAGTGAAAACTATATCTGTTTTCTGAATGTCTGAACTTGTGTTTTAGCTCTTATTAGCATATGTATAGGATATAGTAAGACAAAGGAGTAGGTTCTGTCTACAGACTGCAAGACGGGTGTCACATGATAGGGCGTCACTTGAAGTTATGGAGACCCACATCAAAACTGTGTGGTTGGCAAGATGGTGCTGTACATCAGTTATTAACATTTTACACCTACTTCACGCCCAAAGCCAACCATCATCGTTATTAACGTCTACTCCTTCCCCAAACCTAAACCCAACCATCATAGTTATTAACATCTACTCCTTCCCCAAACTTGAACCAAACCATCATAATTATTAACGCATACACCTTCCCCATTCATCATAGTTCTTAACCAAACCAAACCACCATAATTATTAACGTATATACCTTTCCCATCCATCATCATCATTATTAACGTCTCCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23978
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065504 | Nonsense | 354 | 694 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 29765879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30966130 |
GRCz11 | 21 | 31002825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCAAAAAGCCTCTGATTGGAGACAGCATGGGACACACTCCACCTTA[C/A]ACACATCGACACTCAGGTAAATCTCCCCTAAATAACAAACATAATTGTCT
Long Flanking Sequence:
TAGCTTTAGAAGCATACAGTACTATTTGATCTATAAAATTTGTAAAATAAACATTTGCAGGTTAATGAAACAGCATAGGAGGGGCCTTGGTACAGATGAAAAGTTTAAAAAGTGTATTTGTATATAGAGGGGTAACTAGATAGAATAGACAGAGATAGGTTGATCTCAGCAGCAGCTGCCGAAGAGCTGCGCGCTGCAGACGCAGCTGGTGTGAAAGGCAAACGCCTGCGTGCTGCAACTGCTCGACATACGCGCTGCTCACGCTCTGCTCACGCGCCGCTGACGCTTGCGGTGTGAAACAGGCGTCAGAGTGTAATTTAAGGATCTAATTCTAAATGTCAAATGTTTCAAAAAGAAGATTTAGGTACTTGCTGTAAAATTACCTGAAATTGTGCCCGTTCCTGCAGGAAACGGAGGTATCACACGCGGAGAATCCAGCGGGACATTCTGAAGACCAAAAAGCCTCTGATTGGAGACAGCATGGGACACACTCCACCTTA[C/A]ACACATCGACACTCAGGTAAATCTCCCCTAAATAACAAACATAATTGTCTTTTGGTCGTTTGTTTTGACATTTAAGCTCATTATCTTTTTTTCCAGCTGATCTGGTTAATTTGCCAGAAGAACCTATAGAAGAAGAGGAAGAGGAGGAGGAGGATGGAGAGGAAGACATGGATGCTGATGATCGAGTGGTGGAGTATAAAGATCGAGGAGAAAAGGAGCGAGGGCCACGGCTTGTGGAAGGAGGCCTGCGCAGTCGCTTAGGAGGCCCATCGCCTACATCTTCAGATTCAGATGAGATGGACTACGATCTGGAACTGAAAATGATCTCAACACCCTCCCCCAAAAAGAGCATGAAGATGACCATGTACGCAGACGAGGTCGAAACCAACCTTCGCAGTCTTCGGTGAGTGCAGGTTTCTTATAGAGGCCAGTTTTATCCCAGTTTCTATCCCATTGGCTGATCCAGTTTGAACGTCTTAATAATAATTTCTTTCTTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa707
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065504 | Essential Splice Site | 596 | 694 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 29761979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 30962230 |
GRCz11 | 21 | 30998925 |
KASP Assay ID:
554-0615.1 (used for ordering genotyping assays)
KASP Sequence:
CATGACAATCGCAGTCTCTTCTCTGAACCCCCCAAAGACAAGAAAACAGG[T/C]ACACCTCAGTTCAGCACTCTTCTCAGTTCTCTTCATATTTGCTCTCCAAT
Long Flanking Sequence:
CAATACCTTGATACCATGACTACATGATATTTTTGTTCAAGGTTATCATACCGTCAGAAACATATACCGGCCCATGCCTAGTACAGTGAGGACTTTCATGTCGCTGCATAAGCAGGCGTTGTAAATTACAAAAATTATTGATTTTAAAATTAAATATGCTTTAAAATGTCCTTAAACCTGCTTGTCATGGAAAAAGTGGAAACCATAATGAAAAATTGGGCCAGGAAAATAGTATACAGGCTTTGAATTGTTATCAGTTTTCATCATGAGCAAATGTGGAAGAGACTCACCTGTTTTTTTTTTTTCCTCTCCACAGATGTGAGACAGAGATTAGGCAAGAGACCACACTCCCCAGAGAGACGTCGCTCTGTGTCTCCTGTGATCTCCAGAAAGACGGCGTCTCGGAGAGAGCCTTTGAGCGACGTGCGCAGCAGACTCGGTGTAGCTAAACATGACAATCGCAGTCTCTTCTCTGAACCCCCCAAAGACAAGAAAACAGG[T/C]ACACCTCAGTTCAGCACTCTTCTCAGTTCTCTTCATATTTGCTCTCCAATACTAATATAACATTGGAGTAATGAAGACAAAAAAAAACATTTTAGTAAATTGGTTTAATTCCAAAGGCTTTAATAATTATGGTATTTTTACTGATTACATGTTCTCATAAATTTCAAATGAGATTTCTCATCAATGTTGGAAAGATTGTATACATTTAGCATTTTTGTGGTTCTCGTGTAAATACAAATTTTGTTAAGTTTGTAATTTTAGAAATGTGGTAGCATGGTAAAAACATGGTAACAGAAAAACATTCAAATTGTGATGTGAAAATGGTTGCAAGAGTACATATTTCACTCATTTTGAATGAGCAGCTCGGGGTAATAAGACATGCATTTCAAAATAAGAGTCCTTTGGTATTCTCGGATTGATTGTTTATTAAAGCATAAAACCCCCTTTTTAAATGTATCTATTTTAATCAAAAATTATTAGGCTGAACTGAAATTGGAATC
Associated Phenotype:
Data not yet available