ZMP
si:ch211-102c2.5
Ensembl ID:
ZFIN ID:
Human Orthologues:
AP005242.1, C9orf86
Human Description:
chromosome 9 open reading frame 86 [Source:HGNC Symbol;Acc:24703]
Mouse Orthologue:
B230208H17Rik
Mouse Description:
RIKEN cDNA B230208H17 gene Gene [Source:MGI Symbol;Acc:MGI:2442633]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38472 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40434 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40435 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa726 | Essential Splice Site | Available for shipment | Available now |
sa38473 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38472
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111019 | Nonsense | 27 | 710 | 1 | 16 |
ENSDART00000142753 | Nonsense | 27 | 765 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 28451769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26207067 |
GRCz11 | 5 | 26807220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTGAGCCGGTTGGTCCTATAAAGGACAAGAACATCCCTGCTGGCCTA[C/T]AGTCTATGAACCAGAGTCTGCAGAGAAGATTCGCTAAAGGGGTTCAGTAC
Long Flanking Sequence:
GTTTCTGCAGTGTACTACAACCTAAAAGAGGCTTTTCAAATGTTTGCAACTACAATATAATTATTATATAATGAATTTCAGCTACATTAAGCTTTAAACTGTGTGTGTGTGGTTTTTTTTTTGTCTCCTGTATTTCCAACAGAACAGAAGTAAATCAGCGCTTGAATGAGGAGAACTTGTGATGCTTTTCTGCAAAAGCTGTGTCATACAGTGGAAAAGCATCCAGAGATGAAGACCTAAACGCATACTGAGATATCATGCTGTGCCAAAGCATCTTAATTCATCCATGAAACTAATATAGAAATGCTTTATGAGCATTGCAAGAAAGCAGTCCAACCACAGACAGACAAACTGTGGAGGCAGATTTGAGACGAGAATATTTGATATTTTTATTACGCACCTAGAGGGATAATTTGGTCAATATGTTCTCTGCTTTAAAGAAGCTTGTCGGCTCTGAGCCGGTTGGTCCTATAAAGGACAAGAACATCCCTGCTGGCCTA[C/T]AGTCTATGAACCAGAGTCTGCAGAGAAGATTCGCTAAAGGGGTTCAGTACAACAGTAAGTCAGATTTCTGCTGTCTTTCGGAAAAATGTACAAATAACCCTTGTGTATTGTTCAAGTTGATTACCCCTTCGTTACGTTCGTGGCTGTTTTTGCTCCATTGACTTCCATTATTACCACATTTTTTCATTGCGAAGCCATGACACCATATTATTATGCTTTCTTGATTGTTGGTGGCTTACCCTGTTGGGAAGAGGTACAATTTGTCACATTTGCCTTTGATCACCTGTTGGCAGCAATAACCCTTTAGCTAGGCCTGTGCAAAAATGTTTCTGGCTTTTATATGGAGTTTTATAGAATAAAACAGCTAATCATAGTGTGTATGTGGCTGTGTCTGTATAAATACGCCTATCACAGTAGCCAATATATTGATTTATTGTGGTTATATTGGTTTATCGGACATGACTTTAATAATATTTGGTGATGCAATATATGTTCTCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40434
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111019 | Nonsense | 225 | 710 | 7 | 16 |
ENSDART00000142753 | Nonsense | 223 | 765 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 28459394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26214692 |
GRCz11 | 5 | 26814845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATCCATTATGCAGAATCTTCCATGAAGAACGGCTTTGGTTTGAAATA[T/G]TTGCACAGATTTTTCAACATTCCATTCTTGCAGCTTCAGGTAAGCAGGTT
Long Flanking Sequence:
CAACTCATGTGCCAGTGTGTGTGCTCGGAAATTACAGAGACATGGGAGAACACAGAGTCGTTTTGCCTGATGACATCCGTGACTTCATCACTGGTCTTAATAGGTCAGAACATTACTTTGAACAGAAATGTGTCAATTAACCATTTTAACTCTCTTAAATTTGCATTATTGTAATTGATTTATGACTTCATCAGTAATTAAATGTAATTAGTAATTCATATGTCACTTTATTCTCATTTAACCTGAATAAATGTCACATTATGGAAGGAATTAGACTGTTAATTCTGTTATCTTGTTAGCAGAAGATTGTTGGTGGCGTTTTATCACAAATAGGTTGAGATGAGTTATTGCCAAATTTAATGTAATTTGTTCATTCATGAGTTAATTATGTTGGGTTATTCTTTTGTAATGTTTGATGTCTTCATGATTTGCAGGCCTCTTGGCTCCTCCTATATCCATTATGCAGAATCTTCCATGAAGAACGGCTTTGGTTTGAAATA[T/G]TTGCACAGATTTTTCAACATTCCATTCTTGCAGCTTCAGGTAAGCAGGTTGATGTTTTAGTATTTTGTCTGTTGTATAATTTGACCATAAAAATGTAGTAATAATAATAGTAAAACAGCTTCCAAATCAAGCTAGTGTTTGTTTGTGATTGTTAATATTGTCTAAGCTCTATAAGCTGTGCCTGGTATGTTTGCATGATATCATTTTTTTCCATTACTCAAATTGTCAGAGCTTGAAATGAAACAGTCGTTTTAATTTTGACAGAGAGAGACCCTGTTACGACAGCTAGAGACTAATCAGTTGGACATCGATGCCACGCTAGAAGAGCTATCAGTTCAACAGGAGACAGAAGACCAGAATTATGATATGTAAGAACTTCAAAACAGACACTTCATAACACATACTTGCTGTTCTTGACAATATCAATTTATATAAATACAACTACACCACTGTTTAAAAGACTGGGGTTGGTTTTATTTTCTTTTTCATCATGAGTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40435
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111019 | Nonsense | 236 | 710 | 7 | 16 |
ENSDART00000142753 | Nonsense | 234 | 765 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 28459425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26214723 |
GRCz11 | 5 | 26814876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGCTTTGGTTTGAAATATTTGCACAGATTTTTCAACATTCCATTCTTG[C/T]AGCTTCAGGTAAGCAGGTTGATGTTTTAGTATTTTGTCTGTTGTATAATT
Long Flanking Sequence:
TTACAGAGACATGGGAGAACACAGAGTCGTTTTGCCTGATGACATCCGTGACTTCATCACTGGTCTTAATAGGTCAGAACATTACTTTGAACAGAAATGTGTCAATTAACCATTTTAACTCTCTTAAATTTGCATTATTGTAATTGATTTATGACTTCATCAGTAATTAAATGTAATTAGTAATTCATATGTCACTTTATTCTCATTTAACCTGAATAAATGTCACATTATGGAAGGAATTAGACTGTTAATTCTGTTATCTTGTTAGCAGAAGATTGTTGGTGGCGTTTTATCACAAATAGGTTGAGATGAGTTATTGCCAAATTTAATGTAATTTGTTCATTCATGAGTTAATTATGTTGGGTTATTCTTTTGTAATGTTTGATGTCTTCATGATTTGCAGGCCTCTTGGCTCCTCCTATATCCATTATGCAGAATCTTCCATGAAGAACGGCTTTGGTTTGAAATATTTGCACAGATTTTTCAACATTCCATTCTTG[C/T]AGCTTCAGGTAAGCAGGTTGATGTTTTAGTATTTTGTCTGTTGTATAATTTGACCATAAAAATGTAGTAATAATAATAGTAAAACAGCTTCCAAATCAAGCTAGTGTTTGTTTGTGATTGTTAATATTGTCTAAGCTCTATAAGCTGTGCCTGGTATGTTTGCATGATATCATTTTTTTCCATTACTCAAATTGTCAGAGCTTGAAATGAAACAGTCGTTTTAATTTTGACAGAGAGAGACCCTGTTACGACAGCTAGAGACTAATCAGTTGGACATCGATGCCACGCTAGAAGAGCTATCAGTTCAACAGGAGACAGAAGACCAGAATTATGATATGTAAGAACTTCAAAACAGACACTTCATAACACATACTTGCTGTTCTTGACAATATCAATTTATATAAATACAACTACACCACTGTTTAAAAGACTGGGGTTGGTTTTATTTTCTTTTTCATCATGAGTCCTTAAGTTTTTCAAAAGAGATAGTAATGAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa726
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 |
---|---|---|---|---|---|
ENSDART00000111019 | Essential Splice Site | 325 | 710 | 10 | 16 |
ENSDART00000142753 | None | 354 | 765 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 28461391)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26216689 |
GRCz11 | 5 | 26816842 |
KASP Assay ID:
554-0633.1 (used for ordering genotyping assays)
KASP Sequence:
CCTYCTCTCTCCACCAGCCAAGCTCCCRCGGYGTCTCCCTCCCCATCCCC[G/A]TCCCCTGCTCACCCCGGCCCAGCAGTCTCTGCTGCTCAGGCTCCTGCTCC
Long Flanking Sequence:
TATTATTTCAAAATATCACAGTTTTTTTATCAAATAAATGAAGCCTTGGTAGACATAATATACTTCTTTCAAAAAAAACAAAAACCCCACCCCAAACCTTTAAACAGTGGTGTACATATCCCTCCACAAAAGCTACATTGTTTACATTGTAGGCCTTTCTGAAATGACTGCTTCTCTATTTTTAGTTTGCGAACTGCAGTCAGTGCAGTCTTGACATTTATGAAACGGTGAATATCTGTAATGACTTTCAGTTTCCTGGAAATGAACGACTCCCGTAGTAAAGGCTACAACTCTCCCGGTCCCGCTAACGGACAGAGTCCCTCCTCGGGCTCGCAGTCTCCTGTGGTTCCTCAAAGCGGATGCTCCACCAGCAGCTCCAGCCCCTGTAGCCCTCAGCAGCCTCCCATTCCCTCTCAGAAGTCTCCATCCCCCTCTCCGTCCCCTCCTCCTCCTCCTCTCTCCACCAGCCAAGCTCCCGCGGCGTCTCCCTCCCCATCCCC[G/A]TCCCCTGCTCACCCCGGCCCAGCAGTCTCTGCTGCTCAGGCTCCTGCTCCTCAAAACCAGAAACGCAGCTTCATCTCCAGGCTCTTTGGCTCCGTTTCCACCCAGGATCCTCCAGCCGTCGCTCAGGGTGAGTTTTAGCTTGATGTTAATAAGTAAAAGTGATGGTAAGACATTTGGCAGTATTTGTAGTAACATATCTTTAAATCTCAGAATTATAAATAACACATCTCAGAATATTAATTGTTGAATATTGAGTTGTAATTAAATTTGAGTTTGCTTTTTATATTAGAAAACACTGCTAATATTTTTTTGGGGGGTGGACAAGAGAGCTTTTTTCTCTTCAAATGTTCAGTGGCCCATTGTTAAAGGACTTCCCTAATGCTATGAACTGCAGAAGGGATTTGAAGGCTGAGAGGAATTCATTCACACACACACACACACACACATTCTCTCAGAAAGATTTTTTTTTCCCTCGAGCAAGACCTACAAAGCCGTGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38473
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111019 | Essential Splice Site | 423 | 710 | 12 | 16 |
ENSDART00000142753 | Essential Splice Site | 453 | 765 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 28465381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 26220679 |
GRCz11 | 5 | 26820832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAATAAAACAAGTTCAATTTGCATCTATTCTTGTATCGTGTTTGTTTT[A/G]GTGAAGGGGAAGGAAGAGAAGGCAATCCCATGGTTGCTGGCTTCCAGGAT
Long Flanking Sequence:
TCTGAAAAAGCCTTTATCAAACAGTCTTAAAAAACAAACCTACAGTAAAATGAGGCGAATAAACAAATTTACAGGTGCAATCATACAAAGTGCCTACAGCAGCAGGATGTGGCATACCAATCTATTATAGTCACCAATTTTGTCAACACACTGTTTTTTCCACAACTTGGCAACACAAAACATCTTTAAATCCTCTGAGGATTTTTTTAGTTTCATGCAGTGTTTGCATCTGGGATGCTCACATTCCTTTGATGGCAAGGTCTCCAGTGTTTTGGCCTTCTTTAAAAAGGACAACATTTAGAAATATTTTGTAGCAACATGAATGTCTTCACTGTTGATCAGTTTAATGCATCCTTTTGATTATTTTTGAACTGTATTTTTACATGTAAATGAACTGAGTCAGTGGTTTCTGTCAGGTTTTGAATATTCAAAAGTGTAATACATTGAAGCTGGAATAAAACAAGTTCAATTTGCATCTATTCTTGTATCGTGTTTGTTTT[A/G]GTGAAGGGGAAGGAAGAGAAGGCAATCCCATGGTTGCTGGCTTCCAGGATGATTTGGACCCTGATGATGCAGAAATAAAACCCAAAGCTGCTATTTCAAGTAAAGACTTGGATATCACCCTCTCCAGTGACGAAGAGGTTCCAAGACCTTCTGTTGCTCAGGATGAAGACCTGGACCCTCAAACACACCTGTAAGCATGAAATCCTCAAGTGGCTTTAAAACTTCTTTTTTTTTGAATATCACTTAAAGAATCTTGGAAACCGGTTGCTATTGACATCTGTGATGGTATAAAAATGTAATAATCATTTTAGATTTTGTTTCAAAAGGAAAGTTCAGACGATGCACTATATCACAACTACTATATAACAATACTGATTAATTGTTGAATTCAGTTTCTTAACAATTATTTGAGTTGATGCACCAATTAAAGACTGACAGCCAATCAGAATCCATTCTGTCATGAAGAACTCAAGCACTTAAAGTGACAAAAGCTGGAGAAA
Associated Phenotype:
Not determined