ZMP
wu:fi37d12
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17873 | Nonsense | Available for shipment | Available now |
sa2212 | Essential Splice Site | F2 line generated | Not yet available |
sa33526 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33525 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17873
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 |
---|---|---|---|---|---|
ENSDART00000113716 | Nonsense | 423 | 748 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 5600877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 5140126 |
GRCz11 | 5 | 5632406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAAAGGTGCAGAGTGTGGATGAATTTGTGCCGGAGGTGGGATTGGAC[C/T]GAACCTTTYTGGATGACGGTGGAGCAGCAGCAGCRGCNNNNNNNNNNNNNNNAGCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGGCTAAATCA
Long Flanking Sequence:
CCTTTATTAATCTGGGGTCGCCACAGTGGAATGAACTGCCATTTTATCCAGCACATGTTTTACGCAGTGGATGCCCTTCCAGCCGCAACCCTAAACTGGGAAACACCCATACACTCTTACACATGCTCTCATACACTGCGGCCAGTTTAGTTTATTTAATCCACCTATATCACATGTGTTTGGACTTTGGGGGAAACCCGAGCACCCGGAGGAAACCCACATCAACATGGGGAGACTCAAACTGACTCAAACTCCACACAGAAATGCCATCTGGCCCAGCTAGGGCTCGAATCATCGATCTTCATGCTGTGCTACCCACTGAGCCACCGTGATGCCAGAAACACAAACATTAACCTGAAACTTGCAGTAGCACACTGAATTTCCTGATATTAAAACCTCTTGTGGGCTTGTCTTCATCAGAGTCTACAGGCTCTGAAAGCGTAAAGGCCTCTGGAAAGGTGCAGAGTGTGGATGAATTTGTGCCGGAGGTGGGATTGGAC[C/T]GAACCTTTCTGGATGACGGTGGAGCAGCAGCAGCAGCAGCGGCTAAATCAAAGAACAAACCTCCAGCCTCAGCTCCCATCCTGGACAGTGACAGGTGAGCTTTAATAACTAATAGATTGTTTAAAAAAAAAAAAAAAAAACTCATCCAATCAGCATTTAAAAGGCACCTATTATGCAAAAATCACTTTTATAAGAGGTTTATACACAGTTGTATGTCAGTAGTGTGTGAATATAACCAGCGTCTAAAGCAGGTCGCACACCAGAAGCGCCGCTCAGTGATGAGCCACGTAGCGCCATGCAGCGTCATGCATTTTAGATTTCTAAACATTGGTTTCTATCAGGGTACACACCGGCGCCGCAAGTCGCCGGCGCTCAGCCATGACTCAGTACACAGCCGCAGCACAGAGCGCCATCTGATTAGTTTTATGTTAAATTTCATGCGAATGTGCACGTCTGGTGTGTGATACTTTACACTGTCATGTGCGTGCCGTGTTGCGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2212
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113716 | Essential Splice Site | 454 | 748 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 5597593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 5136842 |
GRCz11 | 5 | 5629122 |
KASP Assay ID:
554-2679.1 (used for ordering genotyping assays)
KASP Sequence:
CTAATTTTGGTCCCGCATTAAACTCATGCAGTTTTCCTGTGTTTTCCTCA[G/A]TGATGGAGAGGGACGGGGAAATCCTCTGGTCTCCGGCTTCCAGGATGATT
Long Flanking Sequence:
CAAACAATTAATTATTTATAGGCTAATTGATGTCTGTGCGTACAAGGTTTCCCTATCCATGAGAGCGAAAGTGAAAGTAGATAATAAGGAGACTTATCTCTCATTTTCGCGCTGCAGATGCTCTGTTTAACTGTTTTCTTGTAAGTGAAATGCTCAGATTTTCCACTTACGAAGTCCGTCATGTAAATAGCAAATGCAAATGCGCTTTGGCACGGTGCAACTGGCTCTTAAAGGGAATGGGGGATGAGACTCTGATTGGCTTATTCCCAAAACACACCTATAACTCAATAAGAGAATAAGCTCAACCCTGTTAGACCATGCGCCACGGTGCAAAGAGGCTTTTTCCATCTTTATTTTAGCAAAAGTGGATTCTGACACACCCTGAAAGCGTTTGCGCTTTGCACTTTGTGCATGAACCATCAAAATAGAGCCCTAAGAAGTGAAACGGGTCTAATTTTGGTCCCGCATTAAACTCATGCAGTTTTCCTGTGTTTTCCTCA[G/A]TGATGGAGAGGGACGGGGAAATCCTCTGGTCTCCGGCTTCCAGGATGATTTAGATCCAGATGACAGAGTGCCGAGTCAGCCTGCAGTTAAAGCAGTGGTGCCGAGCAAAGACATCACACTGACCAGTGATGAAGAAGCGGAAGATTCACCTGTTCACCAGCAAAAAGCCATCAGCAGCTCAGGACCAAACACAAAGGGGTAACATAAAAAAAATAAAAGCATCTTAGCAATTCCAGTGTTATGGATGTGACGTTTGCAGTGAAAACTTTAAGAGTCACGAAACACCAAAACACATTATTTGAGCTGTTGACAGTCATATTTGTGTCCTACGCTGCTATAAACATTATTAGGACACAAATATCTCACAAAAAAGTGAAAATTGGTTGTTCTTGTATTATTTCGAGCAAATTCGTTCTTCCGGTTTTAAACTAATTTTTAAAGATGCGTCACGGAGATTAGATACTTGTCTACTTGTGTGTATTCCAGTGTGGAGAGTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33526
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113716 | Essential Splice Site | 520 | 748 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 5597393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 5136642 |
GRCz11 | 5 | 5628922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTCACCAGCAAAAAGCCATCAGCAGCTCAGGACCAAACACAAAGGGG[T/C]AACATAAAAAAAATAAAAGCATCTTAGCAATTCCAGTGTTATGGATGTGA
Long Flanking Sequence:
TGCGCTTTGGCACGGTGCAACTGGCTCTTAAAGGGAATGGGGGATGAGACTCTGATTGGCTTATTCCCAAAACACACCTATAACTCAATAAGAGAATAAGCTCAACCCTGTTAGACCATGCGCCACGGTGCAAAGAGGCTTTTTCCATCTTTATTTTAGCAAAAGTGGATTCTGACACACCCTGAAAGCGTTTGCGCTTTGCACTTTGTGCATGAACCATCAAAATAGAGCCCTAAGAAGTGAAACGGGTCTAATTTTGGTCCCGCATTAAACTCATGCAGTTTTCCTGTGTTTTCCTCAGTGATGGAGAGGGACGGGGAAATCCTCTGGTCTCCGGCTTCCAGGATGATTTAGATCCAGATGACAGAGTGCCGAGTCAGCCTGCAGTTAAAGCAGTGGTGCCGAGCAAAGACATCACACTGACCAGTGATGAAGAAGCGGAAGATTCACCTGTTCACCAGCAAAAAGCCATCAGCAGCTCAGGACCAAACACAAAGGGG[T/C]AACATAAAAAAAATAAAAGCATCTTAGCAATTCCAGTGTTATGGATGTGACGTTTGCAGTGAAAACTTTAAGAGTCACGAAACACCAAAACACATTATTTGAGCTGTTGACAGTCATATTTGTGTCCTACGCTGCTATAAACATTATTAGGACACAAATATCTCACAAAAAAGTGAAAATTGGTTGTTCTTGTATTATTTCGAGCAAATTCGTTCTTCCGGTTTTAAACTAATTTTTAAAGATGCGTCACGGAGATTAGATACTTGTCTACTTGTGTGTATTCCAGTGTGGAGAGTGGATGTCTGTAACGGCATGTACAATGTGACGCGTTTGAGTGTGCAGCATTAATTCATGAGAAAGACTTGGTTCAAACCAATCAGCGCTCTCTATTGTGAATGGGGTGCAACTTCAGTACACTTTTTCTCAGTGGCTTTGGTGCATTTCTCACAACACTGTTTACATTTGCACAACAGTAAATGCATTTCTCAAAACAATTAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33525
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 |
---|---|---|---|---|---|
ENSDART00000113716 | Nonsense | 690 | 748 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 5581677)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 5120926 |
GRCz11 | 5 | 5613206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTGAAATTCTCTTGTTGTTTTAGGAGGATGAGAAAAGCAGCAAAAAA[C/T]GACACAAGCACAAGAAAAAGGAAAAAGAGGAGCCCGGAACGGGAGATGAG
Long Flanking Sequence:
AAGCTCTGCTTCAGTTGCTTGACGCGTGTCCACGTGAAGCAGCCAGTGAGCGGCAGCGCACACACATACTATGAAAATCTCGACATGCGAAAGTGTTCCCCCACATGTTTTTTATCAAAGTTGTTCACAATACCAATCCATCCACAGAGTTTGTAATTGTTTACAAATACAAGCGCAGCCGTTTAGAGCTCATTTCTGGTTAATGATGTCATAATTTGCCAATATTTTAGAATGGATCTTTGGAACGTTCTTTCCAGGAAAAAAAAACTTTTTTGTCTGTGTGAACAGCGCTTTTTTGAATATACCGGTAAAGTTGTTCCAGAAATTTTCTGGATATTTACTGGTATCACTGTGTGAAAGGGGCTAGTAATATATTAATTACGCTTGAAGCTCATTCTGTTTGTTTTTTTTTTTTATATATATATTCTGTTTTCTGTCCCACTGTTTAGTTATCTGAAATTCTCTTGTTGTTTTAGGAGGATGAGAAAAGCAGCAAAAAA[C/T]GACACAAGCACAAGAAAAAGGAAAAAGAGGAGCCCGGAACGGGAGATGAGAAAGACAAGAAGAAGAAGAAGAAATCCTCCAGGACCAAGAAAGCAGCAAATGTGGATGATCTTGAGGCTTTCCTGGCGGGAGGAGACGGACCCGGAAACAGTGAGGGCGGAGACTATGAAGAACTCTAACCAATCAGGATTCGACACCATGTGACATCATCGCCAGGTCATTTTCCAATCCATTCCACCTGTTTTCTCAGTGCCTAACCTTTTGGATCTCCACAGCGTTTGTTTGTTCTTCCAGCGTCGCAGCTTTACGTCGTGCTTTCTCAAAATTGCTACATCACACAATTTTCCAAAGTTATTCATACTTTCAGACTTTTAGATGCGTCAGATTTCACACACATGATCAAGAGATATTCCGTTATTAACTGATTAAAAAGTCATTCCAGCAAAACTATAGTGTTCAACAAAGACTTGAGGACTTGTTTAAGCTTTATTGGGGTTTTT
Associated Phenotype:
Not determined