ZMP
C2orf86
Ensembl ID:
Description:
chromosome 2 open reading frame 86 [Source:HGNC Symbol;Acc:28027]
Human Orthologue:
C2orf86
Human Description:
chromosome 2 open reading frame 86 [Source:HGNC Symbol;Acc:28027]
Mouse Orthologue:
AV249152
Mouse Description:
expressed sequence AV249152 Gene [Source:MGI Symbol;Acc:MGI:2144467]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23077 | Essential Splice Site | Available for shipment | Available now |
sa13922 | Nonsense | Available for shipment | Available now |
sa39162 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23077
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112665 | Essential Splice Site | 180 | 707 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 24221479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24374921 |
GRCz11 | 17 | 24393322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGATCTAGCAAGACACATGGAGAAACTCACAGCTGCAGAGATTAAGG[T/G]AACACACACACACACACACACACACACATACCTCTTACACACATCTTTTG
Long Flanking Sequence:
TATTCATTTAAAATTCAAAAGATGAAATCAATGATGCTTGAACCAGCTAGTTGAATGTCATGTAGAAACGTCATTTCATGAATGTTGCATTGGGTTTAGTTATAAATGTGTCTCATTATGTTCAATAAACAACCTATCAGGGATATTCGGGGACACCATCATTTGAAAAAAGCAAAAATCTGTAAGTAAATTAAATAATATTTTCTAATGTTTTAAATGGCAAAGCTTTTCTATTAGAGGTATATATGATTTGAGTGAGTCTATAGTAATAATAATATGTAATTTAGATAGCAAAGTAAACGCTTTGTTTTCTGGCAAGGTCATATGAGTTTTGACCTTTGACCTCGCCCTGTGGTTTTCAGCGGTGATTGGCGATCGCTTCCTGCTGTTCTCCCTGATGGAGAGGAGTCAGGTGTGTCAGGTTTACCTGAACAGGAAGAACCAGAGCTCACCTGATCTAGCAAGACACATGGAGAAACTCACAGCTGCAGAGATTAAGG[T/G]AACACACACACACACACACACACACACATACCTCTTACACACATCTTTTGAACGCTCGCCCAAAGACACACACACTCTTGAATACGCACGCATTAGCACATTTTAGGAGGAAAGGCAGACCAGCCTCTCCTGCTTTCAATTAAAAAGCTTTAATGAGGCTGGTCTGGCTCTTTCCACAGGGCTTTTAGCTCTAATAATTGCCTGGCTTTTCTTGCTTTCTTTTACCACTGGGACAGGTAACACTGTGATTACTGGAGCTCCTCTCTAATGCACACCTGTGGGGAACATCAGGTCCAAACACACAGCACTCGTGTCTTTATAGAGAGATCACATCCGTTATGACAGTGCATCTGTGTGTGCCTGAGAACTGTTCTTTCCCTCATTCTCAATTTCCTTTTGTTTAATTACTGAAACCTGAAAAAATAAAAAAGGGCAGCCAGTTGAAGATCATTGTGTAATTGCTGTAATAATTCTTATGCATCAAATATAAAAAGAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13922
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 |
---|---|---|---|---|---|
ENSDART00000112665 | Nonsense | 346 | 707 | 9 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 24192707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24346149 |
GRCz11 | 17 | 24364550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGGGTTGTYCWGGGGCTTCAAGATTGCTCTGTGGTTCWTTTCGACCCA[C/T]AGACAGGMCTCTCCCAGTGGGCCACTTGCTCCATGATGCCGGCGGTGCTA
Long Flanking Sequence:
AGAAATATACATCATTATTTACCTTTGCAGGAAGAAGTACATAATTTCTTGCATACATTTGCCAAAAGATTTGTCTTTCTGACATTTTCAGTTGTGGATCAGAGATACATGACCAGAATGAATTTCAAACCATAGATGACAAGTGTAAATGAGAGTCAGTCTGTGACTTTTTTGTTTCTGTTTTTTCATCCGTGTAGGTTTTGAGCTCTATCCGAACGGACGGGGATCCTATAGACTGCAGATTTAGTCTGACCCAACCCTACCATATCCTGACCGTGGAGCTGCACCAAGACACCAAACACTCCACATCTGAGTCCCTTGAGGAAATTCAGCATCCTGACATCCAAACCTGTGTGTATGAATTGACTCGTGGCCGTCTCCAGCGTCTGTCCAGCATATCTTTAACCCTCACATCCAAACCTATAACCTGTAGTCGTGACCCCTTAGAGCGTTGGGTTGTTCTGGGGCTTCAAGATTGCTCTGTGGTTCTTTTCGACCCA[C/T]AGACAGGACTCTCCCAGTGGGCCACTTGCTCCATGATGCCGGCGGTGCTAGCATGGCATCCTTCTGGATCACTGCTGGTGGTGGGTGGAGGTCAAGGCGAGCTTCAGTGCTTTGATATGGGCTTCTCGCCTCTCCCACTGCGGTTAGTGAGTGAAGAACCGGTCCCTGGCTCTGTAGGCTCCAGCCTGCAGCTCTCTCAACACTTCAATACCTCTGAGGGGCTAGAGGGGATCCAATGGGCCTACTGTCCGATATCTCAGGGAAACGAGAGTCTAGAGGTGCATGACTTGCTGCTGCTTCGGTTTCATGGAGGACCACTTGCTGCGCTGAGGTTAAAACTGGGTTAGTGGGACCTTTGTAATAATTGATTAAAATCCAGGGTAGAGCATGTAAGATGTAGAGCTAAAGGGTTTAACTGGATTGTATTTAGGTAGCTGGAGGGCATAAAACACAGTCTTAGCTATAATAGCATTTAAATACAGCCATTTAAATGTAGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39162
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112665 | Nonsense | 470 | 707 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 24181683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24335125 |
GRCz11 | 17 | 24353526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGTGTTCTATGTGCAGGTGTGTTTAATGGTGCTCAGCTTGGCCCATG[T/A]GATCTGATACTGCACCGTCTGCTCTGTGAGGAGGTAGATGCAGCTCTGGG
Long Flanking Sequence:
TATTTATTTTATTTGTCATGAACTGGTGAAAATATAGACATCTGAACTACCAAACAGGAAAAAAATTGTTAGCCTCACCCTGGCATCTTTGGTACTTTTTTGTTAGGGTAACTAATTTATCAGCAACTGTTAGTGATTATTTTTTTCTTCAAATATTTCTGCTATTATTATAAAGTACTATTTAATGGAAAGGACATATTTTTCAACACAATTTAAATTATAATATATAATATTAAATTTATACATAATAAATATATAAGAAAAACTGAAATTATTTTTTGCTTTGTTAAATATTAAAAAAAGAATTAAGATTTCACAGAATGTGTCCTCTACTATTACTAAAGCAGTGTTTGAAAAATTTTAATTGATTTTGGAGAAAGTGAGCAATCGTATGATTGATTTGGGTCTCCAAAAACATGGAGCATTTTAATAATATACTGTAATAGTTATAAATGTGTTCTATGTGCAGGTGTGTTTAATGGTGCTCAGCTTGGCCCATG[T/A]GATCTGATACTGCACCGTCTGCTCTGTGAGGAGGTAGATGCAGCTCTGGGAATTCTGGGTAATATGGACTGGGCTATTATGGGGGCAGAGTGTTACAGGTCACTCATCTCCATCACTGATCACCTGCTGAGAAAACCACTGGACCAGCAGACTGAAGGTAAAGACCCCAGACCTGCAGGCTTTGATTTCTGAATGGAGACTAAACCTAAACTTAATTAGTGTCAGGGAAAATGTACAGTAATCTCAGCTTAGAATTAAATACGGTCTTTACTTGTGAAAATAACACCTTTTAAATCACATTATATGATCTGGTTCTGAATGTAGTTTGCAAACAGGACAATTCAGCACATTAAAAACCAATGATAAATTATTTTATTTATTGAGAATTTACATTTATGGCCCCCAATAGTATTTTAGTATATCTGTTTTGTTGGTCACTTTTACTTTTTTTGTTAGTTCCCCAAAGGACAAGCTACTGACTATAAGTATATTTTTTAAGT
Associated Phenotype:
Not determined