ZMP
si:dkey-228b2.4
Ensembl ID:
ZFIN ID:
Description:
ODF2 [Source:UniProtKB/TrEMBL;Acc:Q1WCB5]
Human Orthologue:
ODF2
Human Description:
outer dense fiber of sperm tails 2 [Source:HGNC Symbol;Acc:8114]
Mouse Orthologue:
Odf2
Mouse Description:
outer dense fiber of sperm tails 2 Gene [Source:MGI Symbol;Acc:MGI:1098824]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16482 | Nonsense | Available for shipment | Available now |
sa39320 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12668 | Essential Splice Site | Available for shipment | Available now |
sa12576 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16482
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 |
---|---|---|---|---|---|
ENSDART00000022708 | Nonsense | 20 | 831 | 2 | 20 |
ENSDART00000081426 | Nonsense | 20 | 831 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 11331440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13032805 |
GRCz11 | 21 | 13129793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAGTGAGAACAAGGTCCTCCTCCCCACCCCTGCATGTGCAYGTGAAY[G/T]AGAGCACACCTGTGCATGTTCATGTGAAGAAGAGCACGAAATGCAGCCCT
Long Flanking Sequence:
TGATATTTAAAAAATAGAAAATAAAATATTTCTTTTCCGTAACAGGGATCAATGTAATTTTAACATAAATTCATATATAAATTATATTAATTTATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGAGTAAAACATAAAACCTATATGAAATTAAATTTAAGTCAATAATTTTATAAACATGGGAAGCATATAAAATGTAAATAAAGTGTCTATTTAGATATTTGAATTTCCCTTTGTTGAATGAAATGTTAGAATGTGGGCAAAATAATGATTTGTTCAGTCGGACAGATGTTTTTGTACACTCGAAATAAAATTGATATATTATTGATATTTATCTTTTTTATACAGAAGAAATCAGTGAGAACAAGGTCCTCCTCCCCACCCCTGCATGTGCACGTGAAC[G/T]AGAGCACACCTGTGCATGTTCATGTGAAGAAGAGCACGAAATGCAGCCCTACCAAGACAGCCCAGGTATGACATCATCAAATAGTCTGTGCATATACACTTGTTCCCAAATTACTGTTTAATAATATATACAGGATTCCCACAAATTATGAAATTTCTGGAATTTCATATATATGAAGACAAGAATTATAAAATAAAAAAAATAATGTATATATATTTCATACATTGAAAGTCATGGATTTTATAAGTGTTTCTAGTGTTTCACATTTTGCCTATTGTTTTATTTAGGCTATTTTTAAGCACAATCTTATTCATTCTCCACTACGCAGTTGTGGTAAATAAGGTTATTAAGATTACTAATTAATTAGTAGTATGCAAAACACAGCAGTGCCTTGTTTTTTATGGAAATTCAGCTTTTTAGTCAGGAAATGTATATAATAACCTATAATGATACTTTGTTTTTTTAAATTACACAATTAGTAAAGTTCCAAAATATGTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39320
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 |
---|---|---|---|---|---|
ENSDART00000022708 | Nonsense | 648 | 831 | 16 | 20 |
ENSDART00000081426 | Nonsense | 648 | 831 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 11346508)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13047873 |
GRCz11 | 21 | 13144861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAAATAAATCATGTTGTATTCTGGTGGATTGGGTATAGGCAGAGCAA[C/T]AGGGAAGCTTGGCGGAGATGTTGAGGCACAAAAACATGCTGCTACAGGAG
Long Flanking Sequence:
GGGTTGAAAAAAAATAGATATTTTATAAAACATTCAGAAATAATATTTTTATAACTTACTGGGGGTCTTGAGGTATGTCTATGCAGATTTTATTGATTTGTAACACTTCGTTGTTAAACAATAAATAAATATATTAATTTATTAATTTTCCTTTGGCACATCAATACACCTTCTCATTCACACAGACACACTTGTACACTACGGCCAATTGAGTTAATCCAATTCACTTATAGCGCATGTCTTATGTCTTTGGACTGTGGGGGGAAACCGCAGCACCCGGAGGAAACTTATGCAAACACGGGAAGAACATGCAAACTCTACACAGAAATGACAACTGGCCCCTCCCAGACTCAAACCAGCGACCTTCTTACTGAGAGGCAAAAGTGCTAACCACTGAGCCACCGTACAACTATAAGTAAATATAATTGTATTTTATTTTATTGTATTGGATTATAAATAAATCATGTTGTATTCTGGTGGATTGGGTATAGGCAGAGCAA[C/T]AGGGAAGCTTGGCGGAGATGTTGAGGCACAAAAACATGCTGCTACAGGAGGAAAACAAACAGCTTCAGCACAAAATGGAGAGCCTTGAACGGTCTGTTGCCTTGTCTTATATCCCTCTGTCATTCATTTTAAAGTATTTTATCTTTTAAAGTAATAATACATCTAAAAGTGAAAATTGAAAGTGAAAAAAGTAGTAGTCTCTATTTTTATTTACTTATTCATTTGAAGTAAAAATTGGTTTCAGATAATGATGGAAGAATTTTCATTTTTGGGTTTTGATTTGCTCTTTTCAGGAAGCAAGAGGAGGCTAACTCGCAAAATCGAGATCTCATCCAGGTCATTTCAAAACGGGAAGAGACGATTCATAGCAGCCAGGTGCGTCTGGAAGAAAAGTCTCGAGAGTGCAGTATTCTGACCAAACAGCTGGAGGAGGCATTGGATGATGCCCGTCGACAGGTCTGTCCCCAACTATATCTTGTTAAAGGGATAGTTCACTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12668
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022708 | Essential Splice Site | 678 | 831 | 17 | 20 |
ENSDART00000081426 | Essential Splice Site | 678 | 831 | 17 | 19 |
ENSDART00000022708 | Essential Splice Site | 678 | 831 | 17 | 20 |
ENSDART00000081426 | Essential Splice Site | 678 | 831 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 11346800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13048165 |
GRCz11 | 21 | 13145153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATAATGATGGAAGAAYTTTCRTTTTTGGGTTTTGATTTGCTCTTTTC[A/G]GGAAGCAAGAGGAGGCTAMYTCRCAAAATCGAGATCTCATCCAGGTCATT
Long Flanking Sequence:
CAAACACGGGAAGAACATGCAAACTCTACACAGAAATGACAACTGGCCCCTCCCAGACTCAAACCAGCGACCTTCTTACTGAGAGGCAAAAGTGCTAACCACTGAGCCACCGTACAACTATAAGTAAATATAATTGTATTTTATTTTATTGTATTGGATTATAAATAAATCATGTTGTATTCTGGTGGATTGGGTATAGGCAGAGCAACAGGGAAGCTTGGCGGAGATGTTGAGGCACAAAAACATGCTGCTACAGGAGGAAAACAAACAGCTTCAGCACAAAATGGAGAGCCTTGAACGGTCTGTTGCCTTGTCTTATATCCCTCTGTCATTCATTTTAAAGTATTTTATCTTTTAAAGTAATAATACATCTAAAAGTGAAAATTGAAAGTGAAAAAAGTAGTAGTCTCTATTTTTATTTACTTATTCATTTGAAGTAAAAATTGGTTTCAGATAATGATGGAAGAATTTTCATTTTTGGGTTTTGATTTGCTCTTTTC[A/G]GGAAGCAAGAGGAGGCTAACTCGCAAAATCGAGATCTCATCCAGGTCATTTCAAAACGGGAAGAGACGATTCATAGCAGCCAGGTGCGTCTGGAAGAAAAGTCTCGAGAGTGCAGTATTCTGACCAAACAGCTGGAGGAGGCATTGGATGATGCCCGTCGACAGGTCTGTCCCCAACTATATCTTGTTAAAGGGATAGTTCACTCAAAAGTGTACATTCTGTTAATAATTACACACCCTAATATAGTTAAAATTAAGATATTTTAGATGAAATCCAAAAGCTATCCGACCATAAATAGACAGCAATGGTCCTAATTTGTTCAAACTCCAAAAAGGAACTAAAAAACATCTTTAACACAGTCCATCGGTCTACTGGTTTGATTGGAATATTATCAAGTTACGAAAATAGCACATAAAACAAAAATGAGAACTTTATCCAACAGTTTCTTCTCTTCATGTTTTTTTTTCTGGACTTCTTCAGGGATGAGAGAGCTCTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12576
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022708 | Essential Splice Site | 678 | 831 | 17 | 20 |
ENSDART00000081426 | Essential Splice Site | 678 | 831 | 17 | 19 |
ENSDART00000022708 | Essential Splice Site | 678 | 831 | 17 | 20 |
ENSDART00000081426 | Essential Splice Site | 678 | 831 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 11346800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13048165 |
GRCz11 | 21 | 13145153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATAATGATGGAAGAAYTTTCRTTTTTGGGTTTTGATTTGCTCTTTTC[A/G]GGAAGCAAGAGGAGGCTAMYTCRCAAAATCGAGATCTCATCCAGGTCATT
Long Flanking Sequence:
CAAACACGGGAAGAACATGCAAACTCTACACAGAAATGACAACTGGCCCCTCCCAGACTCAAACCAGCGACCTTCTTACTGAGAGGCAAAAGTGCTAACCACTGAGCCACCGTACAACTATAAGTAAATATAATTGTATTTTATTTTATTGTATTGGATTATAAATAAATCATGTTGTATTCTGGTGGATTGGGTATAGGCAGAGCAACAGGGAAGCTTGGCGGAGATGTTGAGGCACAAAAACATGCTGCTACAGGAGGAAAACAAACAGCTTCAGCACAAAATGGAGAGCCTTGAACGGTCTGTTGCCTTGTCTTATATCCCTCTGTCATTCATTTTAAAGTATTTTATCTTTTAAAGTAATAATACATCTAAAAGTGAAAATTGAAAGTGAAAAAAGTAGTAGTCTCTATTTTTATTTACTTATTCATTTGAAGTAAAAATTGGTTTCAGATAATGATGGAAGAATTTTCATTTTTGGGTTTTGATTTGCTCTTTTC[A/G]GGAAGCAAGAGGAGGCTAACTCGCAAAATCGAGATCTCATCCAGGTCATTTCAAAACGGGAAGAGACGATTCATAGCAGCCAGGTGCGTCTGGAAGAAAAGTCTCGAGAGTGCAGTATTCTGACCAAACAGCTGGAGGAGGCATTGGATGATGCCCGTCGACAGGTCTGTCCCCAACTATATCTTGTTAAAGGGATAGTTCACTCAAAAGTGTACATTCTGTTAATAATTACACACCCTAATATAGTTAAAATTAAGATATTTTAGATGAAATCCAAAAGCTATCCGACCATAAATAGACAGCAATGGTCCTAATTTGTTCAAACTCCAAAAAGGAACTAAAAAACATCTTTAACACAGTCCATCGGTCTACTGGTTTGATTGGAATATTATCAAGTTACGAAAATAGCACATAAAACAAAAATGAGAACTTTATCCAACAGTTTCTTCTCTTCATGTTTTTTTTTCTGGACTTCTTCAGGGATGAGAGAGCTCTTTAAT
Associated Phenotype:
Not determined