ZMP
si:ch211-251j10.4
Ensembl ID:
ZFIN ID:
Description:
outer dense fiber of sperm tails 2-like [Source:RefSeq peptide;Acc:NP_001116704]
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 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21332 | Nonsense | Available for shipment | Available now |
| sa31661 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21332
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 |
|---|---|---|---|---|---|
| ENSDART00000077361 | Nonsense | 62 | 799 | 2 | 19 |
| ENSDART00000124213 | Nonsense | 62 | 234 | 2 | 7 |
| ENSDART00000130870 | Nonsense | 62 | 173 | 3 | 5 |
| ENSDART00000143604 | Nonsense | 62 | 810 | 2 | 18 |
The following transcripts of ENSDARG00000020702 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31864820)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31007546 |
| GRCz11 | 8 | 31016778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGTCCGAGCTCCATGGGTTCCTCCTGGAAAGAGCTCAACACGAAGA[C/T]AGTACAAATGGGAGGTTTGTTTAGCCCTGTTTTACTTTATTCACCAGCGT
Long Flanking Sequence:
ACGAATTGCTTTTTCAAACGTATTTCCGATCATGCCGATTTAACTGGTTGCAGTGCGTAAACTAAAATAACGACTCAGAACTACAAACATCGTTGAATGTGGACAAAGTGGACGCTTGTTTCGTAACACTTCTTTTTTATTTTTCTTACAAGTTTCTGACACACATCTGGGACACTTTTTCATACCTGTAACTGTTTTAAGACCGTCTTACTAAAGTGAAGGGATGAAAACACGGTCGTCTTCTCCGCCCGTTCATGTTCATATCCCAGACTCCACATCTGTGCATGTTCACCTGAAGAAGAGCCCACAGAGGAGCCAGGTTTGACCATATCCTCCTCTTGTTCCAGTTTAAATAAATATTATCTGAATTACAGAAACAGTTAAGTCACTCATCACCATTACTGTGTTTTTAGCAGGCAAAAGTGAGCAGTTTGCGATCCACTGCCAGTGTGAAGGTCCGAGCTCCATGGGTTCCTCCTGGAAAGAGCTCAACACGAAGA[C/T]AGTACAAATGGGAGGTTTGTTTAGCCCTGTTTTACTTTATTCACCAGCGTGAAATAAAAATCTTTATTATTAATAACAATTATTAAAATCATTTTATCTGTAAACACACACAAACACATACATTTATAAATGCCCTTGTATTTTTTAATTAAATATACTTAATTTTACTCTTAATGCAGCAACCTTTCCTGTGTGAGGGCCGGACAAATCATGTCACATCATTCGTTTTTTTATTACCTCACCCTGTTTACCATGTACTTTCACTTTTGCTTTATTTCAATTGTGTCACTTGCAAAATTTGAGAACGACCAATGTCAATAAATAGAGCAAGAGTTTTTCAGTGCATTCGTACACTAAATAAGAAAAACACAATAATATTACATACCTACATTCACTGCTACACAGTTTCTACTGCAGCTCCATGACCAAAAGTTCAACAGTGCATTGTGTTGTTATGTCACATTCCCATTCTCTAGTAAACCACAGCCATACAGTCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31661
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077361 | Nonsense | 347 | 799 | 10 | 19 |
| ENSDART00000124213 | None | None | 234 | None | 7 |
| ENSDART00000130870 | None | None | 173 | None | 5 |
| ENSDART00000143604 | Nonsense | 352 | 810 | 9 | 18 |
The following transcripts of ENSDARG00000020702 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31868161)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31010887 |
| GRCz11 | 8 | 31020119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACCCGCAGTCGCTTGCAGAACAATCTGCTTAAGAAGGAAGCTGAAAAT[A/T]AACGTCAGGAGGCTCAGATCCAAGTAAGCCAACAAATTTATACTTTGTTC
Long Flanking Sequence:
GTTTTAGATCAAATAAATGTTGCAGTGGTCCATATAAGGCAGAATTTAGTTAAAACTCCAAGAATCTTACCAACCTCAAAATTCCAAATGGTAGTTAATTATTGAATGCAAAGCTGTTTCCTTTCTCTCAAGCTAGACTTGTTGTTTACTATTACTAATAAATATCATTTCTGTTGTAGAAACTTGAGACTAAACTTAGCAGGAGAGAAAGAGAGGCCAATCAGATGGCTGAGAATTTGGAAACTGAAAAGGTAACAGTAATTTTTCTTTATGCATTTGTGTAGCATTCTTCTACAGCATTACTTAATACCTTCAATACTTCAATATTGTGGATTTGCATCTAATTTTCTTCTGCGATGAGTACTTTAAAATCTGAAAAATATTTAAAAGACATTGTTTCATGACAGGAGCATATGAAAGCCACAGGAGAGCTGTCCAAGGTTCTTGAATCAACCCGCAGTCGCTTGCAGAACAATCTGCTTAAGAAGGAAGCTGAAAAT[A/T]AACGTCAGGAGGCTCAGATCCAAGTAAGCCAACAAATTTATACTTTGTTCTCGGTTTTTGTTTGACACAGTAAAGTGAGACTGTAAACATGTCCTGCGACACAGAGACTGGAAGAGACACTGCAGCATCAGCAGGATGAGGTTCAAGGCCTGCTGGAGCAGATGAGAGAGTTGAAGCAGCACTGTGAAGGAGACGTCCACAAACAGGTCTTGGAGGAACACAGAAAACAGGCAGAGAAAAGTGTGAATACTGCTGCACAGCTTTCTGCACAGCTCCTGGAAAAGGTAATGTAGAAAAGAAAAAGATTTGGATATCCTACCAAAGACAAAAACCAGAAGTCAGAATTATTAGTTCTCCTGTTAAATTTTTATTCTTTTTTATTTTTTCCCATAATTTCTGTTTAACAGATAGATTTTTATCTAAAAATACTTTTTTTTATCTAAAAAAACTTTTCTAAAAATAATAGTTTTAATATCTAATTTCTAATAACTGATTTATTT
Associated Phenotype:
Not determined