ZMP
si:dkeyp-92f1.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
FAM129A
Human Description:
family with sequence similarity 129, member A [Source:HGNC Symbol;Acc:16784]
Mouse Orthologue:
Fam129a
Mouse Description:
family with sequence similarity 129, member A Gene [Source:MGI Symbol;Acc:MGI:2137237]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19741 | Nonsense | Available for shipment | Available now |
| sa32908 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19741
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099690 | Nonsense | 218 | 817 | 6 | 14 |
| ENSDART00000141315 | None | None | 347 | None | 5 |
| ENSDART00000143187 | Nonsense | 218 | 377 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22769955)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 23656660 |
| GRCz11 | 2 | 23312311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGTACGGCACATGAGGTGCAGGCTTTCCTGAAGGCCATTCACTTCTA[C/A]AGGCAGGAGAAGGGCCACTATGAATCATGGGATATGCTGGTGGGCACTGA
Long Flanking Sequence:
CTTCTTGTGTTTATAATAGTTATACAAGTTATATTATATATATTATATGTTTATATTAGTTAGTATATTAGTACATCATGCCACTTCTCTATAGTGCATTATAGTGTTCAAAATGTAAAATAAATGTAGCAAATGTAGCAATGTTGCAGTTTTTATCCTATTTAAAGTGGCCAATTCACGGAAAAGATTTTTTAAAGACATTGTTACGCCATGAAAGCACAGTCATGCATGTGGTGTGGCAATGTTTAGTTAGTTACGTTCAACCCTTTGTGACAACTGTTTATTATTTCCTTTTTTTCATATTATTTCATCACTCTTACTAGTCTTTTCCCTTCTTTCTTAAACCAGAAAAGAGAAGTTTCTAACAACTTCTCACATGATTGAGTATTACGCAATCCTTTCATTTACCAGAGCTCTTCTCCTCTGTCTGTTGTGTGTGCAGATTTTGTGAAGAGTACGGCACATGAGGTGCAGGCTTTCCTGAAGGCCATTCACTTCTA[C/A]AGGCAGGAGAAGGGCCACTATGAATCATGGGATATGCTGGTGGGCACTGACACCCAGGTGGGCCTCTTGATCTCCAAATTACTCACAAGCATCTTTACAATGAGTGTCTGGGAAAACTAGTGTCTGCTTCATTTGAATGAATGAGACGAGTCATGCTTCTGTCATGTTCTAGTGACCACAGAGGTGAACAAATGCTCTGTGACATCATAGTGTGGTCATCAGACTGAATTGAGTGGATTTAGGAGCGTCATGCTGTTAACATTTCATTTGTGGCTCATTGAACTGTCAGTTCATGCTTGACTGAAAGTATTTAATGCATGTTTATGTTTTACGAGGACTGATTTTGTACATATATTTAGTGTAAATGTTTTAGAGGAGATGTATTTGTCATTTCCACGTGCTCCAGGAAAACATTTACATTTATTTTATAGACAATGATTATATTTAAAGGGATAGTTCACCCAAAAACAAAAATTCTGTCATCAGTTTTTACTCATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32908
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099690 | Essential Splice Site | 475 | 817 | 11 | 14 |
| ENSDART00000141315 | Essential Splice Site | 78 | 347 | 2 | 5 |
| ENSDART00000143187 | None | None | 377 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 22757977)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 23644682 |
| GRCz11 | 2 | 23300333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACAAACAGGCATCGGTTATGGAGAAAGCCAAGCTCCGCGTCCTGAAG[G/A]TTGGCCTCAGAATATATTCACCAGCAATTGAACATGATCTTAATAATAAA
Long Flanking Sequence:
CAGCTCCAGGAACTGCGCAACCGCTTCAAGTTCTCCAACTCGTCTCGAGTGGTTCACTGCACACAGGGTCAGATGCAGCAGGTGGGTGTGTTTCGTGCTCTTGACTGGGCGTTGGTTAAACTTGGTGGGGCTTTTAGATGTTTTATGTTCATGTAATGAAACTGGCGCTCTGACTCAATTGTAATCACATAAATCTTTTCTAGAGCTCAGTAGAGGAAAAAAAACGACTACTGGAATTAGTTGTGTCACAGACTGCTCCACCAAAAATGAAGTCAGCGGAGAGCATTGCTTCATTTTGTCATGATCTTTGGTTCCCCCTACAGGTCAAGGGAGTTGAAATGAACTGAAGCATGTCTGTTGATTTTTTTTTCACCCCTCAAACTGTTTAGTTGATGGAGAATGCTGTGTACACGTTTGAGCTGCTGCTCCAGTCTGCTTTAAAGGATAAACCTGACAAACAGGCATCGGTTATGGAGAAAGCCAAGCTCCGCGTCCTGAAG[G/A]TTGGCCTCAGAATATATTCACCAGCAATTGAACATGATCTTAATAATAAAATAATTCTAATAAATAAAATATTGTCATGAATCTCTTTATTCTCATCAGCAATTTGACTATGACAGCAGCACAGTGAGGAAGAAGATTTTCCAGGAGGCTCTTGTTGACATCACTCTGCCAGCCATCAAGAGGAGTCTGGCCCCTGCCTGCAAAACTGTACGTTCAATTTATCTCTTAAAGATATTCCCCTGAACACTTAGACAATACACCCTCTTACTTAAATGAACACTCCAGTTTTTTAAGAAAAGGCTCATTAACTACTCCATCTTCCAAGTCTGGCAGGAGCACTTTTATTTTAGCTTAGCATAGAATAATCAAATCAGATTAGACCAGAGATGCCAAACTATAGGGCCCGTGGGTCAAAGTTGGCCCATGGTAACCTTTGATTTGGCCCACCATCCCATCTGAGAAGAAAGGGAGAATGATAGGGATGGTTAAGAGATTTGTTG
Associated Phenotype:
Not determined