ZMP
zgc:110527
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC503537 [Source:RefSeq peptide;Acc:NP_001012519]
Human Orthologue:
SLC29A2
Human Description:
solute carrier family 29 (nucleoside transporters), member 2 [Source:HGNC Symbol;Acc:11004]
Mouse Orthologue:
Slc29a2
Mouse Description:
solute carrier family 29 (nucleoside transporters), member 2 Gene [Source:MGI Symbol;Acc:MGI:1345278
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39333 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23957 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39333
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011551 | Nonsense | 90 | 415 | 5 | 15 |
| ENSDART00000115338 | Nonsense | 90 | 415 | 5 | 13 |
| ENSDART00000131646 | Nonsense | 125 | 450 | 5 | 13 |
The following transcripts of ENSDARG00000001767 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 26805658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 27374569 |
| GRCz11 | 21 | 27411264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGAAATGGACCGGGACAGCTTCTTTTCCATTACCATGGCAACCATCTG[G/A]TTTATTAACAGTATGTCTCTTATCATTTTAAAGTTAGATGCTGTACATAC
Long Flanking Sequence:
GGAATGGGAACTTTGCTTCCATGGAACTTCTTCATAACTGCAATGACGGTAAGACATTTACCGATCTTACTTTAGGTCTTCTTTAAATCGTACATGCTTGAACTCCTTTCTTTTTTTTACTTGCAGTATTTCACCGACCGTTTGAAAAATGGTACAAATTCTACGCAGCCAGACACGTATATGTTCAGTAACAACAGTGTGCTGCTAGCCCAGCTTCCTTTACTGCTATTCACACTCCTCAACTCCTTTCTATACCAGCAGTGAGTATTCGGTTCAAACAACATGTAGCTGCAATCCTGCATACAGATAAATACCTATAATTATGATAATTTGTTTTATCATGACCAATTTGTTTTCTTTTGTACATGTAGCATTGCAGAAAAGATCCGGATTGCTGGCAGCATGGTCGCTATATTACTTCTCTTCATTCTCACAGCCATTTTAGTGAAAGTTGAAATGGACCGGGACAGCTTCTTTTCCATTACCATGGCAACCATCTG[G/A]TTTATTAACAGTATGTCTCTTATCATTTTAAAGTTAGATGCTGTACATACAGTATATTTTCATTCCCCTTTTCATTTTGAATTGAATAGTGTGTTCAATTTCCACTTTAATTAGCAAATCATCTTATAGAACTCATCATTTTTTGCACAGTGTTTGGGGCCATTCTGCAAGGTAGTCTTTTTGGTTTGGTTGGGAAACTTCCTTCTAGATTCAGCTCCGTGTTCATGAGTGGACAGGCAGTGGCGGGAATCTTCTCTGGTCTTGCCATGCTGTTTTCAAATATCTGTGAGTACCTGAATATCTACATTTTGGACAATAAATACAATGGGATAATATACGCAGAGGAAAATAAGTATTTATAACATTTATTTATAACATTTTTCTTAGAAAAAATGTTTATAAAGTTCCTGTTTTCCTTAATAAAACGAAATGACGTACTTGTCACTAGGGTTGGGTCGATAGACGATGCCATCGTCCATCCCCGACGGTTAATAGACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23957
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011551 | Essential Splice Site | 94 | 415 | 6 | 15 |
| ENSDART00000115338 | Essential Splice Site | 94 | 415 | 6 | 13 |
| ENSDART00000131646 | Essential Splice Site | 129 | 450 | 6 | 13 |
The following transcripts of ENSDARG00000001767 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 26805508)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 27374419 |
| GRCz11 | 21 | 27411114 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCACTTTAATTAGCAAATCATCTTATAGAACTCATCATTTTTTGCACA[G/T]TGTTTGGGGCCATTCTGCAAGGTAGTCTTTTTGGTTTGGTTGGGAAACTT
Long Flanking Sequence:
GGTACAAATTCTACGCAGCCAGACACGTATATGTTCAGTAACAACAGTGTGCTGCTAGCCCAGCTTCCTTTACTGCTATTCACACTCCTCAACTCCTTTCTATACCAGCAGTGAGTATTCGGTTCAAACAACATGTAGCTGCAATCCTGCATACAGATAAATACCTATAATTATGATAATTTGTTTTATCATGACCAATTTGTTTTCTTTTGTACATGTAGCATTGCAGAAAAGATCCGGATTGCTGGCAGCATGGTCGCTATATTACTTCTCTTCATTCTCACAGCCATTTTAGTGAAAGTTGAAATGGACCGGGACAGCTTCTTTTCCATTACCATGGCAACCATCTGGTTTATTAACAGTATGTCTCTTATCATTTTAAAGTTAGATGCTGTACATACAGTATATTTTCATTCCCCTTTTCATTTTGAATTGAATAGTGTGTTCAATTTCCACTTTAATTAGCAAATCATCTTATAGAACTCATCATTTTTTGCACA[G/T]TGTTTGGGGCCATTCTGCAAGGTAGTCTTTTTGGTTTGGTTGGGAAACTTCCTTCTAGATTCAGCTCCGTGTTCATGAGTGGACAGGCAGTGGCGGGAATCTTCTCTGGTCTTGCCATGCTGTTTTCAAATATCTGTGAGTACCTGAATATCTACATTTTGGACAATAAATACAATGGGATAATATACGCAGAGGAAAATAAGTATTTATAACATTTATTTATAACATTTTTCTTAGAAAAAATGTTTATAAAGTTCCTGTTTTCCTTAATAAAACGAAATGACGTACTTGTCACTAGGGTTGGGTCGATAGACGATGCCATCGTCCATCCCCGACGGTTAATAGACATCATGATGCTGACCCGGCATTGCGGTCTTCCGCCTCGCCCCGTCGCAGCAACCCGCTCGCAAAAAATACACACTCAGGCCCCATTTACACACTAATAAGTCTTAGTTTTAAGATGGCATTATAGAACGAAAACAATCAACGTCCACACTGGC
Associated Phenotype:
Not determined