ZMP
si:dkey-48j7.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens SLC38A3, solute carrier family 38, member 3 (SLC38A3) [Source:Uni
Human Orthologue:
SLC38A5
Human Description:
solute carrier family 38, member 5 [Source:HGNC Symbol;Acc:18070]
Mouse Orthologue:
Slc38a5
Mouse Description:
solute carrier family 38, member 5 Gene [Source:MGI Symbol;Acc:MGI:2148066]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41216 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41217 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16895 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41216
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062385 | Essential Splice Site | 91 | 491 | 4 | 15 |
| ENSDART00000133983 | Essential Splice Site | 40 | 440 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 26472328)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25600246 |
| GRCz11 | 8 | 25619385 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTGTTTTGTTGCCAATACCCAAGTTAATCATTTGTGTCTTTTTCTTC[A/G]GATTTCTGTTGATAACCATCGCTTTGCTCTCTTCTTACTCTATCCATCTG
Long Flanking Sequence:
ATTATTTTGCTAATACTATGAAAGTCAATGGGATTTGATATTGTTTTGATTCCTAAAGAATTTCACTGGATAGGCAAACACATTCTTCAAAACATCTTCTTTGTTCTACAAGCGAAAGCCTTCGAATGACACAAGTTAGGAAATATTGGCAGAATTTTACTATCATTATTTAGTTTTCTGCGAATTATCTCTTTAAATCTAAATGCACTGCAAAAAGCGATTAGTTGACTTTGTTTTTTTAGAAAATGAGCAAACACATTGCTTTTGAAATATCTAGTTGGGTTTACTTAAAAGATAAGCAAGCCTGTTGCCTTTAAATGAATAAGTAAATTAACTATAACCAGGTTTACTCTTTATTTTTTAAAGTAAAGTCAACTTGTCACTTTTAAGGCAATGTGTTGTAATTTTTTAATTACAGTAACTTAATTGCTTTAAACAGTGTGGGAAGTTGTATTGTTTTGTTGCCAATACCCAAGTTAATCATTTGTGTCTTTTTCTTC[A/G]GATTTCTGTTGATAACCATCGCTTTGCTCTCTTCTTACTCTATCCATCTGCTTCTGAGGAGTGCAGGAGTGGTTGGTGAGAAACATTTTCTCTTTTATGTCTCTAAAGACAGTCCTAACAACATTGCATTATATGATAAATCAGCATCTGAACTTTCCATTATGTTTGTTTTTTTTAGGCATCCGTGCATATGAACAGCTGGGGTACCGTGCATTTGGTACGCCTGGAAAAGTTGTTGCAGGATGTATTATAACATTGCACAACATTGGAGGTACAGCATATGTAATTAAATGATTACACTTTGATTCCATTACCACTCAGTACAACACGAGTGCTGAATACAGATCCACGAAAACTATTCATGCTGTCTTTCTTTGACTCAACAGCAATGTCAAGTTACCTATTTATTGTGAAGATAGAGTTACCTCATGTCATTGAAGGTCTCACAGGACTGCCAGACAACTCTGGGTGAGTACTGAAAAATACTTCTGATGGGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41217
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 |
|---|---|---|---|---|---|
| ENSDART00000062385 | Essential Splice Site | 174 | 491 | 6 | 15 |
| ENSDART00000133983 | Essential Splice Site | 123 | 440 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 26472797)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25600715 |
| GRCz11 | 8 | 25619854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTACCTCATGTCATTGAAGGTCTCACAGGACTGCCAGACAACTCTGG[G/A]TGAGTACTGAAAAATACTTCTGATGGGTTCAGCTGTTTGAGACCATGTTA
Long Flanking Sequence:
ACCCAAGTTAATCATTTGTGTCTTTTTCTTCAGATTTCTGTTGATAACCATCGCTTTGCTCTCTTCTTACTCTATCCATCTGCTTCTGAGGAGTGCAGGAGTGGTTGGTGAGAAACATTTTCTCTTTTATGTCTCTAAAGACAGTCCTAACAACATTGCATTATATGATAAATCAGCATCTGAACTTTCCATTATGTTTGTTTTTTTTAGGCATCCGTGCATATGAACAGCTGGGGTACCGTGCATTTGGTACGCCTGGAAAAGTTGTTGCAGGATGTATTATAACATTGCACAACATTGGAGGTACAGCATATGTAATTAAATGATTACACTTTGATTCCATTACCACTCAGTACAACACGAGTGCTGAATACAGATCCACGAAAACTATTCATGCTGTCTTTCTTTGACTCAACAGCAATGTCAAGTTACCTATTTATTGTGAAGATAGAGTTACCTCATGTCATTGAAGGTCTCACAGGACTGCCAGACAACTCTGG[G/A]TGAGTACTGAAAAATACTTCTGATGGGTTCAGCTGTTTGAGACCATGTTAAAAGTTTTAGTTATATAAACAGAAGAAGGAATCTGAAACAGATGAAAGGAAGAAAGAGCATCATGTCAATTACATTTGATCTGTTCTTTCCCTTCATTATTTAAACAAGAAAATTGCTAGTGAAATACTTTGAGGCACAAAGTGGATCCTTCTCAAATATTACTGAAGAATATGTCAGTCATTTTGTTATTCTGTTTTTTTTATGTTCTGTAATGTATAAAAACATCTAAACAAAACTATTGTCAAACTAGTGGTCTCAGACATTTGATCCTTGTTAACTGAATTTTCCTCTCTTTTCTCAAAATCCTCTTTTTTGACTTCATTTTTTTTTTTTACTCTTCATCAGTCACTGGTATGTAGATGGGAGATACCTCATCATTATTGTTAGTGTCTGCGTCATTTTCCCACTGGCACTTATGAAAAGACTTGGTAGGTTACAACTACTTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16895
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062385 | Essential Splice Site | 424 | 491 | 14 | 15 |
| ENSDART00000133983 | Essential Splice Site | 373 | 440 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 26476137)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 25604055 |
| GRCz11 | 8 | 25623194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCTATCATTCGAATGCAGCACTTTGTGATACATTTTATACTATATTTC[A/T]GGTGCARCATCTGCTCCCAGCCTCATTTTCATTCTGCCAGGAATATTCTA
Long Flanking Sequence:
TGAGGGTCTTAAAAATACGTATTTTAAAAGAAATTATATTAACAAATGATATTTGAAACTCTCTCTTCTGGGTCAAAATGATCTCAAATGCATTATGAAGATCAACTGACAAAACTATTGGACATCCCTTAAACGTGTTTCCTTAAGAAATAAAACACTTGTGCATACAAAATGTCTCCAAAGCACAGCTGCACAATAATCTGCTTCACACATAACATCAATCAATGTCTGAACAACATACAACACTTTTGACGTCTCCTATAATCATGTTTTCTTCTAGATCCGCCGTGCCGTCTTGCAGCTTCTATTCCCTGAAAAGCCTTTCAGCTGGGTGCGTCACATCATCATCGCCATGTGCCTCCTGTTTGCCGTCAATCTGCTCGTCATCTTCGTCCCCAACATTCGTGACATCTTCGGCTTCATCGGTGAGTTGGATTTACCACATAGAAGATTCTATCATTCGAATGCAGCACTTTGTGATACATTTTATACTATATTTC[A/T]GGTGCAACATCTGCTCCCAGCCTCATTTTCATTCTGCCAGGAATATTCTACATTTACATCGTCCCTGAGGAGCAGGAGCCATTAAAATCTCGACCAAAGATTCTGGTGAGAATAAAGACAGAGCATGCAGAACTCCACTCTCACTCTTTTCTTTTTCACTTTCTCACTTCCTGTTATGTTTTCCAGGCGATTTTGTTTGTGACCCTGGGGTTCATCTTTATGATTATGAGCATTACTTTCATCATAATCGAGTGGGTCAATGGAAAGCAGTCGGTGGGCGGTCACTGACGGAGCTGAGACAGCGAAACAGATTCCAGCACTTAAAGACCAAATACAGCAAACACAAAATGCTGAGCCTGAAAACATGATTCAGGTTCAGGTTCATCCATCAGATAAGTCCAAAATGAAAAATGGTTTTCAGGAAGACTTTTACTATTTTTATAAAAGCCAGTTTTACTTGAAAAGTATTGCTGTTATGAATGGAATCAGATGGAATCTCC
Associated Phenotype:
Not determined