ZMP
im:7152917
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC36A4
Human Description:
solute carrier family 36 (proton/amino acid symporter), member 4 [Source:HGNC Symbol;Acc:19660]
Mouse Orthologue:
Slc36a4
Mouse Description:
solute carrier family 36 (proton/amino acid symporter), member 4 Gene [Source:MGI Symbol;Acc:MGI:244
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39066 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35979 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39066
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 |
|---|---|---|---|---|---|
| ENSDART00000057972 | Essential Splice Site | 74 | 488 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 39753001)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 41269708 |
| GRCz11 | 15 | 41227104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAGGATTGCTCGGGCTTCCTCTAGCAGTGAAGAATGCTGGCATAGTG[G/A]TATGTATTAATAAACTAGGTCAAGGTTAACATCAGCATTTTCAATTCAAT
Long Flanking Sequence:
CATAAAGTTAATCTGTAAAAAAAACAATTTGAATATATGAACACCATACATTTATAAAGAGATGGTTCACCCAAAAATGACAGTCCTATCACCATTTACTCACCCTTTACTTACTTTCTTCTGTTAAACATAAAAGAAGATATTTTGAAGAATGTTGGGAACCTGTAACCATTGACTTTCATAGTATTTGTTTTTCCTACTATGGAAGACATGGGATACAGATTTTCAGCATTCTTCAAAATATCTTTTTTTGTGCTCAACACAAGAAAGGTTTGGAACTACTTGAAGGAGAGTAAGTATTGAGTAAACTTTAATTTATGGGGTAAACTATCCCTTAAGTTCATGCTGTAATCTTCTGACATCTGAAGTAACATCACTGGTGTGGATTTCTTCTTCTTCTGTGTTTCAGGTTTACTCAAACTCTGCTGCATCTTTTAAAAGGGAACATCGGCACAGGATTGCTCGGGCTTCCTCTAGCAGTGAAGAATGCTGGCATAGTG[G/A]TATGTATTAATAAACTAGGTCAAGGTTAACATCAGCATTTTCAATTCAATTCAGCTTTATTTGTATAGCACTTTTACAATATAGATTGCGTCAAAGCAGCTTCACATAGAAGATCATAGTAAATTGGCACATTGTAGTTCAGCTTTTAGTGTTTAAGTTTAGTTCAGTTTAGCTCAGTTCAGTGTGATTTAATAGTCACTACTGAGAGGCACACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATGACAAATAAAATAAATCAGTTATTAGAAATGAGTTATTATGAGTTATATTTATGTTGAGAAATGTGTTAAAAAAATCTTCTCTTCGTTAAAAAGAAATTGGGCAAAAAATAAACAGGGGGTCTAATAATTCAGGGGGGTTAATAATTCTGACTTCAACTGTATATAGTCACTAATTTACTAATTAAAAATATATATTAAAATATTATTCAATAGTTTCCCAGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35979
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000057972 | Essential Splice Site | 104 | 488 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 39750373)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 41267080 |
| GRCz11 | 15 | 41224476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACTGCATGCACATCCTGGTCAACTGCAGCCATCAGCTGAGTGAGCGG[T/A]AAGAATACACCAATCAAAGCCCTCCGCCTCAGTCTGCACAGCCAGTCACA
Long Flanking Sequence:
GGCAGCAACCTAGCTTTCCCTTGTGGTCTCCCATCCAGGTACTGACCGGGCGCAGCCCTGCTTAGCTTCAGTGGGCGACCAAGTAAGAGTTGCAGAGAGCTAGCTGCCGGCTGAATAATCTGAATAATCAAGTGAAACTGCATCTGAAATATGAAAAATGTAGGACAGGTCTTGATTTTATCATTCAGGAATTGATTGGTTGGTCGTGGTCTGCTATTGGTGGATCTCATGTGATTAACGGGATGATTCCACCATTGTGACATCATATATAAATATAAAATATGTTATAGTAGAGGGAGAGAAAGGTATTTTGATTAAAGAATTAAAATGTGTTTGTGCAAAACTGATAACAGATAGTGTCTTAAAAACACATTTTACTGATCATGATTGTGTTGTTTTTCTTCCTCCAGTTGGGTCCGGTTAGTCTGGTTCTGATGGGTGTAGTGTGTGTCCACTGCATGCACATCCTGGTCAACTGCAGCCATCAGCTGAGTGAGCGG[T/A]AAGAATACACCAATCAAAGCCCTCCGCCTCAGTCTGCACAGCCAGTCACAATTCATCCACACCGAGATCATATTTTTAGGGGAGAAAAAAAAAGTGTACTTTTGCCAACTGTTTTCTCCCATTCACTGCGCTCTAAGGCCTCGTTTACTCTTAATACGTTTTAGTTTTAAAACGCATAAGTTCGGCTACGGTTACGCCATCCATCCACACCACGCTGTAGTTTTTGAGTGCAGAAAGCAAAGCATTTTGATAACGCTGGAGAGGCCATTTTCATTTTAAAACGTTGCTGCTCGGTGTCAGTGTGGATGGGGAAAAACGGAGACATCTGAAAACGGAGGCGTGGCTGCAGACATTCGCCTCTCTGATTGGGGCTTTTTACTCAATACTACGTAGACTACATACAATTCAGTCCTGCATCCTCTCCTAGTTCAGACTACGCAAGTTTGATATGGAAAACAGACTCTCGAGGACACGTCGGGTAAATCTTCAAAGGACACTGT
Associated Phenotype:
Not determined