ZMP
zgc:63767
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 15 member 4 [Source:RefSeq peptide;Acc:NP_957251]
Human Orthologue:
SLC15A4
Human Description:
solute carrier family 15, member 4 [Source:HGNC Symbol;Acc:23090]
Mouse Orthologue:
Slc15a4
Mouse Description:
solute carrier family 15, member 4 Gene [Source:MGI Symbol;Acc:MGI:2140796]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41259 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18451 | Nonsense | Available for shipment | Available now |
| sa25401 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34450 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41259
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 |
|---|---|---|---|---|---|
| ENSDART00000061691 | Essential Splice Site | 114 | 501 | 3 | 10 |
| ENSDART00000076101 | None | None | 240 | None | 5 |
| ENSDART00000128499 | Essential Splice Site | 168 | 428 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 37374458)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36230605 |
| GRCz11 | 8 | 35959953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGTGGGAGCTGTCAAATCAAATATCACTCCATTCGGGGCAGATCAG[G/A]TAATGCAGGGGTGTAAGAGTTGAATTTTGGGGGCCCTCAGAGGGCAGCAA
Long Flanking Sequence:
TGTTCAATGGCAGGAGACTGGCATGTGCTGCCATCCTGCTGGCAGAGTCTTTGGAAAGAATGGCCTTCTATGGCATCACCTCAAACCTGGTGCTCTTCCTCAACAGCAGCCCCTTCTATTGGGAGGGCACTTTGGCCAGCCAGGGTCCCTTGATCTTCATGGGAGTCACTTATTTAATATCTCCATTTGGTGGCTGGCTGGCAGATGCGTACCTTGGCAAATTCTTAACCATAGCCTTGAGTTTGGGCCTTTACTTGCTCGGGATGCTGCTTTTCCCTTTTGTGGCCAGTGATAATACTAGGAACTATCTGTGTGGAGAGGAGATGGCATTTCCAGTGCAGCCAGCGGAGTGTTTTCCTGAAAATGGGACAGTCCCTGCTAATGTGACCTGCGTCAATCGGCCGTCGTACTGCAGGCCTGCGATCTACAGTGGTCTGGTGCTGGTGGCCCTTGGAGTGGGAGCTGTCAAATCAAATATCACTCCATTCGGGGCAGATCAG[G/A]TAATGCAGGGGTGTAAGAGTTGAATTTTGGGGGCCCTCAGAGGGCAGCAACGGAGTCTTAGTGGGTCTGTTGAAAAGTTCGAGAACATATTAGTAAAATAATGTAATAATAGAAAGCAGATTAGACTAATAGTATGGAAAAAAATGGTATGATTAAATAAAGAAAACAAACTTATATTGGCAAGAAAAACATAATATATTTAACAGTGTATTCAAAATTGTTATCAAAATTGAAAATTGACACACAAGGTGTATCTAGAATTGATTTGAGACTCATTTCATAACTATTTTTTATGTCAGATAAACTGTCCTCCAATCATTTATGCACAAAAACTCAAGTGGTTTCATGATAATTCAATAAAAAAGGTTCAGTTTATATAAAAAAACTATATAAATATATTATTTATATAAAAATTATCTATAATAAATGCATAATATTTTAAAGTTGGATGCATGTCTTGAAATGATAAAATTAATAATAATAATAATAATAATAGTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18451
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061691 | Nonsense | 129 | 501 | 4 | 10 |
| ENSDART00000076101 | None | None | 240 | None | 5 |
| ENSDART00000128499 | Nonsense | 183 | 428 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 37365219)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36221366 |
| GRCz11 | 8 | 35950714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTACAGGYGAARGATCGAGGTCCTGAAGCAACGCGGCGGTTCTTTAACT[G/A]GTTCTACTGGTGCATTAATCTTGGAGCGATCTTCTCTCTGGGTGGTATAG
Long Flanking Sequence:
GCCAAATAAGGGCATCTAATTGGATTTGCATTGTAAACATTAAACAAAATGTATTATTTTTTATTCCATATATTAGTTATGATACTGCCAAAATCATTCCGCAAAAAATTTGATGATTTTCTTTCTTTTTTTTTTTTTTTTCGAAATTCTGCCTAGAAATAACAAAAAATGTCTGCAGATTCTATCTGGCCCTTCTAAATGATGTAAATTATTACTGAAACCAAAGTGTAACCAAATGTCTTGGTCTTGTGGTGTACTGGCTTTGCAGTGTTATTGCTCTCTTTGTTTGACATAAACCACTTTCGGTGTGTTGTTATGGAATTTAAACTGATAAAAAGAGAGTTTTTTTTTTAAAGGGAGTTTTAGCTGTTGCGACAAAACAATAAAGAGAATAAATAAAATAAATAAATGTATGATTAGAAATCCACTAATTTTCTTTTTATTTATGTTCTTACAGGTGAAGGATCGAGGTCCTGAAGCAACGCGGCGGTTCTTTAACT[G/A]GTTCTACTGGTGCATTAATCTTGGAGCGATCTTCTCTCTGGGTGGTATAGCTTACATCCAGCAGAACATTAGCTTCTCTATAGGCTACATCATCCCTGCCGTCTGCCTTGGGGTGTCCCTCATCATCTTTTTTCTGGGCAAAGCGGTTTTCATAACCAAACCTGCAGATGGCAGTGCCTTCAGCGACATGTTTCGGATCCTGGGCTCAGCCCTCTGTGGACGTGGACCGAAAGAACCCAGTCTGCTGAGGTGAGAGCAACATTTATTCACTTATTAAAGGATCAGTTCACCAAAAAAAATGTAATTCTGTTATTAATTACTCAACCTCATGTTGTTCCAATCCCCTGAGACCTGAAGATATTTTAGATGAAATCTGAATTGATAAATTGGGTCTAATTAATAAAATATGTGTAGAATCTTTTCTAAAAGTGAACATACACCAGAATATATTTTCATTTATTTATTTATGGATGTGGCTGATATGATTATTTAAAGTGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25401
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 |
|---|---|---|---|---|---|
| ENSDART00000061691 | Nonsense | 254 | 501 | 5 | 10 |
| ENSDART00000076101 | Nonsense | 43 | 240 | 1 | 5 |
| ENSDART00000128499 | Nonsense | 308 | 428 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 37359885)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36216032 |
| GRCz11 | 8 | 35945380 |
KASP Assay ID:
554-7854.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATCGCTGGTTAAAATACTTCCTGTTTTCCTGGCCCTCATTCCATACTG[G/A]ACTGTCTATTTCCAGGTAAGGCTACTATACATCTTTCAGATCTGTCAGCT
Long Flanking Sequence:
TGTGTGAAGCTGTACATTTATGAGGCTTTTTTCAAGCTTTCACATGACTCTATTAGTGTGTGATGTTATCCCTCACCTACCTTTTGATCCAGCTCTCCTGTCTGTCTCACACGCAGTGCTATTCATCGTGTCTCTGTGGTATAACTTACTGTCAAGTGCTGTACCCTTTCTTTAAACCAAAGAAGAACTCTTTATAAAAACCTGACATTAGAATCTTGGAATTAGAGGAAACAAGTCAAAATCCTTGCTCATTTGTTTCTTTGCTTTTTTTTTTCTTTCTTCCTGAGCTGTTGATAATCTCACAAATATTGCAATGATGTGATTTAATAATGTCTACACAGAAAAGCTTGTTACAAACCATGTTTTCCCTTTAGGCCAAAGCCCACTGTTCTGGATGGTGCTAAAGTAACATACGGCGGCCGCTTTTCAGACGAGAAGGTGGAGGAAGTGAAATCGCTGGTTAAAATACTTCCTGTTTTCCTGGCCCTCATTCCATACTG[G/A]ACTGTCTATTTCCAGGTAAGGCTACTATACATCTTTCAGATCTGTCAGCTATTAAAAAAAAGGGAGTTGTACAGCTGGCATATTAACTTAAAGGTCTCGTGAAATTGAAATAAAAAAAAATAATAATGTTAGTTCCCTTCAGTTACACTGCAGGCAAATGTGACCCAAATCTGGTTTTCTTTTGTCCACATGTGACTCATTTTGGTTATGACAGTGTGAACGGCTCAAACATCATGGAATCTAATCTTTTCAGTTCTGATTTGTCCCACTTTCATATGTGGTACTAAATCAGATACAGATCTGATGTTTTGCATTGTGACCGCAGTGTGAACCGGTATGTAGGAATTCATGTGACCCTTACATGATTTTGGATCGACGTGCATCATCATTCTGTGCTGCAAACATCTTCAACAGCATAGTACAATAGCACACAGGGCAAATACTTTACCACAAAAAGTTGGTTGTTCATTTTGAATATTTTCTTTTAAGCAAAACTGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34450
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061691 | Essential Splice Site | 259 | 501 | 5 | 10 |
| ENSDART00000076101 | Essential Splice Site | 48 | 240 | 1 | 5 |
| ENSDART00000128499 | Essential Splice Site | 313 | 428 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 37359868)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36216015 |
| GRCz11 | 8 | 35945363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCCTGTTTTCCTGGCCCTCATTCCATACTGGACTGTCTATTTCCAGG[T/C]AAGGCTACTATACATCTTTCAGATCTGTCAGCTATTAAAAAAAAGGGAGT
Long Flanking Sequence:
TTATGAGGCTTTTTTCAAGCTTTCACATGACTCTATTAGTGTGTGATGTTATCCCTCACCTACCTTTTGATCCAGCTCTCCTGTCTGTCTCACACGCAGTGCTATTCATCGTGTCTCTGTGGTATAACTTACTGTCAAGTGCTGTACCCTTTCTTTAAACCAAAGAAGAACTCTTTATAAAAACCTGACATTAGAATCTTGGAATTAGAGGAAACAAGTCAAAATCCTTGCTCATTTGTTTCTTTGCTTTTTTTTTTCTTTCTTCCTGAGCTGTTGATAATCTCACAAATATTGCAATGATGTGATTTAATAATGTCTACACAGAAAAGCTTGTTACAAACCATGTTTTCCCTTTAGGCCAAAGCCCACTGTTCTGGATGGTGCTAAAGTAACATACGGCGGCCGCTTTTCAGACGAGAAGGTGGAGGAAGTGAAATCGCTGGTTAAAATACTTCCTGTTTTCCTGGCCCTCATTCCATACTGGACTGTCTATTTCCAGG[T/C]AAGGCTACTATACATCTTTCAGATCTGTCAGCTATTAAAAAAAAGGGAGTTGTACAGCTGGCATATTAACTTAAAGGTCTCGTGAAATTGAAATAAAAAAAAATAATAATGTTAGTTCCCTTCAGTTACACTGCAGGCAAATGTGACCCAAATCTGGTTTTCTTTTGTCCACATGTGACTCATTTTGGTTATGACAGTGTGAACGGCTCAAACATCATGGAATCTAATCTTTTCAGTTCTGATTTGTCCCACTTTCATATGTGGTACTAAATCAGATACAGATCTGATGTTTTGCATTGTGACCGCAGTGTGAACCGGTATGTAGGAATTCATGTGACCCTTACATGATTTTGGATCGACGTGCATCATCATTCTGTGCTGCAAACATCTTCAACAGCATAGTACAATAGCACACAGGGCAAATACTTTACCACAAAAAGTTGGTTGTTCATTTTGAATATTTTCTTTTAAGCAAAACTGCCTATGTTGTTTATAACGAA
Associated Phenotype:
Not determined