ZMP
zgc:158635
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC791217 [Source:RefSeq peptide;Acc:NP_001074168]
Human Orthologue:
SLC45A1
Human Description:
solute carrier family 45, member 1 [Source:HGNC Symbol;Acc:17939]
Mouse Orthologue:
Slc45a1
Mouse Description:
solute carrier family 45, member 1 Gene [Source:MGI Symbol;Acc:MGI:2653235]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9841 | Nonsense | Available for shipment | Available now |
| sa19012 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9841
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043016 | None | None | 148 | None | 4 |
| ENSDART00000102760 | Nonsense | 266 | 802 | 4 | 9 |
| ENSDART00000134560 | Nonsense | 266 | 802 | 5 | 10 |
| ENSDART00000043016 | None | None | 148 | None | 4 |
| ENSDART00000102760 | Nonsense | 266 | 802 | 4 | 9 |
| ENSDART00000134560 | Nonsense | 266 | 802 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 42133809)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 40393590 |
| GRCz11 | 11 | 40657735 |
KASP Assay ID:
2260-4647.1 (used for ordering genotyping assays)
KASP Sequence:
TCGGTGGAGGCTTCGGCTACATAGTGGGTGGCATCAACTGGGACAAAACT[G/T]AGTTCGGAAGGACAATGGGCGGTCAGCTCCGCGTCATATACCTGTTCACC
Long Flanking Sequence:
GTGACTGTCGCTAGTGCACCTTTTGAGGTCAGAGGAGTGAAGTTTATCTGCACAGCACTTCACTAGCTGGCCTCCATTACATTGGCATTTCTGTGTGGAGTTTGCAGGTTCTCCCCATGCTGGTGTGGATTTCCTTCTGGTGCTTCGGTTTCCCACACAAGTCCAAAGACATGCGCTGAACTGGATAAACTAAATTAGACTTAGTGTATGCGTGTGTGTGAGAGTGTATGGGTGTTTTCAAGTTCTGGGCTACGGCTGGAAGGGCATCCACTGTGTATAGTTGGCAGTTAAGTCCGCTGTGGAAACCATTGAGAAGTAAGGGACTAAGCCAAAGGAAATTGAATGAATAAATGAATGAACTTTCATATCAGGAATGTTTTTTAAATGACATTTAATAGTTTGCCATGACTGAACTCCATACTTCTGCATCTCTCATGTATAACTCAGGTCTCGGTGGAGGCTTCGGCTACATAGTGGGTGGCATCAACTGGGACAAAACT[G/T]AGTTCGGAAGGACAATGGGCGGTCAGCTCCGCGTCATATACCTGTTCACCAGCATCACCCTGGCCGCCGCCACAGCCATGACCCTCACTAGTATCCCAGAGCGGCCTTTACCCCAATCCCAACCTCAAACCAGAAACACTCGAAACCTAAAGAGCCCCAATCTCCCTCTGCCTCCATCCCCGCCACCGCCTCCTGGAGCTGCTGCAGATCAGGATGAAGAGGATGAAGAAGAAGCTCTATATAACAGCCAGTTCTCCAATTGCCGCAACCCTGATCTTTTCGGCCGCTCCAGCAGTGCAAACGCACGTTTATACGCAGGCCTCACCAGCCCAATCTCCCCTCTAAGTCCTTTGACACCCAAATACGGCAGCTTTATAAGTCGAGATAACTCTCTCACGGGCATTAATGAGTTCGCATCCTCTTTAGGCACCTCCTATATAGACAGAGTATTAATTGAATGTTACACCGGACAGCAGACGCCGCAGCCAATGGAATGCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19012
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043016 | None | None | 148 | None | 4 |
| ENSDART00000102760 | Nonsense | 266 | 802 | 4 | 9 |
| ENSDART00000134560 | Nonsense | 266 | 802 | 5 | 10 |
| ENSDART00000043016 | None | None | 148 | None | 4 |
| ENSDART00000102760 | Nonsense | 266 | 802 | 4 | 9 |
| ENSDART00000134560 | Nonsense | 266 | 802 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 42133809)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 40393590 |
| GRCz11 | 11 | 40657735 |
KASP Assay ID:
2260-4647.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGTGGAGGCTTCGGCTACATAGTGGGTGGCATCAACTGGGACAAAACT[G/T]AGTTCGGAAGGACAATGGGCGGTCAGCTCCGCGTCATATACCTGTTCACC
Long Flanking Sequence:
GTGACTGTCGCTAGTGCACCTTTTGAGGTCAGAGGAGTGAAGTTTATCTGCACAGCACTTCACTAGCTGGCCTCCATTACATTGGCATTTCTGTGTGGAGTTTGCAGGTTCTCCCCATGCTGGTGTGGATTTCCTTCTGGTGCTTCGGTTTCCCACACAAGTCCAAAGACATGCGCTGAACTGGATAAACTAAATTAGACTTAGTGTATGCGTGTGTGTGAGAGTGTATGGGTGTTTTCAAGTTCTGGGCTACGGCTGGAAGGGCATCCACTGTGTATAGTTGGCAGTTAAGTCCGCTGTGGAAACCATTGAGAAGTAAGGGACTAAGCCAAAGGAAATTGAATGAATAAATGAATGAACTTTCATATCAGGAATGTTTTTTAAATGACATTTAATAGTTTGCCATGACTGAACTCCATACTTCTGCATCTCTCATGTATAACTCAGGTCTCGGTGGAGGCTTCGGCTACATAGTGGGTGGCATCAACTGGGACAAAACT[G/T]AGTTCGGAAGGACAATGGGCGGTCAGCTCCGCGTCATATACCTGTTCACCAGCATCACCCTGGCCGCCGCCACAGCCATGACCCTCACTAGTATCCCAGAGCGGCCTTTACCCCAATCCCAACCTCAAACCAGAAACACTCGAAACCTAAAGAGCCCCAATCTCCCTCTGCCTCCATCCCCGCCACCGCCTCCTGGAGCTGCTGCAGATCAGGATGAAGAGGATGAAGAAGAAGCTCTATATAACAGCCAGTTCTCCAATTGCCGCAACCCTGATCTTTTCGGCCGCTCCAGCAGTGCAAACGCACGTTTATACGCAGGCCTCACCAGCCCAATCTCCCCTCTAAGTCCTTTGACACCCAAATACGGCAGCTTTATAAGTCGAGATAACTCTCTCACGGGCATTAATGAGTTCGCATCCTCTTTAGGCACCTCCTATATAGACAGAGTATTAATTGAATGTTACACCGGACAGCAGACGCCGCAGCCAATGGAATGCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41906
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043016 | None | None | 148 | None | 4 |
| ENSDART00000102760 | Nonsense | 490 | 802 | 4 | 9 |
| ENSDART00000134560 | Nonsense | 490 | 802 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 42134481)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 40394262 |
| GRCz11 | 11 | 40658407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCGTTGCAGGCCGATGAGCAAAAACAAGCCATTGAGCCTGACGAGCAG[C/T]AGAATGAAGCTGCGGCAGGCTCTCAGAGAGGCAGTAGCTCAGGGATATTG
Long Flanking Sequence:
CTCCATCCCCGCCACCGCCTCCTGGAGCTGCTGCAGATCAGGATGAAGAGGATGAAGAAGAAGCTCTATATAACAGCCAGTTCTCCAATTGCCGCAACCCTGATCTTTTCGGCCGCTCCAGCAGTGCAAACGCACGTTTATACGCAGGCCTCACCAGCCCAATCTCCCCTCTAAGTCCTTTGACACCCAAATACGGCAGCTTTATAAGTCGAGATAACTCTCTCACGGGCATTAATGAGTTCGCATCCTCTTTAGGCACCTCCTATATAGACAGAGTATTAATTGAATGTTACACCGGACAGCAGACGCCGCAGCCAATGGAATGCGAGGCTGTTGCTGTGGCCCCGCCTCTTCCACCAGGAGACACGCCCCCTCCTCATGGACAAAGTGAAACGCTTGAAGTTCCACAGCAGATTAAGGTTTCACAGCCGAATGGAGAGCTGGCGACTGATGCGTTGCAGGCCGATGAGCAAAAACAAGCCATTGAGCCTGACGAGCAG[C/T]AGAATGAAGCTGCGGCAGGCTCTCAGAGAGGCAGTAGCTCAGGGATATTGAAGAGGCCACAGAGTCTGGCCTTAATGGAGGATCCGCTGATTGCTCCGAGCGCTGGATTGGATAACGGTCGTAGACGCACTGTTACTTTCAGTCAACAGGTCTGTACATTTACATTGAATCATTTGCCAAACTCTTTTATCCAAGTGATGAGAAATGATCAATGCAACAATAGAACAAACATGTGGATAATATGAAAAGTTTTAGTAAGTGTGCAATTTAAATTTGTGCTGTCAAAAGATTTATCGCGATTAATTGCATTCAAAATAAAAGTTTGTATTTACACAATACGCACACACACACACATACACTACCTGATACAAGTGTTGTTGCTTGCTTATCCAAGTTTTAAGAACAACAAATAATAACTTGACTTCTAGTTGATCAGTTGGTTTTAGAAGTGGCTTATATGAAAGGCAAAGGCCTCTAAATTACGCTTATTTTACCAAAAT
Associated Phenotype:
Not determined