ZMP
zgc:114103
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein adipocyte-associated 1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q4V8X0]
Human Orthologue:
TPRA1
Human Description:
transmembrane protein, adipocyte asscociated 1 [Source:HGNC Symbol;Acc:30413]
Mouse Orthologue:
Tpra1
Mouse Description:
transmembrane protein, adipocyte asscociated 1 Gene [Source:MGI Symbol;Acc:MGI:1345190]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9949 | Essential Splice Site | Available for shipment | Available now |
| sa11107 | Essential Splice Site | Available for shipment | Available now |
| sa9851 | Essential Splice Site | Available for shipment | Available now |
| sa18832 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38533 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9949
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077209 | Essential Splice Site | None | 378 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 1655877)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 1600494 |
| GRCz11 | 6 | 1553166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACACYAAAGCACTTCAGAATCTGAWCTGAGACYACCAGCGCTYAAAGG[T/C]GAGTGTGTTTTTGTGAGGTTGAGCAGCTGATTTATCCGTGCAGCGTTTGT
Long Flanking Sequence:
CCACTTGTTCCAAACCTAAGATAACGTTACTGTCTTCTGTTTAACACACAAGAAGAAGATATTTTGAAGAAAGCTGAAAACCATTGACTTTCATAGTATTTGTTATCGCTACTATGGGTGTTAATGTCTTGTTTAGCTTTCTAACTTGTCTTCTTTAGTGTTCAACAGAATTGAAAACAAATTGAAACCACTTGAAGGTAAGTAAATAGTTCATTTCATCATAATATGTTCATTTTGGCGTGAACTATCCCTTCAACAAATATGTGTTGAACTTTTATTTTGAAGTGTCTCCTAGAGGGCGGCCATCTTTGATACGAGAACGCCTTCACGCTGACTTTTATCTGACAAGCGCATCGCGACTGACGCATCAGTTTCTTTCCGCCTGTAAACACCGAGTCAGAGACACAAACATAAAGTTAATATGCCTCAACCAATGCCTTATGATCGCATTAACACTAAAGCACTTCAGAATCTGATCTGAGACCACCAGCGCTCAAAGG[T/C]GAGTGTGTTTTTGTGAGGTTGAGCAGCTGATTTATCCGTGCAGCGTTTGTGAATTGTGTCATATGATACATATCCTAATGTAAACACATCACTTCAGTGTGACACACAGACGAGTTTTGTTCTTAAATGCTTTATATTTGTGTCTGAATGCGTGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTTTTAATCGCTCAGACTGTTATGTAACGATATATAAGCCTAAATAAACACACATTCCAGGGGAGTAACTTTCGCAGACCCTAAACAGCCTGTTTGCTAATGAAATATATAATTAAAAACATTATTTCGCCTGTAAATTAATTTATGATTAATTCAAGAAGCGATAAATGTTATTCACACAGTAATTAGATGTGAGTCATTGCTAATTTTGTGTTATTTATGCACTATTGTTGATTTTTATTAACATTTATCTGTTATTAGTGTAACATTTGAGTGTCTTTGTTCAGTTTTGTTTATTTATCTTTTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11107
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 |
|---|---|---|---|---|---|
| ENSDART00000077209 | Essential Splice Site | 99 | 378 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 1649816)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 1594433 |
| GRCz11 | 6 | 1546687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAGATCCGCTTGACCTCCAGCCCCATATTTGTGGCGTTTTACATATTG[G/T]TAAGCAGCCRATCCATCCTAAAGCATCCATATATTYTCAACACYGGCAGT
Long Flanking Sequence:
GTGTGTGTGTGTGTTTTGTAGTGTTTGTGTGTTTCTCTTTTAGTGTGTGTGAGGGTGTGTTTGTTTTGGATCTGTGTGTGTGTGTGCGTGTGTGCGTGCGCGTGCGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTCTTTTGTGTGTGTCCTGTATTAACAGTTATAAATGTCTGTTTTCTGTAAACCTGTTTAACACACACACACACACACACACACACACACACACACTCTCACACACTCACACACACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAGTTTAGTGCGTGTGTTTTGGTCTGTCCCGTCACCCATGGTGTGTGTTTTGTTTCTCAGGGTCCGCTACTGGGACGTGATGCTGCTCATCCCAAACGTGGCGTTCCTGGTTTTCCTGATGTGGAAGCTTCCGTCTGCGCGAGCCAAGATCCGCTTGACCTCCAGCCCCATATTTGTGGCGTTTTACATATTG[G/T]TAAGCAGCCGATCCATCCTAAAGCATCCATATATTTTCAACACTGGCAGTGCATCAAAAGCATCCATTCCTAAATAGAATGATCAGTTCTGTCTGTGTTTGCTTTTCTTAATGACTGAACACTGAGTGATATTAATATCCCAATAATAGAACATGATAATAACAGACTCAAAAGGAGAGAGTCACCCGTCAGTTTTTCAGAAAATAAAATGTTGAAGGGAAGAAATGTAGATTTATTTTATTTAAATAAGGTTTTTGCAGTGTGTTATTATTGCTATATGGTGTTCTATTGCCAATTTTTTTTATTTAATTTATGCTGTTATGTAGTGGTGGCACGGTGGCTCAATGGCTAGCACTGTGGCCTCACAGCAAGAAGGTCGCTGATTCGAGTTCTGGCTGAGCCAGTTGGGATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTGGCGTGGGTTTCCTCCGGGTGCTCCTGGTTTCCCCCACAGTCCAAACACATGCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9851
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 |
|---|---|---|---|---|---|
| ENSDART00000077209 | Essential Splice Site | 129 | 378 | 5 | 11 |
| ENSDART00000077209 | Essential Splice Site | 129 | 378 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 1647089)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 1591706 |
| GRCz11 | 6 | 1543982 |
KASP Assay ID:
2259-6982.1 (used for ordering genotyping assays)
KASP Sequence:
CACACACACACACACACAYGTTTGGTTCTGATATTGTCAGTGTGTTTGCA[G/T]GTGCTTTGGGAAATCACAAGGTTCTTTTTATTGGCTATTGAGCTCAGCGT
Long Flanking Sequence:
CTGGAGAAAGTCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTATAATTTTTTAAAACCCTATTTAAGGTCGATATTATTAGCACCTTTAAGCAATATTTGTTTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTGCTTAATTACCTTAATTAACTTAACTTAATAAACCTAGTTATGCCTTTAAATGTCACTATTAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGTCATCATGATAAAGATAAAATCAGTTATTAGAGATGAGTTATTATTAAAAATGTGCTGAACAAAATCTCATTAAAAAGAATTTGGGGGAAAAATATACAGGAATTAAAATGTGACAGGAGGACTAATAATTTTTAATTCAACTGTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATGTTTGGTTCTGATATTGTCAGTGTGTTTGCA[G/T]GTGCTTTGGGAAATCACAAGGTTCTTTTTATTGGCTATTGAGCTCAGCGTCATCATACTCGGATTGGCTTTTGGTAAGTGAACGATTCCACCTCTAATAATTAACTATTGTTATTTTAGTATGATTTAGTTATATTTAATTATAAATGTCTTTTTCAAAAACTTTTAGACTTTTTAAACTTTTAGTTCCTTCAAAAATGAATTTATAATGTATTATTTATTAGTATAATAAATAATATAATGTATTATTTATTAGAATTAATTAATTTGACCTATTTTGTTATGTACTTTTTTATTTTGTTCTATTTTATTAAAATAAAATGAATTAAAATAAAAATAATAATATATATATATATATATGTGTGTGTGTATATATATATATATGTGTATTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18832
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077209 | Essential Splice Site | 129 | 378 | 5 | 11 |
| ENSDART00000077209 | Essential Splice Site | 129 | 378 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 1647089)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 1591706 |
| GRCz11 | 6 | 1543982 |
KASP Assay ID:
2259-6982.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACACACACACACACATGTTTGGTTCTGATATTGTCAGTGTGTTTGCA[G/T]GTGCTTTGGGAAATCACAAGGTTCTTTTTATTGGCTATTGAGCTCAGCGT
Long Flanking Sequence:
CTGGAGAAAGTCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTATAATTTTTTAAAACCCTATTTAAGGTCGATATTATTAGCACCTTTAAGCAATATTTGTTTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTGCTTAATTACCTTAATTAACTTAACTTAATAAACCTAGTTATGCCTTTAAATGTCACTATTAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGTCATCATGATAAAGATAAAATCAGTTATTAGAGATGAGTTATTATTAAAAATGTGCTGAACAAAATCTCATTAAAAAGAATTTGGGGGAAAAATATACAGGAATTAAAATGTGACAGGAGGACTAATAATTTTTAATTCAACTGTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATGTTTGGTTCTGATATTGTCAGTGTGTTTGCA[G/T]GTGCTTTGGGAAATCACAAGGTTCTTTTTATTGGCTATTGAGCTCAGCGTCATCATACTCGGATTGGCTTTTGGTAAGTGAACGATTCCACCTCTAATAATTAACTATTGTTATTTTAGTATGATTTAGTTATATTTAATTATAAATGTCTTTTTCAAAAACTTTTAGACTTTTTAAACTTTTAGTTCCTTCAAAAATGAATTTATAATGTATTATTTATTAGTATAATAAATAATATAATGTATTATTTATTAGAATTAATTAATTTGACCTATTTTGTTATGTACTTTTTTATTTTGTTCTATTTTATTAAAATAAAATGAATTAAAATAAAAATAATAATATATATATATATATATGTGTGTGTGTATATATATATATATGTGTATTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38533
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077209 | Nonsense | 244 | 378 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 1642275)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 1586892 |
| GRCz11 | 6 | 1539123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGATGATGATCAATGTGTTTGTGCAGCGAAGAGGAGTTTTTACGTGTA[T/A]TCGGGGATCCTGGCGCTGCTGAATCTGGTTCAGGGTTTGGGAAGTGCTCT
Long Flanking Sequence:
ACTGTAATGAAGTTCACAGCCCTTTGGCCGCCGGGAAGGAGGAGGCGGAGAACCGACGCAGTTTTTGAATATTTATTAATAACAGTGACGGCAGCTCCTCACGGAGACTGCCATCTAAACCAAAACAAACGGACGCCAGCTCCTCACGGAGACTGCCGTCAAACTGAAAGCAGAAGTAAAATATGTCCGGGCCCGGTCCTCTCTCGGCTTCCTCTGCCATCATTCCTCCCTTTATAGTCCAGAGCTCCTTCCGTGGGATTCGAGGCAGGTGCGCACCACAGGTGTATCCACTTACGCGGTGGCCTCACTCCGTTCCCACGGCTCTCGGCCACGCCCCCTCGCCACATTGGTGTTTACGTTTACATTTTTTATGCGATTTTCAAAAATGTGCATATAATAGATGGATGGAAACATAGTTTGTGTTTCAGTGTAGATTCAGATGATGATGATGATGATGATGATCAATGTGTTTGTGCAGCGAAGAGGAGTTTTTACGTGTA[T/A]TCGGGGATCCTGGCGCTGCTGAATCTGGTTCAGGGTTTGGGAAGTGCTCTGCTCTGTGCCGACATCATTGAAGGCCTGTGGTGAGACTTCAGCTCTTTCTTACACTCTTGCTTTCTGCTTTTCTGTAGTCTCATTTTAACTATTAAAATACGCCTCTTTATGGATTTTTTAGTTAACGTTTTCTTTTTACTGTAAGAACAGTAGCTTATCATTTTAAATTACTTTAAAAAGCTCATTTTAAACGTCGACTTTTTATTTTTTATTGTTTTTTTTATCTATAAGCACAGTACAGTGTTAATGTTCAAACTATTTATAATGATTAAAGTGGCTGACAATAATAAATATTATTAATAAAAGGAATTAATCTGCCTGGTCCTTATGGTGGTGTTTGAAAAAAACAATTCTGAAGAGGTACTTGATGAAAAGAGTTTGAGAAGCGCTGCCTTAATTATTAATTATTATATATTAATTTTAGTTTACATAATTTATATCATTTTGTA
Associated Phenotype:
Not determined