ZMP
zgc:171581
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100136868 [Source:RefSeq peptide;Acc:NP_001108058]
Human Orthologue:
ABCA1
Human Description:
ATP-binding cassette, sub-family A (ABC1), member 1 [Source:HGNC Symbol;Acc:29]
Mouse Orthologue:
Abca1
Mouse Description:
ATP-binding cassette, sub-family A (ABC1), member 1 Gene [Source:MGI Symbol;Acc:MGI:99607]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42341 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42342 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa22420 | Nonsense | Available for shipment | Available now |
| sa18382 | Essential Splice Site | Available for shipment | Available now |
| sa16400 | Essential Splice Site | Available for shipment | Available now |
| sa22421 | Essential Splice Site | Available for shipment | Available now |
| sa8542 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42341
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 |
|---|---|---|---|---|---|
| ENSDART00000051556 | Essential Splice Site | 54 | 2282 | 3 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6410584)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6137971 |
| GRCz11 | 14 | 6444698 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCCGTCTTCAATGAGGTAGTTAATTTAGTCTCTCTCTATTCATTACA[G/T]GTCACTTTCCCAACAAAGCCATGCCCTCAGCAGGCACCCTGCCCTGGATC
Long Flanking Sequence:
GTTCGAGGCAACTGTACCTAGTGTGAGTACGGCCTAAATATTCACTCTGAAATAGCATGGCAGTTTGACTTGCTCGCCACCGGACAAGCACTAGTCGCTTTTAACACAAGAGAGTTTTTTTTTGCTGTTCTCGTGTTTAAGGAGGTGTGGCTCTAGACGGCAGGAGAGAGAGTGTTATTCAGAGATTTATGCTAAGCTGTTAGCATTGTGAAAGATCACCTACTGCACCTTTAATTCCTTCATGTTGCCCCAACACAAATCAATTATGTGGAACCCACAGTGAATTACACTCATTTGAGGATTTGTAATCCATTACTTTACACCGATGAAATTTGATTTATTGAAAGAAATGTTTTTAGGATTAAATGTTTTCTGATTTTGTCTTTGTTCGCCAGTGTACACTTTCTTCTCTTCTGCCACCCTGACAAGGCCTTAATGTGGAAACTCTTTTCACCCGTCTTCAATGAGGTAGTTAATTTAGTCTCTCTCTATTCATTACA[G/T]GTCACTTTCCCAACAAAGCCATGCCCTCAGCAGGCACCCTGCCCTGGATCCAGGGCATCGTCTGCAATGCCAACAATCCGTGCTTCCGCCACCCAACCCCAGGGGAATCTCCCGGAGTCGTTGGGAACTTCAACGATTCCATGTAAGCGGTCGCCTGCGGCTGAAGATTTCCAAATAACAGCTGTCAGCTCTGATGTAGCCTGTTACACGTAATATAAGACATTGAGTATTGCACAGTCTAGTAGTAATCATGAGTTCTTTTTTATTTCAGAATCTCACGCCTTTTTTCTGATGCCAAGAAGATCTTGTTGTATAGTCAAAATGACAAGAGCTTGGATGGGTTCAAGGAGCTCATCGACGCTGTAAAAGTCATGCAAAATAACACGGCCGGTGAGTAGATTAGTCTACAATTTAACCCTCATTGGAAAGACCATTTGGTTTTATTGGGAGTTTTTTATGACTTGAAAAAATTTATATTGTAATCAACGTCAATGATGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42342
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 |
|---|---|---|---|---|---|
| ENSDART00000051556 | Nonsense | 168 | 2282 | 5 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6426079)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6153466 |
| GRCz11 | 14 | 6460193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACCCTCTCTACCTTCCTCCTACAAAACGCCTCATTTACAGAGAATTA[T/A]GTTACGAATATTCTGGACGCTGATGTGAATCTTGAAAAGGTGAGAAAGGA
Long Flanking Sequence:
AATGAATCAGTCGCCGTTTCTCTCCACGCCCAGGAGAACCGCTCTAGCTGGCCTGCTCAGACATGCGCTTGAACTTTGAAAAGAGGAATGAAATTTAAGGAGAGCGCACCAGCGTGTAGTTAACACTCTCAAAGGCTCCACACCTGAATGAACAGCGCTCAATTTCAGCAAGTGAGCGCATGCACGGGGAACAAAAGGTTTGAGGTTTTGTAAGAATGCAAACCAAATGTAAATTAATGAAGAGCGGGCTGCATTTCCAAAAAAACAAAATTAATCCTAAAATGCAGGGGTGGGTCTGCTGAAATTGAAAGTTTGGTCAATTTGCTGAAAACTGATAACTGCAGCCATTGTATGGTGGATTTGTAAAGCACTCCTTAACACACACACACTTACACTAAAGCAATATGTTTGTCCCCAGGATTCAAGCTGAAGGACTTCCTGCATGAAGACGAGACCCTCTCTACCTTCCTCCTACAAAACGCCTCATTTACAGAGAATTA[T/A]GTTACGAATATTCTGGACGCTGATGTGAATCTTGAAAAGGTGAGAAAGGAAATGCACCGTATGGAAACATTAATGGTGCCTATGAGAGTTGATTTGCATAAACGTGCTTGTGTTTCCCCTAACAAACTTTAGGAAGGTGACAGAATGTTGGAAATATGGATTTATAGCCATAGACAGGGTTTCTGCAGGTCACATTTAAGACTTTTCAAGACCTTTTTAGGACTATTATGAATTAAATTTTGTAAAGGGCAGATGATTTTTTTTACTTGACCCAGTCAAATTTAAATTCAGTTATTTTTTAGCCGAACATTTTAAATAACGTGTCGAAACAAGCAAACTCTAGATGTATACATGTATACACTCACCGGCCACTTTATTAGGTACACCTACTACTAGTACCGGGTTGGTCCCCCTTTTGACTTCAGAACTGCCTTAATCCTTTTTGATCGGATGTGCACAAAAATGTTGTCCTGATTTGTTCTGACAGCCTAAACAAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22420
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051556 | Nonsense | 328 | 2282 | 8 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6439374)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6166761 |
| GRCz11 | 14 | 6473488 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGACACCCTGAAGGCGGTGGCCTCAAGATCAAATCCCTCAACTGGTA[C/A]GAAGACAGCAACTTCCAGGCGCTGTTTGGCAACCACAACGACAGCGATGA
Long Flanking Sequence:
GAGGGACTTTGGCCAGGACACCGCAGTCCAGTGCAGTTCTCCTGAAATTATGTGTTCGGCATGTTATTCAAAACCAATATTGCTCTTTCATCTGTGAAACACAAAAGAAGTCATGCTTTCACTTCTTTTCAATTATAACAAATAGTAACTGGAGCCTTCATGCTTCAAAAAGAACACAAAAGCTACCTGATAGTGGTCTAAATCACTTGTGCACTACAGTATTCCATTGAAGCCTATAGATTCTGTTTAGCTAACCAATCAAAATCTCTTTTAACTTCTTGTGTGTCTATATATCAGTATTCTTAGCTCTGATTAAAATGGTACCCACTTCCATTCTTTCAGCTGGCCAGTATGAGGAGTTGGAGTGACCTGCGAAACGAGATCCTGTTTCTGACCGAAAATGCCACTGGCTCCCCAAGTCTGATGTACCAGGCTGTGTCCCGTATCGTGTGTGGACACCCTGAAGGCGGTGGCCTCAAGATCAAATCCCTCAACTGGTA[C/A]GAAGACAGCAACTTCCAGGCGCTGTTTGGCAACCACAACGACAGCGATGACCAACCGGTTCCAGTCTACGACAACACAACCAGTATGTCAAGCATATAAAAGTGTTTATTATTATTTAAATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATCTATTAATATTTAAAAGTTTTGTTTTTAAGTTTAAGCATTTTATTTAATATTTTTATAATATCATTCTAATCCTTTTCTCATCTCCTAAACAAAAGAGAGATTACTGTCTCTCTACTGAAAAACAACTCGTTTAAAAGTATTGACAAAATGTTGATTGGTGAGTATAAACAGAAGCTTTTAGGCTCATAGAACTATTGGTGGAAGTACCAGCATTTCAGCATCTTCATAACACAGGAATTACAAATTATTTTGGTTATAGGAACACCTTATGTGGGAACTAAATTAGCACAAAATGTTTTGTTTTTTCAAAGTCTACCTACATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18382
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 |
|---|---|---|---|---|---|
| ENSDART00000051556 | Essential Splice Site | 1728 | 2282 | 34 | 46 |
| ENSDART00000051556 | Essential Splice Site | 1728 | 2282 | 34 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6460131)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6187518 |
| GRCz11 | 14 | 6494245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAATATGCCAAGTATCTAAATGCACATGTCTKTYTGTTTTCTGCTACA[G/T]TGCAATTATGTTGTTCCTGCCACTCTGGTGATCCTGATCTTTGTGTGCTT
Long Flanking Sequence:
GTATTGGGGCCTTCCTCAATGTAATGAACAACGGTATCTTGCGTGCAAACTTACCACCCGGTAAAGACCCCAGTGAGTTTGGCATCACTGCGTACAACCATCCACTCAATCTGACCAAGGAACAGCTTTCTCAAGTGGCGCTGTAAGTCCTGAAATAATGATTCAATTAAATATTAATAACAAAAATAACATATTTAATGGATTAACACAGTTTTACGATCTCTGATTGATGGCCTTTCAGGATGACTACCTCGGTAGACGTGCTGGTTTCCATCTGCGTGATCTTCGCCATGTCTTTCGTCCCTGCTAGCTTTGTTGTCTTCCTCATCCAAGAGCGAGTGAACAAAGCCAAGCACATGCAGTTTATCAGTGGAGTTCAGCCATATCTCTACTGGCTGGCAAACTTTCTCTGGGATATGGTGAGTGTCTGCTTTATATGCTATAATCCTCCCAAATATGCCAAGTATCTAAATGCACATGTCTGTCTGTTTTCTGCTACA[G/T]TGCAATTATGTTGTTCCTGCCACTCTGGTGATCCTGATCTTTGTGTGCTTTCAACAAAAAGCCTACGTTTCCGCCACCAACCTGCCTGTTCTTGCCCTGCTTCTGCTTCTATATGGGTAAGACATTCTTATGGAGCTAGTATGACGATCACTCGCAAATTAGGAACATTTTCTGTAGATATGGGAGTTGTGCTGGCTTTTGCACAACAGGTCTTTAAGCAGCAGATCACTACATGCATTTTTCTGATCGGATAGCTTTCTGTTTGTAAAAAGGGAAGGTGTAAATGCTTTCTGAAATGCATTTGAGATGGATATGAATCCAATCTCTCAAATAACTTTAGGAGGTGGTCTTTGATGCATTCCAGACGAACCTGGACAAGTCTAAATGTTGGATCTTACTCCTTCCAAAATGTAAATAAACAAGTGAGACTGTGGCCCCGTTTACACTAGTGCGTTTTAGTTTTAAAACGGCGTTTTAGAATGAAAACGATCCGCGTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16400
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051556 | Essential Splice Site | 1728 | 2282 | 34 | 46 |
| ENSDART00000051556 | Essential Splice Site | 1728 | 2282 | 34 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6460131)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6187518 |
| GRCz11 | 14 | 6494245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAATATGCCAAGTATCTAAATGCACATGTCTKTYTGTTTTCTGCTACA[G/A]TGCAATTATGTTGTTCCTGCCACTCTGGTGATCCTGATCTTTGTGTGCTT
Long Flanking Sequence:
GTATTGGGGCCTTCCTCAATGTAATGAACAACGGTATCTTGCGTGCAAACTTACCACCCGGTAAAGACCCCAGTGAGTTTGGCATCACTGCGTACAACCATCCACTCAATCTGACCAAGGAACAGCTTTCTCAAGTGGCGCTGTAAGTCCTGAAATAATGATTCAATTAAATATTAATAACAAAAATAACATATTTAATGGATTAACACAGTTTTACGATCTCTGATTGATGGCCTTTCAGGATGACTACCTCGGTAGACGTGCTGGTTTCCATCTGCGTGATCTTCGCCATGTCTTTCGTCCCTGCTAGCTTTGTTGTCTTCCTCATCCAAGAGCGAGTGAACAAAGCCAAGCACATGCAGTTTATCAGTGGAGTTCAGCCATATCTCTACTGGCTGGCAAACTTTCTCTGGGATATGGTGAGTGTCTGCTTTATATGCTATAATCCTCCCAAATATGCCAAGTATCTAAATGCACATGTCTGTCTGTTTTCTGCTACA[G/A]TGCAATTATGTTGTTCCTGCCACTCTGGTGATCCTGATCTTTGTGTGCTTTCAACAAAAAGCCTACGTTTCCGCCACCAACCTGCCTGTTCTTGCCCTGCTTCTGCTTCTATATGGGTAAGACATTCTTATGGAGCTAGTATGACGATCACTCGCAAATTAGGAACATTTTCTGTAGATATGGGAGTTGTGCTGGCTTTTGCACAACAGGTCTTTAAGCAGCAGATCACTACATGCATTTTTCTGATCGGATAGCTTTCTGTTTGTAAAAAGGGAAGGTGTAAATGCTTTCTGAAATGCATTTGAGATGGATATGAATCCAATCTCTCAAATAACTTTAGGAGGTGGTCTTTGATGCATTCCAGACGAACCTGGACAAGTCTAAATGTTGGATCTTACTCCTTCCAAAATGTAAATAAACAAGTGAGACTGTGGCCCCGTTTACACTAGTGCGTTTTAGTTTTAAAACGGCGTTTTAGAATGAAAACGATCCGCGTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22421
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 |
|---|---|---|---|---|---|
| ENSDART00000051556 | Essential Splice Site | 1899 | 2282 | 37 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6468142)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6195529 |
| GRCz11 | 14 | 6502256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTCATTATCACCGTCCTCATCCAGTACAGATTCTTCTTTGAACCCAA[G/T]TAAGCATCATTAACCAATGAAATTATGGATGGAAGTAGTTTCAAAGATCT
Long Flanking Sequence:
TTCTAGAATTCATTTTCTGAGAATTCTTTCAGAAGTTGCTAGATGGAAAGCTGCATTTGTGAGGAAAAAAACGCCAGAAATGTGACAAAGTTTTCTTTTTTTACTTTGGCTTAAACAGGCTTCCATAAATTTCTTATAATTATCATGAATAAGTATTTCATTTAACTTAACTTATTACCTTGTTAGGTTTCCAGTTCCAGTTATTTATAGGAATGCAGGCATCATTCTTCAATTTAAATAATTCCGATATGTGAAGACTAAATATTATCGTTTAATCCTTTAAAAGTGCATTGTCCGCTGTATTTTGAAGTAATTAATTACTACTGAGGCATATGTATTAGATGCTGAATTCTTTCTTACCTTACATAAGGTGAGAACCGTTTCCGTTCTCCACTGGAGTGGGACATGGTGGGTAAGAATCTTTTCGCTATGGCTGTGGAGGGTGTGGTTTTCTTCATTATCACCGTCCTCATCCAGTACAGATTCTTCTTTGAACCCAA[G/T]TAAGCATCATTAACCAATGAAATTATGGATGGAAGTAGTTTCAAAGATCTAAAGCCATGCTTTGGTCCTTTTCCTTAGGTCTTTATGTCCTAAATTGAGTCCGATTGGAGAGGAAGATGAAGATGTAGCCAGAGAGAGGCAGAGGATCATGAGTGGGGCCGGACAGGGAGACATTCTCGAACTCCGACAGCTCACTAAGGTCAGCTGATGATCACACACAACAACCATAACTACAATTCAGTGATGAGACCTTCAATAATGTTGTCTACTATATTTACAGGTGTACAAGCGGAAACAAAAGCCTGCAGTGGATCGTCTGTGTGTTGGCATTCCTCCAGGAGAGGTAATTCATGACACCTACTGGTATAACTTTACTTGAAGGGGGTATTTTTGCCCTATTGACTTTCATTCATGTTCAGTCTGCAAACTCAAGCTCAAATGACAAGTTTCGCATGTTACTGCATTCGAAAGTTCAAGTCTGGACCCTGCGATTTTGCGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8542
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 |
|---|---|---|---|---|---|
| ENSDART00000051556 | Essential Splice Site | 2154 | 2282 | 44 | 46 |
Genomic Location (Zv9):
Chromosome 14 (position 6478135)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 6205522 |
| GRCz11 | 14 | 6512249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAACGGCAGGTTTCGCTGTCTGGGCAGCGTCCAGCACCTCAAGAACAG[G/A]TAAGACCACTGCTAGTGTGGAGTATCCTAGAGTNNGGGGGGTGGGGGTTAG
Long Flanking Sequence:
AGCAGGTGGGACAAAATGTTTGGCCCCATTTACAGATTTATGTTGCTTGTTCAAGCTACTTATTTATAATGAGCTAAACCAACACAATTCTTAAGTTTTGTTTAATGCTCAATCCACTTAAATTTGTAAAAACGATTCAGTTAACTTTATCGATTTGTGTTGAGTCAACATGAAGGAATTATGTGGAAATCAGCATTATTTACAGTGTGACAAAACCAGAATGATCCAGTTTTAAACAGGTGCACTGAGCAAAACAGCAGCACTAAAAACACAAACACACAACACAATGTCAAACACAAACACACACAGGGATTGACTAATTATTTTAGCTTAGCTTAGACGTCCAGCTGTCACTATGTGTCAGTGGCAGTTTTCCTCAAACTGACCCGTGTTCTGTTCTCTCTCAGCATGGAGGAGTGTGAAGCTCTGTGCACCAGAATGGCCATCATGGTGAACGGCAGGTTTCGCTGTCTGGGCAGCGTCCAGCACCTCAAGAACAG[G/A]TAAGACCACTGCTAGTGTGGAGTATCCTAGAGTGGGGGGGTGGGGGTTAGTGGGAGGGGGTAAAACGGTCAATCATTTTAATAAGAAGTTAGTTCAAACCTTACACTTTATCACAGATTATTGCAATCTAATTAAGCGATTTAAAATCCGCATGAACTGGAAGATTTTTTCTCCGTATTGTGACGCATTCTTAGAAAAAATAGAATGTTATATGAGCAGACAGTGGGTGTGGCTTGTTTTTTCTACTGCGAGCTGATTGGATGTATTAAAGTGGGCATTTCATTCAAAGAGATTGGGAAAAGGGTTTAGGGAGGGTTATTACAACATAACAGACTCATCCTCCTCACCATTTCTGTTTGTTGTCATAGCACTGACAGTTGGAAGGGGCGTGGTTACATATGTTAGCCCCGCCTAATACCTCAGACTAAATCTGAGAATTTACCTGAAAACAAACAGGAAGCGTCCAAAAGGGCATACTTCCATACTATATAGTTTGCTAA
Associated Phenotype:
Not determined