ZMP
abca5
Ensembl ID:
ZFIN ID:
Description:
ATP-binding cassette sub-family A member 5 [Source:RefSeq peptide;Acc:NP_001092716]
Human Orthologues:
ABCA10, ABCA5, ABCA6, ABCA8, ABCA9
Human Descriptions:
ATP-binding cassette, sub-family A (ABC1), member 10 [Source:HGNC Symbol;Acc:30]
ATP-binding cassette, sub-family A (ABC1), member 5 [Source:HGNC Symbol;Acc:35]
ATP-binding cassette, sub-family A (ABC1), member 6 [Source:HGNC Symbol;Acc:36]
ATP-binding cassette, sub-family A (ABC1), member 8 [Source:HGNC Symbol;Acc:38]
ATP-binding cassette, sub-family A (ABC1), member 9 [Source:HGNC Symbol;Acc:39]
ATP-binding cassette, sub-family A (ABC1), member 5 [Source:HGNC Symbol;Acc:35]
ATP-binding cassette, sub-family A (ABC1), member 6 [Source:HGNC Symbol;Acc:36]
ATP-binding cassette, sub-family A (ABC1), member 8 [Source:HGNC Symbol;Acc:38]
ATP-binding cassette, sub-family A (ABC1), member 9 [Source:HGNC Symbol;Acc:39]
Mouse Orthologues:
Abca5, Abca6, Abca8a, Abca8b, Abca9
Mouse Descriptions:
ATP-binding cassette, sub-family A (ABC1), member 5 Gene [Source:MGI Symbol;Acc:MGI:2386607]
ATP-binding cassette, sub-family A (ABC1), member 6 Gene [Source:MGI Symbol;Acc:MGI:1923434]
ATP-binding cassette, sub-family A (ABC1), member 8a Gene [Source:MGI Symbol;Acc:MGI:2386846]
ATP-binding cassette, sub-family A (ABC1), member 8b Gene [Source:MGI Symbol;Acc:MGI:1351668]
ATP-binding cassette, sub-family A (ABC1), member 9 Gene [Source:MGI Symbol;Acc:MGI:2386796]
ATP-binding cassette, sub-family A (ABC1), member 6 Gene [Source:MGI Symbol;Acc:MGI:1923434]
ATP-binding cassette, sub-family A (ABC1), member 8a Gene [Source:MGI Symbol;Acc:MGI:2386846]
ATP-binding cassette, sub-family A (ABC1), member 8b Gene [Source:MGI Symbol;Acc:MGI:1351668]
ATP-binding cassette, sub-family A (ABC1), member 9 Gene [Source:MGI Symbol;Acc:MGI:2386796]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12201 | Nonsense | Available for shipment | Available now |
sa15733 | Nonsense | Available for shipment | Available now |
sa22162 | Essential Splice Site | Available for shipment | Available now |
sa22163 | Essential Splice Site | Available for shipment | Available now |
sa35362 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12201
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112302 | Nonsense | 2 | 1673 | 1 | 39 |
ENSDART00000127464 | Nonsense | 2 | 1673 | 1 | 40 |
Genomic Location (Zv9):
Chromosome 12 (position 40351448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38633191 |
GRCz11 | 12 | 38807692 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAACAACAACGCRAATCTGGAGGACAGGAAAGACATGTCTTAATGTA[T/A]TTCATACGTAAGTGCGCTTCTTTGTTTARGCATGAGGGAAAGCTRTTAGC
Long Flanking Sequence:
GTATATTTTATATTTCAATTGAAATGTTTTTATACATTTATATACATCACATTTTAGATTATTCATTCAAACCCTTGTAATATTATTTGCACAATATAACCCGCTTTAATATTTAATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACTACGTACACAGTACAGTTCATAGCAGCTGCCGCCAGATGTGTTGTGATGACGTCAATCACAAACTAAAAGACCAATCCGCGCAGTCTTACAAGTTCTGAGTCTCGGGATTGGCTCCCTCGGTACCGACGAATCCCGAGTCTAGTAACTTGTAGGGCTGCACTGATTGGCTGACTGACTGGTCGGTCCAGCTGATGGCAGAGGCGCAAGTAGTGTTGACAACGCCGCCCTGGATCTCTTCTGTTTTTATTTATTTCCCAAAGGTTTTTTATTTGGAAACAACAACGCAAATCTGGAGGACAGGAAAGACATGTCTTAATGTA[T/A]TTCATACGTAAGTGCGCTTCTTTGTTTAGGCATGAGGGAAAGCTGTTAGCCAGTTAGCGTTAGCTGTCAGTGTTTACACAATGATAGCAGGGAACAAAACTCACACTTGCATCGACAATTTGCACGTTTGGCTCGAATATTGTATATTAACTAGAAGAACACATTGGTTATCTACATTTAAGAAAATAGGAAGGGGCGAAAGCCCAACCCAGTCGTTATTGACCTGCACCGCGCGCGCTTGCGAGCACGCGCAACACGTCGGGTGCACGCGACCTCCTGCACGCGCAGAAATATATAAATATATTCTGCATAGAAATTGCAGTTTGACTGACTGTACATCGTAGTATTTAGCAGCATTTGAGGTAAAGTTGGTTTAATATTCGCACATTCGTTTAGTGACAACTTGTGACATGCTCCCTATATTGTTTGCCATGGTTCTTTGAATATTCGGTCTAAAATATGTAAGGATGACTTTAAAACAACATCAGCACTATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15733
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112302 | Nonsense | 694 | 1673 | 15 | 39 |
ENSDART00000127464 | Nonsense | 694 | 1673 | 15 | 40 |
Genomic Location (Zv9):
Chromosome 12 (position 40378304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38660047 |
GRCz11 | 12 | 38834548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTACTGAAGAGCCGTAGAGCAGGCAGAGTTACWGTTCTCAGCACTCACTA[T/A]ATGGATGAGGCTGATATACTTGCAGGTGCTTCTCTCATTTTTCTCTTCCA
Long Flanking Sequence:
ATCATTCCAATGCGTTTTTTAATGGTTATGAAATCTTTATTTATTTAATATTTTATTATATAAAATTTCATTTCAAACATTATTATACATTTATTATTCAATAATTCAATAAATGATTTTCCAGGCATCTTTTTTTTGTGTGTGTTTTCTGCTTTAAAATATCTCTCTTTTTAAGGTAAGGAAAGTTCTAAAGGATCTGGATTTGGAAAAGATTATGGATGCTCTGGCAAAAAACCTCAGTGGAGGCCAGAAGAGGAAGCTCTCTGTGGGCATAGCCATTCTTGGAGATCCCAAGGTAAACGTCTGACAGCTTATAACTCTGACTTGTTGATCCGTTATCTTATTTATCCATCTACTTCAAATTTTTTTTTTTCGTTTATGAATCAGATCCTCCTTTTGGATGAGCCTACAGCTGGTATGGACCCAGTGTCTCGGCACCAGGTTTGGTCTTTACTGAAGAGCCGTAGAGCAGGCAGAGTTACAGTTCTCAGCACTCACTA[T/A]ATGGATGAGGCTGATATACTTGCAGGTGCTTCTCTCATTTTTCTCTTCCATCAGTCATTTTCTCAGTCTCTTTTCTCATGCACCTCTCTGTGTTTTCTGTAACACAGATCGTAAAGCTGTCATCTCGCAAGGACAGCTCAAGTGTGTTGGCTCTTCTTTGTACCTGAAGACCAAGTGTGGAGTTGGGTATCATCTTAGGTTAGTTTGGTATTTGTTCTAATGTAAAATACTATTGTGTTGTATTATAAAGTCATGGTTTGGCATGTGTTTAGGGCAGCAGGCTGGAAAAACTCTTATGTCCTAAAGGGATAGTTCACCCAATATTGAAACTCAAGTGGCTCCAAACATTATTTCTTACTTCTGTTGAACACATAAGAAGATATTTTGAAGAAAGTTGAAAACCGGTAACCATTGACTTCTATAGTAGAAACAATACTATGGAAGTCAATGGTTACAGGCTTCCAACATCTTTCGAAGTATCTTTTTTGTGTTTAAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22162
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112302 | Essential Splice Site | 1031 | 1673 | 22 | 39 |
ENSDART00000127464 | Essential Splice Site | 1031 | 1673 | 22 | 40 |
Genomic Location (Zv9):
Chromosome 12 (position 40387218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38668961 |
GRCz11 | 12 | 38843462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAATGGCACTGGACACATTAGAACATGGTCCAAACCCTTTGATTATG[T/G]AAGTGCAGTGCTCTAAAACATCAAAGTCAACACATTAATTTTGCGGTTTT
Long Flanking Sequence:
ATGTTATTTTCTTTTGTTGTTTTTTTTTTGTAGCAAATAAAACTAAGAGAGCTAAACTACAAGTGTAAACACTCTTAAAATAACTGCTAATAATTGGATTGTTTATTTGTTTATTTATTTATTTTATTTTATTATATTATTTATTTTATTTTAATATATATGAGAGTAGTAAGATTTATTTACAGATAAGTAACATATCTTAATTAATTTTTTTATTTATCTCATTTATTTTGTTCATATTTATTTCATATTTATTTATTTATTTACTAATATTTTTTATTATATATTTTTTCTTTGGCATTTTAAAATGTTTGTTGTCCCATCTCTAATCCTTTCTTTGTTCTCTTTGTGTGACTTACAGGATTTTACCTACATTTTAGCGTTTAACAGCACCACTGTGCACTCTTTGCCCATGGCTGTGAATGTGCTCAGTAATGCTCTCCTGAGAGGTTATAATGGCACTGGACACATTAGAACATGGTCCAAACCCTTTGATTATG[T/G]AAGTGCAGTGCTCTAAAACATCAAAGTCAACACATTAATTTTGCGGTTTTCTGTTTCTAGAAACATTTTGTTTGTGTTTTTAGCAAATTCCAGATAAAACATCTTATGCACTGGTTTACATTGAAGCTGTGATTCTTGGGATGCTGGCTGCTGGGATGCCAGCTTACTTCGCAATGGACCACACAAGAGACAGAGAAGTATGTCGTTTGGGTTGTAATTTATTTCAATTGACCATTTAAATTTAACTAATAAAACACATTCTTAGTTATGCATATACAGATCTACAGTACTTTTTACTATAAACTCTAAAGAGTTAGAGTTAATAATCTTTCTTTGTATTATAAATTAATTCTATTATTTATATGAAATATAAATTGGACAAAATTAAAATTAAGCAAAACAACTTTTTTTACACTTTCATTTTTTTCTATAAATTATATGAATTGTCCTATATATATAAAAAAAAACAATCCTCAAAAATATTAGGCTATGCAGCACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22163
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 |
---|---|---|---|---|---|
ENSDART00000112302 | Essential Splice Site | 1608 | 1673 | 37 | 39 |
ENSDART00000127464 | Essential Splice Site | 1608 | 1673 | 37 | 40 |
Genomic Location (Zv9):
Chromosome 12 (position 40394979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38676722 |
GRCz11 | 12 | 38851223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGAAGATGTGAAGTCTTTAGCCAAGTCTTTTGCCCAGTTAGAAAGTG[G/A]TAAGAGATGGACACCATAACAATGAGAAGAATTTGAGAAGAATTGAAAGT
Long Flanking Sequence:
CGTGTGGCGATCATGGTATCTGGTCAGCTGAGGTAAACACTGACTACAACTAAAGATCTCAATTTTTAAAAAATGTTATGCAAATGAATTTGAAGCAAGTCCATAATTTGGAATAGAAAGCCCTTTTTTGTTGCCCCCCCTGCAGGTGTATTGGCTCAATCCAGCACCTGAAGGGGAAGTTTGGCCGAGGATACAGCCTAGAGATTAACCTCAGGGAGGAGCTCACAGGTCTCCAGCAGGTAGCGCTGTTGCACAAAGAGATACTGAAGATATTTCCCCATGCTGTTCGTCAGGACAGGTGAGATGGGTTTAATTAAATGAGAAAAGGTTTAATCAAATGCACCAAAACAGAAATGTCTTTTTAAAAATGAGAATGTAAAATATTCAGTCGTTTTTTTTCCGATATGTTTTGGGTTGTAGTTTTGCCACTATGATGGTGTATAAAATCCCAATGGAAGATGTGAAGTCTTTAGCCAAGTCTTTTGCCCAGTTAGAAAGTG[G/A]TAAGAGATGGACACCATAACAATGAGAAGAATTTGAGAAGAATTGAAAGTACTATTTTAATCTTTAACCATTGTTTTTTTTTTCCTCCACAGCTAAACAGAACTTCAACTTTGAAGAGTACAACTTTTCCCAGTCAACTCTTGAACAAGTATGTCAAAATGTTCTTATTTAAAAAGTATTATTTTTGTCAACATTTTAAAATAGGCAAGGCAAACTTTATTTATAGAGCACAATTTTATACAACCGTAGTTGATCCAAAGTGCTTTACAATGAAATAAAATATTTAAGAAAATAAAATAAAACTTGTATTAAAAATATAAGGAAATCAAATAAATATGTATATATGTAATACTAAAATACAGATAAGAAATTACATGTATGAGTCACTCAAAAGCAAGGGAGTAAAAATAAGTCTTTAAATTAGATTTAAAAGTATCCAAGGATGGAGAAATCCTCATGTTCAATGGGAGACTGTTGCAGAGCCTTGGGGCCACAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35362
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 |
---|---|---|---|---|---|
ENSDART00000112302 | Nonsense | 1644 | 1673 | 39 | 39 |
ENSDART00000127464 | Nonsense | 1644 | 1673 | 39 | 40 |
Genomic Location (Zv9):
Chromosome 12 (position 40398344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 38680087 |
GRCz11 | 12 | 38854588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTTCATGGAGTTTGCCAAGGAGCAGGAGAACGAGGAAGAAGAGGTC[G/T]GATCACTAAGCACGACTTTTCAATGGCAGAGACTGAGACAGGACGGCCCT
Long Flanking Sequence:
AATGCGGTCTCCTTTAGGTCGCTTTATAAATGAATAGAAAAAAAAATGGATGTCTTTGGAAAGATGACTGTAATTTAAAATTCAATGTAATAACGTTTTTGTTTTGTTTTTATTATTATTTTTATATACGCACACACATTGGTCAATTTGAATGTATTTTATTTTATGATTTATTTTAAATGTCTTTTCTGTTTAGCAAATGTTGCGGTGGGAAAGTTAATATTCTGTATTGTTTGCTGGGTTTTATAATATAATTCAAATCAATAAAAACAACCTTGGGAAAAAAAAAACATATAAAGTGTAAAAAAAAAAAAAAAAAGAATTAAATAAATAAATAAATAAAATAGTTGACAAGATCAGTTTACTGAAAATAATTAGGATTATTGCTTTATTTATCTCTGTCTACATAACCTGAACAAGAGAATTTAATTAACCATACACCCGTTCTGCAGGTTTTCATGGAGTTTGCCAAGGAGCAGGAGAACGAGGAAGAAGAGGTC[G/T]GATCACTAAGCACGACTTTTCAATGGCAGAGACTGAGACAGGACGGCCCTGTATCTATTAATCACGCTGACAGCATAGTACACCAGCTATGAACCAATCCTGTTCCCTGAAGCGTTCTGCCCTTGCCTCTTTCTCCTTTTCCTTCGTTCTGCATGTGCCGTCTTTTGCCTTAAGAGCCTTAAACCCATGGGACTCACAGGACAATCGACTCCAGAGACTCCAATGGCCACTAACGCACACTAATAACGTGTGTATGTGTGTGTGTGTTTATGTGGCTCTGGCACTGGCACTTGCTCAGAAGGAATCAGACACACGACTTGAGTGTCATCCGTTAAACACAGAGCTAGACTCGTCGTCATCTGTTTTTACAACGACAAAAAAAAAAAGATTTTATTTTTTAAACTCTCACTTCTACTTGTATCTATCAAGCTCACTGTTTTCTTGTGTCCATATAACACACGTCTATCACTGGGAAATGAATTTGCATGAAGCGGGTTCCA
Associated Phenotype:
Not determined