ZMP
si:dkey-7j20.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to ATP-binding cassette, sub-family B (MDR/TAP) [Source:UniProtKB/TrEMBL;Acc:B
Human Orthologue:
ABCB6
Human Description:
ATP-binding cassette, sub-family B (MDR/TAP), member 6 [Source:HGNC Symbol;Acc:47]
Mouse Orthologue:
Abcb6
Mouse Description:
ATP-binding cassette, sub-family B (MDR/TAP), member 6 Gene [Source:MGI Symbol;Acc:MGI:1921354]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21450 | Nonsense | Available for shipment | Available now |
| sa34589 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21449 | Essential Splice Site | Available for shipment | Available now |
| sa21448 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21450
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113953 | Nonsense | 145 | 648 | 4 | 18 |
| ENSDART00000135458 | Nonsense | 145 | 627 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 9 (position 14542276)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 14294841 |
| GRCz11 | 9 | 14266044 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGGGGTTTGTCAGTAACTTGCGCAGCTTCCTATGGACTCATGTGCAG[C/T]AGTACACCAGCCGTGTGGTGCAGGTGCGTCTGTTCGCTCATCTGCATGGC
Long Flanking Sequence:
TCATTTTTAGGTTAACTGTCACTATAAGCATCGCAGCTCTTTTTAATGTCACAGGGATGCATTTGATTTTAAAATATAAAAACCAAAATTTGTTTACTTGAAATTTTTGTTTGACTATATCACAGATCTTACTGTTTTTAAGTAAACAGCCTTAATAAGCATTAAATATTTCAAATCATGTTTAGCTAATCCAGCACAAGTTTTGGTGCACTCTCATTTTCTCTTCTTTGTTTCTGCAATCATGTTATTCCAGTAAATCAGCTGTCAGCAATGGAGAACTGGAGAACCCTGGCCATCACAGTCTGTGTTTACGTCCTCCTTAAGTTCTTCCAGGGCGGAGGGGTAGGTGAGGCTTAATTTTTAGTGGTATTTTTAGAAAAATAAAGGATAAGCTCTTTTTCAAATGTCACACCTTGTGCAAATCATCATCTGTCTCACTTCTCTCAGGGACATCGGGGTTTGTCAGTAACTTGCGCAGCTTCCTATGGACTCATGTGCAG[C/T]AGTACACCAGCCGTGTGGTGCAGGTGCGTCTGTTCGCTCATCTGCATGGCTTGTCTCTTCGCTGGCACCTGGGTCGCCGCACCGGAGATGTCCTGCGCAGCATTGACCGTGGGACATCTTCAGTCAACAACTTGTTAAGGTCTGATTACTTACAGATTTTACCCTACATGCTGTTTTCTACAATGTAAATGTTTAAATCTTTTTCTTAATGAAATGTTTGAGGTTTTTTTTTTTGGTTTGGGTTGCAGCTATATTGTGTTCAGCATTGTACCCACTATTGCTGACATTGTCATTGCCATCATCTACTTTGTGACGTACTTCAGTGCCTGGTTTGGCCTCATTGTCTTCATTTGCATGTTTCTCTACCTCAGTAAGTGCAGCACAAATACACTGTAACAAATGACAAAAAGCCATCACAACAAAAGCTTTTGTGTTACTTTTAGGGATGTTCATAATAACCGAGTAATTGTTAACCGAAAGGGTGCTTTTCATAGATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34589
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 |
|---|---|---|---|---|---|
| ENSDART00000113953 | Essential Splice Site | 332 | 648 | 8 | 18 |
| ENSDART00000135458 | Essential Splice Site | 332 | 627 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 9 (position 14537061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 14289626 |
| GRCz11 | 9 | 14260829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGGATCATTGCTTTGTGCATACTATGTTACTGTGGACAAGTTTCAA[G/T]TATAGTAATCTCCACTCATACTGTAAAATCTACTTCTTATTGGTCTGGAG
Long Flanking Sequence:
TGTACAATTTACAATTGTAAATATGCTGACCTGTTTTTTAAAAAGTGCACATTTGAAGATATGTTGTGTTTATAAGTACTAAGAGTTTTGAAAATGTTCTAAATGGTTGTAAAATTTGCCCAAACCGATAATATAAAAAAACATAAATGCTGACAAACCCTGGGTCATGTAATTTTGTTAACACTTAACCCTGCAAAAATGCATTTCTCCATGCAGGTTAAGTACTATAATTCAGAGGGTTTTGAAGTCAGGCGCTTTGAGGATGCTATCCTGAAATATCAGGTGATGTAATCATTTAACAGGATTACACTTCTTGAGCAAATCCAATTAATATGAGATGCTGATTTGAGTTTTTTTTTTTTTTTTTTGCTTAGGCATGTGAATGGAAGACCAATGCCTCCCTGGCCCTTCTTAACCAAACACAGAATCTGATTATTGGATTAGGACTTTTGGCTGGATCATTGCTTTGTGCATACTATGTTACTGTGGACAAGTTTCAA[G/T]TATAGTAATCTCCACTCATACTGTAAAATCTACTTCTTATTGGTCTGGAGGGGTATTTTTGTTCACGCTCTTCTGGTGTTCTCATAGGTTGGTGACTATGTTCTCTTCGGAACCTACATTGTTCAGCTCTACACGCCACTCAATTGGTTTGGCACATATTATAGGTAAGACTAGAAAATGACAATATAGGGTGTTGACAATTTCCCTGTGCATTTTTTTAAATGGGTTCTTCTGATATGCCATTTTAACAAGATGCAGTATGAATCTCAAATGTTCAAGTGAATTTCAGTTTCAAATCCTCCATGGACCATTTTTACACCATACTATTACACCATACTATTGAGGCCAGCTAGCAAAGTGCCATGCAGGTAAAACCTCTTTCCTTTGACCTTAAAAGATGCTCTAGAGGCCATGGTCTTTAGCCTCCTTGTTAGAGCAACCAATTCCTATGCAAAGTATTGCCGGTTAGATCCCAGCTCAGACCGGGCTGGGTGCAGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21449
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 |
|---|---|---|---|---|---|
| ENSDART00000113953 | Essential Splice Site | 358 | 648 | 9 | 18 |
| ENSDART00000135458 | Essential Splice Site | 358 | 627 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 9 (position 14536896)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 14289461 |
| GRCz11 | 9 | 14260664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATTGTTCAGCTCTACACGCCACTCAATTGGTTTGGCACATATTATAG[G/T]TAAGACTAGAAAATGACAATATAGGGTGTTGACAATTTCCCTGTGCATTT
Long Flanking Sequence:
CATGTAATTTTGTTAACACTTAACCCTGCAAAAATGCATTTCTCCATGCAGGTTAAGTACTATAATTCAGAGGGTTTTGAAGTCAGGCGCTTTGAGGATGCTATCCTGAAATATCAGGTGATGTAATCATTTAACAGGATTACACTTCTTGAGCAAATCCAATTAATATGAGATGCTGATTTGAGTTTTTTTTTTTTTTTTTTGCTTAGGCATGTGAATGGAAGACCAATGCCTCCCTGGCCCTTCTTAACCAAACACAGAATCTGATTATTGGATTAGGACTTTTGGCTGGATCATTGCTTTGTGCATACTATGTTACTGTGGACAAGTTTCAAGTATAGTAATCTCCACTCATACTGTAAAATCTACTTCTTATTGGTCTGGAGGGGTATTTTTGTTCACGCTCTTCTGGTGTTCTCATAGGTTGGTGACTATGTTCTCTTCGGAACCTACATTGTTCAGCTCTACACGCCACTCAATTGGTTTGGCACATATTATAG[G/T]TAAGACTAGAAAATGACAATATAGGGTGTTGACAATTTCCCTGTGCATTTTTTTAAATGGGTTCTTCTGATATGCCATTTTAACAAGATGCAGTATGAATCTCAAATGTTCAAGTGAATTTCAGTTTCAAATCCTCCATGGACCATTTTTACACCATACTATTACACCATACTATTGAGGCCAGCTAGCAAAGTGCCATGCAGGTAAAACCTCTTTCCTTTGACCTTAAAAGATGCTCTAGAGGCCATGGTCTTTAGCCTCCTTGTTAGAGCAACCAATTCCTATGCAAAGTATTGCCGGTTAGATCCCAGCTCAGACCGGGCTGGGTGCAGTAGGACATGGGGGGGCTCGTGGATCACATGTAATCCACTGGTCCTACTGCTCATAACCCGGTTTGAGCTGGGATCGAACCAGCGATTCTTTGCATGGGAGTCGGTTGCTCTAACAAGGAGGCTTAAGACCATATCCCGTAGAGCATCTGTCTGTCACTAGAGCACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21448
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 |
|---|---|---|---|---|---|
| ENSDART00000113953 | Essential Splice Site | 590 | 648 | 16 | 18 |
| ENSDART00000135458 | Essential Splice Site | 590 | 627 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 9 (position 14503061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 14255626 |
| GRCz11 | 9 | 14226829 |
KASP Assay ID:
2260-1622.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTGCTAAGGTGTGTGCCAACCACACCACTCTCGTCGTCGCACATAG[G/A]TAAGTCTGCTTAATCCATTAACAGAATTGCTAATGCAACTTGAAGAGATA
Long Flanking Sequence:
TCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAAGTATAATTTTATGTAAAATATTAAAAAATAAATAAATCCAAAGGGGGGCTAATAATTCTGACTTCAACTGTATATATTTTGAACAGTAGGTAATGATTAATCAAAGTTTTGAAGGAACAATACATGTAGTATGACAATAACATGTGGTGACATTTGTCTCTGTATCATTATTGCAGGATATGATACAGAGGTGGGTGAGAGGGGTCTGAAGTTGAGTGGGGGAGAGAAACAGAGAGTGGCGATTGCCCGCACAATCCTGAAATCGCCACGAATTATTTTGCTTGATGAAGTAAGCAAATGTTTTCCTAAAAGTTGATAATTTATGATGTTGGTATGTATTAAAGCCTGCAACTGGAATTTTACTTTCAGGCCACATCTGCTTTAGACAGTCAAACAGAGCGCAACATTCAGGCTTCTCTTGCTAAGGTGTGTGCCAACCACACCACTCTCGTCGTCGCACATAG[G/A]TAAGTCTGCTTAATCCATTAACAGAATTGCTAATGCAACTTGAAGAGATAGTTGCCCTCCAAAGTAAGAATTCTGTTATCATTTACTTATGCTCAACTTTTACAAAACATATTTGAGTTTCTTCTGTTGAACACAAAGGTAGAAATACTGAAAAATGTTGGAAATAAGCTGTCATGACTATTTTTTGTTCCCACTATAGATATCAAGGGCTGCTTTTTTCCAACATCCTTTATTATATCTTTCTTTGTGTTCAACAGAATTAAGAAATTTATAAACATTTAGAACCACTTGAGTGTGTGTATATGGTAAGGATATCTTCATATAGAGGTGAACTATCCCTTTAAAACTAATTTTTGTTGAGTGCAAGCCTCTGAAGTTGTTAAACTGATCAGTAAACAGTAAATCATCAGCATTGCAATAACATTAATAATGTAAAACTTAATATTCATGTATATATTTTTAAAATGTACCACATAACAAAATATACAAAATCTGAAACT
Associated Phenotype:
Not determined