ZMP
abcb11a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ATP-binding cassette, sub-family B (MDR/TAP), member 11 (ABCB11)
Human Orthologue:
ABCB11
Human Description:
ATP-binding cassette, sub-family B (MDR/TAP), member 11 [Source:HGNC Symbol;Acc:42]
Mouse Orthologue:
Abcb11
Mouse Description:
ATP-binding cassette, sub-family B (MDR/TAP), member 11 Gene [Source:MGI Symbol;Acc:MGI:1351619]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34768 | Essential Splice Site | Available for shipment | Available now |
sa18599 | Essential Splice Site | Available for shipment | Available now |
sa21601 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34768
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 |
---|---|---|---|---|---|
ENSDART00000047401 | Essential Splice Site | 160 | 1281 | 4 | 25 |
ENSDART00000134566 | Essential Splice Site | 154 | 609 | 3 | 12 |
ENSDART00000139631 | None | None | 635 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 49811110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49066306 |
GRCz11 | 9 | 48763791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGTTTGACTGCAACTCTGTGGGGGAGCTGAACACGAGGATGTCTGAG[T/C]AATGTCCAAGTCTATCTGTGTTATCTTAAACCATTGTTAGCTTTGCTCAC
Long Flanking Sequence:
AGTGCACTAATTATTTTTAGAGTTTTTAGTGTGAACACACTACTTGCACTATTTATACTACAAAATGGCGTAGAATAGTGCATAAGTATGTGATTTGGGACGCAGCTTCAGTCCTGGAGAGCCAGTGTCGGAATTTAACGCCAACCCCAATCAGACACACCTGGACTAGCTAATCAAGCTCTTACTAGGCTTTCTAATAACATCTGTGCAGTTGTGTTGAGGCAAGTTGGAGCTAAAATCTGCAGGACACCAGCCCTCCAGGACCAAGTTTGAGCACCCCTGATTTAAGTAGTGCATATTTATAATAGCAAAACCTCATCTGGTTTGCACATTGTCAGTCTAAATGAGCTTTTCTGCGGTTTCAGATCACGTTTTGGGTTTCTGCAGCTGCCAGGCAGATCCAGCGCATCCGAAAAACCTACTTCAGAAAGATCATGTGCATGGAGATCGGCTGGTTTGACTGCAACTCTGTGGGGGAGCTGAACACGAGGATGTCTGAG[T/C]AATGTCCAAGTCTATCTGTGTTATCTTAAACCATTGTTAGCTTTGCTCACAAGCCTGTGATTAGTGGTGTTAAATATTAAACTCGGGTTCTAAAAACAGGTGTCTTCAATAGCTATTCGATCTGTATTTGGTGGAAGATGGGGATAAAAGTTTCTTATTGTGGAGTTAGACTATTAGTGTGTTTCATAAAATTTTGTTTTATTTCTAAAGATCTGGGCCTGGTTGTGCTTTATGAAAGCTTAAGCTAACAAACCCCTTTATTATAAAGTTGGAAGTTGGGTGACATGATGGCTCAATGGTTAGCATTGTCACCTCACAGCAAGAAGGTCATTGGTTCGAGCCTCTGCTAGGTCAGTTTGCATTTCTGTGTGGAGTTTGTATGTTCTCCCCGTGCTGGCGTGGGTTTCCTCTGGGTGCTCCAGTTTGCCTGACAGTTTGCCTAAGACATCTGCTAAGGTGAATTGAATCAGCTAAATTGTCTGTAGTGTATGTATGTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18599
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 |
---|---|---|---|---|---|
ENSDART00000047401 | Essential Splice Site | 317 | 1281 | 7 | 25 |
ENSDART00000134566 | Essential Splice Site | 311 | 609 | 6 | 12 |
ENSDART00000139631 | None | None | 635 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 49824965)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49080161 |
GRCz11 | 9 | 48777646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAACTGGTCATCGAGACCCAGGAGCKCACACCTGGAGGACTCGTTCAGG[T/G]AGAAATGACTCTCAGAATTTAATTTTTCTGTTCAAAACAAYATCTTCACA
Long Flanking Sequence:
CTATTCCTTAGTTGTGTATTTATTTAAGCAGGGATATATATATATATATATATATAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAATTATGTGTAAAGTGCTAATTTTGATCAAGTCATCATTTTTTTTTGTCTTAGTTCATTAATTTGAGCCTAAGAATTGCATAATTTTGATTTGGTATACATTAAAATGATGACATCAGTCAAATTTGGGAGATAAAAAGTCAAACTTTTGACATATGATGCTAAATTGCTGGCTGGCAAAAGCTGTACAGGCAGAAACTGTTGTGTGGTTTATGCCCGCAGGTATGACAGGAATCTGGTGCAGGCGCAGGAGTGGGGCATAAAGAAGGGCATGATCATCGGGGTGTTTCAGGGCTATCTCTGGTGCATCATATTCCTGTGTTACGCTCTCGCCTTCTGGTTCGGCTCTAAACTGGTCATCGAGACCCAGGAGCTCACACCTGGAGGACTCGTTCAGG[T/G]AGAAATGACTCTCAGAATTTAATTTTTCTGTTCAAAACAACATCTTCACACATTTAAACTCCGGTCTGTTCCTTAAGGGTATTATTTGTAATTAAAACTATTAAATATGTTTGTTACCTTACTCTTTCCCTGCCGGCGTTTAGAAAAAAAATAGTTGCCAGCCACCAACATTTTTAATATTTTTTTCCTACATTTTTAAATATTTTCTGCTTGGAATATATGAGCATATTATATATCAAAATAAAGAACCAAGACTCTGCTTTCAAACAAAAAAGCATTTTATTTTTCATGTGTTCATGTTGTAATCCTATTTAAATGCATGTATGCAGGGTGTCAATAAACAAGCAACAAAAACTAAATCATATATTAATATTTCGGATGAAGTAGTTCGATTTTTAAGCACAAGTGAAAATATAATTTATTGTGGACTTTGAATTAAACTAACAAACATCATATACACAAGTAAATCCTCTGAGTAAAGTTTACTCAGTTTAGATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21601
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 |
---|---|---|---|---|---|
ENSDART00000047401 | Essential Splice Site | 559 | 1281 | 12 | 25 |
ENSDART00000134566 | Essential Splice Site | 553 | 609 | 11 | 12 |
ENSDART00000139631 | None | None | 635 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 49833688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49088884 |
GRCz11 | 9 | 48786369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGCTGGATAATGAGAGTGAGGCTGTCGTACAGGAGGCCTTGGACAAG[G/A]TGAGACTAATGATATCCTCACCAGCTGATGCTAAAATATAACTTTGGCAC
Long Flanking Sequence:
TAGAAAATTCCTGGCAGGTGTGTTGAAGCAAGTTGGAGCTAAACTATGCAGGACACCGGCCCTCCAGGACTGAGTTTGAACACCCCTGTATAACCGTATCTCAGTCAATGTTGGGTGTAATGCGTAACAAAATACACTCAAATTATTTTTGCTGCTCTTTCAAACTACTTATTTAAAATTAGATAAATCGACACAATGTTTCAGATTTTTTTCAGCTTAATTGTTTCATGTTCAACGTTTTTAATAAAAAATACCTTTTTTATGTTAGCTCTGCAATTTTTGCATATTAATTCTGGAGATCAAACTAATTAAAGCGTGGTGCTTTGCAGACATTTGACACATTGGTTGGTGAAGGTGGAGGGCAAATGAGCGGAGGACAGAAACAGAGGATCGCCATTGCTCGAGCGCTGGTCAGGAATCCCAGAATCCTCCTGTTAGACATGGCCACATCAGCGCTGGATAATGAGAGTGAGGCTGTCGTACAGGAGGCCTTGGACAAG[G/A]TGAGACTAATGATATCCTCACCAGCTGATGCTAAAATATAACTTTGGCACAGTCATTCTTTTATCCTGCTGACTATATTATATGCATTCTAATTAATCCAATTATTGGTTTTCCATAAGTGACAAATGGGATCTCAATAAGCACTTGTTTATTAGTCAGTGCACTGATCAGGGCGTGAGCCATTTTAAGTGTTGTCTCAATTACACAAATTTTCCAGTGCACTGAAACGCCTGCACCCTGAAAAGTCCCACAATGCACAGTGAATTCATCGAAATGCAGTATGCACCCTTAATGGAAGCTTAGAAGCATGAAATGTGAATCACGTGGCTCAAATCGTCAAACGTAATTACAAATGAGAGACGTTTTTCTCATTTGAGAAGAAGAAGAAGAATCTGATATTTTTTATTTTAACATGAACAAACAAAGCTAGACACAAAAAAAATCTACATTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTT
Associated Phenotype:
Not determined