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 |
---|---|---|---|
sa44714 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34768 | Essential Splice Site | Available for shipment | Available now |
sa18968 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18599 | Essential Splice Site | Available for shipment | Available now |
sa45380 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21601 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44714
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047401 | Nonsense | 5 | 1281 | 1 | 25 |
ENSDART00000134566 | None | None | 609 | None | 12 |
ENSDART00000139631 | None | None | 635 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 49806243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49061439 |
GRCz11 | 9 | 48758924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATGGTGAAGTCAAAAAAAAAGAGAAAGCACCGACTGTCGGATTCTTT[C/T]AGCTGGTAAGCATCTCAGTAGTACTCTACGACGTTTTTTCGTTACCTGGA
Long Flanking Sequence:
CTCGACTAAAAAAAGCCTCAAAAGTACATTATGTTGTCCAACAGCTGCATTATTTGTCAAACTGTAGTGAGTCTATTGATCTGCTGCCACTCTCTGCAGGTGGAGTGAAACAAAAGGGTGAAGAGGATGTATGAGTGCTGTTATTGCAGAATATATCTCGGCTATCAACCAATCAGATTCTAAAACCAGACAGAACTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACAGTAAATACAAGCTTTAAATTTGAATTTGATTAATTGTGATTAATCATTTGACAGCACTAATATAACAGTAAATTTGTAAAAATCTATTTTAGCTTGACCAAAATATCAATAATAATCTGATTTAGGTTTCACTACAGCTACAGTTTCTAAAATATTTCTGTGTTTGAAGGAATGGTGAAGTCAAAAAAAAAGAGAAAGCACCGACTGTCGGATTCTTT[C/T]AGCTGGTAAGCATCTCAGTAGTACTCTACGACGTTTTTTCGTTACCTGGATCAAAATATTAAATTATTAACTGAATGTTTTTAACAACTGAAGTTGGGCAGCAAAAAGGTCACTGGTTTGAGTTCTGGCTAGGCCAATTGGCGTTTCTGAGTGGAGTTTGCATGTTCTCCCTGTGTTGGTGTGGGTTTCTCCGGATGCTCCGGTTTCCCTCACAGTCCAAAGACATGCAGTATAGGTGAATTGGATAAACTAAATTGGCCCTAGTGTATGTGTGTGAATGCAAGACTGTATGGGTGTTTCCCTGTGATGGATATCCGCTGCGTAAGACATATGCTTTATTGCCAGGTATGTTCATACATTCGAGGAATTTGTTTTGGTGACAGAGCTTCTACAGTGCAACAGAATGACAAAGACAGGATATAAAACAGATAATAAATATATTTAATAAAAATAGAAGTAGTGAATGCCAAGGCTGGAGTGGGACTCCTTCAGCCCTGGAG
Associated Phenotype:
Not determined
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:
sa18968
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 |
---|---|---|---|---|---|
ENSDART00000047401 | Essential Splice Site | 160 | 1281 | 5 | 25 |
ENSDART00000134566 | Essential Splice Site | 154 | 609 | 4 | 12 |
ENSDART00000139631 | None | None | 635 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 49816762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49071958 |
GRCz11 | 9 | 48769443 |
KASP Assay ID:
2260-2534.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTTGCATAGATACTAGTTTAATTTAGCATGTTTGTTACTTTTTTGCA[G/A]TGACATCAACAAAATCAACAACGCTATAGCGGACCAGGTGTCCATCTTCA
Long Flanking Sequence:
GTAACAGACACACTGTACCTCTTCCCAACAGGGAAAAACATAAACAATCATGAATGCATGATTATATGGTGTCATAGCTTTGCAAACAAAAAAATGTCATTTTAATGGAAGTCAATGGGGCAAAAACAGACACCAACATAACGAAAGGATAGTAAATTTGCCCAGAGTGTATTGTTGTTTTTTTTATTTTATTTTTTTTTTATTAAGATTTTAGAGCATTTTCTTAAAATGTGTGTCAAAATAAAATTTGTCACCAAAAATCACCCTATTTGCTGAAACAGATATTTGTGGCCAAATTAAGACTCAAACTCCCCTCAGAGTGGATGAAAACATCCCCAAGAGCACACGAGGGTTAACTTTGCTGGAGCTGTAGAAAAAAACAACAATGTTGTGCATGAAATGAAAAATTAATCTCACAGTGAATGCATCTTTAAGTATTTCTGCTCATTTCATCTTGCATAGATACTAGTTTAATTTAGCATGTTTGTTACTTTTTTGCA[G/A]TGACATCAACAAAATCAACAACGCTATAGCGGACCAGGTGTCCATCTTCATTGAGAGGATCTCCACGTTTATATTCGGCTTCATGGTGGGCTTCATCGGCGGCTGGAAGCTGACACTGGTGGTCATCGCAGTCAGTCCTCTATTAGGCCTCGCCGCAGGACTCATGGCTATGGTCAGTTTCACCACAGACAAATCAATATGAAGGAGACTGGAGTCAGGGATTGTGTGGGGTTTACAAACACTTAATTCAACATATTACAGATAAAGGCCTTAAAGGGAGAGTTCACCCAAAAATGAACATTTACTCACTATTTATTCACCCTCTTTTTTTCTTCTTCTGTTGAACACAAAAGAAGATAGAGTATTTTGGAGAAAGCTGAAAACATGTAACCATTCACTTCCATAGTAGGAAAAACAAATACTATGGATGTCAATGGTTACAGGTTTACTGCTTTCTTCGAAATATCTTCTTATGTCTTCAACAAAAGAAAGAAACTTTT
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:
sa45380
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047401 | Nonsense | 422 | 1281 | 10 | 25 |
ENSDART00000134566 | Nonsense | 416 | 609 | 9 | 12 |
ENSDART00000139631 | None | None | 635 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 49832217)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 49087413 |
GRCz11 | 9 | 48784898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACGACAGCGTTTGTTGGACCCAGCGGATCAGGAAAAACCACAACAATA[C/T]AACTCATCCAAAGGTTCTACGACCCAAGTGAAGGAATGGTACTGTCATTT
Long Flanking Sequence:
TATATTTCGCCTTAAATTAATATTGTTCGCTGTTCTCTGTCATCCTGAGGCCACCGGCCGGCGTTGAGCCCGGGTGCGAGGTTCCGTTTATCGCTGCTTGCAGCTTTAATTTGTTTTGTATTTTTCATAGGTTTTATATGTTTTAAAAGTAACCTCAAAGAAATGTAATTAGTAATCTGATAACTTTTTACATGAAGTCATTAGTAATGTGATAAGATTACAATTTTGCAGTTGTCAGTAATTTGGAATCAGTGTTGTTTTTTTTAAAGTAACTTACCCAACACTGCTTCGTAATGTGTTCAACAGAAGAAAGAAACTCAAAAGAGTGAGAAAGGAGTGAATAAATGTTCATTTTTGTGTAAATTATCCCTTTAGATTATGTCTAGTATTACCTGAGTATTTCTTGTGTTCAGATATTAGATGATTTGAACATTGTGGTCAAAGCTGGCGAGACGACAGCGTTTGTTGGACCCAGCGGATCAGGAAAAACCACAACAATA[C/T]AACTCATCCAAAGGTTCTACGACCCAAGTGAAGGAATGGTACTGTCATTTGATCCAGTAATATTTTGATATTATTAATATGCCTTCTGGGTGGCACTGTGGCTTAGTCTTTACCACCTCACCTCATAGCAAGAAGGTCACTGCTTTGAGTCCTGGCTGGGCCAGTTGGCATTTCTGTGTAGAGTTTGCATCTTCTCCCCCTTGTTGGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCTCCATAGTCCGAACACATGCGCTGTAGGTGAATTGGGTAAACTAAATTGACCGTAGTCTATGAGTGTGTATTGGTGTTTCCCAGTACTGGGTTGCAGCTGGAAGTGTATCCGCTGCATAGCCGTATGTCGGAATAGTTGGCGGTTCATTCCGCTGTGGCGACCCTTAATAAATGAAAGGACTAAGCTGAGAAAAATTAATAAATGAAATGATTTATGTTTGAGCAGTGTGTATGTAATTATGCACATTGTATTTATTAGCAAA
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