ZMP

ABCB11

Ensembl ID:

ENSDARG00000070078

Description:

ATP-binding cassette, sub-family B (MDR/TAP), member 11 [Source:HGNC Symbol;Acc:42]

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6199	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa6200	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6199

Status:

Mutation detected in F1 DNA
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
ENSDART00000102557	Essential Splice Site	969	1352	22	28

Genomic Location (Zv9):

Chromosome 11 (position 13440918)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	13197741
GRCz11	11	13255400

KASP Assay ID:

554-5479.1 (used for ordering genotyping assays)

KASP Sequence:

TTACTGGATTCGCCAAGCAGGACAAAGAGGCCATGGAGACAGCAGGGCAG[G/A]TGAGCTCATGCTACACTGCAGTAGTGGAGATCAAAATTAGAACAATTTAT

Long Flanking Sequence:

ATTGTTGGGTATTTGTATTTATTTCCAGGGCTATGCATTCTCTAAATCCGGCGAGCTGCTCACTCGTAGATTGAGGCGTCTGGGCTTTCAGGCAATGTTGGGGCAGGAGATCGGCTGGTTTGATGATCGCAAAAACAGCCCTGGTGCTTTAACAACACGACTGGCTACAGATGCCTCGCAAGTCCAGGGAGTAAGAAAATCACTTAGCTGAAATGTTTCCATTAGCTCCCACATGTTATGTGACCCTTTTCAATCAAAATAAAACTTTATTAAGACTAAATAAACTCTCACCCCAGGCCACAGGTTCTCAGATCGGCATGATTGTGAATTCTCTGACCAACATCGGTGTGGCTGTTATCATCTCCTTTTACTTCAGCTGGAAGCTCACTCTGGTCATCCTGTGCTTCCTTCCATTCTTGGCTCTTTCTGGAGGGTTTCAGGCTAAAATGCTTACTGGATTCGCCAAGCAGGACAAAGAGGCCATGGAGACAGCAGGGCAG[G/A]TGAGCTCATGCTACACTGCAGTAGTGGAGATCAAAATTAGAACAATTTATAAACACTCGATATCTTTCATAAACAATCATAATTAATAATAATCCAAATTTAGACCTTTCCCAGAAAGCATTTTGTGTTTTTAAAAAATGTCTAATACATGTCTAATAGGCGTCTAAACATAGTCGTCTTGGCTAAAACAGAGCTAAATTTACACTGTCAGTTAAAATCTAATACACGTCTAAAAATAGGTCAACACTAGACTAGTCATCAAATAAACAGAAATGATTGACTACACATATAAAGTCACTTTAATCAGTCGATTTGACGACTAGTCTAGTTCCGGGCTATTCTTAGATGTCTATTAGATTTTCACTCACAGGCCAATCTTAGCCTTGTTTTAGAAAAGCTCTCTGCATTTAGATGTCTATTAGACGTCTATTATCACAAAATTGTTTGCTGGGATAGATTTCCTGCATCCCAATAAAGACTATTACTCAGTTGTAGATTAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6200

Status:

Mutation detected in F1 DNA
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
ENSDART00000102557	Essential Splice Site	1286	1352	27	28

Genomic Location (Zv9):

Chromosome 11 (position 13453822)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	13210645
GRCz11	11	13268304

KASP Assay ID:

554-4611.1 (used for ordering genotyping assays)

KASP Sequence:

TACTGCTTCTRGATGAGGCCACCTCAGCACTAGACACAGAAAGYGAGAAG[G/A]TGAGCAGGAAAGCYAGCAAAACGAGTTTTAGAAGATGTTTAAGAGGTCAT

Long Flanking Sequence:

TTGTGATATAAAGTCCCCTGTTTTTATATTTGAAATGATTTCAAATGTGTATTAAACTATAACTATATCTTTATTGTTATCTAGTTACCATGCAGGATGTGAACAGGCCTTACATTAGTAGTAGTTTAAATAAAATAAAAAAAGTAGTTTAAATTCTGAAGCAGTTTTAGTTTTAAAGTGGTTTTAAGTGGCTTTTGCTAGGCAGTTGTTGGATGGATGCTACATGCAAGTAGATACTATACTACTGTTTTGATTGGTTGCTAGGGTCTTTCTGGGTGGTCACTGGGATGTTTTTGGCATGGTCTTATGTAGAAAAGAAGATCTCATTAATACATCTTCCTCCCATGATGCAGAAATACGACACCAATGTTGGTTCCCAAGGTTCCCAGCTTTCCCGGGGTCAAAAACAGCGTATTGCCATAGCCAGAGCGATCATAAGAGACCCCAAAATACTGCTTCTGGATGAGGCCACCTCAGCACTAGACACAGAAAGTGAGAAG[G/A]TGAGCAGGAAAGCTAGCAAAACGAGTTTTAGAAGATGTTTAAGAGGTCATTTAGGAACTCGTAGTCTATGTTTGTTTGTGTTTCAGACTGTACAGGAGGCCTTGGATAAAGCCAGAGAAGGCAGAACATGTATTGTCATCGCTCACCGTCTGTCTACTATCCAGAACTCTGACATCATAGCTGTGATGTCAAGAGGATACGTCATTGAGAAGGGCACGCATGACTATCTGATGGGCCTGAAGGGGGCGTACTATAAACTTGTCACGACTGGAGCTCCAATCAGTTAATCTTACTCTCAACGAGGCAGATAGAAAGACCAATCAGCACTGTAGACCTGGTGTGGACATGGATGTGCATTATTTTCTTATGTTTTTAAAGACCAAGGTCTATTATTCTGCCTATGATAGTCAGCGAAACTAAAGATATCCGTTAGATGTTGCATTTCAAGCTTGTTTTCAGATTTTTATCTTCAAAGATGTATGGGAGGTGGGTGTGATTTT

Associated Phenotype:

Not determined