Busch Lab

ZMP

LOC568482

Ensembl ID:
ENSDARG00000013050
Human Orthologues:
ABCC11, ABCC12
Human Descriptions:
ATP-binding cassette, sub-family C (CFTR/MRP), member 11 [Source:HGNC Symbol;Acc:14639]
ATP-binding cassette, sub-family C (CFTR/MRP), member 12 [Source:HGNC Symbol;Acc:14640]
Mouse Orthologue:
Abcc12
Mouse Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 12 Gene [Source:MGI Symbol;Acc:MGI:2441679]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa18406 Nonsense Available for shipment Available now
sa9287 Nonsense Mutation detected in F1 DNA Not yet available
sa26997 Nonsense Mutation detected in F1 DNA Not yet available
sa45286 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18406
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049974 Nonsense 207 1368 5 30
Genomic Location (Zv9):
Chromosome 7 (position 39572798)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 37909438
GRCz11 7 38180696
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTTTTCCTCACKGAGTTYAGCAAGGCATTTTTTGCATCCGTCCTGTG[G/A]GCTGTGAAYTTGMGGACAGCTGTGAGAGTGAAGGGAGCATTCTCCATGCT
Long Flanking Sequence:
GTACCAAAAAACAACAATTTGACGAGTTCAGATGCAAAAACCTTTAAATGTCCACTGAAACATTCTGCTAAAATGAAATTTTTTCTCAATCTTTAACGTTTATGTTCAGTTGTTTCCCTTGAAAGGCAATGAAAAGAACCTATTTGTCACTATAAATGTAAAATTTCTAAGCCAATACACAAGAGTTTAAGAAAAACGCTCATTTTTTAAGAAAATATCAAACGGCTTTTAGAGGTTTTTGCATCTAAACTCTTAATTTGTAAATATTGTCCATGCTTGTAGTGCTTGTGTGTAGTGTTATTTGCTGTCATACACCATAAATCTGTTTGAAAATGTTGGCTTATGTATACATTTTGTCTTTTTTTCTAGTCAATTCTAGTATATGAAATCCTGAACTATGTCGAGCAGTCTGAACCGTCTACAGTGGTGCATGGTGTCGGTGTGTGTGTGGCTCTTTTCCTCACGGAGTTCAGCAAGGCATTTTTTGCATCCGTCCTGTG[G/A]GCTGTGAACTTGAGGACAGCTGTGAGAGTGAAGGGAGCATTCTCCATGCTTGCTTTCAAGAAAATCATCTCTCTTAGGAGTCTTACTACTATCACTGTAGGAGAGGTAAGCTACTGATTGTTGGTTCATCAGTGAATACTGCCACAATATTTTCTAGATGCAGAATCTACTTATTAGTGGCTTTATTAGGGCATTAATGTGCTGTAGTAAACTAAACAATTTTAAATGACTATATACAATCCAAAGAGTGTTTGTCATGAACTGTAGTCTTCATTCTTTGTATGTTTTGTGTCTGGTTTAGACGATAAACGTCTTGACGAGTGATGGCTATCGGTTGTTTGATGCGGTCATATTTGGGACATTTCTGCTGTGTGTTCCAGTACTGCTGATCATCTGTATCATATATGCCTGCTTTATTCTTGGATACACAGCACTTATTGGAATTCTAGTGTATTTGATCTTCCTTCCAATACAGGTATGCAGCCTTCTTTTGTGTTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9287
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049974 Nonsense 818 1368 19 30
Genomic Location (Zv9):
Chromosome 7 (position 39565004)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 37901644
GRCz11 7 38172902
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCTTCTTGTGGGATCGMCTGCTTTCAGCAACTGGTGGCTCAGYTACTG[G/A]TTGGACCAGGGATCAGGGGTAAGCACACACACACANNGAAGCACATACAGAC
Long Flanking Sequence:
AAAAAGCACTTTGTTCACCTTTGGTAATCTTTATCATTTCCCTTTAGCGTTTGATATGTCTGATGAGAAACCTGCAACAAACGAAACACCCAAAGACTCTTCAGAAACAAAAGGTAGATTTAGACACAATATCCTCTTCACAATATATAATCACAATATAATCAAGAAAATGTCCACTATATTCATACAAACGTGACTCACACAACACTGTGTATGTTTGTTTTAGGGAAAAAGGATCAATTAGTGACACGAGAAGTGGCCCAAGAAGGTTCAGTTACGTGGAGGACTTACCATCAATACTGCCAAGCAGCTGGAGGTTTCTCTTATTATTTCTTCACTCTCCATATGTGTCTCTCTGCTCATTGCAAATGACATAACACAGTTTTTAAATCTTGATGTGTCTATATTTCTATAGGCTATATACTGTTGTTTCTTGTTGTCCTTCTCTTCACGCTTCTTGTGGGATCGACTGCTTTCAGCAACTGGTGGCTCAGCTACTG[G/A]TTGGACCAGGGATCAGGGGTAAGCACACACACACAGAAGCACATACAGACACATAACAAATCTGGTTTGCTATCCCTATGGGGACTTTCTTGGCCAGAATGATTTTAACACTGTACAAAATATTTAACCTGTCCCCTTACCTCAACCCTATCCTTACCTCATCCCTGATAGTGAACATTCTGTCTTTTGTTTTTACATTTTTAATTTGAGCGATGTTGAGGGCGTACGTAAAAAGTGCTGATTGGCCATTGTGTTCACATGCTCAACAGAAATTACTGTGATTGGCCAGAAGGTCATCAGTTCACTGCTTTTCAAGGAGTGCAAACACAGATACAAGGACACTGGAGCGTTTCAAAGCCATGAAGATCAGTCGTTTCATCAGTGAATCGCTCGTATGTCAGCTCATAGACAGATCAGCTGATTGATGCTGCTTTGAAACGCTCCAGCGTCACTGTATCTGTGTTTGCACTCTGTAAACAGCAGTAAATAATGGTAAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26997
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049974 Nonsense 848 1368 20 30
Genomic Location (Zv9):
Chromosome 7 (position 39564095)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 37900735
GRCz11 7 38171993
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACATCAAACAGCGGTAATATCTCTGAGAATCCGGACCTGTCGTTCTAC[C/T]AAATGGTTTATGGTGTTATTATCATTGCCATGATCGTGCTGAGTATTCTC
Long Flanking Sequence:
ACAGATCAGCTGATTGATGCTGCTTTGAAACGCTCCAGCGTCACTGTATCTGTGTTTGCACTCTGTAAACAGCAGTAAATAATGGTAAATCAATGACCATCACATCCAATCATGGTCATTTCTGTTAAGCACGCAATGGCCAATCAGCTGTGCTCAAGTATGCCCTCAACATCGCTCAAATGTAAGCGGGAAATGGACTTTTAAAAATGTCAGTATCGATTGGTACCGAAGTCGATACTTATTACAATTCTACCCATGGGACCTCAGTTTATGTCCCATTGGTGACATGAGTCTCCATGAGTATGTGCACATTCATGTTTAGTCTCCTCTAGGATATAAAAACAAGGTCACACACATGCACACACTTGAGACTCATTCAAGACCTCATCATCTTATCATTAAATCACTTTTCTCTGTTTGTGTTCTTGAAGAACAATTCCAGCTCTAATGCAACATCAAACAGCGGTAATATCTCTGAGAATCCGGACCTGTCGTTCTAC[C/T]AAATGGTTTATGGTGTTATTATCATTGCCATGATCGTGCTGAGTATTCTCAAGGGCTACACCTTCACTAAAGTCACTCTGCGTTCCTCTTCCAAACTCCATGACACCATGTTCAAACGGGTAAGACAAACAGATAAACGATAATTTAATCTTTACTGTCTCTTATTTATTGATAGATGCATTATTGTCTTGTTCAAGATTCCACAGTTTGCTTGTGTTTGTAAATTGTGTGTGAGGCAATCAAATGAATTGTATTCAAATAATCCAAACTTCCCATCATTATATTCGTAGGCTATAGCATCAATCTTTATTTTGTATTCACTCTCACATCCAGAACATTTCCCCAATATGCATAACGCAGACCTTTATGTCTGCATTTGTCTGAAATCATCATGTAATTTCACAGAATTTATTAATTCACACCTTGATAGGGGAGCTATACGCTACTGATAGTGAAAGCTTGTTGTAGTGTGAGAAGGGAGGGAGGGCTTTGAGAAGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45286
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049974 Nonsense 1365 1368 30 30
Genomic Location (Zv9):
Chromosome 7 (position 39551144)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 37887784
GRCz11 7 38159042
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTCAGAGACCCAACTCTTTATTTGCATCACTTCTAGCAGCAGCGAAT[C/T]AAGTCAACACGTGAAGCTCTCACAAACATTCACATTCTCTTCTAGACATG
Long Flanking Sequence:
TCTCTGTATCAGTTAGCAAGTTTCTGAAAAAAGAGTCATTTACAGCAATAAATGATCCAAGAGGTATTTTAAGCTAAACATTTACACATCTTGGAGGTACATGTAAAAAAAGGCACAGCAGGACTATTTCACTGCAGTCTTTTTTTAGATATGTAGCAGCATCATAGTATATTGATGGTACTGTATTTCAAGAGACACTGAATGGTGTACACACAGACCAAAAAAATCAAACTTGCCATGATTAAAACTAAACACAACAACACTGCTTCTATTTGGAAAACATGCATACCAAAAAACTGTAACTGAACATGTTCACTTTACATTTGTGTACCATTACACCCCACATTAAACTAAATGAGCTAAATTATAGTTTGAGCATTTTAAAGAAATTATTTGAAAGCCTATTTTGTGTTTTCTTTCAGGTGATTGAGTTTGATCCACCGCAGGACCTGATTCAGAGACCCAACTCTTTATTTGCATCACTTCTAGCAGCAGCGAAT[C/T]AAGTCAACACGTGAAGCTCTCACAAACATTCACATTCTCTTCTAGACATGCATTCAAATCTCATACATTTATTCAGGAAGTCAACCTGAAGGAGTTTACCACATCTTTTATACAGAACATTTGTGACTTCATACCTCAATCTTAACATATATGCTATCAATAACATGCCAGAGCACACTTCACACGTTTGAACTGTACATTAACAGGTAAAAGCACATGGATTTGCACTTTTTTATATAAAGTAAGCTGCACAGTAAATTTTTCTCCAGAGATTCACCAGTCTTTTGTGTGTAGACACAGCATTTACAGACGATGTGTAAAATATTTTCATAGGTTCATCAGATGTATATATAAAAATATTTATTTGATTTTTATAAGTATAAAACATGTATTAGGGAAACTGTTCACAAATAAAACCTAATTTCTGTCTTGTATTCTATTCTTGCATACTTTTCCCCCCATGTATCATGAGGCTGTTCAAAATTTGATGTATCAAAATT
Associated Phenotype:
Not determined