Busch Lab

ZMP

ABCC10

Ensembl ID:
ENSDARG00000077988
Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 10 [Source:HGNC Symbol;Acc:52]
Human Orthologue:
ABCC10
Human Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 10 [Source:HGNC Symbol;Acc:52]
Mouse Orthologue:
Abcc10
Mouse Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 10 Gene [Source:MGI Symbol;Acc:MGI:2386976]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa2584 Nonsense F2 line generated Not yet available
sa30944 Nonsense Mutation detected in F1 DNA Not yet available
sa45422 Nonsense Mutation detected in F1 DNA Not yet available
sa38830 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa2584
Status:
F2 line generated
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
ENSDART00000115249 Nonsense 379 1548 2 21
Genomic Location (Zv9):
Chromosome 11 (position 12090520)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11971907
GRCz11 11 11955528
KASP Assay ID:
554-2442.1 (used for ordering genotyping assays)
KASP Sequence:
ACTGGTGGGTTTCATGGAGACTGAAGGAGCACCACTGAGCAAGGGTGTGT[G/A]GTGCRCTGTAGGGCTTTTTGCTAGTACTTTTCTTGCTGCCCTGCTAAAAA
Long Flanking Sequence:
TCCTTTAATTGTTACTTTTGAACCCTTCGAAGAGGTGACTGTTGCTGAGGATGGCAGCAGCTTGCTTTCCAGACTCCTCTATCTGTGGCTCAACCCTTTGCTAAATCGAGGTAAACGTGGAGAGCTGGGGAGACCAAGTGATGTCTTTGAGCTTCCAAGTCGACTGCGCACCAAATCAGTCACCCGCCGGTTCTACCAGTGCTGGGAGAAATGCCTCCATTCACGAGCTCTGGAAAGACCTGAGAGACCGGATAGACGTCCGAGAGGAAACCTGCAGGACAACTCTTGGAGTGAAGCTCAACCGGAAAGGATTTGCGAAGGTGAAGCGGAACATGAAGTCAAGCTTCTGCAAGTGCTGCACAAGGCCTTTGGTTTACGCTACTACCTGTTGGGAGGGTTGAAGCTAGTAGCTAGCATGTTAGCTTTTGCAGGACCCCTTCTTCTTGGTGGACTGGTGGGTTTCATGGAGACTGAAGGAGCACCACTGAGCAAGGGTGTGT[G/A]GTGCGCTGTAGGGCTTTTTGCTAGTACTTTTCTTGCTGCCCTGCTAAAAAACATCTTTGTTTATGAAGTATCAAAGGTTGCCCTGGAAGCTCGGGCTGCTGTGATTTCCACCATCTACTGCAAAGCCTTAAAAGTCAATGCGCCTTCTCTGGCTCGCTTCAACATGGGTGAGGTAGTCAACTTTATGAGCACGGACACTGACCGCGTGGTCAATTTCTTCAACAGCTTCCATGAGGTGTGGAGTCTTCCCTTCCAGTTTGTTCTTGCACTTTACCTGCTGTACCTGCAGGTGGGCGTGGCCTTTTTAGGTGGAGTGGGTGTAGCCGTGCTGCTTGTGCCTTTGAATAAAGTCCTGGCTTCCCGAATTCTGGAAAACAATAAGCATATGCTGCAGCACAAAGATGGCAGAGTGAAGGTGGGACTGCATTGCATATATTTTTAAATATTTCCTGTTAATAATGTTTGTCTTTGTCCAAATACGTTGTCATTCATGGGTCAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30944
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115249 Nonsense 400 1548 2 21
Genomic Location (Zv9):
Chromosome 11 (position 12090456)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11971843
GRCz11 11 11955464
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTTGCTAGTACTTTTCTTGCTGCCCTGCTAAAAAACATCTTTGTTTA[T/G]GAAGTATCAAAGGTTGCCCTGGAAGCTCGGGCTGCTGTGATTTCCACCAT
Long Flanking Sequence:
CTTTCCAGACTCCTCTATCTGTGGCTCAACCCTTTGCTAAATCGAGGTAAACGTGGAGAGCTGGGGAGACCAAGTGATGTCTTTGAGCTTCCAAGTCGACTGCGCACCAAATCAGTCACCCGCCGGTTCTACCAGTGCTGGGAGAAATGCCTCCATTCACGAGCTCTGGAAAGACCTGAGAGACCGGATAGACGTCCGAGAGGAAACCTGCAGGACAACTCTTGGAGTGAAGCTCAACCGGAAAGGATTTGCGAAGGTGAAGCGGAACATGAAGTCAAGCTTCTGCAAGTGCTGCACAAGGCCTTTGGTTTACGCTACTACCTGTTGGGAGGGTTGAAGCTAGTAGCTAGCATGTTAGCTTTTGCAGGACCCCTTCTTCTTGGTGGACTGGTGGGTTTCATGGAGACTGAAGGAGCACCACTGAGCAAGGGTGTGTGGTGCGCTGTAGGGCTTTTTGCTAGTACTTTTCTTGCTGCCCTGCTAAAAAACATCTTTGTTTA[T/G]GAAGTATCAAAGGTTGCCCTGGAAGCTCGGGCTGCTGTGATTTCCACCATCTACTGCAAAGCCTTAAAAGTCAATGCGCCTTCTCTGGCTCGCTTCAACATGGGTGAGGTAGTCAACTTTATGAGCACGGACACTGACCGCGTGGTCAATTTCTTCAACAGCTTCCATGAGGTGTGGAGTCTTCCCTTCCAGTTTGTTCTTGCACTTTACCTGCTGTACCTGCAGGTGGGCGTGGCCTTTTTAGGTGGAGTGGGTGTAGCCGTGCTGCTTGTGCCTTTGAATAAAGTCCTGGCTTCCCGAATTCTGGAAAACAATAAGCATATGCTGCAGCACAAAGATGGCAGAGTGAAGGTGGGACTGCATTGCATATATTTTTAAATATTTCCTGTTAATAATGTTTGTCTTTGTCCAAATACGTTGTCATTCATGGGTCAAATTAGCAAGGATGCATGGAAGGCACAGTATGTAAAGGTAAAATACCCGAAAAACACTTGAACAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45422
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115249 Nonsense 770 1548 7 21
Genomic Location (Zv9):
Chromosome 11 (position 12077025)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11958412
GRCz11 11 11942033
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTGCAAGATAACATTCTCTTCGGCAGGGATTATGACAACATGTTTTA[T/A]CAATCTGTGATACAGGCCTGTGCCCTGGCTGATGACTTAAATGTAAGCGT
Long Flanking Sequence:
GGGTCTGCTCTGCTCTTTCTCGGCTTTATTATGGAGAATAAAGTCTATTTTCTGATATTCAAAACCTCTGGTCTGATAATTTGTAATAAATGAGAAGTCAATATTTACCACAGGGGGCGAATAATTCAGGGGGCTAATAATTCTGGCTTCAGTTGTATATTTGTAAAACTAACTGTATTTTCTTGTGACATGTAAACAACCATTATTATTACTACTACATAATACATTCATAACAATATTTTGCCTAATAGCATTGTTTTAATAATAAAAATTTATATTTAGTGCTAAAATGTAATATGTATAAAAGAAAAACCCATAAAAACTGTAAATGTGCAGAAGTTCTCATAATTGTATTAGTTTCTGTCCTGTAGGTGTGGCGGGGAAGTGTTTGTTCAGGGAAGAGAGCAGGGGTTTGGATTGGCCGTCCAGGAGCCGTGGATCCAGCATGCAACAGTGCAAGATAACATTCTCTTCGGCAGGGATTATGACAACATGTTTTA[T/A]CAATCTGTGATACAGGCCTGTGCCCTGGCTGATGACTTAAATGTAAGCGTATATCTAGTTACTTTTTACTTTATTTAGTATTCTGCTTTGAATTGTAACGATGGAAAGTTAAAGCTGACACTGTTTTGTTCAGATCTTACCTGGTGGTGATCAGACAGAGGTCGGAGAGAACGGCGTGACTCTGAGCGGAGGACAGAAAAGCCGCCTTGCTTTGGCCCGGGCTGTTTATATGGTGCAACGTTTTGTTGTTTTAATGGTCAAAGTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCATTTTCTCAGCATTTTCTTTTTCAGTATACATAAACATTGAGCATATACAACCATTTCTATAGCATAATCAATTACAGAAAAAAATAATGCAAAGGAAAAAAAACAGAACAAAATAAAGATTAATAACAATTACCAACATAGAAAAAAAAGAACCGCTTGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38830
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
ENSDART00000115249 Nonsense 1143 1548 14 21
Genomic Location (Zv9):
Chromosome 11 (position 12064381)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11945768
GRCz11 11 11929389
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTTCCTTGGGTTCTGCTGCCTTTGGTTCCTTTGGGGGCGCTTTACTAC[C/T]AAACTCAGTGTTTTTATCGTTACTCGTCCCGTGAGCTGAAACGCCTGTGC
Long Flanking Sequence:
ATTTTAGAGTATTAAATACGGCCTTGGTGAGCAGAAAAAATATTTTAAGAACTATATAGTTAAATATATAAATATCAACATTTTGACTATTAGTGTACATATTATTTTAATAGTTTAATATTTTAATAATACATTTAATAAATTATTTCTAAAAAGAATTTACATATTTTTTTCTTAATATACTATTTATTATTTACTTGGTAAAAATATATATTATTATTATTATAATTGTTGTTGTTATTGTTATTATTATTCATTTAAAATATTCACATCTCATGCTTTTTCTATTCTAGGCCACTATGACGTTTTTTGACACAACACCATTGGGTCGCATCCTGAACCGTTTCTCCTCAGACATTTACAGTGTGGACGACTCTCTCCCCTTCGTCTTAAACATCCTCCTGGCCAACGTGTTTGGTCTTCTTGGGATGCTCATCGTCATGAGTTACGGGCTTCCTTGGGTTCTGCTGCCTTTGGTTCCTTTGGGGGCGCTTTACTAC[C/T]AAACTCAGTGTTTTTATCGTTACTCGTCCCGTGAGCTGAAACGCCTGTGCAGCCTCACACTCTCTCCAGTTTATTCACACTTCTCAGAAACCCTCAGCGGTCTGTCCACGGTGCGGGGCAGTGGACACACTACCAGGTTTGAAAAAGTGCTGTACTTTTACTCAGATAAACTCATTTAAATATGCATGTTTGTTTCAAAGAACAAAATGAATACTTTGCATAAAGAATACAATGATTTTGTTGTTTGCATTGTGACATTATTTTCATGACTAATGAATTACTGATGCCAAAAATATCAAAATTAGTATACGAAAATGAAATGTTAATAATTTTTGATTAGAATAAATTTATATTGACAAAGCAAATGCAATAATTTTATATTCAAGTAATGTGCTTTGTTTACATGTGATAAAACGTCTATAATCTATGCAGATTTTAATCCTAGAGTCCAAAAATATCTTCATTCATGAATATGTATTCAGTTATTAGTAGTTGTTAGT
Associated Phenotype:
Not determined