ZMP
abcc9
Ensembl ID:
ZFIN ID:
Description:
ATP-binding cassette sub-family C member 9 [Source:RefSeq peptide;Acc:NP_001025325]
Human Orthologue:
ABCC9
Human Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 9 [Source:HGNC Symbol;Acc:60]
Mouse Orthologue:
Abcc9
Mouse Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 9 Gene [Source:MGI Symbol;Acc:MGI:1352630]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26260 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8414 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8868 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18175 | Essential Splice Site | Available for shipment | Available now |
sa17129 | Nonsense | Available for shipment | Available now |
sa38431 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26260
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013990 | Nonsense | 143 | 1558 | 4 | 37 |
ENSDART00000079987 | Nonsense | 55 | 1409 | 2 | 33 |
Genomic Location (Zv9):
Chromosome 4 (position 13730723)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 14666576 |
GRCz11 | 4 | 14665331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCAAACCTAATCAACCTAACCTCTTTCACAGCCTTATTTATTTACTG[G/A]ATTCTGGCTTTCATCACAAAGATGATAAAGTTATGGAAGTTTGCCGAGGC
Long Flanking Sequence:
ACACGTGTGTGAGATCGCTGAGGGAATCGTCTCCAATACGTGGGTTTCATTTCAACATATGCCTGTGCAGTTTATTAATGTGTCTGTACTGTTTTATTTACCTCTTCGTGCATGAATCTTGCTTTGCAGGCAGATGGAGTCTAATCACTTGCACCTCTTCATGCCAGCATTTATGGGCTTTATAGCAGCCACCACATCGGTTGTGTATTACCACAATATTGAAACAGCCAATTTCCCCAAACTCCTGCTGGGTAAGTGTCTATTTCATCATGCAGGTAGGCACTTCATAATAAAATGTACTTGCAGTGTGGTTGTTTCATTATGTTACATTTACTCCTACTCTAATTTAAATAAAGCATAGTCGTTTTGCACGTTGCTCGGTAACGCAATGGTCCAACCATATTTTTAGACATTGTCAGTAGTATTTTTTGCCTAGTGGTTGAGTATGAATATTCAAACCTAATCAACCTAACCTCTTTCACAGCCTTATTTATTTACTG[G/A]ATTCTGGCTTTCATCACAAAGATGATAAAGTTATGGAAGTTTGCCGAGGCGAGCTTGGGGGTACAACATCTCCGCTTCTGTATCACAGCGTTGCTTGTGGTGCTCTACGGCCTACTCATGGCTGTCGAGATCAACGTTATCAGAGTCAGGGTGAGTTTAGACATGTTTATTATTTATTTTAATTTTTTTCTATAAGCACTTAATTACACAATTATATACACAAATAAAATCTAAGCAAATTTCAGGCATTTTATTCAATTAATTTTTTTAATAATTATATTTATATTGTTAGTATTTATCTATTTTATTTTATTTAGTCCAGTGGATTTATTATTCTCAGCTTAAATGATTCAATAAAAACTAATCATGTACACAACTTTATGTATTGCACCAAATATGAATATTTTTCATATCAGGATTACACACACGTACACAAATCTTTTATTTTATTCAATATTTTATTTACTTTTTAACCATTCTTTATTTATTTTTTTTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8414
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013990 | Nonsense | 576 | 1558 | 12 | 37 |
ENSDART00000079987 | Nonsense | 488 | 1409 | 10 | 33 |
ENSDART00000013990 | Nonsense | 576 | 1558 | 12 | 37 |
ENSDART00000079987 | Nonsense | 488 | 1409 | 10 | 33 |
Genomic Location (Zv9):
Chromosome 4 (position 13741511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 14677364 |
GRCz11 | 4 | 14676119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCTTCGTCACACATGCCTACATTGAGGAGGACAGGCTCAGTCCTGCC[A/T]AGGCATTTGCCTCTTTGGCKCTATTCCACATYCTGGTCACTCCACTCTTY
Long Flanking Sequence:
CAGGGCAAAATAATATTCAAGCTAAAAACAATGTAATGTGTTATTACATAATATTGACATTTTATTTTTGTTGTATTATTAAGATACAAGTTCAACATTACATAATATTGACATACTTTTTTATGTTATATTATTAATGCACAAGTACAACAGCATCATGCTTTTTCAGTTTATTAGATTCCATGGAAATTCAGTTTTCTGAAGTGAGAGAATTTGATAATTGGTTTAAACCCTGTAAACTGCTTCCCTTGAAATTTCCCTCCCTCAATCCATACTGTCATTTGCTGATTTGATAGTACATTAACTGAAGTTTTCTTTTTCTTCATCTTCACAGTATTTATGAATGCCGCCATTCCCATTGCTGCAGTGTTGGCGGTAAGAGATGCACAATCACAGGCTTTGATCCGGTTGTATTTTTTCCAGTGTGACCATACGCACTCTTGTTATTGTAGACCTTCGTCACACATGCCTACATTGAGGAGGACAGGCTCAGTCCTGCC[A/T]AGGCATTTGCCTCTTTGGCTCTATTCCACATCCTGGTCACTCCACTCTTCCTTTTGTCCACGGTTGTCAGGTTTGCCGTCAAGGCTCTTGTCAGGTATGTGGCTAAACTAAATCAGCAGTAAAATGTTACTTTGGAAGGATCTAATCATCTGATTGATGTCTGCAGTGTACAGAAGCTCAGCGAGTTCCTGCAAAGTGATGAGATTGGAGACGACAGCTGGAGAAATGGAGATATGTGCATGTCTCTTGAAGTCGGCAAGAAATACAAATACCAAGGCGATGTGAGTAGGCACACACAACCTTTCAACACAATTTCAGATAGTTTGTGTCATGGGTTCTGAAAAATTTGCTCTAATTTGCTCTTATTTAATATTAACCGCACCTAATGGGACTGGTTGACACAATATTTAAGTTACATAACAAGTCTTTTCTTGGCTTAATTTTGGAGACTCTCTGAGATCCACTCTGTCTTTTCCCGTATTTATTTTAAATGTACGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8868
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013990 | Nonsense | 576 | 1558 | 12 | 37 |
ENSDART00000079987 | Nonsense | 488 | 1409 | 10 | 33 |
ENSDART00000013990 | Nonsense | 576 | 1558 | 12 | 37 |
ENSDART00000079987 | Nonsense | 488 | 1409 | 10 | 33 |
Genomic Location (Zv9):
Chromosome 4 (position 13741511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 14677364 |
GRCz11 | 4 | 14676119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCTTCGTCACACATGCCTACATTGAGGAGGACAGGCTCAGTCCTGCC[A/T]AGGCATTTGCCTCTTTGGCKCTATTCCACATYCTGGTCACTCCACTCTTY
Long Flanking Sequence:
CAGGGCAAAATAATATTCAAGCTAAAAACAATGTAATGTGTTATTACATAATATTGACATTTTATTTTTGTTGTATTATTAAGATACAAGTTCAACATTACATAATATTGACATACTTTTTTATGTTATATTATTAATGCACAAGTACAACAGCATCATGCTTTTTCAGTTTATTAGATTCCATGGAAATTCAGTTTTCTGAAGTGAGAGAATTTGATAATTGGTTTAAACCCTGTAAACTGCTTCCCTTGAAATTTCCCTCCCTCAATCCATACTGTCATTTGCTGATTTGATAGTACATTAACTGAAGTTTTCTTTTTCTTCATCTTCACAGTATTTATGAATGCCGCCATTCCCATTGCTGCAGTGTTGGCGGTAAGAGATGCACAATCACAGGCTTTGATCCGGTTGTATTTTTTCCAGTGTGACCATACGCACTCTTGTTATTGTAGACCTTCGTCACACATGCCTACATTGAGGAGGACAGGCTCAGTCCTGCC[A/T]AGGCATTTGCCTCTTTGGCTCTATTCCACATCCTGGTCACTCCACTCTTCCTTTTGTCCACGGTTGTCAGGTTTGCCGTCAAGGCTCTTGTCAGGTATGTGGCTAAACTAAATCAGCAGTAAAATGTTACTTTGGAAGGATCTAATCATCTGATTGATGTCTGCAGTGTACAGAAGCTCAGCGAGTTCCTGCAAAGTGATGAGATTGGAGACGACAGCTGGAGAAATGGAGATATGTGCATGTCTCTTGAAGTCGGCAAGAAATACAAATACCAAGGCGATGTGAGTAGGCACACACAACCTTTCAACACAATTTCAGATAGTTTGTGTCATGGGTTCTGAAAAATTTGCTCTAATTTGCTCTTATTTAATATTAACCGCACCTAATGGGACTGGTTGACACAATATTTAAGTTACATAACAAGTCTTTTCTTGGCTTAATTTTGGAGACTCTCTGAGATCCACTCTGTCTTTTCCCGTATTTATTTTAAATGTACGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18175
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013990 | Essential Splice Site | 645 | 1558 | 13 | 37 |
ENSDART00000079987 | Essential Splice Site | 557 | 1409 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 4 (position 13741793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 14677646 |
GRCz11 | 4 | 14676401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATGTGYATGTCTCTTGAAGTCGGCAAGAAATACAAATACCAAGGCGAT[G/T]TGAGTAGGYACACACAACCTTTCAACACAATTTCAGATAGTTTGTGTCAT
Long Flanking Sequence:
TGCTGATTTGATAGTACATTAACTGAAGTTTTCTTTTTCTTCATCTTCACAGTATTTATGAATGCCGCCATTCCCATTGCTGCAGTGTTGGCGGTAAGAGATGCACAATCACAGGCTTTGATCCGGTTGTATTTTTTCCAGTGTGACCATACGCACTCTTGTTATTGTAGACCTTCGTCACACATGCCTACATTGAGGAGGACAGGCTCAGTCCTGCCAAGGCATTTGCCTCTTTGGCTCTATTCCACATCCTGGTCACTCCACTCTTCCTTTTGTCCACGGTTGTCAGGTTTGCCGTCAAGGCTCTTGTCAGGTATGTGGCTAAACTAAATCAGCAGTAAAATGTTACTTTGGAAGGATCTAATCATCTGATTGATGTCTGCAGTGTACAGAAGCTCAGCGAGTTCCTGCAAAGTGATGAGATTGGAGACGACAGCTGGAGAAATGGAGATATGTGCATGTCTCTTGAAGTCGGCAAGAAATACAAATACCAAGGCGAT[G/T]TGAGTAGGCACACACAACCTTTCAACACAATTTCAGATAGTTTGTGTCATGGGTTCTGAAAAATTTGCTCTAATTTGCTCTTATTTAATATTAACCGCACCTAATGGGACTGGTTGACACAATATTTAAGTTACATAACAAGTCTTTTCTTGGCTTAATTTTGGAGACTCTCTGAGATCCACTCTGTCTTTTCCCGTATTTATTTTAAATGTACGTTATTGCCATAAAGGTGTCAGAAAGTTATGCTACTGAATTAAACCTAATATTTTTTACATTTCCTACAAGCAGTAAAATCCCAGAGAAGGAAAACGTTATCAACCTAGGATGGTTAATTCCGTTGATTTTATTAGTCAGTGACTTTTTTTTCACTGAAAGAAACTAGAAAAAAATAAAATAAAATCAGTTTTACCTGAAAAAATAGACTTTTTCATCAACAAATAAAGATGGAATGAAAATGTTTATAGTGGGGCAATTTGTTAAATGATCCAGTCAGAACCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17129
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013990 | Nonsense | 800 | 1558 | 18 | 37 |
ENSDART00000079987 | Nonsense | 712 | 1409 | 16 | 33 |
Genomic Location (Zv9):
Chromosome 4 (position 13756579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 14692432 |
GRCz11 | 4 | 14691187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAACCAGATATCGACCTCCTTCCTTTTGGAGACCAGACTGAAATCGGA[G/T]AGCGGGTAAGACTGTCTCTGGGCTTGAAACCAGCTCTCTGACCTCAGCTG
Long Flanking Sequence:
ATTTTTAATATTTTCATTACAAATCGCCTACGTTTCACATGACTTTCCAATCAATTCTCAATAGATGAAGTCTAAATGTAATTTTTTTACCTATATTCGTTTGAAATATGTCACATTACAGCCACATAATTGGTGAATGGATATTATCATTGATTTAACAAGGTGCTGTGAACTTGCCATTGTGGTTTGTAGCTTTACCACTGCTTTGAATTTAAATCTGTCAGCACTTACAGATGTTTTTTAAAGTTCGGCGGGTTGAAATTTTTACAATGCTCAGGGCCAGACCTCAGCTAAAATAAAACTCTCTTTGGAAACTCCGGGTCATGACTTTGCTCCCTAGAGAGCTCATGTTCGAGATTCCTAAGCTTTGGTTTTTTGAGGAGACGTTCTTTTATTTTTAAACTTTAAATTTGTTGGACAGATACAAAGCTGTGATTGATGCCTGCTCGCTTCAACCAGATATCGACCTCCTTCCTTTTGGAGACCAGACTGAAATCGGA[G/T]AGCGGGTAAGACTGTCTCTGGGCTTGAAACCAGCTCTCTGACCTCAGCTGCCGTGATGCTAATTGAATAAAGACCTGTTATTGAAACTACCATGACTATTGCATTACGTCATCAGAATCAAAAGTGTTTAACTTGTGTTTGTGTGTTGTAACCCAACAGGGTATTAATCTCAGCGGTGGTCAGAGACAGCGGATCTGTGTGGCCAGAGCTCTGTACCAGAACACCAACATTGTTTTCCTGGTAGGAACAAACTTATGGTGTCTTTCCTCCACCCTGAATAAGTGATATGCCACATGATTGAAATGTTATGAATGACCGCAGCTTTTAATTTGATTTTAGAGGTACTCCCAAGTTGAGATTTCTTAACTGACACATGATAGCACAGGGTACGTTGTGGCAGCGATCGCAGAAAACACAGTGATGTGTAAGGACTGTTATTGGATTACTGGACATAACTACACACCCTTCTGGACAGGATCGTGAATTCATCTCATTCCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38431
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013990 | Nonsense | 1454 | 1558 | 35 | 37 |
ENSDART00000079987 | Nonsense | 1265 | 1409 | 30 | 33 |
Genomic Location (Zv9):
Chromosome 4 (position 13775614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 14711467 |
GRCz11 | 4 | 14710222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCATGCTTTATGTTTGACTTTCGTCCCGCAGACGCTGTGGTGACCGAA[G/T]GAGGAGAGAACTTCAGTGTGGGACAGAGGCAGCTATTTTGTCTCGCCCGG
Long Flanking Sequence:
TAATGACACTTCTATATTACATTTGCCAGTTTTGTAGCTTGACAACCCTAAAAAAAAAGTGCAGCATGAACATTCTATCAAACATCTCCAAATGTCTCTCTCTAAAAAAACTGTGTTTATAGAAACATGAGTTCATCAGCTGTCTATATATGCACTTTCTATAGGTTAAATCTAGACCCCGAGCGCACATGCACCGACGACCGGCTTTGGGAAGCTCTAGAAATCGCTCAGCTGAAGAATATGGTGAAAGCTCTTCCAGGAGGATTGGGTAAGAGCAACAACACACGCCCTCCGAAAACATTCAGCTCTTATCCAGCAGAATGTCAGTCACCTCCTGGTTTTGACACTCACTGGAAATTCTCTACTGAAACGCTGGAGTTTTCTGACCCTTTGACAATGAGTTTGATTTCTGAGGAAAGCGATATTGAGTAAATGTGAACAGCTGTTGGTGGTCATGCTTTATGTTTGACTTTCGTCCCGCAGACGCTGTGGTGACCGAA[G/T]GAGGAGAGAACTTCAGTGTGGGACAGAGGCAGCTATTTTGTCTCGCCCGGGCCTTTGTTCGCAAGAGCAGCATCCTAATAATGGACGAGGCCACAGCTTCTATTGACATGGCCACGGTATAATCACAGATACAGAGGCTCATTTTTTACGACATGAGGAAAACAAATCATGCTTTGTTAAATCATGGCTATGCTAAAGTCACATTTAAAAAAAAAAAAAAGCCATTTTGTGATTAAAAAGTGACATTTTAATAGATTAAAATTAATATTCTTAATATAAATGTAAAAAAAAGTCTAAATTATTTTATAACAAGGTGTGGAATTTACAAATATTTGACAAAAAGTCTTAAATTTCAAACAAAAAGTGATGATTTTGACATACAAATTCATAATTGAAATAGAGGAATTATTGATTTATTTATTAATAATTTAAGCTAGCATATTTTAAGGAGATTTGTATCAATTATGATCATTGAAATTATGATAAACATTGGGAAAAGC
Associated Phenotype:
Not determined