ZMP
abcc2
Ensembl ID:
ZFIN ID:
Description:
canalicular multispecific organic anion transporter 1 [Source:RefSeq peptide;Acc:NP_956883]
Human Orthologue:
ABCC2
Human Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 2 [Source:HGNC Symbol;Acc:53]
Mouse Orthologue:
Abcc2
Mouse Description:
ATP-binding cassette, sub-family C (CFTR/MRP), member 2 Gene [Source:MGI Symbol;Acc:MGI:1352447]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22191 | Nonsense | Available for shipment | Available now |
sa11900 | Essential Splice Site | Available for shipment | Available now |
sa2688 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22191
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016604 | Nonsense | 273 | 1553 | 6 | 31 |
ENSDART00000114538 | Nonsense | 277 | 1564 | 6 | 34 |
Genomic Location (Zv9):
Chromosome 13 (position 556851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 554834 |
GRCz11 | 13 | 685125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTACAGAAGAAGAAAAGCAAGAAACGCAAGACCGTAGATGCTGAGGGT[C/T]AGAACGGACTGGCCAAAGGGGTCAGTCAGGACGTGCTGGTCATGGTGAGA
Long Flanking Sequence:
AGTTTATTGTCTAATGTTTTACTCATTTGAATATGCTGATTACTTGATTCTGATTGGCTGATGAGCATTCTATGCACTGCAAATTGTCTAATTTCTAGTGCAAATATCTAAAACCTCTTAAATCAAGAAGTATTTCTAGTCAAGCACAAAATATAGTTTTATTTTCAGAAATAATGAGTCAAAATGAACTGAGCTTTACATTAAAACAAGCAAAATAATCTGACAATGATGTAAAAATGATCATCTCATGTCAAAAGGAAGAACCAGATTATTGTGCATGGAAACCCAGTCATTGAGTGTGTTTGTGCTCCTCCAGCATGGTGTGGAAGGGCTTTAAAAGGCCTCTGGTTCAGGAGGACATGTGGGATCTGAACAAAAACGACTCCACACACTTCATCTGTCAGACGTTCGAGGACGTGATGGCCAAGGAGCTGAAGAAAGCCCGCAACAACCTACAGAAGAAGAAAAGCAAGAAACGCAAGACCGTAGATGCTGAGGGT[C/T]AGAACGGACTGGCCAAAGGGGTCAGTCAGGACGTGCTGGTCATGGTGAGAGAAAACACACACAATAATGCTGTTCTCAGATAAACTGTTAAATTCATATCCGCTCAGATCAATGTTTAGTTGGCTAATAGTTTAGTTTTGTGGCCAGTTGTCATGTAATAAACAGCAAACTGCAAAAAAAGCTAGTTCATGATGTGTAAAAGTGTCAAAAGGTGGATTTCTCTGCTGAATCAGCTGTTGATCTGCTCAAATAAGCCTCATCTAGAGGACTTTGCCTTTCATATAAGACACTGTTGATACCAAATCATCAACTAGAAGAACAGTTATTATTTGCCGTTCCTAAAACTTGAAGAGGCCACAAGACTTTTATCAGATAGTGTAGAGTTTTTGCCTTATTTCTAGTCCAAATATTTTTAAAAAATCTTAAATCAAGAAGCTTTTTCTAGACAAGTATTAAATATTGTCTTGTTTTCAGAAATAGTAGATCAAAATGAAGTGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11900
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 |
---|---|---|---|---|---|
ENSDART00000016604 | Essential Splice Site | 1142 | 1553 | 23 | 31 |
ENSDART00000114538 | Essential Splice Site | 1152 | 1564 | 25 | 34 |
Genomic Location (Zv9):
Chromosome 13 (position 577918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 575901 |
GRCz11 | 13 | 706192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTMACTGCGGTTGTTGTACCGATGGCTGTTGTCTACTACTTTGTGCAG[G/T]TAACACAGATACCAGTAYTRACGAAAACTGTNNNTATATCAGTGGTGGACAGT
Long Flanking Sequence:
GTGCTCTAGGCTAGTTTATAACAACAGATGGTGCTCTAGGCTAGTTTATAACAACAGATGGTGCTCTAGGCTAGTTTATAACAACAGATGGTGCTCTAGGCTAGTTTATAACAACAGATGGTGCTCTAGTCTAGTTTATAACAGCAGATGGCGCTCTAGGCTGGTTTATAACAGCAGATGGCGCTCTAGGCTAGTTTATAACAGCAGATGGCGCTCTAGGCTAGTTTATAACAGCAGATGGCTTAGAATAGCTTTTAACAACAAACATTGCTCTAGGATAGTTTATAACTAGTTTATAAGTAAATATTTAAAACTTCCTAAACTGAAATGTGTCTTGAATGCAGGATATATTCACTGTGGACGAGATGATCCCGATGTCCTTCAGGTCCTGGATCCTCTGTCTTCTTGGAGTTCTGGGAACTCTTTTCGTCATCTGTCTGGCTACTCCAATCTTCACTGCGGTTGTTGTACCGATGGCTGTTGTCTACTACTTTGTGCAG[G/T]TAACACAGATACCAGTATTGACGAAAACTGTTATATCAGTGGTGGACAGTGAATATATATTTCATTAAAACAAGCTAAATAGTTTGCTAATGGAGTCAGAAATGTAGTATTATTTCAAAGTGAAAACTAGATTATTTTGCTTAGCCCGTTGTCAGTTTATTCTGCTTGTTTTAAGGGAAAACTAATTTTGCCTCATTATTTCTAAACACAAGATTATACATTTAACCTGTCCAGAACATGCTTCTTGGTTTAAGATTTTTTTAGATATTTAGACTAGAAACATGATAAAACCTCAATGAGAAATGGTTTGAAATCAAATAAATTCTTCTTGTGTTGTAGAGGTTTTACGTGGCCACGTCTCGGCAGCTCAGACGACTGGACTCGGTGTCTCGATCTCCCATATACTCACACTTTGGAGAAACCGTATCCGGCCTGTCCGTGATAAGGGCGTATGGACACCAGGACCGCTTCCTAAAGCACAACGAGCACACCATCGACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2688
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 |
---|---|---|---|---|---|
ENSDART00000016604 | Essential Splice Site | 1251 | 1553 | 25 | 31 |
ENSDART00000114538 | Essential Splice Site | 1261 | 1564 | 27 | 34 |
Genomic Location (Zv9):
Chromosome 13 (position 578886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 576869 |
GRCz11 | 13 | 707160 |
KASP Assay ID:
554-2727.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCTCTGAACAGCGGACTGGTCGGACTGTCCATCTCATACGCTTTAAAT[G/A]TAAATGCTTAAATCTGATGTATTTATGACAGTCAGCTGAAAGATCTTCCT
Long Flanking Sequence:
CTTCCTAAAGCACAACGAGCACACCATCGACCAGAACCTGAAGAGTGTTTATCCATGGATTGTTTCCAATAGGTCAGAATTAGTACTGCAATCATTAAAGATAACCTATTATGCAAAAACCCACTGTTATAAGGGGTATAAGTGTGTGAATATCTCCAGCCTCTAATGCTCATTATTTCCTTTTTAAAATTGTATTTATCTCCAGTTTTAGAGTATCCTCTAATCTTCCCTCAGCATGTTTGACGGTCCGCTGTAAAAGTGCATTTCCCTCTGTTGTAGAGTTTGCAGTGTGGCTGTGCACTTGAATTTTTCACTTTCACTTTGCTTTTCTCTGTCAGAATAGCTGAATCTGGAGTGTGTTTGTTGTTTGCAGGTGGTTGGCCATGCGTTTGGAGTCTCTGGGGAATCTGGTGGTGTTTTTCGCAGCTCTGTTTGCTGTCATCTCCCGAGACTCTCTGAACAGCGGACTGGTCGGACTGTCCATCTCATACGCTTTAAAT[G/A]TAAATGCTTAAATCTGATGTATTTATGACAGTCAGCTGAAAGATCTTCCTATTAAGTAGCATATCTGTGTCTTTATTAGGTGACGCAGACGCTGAACTGGCTGGTGAGAATGACGTCTGAACTGGAGACCAACATCGTAGCTGTGGAAAGAGTGAGAGAGTATGCCGAGATCCAAAATGAGGTGCAGTTTTACATTCATTCATTTTCCTTCAGCATATTCTCTTATTCATCAGGGATCACCACAGTGAAATGAACCGCCAACTATTCCAGCATATGTTTTATGCAGCGGATGACCTTCCAGCTGCAATACAGTGCTGGGAAACACCCAAACACACTCATTCACACCCACACTCATACACTACAGCCAGTGTAGTTGATCAGTTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCCAACATGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCCGGGA
Associated Phenotype:
Not determined