ZMP
zgc:63611
Ensembl ID:
ZFIN IDs:
Description:
Zgc:63611 protein [Source:UniProtKB/TrEMBL;Acc:Q7SY15]
Human Orthologue:
AQR
Human Description:
aquarius homolog (mouse) [Source:HGNC Symbol;Acc:29513]
Mouse Orthologue:
Aqr
Mouse Description:
aquarius Gene [Source:MGI Symbol;Acc:MGI:1276102]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16798 | Nonsense | Available for shipment | Available now |
sa23194 | Nonsense | Available for shipment | Available now |
sa17038 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16798
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 |
---|---|---|---|---|---|
ENSDART00000013418 | Nonsense | 245 | 285 | 10 | 14 |
ENSDART00000123746 | None | 270 | 1524 | 11 | 37 |
ENSDART00000130412 | None | 270 | 1524 | 11 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 51629378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51015062 |
GRCz11 | 17 | 51103960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAACCATGTCCATCTTTGCAAAGGCTCTGCTCCCGACCCGCCGTTGGTT[C/T]AACACTGTGCTGGACGATGCTCATCTGATGGTCAAATGCCAGCTGTCTCA
Long Flanking Sequence:
AACAGGGTTGATGGTAACAGTAACAGGGTTGATTGTGACAGTAACAGGGTTGTCGATAACGGTTTTCAATAACAGCAACGGTTGATGGTAACAGTAACAGTTAACAGTAACAGGTTTATTGATAACAGAGTTGACAGTAACAGTTGTTGATAAAAGGGTTGTTGGTAACAGTAATAGTGTTGTCGGTAGTAGGGTTGATGAAAACAGAGTAACAGGGTTGTTGGGGACTGAGTTGACTAACAGGCTTGACATTTTCCACCATACTGTGAAATATAAAGTGAATGAGCCGGTGTGCTCAACATCAACTGCTGCGTGAAGCTTTTTAATCAATTTTGATATTTTTTGCAACATTAGTGTTGCTTTTTGCTTTAGCTTTTTTTTCTCTTTAAGCTCTTCTTCTGAGCACTCGTTCGAGACTGATGTGTGTGCTTTTGTGCAATTGTTATGTAATTAACCATGTCCATCTTTGCAAAGGCTCTGCTCCCGACCCGCCGTTGGTT[C/T]AACACTGTGCTGGACGATGCTCATCTGATGGTCAAATGCCAGCTGTCTCACCTCACCGGCAGAGAGAAAGAGGGTCACCTGTTCTGCCAGGTACAGCACTGAACCACTCCAGGAAAACAAAAACCTTGATTTTAGTCCTCAAATCACACATTTAATAAACACCACATCATGTATGTTTCGGAGTGAAGTCCAGCAATGTATTAAATATAAGTTTGATTTCCCTGTTTAAAAACATGAAGTAATCAATATTGCCTTAAATATTTAACTGTACTGTTGAATAAAATGATTCTGTTACATGTTGCATTGCAATTACTTGTATATATTTAATAATCACAATATGTACTGCAGTACTAATGGTCAAATTCAATTCATTATGCTAAGCTGAGCTAAAAGTGACCATGGCAAAACTAGAAATCGGCTGAATGGATTAAGTCAACCGTTTAACTCTCTGACACTTGTAAAATGAGAGTGTCGCTTTAAGGTTGTCCTTTAATATATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23194
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 |
---|---|---|---|---|---|
ENSDART00000013418 | None | None | 285 | None | 14 |
ENSDART00000123746 | Nonsense | 743 | 1524 | 20 | 37 |
ENSDART00000130412 | Nonsense | 743 | 1524 | 20 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 51606280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50991169 |
GRCz11 | 17 | 51080067 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTTTCCCAGAGCACACGGTCAAGGTGACGGAGGAGGATCCCGCTAGA[C/T]AGATGCCACCATTCAGGTTCATTCATGCTCCGTTTTCAACACAACATACC
Long Flanking Sequence:
AACGCAACAAATTATACACATTTATTTGACGTTAATAAATACTAAAATGATATTACTAATAGTGTTTTAAAAATAATTCTATCGAATATCATCATAGGTATTTCTGTGCAAGAAACGTTTCGTTGTATAGCGTGCGAGACGGATCAAGTGCACATATATTTGTGTTGTTTTTAAAAATCAAGCCATGTGGTATACATGTCCAACATTTAAAACAGGGCTGTGGTCATTTCAGTCATCAAAGATTAACTGTTTATTTATTTATTTTTATTTTGCAGGCTGTGCTGGAGACCATCCGTAACCTCATGAACACCGAGTGTGTGGTTCCCGACTGGCTTCACGACATCATCCTGGGTTATGGAGACCCTGGTAGTGCTCATTACTCAAAGATGCCCAATCAGATCTCCAGTCTGGACTTCAACGACACCTTCCTGTCCATCCAGCACCTCAGATCCTGTTTCCCAGAGCACACGGTCAAGGTGACGGAGGAGGATCCCGCTAGA[C/T]AGATGCCACCATTCAGGTTCATTCATGCTCCGTTTTCAACACAACATACCACTTCCTAGACCTTAAATTTTTTTTTTTTTTTTTTTTTACAATCTATTTAGTTATTCAGGTTTTTTAAAATCTAATGTTTAGGTATTTTAATACTTTTTCCATTTTAAGTTTTAGTAAAGTTTCAGTGCCTCCCACACATTAACTTTTACTTGGCGGGGTCGCCTAGGTATATTAACGGCTGCCCAAATATATGTTTGTGACATTTATTTTTTTACTATTTTCATCCTTTTAGACTTTTTATGTATCCGCCCAATATAACCAAACATCCGCCATCGATTAACCAGTAGAAAACTCTTCTCTCGCACTAAACGTTTCCTACTTCTTGTTGTGTACGCTTGAGAACTGTCAACACTCTCACAGACAATCTCACAAGCTCAGCAGAGACCCACAGAGATGCGCCTTTTTTGGGACTTAAATATGCATCCATTAGAGGTTTCTAAATCTCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17038
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013418 | None | None | 285 | None | 14 |
ENSDART00000123746 | Essential Splice Site | 1081 | 1524 | 28 | 37 |
ENSDART00000130412 | Essential Splice Site | 1078 | 1524 | 28 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 51578398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50963287 |
GRCz11 | 17 | 51052185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCMGCTCARATCCTGGAGATTGAGACCTTCATYCCTCTGCTGCTGCAGG[T/C]ACTGCTCTCGCTCGCTCCCAAATACACCCYGAGTTTTCTTGTAYTATTTA
Long Flanking Sequence:
TTAAGTTCTATTTGTTAAAACCAAAAGTGTCTTGCAGGACTGTTTTTGTAATAATTGGAAAGCAAATTACATTTGTCTCCTCCCCTTTTTGGCTGATCCGAAAAATGGTCCGATCTGTGACTAAAGCACCATAACGTGATCCGAACCGTGAGATTTCTGATCGTTACACCACTAGGAAATAATGTGGAAAAATTCCTGAATCCTTCCAATTTCATTTGTGAAAAATTTGACAAAGGAAAAAAAAATTCACAGAAGGGCGAATAATTTTGACTTTACCTGTATATCGAAGTGAAACTCACATTTATTGTGTTTAATTTAAAACTGGATTGTCTCTTAATGTATGAAATTGTTGCTGTGATTATTATGAAATATATTTTTATTTGTGTTGATCTGAATATCTATTTAACAAAAATTGATTTGTTTGTAGTATGATAATATCCTGATGGAGGAAGCAGCTCAAATCCTGGAGATTGAGACCTTCATCCCTCTGCTGCTGCAGG[T/C]ACTGCTCTCGCTCGCTCCCAAATACACCCCGAGTTTTCTTGTACTATTTATTATCATTAATCTTCTTTATTTAGTTTACTTATTTATAAACTGTTCTACATTTTCTGATCCTATGCATCTTGGTTTCATCTAGAGAATCATTGTAACCAATTCAATTTCAAATGTTCAAGGAACACTTGTTTTGGCTCATTTTACATCTTCCCTAGAGTTAAAATGTTGTTTTACCAGTTTCTGAATCCATTCAGCTGATCTTCAGTTCTGTCTGGAGCACTTTTAGCTTAGCTTAGCTTAGCATAGATCATTGAATCGGATTAGACCGCTAGCATCTCACTCAATTTTCAAAAAAAAAAAAGAGTTTGGGTCGTTTATCTATTTAAGGCTCGACTCTTCTGTAATTACTTGCTGTAGTAAGACCAACAAAAATGAAAAGTTCCTGTTTCTAGACCGATATGACTAGGAACTAAACTCACATTCTGGCATAATAAATAAGGAATTTTGCT
Associated Phenotype:
Not determined