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 |
---|---|---|---|
sa2924 | Essential Splice Site | F2 line generated | Not yet available |
sa16798 | Nonsense | Available for shipment | Available now |
sa7441 | Missense | Mutation detected in F1 DNA | Not yet available |
sa23194 | Nonsense | Available for shipment | Available now |
sa45623 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17038 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2924
Status:
F2 line generated
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013418 | Essential Splice Site | 58 | 285 | 3 | 14 |
ENSDART00000123746 | Essential Splice Site | 58 | 1524 | 3 | 37 |
ENSDART00000130412 | Essential Splice Site | 58 | 1524 | 3 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 51643555)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51029669 |
GRCz11 | 17 | 51118567 |
KASP Assay ID:
554-3291.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTTCAGAWCATTGAAGAGGTTTACCAGAATGAGATCCTCAAATCAAAG[T/C]AAGACCAATCATGCTGGCTTCYTGTAAAAGTTCGYAGCTAGTGTATTTAT
Long Flanking Sequence:
AGAATTATTATAAGTAGAATATAATTATTTATAGAAACCAATAGACCTACACATAATATTAATACTGTTGTTTTACCATGTGTTTGAGAAAAAACAATAATCTCATATTAAGCTTTATTTTACATCTACAGAATCGTGAGAGAATCGTGATCTTTATTTTAAACAAATAAATCGCGATTCCCATTTTAGCCAGAATCGTGCAGCTGTAATATAAAACATTAAGCTAAACACTTGCAATTGATGTACTCTGTGTGTAAATTCAGCACAGACACCAAACACATCCTTGTCTTATATAAAGAGAAGCGTCTTTAATCTCATACAGTTTCTTTACTTAATGGTGCTTAATGATTGATTGATGTTGTTTATGTCCAAAAGTGCTTGTTTTATGGTAGTGAATGATCAACTTCTACGTAAAACCTGGATTTATAATGAATCTGGCAAACATTTTCTATTTTCAGATCATTGAAGAGGTTTACCAGAATGAGATCCTCAAATCAAAG[T/C]AAGACCAATCATGCTGGCTTCTTGTAAAAGTTCGTAGCTAGTGTATTTATTGTTTGTTGTGCTACTTTTGTTGTTATTGTTGTGTTAAGTCCACCTGTCTTGTGTTTGTGCTTTCAAAAAAGGTTGTTCACTGTTTGTTTAAAATGAGCTGAAACAACACAATTCTTTAGGGGTGTTTTTGTGAAAACTCAATTGTTTTATGTTCAATCAACATAAATGAATGTCAAATTTAATAAGTTAACTTAATTCCTTTATGCCGTCCCAACACAAATCAACTGTGTGAATCCCAGTGTACTCAGAATTGTGGAAGTTGTTAAATGCGCAGTTTCAAATGAACATTTTCGACCGATTTGTTTGACTTTGACTTTGCTTCTCTTCAGATTTTCCATCAGAAAAATTATGCTTCTGGAGTTTAGGTTAGTGATGTACACACACGTTTTGACATACATTTAGTGTGTGTGTGTGTTGTCTGTTGATGTTCTTGTTGTATATTTCGCAGT
Associated Phenotype:
Not determined
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:
sa7441
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:
C > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013418 | None | None | 285 | None | 14 |
ENSDART00000123746 | Missense | 624 | 1524 | 19 | 37 |
ENSDART00000130412 | Missense | 624 | 1524 | 19 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 51607530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50992419 |
GRCz11 | 17 | 51081317 |
KASP Assay ID:
554-4235.1 (used for ordering genotyping assays)
KASP Sequence:
CTTYCGTGAAGGTCCTGATCCAAAGCCCAAAYTGAGAGGTGACACCAGGA[C/T]GTACCGAGTGTGGCTGGACTCGAACCAATACCAGCAGGACATGACCAACA
Long Flanking Sequence:
GTTTTGTTAACTATATATGGTAATAAAACTCTCTCAACAAAAATATGTTGCTTTAACGATATATCGCAATAACACTATATCGTCATAGCAATATGTTTTGTTAACTATATATGGTAATAAAACTCTATCTCCACAAAAATATGTTGCTTTAACGATATATCGCAATAACACTATATCGTCATAACAATATGTTGCGTTAACTATATATGGCGATGTTGTCGCGATAACAATATATCCTAATTGGTATTTTACCCTGATTATTGATATTGTCCATTTAGTGAAGAGTTAAATTAGCTTAGAAAGAGGAATCATTCTTGTGATTCTCATTTGTAATTTTGTGGCACCATATTGATTACAGTAAGATGTTCTTGTATTTTGTGAGATTGAATGTTTGGCTTTCTATTCTTTCTGTTTGTTCTGTACAAACTTTTATTTTACCATTTTCTTATGCTTCCGTGAAGGTCCTGATCCAAAGCCCAAATTGAGAGGTGACACCAGGA[C/T]GTACCGAGTGTGGCTGGACTCGAACCAATACCAGCAGGACATGACCAACAGCATCCAGAGCGGAGCAGAAGATCCCTACGAGACCTTCAACGTCATCATGAGGCGCAAACCCAAAGAGAACAACTTCAAGGTCACTCCGACTTTACTGTGTCAAACTAGACGGTGTTTATAGTGCGACATAAAACTATACTATGAATAAAACTGTTAAAGGGTTATTTCACCCAAAAATAAAAATTCTGTTTTTTACTAAAAGACAAAAAAATATTTTGTAGAAATCTGGAAATGTGTAACCATTGACTTCCATAGTATTTGTTTTTCCAACAGTGGAGATCAATGTTTACAGGTTTCCCAGCTTTCTTCAATATATCTTCTATTGCCTTCAACAGAAGAAAGAAAGTCATAAAGGTTGAGTTAGATGGGTCATTTTTTGGATTAACTATCTTTTTACATGAAATACAAATTTGTATCGTCAACTAAAAAAACAGCTTGTTGTTGTTGTT
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:
sa45623
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013418 | None | None | 285 | None | 14 |
ENSDART00000123746 | Nonsense | 859 | 1524 | 24 | 37 |
ENSDART00000130412 | Nonsense | 858 | 1524 | 24 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 51600240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50985129 |
GRCz11 | 17 | 51074027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCATTGCTTCCTACATATCTGTTGTGTGTGTGTGTGTTGTTCAGGCTT[T/A]AAATCAGCTGTTTGAGAAGATTATGGCGCTAGACATCGATGAACGCCACC
Long Flanking Sequence:
GTTGCGCTGGCCTGAAAATAGCAACAAATTACGGCAAACACGTCTTGTGCCTTATTGCGGCAGGTGTATGATAGAGCCCTACATGTTTCCATTTATACTAGTGCTGGGCAAAGATGAATCACATTCAAAATGAAGTTTTGTATAGTCTTTCTGTTTTGTCGTGTGTAAAGAAAGGAAATACATCCTCTTTGTCTCTGTTTAATCTTTTGCTAATACGTCTTTACCCTCTTTCTTTTCTCCGCGCTGTAGGTTGTTGGTCCTCCTGGCACTGGAAAAACAGATGTGGCTGTTCAGATCATCTCCAACCTGTACCACAACTTCCCTGAGCAGAGAACACTCATCGTCACACACTCCAATCAGGTACACACACACTTACAGAATTACAGAAATCAGTCACACACACTGAGAAATCAGGACCAAACATCTGTCAAAAATTCGGTCACACATTACTTGCATTGCTTCCTACATATCTGTTGTGTGTGTGTGTGTTGTTCAGGCTT[T/A]AAATCAGCTGTTTGAGAAGATTATGGCGCTAGACATCGATGAACGCCACCTTTTGCGTCTGGGTCACGGTGAGGAAGAACTGGAGACGGAGAAAGATTTCAGCAGGTATAGCTGTTATACACACACACACACACACACACACAGACAATAGTGACACAGGCTGAATATGTTTTGTTGGGCTTTGGCCAACTAAAACTGAAGACGGAATATGACTTTTAACGGACTGTTTCATATGGATTTATTAATCATTCTTACTTTTCGATGAAAGCAAACTGTCGTAGATTATTAAAGACAAACCCCTCACTGCACGACAGCTGCACCTTTAGCAAACCTCCTAATTACTGCAGCACCAGGACTTTTATGATATTTTATGAGCGTCTAAAGTGGCTGATCTGGTCTTCGAAAAATTTGACTGCATCCCACTGTAACGCCGCCGGTCCTACGCCACCCAACCCGCTCCGAGCTGGTATCGAACCGGCGACCTTCCGCATGGGAGTCGG
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