Busch Lab

ZMP

ca15b

Ensembl ID:
ENSDARG00000040510
ZFIN ID:
ZDB-GENE-040426-2222
Description:
carbonic anhydrase XV b [Source:RefSeq peptide;Acc:NP_998347]
Human Orthologue:
CA4
Human Description:
carbonic anhydrase IV [Source:HGNC Symbol;Acc:1375]
Mouse Orthologue:
Car4
Mouse Description:
carbonic anhydrase 4 Gene [Source:MGI Symbol;Acc:MGI:1096574]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa17825 Nonsense Available for shipment Available now
sa22006 Essential Splice Site Available for shipment Available now
sa35195 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8484 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa27866 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17825
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008362 Nonsense 36 305 4 9
Genomic Location (Zv9):
Chromosome 12 (position 4980137)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4262764
GRCz11 12 4299422
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAAGTCACATGGCCCATCAYTGCAGAAAAACACTGTAACGGCACTCAA[C/T]ARTCTCCAATAAACATYGTAACYGCTAATGTCAAGGCTAATGCTAATTTG
Long Flanking Sequence:
TAAGGGGTTTATTATAACGCGAACAACATTTACAGTTATTTTAAATTTTCAATAGTGTTTTATGGAAATTCTAAGGGTTTTCTTTAAAATGATACCAAATGTTTGCATTTACACCTCTGCATGTGGATTTGGGAAGCTTTTAACTGTGGGTAGGCAAAATCCAGGCGGAAATCCCAAAATAACAGCAGAGTTTAACTGGTTAAAGTACAACATTGTTCACAGTCAAATAAATTGCGCTAATGTTGTTTTGAAGTCATGTTTACATGCCATTTCGGACCAAATATTTAAAGTAGAAAGGTAAATAATATAGACCGTTAAATGAACGAATGTGCAAATATAAAGCCAACTTTACCTCGATTATTTATGGCATCCAGGAATGCTGAGGTCTTGAAACTAGCAAATGTGTTTTGGTGCAAATAACTGTTTTAAAATGCTTTCTCTGCCTCTCAGGTGAAGTCACATGGCCCATCATTGCAGAAAAACACTGTAACGGCACTCAA[C/T]AATCTCCAATAAACATCGTAACCGCTAATGTCAAGGCTAATGCTAATTTGACCTCTTTCACATACGTTGGCTACAATGACAGCACTGCTTTAACTGTGATTAAAAACACTGGCACAAGTAGTAAGTAGATTTATTTTAGTTATTCAATTTTCCGCAAGGTTTTTAATGAATGTTTAACCAGTGTTTTAAGTTCAAGTTACGTTGGATCCGAAGAAGATGCGTGTGGCAGGGGGTAATCTGCCAGGCCGGTTTGCCAGCACTGAGTTTCATCTTCACTGGGGAAATGGCAGTGCCATGCCTGGGTCTGAACACACTGTGAATGGAAAACGATTCCCAATGGAGGTATGGTTAAACAGTCCCATAGAGTTCTGATGTATACACGCGTACAAATGAAACTAGTTCATGTTTGGGTTTTACATAGTCTATATAAAGTGATATTGGTAGTTTGTTTTTTGTTCATTTAGTAGTCTTGATGTTGGTTACCATGTTGCATTTGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22006
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008362 Essential Splice Site 76 305 5 9
Genomic Location (Zv9):
Chromosome 12 (position 4979947)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4262574
GRCz11 12 4299232
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTCAATTTTCCGCAAGGTTTTTAATGAATGTTTAACCAGTGTTTTAA[G/A]TTCAAGTTACGTTGGATCCGAAGAAGATGCGTGTGGCAGGGGGTAATCTG
Long Flanking Sequence:
TTTAACTGGTTAAAGTACAACATTGTTCACAGTCAAATAAATTGCGCTAATGTTGTTTTGAAGTCATGTTTACATGCCATTTCGGACCAAATATTTAAAGTAGAAAGGTAAATAATATAGACCGTTAAATGAACGAATGTGCAAATATAAAGCCAACTTTACCTCGATTATTTATGGCATCCAGGAATGCTGAGGTCTTGAAACTAGCAAATGTGTTTTGGTGCAAATAACTGTTTTAAAATGCTTTCTCTGCCTCTCAGGTGAAGTCACATGGCCCATCATTGCAGAAAAACACTGTAACGGCACTCAACAATCTCCAATAAACATCGTAACCGCTAATGTCAAGGCTAATGCTAATTTGACCTCTTTCACATACGTTGGCTACAATGACAGCACTGCTTTAACTGTGATTAAAAACACTGGCACAAGTAGTAAGTAGATTTATTTTAGTTATTCAATTTTCCGCAAGGTTTTTAATGAATGTTTAACCAGTGTTTTAA[G/A]TTCAAGTTACGTTGGATCCGAAGAAGATGCGTGTGGCAGGGGGTAATCTGCCAGGCCGGTTTGCCAGCACTGAGTTTCATCTTCACTGGGGAAATGGCAGTGCCATGCCTGGGTCTGAACACACTGTGAATGGAAAACGATTCCCAATGGAGGTATGGTTAAACAGTCCCATAGAGTTCTGATGTATACACGCGTACAAATGAAACTAGTTCATGTTTGGGTTTTACATAGTCTATATAAAGTGATATTGGTAGTTTGTTTTTTGTTCATTTAGTAGTCTTGATGTTGGTTACCATGTTGCATTTGAATATTCAATTGGAATTAGCATGCAAGTATGACTTCTAAACAACATTAATGTTGTACTTTAATAATCATTGGCTGCTCATGATTTCCCTATTTAGAGTTTTCAAAGAATCCTTTTCTGAAATTAAGGAGAATGTCTGAATATCCGAATATAAAACCAACCTTACCTCTATTATAAAATGTCACATGCAACATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35195
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008362 Essential Splice Site 149 305 6 9
Genomic Location (Zv9):
Chromosome 12 (position 4978940)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4261567
GRCz11 12 4298225
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGTAACACCAGTGATTCGTTGGCAGTTCTTGGTGTCTTCATTGAGG[T/C]ATACTGACTTTTACTCATATTTGAGATGCAACTTAAGAGGTGGATGATGG
Long Flanking Sequence:
TATCGCAAAAGTGGCTAGATACTGTAGATGCACTGTGAAACCCAGCAGCTAACTTTAAGTAAATTCAGTTAAGGACTCATTTTATTTGATAAAGTACTCGTTTGTAAAGAGTTTTGAACTGCCAGGCTAGTTTCCAGCCAGTTCCAGCCTGGTCTTAGTTGGTCAGGCTGGGAGATGACCAGCTAAAACCAACTTGACCAGCCTTGCCAGGCTGGGAGCCCAGCCAAAACCAGCTATGTCCAGCTTAAACTAGGCGTGGTCATTTAGCTGGTCATTTTCCAGCCTGACCAGGTTGAGGAAAAGGCTGGAAACCAGCCTGTAAGTGGCCAAAACCCCTCTAAAACCAGGTTGGTCAACCAGCTTAGGCTGGTTTAAGCTGTTTTTTCAGCAGGAACATCATGATTTAAGCAAAAGTGTTCTCTCGTTTCAGTTGCATATTGTGAACAAGCCTGTCAGTAACACCAGTGATTCGTTGGCAGTTCTTGGTGTCTTCATTGAGG[T/C]ATACTGACTTTTACTCATATTTGAGATGCAACTTAAGAGGTGGATGATGGAATTGTAATCTCACCCTCAGGCCTCTAATGAAACTGGGAAACCTGAGAGCTGGAAGACTTTAACGTCGTATCTTACAAGGATTGTCAAAGCAGGTGATGCATGGAAATGATTCATCTATGAGGATAGGAGTGCTGCGCGTCAGTGATGTTGATAGATCAATTGTTTCAGGTGATAAAGCAAGCCTTTTCAGAAACTTCTCCATGGATGATCTGCTTTCTGGAGTGGACAGGACAAAATACTACCGGTATTTGGGCTCCTTGACCACACCAAACTGCAATGAAGGTGTGATCTGGACCGTCTTCAAAGACCCAATTAGAGTCAGCAGGGATTTGGTGAGTAAAATGAGTGTTACTTTCCTCTAACCAATGTATTTTGTAAGAAGCCGTGGTCTTGAGTTTGAGCATACAAATTCTGTAGTACAATGCTGCCAGTTTTTTATTTATTTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8484
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008362 Essential Splice Site 150 305 7 9
Genomic Location (Zv9):
Chromosome 12 (position 4978871)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4261498
GRCz11 12 4298156
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTGAGRTGCAACTTRAGAGKTGGATGATKGAATTNGTAATCTCACCCTC[A/G]GGCCTCTAATGAAACTGGRAAACCTGAGAGCTGGAAGACTTTAACGTCGT
Long Flanking Sequence:
TAAGGACTCATTTTATTTGATAAAGTACTCGTTTGTAAAGAGTTTTGAACTGCCAGGCTAGTTTCCAGCCAGTTCCAGCCTGGTCTTAGTTGGTCAGGCTGGGAGATGACCAGCTAAAACCAACTTGACCAGCCTTGCCAGGCTGGGAGCCCAGCCAAAACCAGCTATGTCCAGCTTAAACTAGGCGTGGTCATTTAGCTGGTCATTTTCCAGCCTGACCAGGTTGAGGAAAAGGCTGGAAACCAGCCTGTAAGTGGCCAAAACCCCTCTAAAACCAGGTTGGTCAACCAGCTTAGGCTGGTTTAAGCTGTTTTTTCAGCAGGAACATCATGATTTAAGCAAAAGTGTTCTCTCGTTTCAGTTGCATATTGTGAACAAGCCTGTCAGTAACACCAGTGATTCGTTGGCAGTTCTTGGTGTCTTCATTGAGGTATACTGACTTTTACTCATATTTGAGATGCAACTTAAGAGGTGGATGATGGAATTGTAATCTCACCCTC[A/G]GGCCTCTAATGAAACTGGGAAACCTGAGAGCTGGAAGACTTTAACGTCGTATCTTACAAGGATTGTCAAAGCAGGTGATGCATGGAAATGATTCATCTATGAGGATAGGAGTGCTGCGCGTCAGTGATGTTGATAGATCAATTGTTTCAGGTGATAAAGCAAGCCTTTTCAGAAACTTCTCCATGGATGATCTGCTTTCTGGAGTGGACAGGACAAAATACTACCGGTATTTGGGCTCCTTGACCACACCAAACTGCAATGAAGGTGTGATCTGGACCGTCTTCAAAGACCCAATTAGAGTCAGCAGGGATTTGGTGAGTAAAATGAGTGTTACTTTCCTCTAACCAATGTATTTTGTAAGAAGCCGTGGTCTTGAGTTTGAGCATACAAATTCTGTAGTACAATGCTGCCAGTTTTTTATTTATTTTATTGAAATCAGATGATTTAGACATCGATAAAGCGAGCGGTTGCTCTTTTACATTTCTGTACAGAGAAAGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27866
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:
A > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000008362 Missense 159 305 7 9
Genomic Location (Zv9):
Chromosome 12 (position 4978842)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4261469
GRCz11 12 4298127
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAATTGTAATCTCACCCTCAGGCCTCTAATGAAACTGGGAAACCTGAG[A/C]GCTGGAAGACTTTAACGTCGTATCTTACAAGGATTGTCAAAGCAGGTGAT
Long Flanking Sequence:
CGTTTGTAAAGAGTTTTGAACTGCCAGGCTAGTTTCCAGCCAGTTCCAGCCTGGTCTTAGTTGGTCAGGCTGGGAGATGACCAGCTAAAACCAACTTGACCAGCCTTGCCAGGCTGGGAGCCCAGCCAAAACCAGCTATGTCCAGCTTAAACTAGGCGTGGTCATTTAGCTGGTCATTTTCCAGCCTGACCAGGTTGAGGAAAAGGCTGGAAACCAGCCTGTAAGTGGCCAAAACCCCTCTAAAACCAGGTTGGTCAACCAGCTTAGGCTGGTTTAAGCTGTTTTTTCAGCAGGAACATCATGATTTAAGCAAAAGTGTTCTCTCGTTTCAGTTGCATATTGTGAACAAGCCTGTCAGTAACACCAGTGATTCGTTGGCAGTTCTTGGTGTCTTCATTGAGGTATACTGACTTTTACTCATATTTGAGATGCAACTTAAGAGGTGGATGATGGAATTGTAATCTCACCCTCAGGCCTCTAATGAAACTGGGAAACCTGAG[A/C]GCTGGAAGACTTTAACGTCGTATCTTACAAGGATTGTCAAAGCAGGTGATGCATGGAAATGATTCATCTATGAGGATAGGAGTGCTGCGCGTCAGTGATGTTGATAGATCAATTGTTTCAGGTGATAAAGCAAGCCTTTTCAGAAACTTCTCCATGGATGATCTGCTTTCTGGAGTGGACAGGACAAAATACTACCGGTATTTGGGCTCCTTGACCACACCAAACTGCAATGAAGGTGTGATCTGGACCGTCTTCAAAGACCCAATTAGAGTCAGCAGGGATTTGGTGAGTAAAATGAGTGTTACTTTCCTCTAACCAATGTATTTTGTAAGAAGCCGTGGTCTTGAGTTTGAGCATACAAATTCTGTAGTACAATGCTGCCAGTTTTTTATTTATTTTATTGAAATCAGATGATTTAGACATCGATAAAGCGAGCGGTTGCTCTTTTACATTTCTGTACAGAGAAAGCACATTTTGTTCTTTTATTGGTGTCACGATCA
Associated Phenotype:
Not determined