ZMP
CA12
Ensembl ID:
Description:
carbonic anhydrase XII [Source:HGNC Symbol;Acc:1371]
Human Orthologue:
CA12
Human Description:
carbonic anhydrase XII [Source:HGNC Symbol;Acc:1371]
Mouse Orthologue:
Car12
Mouse Description:
carbonic anyhydrase 12 Gene [Source:MGI Symbol;Acc:MGI:1923709]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9058 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa5708 | Nonsense | F2 line generated | Not yet available |
| sa9295 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10344 | Nonsense | Available for shipment | Available now |
| sa44316 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9058
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 |
|---|---|---|---|---|---|
| ENSDART00000103577 | Nonsense | 53 | 323 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 27665511)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 26355605 |
| GRCz11 | 25 | 26798807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTYAGGACTTGATGGAGAACACGACTGGCCCACCAACTATCCGTTTTGT[G/T]GAGGAGCATTCCAGTCCCCAATCGATTTCCAGACACATTTGCKGAGATAW
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAAACATGTAATCCCTTAGCAACAACAAACCACTTTTACTGCTACTGTTTCTGCAACTGAAACAATGACAATTTCATTTAAAGAGGCTAATTATTGTCATTTGTAAGTTTGTCATTTTATTTATTTTTAAAAAATCTGCTTAGGCAAGTTTAAACTCTGTTGGAAATAAAACCTTCCCTAAAGTAACAAAAATGATCTTTTATTGCTGCGTGTGGTATTCATACAAGAGCATTTATTTTGTAAGGGAGTGCTGTGTGACTGCTGACTTTAGTCTCTGTCTTTGACCAATTTTAATGCTGTTTAATTTAATGCCAACAAATGTTTAATTTAGTGCATCAGTCAGAGAATGATGCTTTCCCTGACTTTTTGTTTCAGGACTTGATGGAGAACACGACTGGCCCACCAACTATCCGTTTTGT[G/T]GAGGAGCATTCCAGTCCCCAATCGATTTCCAGACACATTTGCTGAGATATGATCCAAACTTGCCACCCATCCAGGTCCAGAACTATAACCTGTCAACCAGTGAGCAGCTCACTCTTGGCAACAATGGGCACTCTGGTGAGTACATTATACACTCTCAAAAATAAAGATACAAAATTTGTCACTGGGGCAGTTCTTTTTGAAAAGGTACCACCTCAGTGACAGATTTTGTACCTTTATTTCTGAGTGTGTAGAGCATACCGTTTTTTTTTTTTTTTGTTTCTTTTTTTTTTTTTTAAACACATCTTTTAAAACTTCAACATTTAAAGAAGTTACATTTTATATGGCTAAGTAGACTGTTCATTCCCTATAACAGATGAAAGGATTTGTGGTTGTTAGACTAATGAGACTGTGTGTTACATATAAAAGAAAAATAGACTTTCTTCTTAAGCTTAATTTCTGGTTCACCATGAAGAAAATGACAGAAGGATCTATTTTGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5708
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103577 | Nonsense | 69 | 323 | 3 | 9 |
| ENSDART00000103577 | Nonsense | 69 | 323 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 27665561)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 26355655 |
| GRCz11 | 25 | 26798857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGGAGCATTCCAGTCCCCAATCGATTTCCAGACACATTTGCTGAGATA[T/A]GATCCAAACTTGCCACCCATCCAGGTCCAGAACTATAACCTGTCAACCAG
Long Flanking Sequence:
ATATATATATATATATATATATATATATATAAAAACATGTAATCCCTTAGCAACAACAAACCACTTTTACTGCTACTGTTTCTGCAACTGAAACAATGACAATTTCATTTAAAGAGGCTAATTATTGTCATTTGTAAGTTTGTCATTTTATTTATTTTTAAAAAATCTGCTTAGGCAAGTTTAAACTCTGTTGGAAATAAAACCTTCCCTAAAGTAACAAAAATGATCTTTTATTGCTGCGTGTGGTATTCATACAAGAGCATTTATTTTGTAAGGGAGTGCTGTGTGACTGCTGACTTTAGTCTCTGTCTTTGACCAATTTTAATGCTGTTTAATTTAATGCCAACAAATGTTTAATTTAGTGCATCAGTCAGAGAATGATGCTTTCCCTGACTTTTTGTTTCAGGACTTGATGGAGAACACGACTGGCCCACCAACTATCCGTTTTGTGGAGGAGCATTCCAGTCCCCAATCGATTTCCAGACACATTTGCTGAGATA[T/A]GATCCAAACTTGCCACCCATCCAGGTCCAGAACTATAACCTGTCAACCAGTGAGCAGCTCACTCTTGGCAACAATGGGCACTCTGGTGAGTACATTATACACTCTCAAAAATAAAGATACAAAATTTGTCACTGGGGCAGTTCTTTTTGAAAAGGTACCACCTCAGTGACAGATTTTGTACCTTTATTTCTGAGTGTGTAGAGCATACCGTTTTTTTTTTTTTTTGTTTCTTTTTTTTTTTTTTAAACACATCTTTTAAAACTTCAACATTTAAAGAAGTTACATTTTATATGGCTAAGTAGACTGTTCATTCCCTATAACAGATGAAAGGATTTGTGGTTGTTAGACTAATGAGACTGTGTGTTACATATAAAAGAAAAATAGACTTTCTTCTTAAGCTTAATTTCTGGTTCACCATGAAGAAAATGACAGAAGGATCTATTTTGCATGTCCGCCATAGCAATTTTCTATAAGTACCTGCTTATTACAATAGATCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9295
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 |
|---|---|---|---|---|---|
| ENSDART00000103577 | Nonsense | 81 | 323 | 3 | 9 |
| ENSDART00000103577 | Nonsense | 81 | 323 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 27665597)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 26355691 |
| GRCz11 | 25 | 26798893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTGCKGAGATAWGATCCAAACTTRCCACCCATCCAGGTCCAGAACTA[T/A]AACCTGTCAACCAGTGAGCAGCTCACTCTTGGCAACAATGGGCACTCTGG
Long Flanking Sequence:
ATGTAATCCCTTAGCAACAACAAACCACTTTTACTGCTACTGTTTCTGCAACTGAAACAATGACAATTTCATTTAAAGAGGCTAATTATTGTCATTTGTAAGTTTGTCATTTTATTTATTTTTAAAAAATCTGCTTAGGCAAGTTTAAACTCTGTTGGAAATAAAACCTTCCCTAAAGTAACAAAAATGATCTTTTATTGCTGCGTGTGGTATTCATACAAGAGCATTTATTTTGTAAGGGAGTGCTGTGTGACTGCTGACTTTAGTCTCTGTCTTTGACCAATTTTAATGCTGTTTAATTTAATGCCAACAAATGTTTAATTTAGTGCATCAGTCAGAGAATGATGCTTTCCCTGACTTTTTGTTTCAGGACTTGATGGAGAACACGACTGGCCCACCAACTATCCGTTTTGTGGAGGAGCATTCCAGTCCCCAATCGATTTCCAGACACATTTGCTGAGATATGATCCAAACTTGCCACCCATCCAGGTCCAGAACTA[T/A]AACCTGTCAACCAGTGAGCAGCTCACTCTTGGCAACAATGGGCACTCTGGTGAGTACATTATACACTCTCAAAAATAAAGATACAAAATTTGTCACTGGGGCAGTTCTTTTTGAAAAGGTACCACCTCAGTGACAGATTTTGTACCTTTATTTCTGAGTGTGTAGAGCATACCGTTTTTTTTTTTTTTTGTTTCTTTTTTTTTTTTTTAAACACATCTTTTAAAACTTCAACATTTAAAGAAGTTACATTTTATATGGCTAAGTAGACTGTTCATTCCCTATAACAGATGAAAGGATTTGTGGTTGTTAGACTAATGAGACTGTGTGTTACATATAAAAGAAAAATAGACTTTCTTCTTAAGCTTAATTTCTGGTTCACCATGAAGAAAATGACAGAAGGATCTATTTTGCATGTCCGCCATAGCAATTTTCTATAAGTACCTGCTTATTACAATAGATCAAACCTGTTTGTATTTTAGTCTGGAAAATGCAACAAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10344
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103577 | Nonsense | 81 | 323 | 3 | 9 |
| ENSDART00000103577 | Nonsense | 81 | 323 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 27665597)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 26355691 |
| GRCz11 | 25 | 26798893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTGCKGAGATAWGATCCAAACTTRCCACCCATCCAGGTCCAGAACTA[T/A]AACCTGTCAACCAGTGAGCAGCTCACTCTTGGCAACAATGGGCACTCTGG
Long Flanking Sequence:
ATGTAATCCCTTAGCAACAACAAACCACTTTTACTGCTACTGTTTCTGCAACTGAAACAATGACAATTTCATTTAAAGAGGCTAATTATTGTCATTTGTAAGTTTGTCATTTTATTTATTTTTAAAAAATCTGCTTAGGCAAGTTTAAACTCTGTTGGAAATAAAACCTTCCCTAAAGTAACAAAAATGATCTTTTATTGCTGCGTGTGGTATTCATACAAGAGCATTTATTTTGTAAGGGAGTGCTGTGTGACTGCTGACTTTAGTCTCTGTCTTTGACCAATTTTAATGCTGTTTAATTTAATGCCAACAAATGTTTAATTTAGTGCATCAGTCAGAGAATGATGCTTTCCCTGACTTTTTGTTTCAGGACTTGATGGAGAACACGACTGGCCCACCAACTATCCGTTTTGTGGAGGAGCATTCCAGTCCCCAATCGATTTCCAGACACATTTGCTGAGATATGATCCAAACTTGCCACCCATCCAGGTCCAGAACTA[T/A]AACCTGTCAACCAGTGAGCAGCTCACTCTTGGCAACAATGGGCACTCTGGTGAGTACATTATACACTCTCAAAAATAAAGATACAAAATTTGTCACTGGGGCAGTTCTTTTTGAAAAGGTACCACCTCAGTGACAGATTTTGTACCTTTATTTCTGAGTGTGTAGAGCATACCGTTTTTTTTTTTTTTTGTTTCTTTTTTTTTTTTTTAAACACATCTTTTAAAACTTCAACATTTAAAGAAGTTACATTTTATATGGCTAAGTAGACTGTTCATTCCCTATAACAGATGAAAGGATTTGTGGTTGTTAGACTAATGAGACTGTGTGTTACATATAAAAGAAAAATAGACTTTCTTCTTAAGCTTAATTTCTGGTTCACCATGAAGAAAATGACAGAAGGATCTATTTTGCATGTCCGCCATAGCAATTTTCTATAAGTACCTGCTTATTACAATAGATCAAACCTGTTTGTATTTTAGTCTGGAAAATGCAACAAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44316
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103577 | Nonsense | 282 | 323 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 27671563)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 26361657 |
| GRCz11 | 25 | 26804859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCCAAGACTCTCCTTCCATGCCACTTCATGAAAATTACCGGAAGTCA[C/T]AACTCCCTGATAACAGAGTGGTACTAGTTTCCTTCAGAGAAGGTAAGAGA
Long Flanking Sequence:
TTCTACTGCTGATGCTACTCATGGACTGATTACACACACATATATGCGACTCATTTTGAAACTCTCATCAGTCTTGTTATTCTAAACTGTGAACATTGCGATGCGGTTTCCTTGCCTTCTGTATTTGAACCTTGCTTTGTTTCGTTTATTCTTGTCTGCTGCATGCCTTTGACCATCTGGCTGTTTATTGACCACGACTCTGGATTGCCCGTAAATCTGTTTGCTCCTGTGTTGACTGTTGCTTGCTTGACCATCCTGCTAATAAATCCTGTGTTTGGATCGGCACCCCTGTTGTCAGCGTCACTTCACGTTACACAGCTGCTAAAAGCTAACTAGCCAAATCTTGTCCTTTTAGGTAATAGTAGGTAATAGTTTTGCTGTTTTTAATAATGTTTACTGTTGTACTATTTTTACAGTTTTTGGCATTGGCCACAGCTCTATATGCCTCCTTTGCCCAAGACTCTCCTTCCATGCCACTTCATGAAAATTACCGGAAGTCA[C/T]AACTCCCTGATAACAGAGTGGTACTAGTTTCCTTCAGAGAAGGTAAGAGAATTTATATTGTAATATGTATACAGTTTAGCAGGCCATAACTTTAGCAGTAGATTGCTTTCTCTCTTATTCTCTTTTAACGTCTGCACAAGGATTCAGTTTATGCACTGTTACCTTTATTCCTAAATGAAAAACTACTACTGCAGGCTCCTTTAAAAGGAAAAAAACAATGGCTGTTTTTATAAGCTGCTTCAACTGACATAAATCTTTACCTTTAAACCTGTTTTAGAGTTGCTGCACCACAACATTTGTTTATCAGGTATTTTGTTGCTGTGAGAGAAGCCTGAGTTTGCTGTCTTCACCAGAGGCTTATGATCTGCTTCAGTCTTGCTGTTTCTAACATTCTTGCATGAAGGCTCATTTCATGAAAAACCAAGTCTACCACTTACAGCATGATTTACTGCATGGCAACATTTTCTATGAAGCTGAATGATGGAGAAGAATGGTTGGTC
Associated Phenotype:
Not determined