ZMP
CAMTA1
Ensembl ID:
Description:
calmodulin binding transcription activator 1 [Source:HGNC Symbol;Acc:18806]
Human Orthologue:
CAMTA1
Human Description:
calmodulin binding transcription activator 1 [Source:HGNC Symbol;Acc:18806]
Mouse Orthologue:
Camta1
Mouse Description:
calmodulin binding transcription activator 1 Gene [Source:MGI Symbol;Acc:MGI:2140230]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12769 | Nonsense | Available for shipment | Available now |
sa16711 | Nonsense | Available for shipment | Available now |
sa13525 | Nonsense | Available for shipment | Available now |
sa21967 | Nonsense | Available for shipment | Available now |
sa21968 | Essential Splice Site | Available for shipment | Available now |
sa24895 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12769
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 |
---|---|---|---|---|---|
ENSDART00000046663 | Nonsense | 173 | 1626 | 4 | 19 |
Genomic Location (Zv9):
Chromosome 11 (position 41353171)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 39613261 |
GRCz11 | 11 | 39877406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATRTKTCAGAAGGAAAGACGGAGCACAGCCACAGCGGYGGAAAGAACGGC[C/T]GAGCAGGAGGAGATGGAGCCGCTGGAGCAGGAGGCAGAGAGAAAAGAAAC
Long Flanking Sequence:
ATCACTTGTTCTTATCTGTACTATTTTTCCTGTCATTTATATATGCTGGTTTCTATTTTATGTGATTTATTTATGCATATATGACAGCATGCTATTGTAGTATTGAAACATTTATTTCTATTTATTATGTTTGTTTGTTTATCTTTTATTATAAGCAACTCCATGTACAATAAACATGAGCGTTTGAAACTGATAAACAGAGAAAATGTATAAAAAATCTTCTCATGTGCATTAAAAATTTAACAAACACATGCATTATTTATTTTAAGTGTCAATCTGTTTTGATAGCATTAGTATTAAAACATTAAAGCATCTGTCTGTCCTCTGTAGGTGCTGGAAGCAGCCTGCATCACAAATGCAACAGTGCCAAACACCGTATCATCTCCCCAAAAGTGGACCCACGTGCCGGAGGCGCCTACAGCAGCACCCACTCCGAAGTCCAAAACAACGATGTGTCAGAAGGAAAGACGGAGCACAGCCACAGCGGCGGAAAGAACGGC[C/T]GAGCAGGAGGAGATGGAGCCGCTGGAGCAGGAGGCAGAGAGAAAAGAAACGGCAAAGTGCACAAACCAGCCCTACTCCACCAGAACAGCATGGAGGTGTCCTCGACCAATCAGGTGGAAGTGCCGGACACCACCCAGAGCTCACCCGTCTCCATCAGCAGCGGTTTAAACTCTGACCCGGATATGGCAGACAGTCCTGTGGTGACCGGAATGGGCCATGTAGCTTCAGTAATGAGTAGTCTATCTCAATCCGCAACTGTATTCATGTCCGAGGTCTCTGGAGATCCTGTCTATAGCATGTCGCCCACTGTAGACCCCAACGCTCACCTATTGGGTCCCGACCCAGCCTCCAGCAGCCTGGTGTTAGCAGTGACAGCCGAAAGCCACAAGTTTGCCTTTGCTAATGCGGTAGGGTTAGCGGATCCAGCGTCCGCTGATGGACTGGGTATGTTGACAACAGCCGGTGTGTCCGAAGAACTGGTGCTGTCTAGTAACCTGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16711
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 |
---|---|---|---|---|---|
ENSDART00000046663 | Nonsense | 683 | 1626 | 4 | 19 |
Genomic Location (Zv9):
Chromosome 11 (position 41354701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 39614791 |
GRCz11 | 11 | 39878936 |
KASP Assay ID:
2260-4626.1 (used for ordering genotyping assays)
KASP Sequence:
GAAACCTGTGCAATGACACCGATAATAACACCTCTRATAGTTCCCATCAA[C/T]AGCTCCTGCAGGGAGCCGGGTTGGTACCTKGACTTTTTAGCGCYGTAGGC
Long Flanking Sequence:
ACCAGAACAACTCCGTCTCCACCCAGAACTCTCACGACTCCAATGCCTACATGGGATTGTCAGTAGTCAAAACGGACTCGTCGGGAACCAACGGGGATTTCCACCACCATCACCATACCCTCACAAACCAGCACACTGCCTCCAACTGCAACGGTGGATCTCCAACTGAACGCAACAACGGACAGGCAGGTTCACTTCAGATTCTGCAGTACCAAAACCGCTTTGCGAGTACAGGTCAGGAGCATGAGGAGATGAGCGGTTTGGAGCAGTCGACGGGAGCAGAACAAGAAGGAGGAGGCATTCAGGAGAAAGATTCGGATGGTAGGATGAAGCAAGGCGATCACTTGCAGACTGGTGAAGCTGAGGGTGTAGGAGGCGCTGAGCACTACCTCCAGCAGCCGACGGAGACTGGGGGAGTAGGATCTGGAGGAACGAGCGCAAGGGAAACTGGAAACCTGTGCAATGACACCGATAATAACACCTCTAATAGTTCCCATCAA[C/T]AGCTCCTGCAGGGAGCCGGGTTGGTACCTGGACTTTTTAGCGCCGTAGGCGCACATCAAACCCTGACCAGCACTGGCACCAACGGAGGAGGCTCTATGGAGATCAACTTAGACCATTTTGATGTTTCATTCGGGAATCAGTTCTCAGACCTCATCAATGACTTCATTTCAGTGGAGGGGGGAAGTGGTACAGGGGTAGTCCCAGGTAGCAATGCTCTCTACAGCCATCAGCTGATCACCCATTCGGGAACAGAGGGGCAGGTCTCCTCTGGTACTGCAGCTCAGCAGGGTGGAGATGAAGGAGCTCATGGGGCGAGAGGGTATAATTCGGCAGAGCTTTGCCTACAGCCCTGCTGCAGCCCGCAGTCCTCACAGTCCGGAGCGGTGGCGGCCGAGGCGGGACAGCTGGCATACATGCAGGTTGCTGAGGCAGTGTCGGCTGCTGTGGCTCATGGGAACATGGGAATGTTACAGGCCACCGGGAGGCTATTTGTGGTGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13525
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046663 | Nonsense | 693 | 1626 | 4 | 19 |
Genomic Location (Zv9):
Chromosome 11 (position 41354731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 39614821 |
GRCz11 | 11 | 39878966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTRATAGTTCCCATCAAYAGCTCCTGCAGGGAGCCGGGTTGGTACCT[G/T]GACTTTTTAGCGCYGTAGGCGCACATCAAACCCTGACCAGCASTGGCACC
Long Flanking Sequence:
CTCACGACTCCAATGCCTACATGGGATTGTCAGTAGTCAAAACGGACTCGTCGGGAACCAACGGGGATTTCCACCACCATCACCATACCCTCACAAACCAGCACACTGCCTCCAACTGCAACGGTGGATCTCCAACTGAACGCAACAACGGACAGGCAGGTTCACTTCAGATTCTGCAGTACCAAAACCGCTTTGCGAGTACAGGTCAGGAGCATGAGGAGATGAGCGGTTTGGAGCAGTCGACGGGAGCAGAACAAGAAGGAGGAGGCATTCAGGAGAAAGATTCGGATGGTAGGATGAAGCAAGGCGATCACTTGCAGACTGGTGAAGCTGAGGGTGTAGGAGGCGCTGAGCACTACCTCCAGCAGCCGACGGAGACTGGGGGAGTAGGATCTGGAGGAACGAGCGCAAGGGAAACTGGAAACCTGTGCAATGACACCGATAATAACACCTCTAATAGTTCCCATCAACAGCTCCTGCAGGGAGCCGGGTTGGTACCT[G/T]GACTTTTTAGCGCCGTAGGCGCACATCAAACCCTGACCAGCACTGGCACCAACGGAGGAGGCTCTATGGAGATCAACTTAGACCATTTTGATGTTTCATTCGGGAATCAGTTCTCAGACCTCATCAATGACTTCATTTCAGTGGAGGGGGGAAGTGGTACAGGGGTAGTCCCAGGTAGCAATGCTCTCTACAGCCATCAGCTGATCACCCATTCGGGAACAGAGGGGCAGGTCTCCTCTGGTACTGCAGCTCAGCAGGGTGGAGATGAAGGAGCTCATGGGGCGAGAGGGTATAATTCGGCAGAGCTTTGCCTACAGCCCTGCTGCAGCCCGCAGTCCTCACAGTCCGGAGCGGTGGCGGCCGAGGCGGGACAGCTGGCATACATGCAGGTTGCTGAGGCAGTGTCGGCTGCTGTGGCTCATGGGAACATGGGAATGTTACAGGCCACCGGGAGGCTATTTGTGGTGACGGACTATTCTCCAGAGTGGTCTTATCCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21967
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 |
---|---|---|---|---|---|
ENSDART00000046663 | Nonsense | 1422 | 1626 | 13 | 19 |
Genomic Location (Zv9):
Chromosome 11 (position 41384054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 39643735 |
GRCz11 | 11 | 39907880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGCCTCTAACTTCCTCTCCTGGCCTGGGAACGGTCCACGGTGGAGCA[C/T]AGCCAGAACTTGACGGCCCTCTTGGGAAACTTGGCATTCAGTCCCCTGCT
Long Flanking Sequence:
AGCTGTGCTATAGGATTGAAATAAAGTCTGACAGATCTTGAACACTTGCATTGACTTCTGTCTGGTATCTCGATTGCATTATTGTTAGAAATCTTTTATACCATGTACTGTAAGCCGCTTTTTGGAATTACTTAACATCTCAAGTTTCTAGTGCAGGTTTGAAAGTTCCCAACTCTTTGTTTCAGAATATGAACATGATGACTTTGGCTGAGGAAGTTATCGAGGCGACATCCGATCGCATCAAGAGGGAAAACTTTGTTGCGTCAGACACTTCTCTAGACGGTGTTGGAGTCAGCAGTACCATGAGTTGGTTGGCCAGTTACCTTGGAGATGCAGAGAGGTGATTCATCATAAATGCAATCTCATAAATCTGTGCTCCACAAATATAGTTGCAAACTCTTTTGGTCCTTGTTTGTAATTTTCCCTCAATTGTTCCCAGGTTCCTGTTTAACAAGCCTCTAACTTCCTCTCCTGGCCTGGGAACGGTCCACGGTGGAGCA[C/T]AGCCAGAACTTGACGGCCCTCTTGGGAAACTTGGCATTCAGTCCCCTGCTGAATGGACTGCGCTCCTTAATGCCTCCCACAACAAGGAGGAGCGTGACTTGACCCAGCTGGCCCTGTCGGATCCTGAACAGAGGGAACTTTATGAGGCAGCTCGCCAGGTCCAGAACACTTTCCGCAAGTACAAGGTAGGGCAGGGCTTCACCCAGGTGCCAGAGTCACCCATGCTGGTTATTGGTGGTGTGTTGCCAGTGTTTGTGATGGTCCAGTTTCAAAGGTCTAGATGTACTGTGTTGTGTTGTATGGTGTTCCTGAAGTTAAGGTAAATGATTCATCCGGATCTTTGCAGTCCTGTGTCGTGAAAGGTGATATGATTGTTGTGGTGTGCGCTCTAAAGGCAGAGATAGGGTCAGTGTTGTTGACAAGCATGGGGATATTTGCTTGAGCTTAGCATGGCCTTGCTGTAAGGAATGATTGCATTGTTCCCTCTATCTGTCTGTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21968
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 |
---|---|---|---|---|---|
ENSDART00000046663 | Essential Splice Site | 1484 | 1626 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 11 (position 41384831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 39644512 |
GRCz11 | 11 | 39908657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCCTGTCCTCTCCACCCTACCTTATCCCCCTCTTCCCCCGTCCTGCA[G/A]GGTCGGCCACTTCGGGAGCAGCAGGAACTGGCAGCTGCTGTCATTCAGCG
Long Flanking Sequence:
CTAGATGTACTGTGTTGTGTTGTATGGTGTTCCTGAAGTTAAGGTAAATGATTCATCCGGATCTTTGCAGTCCTGTGTCGTGAAAGGTGATATGATTGTTGTGGTGTGCGCTCTAAAGGCAGAGATAGGGTCAGTGTTGTTGACAAGCATGGGGATATTTGCTTGAGCTTAGCATGGCCTTGCTGTAAGGAATGATTGCATTGTTCCCTCTATCTGTCTGTCTAAATGGGATGCACAGATATCCCTGAGTCCACACCACATTTGGTTGTTCAGAGCAGATTTCTCCCTGTGTTCTGCTGGCGCGCCGTGCTCTGACAAATAACCTTCTCCCAGGTCTCAGAGCATATCGACGCAACTTTGCCAGTCTAAGAGGATACCTTGTCCAGGCACTAAAGGAATCAGATGCCATCATCGCTGTGGCCTATCAGGCCTCCCTGTGAACACTAATCTCTCTCCTGTCCTCTCCACCCTACCTTATCCCCCTCTTCCCCCGTCCTGCA[G/A]GGTCGGCCACTTCGGGAGCAGCAGGAACTGGCAGCTGCTGTCATTCAGCGCTGTTATAAGAGGTACAAACAGGTGAGTTCAGACACTCAGAAACATCTGCGTGTTGTACACTTCTGAGTGGTCAATTATTAAAGGCTTTACAAGAATGCACTCAATACTTCCCTCTCTCTATCCCTCAAGCTGACATGGATAGCCTTGAAGGTAACTCTTCCTGTTTCATCTATAACATCTTCTGCTTTGAATTGGAAGATTGTTATTTGCTTATTAATAATACTAAATATAAAACTTGTACGTGGACAAAAATGAATACTAGCTTAAACTGTACATCTTCGTAAGAACAGATTAGCTATTTAGCAGCCTCACATATGAACCAATAAAAAAGCAGAAAATAATCCCTAGACTTGCACAGGGATTCAAACTACATCTATAACAATATAGTTCACACAAATATGACAATTTACTCACCCTTAAGTAGTTCCAATGCTTTATGGGTTTCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24895
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 |
---|---|---|---|---|---|
ENSDART00000046663 | Nonsense | 1618 | 1626 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 11 (position 41398376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 39658057 |
GRCz11 | 11 | 39922202 |
KASP Assay ID:
554-7797.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTCAAGTTAATTATGTAAAACTCTTGTTTTTGCTCTGTTTTTAGGGC[G/T]AAAGAATTGAAAAAGGCCAAGGAACATGAGAACGCCGCAAAGAGCCCCGT
Long Flanking Sequence:
TTTAAGAATAAGAATAGCCCAAAACTAGACTAGTCATCAAATATACAGATTAGACAGACTTTGTAGTCATTCATTTCTGTTTATTTGATGACTTGTCTAGTTTTGGCCTATTCTTAGACGTCTATGAGATTTTCCCTGACAGCCCAAGTTTAGCCTTGTTTTAGCCAAGATGACTATGTTTAGACATTTATTAGACATCTATTAAAAACAGAAAATGCTAGCTGGGATCATCGCTTGAAGAATTATTAAACATTTAAACTAGAAACAAGAGAAAAACTCAAAGTAAGAAAAGCATTTGTTGTGTTTCTCAAGGTTTAAAAAGTCTTTGTGGTTTATAGTAAGGGCATATTTGTTGTTCCTTGCTGATTCCAGTGAGGAGAAAGAAATGAAAATAGCAGGTTTATTTGCTAATGATCTGTGATTCATGTGAGGGCCCTGAATGTTTGTGAAATCCTCAAGTTAATTATGTAAAACTCTTGTTTTTGCTCTGTTTTTAGGGC[G/T]AAAGAATTGAAAAAGGCCAAGGAACATGAGAACGCCGCAAAGAGCCCCGTCGCAATGTAACATCTCCGAGCAGACCCTTTCTCTTCCACTTCAACTGCGTTTTTACAAGAGACGAACACTTTAGAGGAGGAAAAAAAAGCAAAAATTCTTCAAGAAGCGGAGCGTGTCATCGGACGTGCGGCGGTTGAACTCTAGCAGCGTTGTGACTGATTCTGCATTGTGTATTTTCTCGCTACGGGGGAACTGAAATCAAGACTATTGGGGAAATATGACATTATCTTCATGGCATTTTTGCACTCTTCATAGATTTTTTTTCTTTAGATTATAAGAAAAAAAAGGAAAAAAAAAACGAACGAAGACCAAGGAGCAGAGGCTTTTTATTCTGACGACGCTTGTAAAATATCACGCGACATGAACAGATGGAAATCAGAAAAACGTCATGCTGGAAGCCGCTTCAGATTACATTTTTATATTTTGAAAGGAAAAACACAGCAATCAGT
Associated Phenotype:
Not determined