ZMP
sec24c
Ensembl ID:
ZFIN IDs:
Description:
Sec24 family member C [Source:UniProtKB/TrEMBL;Acc:D5LHQ7]
Human Orthologue:
SEC24C
Human Description:
SEC24 family, member C (S. cerevisiae) [Source:HGNC Symbol;Acc:10705]
Mouse Orthologue:
Sec24c
Mouse Description:
Sec24 related gene family, member C (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1919746]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22150 | Nonsense | Available for shipment | Available now |
sa31889 | Nonsense | Available for shipment | Available now |
sa35346 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17715 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22150
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 |
---|---|---|---|---|---|
ENSDART00000085476 | Nonsense | 20 | 1241 | 1 | 22 |
ENSDART00000109159 | Nonsense | 20 | 1142 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 12 (position 35748533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35473212 |
GRCz11 | 12 | 35574275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAGCAACCTCACATGGCCTCTCCTTATGGGCAACCTCAGCCAGGGTA[T/A]CAGCGCTACCCTCAGCCTGGGTATCAGCGCTACCCTCAGCCAGGGTATCA
Long Flanking Sequence:
TAAATCACATTTCCTTTTTACTTTTTGCACTGGACAGTTTCTGCTAAAATGGGTTGTGGCACCAAAACAAATCATATCAATTCTTGTGCTTCAAATTCGTGTGAAATGCTCCTGTTATTTGTTTACTCATCAACTTCTCCATGTTGTTCGCTTTAAGAAACCTCAAAGCTTTTCCGCCTTGAAGTGCGAAATAGCTTTTCTGGCAAAATTTCTCATTTATGTCAACACTTGCTGCACTGGTCTGAGCTTAAATGATTAGTTGTGAGTTTTGCTGTGCCAGCAGTCCAGTGGCACATGGCTTTAGACCCCTGAAAGCACCAGGGGGGCTAACAAGACGTCTTAAGCACTTCTTATAGGCATACCTCATAAATATAGATTTACTTACTCACTTTCTCCTTATCCTTTTTCCCCTCTTTTCTTCAGATTAGGGATGAACTGAGAATGAATGTCAACCAGCAACCTCACATGGCCTCTCCTTATGGGCAACCTCAGCCAGGGTA[T/A]CAGCGCTACCCTCAGCCTGGGTATCAGCGCTACCCTCAGCCAGGGTATCAGCGCTACCCCCAGCCTGGATACGGGGGTGGCCATGTGCCATCGGCGTATCCAGCTCAGTATGCACCAGATAACGGCCCGGGCTCTGGCTACCAACAAGGTCCACCGCAAGGTAAGAGAGGTTGAAAGTACACAATGATTGTGACTTGTTCAGGAGACACGTTTATGATGGGTTATCATTAGGAATGCTCATTTCGGTTAATTTTGCTAACCGACAACCGCCGCTCGTAAATCGAATATTAACGGTTAACTGTTCAGATTAATATTAAATTATTATAAAATTATTGTATAAAAATTGACGTGTCTATTTTGTGTCTGACACATTATATATTGCATTTTAAAATTCTGATTTATTTTAACATGCAAACATATTAATAGTAGAACATAACAACAGAGCATCTTCATGCACCTGTAGTGTTTCCAACAGCATAGAAAAACAGAAAAAACTAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31889
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 |
---|---|---|---|---|---|
ENSDART00000085476 | Nonsense | 92 | 1241 | 2 | 22 |
ENSDART00000109159 | Nonsense | 92 | 1142 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 12 (position 35753286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35468453 |
GRCz11 | 12 | 35569516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAACCCCCCACCTCAGGGACACCACCTGTCTCAGGTGCCCAGAGCTA[T/A]TCGCAGTTTGGCCAAGGAGAGACTCAAAATGGACCACCTCCAATGGTAGC
Long Flanking Sequence:
AATTTGAGTGTTCCCTATGTAATGTCCGAACTAGTTTATTGCACACAAAATATTTAAAGGAAACCATTTAGAAAGATAAAATCTTAACATTTAGCCAAGAAGGTTTTTGTATGAGATAGGTAGTCAAAACGTAGTCTTGTGGAGAGTCGTCCAATGTGTTGCGTGGTTGAGCTCTAGGTGTTCTGGTTTGGGGAAATGTTCTTATTCTGACCACTGTCTTTCAAACTTTACTTTTTATCATGTGTGTATTCGTCCATCATAATAAAGGCAAACATGTCTAAACAAACTTTAAAAATCCCCTGCTATTCAATGTAGGTCCCACATATTTTACAGCTAGATTATTTACCTAAAATGTCTTTGTTTCTTAAAGATGATCATAAAAGTTGGAATTTAAAAAGTGTTTCTATAAGATGTATTTATTTGCTTATTGCCTGTTCCCATGAAGGCATGAGAGAACCCCCCACCTCAGGGACACCACCTGTCTCAGGTGCCCAGAGCTA[T/A]TCGCAGTTTGGCCAAGGAGAGACTCAAAATGGACCACCTCCAATGGTAGCTCCACCACAGGGGTCAGTGAAGTCATTTTGCTTTCACTCTCATATCTTATATGTTAATATACACTACTGTTCAAAACTTTGGGGTCCGTGGGATTTTTAAGTGTTTTAAAAATAAGCTTCTTCTGCTCACCAAGGCTGCATTTATTTAATCAAAATACAGTACAAATTGTACAGTTGTGAAATTTTATTGCACTATAAAATAACTGTTCAAAGTAGTTTAGAATTTAATTTAATCATATCTTCCAGCTATTTTAAAGATGAATTTTCAGCTTTATTACTTTAGAGTCACATGATCCTTTAGAAATCACTTGAGTATTATTTTTTTGTTGTTGTTGTTATTATTTTTATTATTAATGGTCATAGTAATAAAAACAATAATGACAGGATTAATAATTTCATTTGAAACTCAAATACAGTAATTTAACAATTTGTTTACATTTATTAAATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35346
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 |
---|---|---|---|---|---|
ENSDART00000085476 | Nonsense | 602 | 1241 | 8 | 22 |
ENSDART00000109159 | Nonsense | 503 | 1142 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 12 (position 35763784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35458073 |
GRCz11 | 12 | 35559136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGAAGGTGGCCGTCGTTTCCAGTGTGGCTTCTGCAGCTGTGTCACC[G/T]AGGGTTGGTTTTGCTGCCATAACAGGATTATCATTTTGGATTCATCAGAA
Long Flanking Sequence:
GAGGTCAAGCTCCACCTCTAGTAACCACCAGATTTCAAGTGAAAGATCAAGGTAAAAGCATAAATTTAGGCTTCATTTAAGAACAAAATGGTTTTATTCCATTATATTATGCTTTTTATCAATATGAATCTCTTTAAAGGGAATGCAAGTCCACGCTACATTCGTTGTACTGCCTACAACATGCCCTGCAATTCTGACATGGCCAAACAGTCCCAGGTTCCTTTGGCTGCTGTCATTAAACCCTTGGCCACGTTGCCTCCAGATGAGGTAAAAGGACACATTTGAAAGCTCAATATTGTGATTTGTCTTTAAAATGAATTCAGAAGTATTAACGAAAAGCCCATGTCATTCTTTTTGTCCCGCAGTCACCGCCATATCTCGTGGATCATGGAGAAAGTGGTCCCATTCGCTGTAATCGCTGTAAGGCCTACATGTGCCCATTCATGCAGTTTATTGAAGGTGGCCGTCGTTTCCAGTGTGGCTTCTGCAGCTGTGTCACC[G/T]AGGGTTGGTTTTGCTGCCATAACAGGATTATCATTTTGGATTCATCAGAAATTCATCTAACGTTATGGTTTTTGGTCTGCTTTCTCCCTCTCAGTGCCTCCCCATTACTTCCAGCATCTGGATCACACAGGGAAGAGAGTGGACTGCTATGAACGACCGGAGCTCTCGATGGGAAGTTATGAATTTATGGCTACTGTGGACTATTGTAAGGTACAGTGTGTTTCTTTCAGGCCACTACAAGCCAAAGGAAATGATAAGGTGTTGATATGCATGGGATTGCTTATTTGAATATTATTTCTTGGCAGAACAACAAGTTTCCTCAGCCACCAGCCTTTATTTTCCTAATTGACGTGTCCTACAATGCTGTAAAAAATGGCATGGTGGGAATGGTTTGCCAGGAGCTGAAGACATTGATGGATTATTTGCCCAGGTGAGAGTGTAAAAGAGAAACTGTTTGGAAACGCAGAGAATGTTTATGTTTTTGGCATCTACAGCAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17715
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 |
---|---|---|---|---|---|
ENSDART00000085476 | Essential Splice Site | 874 | 1241 | 14 | 22 |
ENSDART00000109159 | Essential Splice Site | 775 | 1142 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 12 (position 35766594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35455283 |
GRCz11 | 12 | 35556346 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGCCCACTTCAACAGGCGGCTCSATCWATAAGTACACCTACTTYCAGG[T/C]ATAGAAGAAYTGCATCTGAGTCACCATAACCATACAAGAGCAGCTAAACA
Long Flanking Sequence:
CTAGGCCGCAGACTGTGCTGGAAAGCTGTTTATTTTCCACTCATCTCTCCCCATTGCCGAGGCTCCAGGCAAACTGAAGAATAGGGAGGATAAGAAACTAGTGGGCACTGATAAAGAAAAGGTACCTTGACCTTTTCTCTAAAAAGCACTCACACGTATTGCATTTGTATCTGAAAGACGCAACCTTAAACCAACAGTGATGCTTTGAAAATATGTTATCAAGCATGGAGAATTAAGAAAACTTCACTACAGGAAGCTTTTCAATGTGCTTGTTATTGGGTAGGTTTTAAGGACCACGCTTCCTGAAGTTGACCTGTTTCTTTTGCAGTCATTGTTCCAGCCGCAAGTTAGTTTTTACAACACCCTAGCCAAGGATTGTGTGGCGCAGGGCTGCTGTGTGGACCTTTTCCTATTTCCCAACCAGTATGTTGATGTAGCAACGTTAGGGGTGGTGCCCACTTCAACAGGCGGCTCCATCTATAAGTACACCTACTTCCAGG[T/C]ATAGAAGAACTGCATCTGAGTCACCATAACCATACAAGAGCAGCTAAACAACAAAAAATAAAATAAAAAAATTGGTTATACACTTTTTCTTTTCCTTTTTTAGGCTTCATCTGACCAGGAGCGTTTCCTTAATGATTTGAGGCGAGATGTGCAGAAGCAGATGGGCTTTGATGCAGTGATGAGGGTCCGCACCAGCACAGGTGAATACATCGGGCTACATGTAAATTGCTCAGCGTAAAGGAGGATGCTTTACAGGATGCTTTTCAGTGTTAATTTGTGCATATTCGGGCTGCACAGTATACCGTTTTATATTCGATATCGCAGTGTGCGCATCCGCAATATTCACATCGCAATATATGCAATGTTGAGTCTGAATTATACACCAGGAGCTTCAGAACACATGTGGTTTGAGGAATCACTGCTAGGTTTAACTATAATATAGTGAAGGTTTATCATTTGCATGTGTTTTTAAGGCCTGTAACTGTATGAGCATTTCAAGA
Associated Phenotype:
Not determined