ZMP
sec22c
Ensembl ID:
ZFIN ID:
Human Orthologue:
SEC22C
Human Description:
SEC22 vesicle trafficking protein homolog C (S. cerevisiae) [Source:HGNC Symbol;Acc:16828]
Mouse Orthologue:
Sec22c
Mouse Description:
SEC22 vesicle trafficking protein homolog C (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2447871]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37875 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8381 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7516 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37875
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092591 | Nonsense | 33 | 305 | 1 | 6 |
ENSDART00000142848 | Nonsense | 33 | 303 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 21268446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20515575 |
GRCz11 | 24 | 20659994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTCTCTCCGCCTCCACTGATTTCCTGCATAACAAGGAACTTCAGGAG[A/T]AAAAGCAACAGATTAAAATCATCTCGAAATCCTTGAATGTCTTACCAGAG
Long Flanking Sequence:
GATTTAATAAATGTTTCTACCTGAAGGCTAATTATGCTTTTAAATGTTTAAAATTAGTTTCTTAGATGCATATAATGAGTATACATATTCCTACATATAAATTCTGCCGTTGTATGATTTAATTCTTTTGATTCAGATATAAAAAAAAACATTCATGACTTTTATATACAACAAAAGACTATTATTATTTACAGAAAAAAACATATAGTTTAAATAATTTATTTGTTTTAAAATCAATATCATTAGATCGATACACACTTCAGAAGTATTATTTATTGTTAGTCCTTGTTAACTCATGTACTTAACAGGGAATAATAAGGTGAAAAACACATTTAAAAATAACTATCTGTTTCTCTCCTGTGCTGTGTGTTCAGGATGTGTTCTCATAGAGCTTCACGAGGAGCATGTCACTGATCCTGTTTGCTTTTGTGGTCCGGGTCAGGGACGGACTCCCTCTCTCCGCCTCCACTGATTTCCTGCATAACAAGGAACTTCAGGAG[A/T]AAAAGCAACAGATTAAAATCATCTCGAAATCCTTGAATGTCTTACCAGAGAGAGGGACAGTCAAGGGCCATGAGCTCAACATTCAGTAAGTGCACTATAGTGTCTTGAGCTTAAGTCACCCCATATTATTACCCTAATGATACATGATAAATTGCTAAAAATGCAGAAGAATAAAGAGGATATGTGAATTATGTAAGGGTATAACTGTTCACCGTTTCTCAATATATTGCAACTGCAGTGACGCAATGTGCATTAGTGCTTCAGCAGTTTTTCTGTTACAGAATATTTTCCTATAGGCATTTAAAAAAAAGAGTCTTAGTTAAAGTGTTATACGCCATGAAGAGAAACAAAAAGCTACAAGGAGCTATAACATTACAATTTTTGATTTTTAAATCAGAGCAGTATATAAAAATCAGTCAGCAAAGGTACAAAACTTATAGCATACAAATGTTTAAACACAGTTACGTAAAAAGGAAATTGTTCAGAGTTAAACTATCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8381
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092591 | Essential Splice Site | 61 | 305 | 1 | 6 |
ENSDART00000142848 | Essential Splice Site | 61 | 303 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 21268532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20515661 |
GRCz11 | 24 | 20660080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGTCTTACCAGAGAGAGGGACAGTCAAGGGCCATGAGCTCAACATTCA[G/A]TAAGTGCACTATAGTGTCTTRAGCTTAAGTCACCCCATATTATTACCCTA
Long Flanking Sequence:
ATTCCTACATATAAATTCTGCCGTTGTATGATTTAATTCTTTTGATTCAGATATAAAAAAAAACATTCATGACTTTTATATACAACAAAAGACTATTATTATTTACAGAAAAAAACATATAGTTTAAATAATTTATTTGTTTTAAAATCAATATCATTAGATCGATACACACTTCAGAAGTATTATTTATTGTTAGTCCTTGTTAACTCATGTACTTAACAGGGAATAATAAGGTGAAAAACACATTTAAAAATAACTATCTGTTTCTCTCCTGTGCTGTGTGTTCAGGATGTGTTCTCATAGAGCTTCACGAGGAGCATGTCACTGATCCTGTTTGCTTTTGTGGTCCGGGTCAGGGACGGACTCCCTCTCTCCGCCTCCACTGATTTCCTGCATAACAAGGAACTTCAGGAGAAAAAGCAACAGATTAAAATCATCTCGAAATCCTTGAATGTCTTACCAGAGAGAGGGACAGTCAAGGGCCATGAGCTCAACATTCA[G/A]TAAGTGCACTATAGTGTCTTGAGCTTAAGTCACCCCATATTATTACCCTAATGATACATGATAAATTGCTAAAAATGCAGAAGAATAAAGAGGATATGTGAATTATGTAAGGGTATAACTGTTCACCGTTTCTCAATATATTGCAACTGCAGTGACGCAATGTGCATTAGTGCTTCAGCAGTTTTTCTGTTACAGAATATTTTCCTATAGGCATTTAAAAAAAAGAGTCTTAGTTAAAGTGTTATACGCCATGAAGAGAAACAAAAAGCTACAAGGAGCTATAACATTACAATTTTTGATTTTTAAATCAGAGCAGTATATAAAAATCAGTCAGCAAAGGTACAAAACTTATAGCATACAAATGTTTAAACACAGTTACGTAAAAAGGAAATTGTTCAGAGTTAAACTATCCATTTAAAGTTGTTGGTTGCATCTGTAGAAACAATATACACCACCTGACAAAAGTCTTGTCACCTATACAAGTTATAGGAACAACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7516
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 |
---|---|---|---|---|---|
ENSDART00000092591 | Missense | 109 | 305 | 2 | 6 |
ENSDART00000142848 | Missense | 109 | 303 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 21270518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20517647 |
GRCz11 | 24 | 20662066 |
KASP Assay ID:
554-4143.1 (used for ordering genotyping assays)
KASP Sequence:
GGAATTCACAGCATGCTTTGACAACTCTGCAGTGGCCATGGCAAACAGGC[C/T]GTACCCATTTCTGGAGTTTGGTAGGGTGATTAAAATKTTAATGGATGTAW
Long Flanking Sequence:
AAAAATGAGTTTTCTTATAGAAATAAAATAGTTTTTATTTTTTAAATCTAAATATGCACCATGTTTATGTGTCATAAGTTTTGGATGGAGAATAAACATATGCATTTAATGTAATTCTGTATATTTAAACAAATGTTTAGAAAATTCCTTAAACATAATAATAATAAAAATATATATATCATTAGTTCTATATCGTGTTATCCGGAGCTGCATTCAAGTGTTGCCGTATCAGATTCAGGAACTATAAGAAAGCGCCTGACATTGTTTGCCTCCATTCCAGAGTCCAAGATAAGCCAAGGAAACCGGTGGCCGCCCTGTGAAGTCATTTGTCAACTAATTGGTCTCTCTGTGTTGTAGCTTCCTCTCATGTGAGGGTGTGTCCTACATGAGCGTATGTGCCTGCACGCTCCCTGCTGCCACGGCCTTCTGCTTTTTGGAGGACCTGCGCTGGGAATTCACAGCATGCTTTGACAACTCTGCAGTGGCCATGGCAAACAGGC[C/T]GTACCCATTTCTGGAGTTTGGTAGGGTGATTAAAATGTTAATGGATGTATAGGCTTAAGATGATTTAGGAGTAATGGGTGTATTTTTTTATTTTTATTTTTAAATATTTCCCAAATTATGTTTAACAAAAAGGAGAAACTTTTACTTGTTTTATTTTGGCTAGACTAAAAGCAGTTATTATTTTTTTAAAACCTTTTTAAGGTCAAAATTATTAGCCCCTTCAGAGCCGTTACTCGCTGCAGAAGTTGGGACTTTCTCAACTTTTCAGATCGCTGTATGCAAATACACCAGCTCAGACATTGGCCTATTGCTGACTAATTTCATTGGCTGACGCTGCTATGATGATTGCGTTAGCCCACACTTCAGACACGCCCTCTGGAAGCCCTGTGTGAATTGGGCGTTACACATCAAGTTATTTATGAAATCAAAATTTGCAATATTTATTTTGCTTGCACACATTGTTAGATTTAAGTTGAAGTTTTTCTGTGAAAGGTAATCCC
Associated Phenotype:
Not determined