ZMP
sec31a
Ensembl ID:
ZFIN ID:
Description:
Protein transport protein Sec31A [Source:UniProtKB/Swiss-Prot;Acc:Q7SYD5]
Human Orthologue:
SEC31A
Human Description:
SEC31 homolog A (S. cerevisiae) [Source:HGNC Symbol;Acc:17052]
Mouse Orthologue:
Sec31a
Mouse Description:
Sec31 homolog A (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1916412]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1082 | Nonsense | F2 line generated | Not yet available |
sa41581 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34821 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31763 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1082
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108587 | Nonsense | 146 | 1250 | 5 | 28 |
ENSDART00000138537 | Nonsense | 146 | 1237 | 5 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 5133149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 5129443 |
GRCz11 | 10 | 5129747 |
KASP Assay ID:
554-0984.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTCTTTAACTTAGTCAAACCTTGTGGCGTCTGGTGGAAATGAGTCC[G/T]AAATCTACATTTGGGATTTGAACAACTTCAGCTCCCCAATGACACCAGGA
Long Flanking Sequence:
CCGCTGCGTTAGATGTTAATCTGTCTTTTGAAATGGAGAGTTATTCTAAAGTTATACAAAACTGACGTCATTAGATGTTTGATTATATAATAATAAAAAAAAAACATTACTTAATGTTGTACTTTCTCAAAGTCAGTTAATTTTGAAATCTTGTAGTAACCTTTTTGTCCAATTTCTAGATACCACAAGCTAGTCTGGGGTCCGCATGGCATTGAAAACCAGGGCTTGCCATCCGGCGTTCTCATCGCTGGAGGGGAGAATGGCAATATTATCCTCTATGACGCCTCCAAAATTATTGCTGGCGATAGTGAAGTGATCATTTTACAGAGTGAAAAGCATACAGGAGCAGTAAGAGCTCTTGACGTCAACTCATTTCAGGTAATCACTTCTTGCAAGAACATTTGTAGGTGTAGTTCTGATTAATGTGTAAATGTAAATGACTCTTTTTTTTTTTTTCTTTAACTTAGTCAAACCTTGTGGCGTCTGGTGGAAATGAGTCC[G/T]AAATCTACATTTGGGATTTGAACAACTTCAGCTCCCCAATGACACCAGGACCGAAAACACAAGTAAAAACACATCTAATTATTTACTCTTAAGACATCCTGTAGTTTTGTTTAATATTCTGCAATTTTATTGTTTATATTAAGAATGCACTGATAGGATTTTATTTGAGCCAGTTTCAGCAAAACTCTTTCGGCTGATAGAGATAATATATTGGTCAGTTGCATACAGTACTAAACCGTGCTTGTTAGGTAGTTTTTCTCCATTAGGTACATTATATTGAACATTAATCGGATGCATTTAACATTGAACTGTCTAAACTTTTAACAGAGGCCAAGTTAAGATGACAAAAATTACATTATGACAATCTTCTAAGGTCATTTTTGCTATTCAGAGTTTCTTTTAACAACAGCCAGTACTATTGCTATAATAGTGTAAATTCTAAATTTTACTGCTCCAGAAAAGTACTCAGTTTAGCTCATTCCTGCGCTTTAGCATGGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41581
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108587 | Essential Splice Site | 399 | 1250 | 10 | 28 |
ENSDART00000138537 | Essential Splice Site | 399 | 1237 | 10 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 5128238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 5124532 |
GRCz11 | 10 | 5124836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAAACCTCCAAAATGGATCCGTAGACCAGTTGGAGCATCTTTTGCTG[T/A]AAGTGGCTCTAAATCTAGCATTGCACATTGAATATGCACTAATAAATGTG
Long Flanking Sequence:
TGGTTTCACACCAAATATTGATTGAGGCGAGTTCCGCAAATGCATTCTGCATCGTTTGGCTGTTTGCATTGACTTTGTATGTAACTTACTCACATGAATACTCTGTGGTCAGTGTGAACTGTGCATAAAAGGCTCTTATTACCACCTGTTGGTTTGGCCCTTAACAGTTTATCACAGTGCATTTTCATGTGGACAGATGTTTTTTTTTTTTTTTAATGAAGGCAGAGAAAGCTCAGTTTATAAGAATATCTTTGTACGTGTGGATGGGCTCAGTATACAAGATAACGCTCTTAAGCTAGCATGAACATCTTCTCACAGTCGATCCTGATGTGTTTTGGATCAATAGTTAAGTAGCTCATTTGGAAATATGGATCCATTTGGGACGGGGAAGACATTGCCACCGTTACAACTGCCCCAGCAAACGTCCCCCCAGAGCACCATCACACCTCTGAAGAAACCTCCAAAATGGATCCGTAGACCAGTTGGAGCATCTTTTGCTG[T/A]AAGTGGCTCTAAATCTAGCATTGCACATTGAATATGCACTAATAAATGTGCTTGTTCTAAATCTGCTTTGTTTTTGTGAACAGTTTGGTGGGAAACTTGTTACTTTGGACAACATTAAGCCAACTGCTCAACAGCCCCAGCAGACTGCTGCTCATGTTGTTCACATCAGTCAGGTTGTGACGGAAACAGATTTCATTCATCGATCAAACCAACTCCAGACGACTCTCAATGCTGGAAATTTTCTTGAGTACTGCCAAAACAAGATTGAAACTGTTCAGAATGAATTTGAGAGGACTGTTTGGTCATTTCTGAAGGTAAGACACTCGATTAAGAATGCTTAATTGTGTGCACAGGAACAGGTTAGGTAACTTTCTATCAGAGTTGTAACCAATAGATTCATCTTTTTAGGTAAACTTTGAAGAAGATGCACGACTGAAATATTTGGAACTTCTAGGATATGAGAAGGAAGAGCTCGCCTTAAAGGTGTTGTGTTCATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34821
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 |
---|---|---|---|---|---|
ENSDART00000108587 | Essential Splice Site | 476 | 1250 | 11 | 28 |
ENSDART00000138537 | Essential Splice Site | 476 | 1237 | 11 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 5127923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 5124217 |
GRCz11 | 10 | 5124521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAACTGTTCAGAATGAATTTGAGAGGACTGTTTGGTCATTTCTGAAG[G/A]TAAGACACTCGATTAAGAATGCTTAATTGTGTGCACAGGAACAGGTTAGG
Long Flanking Sequence:
CAGTCGATCCTGATGTGTTTTGGATCAATAGTTAAGTAGCTCATTTGGAAATATGGATCCATTTGGGACGGGGAAGACATTGCCACCGTTACAACTGCCCCAGCAAACGTCCCCCCAGAGCACCATCACACCTCTGAAGAAACCTCCAAAATGGATCCGTAGACCAGTTGGAGCATCTTTTGCTGTAAGTGGCTCTAAATCTAGCATTGCACATTGAATATGCACTAATAAATGTGCTTGTTCTAAATCTGCTTTGTTTTTGTGAACAGTTTGGTGGGAAACTTGTTACTTTGGACAACATTAAGCCAACTGCTCAACAGCCCCAGCAGACTGCTGCTCATGTTGTTCACATCAGTCAGGTTGTGACGGAAACAGATTTCATTCATCGATCAAACCAACTCCAGACGACTCTCAATGCTGGAAATTTTCTTGAGTACTGCCAAAACAAGATTGAAACTGTTCAGAATGAATTTGAGAGGACTGTTTGGTCATTTCTGAAG[G/A]TAAGACACTCGATTAAGAATGCTTAATTGTGTGCACAGGAACAGGTTAGGTAACTTTCTATCAGAGTTGTAACCAATAGATTCATCTTTTTAGGTAAACTTTGAAGAAGATGCACGACTGAAATATTTGGAACTTCTAGGATATGAGAAGGAAGAGCTCGCCTTAAAGGTGTTGTGTTCATTATTTGTAAATTGATTTGTAGTGTAAATGCCTGAGATTCTTTCTCTGTGTGTCAGAGTTTTGGACTTGATTCATTTTTGGTTGTGGATTTCAGATTGCATCAGCGTTAGAAGGAAATTGCAAACCTAAAGAGGCCGATATGGTAAGTGGACCAATCATTGGGTTCTATATAACGGTTCCAGGTTTCTATCTTTGCAACTTGTTCAGGTAACCTCGGAATCCAATTTCAAAAATTGCTTTTTGAGATCACAAAAAGAAGATTTATTTTTACTAAACAAGAGCAAAATAACTTTTGTTTTGTGCGCTTCCTAGCAAGGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31763
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 |
---|---|---|---|---|---|
ENSDART00000108587 | Nonsense | 786 | 1250 | 19 | 28 |
ENSDART00000138537 | Nonsense | 788 | 1237 | 19 | 28 |
Genomic Location (Zv9):
Chromosome 10 (position 5114209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 5110503 |
GRCz11 | 10 | 5110807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGATGATTTTTATTTTTAGGTTTCTGTGCAGCAGTTGCGAGAGCGTT[T/A]AAGCAGAGCTTTAGGACAGCATCAGCATCCTCAACAGCCTGCAGCTGCAG
Long Flanking Sequence:
CTAAGTGAAATTTTTTTTAAATCTGAATCCTTCTAAAATTGTTGAATTTTTATCAAAAGGAAACCTTAAAAACTGTTTTAGATTTTTATCATATATATTATCATTATTATTATTATTTATGTATTTTACCTTGTTTATTACTTATTTCTGTTAATGACTTAATTTTTAGGACTTTTTTAAATATATAGAAAAGTGATATTTATAAAATGTAGAAACCTTGATCTGTTTTTTTTTGCCATGACATAGCCATAGAAGCTGAAATGGCAATAAAATTAAAACTCTCTCTCTCTCTCTCTCTCCTCTGTAAGCACATAGTAGTTAAGGCCACTTAATATGAAGTGGGACCGGAGTTTCAATGTTATACATTTTTTGCGTTATGATGGATGATTGGAAAAGTTGCCACAACCGTTCACTCATGCTTAATGGATGAGAAATTATGTCAGCTTTGTAATTTGATGATTTTTATTTTTAGGTTTCTGTGCAGCAGTTGCGAGAGCGTT[T/A]AAGCAGAGCTTTAGGACAGCATCAGCATCCTCAACAGCCTGCAGCTGCAGTCACTGGCATCCAGAAAATGCATCAGACGCGTCCTGCTGCTGTACCAATGCAGACATACTCACAACCTCAACCTCCTGCTCAGCCCGCTGCGCCTGCTGTACCTCCTCAGTATTACCAGCAGGTACGATATACACTCACGCACAGCTGAATAGCACACGCGCAGGTCCATTATTTGTGGTCCTGTGGCCGATACCAGAGTGTGTTTGTGTTTGTGTTGTGTTCAGGGTAGATCCGCCACTACTGTCACATCCTGGAGTAACCAAACCCCAACAGCTCTGCCCAGTGTCCCTCGCCAGCTAGTGCCCTCCTCTGACCCGCAGGTACAGACTGACAGAGCTGTGCCCGCGCTGCGCACACTGACAGATACAAACTCTACATCCCGCACGGGCAATAACAAAGATCTAAAGGCCCCAAAATGCTCACAGTTAACTTCTGTTTTGCTGTTTGGA
Associated Phenotype:
Not determined