ZMP
sec31b
Ensembl ID:
ZFIN ID:
Human Orthologue:
SEC31B
Human Description:
SEC31 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:23197]
Mouse Orthologue:
Sec31b
Mouse Description:
Sec31 homolog B (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2685187]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42099 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42098 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa873 | Essential Splice Site | Available for shipment | Available now |
sa10739 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42099
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014190 | Essential Splice Site | 27 | 1171 | 1 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 49760449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 48483822 |
GRCz11 | 12 | 48467144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAGGCGTGGAGTCCTGCCAGACAACACCCGGCCTACCTGGCCTTAGG[T/C]AAGAGTGTGTGTGTGTGTGTGTTGTATGATTGTATGTTTGTGTAACACCC
Long Flanking Sequence:
CTTGTTTTTAATGATAAACACGATGTTATAATGTTTTATTGTATGTGCTACTGTTCTCTTCTCCGTGTGTTGGTGTGTTTTTGAAGCGCAGACAGTGAGCAGCAGGTTAATGCTAACGCTAACAGCAGCTGATGAGGAATAAACAAACGAGATTATCAATATACACTTAAACTCTATATGAACTGCACGCTGTTTATTACACACTCAGTTCATTAGGATTATTGTTTACTATTAAGAATACAGATTGCTGCAGTCTGGGTGACATTACAGGGTGTGTTTCAGTTCAGATTTTGTGATTTCTGTGACGGGATTGTGCTAGTTCAGTTACCTGGTAAAGTCGTGATTCAGGTAATTTGATTTGAAGTGTGCAGTGAGGGTTGACAGCTCCTTGTGCTGCTCTTCTGTCTTCAGGTGAGGAAGATGAGGGTGAAGGAGATCCTCAGGACGGCCACACAGGCGTGGAGTCCTGCCAGACAACACCCGGCCTACCTGGCCTTAGG[T/C]AAGAGTGTGTGTGTGTGTGTGTTGTATGATTGTATGTTTGTGTAACACCCAACCTACCCGCCTTAGGTGTGTGTTTAAGTGTGACACTTGGCCTACCTGGCCTTAGGTAAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATTGTATGTATGTGTGTGTAAGTTAAGAGTGTGTGTGTGTATGTATGTATGTATGTATGATTGTATGTGTGTGTAACACCCAACCTACCTGCCTTAGGTGTGTGTGCAAGTGTAACACTTGGCCTACCTGGCCTTAGGTAAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGAGATTGTATGTGTGTGTAAGTTAGGAAAGAGAGAGAGTGTGTGTGTGATTGTATGTGTGTGTAAGTTAAGAGAGAGTGTGTGTGTATGTGTGTATGTATGTATGATTGTATGTGTGTGTAACACCCAACCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42098
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 |
---|---|---|---|---|---|
ENSDART00000014190 | Nonsense | 133 | 1171 | 3 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 49752577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 48475950 |
GRCz11 | 12 | 48459272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTAATAAACACACGGGACCTGTTCGAGCCCTCGACTTCAACCGCTTT[C/T]AGGTAAGCCATATCAACCCATATGATTAGCTTCAGTATATCATTCATTCA
Long Flanking Sequence:
AACAACCAATTTACACTTTTTAGCAAAATATAGGTGTCCTAATAGTGTTTTTAGCAGTGTGGGACACATATACCACTGTCAACAGCTCAAACACATGTGCTCTGGTGTTTCTTGACTCTTTAAAAGCATCCGCCCCAACCCTCTCCATCATTCTCAGATGGGCCAAATCAAAGGTTATAATGGACCAACTCCAGCCTGCGGGCTCTGCTTTGGGCATCGCTGCTCTAAAGCATTAACAGGAACATCACTCATGCATGATTGTGAGTGTTGTGTGTGTATTTGTGTTGATCTGAGTGTGTGTTTTCAGGTTTCACAGTCTGATCTGGGTGGCGTTTGGTATGGATGTCCAGCCGTCGTCGGGTCGTCTCATCGGAGGCAGTGAGAATGGTAGCGTGACCGTCTTCAATCCCGACGTGATTCTGACCGCAGGAGAGGATGCTGTGATTGGCCAGTCTAATAAACACACGGGACCTGTTCGAGCCCTCGACTTCAACCGCTTT[C/T]AGGTAAGCCATATCAACCCATATGATTAGCTTCAGTATATCATTCATTCATTTTATTTTCACCGTAGTCCCTTTATTAATCAGCGGAATGAACCGCCAACTATTCCAGCATATGTTTTACGCAGTGGATGCCCATCCTGCTGCAGCCCATCACTGGGAAACAACCATACTCAGTCACACACTTACAAACTAGCTTACCCAATTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAGCACCCGGAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAGACACCAACTGACCCAGCTGGGACTCAAACCATGGACCTTCTTGCTGTGAGGCGATTGTGCTACCCACTGTGCCACTGTGACGATCCATCTAACTTGCTAATCATGCTAATCCATACTGAAAACATGCTAGAAACATGCTAATCCATCCTGGAAGCCTGCTAGCAACATGCTAAATTATACTGGAAATATGAAAGCAACGTGCTATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa873
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 |
---|---|---|---|---|---|
ENSDART00000014190 | Essential Splice Site | 260 | 1171 | 6 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 49747188)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 48470561 |
GRCz11 | 12 | 48453883 |
KASP Assay ID:
554-0775.1 (used for ordering genotyping assays)
KASP Sequence:
GATCTTCGGTTCGCAACATCACCTCTAAAAGTGCTGGAGAACCACACCAG[G/A]TAGAGAAACCCGCATTTCTACTCAACATTAATAATATCACATCATTATTA
Long Flanking Sequence:
CGAACGTATTTCTTGTTTTACATTTTCAATTTCCATAGCATCCGAGAGTCCTGAAAGGTCCACATATTGATAAGGTTATGATAGCTGATTTAACGTTAAGTTATGAATGAATTGCCTCTTGTTACAGTTATGAAATAGTTTAAGAGCAAGCATGAAATATTCATGGCCAAAGACATTGCCACATTGAAATGGTCTATAGTTTTTGCTCTTTATAGATGTGAATTGCTTTGTGATGATGAGAGTATGGATGGGAAATGTGTATGATTGTCATGAAAATAGTGTCACAGTGTGTTGATGATCCAAAAGTTAGCGTTGTTTTTTTTATGAAGAATATATTGTGTGCATGTGTGTGTTCAGATGCACTGCTCAGGGATGCTGTGGCATCCAGATGTGGCCACTCAGCTGGTTCTGGCCTCAGAGGACGACAGGCTGCCAGTCATCCAGATGTGGGATCTTCGGTTCGCAACATCACCTCTAAAAGTGCTGGAGAACCACACCAG[G/A]TAGAGAAACCCGCATTTCTACTCAACATTAATAATATCACATCATTATTATTATTATATTTAAATTACTTTTCTGATTGCTTTGTTTGAAAAGTAATTTAACACTTGTGTTGGGTCGTTTTTATCCACTCTGGGCTGATTTTGAGTCTTAATTTGGCTACAGCTTTCTTTCTGTTTCAGCAAATGTGATGATTTTTACATCTTATTGTGACACATATTTTGGGAAAATGCTTTGTTATGCTATTAAAAAAATATTATTATTATTATTATTATAGCATAATTTATTACACACAAATGCATTATAATTATTATAGCATAATTTATTATACACAAATGCATTATTATTATTATTATTATTATAGCATAATTTATTATACACAAATGCATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATAGCATAATTTATTACACACAAATGCATTATTATTATTATTATTATTATTATTATTATTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10739
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 |
---|---|---|---|---|---|
ENSDART00000014190 | Nonsense | 578 | 1171 | 14 | 27 |
Genomic Location (Zv9):
Chromosome 12 (position 49736732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 48460105 |
GRCz11 | 12 | 48443427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTGTATGTCTATTTTGTTACTAYCTGTGTGTGCAGATACAGACGGTT[T/A]GATCAGTCAGGCGCTGTTAGTGGGAAACTTCGAGGGCGCTGTGGATCTGT
Long Flanking Sequence:
ACATCGGATGGCCTTCCAGGCGCAACCCAGTACTGAGAAACACCCATACACACACTCATTCACACACACACTCAGACACTACGGCCAATTTAGTTCATCAATTCCCCTATAGCGCAAGGATTCACTTAAGGAGACCCTAAAAAGGCCCAAACATTGTGTTTTTAAGGCCTTGCAGATGAGTAAATAATCAATTTTCAAGTTTTTTTTATGAACTAACACTTTAATAGGTCAAGATCAGGTCATATCCAGATAGTCATATAAACAGAGGTTAGTTAAGTTAGTTAACTTTTTATTTGTCCCCGTAAGGAAATTTAATTTGTCTCAGAGACCTTTGACATTTCACATTTGGCATTTATATAAATAAATTATTAAATAAATATCCAGTCTAAAAGCTGTAACTGTCTCTGAAGCTTTTTCCATATACAGTCAGTCCATACATCCCACTTAAGTTTATTGTATGTCTATTTTGTTACTACCTGTGTGTGCAGATACAGACGGTT[T/A]GATCAGTCAGGCGCTGTTAGTGGGAAACTTCGAGGGCGCTGTGGATCTGTGTCTGAATGACGGTCGGTTTGCGGAGGCCATCCTTCTGTCCATCAGCGGAGGAGAAGAACTGCTGAAGAAAACCCAGCAGAGATACCTGCAGCGACAGACCAACAGCATCTCCATGGTGAGCATGCATCACTGATGACAGCACATTTCAGCATCAAATCATTTTCATTCAAAGCACATTTACTCAAGCGCAGACCAAGCAATGAAGGTTATATGGGAATAACTATAATTATATCACATTTCCTAGTTGTTAAAATTAATGCTATATTCAAATGATTTTTTTGAAACGTTACATCAAACAATATTCGTGAAACAATGCTTGATATATATATATATATTTTTTAGGGGGGAGGCAATGCATTTTGCAGCAATGCACAAATCACAAAGGATCATGCTAAATAAAGACATTTATTACGTTTATAACTGTAAATATATCTTGCTTAATTTTGTTT
Associated Phenotype:
Not determined