ZMP
si:dkey-239i15.3
Ensembl ID:
ZFIN IDs:
Description:
STT3, subunit of the oligosaccharyltransferase complex, homolog B [Source:RefSeq peptide;Acc:NP_955
Human Orthologue:
STT3B
Human Description:
STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) [Source:HGNC Symbo
Mouse Orthologue:
Stt3b
Mouse Description:
STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae) Gene [Source:MGI S
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42789 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22917 | Nonsense | Available for shipment | Available now |
sa5896 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22916 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42789
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 |
---|---|---|---|---|---|
ENSDART00000041980 | Nonsense | 204 | 244 | 3 | 5 |
ENSDART00000102525 | Nonsense | 204 | 805 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 42101910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 39485360 |
GRCz11 | 16 | 39435392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTGTACCAGGCTACATTTCCCGCTCTGTGGCTGGCTCTTTTGACAAC[G/T]AGGGCATTGCCATTTTTGCCTTGCAGTTTACTTACTACTTATGGGTAAGT
Long Flanking Sequence:
ACTGCTGGAGTTGGTTGATGCATGGTTTTTATTCTAACAGTTATGCTTTTTTAGGAGTAGGCTTTTTTTTTTTTTATTGTGCATTTGGGCGGGTTTTGGACTGCTTTTGGGCTGGAAAAAGTCAAGTGAATCAAATATTTAGGAATGTTTACAGACTTTCTCAAACATTTTTTTCATCCCTCTCCTGAATTACTCCAGGCAAAAGTCTGCTTGATCGATTGGTGTTAATGGCATCTCTCATATCTGCTCTTTTACAGGTGTATCCTGGTCTGATGGTGACGGCGGGCCTGATTCACTATGTACTGAATCTGCTTCATGTGACGGTGCATATACGTGATGTTTGTGTGTTCCTGGCTCCTGTCTTCAGTGGCTTGACTGCCATTTCTACTTTCCTGTTGACGCGGGAGCTGTGGAACCAGGGCGCTGGACTATTGGCAGCGTGTTTCATCGCCATTGTACCAGGCTACATTTCCCGCTCTGTGGCTGGCTCTTTTGACAAC[G/T]AGGGCATTGCCATTTTTGCCTTGCAGTTTACTTACTACTTATGGGTAAGTTGTATTAATTGCACCGTTTTGTGTTTGTCTTTATTGTTGTTTTCTCATTATCTTTATTCAGTACAATTATCCAGTTTGATTATGTGGAATATATATATATATATATATATATATATATATATATATATATATATATATATAATTAATACGATAATATACGATTAAAGTATTTTTTTTCTGAAAAGTAGCCATGCCAACTTTAATTTAATACTGTTTGGTTTATTTATCTTCAGCCCACCACCCTCAATCAAGTTTGGTTTTTGGCCCTTATCAAGAAACTTTTGCCACCCCTGGTTTAAATTAATTAATTAATCAGGAAGATAAAGTTATCTGGTTGTTATTAGTCGGGTCTTTGAATCACATAATTCATGGTTTCTGCTACATTCATTCTTCTATGGTGGGGCGCCACGCCAAAATTTATCCCGCTACGGCTACATTACAGCTTCCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22917
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 |
---|---|---|---|---|---|
ENSDART00000041980 | None | None | 244 | None | 5 |
ENSDART00000102525 | Nonsense | 320 | 805 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 42080038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 39463488 |
GRCz11 | 16 | 39413520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTGCAGGTGTATTCGCATTGCTTCAGGCTTACGCTTTCCTGCAGTA[T/A]CTGAAGGACAGACTCACCAGACAAGAGTTCCAGACACTGTTCTTTCTAGG
Long Flanking Sequence:
GAATTTTCATTTTTGGGTGAACCATCTCTGAAAGAGCTGTCTTCATCCATTTGTCCTCCGCTGTTTTGAAATGCTCACAGTTGCCATCTGTGCACACCAAGTTTGACAGTTCTGCTAGTCTTCTTTGCTACTCACCTCATTTTTGCTCTTCTTTTCTTCTTCTCAGCCTACAGCACCTTTTATATAGTGGGATTGGTGCTGTCCATGCAGATCCCCTTTGTTGGTTTCCAGCCCATCCGGACGAGTGAACACATGGCTGCTGCAGGTAAGACTGGTTTAACGCCATTCCTCATCAACTGTTGCTCTTTTACATTGATTTATAGAGCCGTTCTCTCAGCGCGAATCCATCTGGGAGATTGTTTACGCGACAACAGATCAGCAGCTGGAGTTCATGAGTGTTGGGAAAATGTGAGAAGCAGTTAAGTACGTGGGTTAATGGTGCATGTATTTGTGTTTGCAGGTGTATTCGCATTGCTTCAGGCTTACGCTTTCCTGCAGTA[T/A]CTGAAGGACAGACTCACCAGACAAGAGTTCCAGACACTGTTCTTTCTAGGCGTTTCTCTGGCTGCGGGGGTGGTTTTCCTTACGGTTATTTATCTTACGTACACAGGTGAGTGCAAAAAAACAGTTGAAGAGTTACTTGTTGTTAACCTTGGGACTACAACAATAGACACAGACATATCCTGTCTTCTGATTGAACTAAGATTGAACTGTTTGGCCATAATGATCAGTGTTACATTTAGAGGACAAAGGGGAAAGCTTACAAGCCTAGGAACACCATCCCAACTGTGAAGTATGGGGGCAGCACCATCATGTTGTGGGGCTGTTTTGCTGCAGGAGGGACTGGTCCACTTCACAGCATAGTTGGCATCATGAAGAAAGAAAATTATGTAGAAATACTAAAGCAACATCTCAAGACATCAGCCAGGAAATTAAAACCTAGCCACAAATGGGTCTTCCAAACACACCATGACCCCAAGCATACTGTCAAATTAGTAAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5896
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041980 | None | None | 244 | None | 5 |
ENSDART00000102525 | Nonsense | 469 | 805 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 42065557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 39449007 |
GRCz11 | 16 | 39399039 |
KASP Assay ID:
554-3865.1 (used for ordering genotyping assays)
KASP Sequence:
CTCGGCCATCGCCTTCTCCAGCGTCTTCGAGCACTACCTAGGGGACGATT[T/A]GAAGCGTGAAAACCCACCGGCTGAGGACAGCAGTGATGAGGATGACAAGA
Long Flanking Sequence:
ATGATCAATTTTAAGCTGTAGTGTTTGTATCCTCTTTGTACCTCTTCGATTTTGATGTCTGCATCGAGCATTTTCATTTATGGAGAAACTTGAGAACAGGATGCACTGAAATAGTTTCAGTCCCCTGAAGAGTTTGTTTTATTATTATTAATTTTTTTTAATGGCTGTCATGACGGTCCTGATGCCTTTTGAGCAGAACAAACAAGGGAACGTGAACAGACGACATGTCGCGGCATGTTTAAAGGCTTGTTTCTGTGCTGTTGAGATTCTCTCTGGAGTCATTATTCAGTGCAGGGTTATAAACACTAGGTAGCAGTTAATTATCTGCAGGAATAATAGCTGGTGTTTTCTCTGTCGCCCTCTAGTGGCTCTGTATGCCATCAGCGCAGTCTACTTTGCTGGAGTGATGGTGCGTCTGATGCTGACACTCACTCCAGTGGTTTGCATGCTCTCGGCCATCGCCTTCTCCAGCGTCTTCGAGCACTACCTAGGGGACGATT[T/A]GAAGCGTGAAAACCCACCGGCTGAGGACAGCAGTGATGAGGATGACAAGAGGAATCAGGGCAACCTCTATGATAAGGTCAGTGAAGGTTCAGAGGTCAGGCTCAGTGGGAAAAAAAAGTTTGAAGCTTTACTATACAATTAGATCTGCATTTAAATATAAAAATAATTTCAATAAGTAAATTTAAAAAAAATGTGCGTTTATACTTTTTCGTAAGGTGATACATTTAAGAACAATATATTATAATAATTTATAATTTGATCTTTTAATATTTAAATCTATAATTTAAAACAAAATATTACAACTTAATGTTTTAATAAAGCTTTTATAGATTAAAATGAAACTGTTGGCAAGTTTCTGTGTTTTTATTAGCTATTTTAGATTTGTTTGTTGGGCATAACAACAATTTGGTATGGTTAAAGATCTTAATTAGGGATGCTACAATTATAGATTTTAGTGGTACGATTATAGTGTGAGGATTAATCATGGTTAAAAACTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22916
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041980 | Splice Site | None | 244 | None | 5 |
ENSDART00000102525 | Nonsense | 791 | 805 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 42053617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 39437067 |
GRCz11 | 16 | 39387099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCGTTGGTTCACAGACAGCCAAGAGGAAGCGGGGGCACATCAAAAAC[A/T]AGCTGGCTCTGAAAAAAGGCAAGAAACTGAACAAGAAGTCTGTTTAGCTG
Long Flanking Sequence:
GAATGAAGAGACCCGTGAAATGGTAATAATTAACGTTTACAAATCGATTTAATACATTCGAAAATCAACATGGCAGTATATATGTCCATGCCTAATATCCGATGGCCAGAAAGGGATTAGTTTTTTATAAATTGTAAAATTTTTGTTATTTGTTATGCAGCAAGCCCAGAGATTGTTGTGTACACTATTACTTTATGTAAAATTAACTTTAATGTGTGATAGGAATAAAACGTGATCATAAACGAATGATTTCTCCGCTCAAATGAATGGCAGCTTGTACCCGGAAACAGTATTACATACGTCACAAACACGTCACCACTTAACAAGCGGATTGGTCTGGCCCTCTAAAACTGCCCCAGAGTCTAAGGTGGCCCCTTGGAAAAATGAATTGCACATTCATGGTGTAGATACTTGCATTTTAAAATGACTTTATGACTTTTTTTTTTTTTTCTTCCGTTGGTTCACAGACAGCCAAGAGGAAGCGGGGGCACATCAAAAAC[A/T]AGCTGGCTCTGAAAAAAGGCAAGAAACTGAACAAGAAGTCTGTTTAGCTGTTGAATGCGAATGTTGAGAACGGAAAACGAGGAAAACAAAAGACAAGGACCGATGCAACTAGTAAGTAATCCACCAATCAAAAAGAAGAACAAGCAAACATGTTGTCTGGCTCCGCCCACCTGCCGACGTTTGGTTGGAGGCTTTTGATCCTGCGATTGCCATGACGACACTGAGGTTCATGACTGGGTTGAGGAGGAGGATCTGCACCGCGGTTTTAATCTGACAACTCTGGACTTTGTTTTTCTTCTTGTGTTTATTTTGTTTGTTTTGCTTTTGTACTTGAATGTTCTGGTGAAGCGAGAGCTCTAAAAACGGCAGGCACTATTTTGTGGTACAGTTTAATAATAGTATCCAACCGAATGCTAAAACAACAAACACATGAATTTCATTGAGCTCAGTGAACCTTGGAGCACCAAAGAGATTTAGTTTTGTTTTTAGTTTTCTTTTTT
Associated Phenotype:
Not determined