ZMP
smg7
Ensembl ID:
ZFIN ID:
Description:
protein SMG7 [Source:RefSeq peptide;Acc:NP_001038548]
Human Orthologue:
SMG7
Human Description:
Smg-7 homolog, nonsense mediated mRNA decay factor (C. elegans) [Source:HGNC Symbol;Acc:16792]
Mouse Orthologue:
Smg7
Mouse Description:
Smg-7 homolog, nonsense mediated mRNA decay factor (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2682
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32963 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa853 | Nonsense | F2 line generated | Not yet available |
sa19816 | Essential Splice Site | Available for shipment | Available now |
sa18100 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32963
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 |
---|---|---|---|---|---|
ENSDART00000085976 | Essential Splice Site | 20 | 1130 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 2 (position 35773618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36070328 |
GRCz11 | 2 | 36052785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTTGTTTTGAGCAGGCAGGCAGAGGCCCTGAAGGCTGACATGACAGG[T/C]ATGTTACTATGTCCTTTAATGTATTTACTTTAAAATGTTTGTTAAAGTCT
Long Flanking Sequence:
GTGTGTGTGTATGTGTGGATGTTTTCCAGAGATGGGTTGTGGCTGGAAGGGCATCCGCTGCGTAAAAAAACAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGTTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATATCATGAAATGCAATCATAAATCATCCATTATCATTTTCAACAAGTGATTTTTCCAAAGGCTCTTTAAATAATCTAAATAAACTAATGTCATTTTCTACAATTTGTCTTTTGCCATTTTAAACTATGTGCGTTTATGGACAAATGAACTGAGTCCAAAATGGCCTTGAGTTTGAGAATGCATAAAAATGAAGCTACCAAACTGCGAAGCTGTTATGCTCATTTCAAAGATGTTCACCAGACCTTGCCAAATCATTCTCTCTTAAATCTTCTCCTCATTAACATATTCATTTCTTGTTTTGAGCAGGCAGGCAGAGGCCCTGAAGGCTGACATGACAGG[T/C]ATGTTACTATGTCCTTTAATGTATTTACTTTAAAATGTTTGTTAAAGTCTTTCTGATGGTGTGCTGTTTTAGACTGTCTTATAAATATCTCTATAATAACCATATATAAGAATAGAGATGGTCACAAGTTGCGCATATTACTCAAATTATTGATGTGATGTAAGGGCTTGCTTGGAGTCTATTGCTGTGTTTCATATTTGTCATCTTATCCCTGTCACTCTGGTAACCATGGCATTGAATGTGGTTACTAAGACGTGCAGATCTTTCTCTAAATGAGCTGAAAGGCGCTGTTAGACTCAGTCAGTCACGTTCTGCAGTGAGGTTGAATCATTAGCTGTTTAACATGTTCAACTCCACGTGTCATGCAGATTCTAAGCTTGGTGCCGCGGAGGTCTGGACGTCACGACAGGCTCTTCAGGACTTGTACCAGAAAATGCTGGTTACGGACCTGGAGTACGCCCTGGACAAGAAAGTTGAGCAAGATCTGTAAGATTACTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa853
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085976 | Nonsense | 33 | 1130 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 2 (position 35774025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36070735 |
GRCz11 | 2 | 36053192 |
KASP Assay ID:
554-0756.1 (used for ordering genotyping assays)
KASP Sequence:
CGTGTCATGCAGATTCTAAGCTTGGTGCCGCGGAGGTCTGGACGTCACGA[C/T]AGGCTCTTCAGGACTTGTACCAGAAAATGCTGGTTACGGACCTGGAGTAC
Long Flanking Sequence:
CCAAATCATTCTCTCTTAAATCTTCTCCTCATTAACATATTCATTTCTTGTTTTGAGCAGGCAGGCAGAGGCCCTGAAGGCTGACATGACAGGTATGTTACTATGTCCTTTAATGTATTTACTTTAAAATGTTTGTTAAAGTCTTTCTGATGGTGTGCTGTTTTAGACTGTCTTATAAATATCTCTATAATAACCATATATAAGAATAGAGATGGTCACAAGTTGCGCATATTACTCAAATTATTGATGTGATGTAAGGGCTTGCTTGGAGTCTATTGCTGTGTTTCATATTTGTCATCTTATCCCTGTCACTCTGGTAACCATGGCATTGAATGTGGTTACTAAGACGTGCAGATCTTTCTCTAAATGAGCTGAAAGGCGCTGTTAGACTCAGTCAGTCACGTTCTGCAGTGAGGTTGAATCATTAGCTGTTTAACATGTTCAACTCCACGTGTCATGCAGATTCTAAGCTTGGTGCCGCGGAGGTCTGGACGTCACGA[C/T]AGGCTCTTCAGGACTTGTACCAGAAAATGCTGGTTACGGACCTGGAGTACGCCCTGGACAAGAAAGTTGAGCAAGATCTGTAAGATTACTAATGATGAAAGATTGCACAATGATTCTATGAATTTACATTAATCGTGTCTTGTCTGATTTTTGTGGTTTAATATTTGGTTGACCTTTATTTTGTCCCCAATATACTTGCATTTCAGCTGGAACCATGCTTTTAAGAATCAAATAACGACATTACAGAGTCAAGCTAAGAACAGGGCCAATCCCAATCGAAGTGAAGTACAGGCCAATCTCTCCCTGTTTCTTGAGGCAGCTAGTGGATTCTACACACAAGTAAGCTGAGTTATTGTATTGTTCATGATAGGGTTGTCAAAAGTATCGATTTTAGTACCAATTGGGACAGAAATTTTAAAATCGTCCATTTGCTGCTAACATTCATTGCTAAAGGTGCGATTTTCAAATCGCAAAAGCTGCTATTATTTTTTTTATTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19816
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085976 | Essential Splice Site | 335 | 1130 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 2 (position 35782936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36079646 |
GRCz11 | 2 | 36062103 |
KASP Assay ID:
2259-2308.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAAGCATTATTTTGTGCAATATTGTGATGTTCTGATGGTCTTTCCCCA[G/T]TGTCTTTTCTGGGAGTGATGCTAAGTCGAGCTTTACTGAATAAGAACCGA
Long Flanking Sequence:
CTGTCTTTTCTTGATTTGACCAGCCTTTACCTGATCCTTCAGAAATTGTATGCTTATTTAGTACTAAAGAAACATTTTTCATCTTTATCAGTTGAAAACAGGTGCTATTCTTTCATTCAACATTTGTTTAAACAGATTTTTCTATGCAAAACAAATGGTTTTGGCCAAAAAATGTATTGTAATAAATATTTATCTCGGAGGAATTGAAAGCTATTTTTGATATATATATCCAGAAATTTTCAAACCAGACGATAACCTTATCAAATGCATAGAGCTAAATATACAAGCATTACATTTACCTATTGTTTAGAAAGAGCCATTTCAATTGTAAAAGGCCAACTGCTGCCTTAAAAAACTGATTTCATCCTATTGAAATGTAAAATATTGTCTTTTTTGTAAAAAGAAAAAAGGATAGCTCCCACAAAATGAAACAAACTTGAAACTAAGCCTCACAAGCATTATTTTGTGCAATATTGTGATGTTCTGATGGTCTTTCCCCA[G/T]TGTCTTTTCTGGGAGTGATGCTAAGTCGAGCTTTACTGAATAAGAACCGAGAGGAGATTATGGGAGAATGTCCACTGCCTGCCATTAAAGTATCTCTGGACTGGCTGAGGCTTCGACCCACTGTGTTTAATGAGAGTGCCATGGACAAGCGACAGTAGTAAGAAAACCTTTTTTTTCCCACCAAAATTAGAAATATTATTAATAAATAGTGGATGATTTAGTATTTTTGTGTTTGTATTAAGTGGGGAACCTATTGTCTCTTAAAAGGATGATTTACTGGATCTCAATTAACAATTTGTTTAGTCCCAACTAAAGAAAAACAAATAATTAGATTTGCTGATATTTTTATATATATATATATATATATATATATATACATATATATATATATATATATATATATATATATATATATACATATATATATATATATATATATATATATATATATATATATATATATGTGTGTATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18100
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085976 | Nonsense | 937 | 1130 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 2 (position 35793632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36090342 |
GRCz11 | 2 | 36072799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGAAACAATATTTAWGTTTGCTGCTGTTTTACAGGATAACTCCTAC[C/T]ARAAYAACAGCATTTTTAGTGAGGCCTACGGTAAAAACATGACACCTTCA
Long Flanking Sequence:
ACTGTGGTCTGCTTTGAGTTGTTGGAATATACATGCGTTTTGCAGATTACTTATAATTGTGCTTCTGTCTCTCTGTAGTTGCCAAATCAGTCTCGGCTTGACAGTGGAGCTGATGTGATTGGTCAGTCCTCCCTTCTTCCTCGATTTTCCATTCAGGTAAGCATGCATCTCTTTGTATCAACTTGCTCTTTAGGCCCTCCTTGCATGAACGATTGAAAGTCACTAGGTGGCAGTGCTGTCCTACAAAACGAGATTGGATTATATTTTTTGCTTTGCTGGATGTTGTATACCTGGATTTGACAGCAAATGCAATTAAGTTGTTTACACTGACAGGTAGACTTTTAGGTAGAAGTTTGAATCAGACCTGCGTTTATTTCCTTATACTGTTCTCTCTTTTTGTTCTGTCTTCACTGAATCTATCAAAATAAGGCTGATAAACAAATCAAAACAATGATGAAACAATATTTATGTTTGCTGCTGTTTTACAGGATAACTCCTAC[C/T]AGAACAACAGCATTTTTAGTGAGGCCTACGGTAAAAACATGACACCTTCATCTAAGCCGGATGCACCCATGATGCATCAGGAGCCCTCACTCTATTCCCTGTTTGAAGGAAATCCCTGGTCTCCCTCCCTTCCTGCCAGCTCAGGTACCAATATTGAGATCTGTGATGTCTAAAGCATGTGAGAAGCATGATTTTTTAAATCATTTCTACCTATGATTTGTTATTGTAGATCACTCAACCCCAGCAAGCCAGTCCCCTCACTCCTCCAATCCCAGCAGTCTGCCTTCATCCCCACCCACCCACAGCCATGGCTCCATGCCCTTCTCCAACTTTGGCCCCATCGGGACGCCAGACAGCAGAGACCGCCGAGCAAATGATCGCTGGAAGGCTGAGAAGACTGGTAATGATGCTGAGCACGCTGTTGTGGTTCTGTTAACAAATAGTAAGGGTACAGTAAATAAATTAAAAGGATTTCATAAATATACATCCTAAAATACCTG
Associated Phenotype:
Not determined