ZMP
LOC100334474
Ensembl ID:
Human Orthologues:
SAMD9, SAMD9L
Human Descriptions:
sterile alpha motif domain containing 9 [Source:HGNC Symbol;Acc:1348]
sterile alpha motif domain containing 9-like [Source:HGNC Symbol;Acc:1349]
sterile alpha motif domain containing 9-like [Source:HGNC Symbol;Acc:1349]
Mouse Orthologue:
Samd9l
Mouse Description:
sterile alpha motif domain containing 9-like Gene [Source:MGI Symbol;Acc:MGI:1343184]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6877 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45127 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6877
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 |
---|---|---|---|---|---|
ENSDART00000108630 | Nonsense | 438 | 954 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 6850978)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6674672 |
GRCz11 | 3 | 6560512 |
KASP Assay ID:
554-4830.1 (used for ordering genotyping assays)
KASP Sequence:
CTAACATTCTGCTTACAACWGAKTTATTTTAYGAGTACACTCTGGGAAAA[C/T]AAAAATTAATGCAGGATGTTCACARCATGTTGGTGAGGAGGCAGAATTCA
Long Flanking Sequence:
TATCTGAAAAGGAACAGAAACTGTTTGAAGAAAAGCTAAAGGAGATTGAGAAGACCAACAGAAACACTAAAACGTTTTATGGATTCATGATTCTAAAGTCCAACTATTCTTCCACGTATATACAGGGTGTTGTAAAAAGCACCCTCATTGGATTCAATCTCCAACACAAGCATGCTCAGCTTTTTGCAGTTCTTGTCCTCTTGCATGTCTACTGCAAGAATGCAGTGCTGTCAGTCTCTACATGTGAAGAGTTCCTTGGTTTGGAAACGAAAGCAGACTCTACATCCTGCAATGTGGAAAATGGGTTCAAGAAGTTTTCCACTCTTTTGAAAAAATGCCCGGTTGATTATAAAATTTCCTTTGAGGGCGTGCGGGTGATTCACTCAAGTATAGCTCAACACTGCTTGAAGGAGCTTTCAGCTTCTCATGGAGTGACGAAGGCAGAAATCACTAACATTCTGCTTACAACAGAGTTATTTTACGAGTACACTCTGGGAAAA[C/T]AAAAATTAATGCAGGATGTTCACAGCATGTTGGTGAGGAGGCAGAATTCAGTTGAGGCTGAAGACTCCCTTTTTTCTCCACTTATCCAAGATATAATGAAAGAGACACCAGGGATGGAAGAAACTGTTCTTCTCAATGCAGTAAAGTGCTATAGAAAAGATGTAGCAATACCCCAGCTTCTCGCCAGGTACTATTACATTAAGAAACAAGACTTTAGTATGGCCAAGGATTGGGCAAAGAAAGCCAAAGACCTTTCAGGGGAGAACTCATACATGTGTGATACAGTATCACAGGTATATGTGAATGAGCTGAAATGTGCTTTTCGCGAAGATAAAGATGATCCCATCAGCCCAAACAGTCTTGATAGATATCTTACATTGGCTAAGACGGCAACAGAAGCTTGCAAAGAAACACAACAAACAGCAAACAAAGAAGCCATTACTCGACTGCAAAGACAAAAGGATTATACTACCTACAACACTGCTGGCCATTTCTGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45127
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 |
---|---|---|---|---|---|
ENSDART00000108630 | Nonsense | 520 | 954 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 6851224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6674426 |
GRCz11 | 3 | 6560266 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTAAGAAACAAGACTTTAGTATGGCCAAGGATTGGGCAAAGAAAGCC[A/T]AAGACCTTTCAGGGGAGAACTCATACATGTGTGATACAGTATCACAGGTA
Long Flanking Sequence:
AAGAGTTCCTTGGTTTGGAAACGAAAGCAGACTCTACATCCTGCAATGTGGAAAATGGGTTCAAGAAGTTTTCCACTCTTTTGAAAAAATGCCCGGTTGATTATAAAATTTCCTTTGAGGGCGTGCGGGTGATTCACTCAAGTATAGCTCAACACTGCTTGAAGGAGCTTTCAGCTTCTCATGGAGTGACGAAGGCAGAAATCACTAACATTCTGCTTACAACAGAGTTATTTTACGAGTACACTCTGGGAAAACAAAAATTAATGCAGGATGTTCACAGCATGTTGGTGAGGAGGCAGAATTCAGTTGAGGCTGAAGACTCCCTTTTTTCTCCACTTATCCAAGATATAATGAAAGAGACACCAGGGATGGAAGAAACTGTTCTTCTCAATGCAGTAAAGTGCTATAGAAAAGATGTAGCAATACCCCAGCTTCTCGCCAGGTACTATTACATTAAGAAACAAGACTTTAGTATGGCCAAGGATTGGGCAAAGAAAGCC[A/T]AAGACCTTTCAGGGGAGAACTCATACATGTGTGATACAGTATCACAGGTATATGTGAATGAGCTGAAATGTGCTTTTCGCGAAGATAAAGATGATCCCATCAGCCCAAACAGTCTTGATAGATATCTTACATTGGCTAAGACGGCAACAGAAGCTTGCAAAGAAACACAACAAACAGCAAACAAAGAAGCCATTACTCGACTGCAAAGACAAAAGGATTATACTACCTACAACACTGCTGGCCATTTCTGTGAACTTCAAGTTGCAGCTACAGTCATAGAAATCCTGCAAAAGACACCACCGTATAAATCACAGTCAGAGCTAGCGGGATCAAACACAAAACAGTCGACTGATGCAGAGAGTGAGCCATATTACCAAGTACTGGGGAGGCATGTCGACTTTCTAACTCAACATAAAGCAATGATGAAGCAAGATTTTGTTTTTCTTGAGACCTTTTTTGTCAACTTGGTTCCCTTTTTTGCCGGGAAAGACAAACAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33084
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 |
---|---|---|---|---|---|
ENSDART00000108630 | Nonsense | 634 | 954 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 6851566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 6674084 |
GRCz11 | 3 | 6559924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACACCACCGTATAAATCACAGTCAGAGCTAGCGGGATCAAACACAAAA[C/T]AGTCGACTGATGCAGAGAGTGAGCCATATTACCAAGTACTGGGGAGGCAT
Long Flanking Sequence:
AAGATATAATGAAAGAGACACCAGGGATGGAAGAAACTGTTCTTCTCAATGCAGTAAAGTGCTATAGAAAAGATGTAGCAATACCCCAGCTTCTCGCCAGGTACTATTACATTAAGAAACAAGACTTTAGTATGGCCAAGGATTGGGCAAAGAAAGCCAAAGACCTTTCAGGGGAGAACTCATACATGTGTGATACAGTATCACAGGTATATGTGAATGAGCTGAAATGTGCTTTTCGCGAAGATAAAGATGATCCCATCAGCCCAAACAGTCTTGATAGATATCTTACATTGGCTAAGACGGCAACAGAAGCTTGCAAAGAAACACAACAAACAGCAAACAAAGAAGCCATTACTCGACTGCAAAGACAAAAGGATTATACTACCTACAACACTGCTGGCCATTTCTGTGAACTTCAAGTTGCAGCTACAGTCATAGAAATCCTGCAAAAGACACCACCGTATAAATCACAGTCAGAGCTAGCGGGATCAAACACAAAA[C/T]AGTCGACTGATGCAGAGAGTGAGCCATATTACCAAGTACTGGGGAGGCATGTCGACTTTCTAACTCAACATAAAGCAATGATGAAGCAAGATTTTGTTTTTCTTGAGACCTTTTTTGTCAACTTGGTTCCCTTTTTTGCCGGGAAAGACAAACAAAAAGAGGCAATCAAGCACAAGGTTTGCAAATATTTTCAACAGTATACTGAAGTCTTCTGTAAAATCAATTGGAGTGAGCTACGTAACAAAGAGTTTATGAACCGACCAAATAAAATAGCTCAGATTCATGAATGTCTGGAGAAGAACAGGGGTGATACATATACTGGCCTTCTGGAATACTTGTATGAGGAAAATTCTTCATCAACTCTTGAAGAGATCATCCAGCAGTATCGTTTCTTTCTGGATCCCAAAACAGAGGACAGAGAAGTAATGGATACTATCAACTTTATTTATGCCAATGTAATTCTAGCCAACATCAAACCTAAATCTCAGTACATCATGCCC
Associated Phenotype:
Not determined