ZMP
ENSDARG00000044796
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 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa3332 | Nonsense | F2 line generated | Not yet available |
sa34261 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38658 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12252 | Nonsense | Available for shipment | Available now |
sa16173 | Nonsense | Available for shipment | Available now |
sa21162 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa3332
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065841 | Nonsense | 95 | 1636 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 76802470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73578365 |
GRCz11 | 7 | 73801653 |
KASP Assay ID:
554-2674.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTATTGGTCAGAGAAAGAAGACCGASCATTTGTCAAACGGAATGGCTA[C/A]MACAGTTTGGTAGAGTTAATCAACAAAAACAAAAGGAAAATATGGAGTGT
Long Flanking Sequence:
AAAGGGCCAAATGATTATTGAGAGGAAATGTTCGGGGAGCTGCTGGAATTTTAGAGATGCTGAGATTTGAGGAGACTGAAGGATGCCGAAACAGCGGATACCAGAGCAATGCCATTTAAGTTGTGCTCCTGCAGTTGATGGAAAGGTAAGATGTTTTACACCTTATAGTTAAGCTTACATTTTGGGTCTCTTTTATTTTGTCTTATGCATTTTGAAATCCACAGATACACTCCATTAACACCAAATAACCAAAACGGTCCAGAGATGGAAGGTCTTACTATACCTTCATTTAAGGGTGGGACAATTCATATCTCACCCGAAGTCATAGAAACCCTTTCGCTTCTTGACATTGTGTGGTCCAATAAGTTCGAGAATGAGAACATTGATGCAGATGATGCCAAACAAAGAGAAGCTGATTTTCTGAAAGGAGCTCCACCCCAGTGGCTGCAGTTTTATTGGTCAGAGAAAGAAGACCGACCATTTGTCAAACGGAATGGCTA[C/A]AACAGTTTGGTAGAGTTAATCAACAAAAACAAAAGGAAAATATGGAGTGTCATCGACATGCATTTGTTTTACCAACCCGGGAGTGGAGGGTCAACCCTGGCGATGCAGGTTCTTTGGAAATTTCGTAAGGAATTCAGATGTGCCAGAGTTACAAACTCTTCTCTGGATGTCGCAGAGCTTTCAAAGCAAGTAGTCAAGTTTTTTATGGCGGGAGATGATCAGGATCAGAACACTGTGCTGCTTTTACTGGACATCAAGGAAAAGATGAATGAAGATCAGCCATTTAAGAGAATTCTACAGGACAGCCTGATCAAGGAAATCAACGGGCAGAACATCAAAGCAAACATTCCAGTTGTGATCATTTTAAACTGCAGCATAATGGACTTCACAAGAACAGATACACTGAGCCTTGAAGCAAACTTGACTGAAGGTGAAGAAATAAAACTAAGGGAGAAGCACAACGAAGTCACTACGAAGCACAAGGAGCATGAACGATTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34261
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065841 | Nonsense | 806 | 1636 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 76804603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73580408 |
GRCz11 | 7 | 73803572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTATCATAAAGATGCCTTCTATCCGCAGGCTCTAGCACGGTTCTACTA[T/G]ATCAAATTTGCAGATTACACAAGGGCTGAAAGGTTTGCAAAAAATGCCAT
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGAATTCTTTGCAAGTCAAGGTTCTCATGCAGGTGACACAATCACACACATAATGACTCCCTTCATGGATCTTTTGGTGATATACAGTGCAGAGCACTGTGAGGACAAATGTGTCCGCATTGCACACCCTATGATTGCTGATGCATGCATCCACAAGCTGTTCACCTTGTCTATACCAAGAGGTGAAATAACACACAACTTTTTGTACTTCATAGTGAAAGCGTTAAAGAAGCATGCTGACTTTCTGCACATTTGCAAAGACATTCTGATCACCAGACAGAAAGGAGATCAAGAGCATGACAAGTTTTCAAAACTCATTCTGGACATCATGGAGGAAGACCTCTATACAAACTCTGCGAACTGCATATCTGTGTTAGAGTTTGCCTCTAATCTCTATCATAAAGATGCCTTCTATCCGCAGGCTCTAGCACGGTTCTACTA[T/G]ATCAAATTTGCAGATTACACAAGGGCTGAAAGGTTTGCAAAAAATGCCATTCTAAGAGATCCAAATAATTCTTTTATGAGAGACACACTTGGACAAGTGTACAAAAACAGACTGAGGAAGACCGTCAAGGACAAAATGTCTCCGAATTATTCTCGCAGAGTCTTGGAGAATGCCGTTTCTGCTGTTAAAGCATTCAAAGAGGAGACAAAGACAGCTGAAGAGGAGCAGAAATCCGATGTCAGGGACAGCAATGCTCCTAGCACCTTTAATATCAGGGGTATATTTGGTTTCATCCAAGTTCTCAAGATTCTCTTCGATGCCCTCACACATCACAGTTCAGAGTGGGCAGACTTTCTAAGAGGGAAAACATCTATCACGTCTCTTGGCACTTCATTTAGAGACCAAAAGCTGAAAAGATACAATGATTTCCTCAGCAGCCTCAAAGAAGAAATCAAAGAGAAATTTCATGTTTTTCAGTATTACCTCACGTACTCAAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38658
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 |
---|---|---|---|---|---|
ENSDART00000065841 | Nonsense | 1096 | 1636 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 76805472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73581277 |
GRCz11 | 7 | 73804441 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCAAGAAAGAAAGGGAAGAAGCCCGGAGTTTTATCTGTTGGTCCTTT[T/A]GTTGTTTTGGCCTGGAGATGATCAACAGAGTACACCAAACTCGCCAAACC
Long Flanking Sequence:
ATCTATCACGTCTCTTGGCACTTCATTTAGAGACCAAAAGCTGAAAAGATACAATGATTTCCTCAGCAGCCTCAAAGAAGAAATCAAAGAGAAATTTCATGTTTTTCAGTATTACCTCACGTACTCAAAGCCAAGCATTGACAGAGAGGAACCGCCATACTTTTACCGAGATGTTGAAGATTGCTTCAAGAAATATGTGATTCAACAGGAAAAGGCTGCTCAAAGTAAACTGAGAATGCTTGAAATAAAAAAGGCAGATACATTTCCAGGGTTGTTGAACCTCTTAGATCAAGACACAGCTGTGACAGAGTTAGAGGAGATTCTCAGTCTAATTAATGTTAATGACAGCCAAATTTACATTCTTGCCAACATTATTTTGTGCAACAAGTCTCCCACATCTCAGTCTCTCGAGTCAAAACGAGAGCTTCAGTACATGATGTGGAGAGACTGGCAGCAAGAAAGAAAGGGAAGAAGCCCGGAGTTTTATCTGTTGGTCCTTT[T/A]GTTGTTTTGGCCTGGAGATGATCAACAGAGTACACCAAACTCGCCAAACCTTGCAGAGTGTGTAATATATATGCACCAAGCCTTTGAGAGGACCTACAGACTGCACCTTCGCTCACGTTACCTGGTGCCCCTCTTTTTCCTTGGAAAAGGTGATCATTTGCAGAGAGTTGTGCATAGATCAAACATAGAGCAAAATCAAATGGACGCCCTGACCAAAGGGGATGAGAAAGCTGAAATCCAGGACCTTCAACGAGTCCAAGGGGAGGTTAGAGACCACAAGGTGTTTGCTCTGAGGGGAACAGTCCAGATTGAAGTAACTCCTCACCATCCAGCCAGCGTACGTGGCCAAAGCCTTGTTTCATTTTATCTGGGCTTTAACATCAGAGGGCCCGTAGCTTACAACATCAGACGTGAGTAATAATTGAGATGCATGCATTGCATCAGACTCTGTATTTCATTTTAACATCAGATGATCCTACTTTATATTAAATGGCCTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12252
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065841 | Nonsense | 1101 | 1636 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 76805486)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73581291 |
GRCz11 | 7 | 73804455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGAAGAAGCCCGGAGTTTTATCTGTTGGTCCTTTTGTTGTTTTGGCCT[G/T]GAGATGATCAACAGAGTACACCAAACTCRCCAAACCTWGCAGAGTGTGTA
Long Flanking Sequence:
TTGGCACTTCATTTAGAGACCAAAAGCTGAAAAGATACAATGATTTCCTCAGCAGCCTCAAAGAAGAAATCAAAGAGAAATTTCATGTTTTTCAGTATTACCTCACGTACTCAAAGCCAAGCATTGACAGAGAGGAACCGCCATACTTTTACCGAGATGTTGAAGATTGCTTCAAGAAATATGTGATTCAACAGGAAAAGGCTGCTCAAAGTAAACTGAGAATGCTTGAAATAAAAAAGGCAGATACATTTCCAGGGTTGTTGAACCTCTTAGATCAAGACACAGCTGTGACAGAGTTAGAGGAGATTCTCAGTCTAATTAATGTTAATGACAGCCAAATTTACATTCTTGCCAACATTATTTTGTGCAACAAGTCTCCCACATCTCAGTCTCTCGAGTCAAAACGAGAGCTTCAGTACATGATGTGGAGAGACTGGCAGCAAGAAAGAAAGGGAAGAAGCCCGGAGTTTTATCTGTTGGTCCTTTTGTTGTTTTGGCCT[G/T]GAGATGATCAACAGAGTACACCAAACTCGCCAAACCTTGCAGAGTGTGTAATATATATGCACCAAGCCTTTGAGAGGACCTACAGACTGCACCTTCGCTCACGTTACCTGGTGCCCCTCTTTTTCCTTGGAAAAGGTGATCATTTGCAGAGAGTTGTGCATAGATCAAACATAGAGCAAAATCAAATGGACGCCCTGACCAAAGGGGATGAGAAAGCTGAAATCCAGGACCTTCAACGAGTCCAAGGGGAGGTTAGAGACCACAAGGTGTTTGCTCTGAGGGGAACAGTCCAGATTGAAGTAACTCCTCACCATCCAGCCAGCGTACGTGGCCAAAGCCTTGTTTCATTTTATCTGGGCTTTAACATCAGAGGGCCCGTAGCTTACAACATCAGACGTGAGTAATAATTGAGATGCATGCATTGCATCAGACTCTGTATTTCATTTTAACATCAGATGATCCTACTTTATATTAAATGGCCTTAATGACTAGGTAGGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16173
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065841 | Nonsense | 1444 | 1636 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 76808805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73584610 |
GRCz11 | 7 | 73807774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGCTATTTTAAAGCCSGGACCGGAATGYTCGCTTCAGATGAAGACTTG[G/A]TTTTTAATGYGGACGCTGGAGAAAATGAGGAAATCTGCTTGTCATTCTGR
Long Flanking Sequence:
TCTGGAAGATCCATTTTACTATTTCAATGAATGACCCATTTAAGTTTAAATTGACTCAATACTGCATGATTATCATCAGCACATTTACCACAAATGCAGGTGGACCTCCAGTCGGCGTGAGAATTCTCCACGTTGAAGACAGTGGAGTTTCATTCGAGAAATGCAAGTTAACCAGGTTCCACGCCAAACTTCTGGACCACACGTTTTCCCCTAAAGGTCTTCTTATGAAAAGTGGACGCTCTGTGAACTATCATTGTGAAACGCTGATCTACCAAACTCTCAAATCTCACCTGACTCTTCACGTGTACTTGATTCCAAGCGATAAAAAAATGATAGAGGTAAGAATTTAATAATAACACCAAAGATCAGATAACTGCTTTTCAACTATCTGTGCTCCAGAGTACTTCAATTTATTTCCTCCAGGCTGTTAAAGAAAATGAGACTGAGAGCAAGGCTATTTTAAAGCCGGGACCGGAATGCTCGCTTCAGATGAAGACTTG[G/A]TTTTTAATGCGGACGCTGGAGAAAATGAGGAAATCTGCTTGTCATTCTGAAGTCCTACCCGAGGTAATTGAATACGCCTATGTGAGTTATAGTTGTGCAAGCAGTGTGGTTTATTAGCTTCAATTGTGTTTCTCCAGAGATCACATTTGTCAGTCTCAAGGGGGTTGTTTAACTGATTTAATCTGGAAGATGCAAGGTATCGCTGCAGCCTGGAGACCTCCAAGTTGGAGGGATAATGCCACAAGTAGATTGGGTGACCTCCAAGTGGATTGCAGATTGCAATTTGGCACTTCTGTATGATTTTTTGGATCCCAACAAGCATTTTTGTGTTTAAAAGACAACTAATAGATGTCATTTCAAGAGTTAGCTGATGATTGATTATAAAGCTTGTTTGGCATGCTGTTCCGGGAGAGCATCCTCAATCCCAGGGCTCCCTCCTGTTTGCAAGGCAAGAGGGGAGTTTGAGCTCAGGTGAATCTGGAGAACTCCCCTGCTGTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21162
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065841 | Nonsense | 1539 | 1636 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 76811571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73587376 |
GRCz11 | 7 | 73810540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTTATGTGTTTGTTTGTTTGCAGATGAAAGCAGAGATTTCCCCAGTT[C/A]AAGCGGTAGGTCTCTAGCACTTATTCACAACAAAAGACTTCGTCTTGGCC
Long Flanking Sequence:
AATTCTGATGTTTCTGTTTCTCCCTTTTCAGCTGACTATAGTCAGAGTACTTCTTCAGTCGGTATGTGACAATATTGTTTTAACAGTGATCCAAGCATATGACCAGTAAACAATGCCCATTTTATCTGATCTCTAACCAATTTGCTGCTTTTGCAGATGCTCGCAAAGAATCTTATTGCTCAAATGGTGAGAATTATACTGTGCTGTAATTGTGATTATTAGTGTAGGATTTAAATGGCAACATTGCATAGTTTTTATATGCAAATGTTTTGTTTACATAAACATTATATAAGTATGAAAATGATGAAATTGGATACACTGCTCTGCTGAATTAGGTTTCACTTTGGGTTTTGTCTTGTGTTTGAAATATGTAAAAGCATTTCTGAAAAGAATAATACATTATGTTGAGGTTCTGAACTGTGGGCTGTTTTTATATAGTGATTAATGCTGATGTTTATGTGTTTGTTTGTTTGCAGATGAAAGCAGAGATTTCCCCAGTT[C/A]AAGCGGTAGGTCTCTAGCACTTATTCACAACAAAAGACTTCGTCTTGGCCCCATAATTTAATTTATTTGAATGTTCTTCTTACTTAATCACTGAAAGAGATTTGCAATAATTACATATGATCAGTGCAGCTGGAGTAGCAAACAAGCAGCAGGGAATGCTGGGAATTCTTTTGAGCAAACATCTTAGTTTTCATATTTCACTTTTGAAGCTACTTTAGACCTGTGCTAATTCCGAATATTAATAAATCAATTCAATGTATTGAATTCTTACAATTAAATGAATTCAATGTACACGTTTAAGACAATTTACAGAAAGGGAAATGAGTATCAGAATGAGGAAGAAATGCCCCAGCAGGCACACAACATCCAAGTATAAGGTTAGAATTAGGTCGGGGTGGCACAGTGGCACAGTTGGTAGCGCTCTCATCCCATAGCAAGAAGGTTGCTGGTTCGAATTCCGGCTGGGTCAGTTGACGTTTCTGTGGTGAGTTTGCATGTTC
Associated Phenotype:
Not determined