ZMP
stam
Ensembl ID:
ZFIN ID:
Description:
signal transducing adapter molecule 1 [Source:RefSeq peptide;Acc:NP_956414]
Human Orthologue:
STAM
Human Description:
signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 [Source:HGNC Symbol;Acc:11357]
Mouse Orthologue:
Stam
Mouse Description:
signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 Gene [Source:MGI Symbol;Acc:MGI:13
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11405 | Essential Splice Site | Available for shipment | Available now |
sa14697 | Essential Splice Site | Available for shipment | Available now |
sa31282 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11405
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 |
---|---|---|---|---|---|
ENSDART00000026966 | Essential Splice Site | 13 | 509 | 1 | 16 |
ENSDART00000141170 | Essential Splice Site | 13 | 516 | 1 | 14 |
The following transcripts of ENSDARG00000002127 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31153464)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31454524 |
GRCz11 | 2 | 31437742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTCGGCCATGCCTCTCTTCACGACAAATCCATTTGATCAAGATGTTG[G/T]TAAGTTTGAGCTGTCATGCATTTAGCGGTCGAGCTAACGGAGCTCWGCTG
Long Flanking Sequence:
AATGAAAAAAATCACAAATTTAGATTTTTAACCAAATAAACAAAACAAGAGGGGGTGAATGTAAATATAATCTCGTGACTGCTGAGTCAGAGAGCCTGTCGTACCATGTGATGATCAAGTCATATGATTTGTCACCGAACTGTCCTTAACTCCTATAAATCATTGTTTACACCACATGATTAATAAACCCCACCGTCCAAACACCAATCCTTTACCAGGGGAATCATATTTATTTGGCTATGCCCGTCTGTTTGTATGTTTAACTGTGCGGCGTGTGTATTACCCAGAATGCACCACTGCAGGGAGTGAGTGACTGAGTAGGGGATCCCGATTCCCGTCAGCGACACTGAGCGGAGTTTCTGTTCTATTATGTTTATTCATTCACTTTTAATCAAGTGCTGACAGGGAGAAGCACAAGAAGAGGATCGAGTTTAGGTTTGGTAGCGTGTATTTCTCGGCCATGCCTCTCTTCACGACAAATCCATTTGATCAAGATGTTG[G/T]TAAGTTTGAGCTGTCATGCATTTAGCGGTCGAGCTAACGGAGCTCTGCTGTGTCTATTGTTGTTCACGCCAACACACCGGCTTTATGTATCGCTTCAGTTTTACTTGAAATACTCGAGACATTGCCGTAATGGTGTTCCGGTGAATGAATAATCAACAATCGCGAATTTATCTTGAGGTTATTAACATGACAACACGCTCACAACTCGTGAGCTTAACATGTTATTAGCCTGATTGCTAGCCAAGTTTGTTGCCGAAGGAGCTGGGACTGTCGACTCGCTTTGTTTGTACGGCCCTGACAGCGCACTATTTGGTAAAAACACGTACTCACGGGTCATATTGTACGATTTAGGACATATTACTACTTTATTATATATATGTATCCAACACTCAAGCTAACGGTGCATACAGTGACGCTGCAAATGACCCCGCCTGCTCCTTTTATGTGTTATGAGCTGTGTATGCTCCTACAATATCCGCTATAGTAGGCTATTATTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14697
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026966 | Essential Splice Site | 14 | 509 | 1 | 16 |
ENSDART00000141170 | Essential Splice Site | 14 | 516 | 1 | 14 |
The following transcripts of ENSDARG00000002127 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31153465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31454525 |
GRCz11 | 2 | 31437743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCGGCCATGCCTCTCTTCACGACAAATCCATTTGATCAAGATGTTGK[T/A]AAGTTTGAGCTGTCATGCATTTAGCGGTCGAGCTAACGGAGCTCWGCTGT
Long Flanking Sequence:
ATGAAAAAAATCACAAATTTAGATTTTTAACCAAATAAACAAAACAAGAGGGGGTGAATGTAAATATAATCTCGTGACTGCTGAGTCAGAGAGCCTGTCGTACCATGTGATGATCAAGTCATATGATTTGTCACCGAACTGTCCTTAACTCCTATAAATCATTGTTTACACCACATGATTAATAAACCCCACCGTCCAAACACCAATCCTTTACCAGGGGAATCATATTTATTTGGCTATGCCCGTCTGTTTGTATGTTTAACTGTGCGGCGTGTGTATTACCCAGAATGCACCACTGCAGGGAGTGAGTGACTGAGTAGGGGATCCCGATTCCCGTCAGCGACACTGAGCGGAGTTTCTGTTCTATTATGTTTATTCATTCACTTTTAATCAAGTGCTGACAGGGAGAAGCACAAGAAGAGGATCGAGTTTAGGTTTGGTAGCGTGTATTTCTCGGCCATGCCTCTCTTCACGACAAATCCATTTGATCAAGATGTTGG[T/A]AAGTTTGAGCTGTCATGCATTTAGCGGTCGAGCTAACGGAGCTCTGCTGTGTCTATTGTTGTTCACGCCAACACACCGGCTTTATGTATCGCTTCAGTTTTACTTGAAATACTCGAGACATTGCCGTAATGGTGTTCCGGTGAATGAATAATCAACAATCGCGAATTTATCTTGAGGTTATTAACATGACAACACGCTCACAACTCGTGAGCTTAACATGTTATTAGCCTGATTGCTAGCCAAGTTTGTTGCCGAAGGAGCTGGGACTGTCGACTCGCTTTGTTTGTACGGCCCTGACAGCGCACTATTTGGTAAAAACACGTACTCACGGGTCATATTGTACGATTTAGGACATATTACTACTTTATTATATATATGTATCCAACACTCAAGCTAACGGTGCATACAGTGACGCTGCAAATGACCCCGCCTGCTCCTTTTATGTGTTATGAGCTGTGTATGCTCCTACAATATCCGCTATAGTAGGCTATTATTAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31282
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 |
---|---|---|---|---|---|
ENSDART00000026966 | Nonsense | 48 | 509 | 3 | 16 |
ENSDART00000141170 | Nonsense | 48 | 516 | 3 | 14 |
The following transcripts of ENSDARG00000002127 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31158651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31459711 |
GRCz11 | 2 | 31442929 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTGGTAAAATATTATTTGTTGTCTTCTGAAGGCCTAAAGAATGCCTG[C/T]GATCTATAATGAGGAGAGTGAATCACAAGGATCCCCATGTTGCCATGCAA
Long Flanking Sequence:
GTTAATAGTGAAATCAGATAATCATTACATCCCTACTATGGAGGCAGTCTACCTTTTAGAAAAGTGTTCAATAGTGGACAAGCTCAAAACATGTAAGCCCCTGTTTACACGTTTAGTATTTTCCACTTGTGAGTGGATTGACAAAAACTCATCTTAAAGCCAGCTGTATACATGGCCTCTAGTGTCAGTGATATGAAACAGAACCAGCAGCCTTTCACAAAAATAGATTAATTAATTTGCATATGCAATGTCTGAAAATGAATTGTCATTATGATGAATAGACATTTAAGTTAGCTTTTTTTTTTTTTTTTTTCAGAAAAAGCAACAAGTGAGATGAACACAGCTGAGGACTGGGGCCTCATTCTGGACATTTGTGACAAGATCGGACAGTCTCGCACTGGGTTAGTAAACAAGCATTTAGCATGTTTTTGAGCGTATCTTTTAAGTTAATGGGTGGTAAAATATTATTTGTTGTCTTCTGAAGGCCTAAAGAATGCCTG[C/T]GATCTATAATGAGGAGAGTGAATCACAAGGATCCCCATGTTGCCATGCAAGCGTTGACGGTAAGGCAAGCGACTGCTAATGCTAGTAAATGAGGAGGAAGCATGCTTTTATCTCAAGTATGCAAACATCAGAAGCCATTAATGAGCGGTTGAGACTGAAACAAGTGTTTTCTGTTCCACAGCTACTCGGTGCATGTGTGTCAAACTGTGGAAAGATATTCCATTTAGAGGTCTGCTCCAGGGAATTTGCTAGTGAAGTTAGCAATGTGCTAAATAAGGTATGTAGTTTAGTTTGTTGAGTATATGATGCAATGTTTTGTCCAGCAGTAGGCTGATGTCGAGGTACTTTCTTTTCAAGGGTCACCCAAAAGTATGTGAGAAGCTAAAGGCTTTGATGGTGGAATGGGCCGAGGATTTCCGCAACGACCCTCAGCTCAGCCTGATCTCTGCAATGATTAAGAACCTCCGAGAGCAGGGCGTCATCTTCCCTGCCGTGGGCTC
Associated Phenotype:
Not determined