ZMP
stap2b
Ensembl ID:
ZFIN ID:
Description:
signal transducing adaptor family member 2b [Source:RefSeq peptide;Acc:NP_998474]
Human Orthologue:
STAP2
Human Description:
signal transducing adaptor family member 2 [Source:HGNC Symbol;Acc:30430]
Mouse Orthologue:
Stap2
Mouse Description:
signal transducing adaptor family member 2 Gene [Source:MGI Symbol;Acc:MGI:2147039]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31642 | Essential Splice Site | Available for shipment | Available now |
sa13852 | Nonsense | Available for shipment | Available now |
sa15784 | Nonsense | Available for shipment | Available now |
sa34366 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7128 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38682 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31642
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100516 | Essential Splice Site | 56 | 410 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 19189019)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18633907 |
GRCz11 | 8 | 18664572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGACAAGACAAGATTATTTATACATCAACTGTTTGCTTATGAATACA[G/A]TATATTGAGAAGCTGGAGCTGTCAGATCTCAACTCAGTGTCGGATGATGG
Long Flanking Sequence:
TTTCAGAATCTAATTTAATTGGAACTTGATTGGAAAATGAACATGAAACAAAATCAAGCCTCTGGGTTATGTCTTGTTTCAAAGTGTTCTTAATGAAGAGGGAAAAATTCCTTTGTTTTCGTCATTCCTTTCTTTCTGTCAAACTGGTTTGGTCGTTACTCGTGTATGTTTTATAAACAAACAGAAAACGTATGCTGTTGAGAAACCACATATCCAGATCACATTTAAATGCAAAATGCAATTTCTCTTTGTACAGATGGGTCGTAAACTCTGGACCAGTTTGTGTGGAGATTCACTTTTTTTCTTCAATAGCAGCAAAGACAGTGTGGTAAGTGTATTTTACAAGCTGCATCTTCTATTTAAGACATTGTAAGCCATAACGTTTTCAGTTTATGTGTATTTCTTAATAACATGTTAAATTGCATGGTTAAAATCTGTTTGCTTATGTATGTTTGACAAGACAAGATTATTTATACATCAACTGTTTGCTTATGAATACA[G/A]TATATTGAGAAGCTGGAGCTGTCAGATCTCAACTCAGTGTCGGATGATGGCTCTCGTGAGCGAAACCTGGATGCTGCTGGTTTCACCCTGCACATGAAAAAAGAAGACGTCAGGATGATTGTATGGCTTTTGTCATTTTTTATCCTTTTGTATAAATCAAACTTCTTGCAGTTGATTAATATTGAGTTATTTTTAAATTGGTAACACTCACCCAATGTCATGCACTTTTTTCAGGCTCCCAGTCTTGAAGCCAGAGAGCTGTGGAAAGGCTACATGCTCTCAATTGCTAAGGTTGGTTGTGCTTTTAAAAATATCCTGTCCTGATCAATATCTGATATACAGAGGGTAAAATCAGATATCACTGTTTTTCACTATAAATTCATATCTAAAGGCACTGTTGACTTGAAACCTTCACCAGATACTGGTAACAAACAAATAACGCAAAACTTATGCCTAATTTACACTAGCAGTGACTTTGTAGCCGCCTGTCGCTTTATGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13852
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 |
---|---|---|---|---|---|
ENSDART00000100516 | Nonsense | 141 | 410 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 19187477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18632365 |
GRCz11 | 8 | 18663030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCTGGACAGATTCACGCAATGAAGGAAGTCATCGAAAAAGAGAAAACA[C/T]GACAACGGCTTCCTTCAGCTTCACCGCCAGAGCAGAACTTTGACCCCTAW
Long Flanking Sequence:
ATAGAAAATAAGAACTAGGATCAGAGTTTATAGAAGGAACCCACAGAATCTTACAAAATATTAATTCATTTTCAGTTATTTAATAATTTTTAACACATAACAACATAATTTATGAAATTGTTTGTTCAGTTATTAGGTTGTTGTTTTGTTACCCATTGTACAATGATATCTGAAATCTATATATATATGTATATGTTGAATGTTCTTCAAGTTTATTTGCAGTTAAACCCACATTGCTGAATAATAACCTTGTTTTATTATTAAATAAAGATAACAGTTTGAGTGGTCATTTTTTATACGTGTCTTATTCATCATCTCTTTATTATGGATCTCCAAGTTATTGATTACCCAATGAGAATGTTTTTCACTTGATTTAATCTTCGTAAGCATGTTAGATAATTCTCACTGTTTGTGTCTCTCAGCTCTCTGTGCCAGTGTCTCTGAACCTGCTGCCTGGACAGATTCACGCAATGAAGGAAGTCATCGAAAAAGAGAAAACA[C/T]GACAACGGCTTCCTTCAGCTTCACCGCCAGAGCAGAACTTTGACCCCTATGTTTGCGTATTACCGGACATGCCTATGTAAGTTAAAACGACTTGATTTAATAGCGTAATGTTGAAGCTGACTTGACTTTTTTTGGTGTTAAAATGCTTTACACAACATGAGCTCAAAGATGCATGTTTTTAAGAAAGTGTGTATGTGTGAAAATGTGTGTAACTAAAATTTAGAATACAGCTTAATGATGGCTCTTTCTTTTAAGCTGTTATTAAAAGGATAATTTACCCAAAATATGAAGATTTCCGGGTGATGCGGTGGGGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTTGGCTGGGTTAGTTGGCATTTCTGTGTGGAGTTTTTTATGTTCTCCCCGCGTTTGCGTGGGTTTCCTCCAGGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCAGTACAGGTGAATTGGGTAGGCTAAAATTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15784
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 |
---|---|---|---|---|---|
ENSDART00000100516 | Nonsense | 157 | 410 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 19187427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18632315 |
GRCz11 | 8 | 18662980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGACAACGGCTTCCTTCAGCTTCACCGCCAGAGCAGAACTTTGACCCCTA[T/A]GTTTGCGTATTACCGGACATGCCTATGTAAGTTRAAACGACYTGATTTAA
Long Flanking Sequence:
TTACAAAATATTAATTCATTTTCAGTTATTTAATAATTTTTAACACATAACAACATAATTTATGAAATTGTTTGTTCAGTTATTAGGTTGTTGTTTTGTTACCCATTGTACAATGATATCTGAAATCTATATATATATGTATATGTTGAATGTTCTTCAAGTTTATTTGCAGTTAAACCCACATTGCTGAATAATAACCTTGTTTTATTATTAAATAAAGATAACAGTTTGAGTGGTCATTTTTTATACGTGTCTTATTCATCATCTCTTTATTATGGATCTCCAAGTTATTGATTACCCAATGAGAATGTTTTTCACTTGATTTAATCTTCGTAAGCATGTTAGATAATTCTCACTGTTTGTGTCTCTCAGCTCTCTGTGCCAGTGTCTCTGAACCTGCTGCCTGGACAGATTCACGCAATGAAGGAAGTCATCGAAAAAGAGAAAACACGACAACGGCTTCCTTCAGCTTCACCGCCAGAGCAGAACTTTGACCCCTA[T/A]GTTTGCGTATTACCGGACATGCCTATGTAAGTTAAAACGACTTGATTTAATAGCGTAATGTTGAAGCTGACTTGACTTTTTTTGGTGTTAAAATGCTTTACACAACATGAGCTCAAAGATGCATGTTTTTAAGAAAGTGTGTATGTGTGAAAATGTGTGTAACTAAAATTTAGAATACAGCTTAATGATGGCTCTTTCTTTTAAGCTGTTATTAAAAGGATAATTTACCCAAAATATGAAGATTTCCGGGTGATGCGGTGGGGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTTGGCTGGGTTAGTTGGCATTTCTGTGTGGAGTTTTTTATGTTCTCCCCGCGTTTGCGTGGGTTTCCTCCAGGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCAGTACAGGTGAATTGGGTAGGCTAAAATTGTCTGTAGTGTACGAGTGTGAATGAGTGTGTATGTATGTTTCCCAGCGATGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34366
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100516 | Essential Splice Site | 166 | 410 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 19185152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18630040 |
GRCz11 | 8 | 18660705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCATGCCTGTTATGTAATAATACAATAATAATGATGCATATTTAACA[G/T]GTGTTTTCATAAAGTGTCTCGTGTGGAAGCTGAAATTTTGTTGGAAAGGA
Long Flanking Sequence:
TGATCACAAGTGGTCAGCTGAGAGTTTACATTGCTTTTGTTTAGCGTGACCATCCACTGAATGAACAATCCCATGTTGCATGTTTTGTGAGTGGTAAAGCATGTGAATGAAAGGGATGTGAATAGCAACTATGATTTTGATTGCAGTCTGCATTTTTTTTTTTTTTTGTAAAATGCACCAAAGTACAAACCCTTATTTTGGTGTTTCTAACAACATACAACATAAAGGTCAGATCAATAGACTGAGAGTGCATTTGAGAGTGTTTACACTACACAAGCAATCCAAAAAAGACATTTTCAATATGAACTCATTTCAGACCCTGTTTACACCTGCATTTACTCTCATGATCAGATTTAAAAAAACAATGTAAATGAGATTAAAATGGTTTAATACATTTCATGTAAATCCAAACACCACTTTTGTTTTTTTGTTTTTCATGTACATCTAAATAAGCCATGCCTGTTATGTAATAATACAATAATAATGATGCATATTTAACA[G/T]GTGTTTTCATAAAGTGTCTCGTGTGGAAGCTGAAATTTTGTTGGAAAGGAATCCTAATGATGGAAACCTTCTGCTGCGGCCGGCTCAAGATCTTTCTCTTTCGTCGTTCTCTCTCACCACTCGGCAAGAAGTTAATGGGTAAAACACACTCTTTCATCTCTACTCAATACAGAATCATGTTGAATACATACGCTGGACAGCCAGCTTCCAAATGCATTATCTGATGCACTGAAGAACTTAATTTATTGCTATTTATCTTCTGAATTGCTCCCTGTAATTCAATAGTTTTGAACCTTAGACCTTGATCTGCACAATATGACATGTTACACAATCACATCTTCTGGGAATTTCTGCTTAATATAGTTGTGCTGGTTAAGAACGTATATATCCTGAAGAATCTTTTTGTTGCTTTCAGCAAATCAATATTTAAGCATTATCGAGTTTTTCGGAGGCCTGAAGGAGGATTCGTCATCAATCTCGACTCACCTGTGAGTAATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7128
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 |
---|---|---|---|---|---|
ENSDART00000100516 | Nonsense | 266 | 410 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 19181607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18626495 |
GRCz11 | 8 | 18657160 |
KASP Assay ID:
554-4395.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGAGAAGACCRGTGGGGTTYTGGTGCCTTTCCATATGGAGAAACACTA[T/A]GATCAAGTTCTAGGTACGACTGTTTTGTATTTACTGTAAAGCAAATAAGG
Long Flanking Sequence:
AGTGCTTTAAAAGCTTAACTAGGTTAATCATTGGAGAAAAGTGTTTGTTCTGCAGCTAATTTAAAAACGTCTTAAGGGGGGCAATAATATTGAACCCTTAAAATAAGTGTTAAAACTGAAAAATAAAACTGCATTTACTGCAGCTTAACTAGAAGAAATAAGACTTTTAGAAAAAAATGTTAGGAAATGCTGTGAAACATGTCTTTGCTGTATTAAAAATCACGTTCACTTACAATTTCACCTAAGGGCTTATAATATTGCCTTTAACTGTACTCCATGCTTTGCCTTGGTGTGTATTTATTGTGCAGTCTTCACCACTGATGAAACATATACCACTGCTAGCTGATCCCAGCCATTGATTCCTTTACTATGGCATTGTGTACTGATCACACACTGTTCTCAAACACACAGATCAACTGTGCCACCCTGCACGATGTGGTTAACAGTATGGTGGAGAAGACCGGTGGGGTTTTGGTGCCTTTCCATATGGAGAAACACTA[T/A]GATCAAGTTCTAGGTACGACTGTTTTGTATTTACTGTAAAGCAAATAAGGAAAATCCTGTTTGTCAGCCACACTGGCATACTTGTTGGTATGAATTAATCATCTGGAAAATGTTTACTATAATGAATGACCTAATGACATGAAAGTTATGAAACAAACCTTCATACAGTAAATCACTCCTTAGACATTCCATCTGGCTGACGGAATAAAAAAGCTTGACTGTTTTGTTTTTTTTGACTGACATTTAAGCTAAAATGGCAAGCAGAAACTTGTTTGATAGCTGAAGCAGCTATTTCACTGTGAACACAGTTTCTTAACATAACAAAACTGAAAAGTAGTTTGTTTGGTTGCGTGAACTAATACTTGTCATTCCATTCTGGTCGAAGCTGGTAGTTTTAGTTCTCAGTTTTTTAGACTTAATGAATACCTGCTTTTTTGGAATTGATTTTAAAGTCAAATGATTTACAATTTAAACACACACATAGGTTTGGTTCTGCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38682
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100516 | Essential Splice Site | 303 | 410 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 8 (position 19178813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18623701 |
GRCz11 | 8 | 18654368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAAACCAGACGCTTCATCTACACCTCCAGTGCCCCCACCCAAACCTGG[T/G]AACACATCATCCTCATAGGCACACACACTGTTAATCAACGTATCTACCGT
Long Flanking Sequence:
CAACTTCAAAATTCAACAGAGCAGAGATTAACATGCCATAATGCAATTCACAACTGTAAATAAACAGAAAACACTTGTAAACTCTCAAATAGCAAATATTTTTTACAGTGTAGTCGTTTAAAGAATTGTGGCAAACTCTAAAGATTTAAAATGACGTTTAATTAATATTTGCAAACTGAAATGTGATCCAAATAATCCTCGTTCTAAACAGACTCTTTATTAGTACAGTATGTTTGCTAATGCTACACTGACAGACATTTGTGCTTGTCTTCTGTTAATCGTTATAAAAATGTAGTCAGTATTTCTGGTCAGAAAAAGAATAAACGGGAGACTTTTTAATTTTGTATTTAATTCTAAATCTTTTAACAGCAGTAAACCTGATTGTTATTGTCTTCTCTCTCAGTATATGTTGAGAAAAATGAAGAAAACGGTGAGCTGAGCACACACTGTGCCAAACCAGACGCTTCATCTACACCTCCAGTGCCCCCACCCAAACCTGG[T/G]AACACATCATCCTCATAGGCACACACACTGTTAATCAACGTATCTACCGTTTCAAACAGTGGATTAGCTTTAATAAGTGTCTAACTTAAACTGACAGCTCGACCTATAAAAGTTAGTATGAATAACTCTTTTTTTTTTTTCATTTGCATGTTTAGTCACAAAGGCTCAAAGGTCCAGTTCAGAAAATGAATACCGCAATATCCCACGTAAGTCATCATCCGGCAACTCTCTGTCTTCAGCTTCTTTTAGCGCTGCAACTGCTTCACTTTGAGGACTTGTATTTAATGTTGCTGTTTTGTTGTGTGTTATTTGATTTGCAGGTGGAGGAGACTATGAGCAGGATGAAGCTGCATCTCCTGCACCTCCAGTTCAACCACGTGTTCCAGGTGACACAAAAAGTAGATCAATAATGCCCTATATGTTCTCGCATGATTTTCCCCTAAAGTGAAAGTTCACCCAAAAATGAATATGTTCTCATTATTTACTCATTCTCTGGCTGT
Associated Phenotype:
Not determined