ZMP
si:ch211-241o7.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
SH3BP2
Human Description:
SH3-domain binding protein 2 [Source:HGNC Symbol;Acc:10825]
Mouse Orthologue:
Sh3bp2
Mouse Description:
SH3-domain binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1346349]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9540 | Nonsense | Available for shipment | Available now |
sa34863 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21687 | Essential Splice Site | Available for shipment | Available now |
sa14545 | Nonsense | Available for shipment | Available now |
sa21688 | Nonsense | Available for shipment | Available now |
sa11802 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9540
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 |
---|---|---|---|---|---|
ENSDART00000065012 | Nonsense | 127 | 532 | 4 | 13 |
ENSDART00000137932 | Nonsense | 108 | 494 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 15258321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15271628 |
GRCz11 | 10 | 15229747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGTTTTCCCTTTTAAGATCGTYCACTTCAGTAAGAGACACAGAACATG[G/A]TATTTCTCAGCTGCGAGTGAAGATGAGAGAAAGGTSAGRTTCTGCTGAAT
Long Flanking Sequence:
CTATTGGCAAAGAAATGGTACATTTGCACAAAGCGGTTTGTTCAAATTAATAAACTGTAATACAAAGGATTTGGTGATTGATAATGGTAGTGAAGCCTGACCCTGAAGCACCACTAGCCATCATAAATGTAAAAAGGTTTATCACAGTATTACAGAATTTCACGGTATTACAGAATTTACTGTAAAGTTGTTATTTTTACTTTAATAAATTACAAAACTTTTATTTCTTTGGGCATGTTGGGGGTCTTAGGTGTTTCTTTAATGCACTTTGCACACATTTTGGTAGTCAATAAGTAAATGTTCATGCATCTTTCTTCAATAAAAGTAATAATTTATGTTTACTTTATATATTTTCCAAATGTAAACTTTGGGTTCTGCTAATTCAGCTTCTCGATATTGTTTTTATTGTCTTTCAGAGTCTTGCGAGCAGCAGAAGAAACAACATCAAGCAATGTTTTCCCTTTTAAGATCGTTCACTTCAGTAAGAGACACAGAACATG[G/A]TATTTCTCAGCTGCGAGTGAAGATGAGAGAAAGGTGAGGTTCTGCTGAATGCATTTCAGATCTGCATTTGCTTTGTTTTTTGTGAATATTTAATTTTAAAAAATCATTAATATTAAATTTTATGTGCATGTTTTTTTTTCTCTGACAGGAATGGATGCGGCACTTAAGAAGAGAAATCAACTATTATAATGATAAAAAAGACATCCCACTTCCAAGGTACAATGTACTGTGCCATTTGCTCACATAGTGTTCAAAAAATCTGTTACATTTACGGTAATGTTTATGGGTAACACTTTATAATAATTACACACTATAAATCATCTATTAAGCATTAGCAAATAGTGAATTCATTATCAGTTAAGCATTAACTCTACATTAATAAGCGTCAGTAAGCAGTTTATAACTGCAGCTACAAATGCTGTATTCTTGTCTTATAAGCACCTACATAATGTGTTCAATAATTGTATTTTCATACTTAGTTAATGATTTGTTTTTCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34863
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 |
---|---|---|---|---|---|
ENSDART00000065012 | Nonsense | 172 | 532 | 6 | 13 |
ENSDART00000137932 | Nonsense | 153 | 494 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 15260748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15274055 |
GRCz11 | 10 | 15232174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCTTGTGTTTTTCATAGTGATGATTTGGATGCGGAGTCGTTATATGGA[C/T]AGCTGGAGGAAACGGTGGAAATCAGGCCTGTTGAAGAAGATCCTGAAGAA
Long Flanking Sequence:
TCCAACACAATCTCACGGCAATTTGTAACTTTTTGATTTAGTGGCTAATTCGTATGAATTCGTACAATCTAATTCGTACAATTTTGTACGACTTGCTCATCCCCCTAATGATGGTTGGATTTAGGGGTGGGGTTAGGTGCCATGCCTCCTTTTTAAAATTGTACAATTTCGTATGACTGAACTCGTATGAATTCGTATAAATTAGCCACTAAACTAGCAAAACGTAAAATACTTACGTTTTCTTGTGAGATCAGGCTGTATAATTCAGATCTACTGTATGCATGGTTTATTATTTGACCTAATAGATTAGGGTTACTTATCTGATTTTTACCTCTCAGTCAAACTTTTCTCAGCAATTTGTCACATGCCATCTGTCATCTCTTCCTCTTTCTTGCGAGCACTGCTTGTTTATGTATTTCTTCATCTGAAATGTTTATCTTTTCTCTGGAACGTCTTGTGTTTTTCATAGTGATGATTTGGATGCGGAGTCGTTATATGGA[C/T]AGCTGGAGGAAACGGTGGAAATCAGGCCTGTTGAAGAAGATCCTGAAGAAGGTGTGCAGCATTTTACTTTATAATAATTGCACTTTAAACAATATTCTCATGTTACAAGTTACATAATAAAATGTAGTTTCAATGTAATACAATTATAATATTATATGTAAACGATCGTTCACCAAAAGATATACATTTACCAAAATTTACTCACATTTTTTGAGAGTGCTCTCTTCTGTTGAACACAAAGCAAGAATTCCTGAAGAATTTTAGAAAAAGCAGCCATTGACATTCACAGTAGGAACAAAACAATACTATGGCAGTTTTCTAGCATCATTATTCAGTATGTCCTTTGTGTGTGTTAAACACAATTAAGAAACTCCAAATAGGATTTTCATTTTTTGGGTGAACCCTTCTTTTGTCTATGTATTTATATATATATATATATTATTACACAGAGTTACACAGGCAACTGCTAACGGTGACTGTCTAGTGCCAAAGTGTAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21687
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 |
---|---|---|---|---|---|
ENSDART00000065012 | Essential Splice Site | 188 | 532 | 6 | 13 |
ENSDART00000137932 | Essential Splice Site | 169 | 494 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 15260800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15274107 |
GRCz11 | 10 | 15232226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGAGGAAACGGTGGAAATCAGGCCTGTTGAAGAAGATCCTGAAGAAG[G/T]TGTGCAGCATTTTACTTTATAATAATTGCACTTTAAACAATATTCTCATG
Long Flanking Sequence:
TATGAATTCGTACAATCTAATTCGTACAATTTTGTACGACTTGCTCATCCCCCTAATGATGGTTGGATTTAGGGGTGGGGTTAGGTGCCATGCCTCCTTTTTAAAATTGTACAATTTCGTATGACTGAACTCGTATGAATTCGTATAAATTAGCCACTAAACTAGCAAAACGTAAAATACTTACGTTTTCTTGTGAGATCAGGCTGTATAATTCAGATCTACTGTATGCATGGTTTATTATTTGACCTAATAGATTAGGGTTACTTATCTGATTTTTACCTCTCAGTCAAACTTTTCTCAGCAATTTGTCACATGCCATCTGTCATCTCTTCCTCTTTCTTGCGAGCACTGCTTGTTTATGTATTTCTTCATCTGAAATGTTTATCTTTTCTCTGGAACGTCTTGTGTTTTTCATAGTGATGATTTGGATGCGGAGTCGTTATATGGACAGCTGGAGGAAACGGTGGAAATCAGGCCTGTTGAAGAAGATCCTGAAGAAG[G/T]TGTGCAGCATTTTACTTTATAATAATTGCACTTTAAACAATATTCTCATGTTACAAGTTACATAATAAAATGTAGTTTCAATGTAATACAATTATAATATTATATGTAAACGATCGTTCACCAAAAGATATACATTTACCAAAATTTACTCACATTTTTTGAGAGTGCTCTCTTCTGTTGAACACAAAGCAAGAATTCCTGAAGAATTTTAGAAAAAGCAGCCATTGACATTCACAGTAGGAACAAAACAATACTATGGCAGTTTTCTAGCATCATTATTCAGTATGTCCTTTGTGTGTGTTAAACACAATTAAGAAACTCCAAATAGGATTTTCATTTTTTGGGTGAACCCTTCTTTTGTCTATGTATTTATATATATATATATATTATTACACAGAGTTACACAGGCAACTGCTAACGGTGACTGTCTAGTGCCAAAGTGTAAGACCTCGTTTGGTCAATCAGTCTTCTCTGTAAAGGGAGCCAAACTGTGGAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14545
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065012 | Nonsense | 245 | 532 | 8 | 13 |
ENSDART00000137932 | Nonsense | 207 | 494 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 15263479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15276786 |
GRCz11 | 10 | 15234905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAAACCCGATCGAAAGGACCTCCGCCTCCTCTACCACCTCCATTCAAG[A/T]AACCGTCCTGCCACATCAAAGATACTCCTCCTCCACCTCTACCGTATGCC
Long Flanking Sequence:
AAACAAATGCCATTCTTAATGTAATAAATTAACTCTTTTTTGTTATTTTGTTTTGTAAAGAAAACATCCAAAATAAAAATTTCTTAGCCACAATGGTCTCTAGATTTAATTAACACATTTAAACATAACATTTTGGAAAACTTGTGACACAAAAATAAATGTTTGCCATTCTTAATGAAATCAATGAACTGTGTTAATTGTGATTTTTAACCTATTCGCATGCAGTGTCTTGCCTAAACAATTCCTCAAGGAACCATCAATTCCAATAAGAACCTTTGTATTGTAAATGAATGATTGTCATCTTTTGCATTTGCATTCAGGTTCACAGACAAAACTAACTCACAGAGTGGAATTTGTTTGATGTTTTTTTGGTTTTCTATTTTTTTCCAGGTCGACCCACGGTTCCACCTCCATCGTATCCACCACCGCCAGTTCCGTTTCAGTCGTCTAGAGAAACCCGATCGAAAGGACCTCCGCCTCCTCTACCACCTCCATTCAAG[A/T]AACCGTCCTGCCACATCAAAGATACTCCTCCTCCACCTCTACCGTATGCCCCGCATCTGGAGAAAACAGACTCAAACAGACGCCCTGTCAGCCCCATGCCCCCTTTACCTCCTCCTGTCAGTCTTAAACCTCCGCCAGGCCCATTCTCCACAATGCCTGCCTGCGAAAAGAAGTCCAGCGTCACTTTTAATCACTCACCAGCCACTTTACCCATCGTGGAGAACCTGCAGAAAGTGATGCTGATCTCTGCAAGTAAAACAAGCATTTCGGGTCATCATTTGGAAGTGAAGCCTTCATTCGGACAAAGGCCGCTTTCACCTCATCTGTCCACAAATCACAGCACTCTGGGACAGATAAACAAGCCCCCAGTGCCAAACAAACCCAAACCCGGAAGACCCTCATTCCAGTAAGTGTCTTCTGTTCGTGGTTGTGTATTCAGACATTTATGGCTATGGATGTGTTTACAAACAGCTAAAACCAAGACTTTAAAGGTTTAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21688
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065012 | Nonsense | 414 | 532 | 9 | 13 |
ENSDART00000137932 | Nonsense | 376 | 494 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 15265607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15278914 |
GRCz11 | 10 | 15237033 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAACGAATTCCAGACAGAATTGATGAAAGCTCAGATGAAGAGGACTA[T/G]GAAAATGTGAGTTTCCTTCATTTGATATTTTGCAAACATATTTGATTCCA
Long Flanking Sequence:
TGGTGCAATCATCAAAGTAACTGAAGTTAATCAAGTTAATTGACTATAAATGTGATGTGATGCAGTCATGAAATTAAATGACATTAATAAAATGCAATGCTTCTAAAAATGTCATGTGGTGCACCATCGAAGTAACTGAAATTAATCAAAAATGTAATGGTTCTAAAAATGTCATCCAGCTTAATCATCAAATTAGGTGAAGTTTATTAAATCCAATGACTCTAAAAATCTAATTAGATGATAAAATTATTAAAACAATTATTTTTTAATTACTATAAGAGTAGTAAGTATAATATTTTAAGCATTTAATAGCTTGATTCTTGTGATTTAATTTTACCACAGACTTTATATATATATATGAGATTATTTATACAACTAGCCTGTGCCTTTCTTCTCAGAAGAGCATCGCCGGATGGACAAAGTTTTCGTTCTTCTATTGAAGAGAAGCCTCCAAAACGAATTCCAGACAGAATTGATGAAAGCTCAGATGAAGAGGACTA[T/G]GAAAATGTGAGTTTCCTTCATTTGATATTTTGCAAACATATTTGATTCCATTTTAATAAAGCACCTGTGTAGTTCACCCTGCGGTTTTGAAAGATATGCTGTAAATTTACTCACCCTCACCCTCAGGTCAATCAAGATGTAGGTAACATTTTATCTGCAGTAGAACATAATTGTGGTCATAGACGATTCATGAAATAAATAAATAAAAAAAGCTTTGAGAGTTTAAAACAAAGTATAAATAAAGGAGAAGCAAATTTAATATGTTATTTTGAGAATTGAGGTCTTCTGAAGCAAAATGATCAGTCTATGCAAGAAACTGAACATTGTTTACATAATTATTACCTTTATTTCACACTCACAGACGTCTTTTCATAGCAGTATTATTTTCATTTGCATGTATATGTTTTGTTAGCTCAAGCAGCTGTTTTGAAATTGTTTTATGAATCACCATTCATTTTAGCTTAAAAAAATCTTCTTTAATGTACTAGTAAAGAAAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11802
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 |
---|---|---|---|---|---|
ENSDART00000065012 | Nonsense | 418 | 532 | 10 | 13 |
ENSDART00000137932 | Nonsense | 380 | 494 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 15266311)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15279618 |
GRCz11 | 10 | 15237737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCTTTAACCAAATTTTGTCGTAACAACGTTGTCTTTTGTCATTAGGTA[C/T]AATTGCCTCCCTCTGTCTTTGTGAACACGATGGAAACCTGTAAYGTGGAA
Long Flanking Sequence:
TAAAAAAAGCTTTGAGAGTTTAAAACAAAGTATAAATAAAGGAGAAGCAAATTTAATATGTTATTTTGAGAATTGAGGTCTTCTGAAGCAAAATGATCAGTCTATGCAAGAAACTGAACATTGTTTACATAATTATTACCTTTATTTCACACTCACAGACGTCTTTTCATAGCAGTATTATTTTCATTTGCATGTATATGTTTTGTTAGCTCAAGCAGCTGTTTTGAAATTGTTTTATGAATCACCATTCATTTTAGCTTAAAAAAATCTTCTTTAATGTACTAGTAAAGAAAAAAGACACTTTTGAGAAGCTGAATCGAGTCATTTCCTGTGACACATTCAGTCGAAATAGATTGTGGGGGACTTGACTTCATTTCTCAAATGATCTGTTTTTGTTTAAGCATTGCAACATTTCCAAGATGTATTTAAATAAAAAACGGAAGGTCATCTTGCCTTTAACCAAATTTTGTCGTAACAACGTTGTCTTTTGTCATTAGGTA[C/T]AATTGCCTCCCTCTGTCTTTGTGAACACGATGGAAACCTGTAACGTGGAAAGGTAAATTAAACATTATGTCATTTTGATTTAGCATTTTATATTTTAGTAATTCTTTAAGCATCATAATTACTATAAAAACATGTAAATAATTAAAAAAAGTTTGCTTGAAAGTTTCCCTCAACTAACGCTCTTTAGTTGTTTGTCTTTATATTGCTGCCCTCTAGTGGACAGAAGTTGTATTGCACAGTGAATTGTTTGGTTTTGAATTAGAATTGTTACACTTACAGTTTTTCTCAGTCGCTTTGGTGCATTCTCACAACACCATTTACATTTGCACAACAGTTAATGCATATCTCAAAACAATTAGTCATTTGTGCACATCCTAGTAGCAGTTTCTCATTCCTTCCAACAAATTGCAGATGCTTTTGGACATGCATCAATTGTTTTCATACAACTCTCTGCTATTTATAACATTATCATTTGCTTCTGTCATGTCAGTCAAAATTAA
Associated Phenotype:
Not determined