ZMP
si:dkey-57b6.3
Ensembl ID:
ZFIN ID:
Description:
SH3-domain binding protein 4 [Source:RefSeq peptide;Acc:NP_001116767]
Human Orthologue:
SH3BP4
Human Description:
SH3-domain binding protein 4 [Source:HGNC Symbol;Acc:10826]
Mouse Orthologue:
Sh3bp4
Mouse Description:
SH3-domain binding protein 4 Gene [Source:MGI Symbol;Acc:MGI:2138297]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34634 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41412 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34634
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 |
---|---|---|---|---|---|
ENSDART00000101685 | Nonsense | 48 | 960 | 2 | 4 |
The following transcripts of ENSDARG00000030104 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24416254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23572040 |
GRCz11 | 9 | 23382909 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTCATTTGTTTATTTATCAATCAACAGTCCCTTCACCTAGTTCTTTA[C/T]GACTGGATGCTACTGCCTCATTTGGAGCTGCCAGGGAAGTGATTGCCATT
Long Flanking Sequence:
GCTTTACACTGGTAGGGGCATGAAGAGGGTCCTTTCGTCCTTTATAAATGCACATTACTTACTTACATACTAAAAGTAACTTTCCAAACAACATACACACACACACACATACATACATACACACATACATACATAAATATTCAGAAGAATTAACTGATAATACCATTATCTTTTGCTTTGTTTTAAGGCCACTAATCTGCCGATAAGAAGCTAAACAATGGAAAGAAAAACATAGGTAAAACATAGATAAAAGGAGGAGTTTGGTAGCAATACACACCATGGCTGCTCATCGCATTAGATCAGCGAACAACAACACTGTGCTCCCTCGCTGCAGATCTGAAGGCGCACTAATCGATCTCAATGAAGGAGTTTCAGAGGCCACCCTCACAGATGTCAAAGGTCTCCCTTATCATTTTTACACAATAAACATGGTTAACTTTTGAAATCGTTTTATTCATTTGTTTATTTATCAATCAACAGTCCCTTCACCTAGTTCTTTA[C/T]GACTGGATGCTACTGCCTCATTTGGAGCTGCCAGGGAAGTGATTGCCATTAAGGATTACTGCCCGTCCAGCTTTACCACACTTAAGTTCTCAAAAGGAGACTGTCTTTATGTCATAGACACATCAGGTGGAGAGTGGTGGTATGCACACAACAGCAAGGAGATGGGGTACATCCCAGCTGCTTATGTCCAGCCGATCAATTATCGGGACTCCTCGTTCAGTGACAGCGGCATGATTGACAGCATATGTGACATTTCTGAAGGAGTGAAAGAAATGGACATCTCAGGGGACTGGACGATGTCCTCCAAAACCACAGAATCTAGACATGAAAATCCTTTTGTTAATAAACGCATGTCAAATAACCCATTCCTAAACAGCACACTGCAAGACACCACTGACCAAAACAGCAACCAAAATTCAGCAAATACCTTTTGCTTTGATCATTTCTCACCTCCCATCTCAAACACCAGTAGCACTGTTAATATAAATGGCTTTGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41412
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 |
---|---|---|---|---|---|
ENSDART00000101685 | Nonsense | 738 | 960 | 2 | 4 |
The following transcripts of ENSDARG00000030104 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24414183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23569969 |
GRCz11 | 9 | 23380838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGAAACCTGTTAATTATAAAGGGTCAGATCTTACGACTACAGTGCTTT[T/A]AGAGCAGATCCTGAAGCCCTGCATGTGTCTGACGTACATCTATGCATCGG
Long Flanking Sequence:
CATGATCGCAGCCCGCGATTCTACAGACATTTCAGACTTTACACTGCGAATACAAGTCAAGGATGATAAAGACTGTATTCTGGCCCAATTTTGCGTTCAGACCCCAACCCCACTACCAAAAACAAGCACAAGGAGTTCTGTTCAAAGGCGCTTTCTAAAGAAAAAGGAAGTGAACAAAATAGTCCTCTCTCCTCTTGCAGCAACCACAAAGTATCCCCTATTTCAGGACAGATTAGTCAAAAACTTGAAATTTGCTAAATTGCTGAAAACAGTTGTAAGACAGTCCAAAAGCCTATATTTACTAGAGTATCTCAAAGGTGACGTAATGACTATTGTAAGCGAGGAAAAAATCAAACTGAAAGGACATCTATGGACAAAGGAATGGTATATCGGATACTACCATGGAAGAATTGGGTTGGTGCATGCAAAAAACATTCTTATCATGGGAAAAGTGAAACCTGTTAATTATAAAGGGTCAGATCTTACGACTACAGTGCTTT[T/A]AGAGCAGATCCTGAAGCCCTGCATGTGTCTGACGTACATCTATGCATCGGTTCGGACGATACTGATGGAAAATGTAGCAAGTTGGAGAGCATTTGCTGATGCTTTGGGCTTCGTCAATCTGCCATTGACACATTTCTGCCGGACAGAGCCAGACAGTGAGCCAGAAAAGGTAGCTTGTGTTCTTGAGAAGCTTAAGGAAGACTGCAATGCAGCTGAGGGCAAGGAGAGGAAGTCTTTCCAGAAGGAGCTCATGAAGGTAAGAGTTGAAAGTTTCTAGTAATTCATCCTGCCTGCTTTGAATAATAAAAAAATTCAAAGTTAATAAAGCTGATAAATATTTAAATATTTTAAAGACAGGTTGTGTCAAACTTATGCATCAATTTTGTTTTATGTATTTGTGTTAAGGACACCAGATAGCGCAGTGGTACTGCTAACTATTCTTGACCTTGCTGGTGATTTTTTTATACACTTAAGTACACTAAACAAACGTGTGTATAACA
Associated Phenotype:
Not determined