ZMP
sh3pxd2b
Ensembl ID:
ZFIN ID:
Description:
Im:7155315 protein [Source:UniProtKB/TrEMBL;Acc:Q6DC19]
Human Orthologue:
SH3PXD2B
Human Description:
SH3 and PX domains 2B [Source:HGNC Symbol;Acc:29242]
Mouse Orthologue:
Sh3pxd2b
Mouse Description:
SH3 and PX domains 2B Gene [Source:MGI Symbol;Acc:MGI:2442062]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24036 | Essential Splice Site | Available for shipment | Available now |
sa9265 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37381 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24036
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031308 | Essential Splice Site | 221 | 565 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 42369967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 42773473 |
GRCz11 | 21 | 42768764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAAGCTCAAGATGATCCGGATGATTTCTCACTTCCAGCAGAAGAAGG[T/C]AAAGCCTCCTGAATAAAGCACCTGCAGCTAATATAGTATAATATTGGGGA
Long Flanking Sequence:
TGACCTGACATGGAAAACATAGGTGAACAAGTACTACAGTGTTATTTTTGTTTTGTTTTTTGCCACACAAAGAAGTTTTTAGAGCTTCGTATGATTACAGTTGAACCACTGAAGTGAGAATGTTTTCAAACATCTCTGGACCATTGCTGTCTATGGAGGATGAGAGAGCTCCTGGATTTCTTCTAAAATATAATATTCTTCTAAAACTTCACTCGTGTTTAGAAGGTAAACAAAGATCTCAGGAGGTTGAAAACACACAAGGCTGAGCAATTAATGACAGAATGTTCATTTTTTTGTGTGAACTAACCCTTTAAATGAACAGCTTATTTTGACATGAATGTTTTGCCATTAGTTACTCATGAAGTATTTCCATCTGTAAACGATTTTTGCCCCCCAGGCTGGTGGTTCGTTAGCACAGAGGATGCTCAAGGTTGGGTTCCAGCCACGTGCCTGGAAGCTCAAGATGATCCGGATGATTTCTCACTTCCAGCAGAAGAAGG[T/C]AAAGCCTCCTGAATAAAGCACCTGCAGCTAATATAGTATAATATTGGGGACCTCTTGTTGAATCTGATTTGGCATCTGTTAAAGGTGAAGTGTCAATTTTTTTTTAATGGTCTTTTCTATTTTAATATGCAGAGACTCTAATGCTGGGTTCACAGCAAATGTGAAGGGAACATGTGCATCATGTCAGTCTCTCTAGTTTACTCATTTTATATGTATATAAATACATATCTATATATCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCTATATATATATACCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTTGCACTGAAGACATGATTTAGGCTGATTTAACGCAGTTGAGCATTTCGCAACACTTAATGTGTAATCATATCCTGCAAATGCTTAAATAAGTATATATAAGCACATTTTCACACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9265
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 |
---|---|---|---|---|---|
ENSDART00000031308 | Nonsense | 262 | 565 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 42363276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 42780164 |
GRCz11 | 21 | 42775455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTTAGCAGTTTCTTGGRTGGAACRTTGTCRCCTTNACCCCCACAGGTAC[C/T]AAGGGAAAGAGGGCTGGGCCCCGGCATCTTACTTGAAGAAGGCTGACATT
Long Flanking Sequence:
CTTGGGTATAATTAAATTTGTTAAACTGAATTAAGTCTTACAGTTTTACTTTATTTAATGAAGTAATAAAAAATATTCCAAAGCATTTTGGATTTTGGTTTTCAGCTAAGTGCATCCAGACATTTCCAAGGTTTAGACCAGAGTTTTCATTTTGATACATCCCTAATTATTAGTGTTATATTCGTGCAAAGCAGAGAAAGCTCAAGTGGTAAATAGGCTGTAGTGGTTGGATGTTGTTCATGAATGGCACCTTTAAGTTAAATAATTAAAATAACCCTTTCTTATTCTCAGAGGAAAAGTACACTGCAATCTATCCATACTCTGCACGTGATCAAGATGAAATCGATTTGGAGAGAGGCATGACTGTTGAGGTCATTCAGAAAAACTTGGAGGGCTGGTGGAAGATCAGGTAAAGGGGAATGAGTGAATGCGACTGTTTTCAGAAAAAAATCTTTAGCAGTTTCTTGGGTGGAACGTTGTCACCTTACCCCCACAGGTAC[C/T]AAGGGAAAGAGGGCTGGGCCCCGGCATCTTACTTGAAGAAGGCTGACATTCTCAGCCAGAAGATGGCAGCAGGTGCTCCAGTTCATGCCAGCACTAATGACCTAGACGTGGCTTGCAAACAACAGAACGCTAACAAGGAAAACAAGGAGAATCAACGTGACCGATTTTCACCGTTTTCAGACAGCAAGCGCAGTAAGCAACTTTTTGTTTCTAATGCCTAAATGTGTCAAGTGTTTAGGGTGCAGAAATACAACTTCCCCATATGCTCTAAATATAATGTAGCCAGCAAGTCATTACTGCATAATAATCCCCTTAAGGGAGATCAAGCAACCAAAGCAAAGCCAAGGTAAAATTATTTTGTGTCCCTTGTTGACTCTTTCAAAAAGAACAGGCCAAATCGTGTCTCAATTTACATGATTGGATTGCATCAGGAAGGGTATTTGGCATAAAACAATGCAAATAAATAGATGGATAATCCACTGTTATGACTTCTAATGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37381
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 |
---|---|---|---|---|---|
ENSDART00000031308 | Nonsense | 337 | 565 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 21 (position 42362669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 42780771 |
GRCz11 | 21 | 42776062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTTCTTCTCTTGCAGAAGTAGGGGCACGACAGAGGCCTCCACCACGC[C/T]GAGATCTTACAATAGTAAGGGTTATAATGCTTTTACAGTTGCATGTCATA
Long Flanking Sequence:
CGTGGCTTGCAAACAACAGAACGCTAACAAGGAAAACAAGGAGAATCAACGTGACCGATTTTCACCGTTTTCAGACAGCAAGCGCAGTAAGCAACTTTTTGTTTCTAATGCCTAAATGTGTCAAGTGTTTAGGGTGCAGAAATACAACTTCCCCATATGCTCTAAATATAATGTAGCCAGCAAGTCATTACTGCATAATAATCCCCTTAAGGGAGATCAAGCAACCAAAGCAAAGCCAAGGTAAAATTATTTTGTGTCCCTTGTTGACTCTTTCAAAAAGAACAGGCCAAATCGTGTCTCAATTTACATGATTGGATTGCATCAGGAAGGGTATTTGGCATAAAACAATGCAAATAAATAGATGGATAATCCACTGTTATGACTTCTAATGGGAGCAACTGAATGTAAGAGAGAGAGACTTGCTTAATAAGATTGTTTCTGCCTAAACTATGGCTTCTTCTCTTGCAGAAGTAGGGGCACGACAGAGGCCTCCACCACGC[C/T]GAGATCTTACAATAGTAAGGGTTATAATGCTTTTACAGTTGCATGTCATATGGTATTATATCACGCTCTGAAAGGCACTTCAGAGGGAAAACTATCAAGGCCACCATATTGAGGTGTTGTTTTAAACCAATGTGCTCAAAACTGGCCACTTCAAAGGGCTCTTAGAAATAAAGAATACAACTGATGGACAGTTCGGGCCCCCTTGATCCTTTACACTGGAATGTTGTTTGGTGTCAAACAGAGCCTTCCATTCAGGGGTCAACAAACTTGTTCTTGGAGGGCCGGTGTCCTGCAGAGTTACCCTAATCAAATACACCTGAACAAGCTAACCAAAGTCTTATTAGGTATACTTGAAGGTTCCAGGCTGGTGTGTTGACACAAGTTGGAGCTATACTCTGAAGGGACACCGGCCCTCCAGGAAAGGGATTGGTGACCCCTGCTCCATAGGGTAAACCTGTAGAAGAGATTAAGGCATGGAACTTTGCAAATGAAACTTGCTG
Associated Phenotype:
Not determined