ZMP
si:dkey-261l7.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
PHIP
Human Description:
pleckstrin homology domain interacting protein [Source:HGNC Symbol;Acc:15673]
Mouse Orthologue:
Phip
Mouse Description:
pleckstrin homology domain interacting protein Gene [Source:MGI Symbol;Acc:MGI:1932404]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32455 | Nonsense | Available for shipment | Available now |
sa32454 | Nonsense | Available for shipment | Available now |
sa13928 | Nonsense | Available for shipment | Available now |
sa24372 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32455
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 |
---|---|---|---|---|---|
ENSDART00000008401 | Nonsense | 182 | 1635 | 5 | 34 |
ENSDART00000138106 | Nonsense | 354 | 1805 | 11 | 39 |
The following transcripts of ENSDARG00000015970 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 31559126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31394016 |
GRCz11 | 23 | 31320547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACGGGCAGCACTGATCACATCATTAGGGTTTATTACTTTGGAGGTGGA[C/T]AACCAGAGAAGATATCTGAGCTGGAGTCTCACACTGTACGTAATGCATTT
Long Flanking Sequence:
TCTCGTGTTTCCATTGTTCTGAAAGCTGATAGCAGATTATAGAGTGATGACGGATCGTTTTGGCTTAAACATTTTTCTGCAAAGTGGGGCTATAAATATCTTGTTGTCAGACAGATATCACAGACTTTTTAAAAGAGAGCGCTCGGCACTGCGGGAGCTCTTTAAATACACATTTCTGAAGAAAAAGAAACACTCGGCTGACTTTAGTTCTTTCCTCTTCTGTGTTCACTTGATCTGTTTGAGTTTCTTGCTCATAAACACTCGATTGTGATTATTGGTTATACTTGCATGGTTGAGTCTGCAGGAAAACGATGACAGAACGCTTGCTGATGATGGATTTTGTTCTAGTGTGTGTGTGTTTGTGCGCATTAATGCTGCGTTATTGATGATGATGGTATATTTTATGTAATGTTAAGTGATATTTGATGATTTCAGGTGGGATGTTCTTGGCGACGGGCAGCACTGATCACATCATTAGGGTTTATTACTTTGGAGGTGGA[C/T]AACCAGAGAAGATATCTGAGCTGGAGTCTCACACTGTACGTAATGCATTTGTTTGCATTTCATATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTGTGTGTGAGTGTGTATGTGTGTGTGTGTGCGTGTGCATGCATGAGTGTGTGTGTTTGTGTGTAAAGGAGACATTTACATCTAAATGTAATGTAAAATGTAATTTAGAGTCTTAAAATTTAGAGTATTAAAATCATGTGGAGGGTAAAGCATGCATAGTGGTGTTTTTCCCTATAAACACGCAAATTAGAATGTGGTTTGTGACTTTATAACACCTTGTCACATGCAGAGTATGAATTAGGGGGAGCTGACCTCCCTAATTAATGATTGATCCCCCTCGAAGGATGTGAAAACAAGATGTATGGGTTGTCAGTCTGCATCTTAAAAACTAATATTACTAATTAATTAATTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32454
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 |
---|---|---|---|---|---|
ENSDART00000008401 | Nonsense | 906 | 1635 | 22 | 34 |
ENSDART00000138106 | Nonsense | 1078 | 1805 | 28 | 39 |
The following transcripts of ENSDARG00000015970 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 31530580)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31365470 |
GRCz11 | 23 | 31292001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTGATGATGCCTGGTGGTTTGGTACGATTGAGAGTCAAGAGCCGTAC[C/T]AGGCCGAATATCCAGACTCTCTGTTCCAGTGCTACAACGTCTGGTCAGTT
Long Flanking Sequence:
TATCTCATAGTTTACTATGGCAATGTTGTCGTCATCAACTTTTTAATACCTCTAGACTGAAAACATACTCGTGCTTTAGACTTCAAGCTGTTTCTGCAACAAAGTCATGCCGCATTCATTGCTGTTACTGTGTGAAGTCAAGAGAAGTCACATACACTGTGGACAAGAGGTCCTCGCATAACTGTTAAACATTTTTTTTTTAAATAATATGTGTTTTTTTTTTAAGCACCTGCTGAAGCAGCATATACTATTAATGTAGGGATTTAAGAATCTGTGTTGATTCAGTGAAAACCAGACCTTTCAGTATGTACTGGGTTAAAACAACACAATTTTAAACATGTGCTAAACCAAAAGAGCTGTACCCAAAATTAAATCAGTTAGAATACATACACCCCTAATATAAATATGTTTACCTTGCAATTTCTCTGTCAGGTGATCGTTTCCGGGCAGTGATTGATGATGCCTGGTGGTTTGGTACGATTGAGAGTCAAGAGCCGTAC[C/T]AGGCCGAATATCCAGACTCTCTGTTCCAGTGCTACAACGTCTGGTCAGTTCTGTGTCCATTTTACACATTTTTATACATAAATCACTTCTCATCATTTCACTTCTCTGCCTCTTTGATTTTTAAGTTTAAAGCCAAACAGGGTGTGTATAGAAGCTTAGATAATAATCTTGTGTGTGTTTAGTATAATGTTACAGATATAACAGTAAATGAACTTGACAGCTTTGTGTTAATGTGTGATGCAGCTGGGATAATGGAGATACTGAGAAGATGAGCCCGTGGGACATGGAGGAGGTTCCTGATGAAGGTTTAACATGTTCCTTAAGTTCAACTGGCTAAATAGATCTTTGTCTAGACAGATAGATCCATCAACAAGCTTAAATTCAACATTAAAATCTATATTTTAATTTAGCATGGATGTGTTAATTGTCAAATTTACAGTAAAACTTTAGTCAAATAAACAGTTTAAACCTTAAAGTCTTCACAGGATCCTGAAAACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13928
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 |
---|---|---|---|---|---|
ENSDART00000008401 | Nonsense | 973 | 1635 | 24 | 34 |
ENSDART00000138106 | Nonsense | 1145 | 1805 | 30 | 39 |
The following transcripts of ENSDARG00000015970 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 31528587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31363477 |
GRCz11 | 23 | 31290008 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGAGCAGAAGGCCTTACTGTACAAGCCGCTGGACGGAGAGTGGGGCTCA[C/T]GAACACGCAACCAGGAGTGTGAACGCWTCATCAGGGGCATCAACCAGCTT
Long Flanking Sequence:
ACTCCTGGTTATTAGATATGTTCAGCCTTGATAAAAGATCTTGAGTGCACTTACATAAGTAACTGATTGATTTAATTTTTTTAATTATAAATTATATTATATTTAATATATTATTTATTATTATTTTTATATATTATTTTACATATTATTTAAAAGTAATCGAGTATGTTTACCAAGCATGCTCTTTCCCATTGGATGTGGATAATTTTAGGCTTTTATTGTGCTTGTGGTGACATTTGGTCCTTGTGACATCAACAACGCAGGCGAGTTAGTGCTCATGGCAACCATCAGATTGAGAGTATCAGCTGTTCTGATGTCCAGCTGGCTTTATTTTAATAAGCAATACAGTCAGAGCTGTGATAGTGTCTGGTTTTCCTCTGTCTCATTGTCTCTGTCTGTCTGCAGTAGTATTTCCTGAGGAGCTAGGCCTCAGTATGGCTCTCACTCAGGACGAGCAGAAGGCCTTACTGTACAAGCCGCTGGACGGAGAGTGGGGCTCA[C/T]GAACACGCAACCAGGAGTGTGAACGCATCATCAGGGGCATCAACCAGCTTTGCACTCTGGGTATGGTCTTATTATTTAGCATTAAGATGATATCTGTGATAATAACACTCACAATGCTGTGGTCAGAACTGTATATGAGTCCTTAATATAGTTGCATTCACACACATTTCAAATGTTCACTTATTACATTGAAAGGACTCACACAGCTATATTTTAAGGAAAGCCTTGCCATTTGGTGATCAACCTGTTTGATGTTTTGGATGGAGCTCTGTGAAACTAAGATAGTCAGGGTTTATTTGGTCCTGGAAAACCTGGAAAGGTCATGGAAAATTAACAAGGCATTTTCCAGGCCTTGAAAAGTTTTGGAAAAAACAAATAAACCCAACATGTTTTGGAAAAGTCGTGAAAATTTGTTTAACAAGTATCTGTGTACTTGAATATATTTGAGATGATAATATTGGGTAAATTTTGAAAATAATTTCGCTGGCTGTCTTTTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24372
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008401 | Nonsense | 1515 | 1635 | 33 | 34 |
ENSDART00000138106 | Nonsense | 1685 | 1805 | 39 | 39 |
The following transcripts of ENSDARG00000015970 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 31515105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 31349995 |
GRCz11 | 23 | 31276526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGATGGCGGGGCTTCTTCAACAGCCCAAGACAGTAATCTTTCAGATT[C/A]GGGAGAGTATCCGAAAGCACGAGGCAGACCACGAATCACAAAGACGATAG
Long Flanking Sequence:
TGTACCTAATAAAGTGGCAGGTGAGTGTACATTTTTAAAAAAAAGTTGTTATTTTGTTATTGAATATCCTGTCAGGGAAAAAAATATTATCACTTTGGAAATAATTGAATAAGAATTTAAATTTCACAGGAGAGCTCGTAATTCTGCCTTCAACTTTATGTAAATGTTTCATCTGTACTTACATGCTCATTCTCTCTTAGGTCCAGTTGATCACAGCTCTCCTCCTCAGAACAGTTTGCATTTGAATGGTCACAGTCAAGTGACTGTAGGAATGGTACGAAGAGGCCGGGGCAGACCCAGATTAGACACACAAATAGAGACGCCGGTGGACACGCCGCCACCTCCACTGCCTAAGACCTCTTCTAAAAAAAAAGAACGAAAAAGCAAAAAAGACACGGAGTCCCCACGACGAAATTTCTCCCACGAGGAGGAGCTTATGTTGCCCACCGGGGATGATGGCGGGGCTTCTTCAACAGCCCAAGACAGTAATCTTTCAGATT[C/A]GGGAGAGTATCCGAAAGCACGAGGCAGACCACGAATCACAAAGACGATAGACACTCCAGCTCCTCCAAGCCCCAAAACTCTCCGGCGGAGCAGTCGACGTGGCAACGAAGAGATCACGCCCCATACATCAGGCTCCGCCCAGAGTGAGGAGCCTGAGGTTTATATTGGAGAAGACGGGAGCTCGAAAGGCCAGATGAAAACACGCAACCAGGGCCGAAGGACTGCTTTCTATAATGAAGAAGACTCTGAGGAAGAGCAAAGACAGCTTTTATTTGAGGACGCCTCCATTACTTTTGGGACGTCCAGCAAAGGGAGAGTCCGCAAGCTCACAGAGAAGGCCAAAGCCAATCTTATTGGCTGGTAACATTGCCAACTTTGCATGTCCTCTGCGACACAAACCTCAATCCCGTCCTGTTGGGAAAGGGGGAAACCATTCCTGCTGCTATATCAGACTGTCACGATTATTTGAATCTTTCACTTTTGAACTCTTTCAAGAGTCG
Associated Phenotype:
Not determined