ZMP
plekha7
Ensembl ID:
ZFIN ID:
Description:
Pleckstrin homology domain-containing family A member 7 [Source:UniProtKB/Swiss-Prot;Acc:B6RSP1]
Human Orthologue:
PLEKHA7
Human Description:
pleckstrin homology domain containing, family A member 7 [Source:HGNC Symbol;Acc:27049]
Mouse Orthologue:
Plekha7
Mouse Description:
pleckstrin homology domain containing, family A member 7 Gene [Source:MGI Symbol;Acc:MGI:2445094]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23317 | Essential Splice Site | Available for shipment | Available now |
| sa29048 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43121 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6523 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23317
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 |
|---|---|---|---|---|---|
| ENSDART00000086094 | Essential Splice Site | 28 | 1208 | 1 | 27 |
| ENSDART00000111450 | None | None | 1075 | None | 22 |
| ENSDART00000140444 | None | None | 110 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 27045979)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 27119234 |
| GRCz11 | 18 | 27101612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAACGGCTCTTATGGAGTGTGCAGAGACGGCAGGGTCTTTTTCATTGA[G/A]TGAGGATATATTTATTTACTCTTGCCTAAGAAAGCATTCCTTTCTCATAG
Long Flanking Sequence:
CATGAGTAAATAGCAAGTACATTTTTATTTTCAGGTGAACTCCTTTAACTTGTGTAACAATAGTTGCACTGTATGCATTCATAAAGCACCTAGCAACAGAACAGGCTGTTCTTCAACAGAATCAAACACATAAACAAATTCATTTCAATGCATCATCAATCACTAAAACGAAAACATGCACACAAACACGTCATATAAAAATACAAACGAGTGGGCAACGACTAGCCTATCTCGATCTGTGTTTTATAGCATACTGTAAGGAATTAATATTTTTCCGTCGGCTAATAATCTCGCTCACTGAACGCCAAGTGCAAAGTCAGCCCTCCCCTTTAATCGCCTTTTGCCCGAGCGCTGATCGCTGCACAGGGAGGACAGTGAGGAGGGAATATGAGGTAGACAGGACTTTACACGGGAATAATGGCGGCGCCGCTCCGGCGGGACACCTTACCTGACAACGGCTCTTATGGAGTGTGCAGAGACGGCAGGGTCTTTTTCATTGA[G/A]TGAGGATATATTTATTTACTCTTGCCTAAGAAAGCATTCCTTTCTCATAGCGTTCGAGTGTTTTCCAGCCAATTGCATCGCTAACAGGTGGTTTGTTTTCCTGGCAGCGATGAAGCGCGCGCCACTACTTGGCTTCATCCCCGCACTGGTCAACCTGTCAATTCTGGACACATGATCCGATCCGGTTAGTGCGTTAATGCGTGCGTTTAACCATTTAGATTTAAACATTTATCTGCTTTTTTCGCGTTGCCTGTGCATAGATAAAACGAAAGGCTAAAAGTTTGGCAAATGTGTTCTTTTCTTGCCTCCTAGATCTGCCCCCAGGTTGGGAGGAAGGTTTTACGAAAGAAGGAGCGAGTTTTTTTATTGAGTAAGTGGATGTGTTTATTGTAATTATACCTTATGCGATCCTGTAGTGCTGCAGGTGAATTACAGGTCACAAGCGGGTTAAATATTGTTGTGAGCACACTTGAGCCGCAGAGAATGAATATTAGGAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29048
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086094 | Essential Splice Site | 73 | 1208 | 3 | 27 |
| ENSDART00000111450 | None | None | 1075 | None | 22 |
| ENSDART00000140444 | None | None | 110 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 27046350)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 27119605 |
| GRCz11 | 18 | 27101983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGTTGGGAGGAAGGTTTTACGAAAGAAGGAGCGAGTTTTTTTATTGA[G/A]TAAGTGGATGTGTTTATTGTAATTATACCTTATGCGATCCTGTAGTGCTG
Long Flanking Sequence:
ACAGTGAGGAGGGAATATGAGGTAGACAGGACTTTACACGGGAATAATGGCGGCGCCGCTCCGGCGGGACACCTTACCTGACAACGGCTCTTATGGAGTGTGCAGAGACGGCAGGGTCTTTTTCATTGAGTGAGGATATATTTATTTACTCTTGCCTAAGAAAGCATTCCTTTCTCATAGCGTTCGAGTGTTTTCCAGCCAATTGCATCGCTAACAGGTGGTTTGTTTTCCTGGCAGCGATGAAGCGCGCGCCACTACTTGGCTTCATCCCCGCACTGGTCAACCTGTCAATTCTGGACACATGATCCGATCCGGTTAGTGCGTTAATGCGTGCGTTTAACCATTTAGATTTAAACATTTATCTGCTTTTTTCGCGTTGCCTGTGCATAGATAAAACGAAAGGCTAAAAGTTTGGCAAATGTGTTCTTTTCTTGCCTCCTAGATCTGCCCCCAGGTTGGGAGGAAGGTTTTACGAAAGAAGGAGCGAGTTTTTTTATTGA[G/A]TAAGTGGATGTGTTTATTGTAATTATACCTTATGCGATCCTGTAGTGCTGCAGGTGAATTACAGGTCACAAGCGGGTTAAATATTGTTGTGAGCACACTTGAGCCGCAGAGAATGAATATTAGGAATTGTGCACGAAGGGGGTATCAAAGGTAAGCTGCAGTCATTGTGTTTGAAGACAGGTATTCAAGTACAAAGTCTACAGGTGTAAATGTCTCTTTGGGTTTATGGTGGATGTCGGATGTTGGCTGTGAACGCTGCAATTTCTCTGAATGCTGTCTAGATACAGCTTTGGTGTTTTTAAAGGGATAGTTCACACAAAAATGAAAATGATCTTTTCATTTAGTTAGCCTGAGGGCATCCAAGATGTGGAGACTTTTTCATTTTCATCAGGAAATTAAAGTAGATAGTATGCTGAAAAACTTTATGGTGATTCATAAAGTGGGAGTTAGTGGATATAGAAAACTAAATAATCACTTGTGGGTTCTGATGGTACATTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43121
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086094 | Essential Splice Site | 133 | 1208 | 5 | 27 |
| ENSDART00000111450 | None | None | 1075 | None | 22 |
| ENSDART00000140444 | None | None | 110 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 27156464)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 27229719 |
| GRCz11 | 18 | 27212097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCACTACTGTCACCACCTCAACTGTGGACAGCACTTCAGGCTCAAAG[G/A]TCAGTAACAAAAAGAAATTGTAATATTTTAGGATTTATAAAGTATTTGAT
Long Flanking Sequence:
AATATTCTTATTTCAAGTTTGGGAAAATGCATATTGTGTTACAGGCAATCAACTAAAAGTAACTGAAAACACACAGTAACAAGACACTGAAAATATGGGATCATGAGCTGCTCTAAATGAACACAGAGTTGTGCTTCACTCTAAACATGTATGAGAATCATGAAAATGAAAAATATGTATATGTAAAGACACTGTAAGTAGTTTTCGCTGCTAGAGGACACGTATTCACAACAAACAAAGGCATACTGTACTTTGATGACGCCATGACATCTTCATTACATCCTACATCAAGATCTTTGCAATGTGTCCTATAACAGTTTTAGTCTTTTTCATCAGCAATAATGAAATATGTTGATTCTAAAGCCATTCCTTAAGTTATAAAGCATCTCCATTTCCCCTACAGGCCGGGCGGACGCATGCTGAAGCAGCCCTCCAGCACAATTAGCGAGGCCTCCACTACTGTCACCACCTCAACTGTGGACAGCACTTCAGGCTCAAAG[G/A]TCAGTAACAAAAAGAAATTGTAATATTTTAGGATTTATAAAGTATTTGATTATTTTTTTTTTTAAACCTGATGAGTTTTCTGTGGGAACCTGTGGGACTGTGATTATGTGATTTTATTGTTGTAATGGTTTGAATCAAATGCCAACATCTGATGCATTTTTTTTTCCTACGGTTGATAATAAAGTCAACTGAACTGAACTGATTTTGATAAAGTTCTGGTATTTTGCACCAGATAGTAGAAGACAGCAGGCCCATAGTAGTGTGGTCCAGACCTTTGTATATTTTTTATGCTCTACGAATGAAAAAGGTTTTAAAATAATAATAATACTGTCAAACTGCCAGCTGTGAAACACAGGCTGTGTGAACAAGCTCTTACTTCAAGGGTGCGTGTGCAGCTTTCAATATGTCATGTTGCCAGATATGGTTCTCATAAGCATTGATTAACTGAAATTGTTTTGTAATTCTTTTAATAGTTCATGTCTAGGTTTCGTTTCAATAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6523
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086094 | Essential Splice Site | 422 | 1208 | 10 | 27 |
| ENSDART00000111450 | Essential Splice Site | 289 | 1075 | 5 | 22 |
| ENSDART00000140444 | None | None | 110 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 27197138)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 27270393 |
| GRCz11 | 18 | 27252771 |
KASP Assay ID:
554-4734.1 (used for ordering genotyping assays)
KASP Sequence:
TGGAGCAGGTGGAGAACTGGGTGAAAGTACAGAAGGAGGAACGCCACGGG[T/C]GAGTCTGCAGACGCATATGGATGTGAACATACATCTGTCACACACATTTT
Long Flanking Sequence:
GCACATACCATGTGTTTATGCCACACAGAGACGAGTGTGGTCATCCAGACCATGTGAATGTTTCGGAGAAGCTCAAGAAGCAGGCCGTCCCTCAGACCAACCACATCAACAGCTACGTGATTCCCAAACCGGAGGTCATCCAAAGTGACGGGCTACCGGAGGACAAACGGGAGGGGTTTGTTGGAGAGGTGGAGATCCAGGTTACTCCTAGAGAGATGGAGCAGGCCAGGGGTAAATCTCCAGCCAGCAGGGTAGTGGAGGTGGAGGTTTTAGCTCCAGGGTCGACACCACCCTCCCGGGTTGCCTCTCGAGCTCCTTCCAGGGCCGTCTCCACCCCGCCAGTGGTGCAGAGGAACGGGACACCCATAGAGCAGAACGGCATGCCTGGATGTCAGAGAGGGGCTACACCTTCTGCTCAAACGCCAGTTCAGGTGCAAAGGAGGAGTACACTGGAGCAGGTGGAGAACTGGGTGAAAGTACAGAAGGAGGAACGCCACGGG[T/C]GAGTCTGCAGACGCATATGGATGTGAACATACATCTGTCACACACATTTTATTAAGATTGGATCAAAGCTCCTCAGGAAAGTGCATGCCAAGGGCAAGATTTGGCCACCCCTGTGCTTGATGTTATGCAGAAGAGTCTTGGGTTATATCTCCACCTAGTGGTTGAGTTCATAAGAAGTCATTGTCACCTCACCTTTAATTCAAACTCATTTTACTTGAATAATGTGCCACAAATGTACACAAACTAGACACATGTACAGACTTCAACAAAATTGTTGCTACCCTTTAATTGTTCAAGGCCAGTTTCACTAGTAATCCTTCTCTTGAACCACAATTTAAAAGCAATATGTGATTTTCATTCATTTCTTTTTTAGAATTTTTGAGTAATCGTTATTCTTTCAGTTTCAAGTTATTTCAGTGACCAATTTTCTTTTTTCATTTCTTTTGGTTTGTGAAAACTGATCAATTGGCAGGAAGAAAATAGGTAAACATTAAACATGA
Associated Phenotype:
Not determined