ZMP
plekhh1
Ensembl ID:
ZFIN ID:
Description:
Pleckstrin homology domain-containing family H member 1 [Source:UniProtKB/Swiss-Prot;Acc:Q00IB7]
Human Orthologue:
PLEKHH1
Human Description:
pleckstrin homology domain containing, family H (with MyTH4 domain) member 1 [Source:HGNC Symbol;Acc
Mouse Orthologue:
Plekhh1
Mouse Description:
pleckstrin homology domain containing, family H (with MyTH4 domain) member 1 Gene [Source:MGI Symbol
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39172 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11978 | Essential Splice Site | Available for shipment | Available now |
sa28898 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9622 | Essential Splice Site | Available for shipment | Available now |
sa23139 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39172
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075941 | Splice Site, Nonsense | 69 | 1432 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 38133493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38018390 |
GRCz11 | 17 | 37965975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAACAGAGAGTCATAGAGGCTGACCAGAGAGCAGAGAGCGCCGAAAAG[C/T]AGGTATTGCTATTGAAAACAATGTTGTCTCTTTCAGAATTCATCTGTATT
Long Flanking Sequence:
ATAAACTACACTTAAAGGTAAACAAGTCAAAACAAAGCAAAATCACTTTGCTTTCAGTATGTTCTGAAAAATTAAAATGTGATGCAAAAAACCCAACAGCGTTCATGATGTAGGACTGTGTGGCTTGTTTACAAGGATGTGCCTTAAGGCTTTTCGCCGTGCTGTCAAACCAACATGCAGGTCTTGTTGATAAGCGTAGTGGTTTGTGTCATGAGCATGTCCAAACCCGCAGCTGTACAATATGCCCTGAGTATTTAGAACCGGATTATGATCAAAATCAGTTAGGCATGAAAGATAACAACACTCCAAATCAGATATACAGTACAGTAGATTGTTCTTATAGTTTATCTCACACTTTTAGTTTATATAACCAACACACACACATATACATCCACAGCCTTAACCGAGCAATCCGTGATCCTGTCTGTTTCTTTCTGTAGATGCAGGAGCTGGAACAGAGAGTCATAGAGGCTGACCAGAGAGCAGAGAGCGCCGAAAAG[C/T]AGGTATTGCTATTGAAAACAATGTTGTCTCTTTCAGAATTCATCTGTATTTGAATGTTTTTTAACCCTTTAACTTGCACTCTAAGAATGTTTTGGACAAGTTATTTCTTTGATTAAATTGAGTCACCCAAAGCAAATGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTTGTTGTAATGAAAACCTACAAAAGGTCAACAGACAGTTACAATACAATTATATGGATGAGTGATGATTTAATATATCTAGATTAATGTTTAAAAATATTGCCATGATTAAAAAAAATAATAATAATGTAATTAAATATGTATATGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATGTATATATATATGTATATATATATATATATATATATATATATATATATATATGACAAGACAAAAAAAGGAAGTTCGGTGCGCTTTTTATGTCGCTAGGCAAAGACTGAATTGGCTTGGTATTGTGCGAGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11978
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 |
---|---|---|---|---|---|
ENSDART00000075941 | Essential Splice Site | 760 | 1432 | 15 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 38153646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38038543 |
GRCz11 | 17 | 37986128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCATGGATAAAGAAGTCAAGCCTACAGCGCKAGGCTGGTTAAYAAAGG[T/C]AAGAGTTCACWKGAGTGTTAACAATGYRCTCCATTATTTCGTTTCAAGTT
Long Flanking Sequence:
GTGCGTGAAGTGTCCAACATTCCACACGTCATATTACCAATTGAATAACTGCATCATGCGGATAATCAAAGTGCACTATTCTTTTTTCAGAGTTTTCAGTGTGAATGCACTACTTACACTATTTAAACTACAAAATAGCATAGAGTAGTGCATAAGTATGCAATTTGGTATGCACATAAGGTTTGTTGGATCAAAGTATTTTGTTCACATAAAGTTAAGTTTAATCACAGTGTTGACAAAATCCTATTAAAGGCTGTGTGTAAACGTAATACATTTTTAGAGAGCCACGTTTGTTCTAAACCTTTATCCATCTTTTTTCTCATTTATTTGTTATGACTAGTTAATTACAGAGAAGAAGACCTTTTACTTGGCTGCAGACTCCCCAAATATCCTGGAGGACTGGATCAGAGTTCTCCAGAATGTTCTCAAGGTCCAGGCCAGTGGACCAATTTCCATGGATAAAGAAGTCAAGCCTACAGCGCGAGGCTGGTTAACAAAGG[T/C]AAGAGTTCACATGAGTGTTAACAATGCACTCCATTATTTCGTTTCAAGTTTCCGAATTTTGATTTGGAGGTCTCTTATAGTAAGATTACATGCAACAACAATAAAAAATAACAAAAATTCTCAAAGTGTCTGAAATGGTCCTTTAATAATCTGGTTTCTCTAAAGACCTTCTTTTCAAGAGCCTACACTGTTTTGATTGGTCAGTTGGCCTAGTCTGTTCTACACTGTGTGGAAAACCTGTATGCCATGTATGACTTTCAGCTTTAGAAGCTTTCTCAGCACTTGTATACACAATGCCATGAACAGTAATGATGCAACCAGGCCCAATTCTTTATCTATTGAACATGCATGTAAAGTGGATTCGAATTCGCAGTGCAGTAAACACAGTAACATGCCGACAGCATAAGCATGTTTGTGGGTAGTAGTTATTGAGATGAGATGTTAAACCGAGGTCAAGACTCTCTGTGGTCATTAAAAATCCCAGGATGTCCTTCGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28898
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 |
---|---|---|---|---|---|
ENSDART00000075941 | Nonsense | 782 | 1432 | 16 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 38159138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38044035 |
GRCz11 | 17 | 37991620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAAAGCTTGTGTGGTGTGCCTTAATTGGGAAAGTCTTTTACTACTAC[C/T]GAAACCAAGAAGACAAGGTGAATATCTTCACATTTCTGAATTAAAAGCTT
Long Flanking Sequence:
AAAAGTTTGGGAATCCCTGATCTAAATAACTTTCTTTCCTGCTTGCAAAGGAGGGACTTTTTAGGGTATTTTTCTTTCAGACTCCAAATTTATGAAAAATGAAATTAATTAAATGAATTATCGATGGTAACTTATTAAGGTGTGAGGTAATCAGTTTACTGGCATTCGTAACATTGATCACTCAATAACTCATGTCTTCCCTTGTCTTATGCCTGTGTTTTTAGCAGATTACCCATACTTCATTTTCATTCAGGTTTTTGACCTTGTGCTGTTCTTGGTGAATCACTTTGGTCTTTATGTACTGTAAAAGAATGTACTGTGCTTTTATATTTGCATTGTGTCTGCATCTATCTGCATCTACTGTATGCCACAACACAGATTGAATATATTTGGGCTGTTGTACATCTGGAATTAATCAGTTTTTTTTTCCACTCCAGGTGAAACATGGTCATTCAAAGCTTGTGTGGTGTGCCTTAATTGGGAAAGTCTTTTACTACTAC[C/T]GAAACCAAGAAGACAAGGTGAATATCTTCACATTTCTGAATTAAAAGCTTTTCAAAGTTTTAATTAAAGTCCATGTGTCATCAATATTTACAATTTATATTTTGCTAGTGCACATATTATTCTTTAGGTAAACAAGAAGTCTGTGCAAGTTAATCCACTTAATAAAAATGTTTGTTTTGGTAATCTTTAATCAAAAGCTGATCATTTGCTTCAATGTATGAAGTGGTGGTCCTTCTCTGTTGACGTCAGTTTGACTGCTTCAGTTTGACTTCTCTTATTACTGTTTATTTGCTATGTAGACTTTAAAGGGTCATGAAACACCAAAACACATTTTTTGAGGTGTTGACAATCATATACAGTATGTGTTCCACGATGCTAAAAGCACACACATAAGGACACATATATTTCACCAAAAAGTAAAAATTGGTTGTTTTTGCGTTATTTAGAAAAATGTAAGCTACGTCACGGCGATGAGATCCTTGTGTAAAATCCAGCGTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9622
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 |
---|---|---|---|---|---|
ENSDART00000075941 | Essential Splice Site | 787 | 1432 | 16 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 38159156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38044053 |
GRCz11 | 17 | 37991638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCCTTAATTGGGAAAGTCKTTTACTACTACCGAAACCAAGAAGACAAG[G/A]TGAATATCTTYACWTTTCTGAATTAAAAGCTTTTCAAAGTTTTMATTAAA
Long Flanking Sequence:
GATCTAAATAACTTTCTTTCCTGCTTGCAAAGGAGGGACTTTTTAGGGTATTTTTCTTTCAGACTCCAAATTTATGAAAAATGAAATTAATTAAATGAATTATCGATGGTAACTTATTAAGGTGTGAGGTAATCAGTTTACTGGCATTCGTAACATTGATCACTCAATAACTCATGTCTTCCCTTGTCTTATGCCTGTGTTTTTAGCAGATTACCCATACTTCATTTTCATTCAGGTTTTTGACCTTGTGCTGTTCTTGGTGAATCACTTTGGTCTTTATGTACTGTAAAAGAATGTACTGTGCTTTTATATTTGCATTGTGTCTGCATCTATCTGCATCTACTGTATGCCACAACACAGATTGAATATATTTGGGCTGTTGTACATCTGGAATTAATCAGTTTTTTTTTCCACTCCAGGTGAAACATGGTCATTCAAAGCTTGTGTGGTGTGCCTTAATTGGGAAAGTCTTTTACTACTACCGAAACCAAGAAGACAAG[G/A]TGAATATCTTCACATTTCTGAATTAAAAGCTTTTCAAAGTTTTAATTAAAGTCCATGTGTCATCAATATTTACAATTTATATTTTGCTAGTGCACATATTATTCTTTAGGTAAACAAGAAGTCTGTGCAAGTTAATCCACTTAATAAAAATGTTTGTTTTGGTAATCTTTAATCAAAAGCTGATCATTTGCTTCAATGTATGAAGTGGTGGTCCTTCTCTGTTGACGTCAGTTTGACTGCTTCAGTTTGACTTCTCTTATTACTGTTTATTTGCTATGTAGACTTTAAAGGGTCATGAAACACCAAAACACATTTTTTGAGGTGTTGACAATCATATACAGTATGTGTTCCACGATGCTAAAAGCACACACATAAGGACACATATATTTCACCAAAAAGTAAAAATTGGTTGTTTTTGCGTTATTTAGAAAAATGTAAGCTACGTCACGGCGATGAGATCCTTGTGTAAAATCCAGCGTGTAGACTGGATGTCTGTATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23139
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 |
---|---|---|---|---|---|
ENSDART00000075941 | Nonsense | 1370 | 1432 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 38187095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38071992 |
GRCz11 | 17 | 38019577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGGCTTTGGGCAAAAAGACTGTGGATAAACTTCTATTTGCAATGGCT[A/T]AACCAAAGGTAAGACGTGATGTTACAAAAGGTAAAACAGAGTTTAACAGC
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCTCAGTATTCACTGATGATTAGAAAGTTTAAATTATTTTTTTTAAATAACTTAAAAATATTTATTGCCACTCATGAGAAAATTAATGTGCCATGATTAATTAATGTGCCATGAAAATTAATGTGCCAAAAGATTAGTTTCTCTGACGAAGAGAAAGTTTAAAATGTATATTTATTTTACATTTTTAGTCAATTAACACATCGTTGGCCCTTTGTTGATTTAAAAAAAAATTCGAAGCTTTGAACTCTTGTTTTAGTACACTTTAACAAAAGCCTGTAATCTTCTCAATTGAGTGTGTTCTGCTTTTCTTTAGCACCCACTGGTCACATATCCATACCAGTCGGTGATCACGTTTGGAGGCTGCAAGGAGGATTTCATGCTGGTGGTCAGCCTGATTAAAGACCAGGCTTTGGGCAAAAAGACTGTGGATAAACTTCTATTTGCAATGGCT[A/T]AACCAAAGGTAAGACGTGATGTTACAAAAGGTAAAACAGAGTTTAACAGCATTTACAAATGCGGCCAGTAAAGACAGTATTCTGATACACATGCTGCTTTTAGCATTACCTTTTATTAAATATCTAGGAAATCTGATCTTAAGTGTGCGGGGTGAAATCAGACCTTTTAAACAGCTTAAAAGCCGAGGTAAACTTCTACAACCCCCTCTGAAACCTGAATGACATCTTGATAGTTAAAACAGGTTTTCATTGACGTTTGCACTCATACGGCAAGTGCTAATGGCAGCCAGGATTTCAGCATTTCTGAAGTCAAAATTATAAGCCATTCTGTGAAATTTGAATTCTTCGAATAGAGCTGTTTAACAGAGCAATACTATTATCAATTGATTTCTAAAAACTAATTCATTGTATCTTTGCCATGATAATAATATATAGTGTTTTACTATTTTTAAGAGATACTAATTTTAAGCTTAAATTGCAAAGGCTGTTTAATAGCTAAT
Associated Phenotype:
Not determined