ZMP
si:ch211-215m13.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
PLEKHG6
Human Description:
pleckstrin homology domain containing, family G (with RhoGef domain) member 6 [Source:HGNC Symbol;Ac
Mouse Orthologue:
Plekhg6
Mouse Description:
pleckstrin homology domain containing, family G (with RhoGef domain) member 6 Gene [Source:MGI Symbo
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36087 | Essential Splice Site | Available for shipment | Available now |
sa36086 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11583 | Essential Splice Site | Available for shipment | Available now |
sa39090 | Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28623 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36087
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 |
---|---|---|---|---|---|
ENSDART00000121458 | Essential Splice Site | 7 | 1024 | 2 | 15 |
ENSDART00000133625 | Essential Splice Site | 14 | 150 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 19112022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17142345 |
GRCz11 | 16 | 17050322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTGTTATTGGCTATTAATCATATTAATATAAACTTATCTATCTATTA[G/A]TAATCCATCAAATCCACAAGAAGTGAACAATGTCATGGCCCCGGAGGAAA
Long Flanking Sequence:
TTATAATAGTTCATTTTATGTATACCTATTATAAAAATCATACATATTTTTTATATATAAAAACAAGCAGGATATTGTATGTTCTCATTAAAATAAACAATAATGATGGAGCTTCAAATTGTGTGTATGTGGATTGTAGAATCCAGCTTTCATCAATTAAAAACAAATGTCAATGGAAAGGATATGAAAACACACCATGACAGAAAAACAAGCGTGTTACAGGTATTTTAAGGTCATGTATTTAAAGGTCACACAGCTGGCAATGAGCTTCAAAAGACTAGTTATCATTTCCTTCTAATTGTGGTTTGCAGTTTTCTGTTGGTTATGTATTATTACGCATTAACTTGCCACAATAATAAATGAAGCATAGGCCTATATTTATATTTTTGTGTAATCTCTCAGTGCTGCTGCTACTTTATCCATTCTCCCTACATATATACTTTCATCATTTCCTTGTTATTGGCTATTAATCATATTAATATAAACTTATCTATCTATTA[G/A]TAATCCATCAAATCCACAAGAAGTGAACAATGTCATGGCCCCGGAGGAAACTGCCCTCGGTGAGAAGAGTGACAGACAGCGGCAGGAAAACAATGAACCAGACGTAGACGCTCCTGATGGATTTGTTGCAGTAGCATCAACTGGTCAGCGGAGGGCTCAAGAAAAACACAGATACAACACTATAGGCTACCAGGTACTGGGTTCATATTGGTTTTACAGTATTAGGTTCATACACTGAGTCGAGCTTTCATTCCCTGCTGAAAAAAACAGCTTAAAACAGCCTAGGCTGGTTGGCTGATTTTAGCTGGTCGACCAGCCTGGTTTTTGAGGGGTTTGGCCATTTTTCCAGCCATTTTCAGCCTGGTCTTAGCTGGTCAGACTGGAAAATAACCAGCTAAAATCAGCTTGACCAGCCTGGTTTAAGCTGGACCTAGCTAGTTTTGGCCTGGCTAACAGCCTGGCTTGGCTGGTCAAGCTGATTAAGCTGGTCTTCTGTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36086
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121458 | Essential Splice Site | 214 | 1024 | 7 | 15 |
ENSDART00000133625 | None | None | 150 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 19105884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17136207 |
GRCz11 | 16 | 17044184 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAATCAATTAATCTTTTTCCATTTCTCTCTACATTTATTTCTTTTTTT[A/C]GGTTAGCCCCACGATGCTCTTTTCCGATCTTCCATCTATTCTCGATGCAC
Long Flanking Sequence:
AAGAAAATAATGATAATTTAACATATTTTTCGTTGTTCATATTGTTATTCATGAATTTTACAGTTTATGTTTGTATAAATGATGCACGTCACAGTTGCTAACCCGTTTTATGCACCTTCTCGTTTTTGCACAGCTCGTACTGGCTGCACTTTCATACTGTCATTTAAACGGATTTCTTCAAGAAGTATGTATATCGTCTCATATTTCACATGTTTACATGAAACAAAATGTTTTTCTACTGAACTGACCTTCTAGAGTTACACACTCAGCATATCTAAATGGCAAGCAGACTGAAAAATGGAAAACAAATGAACAAAACTCTACTCAGAACACTACTCTGTGCTCATTTGTGATCTAGTGCATTACTGCTTAATGGAAACATTTTATGCAGACTAGATGGAAAGTAATCTCTCTGGTGTAAAACGTGGGTTACATGTCTGTGGCAATTACCTTAATCAATTAATCTTTTTCCATTTCTCTCTACATTTATTTCTTTTTTT[A/C]GGTTAGCCCCACGATGCTCTTTTCCGATCTTCCATCTATTCTCGATGCACATCGGCTCTTTTGGCATGATGTGATGTATCCAATGTTACAAGAAGTCCGTCTCACTGGACGACCTTTTGACCCTATGAAACTTGAACCAGGGTGTTTGCAGGTGCGATGCAAGTGTTATTCGATTATAGTATTAGGAGCCCAATTTGATCTAATTTTGCATCTCCAAATATGTTTTAATTTCTCTCACTTCATCTCTTTCAGTTTCACAAACGTTTTCCTGCATATTTTGATTACTGTTTCGAAGGGGACAGAAATGTGGAGCTAACACGAAAACAGCTTGAGACGAACCCACAATTTTACACCTATCTCATGGTATTTTATATCATATACCTAAGTTTATAAAAGGAAATGTTTAAATAATATGGAGTCAATTTAGGGCCATATATACTTGCAAAATAAACAAAAATTTTACTACAAAAAATAAAGTACTGAGCACCATTAAAAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11583
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121458 | Essential Splice Site | 300 | 1024 | 8 | 15 |
ENSDART00000133625 | None | None | 150 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 19105519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17135842 |
GRCz11 | 16 | 17043819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACACGAAAACAGCTTGAGACGAACCCACAATTTWACACCTATCTCATGG[T/G]ATTTTATATCATATACCTWAGTTTATWAAAGGAAATGTTTAAAWAATATG
Long Flanking Sequence:
CTGCTTAATGGAAACATTTTATGCAGACTAGATGGAAAGTAATCTCTCTGGTGTAAAACGTGGGTTACATGTCTGTGGCAATTACCTTAATCAATTAATCTTTTTCCATTTCTCTCTACATTTATTTCTTTTTTTAGGTTAGCCCCACGATGCTCTTTTCCGATCTTCCATCTATTCTCGATGCACATCGGCTCTTTTGGCATGATGTGATGTATCCAATGTTACAAGAAGTCCGTCTCACTGGACGACCTTTTGACCCTATGAAACTTGAACCAGGGTGTTTGCAGGTGCGATGCAAGTGTTATTCGATTATAGTATTAGGAGCCCAATTTGATCTAATTTTGCATCTCCAAATATGTTTTAATTTCTCTCACTTCATCTCTTTCAGTTTCACAAACGTTTTCCTGCATATTTTGATTACTGTTTCGAAGGGGACAGAAATGTGGAGCTAACACGAAAACAGCTTGAGACGAACCCACAATTTTACACCTATCTCATGG[T/G]ATTTTATATCATATACCTAAGTTTATAAAAGGAAATGTTTAAATAATATGGAGTCAATTTAGGGCCATATATACTTGCAAAATAAACAAAAATTTTACTACAAAAAATAAAGTACTGAGCACCATTAAAAAAATGCAAACCTCCAAAAATCACAAAGCGAAAATATATTTTTGAAAAAAAAAAGGAATTGCTAACAAAAATAAACAACTGCAAAGGGAAAATAAAAATTTTAGAATTAAGATTAAATTTGCAAACAGAAAAAGAGCAGCAAATAATAACCGAGCAGTGCAAAAAAAAAAAAAAAAACTAAAACATTTGCAAACAAAAATAAATAAATAAACTGGCCTGTAAGGGTGCATTCACACATGTGGATTGATTCTTTTGTTCCGAAACAAGGATTAAAATTGTTACAATGTTGCTCTTTGTTCTTGGTGCGGTTTGCTTTCACACGGCAACAGAAATAACTGATAAACCAAGACTGCTTTCGTTAATAGTTAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39090
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 > T
Consequence:
Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121458 | Splice Site | None | 1024 | None | 15 |
ENSDART00000133625 | None | None | 150 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 19094469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17124792 |
GRCz11 | 16 | 17032769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACTGGAAGAAACTTTGAAGGTTAAAAGAAGAAAGGATACAAAGGCAA[G/T]TGACAAACTGACTATGATTCACTAATGATTATTATTTATTGGCCTCAAAA
Long Flanking Sequence:
GCATTGAAGTTCCCCATCCGAAAGGGAACTACTGTTCCTTAGCATTGCTGTTAAGATGAACCATGGCCCCAAACTGTGAGCCGAAGTTAACCGTGCCTTTGGTGTATCGTTACAGCCCTGAAAGATATGCACTGTTTTTCACTCACTATCTCTCTTTTTCTTGTAGTTGAACAGTGTCAATAATTTTGTGCAGTCTATCAATGACTATTTGCAACTGAAAGCAGATGAGCTGGCCCTTTCTGCCATTGCTCAAAGGATAGAGGGATACAAGATAGAGGGTCTAAGTGAAGAAGTAGACAAGGTAAGCAAAAGATCTTCATTCACCATTAACTCTACCTAGAGTATTAAATTAATCTAATGCAAAGTTTACCAACAGCATGTTCGCGAGATCTGCCGTTTTGATTTGACGAGCCCCATGAGTGGGGTGGGGCCAAATGTAATACGCAAGCAAATACTGGAAGAAACTTTGAAGGTTAAAAGAAGAAAGGATACAAAGGCAA[G/T]TGACAAACTGACTATGATTCACTAATGATTATTATTTATTGGCCTCAAAATTGTAACATTCGTTTCTGGTTATGTTAGGAGTTTGTGGTCCTGCTCTTTACTGATGTGCTGTTGATAACTAAAGCACAGAAGAAATCAGACAAGCTGAAGGTACTGCGCCCCCCAATGCTTGTGGAGAGAATACACTGCATTGAGGTCAAAGATGGCTGTAAGTGTGTCTTCTAATATAATCTGCTCGTTATTGATCTTGCCTGCCCAAAATAAGAAATATATATATTATTACATTAAATTATTGATTCATTCTTTTTCTTGTCGGGTTAGTCCCTTTATTAATCCGGGGTCGCCAAAGCGGAATGATCCGCCAACTTATCCAGCAGATTTTTACACAGCGGATGCCCTTCCAGCCGCAACTCATCTCTGGGAAACATCCACACACACATTCACACACACACTCATACACTGGACAATTTAGCCTACCCAATTCACCTGTACCACATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28623
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 |
---|---|---|---|---|---|
ENSDART00000121458 | Nonsense | 998 | 1024 | 15 | 15 |
ENSDART00000133625 | None | None | 150 | None | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 19069316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17099639 |
GRCz11 | 16 | 17007616 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGGAGTTTTTTGACTTTGAGGACTTAGATTATGAAAACTGGTTTGAA[C/T]AGTCACTCACCTCCAATGGAGTCCGCAGGTCAAAGACAAAACGATCGGAG
Long Flanking Sequence:
TGACAATATAAGCACACAATATAAAAAATAAGCAATATAGGACAAAATATATAAAACCACATATAGAGTATTCCATACATTAGCAAGGAAAATGCATGTGCAGTAATTATTATTATTAAATACAGTTTTTCAACAAATCAATTCCACTTCTACTCTTCAGAAACACAATCAAAAATAATTCAAAACTAAAACCATGAAAGTTTAATTACATTTCTGACTATTTGATTGTACTTTTGGTACTTTTACTATCAACTTTTAGCCTCAACTAAAATTTGAATACACACTGTTTATATTTATTAATGATAATTACTAAAATACTATTTTGCCATGAAATAGACTGCATGTCATAATTTCATAAGACATGTACCCATAACCCCCTGTTTTCTCCTGTTTGAAGCAGTAACGTTCTGGAGGGTATCAGTGTGGACTGGCCAGGCTGGTGTTTTGACGATGAGGAGTTTTTTGACTTTGAGGACTTAGATTATGAAAACTGGTTTGAA[C/T]AGTCACTCACCTCCAATGGAGTCCGCAGGTCAAAGACAAAACGATCGGAGGGCCATGATGATAACGAATGGAGTGAGGTGTAATTATGTTGAACTACTGTACTTACACAAATGAATCATGGTTTTTCTACAAATACCCTCTAATCCCCTTTTACACATGTATTTATATATACATTTGGGGTTATGGTAATCAAAAAAATTCAACCGTTTGAAAAATGTTGTGTTCTTTAAAGGTTTAATAGCATTGTGTGAGAAGTGTGTAAAGAATGTTATATATATTTTTATGATCATGTAGCATGACTATTATACTTAAATGTATTTGAGAGACATCCATAGCTTGTAAATTGTTTTTATAGATATATAATGAAAGATTGATTAACATTGTGTCTCTAAAAGTCAGACTTGTATAAAGAACAATTATTTTTCTGTATAGGTGTATATCCATTTAAGAGACTTGTTTATAACGTATTTACTGTACACAAGAAGCAGTAAGAAGTAATT
Associated Phenotype:
Not determined