ZMP
plekhm2
Ensembl ID:
ZFIN ID:
Description:
pleckstrin homology domain-containing family M member 2 [Source:RefSeq peptide;Acc:NP_001124255]
Human Orthologue:
PLEKHM2
Human Description:
pleckstrin homology domain containing, family M (with RUN domain) member 2 [Source:HGNC Symbol;Acc:2
Mouse Orthologue:
Plekhm2
Mouse Description:
pleckstrin homology domain containing, family M (with RUN domain) member 2 Gene [Source:MGI Symbol;A
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30738 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa29925 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30738
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 |
|---|---|---|---|---|---|
| ENSDART00000109134 | Nonsense | 346 | 994 | 9 | 20 |
The following transcripts of ENSDARG00000078850 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24501363)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 24287929 |
| GRCz11 | 23 | 24214480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGCCTGGCAAGAAACGACGCGGCAGAGGATCATCAGTGAGTAGTGAA[C/T]AGAACGTCATCTCTCCAGAAGTGACTGATGAATGCCTTCAGATTGTAGTT
Long Flanking Sequence:
GCTTCTACAAGACTTAAAACCGTATTAATTATTACATGGTTTTCAAACTTTTTTCTTATTGCAAGTTTCATATTACAAATTCCACATCTTTATGGTAGTTTCTGCACATCCAGGAATAAGTTACACTTATGAGCACTGTAAAACATATGACCACCAGCAATGACACTTTATGTGCATCCATTATAAATGTTTCATTAATGTAATTTGTTATGCTGCTTGCTAATTTGTTTTCTCAGCATAAACCAATACTGCTAAAGAGACATGAAAAAAGATCTTTCAATACTATTTGGTACCACTAACAGTGCAGAAAAGAGCTTTTAAAATCCTTTTACCTGTGACATATTGTTCATTTTATAATGCCGAACAGTTTTATCATTAGCCAGAGGAAATCCACATTTCCCTGTCATGTTTTCACCAGTATGTTTTTGTTTGACAGAATGGCACGGCGACGAAAGCCTGGCAAGAAACGACGCGGCAGAGGATCATCAGTGAGTAGTGAA[C/T]AGAACGTCATCTCTCCAGAAGTGACTGATGAATGCCTTCAGATTGTAGTTGAGAGAGACGTCACAGTAAACCACATCACCGTGGACAGTCGAGTTCCTCTGGAGCGTGCTGACAGCACTGCTTCAGAACCCTTGAGGAATGGGAGACGCGAAGGAGAAGAAGAGGAGCCTGAAACTGGACTGAGGCTTCCAGAAATGACGGACACTTCAATGGACAACGTAGGGCAACCCCTCCGTGAGGTCATGGACAGGCTGAATGGGTCTCTGGATGCTGAGGATGGAGCAGAAGAAATTTGCACCGCTCACGACGGGCCCCCCAATCAGCAGCCCTTTCGAGAGGATGCTGGCGGTGAACCTCCAGACCCAAGCGATGGTTTCCTGCAGGCCCCGCTGCCGCCTGCAGACTTCTACTGCTTTACCTCCCAGAGTCCAGACCCTGCTGCCTCAGGTGGTGGGCGCCATGACTCTGCAGGGCATGGCGAGCCGCAGGATGTTCCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29925
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 |
|---|---|---|---|---|---|
| ENSDART00000109134 | Nonsense | 453 | 994 | 9 | 20 |
The following transcripts of ENSDARG00000078850 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 24501042)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 24287608 |
| GRCz11 | 23 | 24214159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGGATGGAGCAGAAGAAATTTGCACCGCTCACGACGGGCCCCCCAAT[C/T]AGCAGCCCTTTCGAGAGGATGCTGGCGGTGAACCTCCAGACCCAAGCGAT
Long Flanking Sequence:
AATCCTTTTACCTGTGACATATTGTTCATTTTATAATGCCGAACAGTTTTATCATTAGCCAGAGGAAATCCACATTTCCCTGTCATGTTTTCACCAGTATGTTTTTGTTTGACAGAATGGCACGGCGACGAAAGCCTGGCAAGAAACGACGCGGCAGAGGATCATCAGTGAGTAGTGAACAGAACGTCATCTCTCCAGAAGTGACTGATGAATGCCTTCAGATTGTAGTTGAGAGAGACGTCACAGTAAACCACATCACCGTGGACAGTCGAGTTCCTCTGGAGCGTGCTGACAGCACTGCTTCAGAACCCTTGAGGAATGGGAGACGCGAAGGAGAAGAAGAGGAGCCTGAAACTGGACTGAGGCTTCCAGAAATGACGGACACTTCAATGGACAACGTAGGGCAACCCCTCCGTGAGGTCATGGACAGGCTGAATGGGTCTCTGGATGCTGAGGATGGAGCAGAAGAAATTTGCACCGCTCACGACGGGCCCCCCAAT[C/T]AGCAGCCCTTTCGAGAGGATGCTGGCGGTGAACCTCCAGACCCAAGCGATGGTTTCCTGCAGGCCCCGCTGCCGCCTGCAGACTTCTACTGCTTTACCTCCCAGAGTCCAGACCCTGCTGCCTCAGGTGGTGGGCGCCATGACTCTGCAGGGCATGGCGAGCCGCAGGATGTTCCTGTTAGCAATGAAGATGAGGGAGAAGCAGAAGCAGAGGCAGCAGCTGCAGGGCAGGATCCCTCCATCGCCATAGAGACCTCAGAGAAGAAACTGAGTGAGACAGAAGAAGATGATGAAGATGCAACACAGAGCTCTCATGCTGCAGAATTCAAGTGAGATAGTAAATTGGTTATGATTTTAAGTATGTTTAGATGAGCAACAAAACATACTGATAACTAACAAAAATAAGCTCTTTACAATAGACAATGGGCTCTATGCACTGCTAGTGTTTTTCAGCCAATGATAGACTTTCAGTGGTAGCTTAATGTGACTTCGATTTCATAG
Associated Phenotype:
Not determined