ZMP
plekha3
Ensembl ID:
ZFIN ID:
Description:
pleckstrin homology domain-containing family A member 3 [Source:RefSeq peptide;Acc:NP_957501]
Human Orthologues:
AC005795.1, PLEKHA3
Human Descriptions:
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:C9J6N1]
pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 3 [Source
pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 3 [Source
Mouse Orthologue:
Plekha3
Mouse Description:
pleckstrin homology domain-containing, family A (phosphoinositide binding specific) member 3 Gene [S
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13861 | Nonsense | Available for shipment | Available now |
sa35108 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13861
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 |
---|---|---|---|---|---|
ENSDART00000079117 | Nonsense | 33 | 298 | 2 | 8 |
The following transcripts of ENSDARG00000056601 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 30641450)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29517436 |
GRCz11 | 11 | 29764610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCAAGGTGGTTTGTGCTGGACAATGGCATTATTTCCTATTATGAYTCA[C/T]AAGATGACGTGTGCAAAGGAAGCAAAGGCAGTATTAAGATGTCAGTGTGT
Long Flanking Sequence:
CAGTTTCAGACCAAATATTCAAACTAGTGTGGTAAACAATATGTGACTGTTAAAATAAACAAATTTGCAAAAATAAAACCAACATTACCTCAGTGTTGCAGTTTAGAAAGTTCCCGAAAGTGCACTTTTTGCTGAATTGAATGTGTTTGCTTTTTTGGATTTTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCTCTTTTTGGCTTAGTCCTTTTATTAATCAGGGGTCGCCACGGCGGAATGAAGTGCCAACTATTCCAGCACATGTTTTACACAGCGCATGCCCATCCAGCCGCAACCCAGTACTGGCAAATATCTCAGTTAAACTAAATTCACATAACATCTGTTGCTTTCATTTGTAAGTTGTTCTGGGAAAAAAAAGAAGTATGTGCCAAGTGATTAACGTAAATGTTTTGTGGTGTGTTTTCTGACAGGATGGCAGCCAAGGTGGTTTGTGCTGGACAATGGCATTATTTCCTATTATGATTCA[C/T]AAGATGACGTGTGCAAAGGAAGCAAAGGCAGTATTAAGATGTCAGTGTGTGAAATTAAAGGTGAGGTTATTAGTTTCCTTCTGTCCTTACAAGAAAGGAAAACTGGTTATTTTTATGTCATCTTGGACTTCCTTGTGTTTTTCCAGTTCACCCGACTGACAACACGCGTCTGGAGCTCATCATACCAGGAGAGCAGCATTTTTATGTGAAGGCTGTAAATGCAGCCGAGAGGCAGAAGTGGCTGGTGGCTCTGGGAAGCTCCAAAGCCGGACTCATTGACACTCGAACCAAAAAAGAAAGGGGTGGGTTTTCGCTTATTATGTGCTCATATTTATATATCTTTGGGCGGTTATTGAAATGCCTTCTGTGCTTAGCTAAAGACTCAAGCAGAGGACAAATATACATAAAATGCCTGTATAGGGCTTATTGATCTGATTTTTGCAACTAAGATGTTTTATTTATATATTTAAAATGTTGATTAAATAATAAAAAATGTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35108
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079117 | Nonsense | 173 | 298 | 5 | 8 |
The following transcripts of ENSDARG00000056601 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 30638902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 29514888 |
GRCz11 | 11 | 29762062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTACTAAGTGCCACCTGTGAAACCTTCATCAAAACACTGGAAGAATG[T/A]ATGAAGATCGCCAACTCTAAGTTCAAGACTGACATGTTGCAGTCCAGTCC
Long Flanking Sequence:
AATTTGGCTCGTGTATATTTGTTTTTAGTTTATTGTATTTATTTTTAGTGAAGTTAAAATCATTGGCATTAAATTAAAATCGTTGGCATTAAAATAGCCATTTATGTTTCTGACAGTATTAAATAAAAATATATGATACAATAACAAGATATGCACATCACACGGGTTTCTACTGTAAATAAAAGGCTTATTATTATAATTATAAAAGAATTATAAAAGGAATTATTTAAATAATTAGGAATTTATTATTTTTTTATAAACTCTGCTGTACATATTTTGCACGTAAGCTGCATGCACCTCAAATATGAGACATTTATATTTAATTATCTGCCAGTAAGGTGTATCAATTTTAAGAGTTGTAGGCAATGAATTGAACCTTGATTAATCACTGGCATCCTTAATGGAGTTATATTTGTTTATCTGTTTGCCCAGACAAGGAACGAGGCGTCCTCATTACTAAGTGCCACCTGTGAAACCTTCATCAAAACACTGGAAGAATG[T/A]ATGAAGATCGCCAACTCTAAGTTCAAGACTGACATGTTGCAGTCCAGTCCATCTGATTCCATAATGTCTCCTGTGTCCCCATCTCCTGTCCAGATGTCTCGGGTAAAAACAATAGCAGTTTACAAAAAAAAAAAAAATTCTTTATTTAAAATAAAAAAATATAGAAATCTATTGTTATTATTATTATTATTATGCAATTTAAATATGATATTATATTTTAGATATTATTATTATAATATATATATATTTTTAATCTCTATCAATTCTTGTTGCTTTGTGTTTTTAAATAAAATATAAATGACATTTTTGCGAAATTATGTGTGCCTTAGAATTTTCTTGATGATTTTCATGACAATTCAAAACTGAAATTAATAAAAGAAATCTATAAAATTAATCAATCAATTAATTAAAAAAAAATGTATTTGTGGCATTATTGGAATGAAACTTTCTCCTGCTCCACTGTAATGTGAATTAAGGGGAAATATTTATTTGCAATCATA
Associated Phenotype:
Not determined