ZMP
pard3
Ensembl ID:
ZFIN ID:
Description:
partitioning defective 3 homolog [Source:RefSeq peptide;Acc:NP_991298]
Human Orthologue:
PARD3
Human Description:
par-3 partitioning defective 3 homolog (C. elegans) [Source:HGNC Symbol;Acc:16051]
Mouse Orthologue:
Pard3
Mouse Description:
par-3 (partitioning defective 3) homolog (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2135608]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14266 | Nonsense | Available for shipment | Available now |
sa17998 | Nonsense | Available for shipment | Available now |
sa10740 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14266
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018729 | Nonsense | 270 | 1112 | 6 | 21 |
ENSDART00000056402 | Nonsense | 270 | 1127 | 6 | 22 |
ENSDART00000129134 | Nonsense | 270 | 1332 | 6 | 24 |
The following transcripts of ENSDARG00000010583 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 43371681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43421145 |
GRCz11 | 2 | 43270563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCRGTGGGACGTGCGGACACATGCTTGGAGCAMATGGGAGTGAGATCAT[T/A]GGAGTAAGWAACACGAACACTGTAAAAAATGCCACACAATTCCTTCATGY
Long Flanking Sequence:
GGTTCGGATGAAAACTACCTTCAAAGCGGTTTACACTAACACACAAGTAGTGTCTCCGCAGCAAAACATGGACCTGTGGCTTACTACAACTTTAATGAGAGCTTGTGTATGCATGTGTGTGGGTGTTACTGGGATGATAAAGTGACATGAGCTAGTGAACATGAGCTCTTGTGTTCCTCTCACCTGAGCCGCGGTGTATCAGGTGAAACATCTCAGAGGATGAATTCCTTCAAACTGTTTAGAAAAAGAAGAACTGCTTATCTGTCTGCTGAAGTCTTCACCCAGGTCATGCTTTACATTTGTGTTTCATTTCTAATTTATTGACATTGCGCTGTGGTTGTTATTCATGCAAATGGGTTTCTGGAAGGGACTTGTTGAGTGCGATCGATGCATTGTGGGTTTAGCGGTTTTCTTCTTGTTGCAGGATGAGGAGGAGAATGGAAGGATAGAACCGGTGGGACGTGCGGACACATGCTTGGAGCACATGGGAGTGAGATCAT[T/A]GGAGTAAGTAACACGAACACTGTAAAAAATGCCACACAATTCCTTCATGTTGTCCCAACACCAATAGATTAAGTTCACTTTTTTTCCAAATTTAAGTAGATTGAACATAAAACAATTAAGTTGTCCCCAAAAAAACAGATGAAATCAAAGCTAACAATATGATTTTGTTTGCTCACATTACTAGTTTTGTGGAACAATGAACAATTCATCTGTGCATGTCATTAGGAACACCGTTAAATTCTCAATTACGTCTGTCTGAGGTGGGTGTGGTTAACATACTTGACCACACCCCTCCAACTGTCAGTTTTGACAACAGAAATGGTGAGGATGAGGTGTCTGTTAGGTTGTAATAACTCTCCCCAAACCCTTTTCCTGAGTCCTTACCTGAGATTCAAATGCCAACTATATTACATCCAATCAGCTTGCAGTACAAAAAACAAGCCATGCCCACTTTTTTCTCATATATCACAATATCCCTTTTCTTTAAGAACTGCGTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17998
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018729 | Nonsense | 649 | 1112 | 14 | 21 |
ENSDART00000056402 | Nonsense | 649 | 1127 | 14 | 22 |
ENSDART00000129134 | Nonsense | 649 | 1332 | 14 | 24 |
The following transcripts of ENSDARG00000010583 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 43394274)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43443738 |
GRCz11 | 2 | 43293156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGAAGGCTGCGGGTCAACGATCAGCTTATTGCAGTCAATGGGGAGTCGT[T/A]RTTAGGGAAGACAAACCAGGATGCCATGGAAACGCTGCGCAAGTCCATGT
Long Flanking Sequence:
TAAAAATAAAATCTTCCCAGGAAAAAACATGACATGCTCAATAATTATTTCCCCTATTGTAGATGTTCATTCATTCGTTTTGTTTTTGACTTCCCTTTATTAATCTGGTGTTGCCACAGCTGAATGAACCCATACATTCTAATTCACACACATACGCTACGGCCAATTTAGCTTACCCAGTTCACCCATACCACATGTCTTTGGAATTGTGGGGAAAACCAGAGCACCCAGAGGAAACCCACTCTAACGCGAGGAGAACATGCAAACTACACAGAAAAACCACCCGATCAAGCCAAGCCTCGAACCAGTGACCTTCTTGCTGCGAGGCTCTGCACCACCATGTCACCCCACTGTAGATGTTATTAGAAGCATATCTGATATCTATCCATGAGAACGTTTGATATCTCTCTAATCATATATGAATTCTCTTCGCAATCTCGTGTTGTAGGACGGAAGGCTGCGGGTCAACGATCAGCTTATTGCAGTCAATGGGGAGTCGT[T/A]ATTAGGGAAGACAAACCAGGATGCCATGGAAACGCTGCGCAAGTCCATGTCAACGGAAGGCAACAAGCGAGGGATGATTCAGCTGATCGTGGCGAGACGCATCAACAAGCGCCTCGAGGTAAAGATTCAAGAGTCACGTCTGAGAGCTTCATCTGCATTCATTTCATTGTTTGAATATGCTTCATGCATAAGTTATAATTCATTAGTTCAACTTAAAGGAGACCTATTATGCAAAAATCACTTTTATAAGGGTTTTAAGCTCAGTTGTGTGGCAACAGTGTGTAAATATAAGCAGCTTCTAATGGTAAATTTGAATTGATTCTATTTTTTATAATCACACTTGATAAAAAACTGTCTGCAGAAACACTTTGATTGACATTCTCCCTTTGAACGAGTCATAAGAAAGCTTCACCCATTAGTGGTTATCTCTCCTTAATTAGCATAGACAGCCCTAAGTGAGAGGCAGCCATCCTCCATTAGAGTTTTCACATCATACCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10740
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 |
---|---|---|---|---|---|
ENSDART00000018729 | Nonsense | 895 | 1112 | 18 | 21 |
ENSDART00000056402 | Nonsense | 910 | 1127 | 19 | 22 |
ENSDART00000129134 | Nonsense | 895 | 1332 | 18 | 24 |
The following transcripts of ENSDARG00000010583 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 43417739)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43467203 |
GRCz11 | 2 | 43316621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAYGGTGACATGCCGTTTCACCGGCCGCGACCACGGATTATAAGAGGA[C/T]GAGGCTGCAATGAGAGTTTCAGAGCTGCCATTGACAAATCCTACGACAGG
Long Flanking Sequence:
ATTTTCTTCTGAAAAATAACAGCTTTGTTCTACTATTGTAGTATTACAAACACTCAGCCTTATTATATTTAAAAATAGCAAAGAGAGTCTTGACACGCTTCAGTAAGGCACTGCTGCGTGATGAAGATAAATTCACGCAATCTTTCCTGTCCTCCACTTACATTCATTTATCTTCATCACTTAATACAGAAACACTTTCACTCGCTCCCATGGCTGACTACATACAATAGCAGCGCACACACACACTCATAATGTTTAGATAAATGTACCTGCTTTTATCAGTGTTACGCTTGAGATTTGTAGCACGCGGTCTGCGTCGTTGATTGTGTTATGTGGTTAAACTGGTGAACTCTTCCTCAGGCTCTTCCACGCGAGATGTGGGCCCGTCTCTGGGACTGAAGAAGTCCAGCTCTCTGGAAAGTTTACAGACCGCAGTTGCAGAGGTTACGCTCAACGGTGACATGCCGTTTCACCGGCCGCGACCACGGATTATAAGAGGA[C/T]GAGGCTGCAATGAGAGTTTCAGAGCTGCCATTGACAAATCCTACGACAGGCCTGCAGCCAATGAGGATGAAGAGGAGTGCATGGACACACGTACGGCAGTTCCTGATTGGTTTTAGCTAATAATAGTGATGATTTGATTAAAGTGATAGTTCTCCTAAAAATTAATAGTTAATACTTTACAATAAGGTTACATTGGTTATTGTATTTTATTTATACTTTTTAATGTTAGTTATTGAGTTCGTATATGTTGAACTAAGATTAATAAATGATGTAGCAGTATTTTTCATGTTAGTAAATGCATTAACTAATGAAACCTTATTGTAAAGTGTGACCATTGAAAATTCTCTCATCATTTATTCACCCTACAGTTGTTCCAAATGTATCTGAAATTTCGATCATGTTTTGAATGTTGGAAAGCCATTGACTTCTCATTGCATTTTTATTCTTGCAATGGTTTCCAACATTCTTTAAAATCTTTTTTGGATCATTTTTACATAAAC
Associated Phenotype:
Not determined