ZMP
pwp2h
Ensembl ID:
ZFIN ID:
Description:
periodic tryptophan protein 2 homolog [Source:RefSeq peptide;Acc:NP_998212]
Human Orthologue:
PWP2
Human Description:
PWP2 periodic tryptophan protein homolog (yeast) [Source:HGNC Symbol;Acc:9711]
Mouse Orthologue:
Pwp2
Mouse Description:
PWP2 periodic tryptophan protein homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:1341200]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19511 | Essential Splice Site | Available for shipment | Available now |
sa18575 | Nonsense | Available for shipment | Available now |
sa14829 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32693 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19511
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 |
---|---|---|---|---|---|
ENSDART00000110270 | Essential Splice Site | 44 | 937 | 2 | 21 |
The following transcripts of ENSDARG00000037109 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 27880588)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28146146 |
GRCz11 | 1 | 28949978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTCATCAGTCCTGTAGGCAACCGCATCTCCGTCTTTGATCTGAAAAA[G/A]TAAGTATCACACGTTTCACTGCCCGACTAAGTTTATTGGGTCGTGAGCTC
Long Flanking Sequence:
TTTTACTTGCTTCTTTACACAGTATTTGTCATAATTTTGTAATAATGCCGAGGCGACTTTAAAATGCAGATGTAGAGTACTTTTAGTTTGGTAATGATCCGGAAGTATTCTTGAACACGTGCGTTTAGAGTGTGTTTTTTTCACGTGTGGATCCATGGTATTGATGCTTGAAAGATCAGTTGCAACGTCTTAGAAAATATGAAGTTTGCGTACAAGGTATTCATTTTTTTCTTATAAAAAGAGTCTCGTTTTCTTTAAACATTTATGTATATCAGGTTGCCTGCTGGGTAAATTTTTGATAAAGACTGTTGTAAAATAAATATACAAAGTTGTTTGTTTTATCTGTACGATAACATTTAATTTAAACTTATTTTAATTTCTTTTTAGTTTTCAAACTTATTAGGGGCATTTTATCGCCAAGGGAACATATCTTTCTCTAAAAATGGGGATTCTGTCATCAGTCCTGTAGGCAACCGCATCTCCGTCTTTGATCTGAAAAA[G/A]TAAGTATCACACGTTTCACTGCCCGACTAAGTTTATTGGGTCGTGAGCTCAAAGTACTGTTAAGTGAGTTACGTCTTACTGCTTTTAGTTGAGAAAATGTTTTATATTTCCCCAGTAACAAGTCAGAAACCTTACCGGTGTCCACCTCAAAGAACATTGCTTGTTTTGACATCTCTCCAGACGGAAATCTTGCTATACTAATAGATGAAGGTATGTGAAGGTACCCAGCCACCGGCATTTTAACAGTGATGCAACTAAATACCTGATTCAGTCAGGTCTATAGTTAGATCAACGTTGAATTGCCTTTCTGTTTTGCAATTGGTTCAGTGATTTGGTAATCACTGGCAGGCCCGGATTAAGAACTCCGGGGCCCCTGGGCACATTGTCTTGTAAGGCCCCCTACCTGGCCGCACCCCTATAGATGAATTAAAAAAATAAGAATAATATAATAATTTTTAAATAAAATGAACCTATAATTTGTTTCCCACATATTTAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18575
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 |
---|---|---|---|---|---|
ENSDART00000110270 | Nonsense | 224 | 937 | 7 | 21 |
The following transcripts of ENSDARG00000037109 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 27860342)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28125900 |
GRCz11 | 1 | 28929732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGGAAGGCACTTTATGTATATGGGAAAGTGACACTGATCTAGAAGGCT[T/A]ACGAAAGGGCCCAAAATACGCTGAGAGAAAGGAAAAGGAGCAGAAAAAAC
Long Flanking Sequence:
AGGGTGCGCGTCCTCATGGTAGTAAACAAAAAGTGCGTGTGATTCACAGCTGACATGTGATTTCGCGGCTGCGAAAATGTCATTACATGACGACAGAAATTACATTTTACGTGAATTATACCTCATAAATACAGTATGTGACACTTTCAACACCAGTTGGAGGTGACCTTGTTGCTGAGCAACATTTATCAAACAATGTGAAGACTTGTGCGACTGCCTTTCTCCTGACTGTGAAAATATAATTGGCTGTATCCTAAAAAAGTCGAATTAAGATTATGTGTAGGGTCGAATCAAGTTCGCGATCATTTTTCTAATAATCGTGCTCGTGCAGCCCTAGCAGTAATGTTAATTGTCTTAGTCCCCTGTTGCCATTTCTGTATTTTATTATGGTATCTTTCAACTGCTTTTCATTTTTTTTTTTTTTTTTTTTTTACAGATGTACACAGTAAGTCAGGAAGGCACTTTATGTATATGGGAAAGTGACACTGATCTAGAAGGCT[T/A]ACGAAAGGGCCCAAAATACGCTGAGAGAAAGGAAAAGGAGCAGAAAAAACTGAGAGTTTTAGAAATGGAGGAAGATGAAGCTAATGACATTGAGATTATGGGGGAGGATGGAGAGACCAGAGGAGATGTCATCAAAGGAAGTGCCGAAACACCTGAAGAAGTGGAAGGCATAAAAAATGTTCGTTATTTACAGAAAAGCAAGTGAGTATGTTTTGATTTATCCTAATCTCTTCAATCTATGGATCTGTTCTCAAGATTTGTTCACACCATGGTAAATATTTGCGGCAAAAATGTGCAACTTTCCTTTTTTAATTTTTTTTTTTTATCAGGGCTTAATTTTTCCCAATTATTTAAAATGGAAAGTTTCTGAAGCCTTTTTGAAAAGATATTAGAATTTTCTAGGTCAGAGGTCCTCAGCCCTACTTCTGGCGACCCCTCTTTCAAAATTCAATCTACAACATTCTTCAACATACTTGTCTGTATATTTTTAAATTATACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14829
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 |
---|---|---|---|---|---|
ENSDART00000110270 | Nonsense | 286 | 937 | 7 | 21 |
The following transcripts of ENSDARG00000037109 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 27860155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28125713 |
GRCz11 | 1 | 28929545 |
KASP Assay ID:
1641-0485.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAGTGCMGAAACACCTRAAGAAGTGGAAGGCATAAAAAATGTTCGTTA[T/A]TTACAGAAAAGCAAGTGAGTATGTTTTGATTTATCCTAATCTCTTCAATC
Long Flanking Sequence:
ATCAAACAATGTGAAGACTTGTGCGACTGCCTTTCTCCTGACTGTGAAAATATAATTGGCTGTATCCTAAAAAAGTCGAATTAAGATTATGTGTAGGGTCGAATCAAGTTCGCGATCATTTTTCTAATAATCGTGCTCGTGCAGCCCTAGCAGTAATGTTAATTGTCTTAGTCCCCTGTTGCCATTTCTGTATTTTATTATGGTATCTTTCAACTGCTTTTCATTTTTTTTTTTTTTTTTTTTTTACAGATGTACACAGTAAGTCAGGAAGGCACTTTATGTATATGGGAAAGTGACACTGATCTAGAAGGCTTACGAAAGGGCCCAAAATACGCTGAGAGAAAGGAAAAGGAGCAGAAAAAACTGAGAGTTTTAGAAATGGAGGAAGATGAAGCTAATGACATTGAGATTATGGGGGAGGATGGAGAGACCAGAGGAGATGTCATCAAAGGAAGTGCCGAAACACCTGAAGAAGTGGAAGGCATAAAAAATGTTCGTTA[T/A]TTACAGAAAAGCAAGTGAGTATGTTTTGATTTATCCTAATCTCTTCAATCTATGGATCTGTTCTCAAGATTTGTTCACACCATGGTAAATATTTGCGGCAAAAATGTGCAACTTTCCTTTTTTAATTTTTTTTTTTTATCAGGGCTTAATTTTTCCCAATTATTTAAAATGGAAAGTTTCTGAAGCCTTTTTGAAAAGATATTAGAATTTTCTAGGTCAGAGGTCCTCAGCCCTACTTCTGGCGACCCCTCTTTCAAAATTCAATCTACAACATTCTTCAACATACTTGTCTGTATATTTTTAAATTATACTGAAGAGTTTGATATAAATTTATATTAATGGTGCTTCAATACAACTAATAATATTCAGCAGAGGTAAAACCTGTGAACAAGATATGCTTAGAAAATGTGCCATGCGAGCAGTCACCTTTAATAGCCCGTTTCCACTGAGTGGTACAGTATGCTTTTATGGCTGTTTCCACTTTCAAAGGGTACCTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32693
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 |
---|---|---|---|---|---|
ENSDART00000110270 | Nonsense | 393 | 937 | 10 | 21 |
The following transcripts of ENSDARG00000037109 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 27854791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28120349 |
GRCz11 | 1 | 28924181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTGTTTAAACAGCAAGGACACTTTAACAACATGAACTCTTTGGCTTA[T/A]TCACCTGATGGTCAGTATCTTGCTACTGGAGGGGATGATGGCAAGGTGAG
Long Flanking Sequence:
TGACCTCCATCTAAAAAAAAAACTGTAGATTTACTCTCTAAATATACATTTATGCCATTTAATATTTAGGTTTTTTATTCATTTGTGTTCTTGCTACCAATTAAAAATGATAAATATCTTATATTTGAGCTGTACACCTTTGGTTGAATTGACACAAATGACCCAGTTCTTATTTAATTAAGTCTCTTGACCTTTTGTTATTTGTTGCTATAATGCTGTGGCTGTATTTCTATGCTGTTTAATGAATATCATGTTTAGCATTTCAGATCAGAGGATTTCGGCCATTTCTCTGAATCCCACTGGTGACTGGATTAGCTTTGGCTGCTCAGGTGTTGATCTCAAAGTTTTTTTTCCCCTCAGAGTACTGTTTTATACTGTTTCTTAATTCTTTGCTTCTGTCCTGTGTTAGGTCTGGGCCAGCTGTTGGTTTGGGAATGGCAGAGCGAGTCCTATGTGTTTAAACAGCAAGGACACTTTAACAACATGAACTCTTTGGCTTA[T/A]TCACCTGATGGTCAGTATCTTGCTACTGGAGGGGATGATGGCAAGGTGAGTCCTCTAACTCTATAATTTTATTAAGGAAATAAATACATTTTTTTGATGCTTAGGGTGCACATTCTCACACTTAGTCAAGTTGCTTAGTTTCATGAAGAAACCAAGAAGAGTTTGATTCATGTGTTTTTTTTTTTCTTTTCCATACAAGTAGATGTCTCTACCGTATGTGTGTATTTGTGCATTTTTACTGATTTGGGTACACTTTCGCAGTATGTGGGACATTTAGAAAACATTGTTCACATAATTGATACAGACTAGTCTATGAAATCAAATGAACCTAGATGCATTGCAGACCAAAAATTCTAGTGTGGTTGTCCTCCCCAAGTAAAACGGTTGCTTTCCAGGTGAAGGTGTGGAACACCAACAGTGGTCTCTGTTTTGTGACATTCACCGAGCACTCCAGCGGTGTCACCGAAGTTGCCTTTACCTCCAGTGGTTTCGTGGTGGTC
Associated Phenotype:
Not determined