ZMP
polr2a
Ensembl ID:
ZFIN ID:
Description:
Polr2a protein [Source:UniProtKB/TrEMBL;Acc:Q58EF0]
Human Orthologue:
POLR2A
Human Description:
polymerase (RNA) II (DNA directed) polypeptide A, 220kDa [Source:HGNC Symbol;Acc:9187]
Mouse Orthologue:
Polr2a
Mouse Description:
polymerase (RNA) II (DNA directed) polypeptide A Gene [Source:MGI Symbol;Acc:MGI:98086]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35290 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22095 | Nonsense | Available for shipment | Available now |
sa18581 | Nonsense | Available for shipment | Available now |
sa38889 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35291 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42025 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42026 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35290
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 |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 289 | 1965 | 6 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23918277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22441595 |
GRCz11 | 12 | 22562814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAACACACAAGTTGGCTGACATTGTCAAGATCAATAACCAGCTGAAG[C/T]GAAATGAGCAGAGTGGAGCAGCAGCTCATGTTATAGCAGAGGATGTCAAG
Long Flanking Sequence:
TAGCCTTTGTTGCTGACATAACATTCAAAAATACATTACTTTTACTGTACGTCTTCAGGGTCATGGAGGCTGTGGCAGGTACCAACCACGCATCCGTCGCTCTGGCCTGGAGTTGTATGCTGAATGGAAGCATGTGAATGAAGACTCTCAGGAGAAAAAGATTCTCCTCAGCCCTGAACGTGTGCATGAGATCTTCAAGCGCATTGCAGATGAAGAGGACATAATCCTGGGCATGGACCCTAAATACGCCCGTCCCGAGTGGATGATCGTCACAGTGTTGCCTGTTCCCCCTCTAGCTGTCAGACCGGCTGTGGTCATGCAGGGCTCTGCTAGGAACCAGGTTAGTATTTCTTTGTAGCCAGAGGGAAAGTGGGCAGGTGTACCGCAAGGGTTAGTACTGATGACTGTTAGGTTTGATTCAATTGTATGTTTTCACCTTCCACCAGGATGATTTAACACACAAGTTGGCTGACATTGTCAAGATCAATAACCAGCTGAAG[C/T]GAAATGAGCAGAGTGGAGCAGCAGCTCATGTTATAGCAGAGGATGTCAAGCTGCTTCAGTTTCACGTGGCCACCATGGTGGACAATGAACTGCCAGGTCTACCTAGGGTAAGATTTACAGTATAACTCAGATGATGTTTATACACTTTGTAATGGTTATATGCTTATTAACTGGCATGATTTGTTAATGTAGTAGTGTTTATTAATGTTTTGTTAGTGATTGTAAATATAATTTATTGTAAATATATTTATTGTAAATTTTAGGTAGTTGTAATTGTGTAAAAGTAAAAAATGCAGCCTTGTCTATATAAAAATAGATGTTAGAATGCAATGTTTTAGTTTTTTACTTTAAGTGAATCAAACGTTTTTTGTTTTTTTTTTACCATGATTTAAAGAAGAGACACACACTGTCTGGGTGGCCTTTTATAGAATATTAATTTGACAGATTTAAAGGCTTTTCTATTTGGGTTTCTATTCGCAGTGCAGCAGTAATATACTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22095
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 |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 708 | 1965 | 13 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23921025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22444350 |
GRCz11 | 12 | 22565569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATAAGGCGACATATCAGGACATTCAGAACACTATCAAGAAAGCCAAA[C/T]AGGATGTGATAGAGGTGCGGTGGCATTGTTACTAAATATCAAGGCTCTGT
Long Flanking Sequence:
GAGGACAGTGGCCCTTACAAGAACATCTCCCCTGGAGACACAAAGGTGCAGTAGTGTAGCCCAAGCATGGGCATATTTATGCCGTTATTTTTTATTTTTATATATATATTTTTTTTTGATTATTCACTTAATTTTTTGTGTATTTTTGCAGGTAATTGTGGAGAACGGTGAGCTGATCATGGGGATCCTGTGTAAGAAATCGTTGGGAACCTCAGCTGGATCACTTGTCCATATCTCATACCTTGAGATGGGCCATGACATCACAAGACTCTTCTATTCCAACATCCAGACTGTGGTTAACAACTGGCTCCTCATTGAAGGTAAAATAAGCAAATTGAGTTTGAAGGTTTTTCTCCTAATCAGGCTGATATTAAGTTCTAATCAATACGGTGTTTGTTCTTTTCTTCTTGTCTGCTTTAGGTCACTCTATTGGTATTGGAGACTCCATTGCTGATAAGGCGACATATCAGGACATTCAGAACACTATCAAGAAAGCCAAA[C/T]AGGATGTGATAGAGGTGCGGTGGCATTGTTACTAAATATCAAGGCTCTGTTATAAGACGCTTGTGCACATGTTGACTTATTTTTCTGCTTCTGTTCTGCTCACAGGTCATTGAAAAAGCCCACAACAATGAGCTGGAGCCTACTCCAGGTAACACTTTGAGACAGACCTTTGAGAACCAGGTTAATCGCATTCTGAATGATGCTCGAGACAAAACTGGATCCTCTGCCCAGAAGTCCCTGTCAGAGTACAACAATTTCAAATCCATGGTGGTGGCTGGTTCAAAAGGGTCCAAAATTAACATTTCTCAGGTGAGAGCAGTCTTCCTTGTTTTAATGTTTAAAATTTTAATGGGGCGTTCATTGCCGACAACTCAATTTTAACCCTAAACCAGAAATGAGACTTTCTAAAAATGTACATGCAAATATTGTCAGATATCATAAATTTTGGTCTTTTATGCTTTTTCTGTTCACCCGTTTAGGTTATTGCTGTGGTGGGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18581
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 |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 925 | 1965 | 17 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23922284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22445605 |
GRCz11 | 12 | 22566824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCACCTCTTTTTCCAATCACACAGGTTCAAGTTTGACTACGCCAATGAA[C/T]GAGCTCTCCGCCGCACTCTTCAGGAAGATGTGGTGAAAGATGTGATGACC
Long Flanking Sequence:
TATATTATATGAAACTGTCAAAATGTCATCAGGTTTGTCTCCATGATTTTAATTTTTCTACTGAATGTCAGGTTATATTCAGCGTCGTCTGATCAAGTCTATGGAGTCTGTTATGGTGAAGTACGATGCAACAGTCAGAAACTCCATTAACCAGGTTGTCCAGCTGAGGTATGGAGAGGATGGGCTTGCAGGAGAGGCTGTGGAGTTTCAAAATATGGCCACTCTTAAGCCATCGCACAAAGCCTTTGAAAAGAAGTGAGTTTTTTGCATACATTTTGACAGTTAAGTATAAATGTCCAGTATTTTAAATTATATATAAAATGGCTAAATTGCCCTAAATCAAAAGGTTTAAAATTGTTATCACTTGTATCGTTTAAGTCATTTTAGGTCTTTGTTGATAGCCGATAGCGAGTGCCCACGTGATGTATACAAATGTCACTGATTCAACTGTCCACCTCTTTTTCCAATCACACAGGTTCAAGTTTGACTACGCCAATGAA[C/T]GAGCTCTCCGCCGCACTCTTCAGGAAGATGTGGTGAAAGATGTGATGACCAATGCTCATGTCCAGAGTTCTCTAGAGAGAGAGTTTGAGAAGATGAGGGAAGACCGAGAGATCTTGAGGGCCATTTTCCCCACAGGAGACAGCAAGGTCTGTAACATTAAGCACCATCAATGCCCAAACACATGAACATCATTGGATATTTTGTAAATGTCTGAGGTGTGCAAATATAAAGACACAAACTGCTATGTTTTCTATAGGTGGTCCTACCGTGCAATCTGGCCAGAATGATCTGGAATGCTCAGAAGATTTTCCGCATTAACCCTCGGGCACCAACTGATCTCAACCCAGCACGGGTTGTGGACGGTGGGTTCAAAACATTGGTTTGTGGTTTTAAAAATCTGTAAATGTTAGATTTATTGTTTGATATCTTATGATATCTTTATTTTGAAATATCTTTATTTTAACATGCACTTTAAGAGACTGTGTCTGACTGGGTCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38889
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 |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 1013 | 1965 | 19 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23923002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22446311 |
GRCz11 | 12 | 22567530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGTTCATTAAATTTTCCTCTGCTTTTATTTTTGTAGGAGTTAAGGAGT[T/A]GAGTAAGAAGCTGGTGATTGTAAATGGCGATGACCAGTTAAGCAGGCAAG
Long Flanking Sequence:
GTGCAAATATAAAGACACAAACTGCTATGTTTTCTATAGGTGGTCCTACCGTGCAATCTGGCCAGAATGATCTGGAATGCTCAGAAGATTTTCCGCATTAACCCTCGGGCACCAACTGATCTCAACCCAGCACGGGTTGTGGACGGTGGGTTCAAAACATTGGTTTGTGGTTTTAAAAATCTGTAAATGTTAGATTTATTGTTTGATATCTTATGATATCTTTATTTTGAAATATCTTTATTTTAACATGCACTTTAAGAGACTGTGTCTGACTGGGTCTCCCAGCTAAATAAAGACTTTGTGCCATCTATATTAAGCCTGCTGAAGACTGATCCCTATAGCTTACTGCTGGCTTGTGGCAGACCTGTGCAAGCTGATTATAAAGTCTCAGCTTTTGCATCATTCTATACATTGACTAAAGCAAAACAAAACATTTGCTCTATTGTTATGATAGTTCATTAAATTTTCCTCTGCTTTTATTTTTGTAGGAGTTAAGGAGT[T/A]GAGTAAGAAGCTGGTGATTGTAAATGGCGATGACCAGTTAAGCAGGCAAGCCCAGGAGAACGCCACTCTGCTTTTCAACATCCATCTGCGATCAACCCTCTGTTCCAAACGAATGACTGAGGAGTTCCGTCTTAGCACTGAGGCCTTTGATTGGCTGCTGGGAGAGATTGAGACCAAATTTAACCAATCCATTGTAAGTGAATGCATTCTGAGTGCAGCTGAATGTCTGCACCTGGATAAATTGGAAATATTGAGCAAAATCAAATTGATACAATTTTAAAAGTGCCTTCATTGACTGACGCTGTACATTTTTCTTTTCCGTTTACCTCAGGCTCACCCAGGTGAGATGGTAGGTGCTCTGGCTGCCCAGTCCCTGGGAGAGCCTGCTACTCAGATGACCCTGAACACATTCCACTACGCCGGTGTGTCCGCCAAAAACGTCACTCTCGGTGTGCCTCGTCTCAAAGAGCTTATCAACATCTCCAAGCGACCCAAGACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35291
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 1174 | 1965 | 20 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23923624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22446933 |
GRCz11 | 12 | 22568152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGCACACAACCCTGCGCAAGGTCACTGCCAACACAGCCATTTATTA[T/G]GACCCCAACCCTCAGAACACTGTGGTGACTGAGGATCAAGAGTGGGTTAA
Long Flanking Sequence:
GAGTTCCGTCTTAGCACTGAGGCCTTTGATTGGCTGCTGGGAGAGATTGAGACCAAATTTAACCAATCCATTGTAAGTGAATGCATTCTGAGTGCAGCTGAATGTCTGCACCTGGATAAATTGGAAATATTGAGCAAAATCAAATTGATACAATTTTAAAAGTGCCTTCATTGACTGACGCTGTACATTTTTCTTTTCCGTTTACCTCAGGCTCACCCAGGTGAGATGGTAGGTGCTCTGGCTGCCCAGTCCCTGGGAGAGCCTGCTACTCAGATGACCCTGAACACATTCCACTACGCCGGTGTGTCCGCCAAAAACGTCACTCTCGGTGTGCCTCGTCTCAAAGAGCTTATCAACATCTCCAAGCGACCCAAGACCCCCTCCCTGACTGTCTTTCTACTGGGCCAAGCAGCCCGTGATGCAGAGAGGGCCAAAGATATCCTGTGTCGGTTGGAGCACACAACCCTGCGCAAGGTCACTGCCAACACAGCCATTTATTA[T/G]GACCCCAACCCTCAGAACACTGTGGTGACTGAGGATCAAGAGTGGGTTAACGTCTACTATGAGATGCCTGACTTCGATGTGACCCGAATTTCACCCTGGCTGTTGCGTATCGAACTTGACCGCAAACACATGACTGACCGTAAGCTGACTATGGAGCAAATTGCAGAAAAGATCAATGCAGGTGGGTCTGATATTAGTGAATAGACATACTTCTAACACTTTTAACGGGCTATCAAATTTTAATGCTTGTCTGTGTGTTAGGATTTGGTGACGACTTAAACTGCATCTTCAATGATGACAATGCTGAGAAACTGGTACTGCGAATCCGCATCATGAACAGCGACGAGAACAAGTTCCAAGAGGTGTTGTAATTTAACATTTTTATTGGTGCATGAGCATAACTGTCTACTTTCTCTCAATGTTGAATTCGAAATCTTGTCACCAGGATGAGGAGGTTGTAGATAAGATGGACGATGATGTCTTCCTTCGATGCATTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42025
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 1331 | 1965 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23924454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22447763 |
GRCz11 | 12 | 22568982 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAAATCATCATCACAGAAGATGGAGAGTTTAAAGCCCTGCAGGAGTG[G/A]ATCCTGGAAACAGATGGAGTCAGTCTCATGAGGGTCCTTAGTGAAAAGGA
Long Flanking Sequence:
ATCATGAACAGCGACGAGAACAAGTTCCAAGAGGTGTTGTAATTTAACATTTTTATTGGTGCATGAGCATAACTGTCTACTTTCTCTCAATGTTGAATTCGAAATCTTGTCACCAGGATGAGGAGGTTGTAGATAAGATGGACGATGATGTCTTCCTTCGATGCATTGAATCCAACATGCTGACAGACATGACCCTGCAAGGCATTGAGCAGATCAGCAAGGTATACCTCTTTTGGCAGTTTGGCTTCTATGCTGTCTAATACCCGACAGTCCGTTTGGCAGTGCAGGCTTGTCATAAATGACACTTGTATGCACTTCAGACAGCTAATTGGTACCCACCTGGATTATAAAGTGACAATTGGAAGGGCCTACTGTTTTGTGGATGAAATTTAAGTTTCTCCCTCTCTACACTGTTAGGTGTACATGCATCTTCCCCAGACGGACAACAAAAAGAAAATCATCATCACAGAAGATGGAGAGTTTAAAGCCCTGCAGGAGTG[G/A]ATCCTGGAAACAGATGGAGTCAGTCTCATGAGGGTCCTTAGTGAAAAGGATGTGGACCCTGTTCGGACCACCTCCAACGACATTGTGGAGATTTTCACTGTAAGAATTGTGCTGGCCTGTCTAAATGTTGTGATATATTTAAGTCCTCAGATCAAACTTAGAAATTTCTACTCTTGGCCTGCAGGTTCTTGGTATTGAGGCAGTGCGTAAGGCTCTGGAAAGAGAGTTGTACCATGTCATCTCTTTTGATGGTTCTTACGTTAACTACCGCCATCTTGCCTTGCTGTGTGACACAATGACCTGCAGGGGTCACTTGATGGCTATCACTCGTCATGGTATCAATAGGCAGGACACTGGACCACTAATGAAGTGCTCTTTTGAGGAGACGGTAAGGTCGACAGTTGACTATTAAATGTTTTAAAGTGGCAGCCAGGATGGTCTTGTAAATGTCTAAATAATTAAAAATGTAGGTGGACGTGTTGATGGAAGCCTCTTCCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42026
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077495 | Nonsense | 1937 | 1965 | 28 | 28 |
Genomic Location (Zv9):
Chromosome 12 (position 23926720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22450024 |
GRCz11 | 12 | 22571243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCCACTTCCCCCACTTACTCTCCCACTAGTCCCAAGGGCTCCACTTA[C/A]AGCCCCACTTCTCCTGGCTACAGCCCCACCTCTCCAACCTACAGCCCTGC
Long Flanking Sequence:
CCTTCCTACTCCCCCACCTCTCCCAATTACACACCCACCAGCCCCAACTATTCCCCCACTTCTCCTTCATACTCTCCCACTTCTCCATCCTACTCTCCATCCAGTCCTCGCTACACCCCACAGTCTCCCACCTACACCCCAAGCTCACCTTCCTACAGCCCGAGCTCTCCATCCTATTCCCCTACATCTCCAAAATACACACCCACCTCTCCCTCCTACAGTCCCAGTTCTCCAGAGTATACTCCAACATCCCCCAAATATTCCCCTACTTCTCCAAAGTACTCTCCTACATCGCCCAAATACAGTCCCACCTCTCCAACCTACTCCCCAACTACGCCCAAGTACAGCCCCACTTCCCCAACTTATTCTCCAACCTCTCCTACCTACACCCCAACCAGTCCCAAATACTCCCCTACCTCTCCAACTTACTCTCCAACTTCACCGAAATACTCTCCCACTTCCCCCACTTACTCTCCCACTAGTCCCAAGGGCTCCACTTA[C/A]AGCCCCACTTCTCCTGGCTACAGCCCCACCTCTCCAACCTACAGCCCTGCCATCAGCCCAGATGACAGTGATGAAGAAAATAACTAAAGATTGTTTGCGCCGGGCTTTGTCTGACTTCCCTGATGGGCAGTTTGACCCTAGGATAAAGACTGAAGGAAAGCCATCCAGCTGTGATTCACGGGGAAGGCTGAGCAACCTGGGCTCCCATCCTCTTGGTTTCTCTTTTGGACTTCTTGAACTGTTCTTAATTAGCCTCACTAAACAGGCTTCAGTGGTTGCATATGTTATTTCAGAGGTTTGAACTATAAGCCAAACAAGGCTGCCTTTGTACAGACCATTTGGTCACCATGGTGAGGGAGAACCAATAACTCAAAATTGGTGGAAAGATGCAGGTGGCTAACTGCTTTTTGGAGGAAAAAGATCACTTGTAATCCTCTTTCCATCCATCATTTCTATCTCCCTTACTTTTTCTCTAAAATTCAGTGTTGGATGTAAAGGAA
Associated Phenotype:
Not determined