ZMP
rpap2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0UYH6]
Human Orthologue:
RPAP2
Human Description:
RNA polymerase II associated protein 2 [Source:HGNC Symbol;Acc:25791]
Mouse Orthologue:
Rpap2
Mouse Description:
RNA polymerase II associated protein 2 Gene [Source:MGI Symbol;Acc:MGI:2141142]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38314 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32852 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45091 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38314
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056034 | Essential Splice Site | 169 | 601 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 10605273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11030369 |
GRCz11 | 2 | 10813968 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCCAAAAAGTCCACCTGAGATTAAGCTGATGAAACAAGGAGATGGG[T/G]AAGTACTTGCTGTTTCTCTTTAAAAAAAATTATTTAACTTAAGATGTTTC
Long Flanking Sequence:
TTCGACTCCTCTTGTTCTCTTGATGTGAGAAATGAAAAATGATGCATTGTAGCTATGTTCAGATGATAATTATAGTGCATGCTCTCGTCTTAAGTAAATTATTTAGAATTATGTTTCCCATTTAGCCTAATTCAAATAAATATTTAAATAAAAAAAACGAATACTTAAAAAAAAAAAAATGTGGGGACGGTGTCATGGTGAAAAAGTGATGTCACCGGTGTTGCGTCTTAAAACCGGTGTCATCGTCAACACCGTCTATCGTGGCAAGCCTACCTCAGAGTGGAGGAAAACATCCCCAATAGTACATAAGGGTTAAAATGGCAATCTTAACATTTAGTAAAGGACTTGACTAAGCAATTTAATGGATTTTTGCTTAATGACGTTTAATTTTTTAAAGAGAAAATCTTATTGACCCCAAACATTTGAATGCAATTTGTTTTTGTTTTCTTCTCTCTCCAAAAAGTCCACCTGAGATTAAGCTGATGAAACAAGGAGATGGG[T/G]AAGTACTTGCTGTTTCTCTTTAAAAAAAATTATTTAACTTAAGATGTTTCATGAAGGATTATTAAAAAAAGAAAAGATATTATACTTCTGTAAATGAACTAGCCATTTTATTTTTCACCGGTCCACAGAGGCAGCTCAGGACAGGAGATAAAGCTGATTGACAAGCCTATAACAGAAGCAGACATCGACAATCCCATCGAGGACATTCCCGAGTCTAACAAGGACTTGATCCAGGGTGAAAACGGTGACATCGAACAAGACTTTGTCTCCAGTGTGGTGTCCAATCAGCACAAACAAGTTCACTGGGGAAAACTGCCAAAGAGAGATGAAGTGAGTGAAGATGCTGCTGAATATTCACATTCAGAACATGAACAAAGAATCAATGGAGAAAATAAAGATGAAAGCGAATCTTCACAAACTCCTCAACCACAAAAAGACACAACCGATCATCCTGCACTGGAAAAAAACGCCTCTGAAATTGAAGGGACTTTGGAGCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32852
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056034 | Nonsense | 312 | 601 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 10604717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11029813 |
GRCz11 | 2 | 10813412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATAAATCAACCCAACAGGAAGGTGAAAACACAAGCTCTTCACAGCCT[G/T]AATCTGACATCTCTGTTCCTGTGGCTGGCGACCTGAACATTACTCAGGTG
Long Flanking Sequence:
GGATTATTAAAAAAAGAAAAGATATTATACTTCTGTAAATGAACTAGCCATTTTATTTTTCACCGGTCCACAGAGGCAGCTCAGGACAGGAGATAAAGCTGATTGACAAGCCTATAACAGAAGCAGACATCGACAATCCCATCGAGGACATTCCCGAGTCTAACAAGGACTTGATCCAGGGTGAAAACGGTGACATCGAACAAGACTTTGTCTCCAGTGTGGTGTCCAATCAGCACAAACAAGTTCACTGGGGAAAACTGCCAAAGAGAGATGAAGTGAGTGAAGATGCTGCTGAATATTCACATTCAGAACATGAACAAAGAATCAATGGAGAAAATAAAGATGAAAGCGAATCTTCACAAACTCCTCAACCACAAAAAGACACAACCGATCATCCTGCACTGGAAAAAAACGCCTCTGAAATTGAAGGGACTTTGGAGCTTTTGAATCAGGATAAATCAACCCAACAGGAAGGTGAAAACACAAGCTCTTCACAGCCT[G/T]AATCTGACATCTCTGTTCCTGTGGCTGGCGACCTGAACATTACTCAGGTGGGAATGAGTAAAAGATCAGCTGCGGGCCTCAAAGGCCTGTTGAAGGATCATCATAAAGCTAAAACGGCTTCTACAGCCATCAGTCAGTGTCTTCTGGAGCGTCTACGGCAAGCCTTTATAGAGTGGAGAACTAAGGAAACCATGATATTTCTTTATGGTCCGGATTACGCCTCAGGGATGCAACTGTCTACAGCAGGAGCATGGGAAGAGGAGCAGTTGGATGAAGATGACCTGGATGAGGCTGAGGTGGGCGTGAGATCAGCTGAAGGAGGACCTTCCAGAACCAGCGCTCCAGTTCCTGATGTGGAGACTCTGAGAAAAGAGACAGAAATGTTGGAGCTGAGAGTGAGGGAGTTTTACAAAGGAGTGTGTGTTCTGCCGGAAGAGGTCGAGACGGCCGCTGTTAAAGAGACTGAACACACACAGGTGAGGGCTTTTGAAAGTAACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45091
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056034 | Essential Splice Site | 551 | 601 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 10583043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11008139 |
GRCz11 | 2 | 10791738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATTTATTTACATGCTCATAGTTTAAAAATAATTTTGTTTGTTTGTTC[A/G]GGTTAACAGAAGTGTCACCATTGTTGCGAGAGTCGTTGGCGAGCGTGTCT
Long Flanking Sequence:
ACAGAAGCCCAAAATGGAGGAAAAAAATACGCAGTTTTAAATGATGATGATTTATGGCCATATAGAAACTTTTCACAAGACTGTCTTGATGCGTTTATCGGTCATCAGCATCTTAAATCCTTGAAAGTTTTTAGTTGTTTTTTAAAAAAGTATGAATGTTTATGATTGTATTTATGTATGTATTATATCATCTTTTCATTAAATTCCAAAAAATTACAATTACAGCTTATGCAGTGTCTATGTGGTTGGGTAGGACAGGAAATTTGACGTTGTTCTCTTTTCTGGCTGCCATTATCAGCATCACACAATTTCCTTTCTTTTTCTGAAAGTCTTGATAACACCATCATGGAGTTTTGTTTTATTATTTGAGCAAATAGGATTGTAAAAAAATGATTTCTTCCATTCACTTCACTCTGTGTACCCAAATATTGACTGTTTTTACTTTCAAAATGGATTTATTTACATGCTCATAGTTTAAAAATAATTTTGTTTGTTTGTTC[A/G]GGTTAACAGAAGTGTCACCATTGTTGCGAGAGTCGTTGGCGAGCGTGTCTTCGTTAGAATACATCTCCTGTTTCATGAAAGAGCTGAAACTGGAGGACAAAGATCTTCACAACCTCGTGCTGCTCTTCAAACCGTGCGTCCCTATACAAACGTGATGTACAGAACACTCTTTTAGAGATGAAAATAAAAACCTGTCCCAACACAATGGTTCTGTGCTACATTTGAGTGTTAAGTCATTCTGCAACACAGCCTCAGTGGAAATATGTGCTTCAGCCTACATTTCATACATTTGACTGGAGTTTCTAGGTAAGATAAATGTTACAAGGCAATTTGATGCCGATAACTTTGTTCATTTTCACACTAATTTTATTTGCATCAATACATTATAGACAAATAGGGTTCATTAACGTTCAGGTCATCAAATATATTCCACAAACAACTTAACAGTGTCTTTAATTTGTAATGAGTGTTGTGTTTTGTGTTGTGTTGTACATGGTTCC
Associated Phenotype:
Not determined