ZMP
scaper
Ensembl ID:
ZFIN ID:
Description:
S phase cyclin A-associated protein in the ER [Source:RefSeq peptide;Acc:NP_001116519]
Human Orthologue:
SCAPER
Human Description:
S-phase cyclin A-associated protein in the ER [Source:HGNC Symbol;Acc:13081]
Mouse Orthologue:
Scaper
Mouse Description:
S phase cyclin A-associated protein in the ER Gene [Source:MGI Symbol;Acc:MGI:1925976]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa3292 | Nonsense | F2 line generated | Not yet available |
sa12343 | Essential Splice Site | Available for shipment | Available now |
sa25235 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38119 | Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44341 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa3292
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000035382 | Nonsense | 452 | 1551 | 8 | 31 |
ENSDART00000103324 | Nonsense | 328 | 1318 | 8 | 30 |
Genomic Location (Zv9):
Chromosome 25 (position 33546662)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32157064 |
GRCz11 | 25 | 32568021 |
KASP Assay ID:
554-2488.1 (used for ordering genotyping assays)
KASP Sequence:
CCCAAGAYAAATCTCAGGACGTGAGGGAGCAAGAGCCACCCATACCCCAA[G/T]AGCCCAGCAAAGAGATGGAAAAGACCCCGGTCATCGAGGTAATGACGTCA
Long Flanking Sequence:
AATACAAGACTTGCATTCTATGCTAATGAGGGAGAGATTGTCACTAGTGGGTGGGGCTTTCCCCCTCTGAGGGAGAATGGAATGTCAATCAAAGTGTTTCTACAGACTGTTTTGATCAAGTGTGATTATAAAAAAACCTAATTATTCAATTTTTACCATTAAAAGCTGGTTATATTCACAGACTGCTGCCGCACAACTCTGTGTTAACCCTTTATGAAAGTGATTTTCGCATTATAGGTCCCCTTTAAAGGAGATCCGTTAAAGGTGTACTGGTTTATGCTGAGCACTGTATGCATGTCCATCAACCCTTAGCAAAGAAAGATGCAGAAGGCTGGGAGACGGTGCAGCGTGGGCGCTCCATGAGGCCAAGGGCCAAAGTAAGCCCAGTTCTGGTTCATGCGAGCCCCAAAGACGACAGTGACAAGGAGAACCAGCACGTCCAACCCTCACCCCAAGACAAATCTCAGGACGTGAGGGAGCAAGAGCCACCCATACCCCAA[G/T]AGCCCAGCAAAGAGATGGAAAAGACCCCGGTCATCGAGGTAATGACGTCAACCAACCTTCCGTCATTAATTATTTAGAGCCCAGCCATAGATATGAAGCCTCTGAAACATCAGAAAGTGTTTGTTTGGTCACAGTGTGTTCATAGATACACTGTCCAGACAGGCCAGTATCAAGTGGACGGGCATCGATTTTTGAACATGTTTATCAGATTCAATGAGGCCTATTAAATATTGACGATACGATGTCCTGGATTGCGTTTGGAGAATATGCCGAAGCCAAACCAATTGAGCTGCCATGCTATCTACTTCCTCCTGCATAGACACCTGCCTTCTAAGAGACGGAAATAGAAAGTCATCAGTGAGTGATTTGGAGGGTAGGGAACAGCTCTGAAGTGCACGTGTCATTAACACGTCACTCTAATTAGAATAATACATTCTTCAGATTTAAAGGGATAGTTCACCCAAAAATGGAAATGCACTCAATTTAGCCTTCATGAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12343
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 |
---|---|---|---|---|---|
ENSDART00000035382 | Essential Splice Site | 953 | 1551 | 18 | 31 |
ENSDART00000103324 | Essential Splice Site | 720 | 1318 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 25 (position 33567891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32178293 |
GRCz11 | 25 | 32589250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ARCTCACACCGTATGARCGGAAGAAGCAGTGCTCGCTCTGTAACGTTGTG[G/A]TAAGTACWGCATTATGGGATGCGTYAKGATTATATAARGAGCAGATAAAT
Long Flanking Sequence:
ACTTTGAAGATCACCTAAACTCTTTGCAGCTTGAATACTTTTATTTATCGCCCCTGAATGATTATTTTTATTTACTGATAGGGATCGTGAAGAGCGTTTGGCTGCTCTCAGCGCAGCTCAGCAGGAAGCCATGGAGGAACTGCAGAAGAAAATCCAGATGAAGGTAAACTATAGTATTATACTGTGCTACTGGTGTTTGGAGTTTTACTACTGATCATAGAGCTGTGCTTCCCTGACAAGATGTGCATGAGAATCGTGATCTCGATGTCATTAGAATTAATCATTAATTGATTTCAAACACCCTTTTTATGTTCATCACCGTTTACAAAAACTGTTCATGTTTTCAGCACGACGAGAGCAGTCGCAGACACATGGAGCAGATGGAGCAGAGGAAGGAGAAAGCCGCTGAGCTGAGCAGTGGGAGACACGCAAACACAGACTACGCTCCCAAACTCACACCGTATGAACGGAAGAAGCAGTGCTCGCTCTGTAACGTTGTG[G/A]TAAGTACTGCATTATGGGATGCGTTAGGATTATATAAAGAGCAGATAAATGCCATTGCTGGGACCACTAATTGGCAATTTAATTCATTTTGTTTTAGTTTGATTTTGGATCGCTTAGCTTTGTCACGATACTGGAATACCAATCGATATTACATTTAAAAAATGTCCACTGCCGCTAACATTTGAATGCGTTCCTAAACAGCGCTGATTTGCCATTGTGTTCACGTGCTCTGCAGAAATGACTGTGATTGGCAAAGAAGCTCATCAGTTCACCCAACTGTTTACTGAGTGTAACCACGGATACAGAGACACTGGAGTAGTTTAAAGCTGCAATTCATCAGCAGCTTTAAAACGCTCCAGTGTCCCGGAATCTGTAGTACAAGTAACGATGACATTCAACAACTGGAAACATGTTTAAGAAACTGAAAACATATTTAGCTTTTTTTGTTTATATGGTAATGTAAAAAAACATCTTGTGGTATAAAACTTACCTCTGTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25235
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 |
---|---|---|---|---|---|
ENSDART00000035382 | Essential Splice Site | 1057 | 1551 | 21 | 31 |
ENSDART00000103324 | Essential Splice Site | 824 | 1318 | 20 | 30 |
Genomic Location (Zv9):
Chromosome 25 (position 33600018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32210420 |
GRCz11 | 25 | 32621377 |
KASP Assay ID:
554-7761.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCATGGAAGCCAAAAGCCAGACCTCCGACTCTCCGTACAAGGCCAAG[T/G]AAGCCCCCCCTGCTCTGCTTTTTAAGGATCATATACCCAAACAGGGGTGT
Long Flanking Sequence:
GATGTGTGATTGTCAGGAATTTCGCTCGGCGGACCACACCAGTGTTTCAAGCTGACTGACAGCAAACATTATTCTGCTCTGTGACTCTCCAACATTCACAGAAGTAATTCACACCGTCGGCCAATCATCCTTATTTATTTTGCGTTTCTGAACTTAAAGAGTGTGTCGGTATTCCCTGCTGTGAGACTCTCTGAAGACGGAGTGTTTGTGACTCGTTCCTGCTTGTTAGTTTGTGATTGCTGCTAGTGCGGCCCAAAGACTAAATAAACAGTTGGAGGCTCAGCTTGACCTCTCGACCTTCTCTTTGTTCGCCACGTCGTCTTATCTCCTCACGTCTTCTGGCTGACAGCCATCGGACTCCTCTGTTGCTCTCCGTCTGTCTTTTTCTCTCCGTTTTTTTTTTCTGACAGGCTTGTTTGTCTTTCTTTTTCAGGGCTAAAGAGTACGAGACCTGCATGGAAGCCAAAAGCCAGACCTCCGACTCTCCGTACAAGGCCAAG[T/G]AAGCCCCCCCTGCTCTGCTTTTTAAGGATCATATACCCAAACAGGGGTGTTATGCTGAGTATTTAGGTCTTCATGCTGTCTTTCAGAGCTTTAAACTTCAGAAATGATGCCCGCCCCAGGGGTTTCCTTTATTAAAGCTGTATTGTTTTGCTCTAGATGCAACGTCCCGCTTCATACTAAGTGGCCTTAACTATTATGTACTTAACTACATGTTTTTACATTGTACTTATGATTGATTAAATACTTACATGTATCTACACCTTTAATTAATTTCTCCCACACTTAAACCTACCCTTTCCACCAAACCTGTTCCTAACCATACCCGTATCCCACCTCAACAGTGCCTGAAGTGTTCAGCTATACATTATAAACACATTACGTACTTTGCATTTAATTTCAATGCAAGTACATAGTAGTTAAGACAACTTATTATAAAGTGTGGACTAGATGCAATACTGATGTCTTAAGTGGTGTTTTCATGAATCTACTGTTTATAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38119
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:
Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035382 | Splice Site | None | 1551 | None | 31 |
ENSDART00000103324 | Splice Site | None | 1318 | None | 30 |
Genomic Location (Zv9):
Chromosome 25 (position 33601750)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32212152 |
GRCz11 | 25 | 32623109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACAGAACTCTTGGGGAGATCTCACGAATTCTAGAAAAACAGGTTTGTT[C/A]ATCTCTCTCAGGTCTCGTTTGCGCTAGTGCGTTTTAGTTTAAAACAGCGT
Long Flanking Sequence:
ATGGTCAATTCTGATTTTGTGACTGTATGCAATTTTTTTGATGACCTGTTTACATCCTCTTTTAAAAGTGACTCTTATTCGATCGTCTGCATTTACACAGCACACGGCAAAGGCGCAATGACCAGGGAAAAAAAGAGCGGGCGCTGACTAACAGCTGATAATTAAAGAGTGCTCTATTCCTGTATGTGATCTGTTTGCAGCTTTTGACAAGCTGCTTTACTATAGTTTTACTATAGTATATATATATATAATAAACATATAATAATAATATATGTAATATATATATATAATAAACATTAGGAGTCTTTGTAGTGTCCACATATAGATAACAAACTAAACATGCGCATGTGTGTGTCTTTCTTGCAGACTCCAACGTCTGGTGAAGGACCTGGTAAAGCAACAGCAGGGGCAGGACAGTGGCCAGTGGGCCAGTAACAAAGTGTCCGGCCTGGACAGAACTCTTGGGGAGATCTCACGAATTCTAGAAAAACAGGTTTGTT[C/A]ATCTCTCTCAGGTCTCGTTTGCGCTAGTGCGTTTTAGTTTAAAACAGCGTTTTAGAATGAAAATGATCCGCGTCCATACTAGCGTTTCCCCCAGCGTTTCTGAACATCTCTCCGTCTACACCAAGGGTCTCAAACTCAATTTACCTGGGGGCCGCAGGAGGCAAAGTCTGGGTGAGGCTGGGCCGCATAAGGGATTTCACAAAAAAAAGTCCTCAAATGTCATTATTAACAGTTTTAATTATTTCTTCTGAACATGAAGTGTCCTGAACATTAATAGAACATTGAGTGAAGATTATGAACAGTTCTTCTGAACATGGCATCTTTTGCCTACTTCTTGCTGCCAGAGACTTGACAGCGCTTCTTCTCACAAAACTGAACCACATTTGGCTTTAGAGCAGAAGCAGTTGAGACCCTCAGTATGGCTTGAAGATGATCATCATTAAGTCTAGACCTGTACTTTGACTTATTGAAGTCCTAGGGAAAAAAGTGGGGGAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44341
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 |
---|---|---|---|---|---|
ENSDART00000035382 | Nonsense | 1272 | 1551 | 26 | 31 |
ENSDART00000103324 | Nonsense | 1039 | 1318 | 25 | 30 |
Genomic Location (Zv9):
Chromosome 25 (position 33663815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 32274127 |
GRCz11 | 25 | 32681191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGAACGTGGGCTTGATTGACAAGTTGTACGGCTGCTTCCTGTCCATA[C/T]AAGGGCCAATCGATGAGAGTCCCAAGATGGCTGCCTTTCTGGAGCAAGCC
Long Flanking Sequence:
TCTATGTTTTTTGTTTCTGTTTTGGTTTGTTTTTTATTTGTTTTTTTTTGGGGGGGGTTGTTTTGTTTTGCTTCATTTACTTTAGGTTTTGTTTTGTTTTGTTTTGTTTTTAGTTTATTTTTATTTTTGTTTTAGTTTAGTTTGTATTTGTTTTGTTTACTTTAGTTTATTTTGGTTTTTGTTTTGTGTTTTGTTTTGTTAATGTGTGTAATTATATGCTTATTCAGTTTGGGACACAAGTCCGCTGATTTTTGTTTGTATTTACTCTTGTTTACAAAGTTTGGTTCATAAATACCAAAAAAAGAAGTCTACAGAATCTATCTGTTCCTGCTGATAAGGCAAAATGAAATGTTGAATATCAATTTATCTCAAATAAAATGTATGTTCCACTGTTTAATATGATCCATATGTTTTATGTGTGTGTGCTTCTGCTTGTTTCCCTCAGCTATGTGGTGAACGTGGGCTTGATTGACAAGTTGTACGGCTGCTTCCTGTCCATA[C/T]AAGGGCCAATCGATGAGAGTCCCAAGATGGCTGCCTTTCTGGAGCAAGCCACTGCTTTCCTCCATGGCTTGTGCAAGTTGTGTTTTGCAGTGACCGGTCGGTGAGTTCTAGTGTCGACCCACTTTCTTTGGCTTTTTGCGGCACTTTTGTATGCCTCTTCAAAAATTTTAAGTACCATATACAGTTGAAGTCTATTTCTAATTATTAGAAATAATGACTTAAGTTGTTATTTTGAGACGTTAAGTCATTATTTCTAGATATTAAGTGGTTATTTTAAGATGGTGGTCATTTTTTAAGATACTGATTATTTTGAGATGTTAAGTATTTATTACAACATAATATCTTGTTAAAATGAGGTATTAAGTCAATATTTCAAGGTATTAAGTCATTTTTGAGATATCAAGCCATTATTTAGAGATATCAAATCATGATTTCAAGATAATAAGTTGTTATTTCTAGATATTAAGTCATTATTTTGATACCTCAAACTAACCACTTAT
Associated Phenotype:
Not determined