ZMP
si:dkey-21n12.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
RSF1
Human Description:
remodeling and spacing factor 1 [Source:HGNC Symbol;Acc:18118]
Mouse Orthologue:
Rsf1
Mouse Description:
remodeling and spacing factor 1 Gene [Source:MGI Symbol;Acc:MGI:2682305]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34954 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa27652 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31793 | Nonsense | Available for shipment | Available now |
sa10481 | Nonsense | Available for shipment | Available now |
sa15230 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34954
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077161 | Essential Splice Site | 187 | 1369 | 4 | 22 |
ENSDART00000135302 | None | None | 113 | None | 3 |
ENSDART00000138344 | None | None | 707 | None | 11 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 37875617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36687778 |
GRCz11 | 10 | 36631536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAAGAGCAGGATGATTTGGATGGGTCGTCCTGGAAATGTATAGTAAG[G/A]TAGGCATTCTGCATTTAATTTTTGTCCTCTTATTATGCCTTTTTGAAGTA
Long Flanking Sequence:
TTCACACACAGTTCCATATAGCTTTTTATCATGAATTATTTTGGTGCTAAATGAACATATGCATAATGTAATTTCCTATGCTTTTATTGTAGATTTGTCAGGAGTTTAACACCACATGGGCATGGGAGTTGGAAAAGAAAGGTTATCAAGAGTTGACAGTGGAGTGTAAGACAGGAATATTGAAGGTAAGATGAGGAAACCACTGGATTGAGAAACACTGGAAATCAAAATCCAACTATAAAAATTGTTTTGGATTTTTTTATTAACCCAATTTATCTTGTGTTTCTCTACCAGTATTTGTGTGAATGCCAGTTTGATGACAATGTCAAGTTTAAAAATGCTATCAATGAAGAAGACCCGGATAAAATGCGACTTCAGCCTATTGGCCGAGACAAAGACGGCCTCATGTACTGGTTCCAGCTGGACCAAGACCATAATGTAAGGATCTATGTGGAAGAGCAGGATGATTTGGATGGGTCGTCCTGGAAATGTATAGTAAG[G/A]TAGGCATTCTGCATTTAATTTTTGTCCTCTTATTATGCCTTTTTGAAGTATGATTTATTACAAATTTCTCAGAATGAGGCTGTAAATTTACTTGTTATCGACCTTATTCTTTGTGTGCGAGCGGGAGCAACCATTTGAATCTTTTTGTATTGAAGCCTCCGGTCTCATACGTTCATTCATTTTTAGACATTAAAAACAGCTGGTTCTGCTGCTTGATTTTGCAAACGGATATTTTCTTAATATATTATTTTGCCTTGTCTGTATTCTCATGGACACACTTGTTTGTAGAGAAAGTAGTTTCTGGCATTTACTATTCCTAGTCATTTCACGCAGCGGCAACTGAATCTCAAGTTCTAAAACAATCGCAACAATGAGCACACTTCCGCATTGAAGAATGAGGTCAATACAATAGGGTTGTCACGATACTGGAATACGGTACCAATCAATACTGAAGTTTTAAGAACGTCCGTTTCCCGTTAACGTTTGAGTGCTGTTGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27652
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077161 | Splice Site | None | 1369 | None | 22 |
ENSDART00000135302 | None | None | 113 | None | 3 |
ENSDART00000138344 | Nonsense | 270 | 707 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 37862932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36675093 |
GRCz11 | 10 | 36618851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATAACATTTTTTGAAGGTTGAAGTGGAGGAAGAAAAGGAAGAGGTTT[T/A]GGTTAAGGATAAAGCGGAGACGAAGAAGAGCAAAGGCTGGGGACGGAGAT
Long Flanking Sequence:
TAAAATGGTCAAAAATGTTGATTTAAAAATGCTTAATTTAAAATAATACAAAACAATAAAAATAAAATATAAAAGGGGCAGTATAGTGGCTTATTGGTTAGCATTTTTGCCTCACAGCAAGAAGGTCGCTGGTTTGAATGCCGGCAGGGCCAGTTGGCATTTGGTTTCCCCCACAGTCCAAAGACATGCAATATAGGTGAATTGTATGAACCAATTTGGCCATATTGTATGAGTGTGTGTGTGTGAATGTGAGAGTGTATGGTTGGTTTCTAGTACTGGGTTGAGTCTGGAAGGGCATTCACTGCATAATACATATGCTAAAATAGTTAATTCCACTGTGGCGACCCCTGAATAATAAGGACTAAGTTGAAGAAAAATAAATGAATGAATGGTTCTTTAAAAAGTCATTGAAAGTATTTTAATCTCATCCATGAAAAAGTGGGAACCCTGATCATAACATTTTTTGAAGGTTGAAGTGGAGGAAGAAAAGGAAGAGGTTT[T/A]GGTTAAGGATAAAGCGGAGACGAAGAAGAGCAAAGGCTGGGGACGGAGATCAACCAGAGCCAAGAAATACATAAGCTACAGGTATATCTATCTCCTTTGCTCACACAATAATCTTATGGTCTTCATAAATCATCTTTATTCACTTTTTATTGCTCAATCTTGCACAGATTCGATGAGTTTGATGAAGCGATCGAAGAGGCGATTGAGGAGGACATTAAAGAGGCAGAAGGTGGAGGTGAAGGAGCTTTTATTTGCTCTTGCTGTGCAGTATTGTTGATGTTTGAGCTTGAATGACTGATCAGATGTGTGTGTTTTGATCCAGGAGCAGGACGAGGGAAGGACATGGCGAACATCACAGGCCACAGAGGGAAGGACATGTCCACCATCCTGCAGGAGGAAGGCAAAGAGAACGGCCGACCACAAAGAACTAGCGCAGCGCAGAAGAAGAAACGGCGGCGTCTCAATGATCTGGACAGCGACAGCACTGTAGATGAGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31793
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 |
---|---|---|---|---|---|
ENSDART00000077161 | Nonsense | 1125 | 1369 | 19 | 22 |
ENSDART00000135302 | None | None | 113 | None | 3 |
ENSDART00000138344 | Nonsense | 441 | 707 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 37859957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36672118 |
GRCz11 | 10 | 36615876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATCGTGCGAACAGAAGGAAAACGAGCCGGAGTCGAATCCGGAGAAAA[C/T]AACCTCCGCGCAGGAGACGCAGACCCAGAGGATACTCTGATGAAGAGGAG
Long Flanking Sequence:
CTTTAAACCTGTATGGGTGAAAATACTAGTGGCTGCAGCCCTCTAGGAATTGAGTTTGAGACCATTGCTCTAAGACCTTAAAATATTTTACATGAAATCTGAGAGCTCCCTCATCCTTCATAGACAGCAACAGTCCAGAGACATTCAGTCCAGAGTAATCATCCTCAAAACAATCCCTGTGTTTTTTTAGGTGATCCAATCAGAATATTATTAATCAGCTAAAACACTTTTGTGCGCATATTAAGCAAAAATAACCATTTAATTGCAGTTTATTTCTCCTCAGTGTCAGTATAGGGAGCACAGTATGTATCAGTGTAATGACATTTGCTCTACTCTGATTGGTCAGCAGTTCTGAGGAGGAGTTTGTGGCGTCTGAAAACGCTGAAAGTGAAGACAATGCGCCATCCTTAGAGGACAGCGACTTTGACAGTGATGCTCAAGGTTCACGAGTGAATCGTGCGAACAGAAGGAAAACGAGCCGGAGTCGAATCCGGAGAAAA[C/T]AACCTCCGCGCAGGAGACGCAGACCCAGAGGATACTCTGATGAAGAGGAGCTGGAGACTGATGAAGAGGAGGAGGAAGAGGACGAGATGGGTGAGGCACAGATTCATTTGTTCAGGATTGGAAGTATTTTTAACGAAATATTGAGAAATCAAAACATAAGAAAGGTTTTAATAACATCTATTAGCTAATATAAGACCTGTTGTTTAATTGGGTTGCATTTTGAGGCAAATTAAAATGGTAACTTTTTTGTTGGCTAATAAGCATTGTTTATGTATTTTGCTAGTTTTTGTTTAAATTTACTGTGTTGACTGATTGGTGTGTGTTTCTCTACAGTGACGGAGGGCTCTAGTGAGTTCAGTGACAGTGATCTGGACGTCCGCTGTCGACGCTCGTATCGCAGCCGAAAGCAGGAGGTGAATTACTGTGAAACTTCAGATTCAGACGGCTCGCAAGCCAGCACCAACAAAGACAAGAAAAAGAAGCGCAGACGACTGTCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10481
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 |
---|---|---|---|---|---|
ENSDART00000077161 | Nonsense | 1309 | 1369 | 22 | 22 |
ENSDART00000135302 | None | None | 113 | None | 3 |
ENSDART00000138344 | Nonsense | 647 | 707 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 37857301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36669462 |
GRCz11 | 10 | 36613220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTYCCAGTCCAATAAACGACAACACAGCGGAGCCTCCYTCTACTAATGGA[C/T]AGAGCCCTATAAAGGGTCTGGAGGGCGTCGYGCCACGGCCGGGAGCAGGA
Long Flanking Sequence:
AATAGCTTTTTTTGCCTTTAAATAATTTACAAATTGTTATTCAGTAAATTGGGTTGATATCAATCTCCAAAACCAATACATATCATTTTAACATAGTTTAGACTGATTTAATACATACATTTTTGATGGTTTTATTCTCTTTTGCTCCTCCAGCCAGTTTCCAGTCAGCGGAATCGGAAGAAGAAGAGCGAAAACCCAAGAAGATCAGAGCCGACTCGTCTGAGGAGGAGGAATCCAGGAAGCGACGCAGACGTTTATCCCTAAAGCGCCGACGGGAGTCAGAGGACGATGACGATGATGATGATTCAGATGAATCCGAGGAAGAGGAGCGTCCTGTCCGGAAGCGAGTAAACCGAATCGACTCTGACGAAAGTGAGAGCGAAGAAGAGGAGAAGGAGGTGAAGAAGAGTCCGCAGGAGAAAGACACAGAAGAGACGAGCGCTAGTAAAGGTCCCAGTCCAATAAACGACAACACAGCGGAGCCTCCTTCTACTAATGGA[C/T]AGAGCCCTATAAAGGGTCTGGAGGGCGTCGCGCCACGGCCGGGAGCAGGAGCAACGCCTAAAAATGGCAACACACCATCCATAGCACCCAATGGCCTGGAAGCCGGCGCACAGGAAGAAGACGAAGACGATCTTTTGGGCGTCACAGACCTCGTAGACTATGTCTGCAACAGCGAACAGTTATAACCTGGCATTCATCTTCATCTTTTTGTAGACCCTCACCACAGATCTCATCAACAGTCCCTGTTATAAATGTGCCAGCGGAACAGATTGTCCACGACACGTTAATAATAATAATAATAATAGCTGTAAATATTTTACCGAACAAACAGTATCAAGAGAAGGAGACGGCAATCCTTTCCCTGAGATGTTTCTTCTCAAACGAAACTCCTCTCTGGAAGCAAAACCTCAAAAACCTCTTTCTTTTTTTACACTAATCACTCAGCCATCTGACATCGGTCATGTGTTTCGATCTCCACTGCTGTCTGTCGCACATTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15230
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 |
---|---|---|---|---|---|
ENSDART00000077161 | Nonsense | 1362 | 1369 | 22 | 22 |
ENSDART00000135302 | None | None | 113 | None | 3 |
ENSDART00000138344 | Nonsense | 700 | 707 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 37857140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 36669301 |
GRCz11 | 10 | 36613059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAAGAAGACGARGACGATCTTTTGGGCGTCACAGACCTCGTAGACTA[T/A]GTCTGCAACAGCGAACAGTTATAACCTGGCATTCATCTTCATCTTTTTGT
Long Flanking Sequence:
CAGTCAGCGGAATCGGAAGAAGAAGAGCGAAAACCCAAGAAGATCAGAGCCGACTCGTCTGAGGAGGAGGAATCCAGGAAGCGACGCAGACGTTTATCCCTAAAGCGCCGACGGGAGTCAGAGGACGATGACGATGATGATGATTCAGATGAATCCGAGGAAGAGGAGCGTCCTGTCCGGAAGCGAGTAAACCGAATCGACTCTGACGAAAGTGAGAGCGAAGAAGAGGAGAAGGAGGTGAAGAAGAGTCCGCAGGAGAAAGACACAGAAGAGACGAGCGCTAGTAAAGGTCCCAGTCCAATAAACGACAACACAGCGGAGCCTCCTTCTACTAATGGACAGAGCCCTATAAAGGGTCTGGAGGGCGTCGCGCCACGGCCGGGAGCAGGAGCAACGCCTAAAAATGGCAACACACCATCCATAGCACCCAATGGCCTGGAAGCCGGCGCACAGGAAGAAGACGAAGACGATCTTTTGGGCGTCACAGACCTCGTAGACTA[T/A]GTCTGCAACAGCGAACAGTTATAACCTGGCATTCATCTTCATCTTTTTGTAGACCCTCACCACAGATCTCATCAACAGTCCCTGTTATAAATGTGCCAGCGGAACAGATTGTCCACGACACGTTAATAATAATAATAATAATAGCTGTAAATATTTTACCGAACAAACAGTATCAAGAGAAGGAGACGGCAATCCTTTCCCTGAGATGTTTCTTCTCAAACGAAACTCCTCTCTGGAAGCAAAACCTCAAAAACCTCTTTCTTTTTTTACACTAATCACTCAGCCATCTGACATCGGTCATGTGTTTCGATCTCCACTGCTGTCTGTCGCACATTTCAGAGAAAAATGTGGAAGTGGGCGGAGTCTGTGCGAAAGGGGGAGGAGCCTGAGGTGATGCGCTATTCCACTCCGAGGCCATTTTTTTAAACATTCGTCTTTTTTATAATCAACATACGAGCGGAAGTTAAATTTCTAGTGTCATTTTGCTGGGGAATTGTTTT
Associated Phenotype:
Not determined