ZMP
grsf1
Ensembl ID:
ZFIN ID:
Description:
G-rich sequence factor 1 [Source:RefSeq peptide;Acc:NP_001039317]
Human Orthologue:
GRSF1
Human Description:
G-rich RNA sequence binding factor 1 [Source:HGNC Symbol;Acc:4610]
Mouse Orthologue:
Grsf1
Mouse Description:
G-rich RNA sequence binding factor 1 Gene [Source:MGI Symbol;Acc:MGI:106479]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15820 | Essential Splice Site | Available for shipment | Available now |
sa40534 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40533 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15820
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 |
---|---|---|---|---|---|
ENSDART00000074973 | Essential Splice Site | 202 | 325 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 44565748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 42347013 |
GRCz11 | 5 | 42947166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAATGGCTGAAAAGGCCCTGAAGAAAGACAGAGAAATCTTGGGAAATAG[G/A]TTGGTGTATCATCTTGTAATACTAKAAATGAATAAGGACCTTRTACAATG
Long Flanking Sequence:
GAATAAAAAAACGCAAATTTTAAAGCACTTCATAGGACGTTTAAAAGAACACCCTACAGTTTACAAGGAGGCCTTTTTGACATTTGTAGCATGCCAAATAGAATAGATCTCATCAACAACTTTGTCTTGTTTCAGTCCGTGAAGTAACAAACAAAGATGCTGAAGCCATATTAAAAGCTTCAAAGGAGCGTGTGGAGACAGATACAGTGGTACGACTACGAGGGCTTCCCTACAGCTGCACGGAGGGAGACATCATTAGATTTTTCTCAGGTGAGTACTTGTAAAATCTGACACTTGAACATCTTTATGCTGAAAAAAAATACCCATGCTTCATGTGTGTGTTCTGATATTGTTAAAATAGGGTTGGATGTTGTGGAGGACGGAGTTACTATAATTCTCAACCGCAGAGGGAAAAGCTCAGGCGATGCCTTCGTAGAGTTTGCTACAAAGGCAATGGCTGAAAAGGCCCTGAAGAAAGACAGAGAAATCTTGGGAAATAG[G/A]TTGGTGTATCATCTTGTAATACTAGAAATGAATAAGGACCTTATACAATGTGTGCAATTGTGTTTGAGTCCTTTATGACTTACTCACGAATATTTGTATCACTTCACTGTTTTTTAATATCACTTAATAGTGTTGTAACGGATTACAAATCTCACATGTTTTTTAGTCACAGATTGGAAAATTTTTCGGATCAGCCAAAAAGGGGAGGAAACAAATGTAATTTAATTTCCATTTATTACAAAAGTAGTACTGCAAGACACTTTTGGTTTTAACAAACAGAACCTAGAACCTGTAATTTAATTAAAATGAATAAATAATCCGCTGAACAAAAAAGTGCATTCTTAAATATACTACTACTGTTGCTGATAATGCAAAATCTATAAATCTAACATTATAATTTGTACAACCCTTATTTATTTTTAGCCTTATTTTTAATAAATGATTAAGTTTTCACTCATAAAACTTCATGTTTTGTTGCTAGATGTGTCATTTTTGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40534
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 |
---|---|---|---|---|---|
ENSDART00000074973 | Nonsense | 268 | 325 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 44562937)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 42344202 |
GRCz11 | 5 | 42944355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTGAATGACTAGGGGTGTCATTTTTTTTGCAGTTTTTCGCTCCTGTC[C/T]GACTTATGAAGGTTGTTGTAGAGTTTGGTCCTGAAGGAAAACCCACCGGT
Long Flanking Sequence:
AGCTTCTTGGATTGTGTTTTCTTCCTCCAGGCAGAAAAAAAAAAATCCATGTTTTGCGCTTAATTGTTTCAATTTGCAGCAAATTAAAAAATACTGTATTTTGATGGCGCACATTCACTGTTAATGACATGTTTACTGTTCCAAAATACTTTCCATGTTTCCTAAAATATAGTATATTGTGTTTAATGACAGTTAGGAAAATATCATATTTTAGAGCAGTAAGTACAATACCATGAAACAGTGATCTTTTTAATCAAGGTTATTATACCGTCAGAATCTCATACCAGCCCATGCCTAGAGCATACTTACCCAGTGTGGAAATTTGGTGTTAACAATTCAAAGCACAGTACAAACACTAGTTAGCTTTAATTTTGGCATCATTATATTTGAAATGACATTAAACCAGTATATTACTGCCTGACAGATTAATTAATCTTATCCGTTATATAAACCCTGAATGACTAGGGGTGTCATTTTTTTTGCAGTTTTTCGCTCCTGTC[C/T]GACTTATGAAGGTTGTTGTAGAGTTTGGTCCTGAAGGAAAACCCACCGGTGAAGCAGAGGCTTATTTCAAAACACATGAAGACGCCGTTTTAGCCATGTCCAAAGACAGAGAGTTCATAAGTAAGCAAAGACTCCTCCAATGACCCAAATGTTTTACACATCAAACATGAAGTGATGTTTAACTTGATGTGTTTTGTTTCTTTGTTTTTGTTTCTGTCCAGTGGAGCGATATATTGAGTTGTACCTGAATTCATGTCCACCCAGCGAAGAACGATAAGATGAAAGGACACCATATTTAAATGCACTGCATCCCAATCTGCTACAAATTAACCCAGTGTATCATGTACATTGCAAGAACCAACATTAAAAGCGGACTCTACAAATGTTGCCTGATTTTTTTACATTATGTCTGACCAGCAATGTTAAAAAAAAGGAGACGGGAGTAGATGTGGTGTTTTTTAACTTTTCCATAATAACTATTTGTGGAAGCCTTCAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40533
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 |
---|---|---|---|---|---|
ENSDART00000074973 | Nonsense | 325 | 325 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 44562665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 42343930 |
GRCz11 | 5 | 42944083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCGATATATTGAGTTGTACCTGAATTCATGTCCACCCAGCGAAGAA[C/T]GATAAGATGAAAGGACACCATATTTAAATGCACTGCATCCCAATCTGCTA
Long Flanking Sequence:
AGAATCTCATACCAGCCCATGCCTAGAGCATACTTACCCAGTGTGGAAATTTGGTGTTAACAATTCAAAGCACAGTACAAACACTAGTTAGCTTTAATTTTGGCATCATTATATTTGAAATGACATTAAACCAGTATATTACTGCCTGACAGATTAATTAATCTTATCCGTTATATAAACCCTGAATGACTAGGGGTGTCATTTTTTTTGCAGTTTTTCGCTCCTGTCCGACTTATGAAGGTTGTTGTAGAGTTTGGTCCTGAAGGAAAACCCACCGGTGAAGCAGAGGCTTATTTCAAAACACATGAAGACGCCGTTTTAGCCATGTCCAAAGACAGAGAGTTCATAAGTAAGCAAAGACTCCTCCAATGACCCAAATGTTTTACACATCAAACATGAAGTGATGTTTAACTTGATGTGTTTTGTTTCTTTGTTTTTGTTTCTGTCCAGTGGAGCGATATATTGAGTTGTACCTGAATTCATGTCCACCCAGCGAAGAA[C/T]GATAAGATGAAAGGACACCATATTTAAATGCACTGCATCCCAATCTGCTACAAATTAACCCAGTGTATCATGTACATTGCAAGAACCAACATTAAAAGCGGACTCTACAAATGTTGCCTGATTTTTTTACATTATGTCTGACCAGCAATGTTAAAAAAAAGGAGACGGGAGTAGATGTGGTGTTTTTTAACTTTTCCATAATAACTATTTGTGGAAGCCTTCAAACTATTCAGATTTACACGTTTTTGTCTCTGTTGCAGAGGCATGTCAAACCATTAAAGGGTCTTGACAGTTTCTTAATTAAGTTTTTAATGTGGCAAGATGAGTGAAGCAAGATGACGTTTTCTCATTGATTTGATAGAATTTGTTAGATTTGTGCAGCTCTGACGAAGTCCATTAGGTACAAAGTCCAGATACAAGGTTTCTGCAGGGTCTTAATGTCTTAAATCTCAAAATCCAAATTTTAGGCCTTAAAAAGTCTTAAATTTACTGAAATACTG
Associated Phenotype:
Not determined