Busch Lab

ZMP

clasrp

Ensembl ID:
ENSDARG00000061742
ZFIN ID:
ZDB-GENE-060503-837
Description:
splicing factor, arginine/serine-rich 16 [Source:RefSeq peptide;Acc:NP_001037794]
Human Orthologue:
CLASRP
Human Description:
CLK4-associating serine/arginine rich protein [Source:HGNC Symbol;Acc:17731]
Mouse Orthologue:
Clasrp
Mouse Description:
CLK4-associating serine/arginine rich protein Gene [Source:MGI Symbol;Acc:MGI:1855695]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa43146 Nonsense Mutation detected in F1 DNA Not yet available
sa15739 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa43146
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088421 Nonsense 29 560 2 21
ENSDART00000088425 Nonsense 29 645 1 21
ENSDART00000127825 Nonsense 29 642 2 21
ENSDART00000148032 None None 122 None 7

The following transcripts of ENSDARG00000061742 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 34947235)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 36626391
GRCz11 18 36607399
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGGGATGATGGTGGACTACAAACGGCGTGGGGAAAGGCGAAGAGAGTA[C/G]TATGAAAAAATTGTAAGTCATGCTTTGTTTACTGAAAACAGTCTAACCCT
Long Flanking Sequence:
AATTGCAGTGTGATCACGGCATTACTGGTGGAATGGGCAATTAATGAAGATTGGTCACCAGGCTGTTCAAATTTAGCCATGAAACCTTCAACACTAAATTGGCCATAAAGTGTTTCGGTTTTATTGTCCAACCCCTGTATATTAACAGTGTAGTTTTGTAAACAATTGTAGTTTGCAGCTATTGTATTACTTGTGAGAAATGCATACAGGCATTGTATATTTGCATTCTATATAAAAAATATTATTTTCTCTGAGTGTAGCGATGATTTGACTTAGAGTAGCATTATATGTTCCGAGTAGTATGTTTGTTGTCAGTCTAATTAAGTCTATTGTTAGTAGTCAGCTAATCTGAACTCTCTGTGTCCCCTTGCAGCAGCCCTGCCCCGACGCGCCCCAACCCCAAGCGGAGCCGTCATGTGGCAGGAGGCCCGCAAACATGAACGCAAACTGCGAGGGATGATGGTGGACTACAAACGGCGTGGGGAAAGGCGAAGAGAGTA[C/G]TATGAAAAAATTGTAAGTCATGCTTTGTTTACTGAAAACAGTCTAACCCTGGCCTGGCTGATGCTTATAAATGAAGAAACACACTTTCTTTTCTGTGTAGAAAAAGGATCCAGCCCAGTTCCTGCAAGTTCATGGCAGAGCCTACAAAATCCACCTGGATTCAGCTGTCGCCCTGGCAGCTGAGAGTCCCATAAACATGTAAATACCAGACGATATCTATTTATAAAGCACATTTAAAAACCAAAGTTGACCAAAGTGCTGTATAAAGGAGTACTGAAGGCAGAGAAGAAAGCAGAATATAAAAGAAACATTTAGGGAGGGAAAATAGATAGGTCTTTAACATGGACTTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAACTAAAGTGGGATGGTGTGGGAGTGTCTATTTGGGCACGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15739
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000088421 Nonsense 269 560 10 21
ENSDART00000088425 Nonsense 269 645 9 21
ENSDART00000127825 Nonsense 269 642 10 21
ENSDART00000148032 None None 122 None 7

The following transcripts of ENSDARG00000061742 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 34957671)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 36636827
GRCz11 18 36617835
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TWGGTAATGTGTTGTTGTGTTTCCTTCAGGGCCGGCGGTCTCGCAGACAA[C/T]GAAGAGAGTTCAGAGAGAAGTATATGAAAGGCAGGCAGATCAGCCCACCC
Long Flanking Sequence:
GATTTACTTAAATGTAGAAGGTAAGCCCTTTAAAACTAATGTGTTAATGCTTTACCATGTTGTAGATGTTGAGGTGGACGTAGATGAACTGAGCCCTGAACAGGTGTTGGAGATTAACAAGATGGCCACCACTTACGGCATGGCAGACGGAGACTTTGTTTGGTTCGTTTACTCATTCTTTAGCTAAACCACTGATATTCAATTTAGAAGTTTGCTGTTTGAGCATATTATACTTATTACCGAATAAAACATGATCTTGTAATTTTTCCAAAAATTGTATGTGTACTTTAAATTTGATGTTTGTGACAGGATGTTGAGGAAAGACAAGGAGGAAGTGGAGGCCATTAAACACGCTAAAGCACTGGAGGCAGAGAAGGCCATGTACTCTGTATGAACTGACAATTTTTAATTGGTCTTGCTTCTCATTTAAGATGTCTGTCAATATTTGTGTTGGTAATGTGTTGTTGTGTTTCCTTCAGGGCCGGCGGTCTCGCAGACAA[C/T]GAAGAGAGTTCAGAGAGAAGTATATGAAAGGCAGGCAGATCAGCCCACCCAGGTAACAGATCAACACTAACATTCATACTTTAATATAATAGTCTTAATTCTTAGTAGTACATTCACTGAAATTAATATTTGAATTTTCAAAACAGCTATGCCAGAAGAGACAGTCCTACATATGACCCCTACAAACGGCAAGTGAACCATTTGCACACATTTTGAATAATGGAATAATGTTTGACTTTAAATCCATTAATTATAATTCAGTATGCAGCTATAGAAAGGGTTTGAATGATAATAATGTGCTGATTTTATATATATATATATCTGCAGATTTATGCAGAATGATTTTGGGAGTATTGTGACCAAAATCTTTATATATGAAATAAAAAAAAATACATTTTACTTATTACATTTTTACAATTCAAATTCAATTAGATCCACTTATTTGGTTAACAAAGTCTTTTATAATATAATCTAATAAAAGGCAGACGATACTACTTTAC
Associated Phenotype:
Not determined