Busch Lab

ZMP

csrp2bp

Ensembl ID:
ENSDARG00000041708
ZFIN ID:
ZDB-GENE-040718-452
Description:
cysteine-rich protein 2-binding protein [Source:RefSeq peptide;Acc:NP_001002699]
Human Orthologue:
CSRP2BP
Human Description:
CSRP2 binding protein [Source:HGNC Symbol;Acc:15904]
Mouse Orthologue:
Csrp2bp
Mouse Description:
cysteine and glycine-rich protein 2 binding protein Gene [Source:MGI Symbol;Acc:MGI:1917264]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa10298 Nonsense Available for shipment Available now
sa30730 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10298
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
ENSDART00000061131 Nonsense 273 782 5 10
ENSDART00000131811 Nonsense 273 782 7 12
Genomic Location (Zv9):
Chromosome 22 (position 25544731)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 25044637
GRCz11 22 25072261
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGCAGCTGAAAGAAAAGCGTTCTCGAACACAAGAGGCAAAAGAGATT[C/T]GACGTGCACAGAAGGAGGCGGCTGGGTTTCTTGACCGCAGTGCCTCGTCT
Long Flanking Sequence:
CATTCATTTATGTAGTCCTTGGCTTAGGTTGAACCACCAGGAGGCATTACAAATATGGTCGCAGAGTGAACAGACTAAAACCTGGATATATTTGCTTTTTATGGTTTACACACTTAAGAAAGAAGACGTCCACGTGGTGGAGCACAGTGGCAGGATGTCTGTCAGTCGGCAGCCCAACGTTTTTCCGTTCAGGAGCGCAGGAGTTTGGTGAACCGGGTTGGTGGAAGCTGGTTCAGAATCGTCCACCTACTCTTCGCCCTGAGGGTGACAAAAGCTCTGCAGCCTCGGTCAAGGCAAAAGGTAATAATGGTTTTAACATTTTAAAAGTTATGCAGGATTTTCATTTATTTGAAGTGTTATTGTTTTAAGCTGTGTCAAAGCCATCTCTGGACCCCATAATCACAGTGGAGGGTTTGAGGAAGCGGGGAAGTCGTAACCCAGTGGAAAACGCCATGCAGCTGAAAGAAAAGCGTTCTCGAACACAAGAGGCAAAAGAGATT[C/T]GACGTGCACAGAAGGAGGCGGCTGGGTTTCTTGACCGCAGTGCCTCGTCTACACCTGTGAAACTGGGCAACCGTGCTCGACGGCCCGAGCCTTATCTGGAGAAGGGTGAAGTCATTGACTTTTCCTCCCTCAGCTCATCAGACAGAACCCCCCTCACCTCTCCATCCCCATCCCCTTCTCCTGACTTCTCTGCCCCTGGAACCCCTGCCTCACACTCCGCTACGCCCAGCCTGCTGTCAGAGGCCGATCTGATCCCGGATGTCATGCCCCCTCAGGCTCTGTTCCACGGTGAGATGCTACACTTGCTATCCAGCAAATAACTTTTTTATAGTTAATTAGTTAAGACTTAAATTTCTATTTGATTGCTACCTGGTGTCTAGAGGGTGTATCTGTTCTTTTTAGTGTATCAGATGGAAACCAAAATGGATGAATAGTCACACAATAGCCCCTTTATTAATCTGCGTCGCCACAGTGGATTGAGCCACCAACTTATTCAGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30730
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061131 Nonsense 656 782 8 10
ENSDART00000131811 Nonsense 656 782 10 12
Genomic Location (Zv9):
Chromosome 22 (position 25539954)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 25039860
GRCz11 22 25067484
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTACTGCTACGTACGGCCAAATCACATCCCCTCTGTCAACTCCATGTGC[C/T]AAGACATCTTCTGGCCTGGTAATCATCAGTTCATCCAAACTAATCCATGT
Long Flanking Sequence:
AGAGTAACCAGTCTTGGGCTGAAAGGTGATATGGCTGTGGCTAGAAATAAGCTTACATACGAGTACAGCCACCACAACATATTCAACATTTTTTTGGTATCATTTGGGTATTTCAAAAGCAGTTTTTCTGTTTTAGAATGTTTAGTGTGAACAAAATACTTGAACAAGTCTAAAAAAAAAAAAAAATAGTGCATAAATACTCATAAAAGGACATGGTGAACTTTAATTCTCAACAAACTTGCATCTTCAGGTCTCTTTGGCAAGCAGGAGTTTAGACTGACAAGACTAAGACCATTGTAACAACTGTCTGAAAGCTTTGTGCATGTTGTACATAATCTTGCAGGAGAGACTATGAGAGTCGACCACTGAAGCTGCGTTTGCTCTCAGAGATTCGTGCGCATCACCACAGGAATGACCCGAATTGGGTAGCTGAACCTGACGCACCTATAGACTACTGCTACGTACGGCCAAATCACATCCCCTCTGTCAACTCCATGTGC[C/T]AAGACATCTTCTGGCCTGGTAATCATCAGTTCATCCAAACTAATCCATGTCTCTATCAAACAAGATCTTGAAGGAATATAAGTAGGCTTTTTTTGTCCATAAGGTATCGACCTGTCGGAGTGCCTCCAGTACCCAGACTTCAGCGTGGTGGTGCTTTACAAGAAAGTCGTGATTGGTTTTGGCTTCATGGTGCCAGACGTGAAGTACAATGAGGCCTACATCTCTTTCCTGCTGGTGCATCCAGAATGGAGGCGAGCTGGTATCGCCACATTCATGATCTACCATCTCATTCAGGTGAGTCCAAGAAAGCAACTACACCGAGTTCACTCCATTCAGTGTAAAACAGTAATGACCTTTCTCTTCTCTATAGACCTGCATGGGAAAAGATGTGACTCTACACGTATCGGCAAGCAACTCTGCCATGCTACTTTATCAGAAGTTTGGCTTCAAGACAGAGGAGTACATCCTGGACTTTTATGATAAATACTATCCAGTGGACA
Associated Phenotype:
Not determined