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
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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