Busch Lab

ZMP

csrnp1a

Ensembl ID:
ENSDARG00000031426
ZFIN ID:
ZDB-GENE-070912-475
Description:
Novel protein similar to vertebrate AXIN1 up-regulated 1 (AXUD1) [Source:UniProtKB/TrEMBL;Acc:B0S776
Human Orthologue:
CSRNP1
Human Description:
cysteine-serine-rich nuclear protein 1 [Source:HGNC Symbol;Acc:14300]
Mouse Orthologue:
Csrnp1
Mouse Description:
cysteine-serine-rich nuclear protein 1 Gene [Source:MGI Symbol;Acc:MGI:2387989]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa38331 Nonsense Mutation detected in F1 DNA Not yet available
sa1521 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa38331
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041877 Nonsense 110 514 3 5
Genomic Location (Zv9):
Chromosome 2 (position 24067630)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 24140865
GRCz11 2 23796516
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCGGTTTGGTTCGGTTACAGTGTTCCTTTTTCAGCGCTGTCAAGGTTA[C/A]AGCAGTGTGCCCAGTCATGGTGGCTGCACACTGGGCATGGTTAGATGGCA
Long Flanking Sequence:
CTTGCATTGCGGAAAATACTGTAGCTATTTGTGCTGTAAACAGTCTGAAGTGTTACAAAGGCCAGACCAAAAGCAGTCCATCTCACCAAAGAAAATATGTGCCTCAGGAACATTGGTTGTAGTCGTGCCAATATATCTAGAATGTAGAGACAGAACAATACATGCCTGTTTGCTGGTTTGGCTCACCTTTAAACTAGCAATATAAGCAGTTAAACTGAATTGTGCCATTCAATGCAGGTCAGTCTGTTAATGCGGAAAATGTACTGCTGCACATATTTCCAATACAGTAAAAGTTGGCATGTGAAATATTCTGTATTGTAGTTGTATTCTCATAGACTAATCAACAAAATCATGAACCTTTAAATGAGCTAAAAAGTTATTTTACACATATTTTTACTTTCAGTTTCATCCATCCTGAAGAAGACGAAAGGCAGTCAATCCAAAGGCAGTGTTCGGTTTGGTTCGGTTACAGTGTTCCTTTTTCAGCGCTGTCAAGGTTA[C/A]AGCAGTGTGCCCAGTCATGGTGGCTGCACACTGGGCATGGTTAGATGGCACACTGCTCGTCAGCAGTTCACCCTGCCAGAGCACGCAGAGGAACAACAGCGCTTGAGACTAGTGAGAGTGCGTGAGAGACACCAAGAGGAGAAGCTGGAGGCTTTGAGACAGAAGGTGAGTTGCTAATTTTCCACTTGACATATCAGTGAGCCCACCCATCTAATTCACCATGTAGAAAGAGAGCACTCTGCTGTTCAAATAGGAATCAGTGTGCAAAAACAAAAACAAATACAAACAAGCAAACAAAAGTTAATTGACAAACATAATGGATTAGCGGACTATTAGATATATTTGCTCCAGTGAATCCCTCTGTGATGAGTGAGAAGTACTGGAAAAATGGTATGTTAATGCTGCTTTGATTATGGTTTTTATGTGTGCAGCACTAGTTCCAATTTCCCTTTGTGGAATGACTACAGATACTGTCACCTGTGTGTATGGAGAGTTACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1521
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041877 Nonsense 418 514 5 5
Genomic Location (Zv9):
Chromosome 2 (position 24060695)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 24147800
GRCz11 2 23803451
KASP Assay ID:
554-1445.1 (used for ordering genotyping assays)
KASP Sequence:
GCATCCACAATTGATAATSAACAATTAAAAACCAAACCMCAACTAGAGTA[T/A]CTGGATGAAAATGCCAACCAGGTCACGGTAAAATGTGTAAACGATCCTTT
Long Flanking Sequence:
GCTCTGCACCAGTACTGACGGTTTTTATAATGTTAACAGATGGATCGTTCCAACTTTCCCTGTGGATGCTCAAAGGAATGCTGTGGGAATCCCGCAGGCCGCATTGAGTTCAACTCTAGCCGTGTACGGAGCCACTACATCCACACACACATGAAACTGGAGCTGGAGAAAAGGCTCGATGACACCCAACAGCAATCCACAGAGAGAAACAAATCCATCCCAAATCCTGTAGAAAGCAGCTCTCCGCCCTTCAGACAAGCGGAAAACAGCTGGAGCAGCGACACCTCCTGCTCGTCCTCTCTCAGTCTGGACTCGGAAACAGATGCGAGTCCTTCCTCAGAGGACATGGAGGACACTAGACTCACTCACATACTCAGCTTCTCCGATTCAGATGCGGACAGGTGTCCTTACATTAAAGACTACGATCTGTCCAAAGAAGCTGCTCGGTTCGCATCCACAATTGATAATGAACAATTAAAAACCAAACCCCAACTAGAGTA[T/A]CTGGATGAAAATGCCAACCAGGTCACGGTAAAATGTGTAAACGATCCTTTTTTTGATATCCCTAATACACCTTCTGCGTCTCCAGATCACACTGTGAATGGTTACATGGACCTCAGTCTGTCTTCGGACTCTGACTTGATGTTTTTTGACGCTTTTCATGAGTTTAATCATTTTAAAACATACGGTCATATGGACTACATCTCACATCTGCAGTTTCCTCGCTGTCCCAGTCCTGCTCAAACAGAGGATTCAGGAATCAGCCTTCTGGAGTCTCTTGTCGGAAGTTCCTAAGGTTTATTTACAGACAAATTTGTTTTTTTGTACAGTATGGCTTTATTCTCATTTTGTTTGAGAAGAAAAGCGTGAATATTTCCTGAATTGAAGGATATTCCTTGGAAATGTATTTTAGGATGTTGATGTGAGTTTGTGATCATACTGTTAAAACCACTCTGCATGATGTGTTATGCGTTGTGTGTCAGTTTTAATTTTGTTGCCAAATG
Associated Phenotype:
Not determined