Busch Lab

ZMP

csrnp1b

Ensembl ID:
ENSDARG00000038429
ZFIN ID:
ZDB-GENE-030131-1515
Description:
cysteine/serine-rich nuclear protein 1 [Source:RefSeq peptide;Acc:NP_955913]
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa18280 Nonsense Available for shipment Available now
sa44119 Nonsense Mutation detected in F1 DNA Not yet available
sa39443 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18280
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056082 Nonsense 246 433 4 6
ENSDART00000109107 Nonsense 246 566 4 5
ENSDART00000135405 None None 201 None 4

The following transcripts of ENSDARG00000038429 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 24 (position 20258162)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 19564316
GRCz11 24 19708735
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTTCTGTGAGCCAGAGACCTGCAGCTGTAGTTTGGCTGGGATCAAATG[T/A]CAGGTAAGCAATTCCCAACAGACTTCTTTGAGAACATCAYYTACCAAGTT
Long Flanking Sequence:
GCCCAACGTCGCTACACATTGGCAGAGTTTGCGATAGCACAGCGCCACCTACGGCGAGAGAAACTCAAAAATCGAATGAGGGAGGAAAAACTGGAAGCCCTTAAGCTAAAGGTAGCAAATTTAATTCTTGCACATTCTGGTCAAACAAGCTGCATTTGAATCAAAGCATCATCATAATCATGCAAATATGCTTTCTTCCTTTGATAGCTCACCAAAAACGGTACCCAAGAGTCTGAAGAAGCTGAAAAGTTAACTGTCGATGATATCCCAGAGGATGAAATTGACCTCAGTGGAGTAAATGTGGATGACGGCTCCTTCCTGCATCCATACCCCTCAAAGAAAAGGTACGCCATCCTTAAAGCTGCTGGTGTGAAGAAAATCGATAGAGAAGAGAAACGTCAACTTCATGAGCTGCGGACATCGAGAGAAGACTGCGGATGTGACTGTCAAGGCTTCTGTGAGCCAGAGACCTGCAGCTGTAGTTTGGCTGGGATCAAATG[T/A]CAGGTAAGCAATTCCCAACAGACTTCTTTGAGAACATCACTTACCAAGTTTGTGGGTAATATTCACAAGTATCATCCATGACAGCAGAAAGTAACGCATTATTCTTTGGCTTCACAGATGGACCACTCATCCTTCCCATGTGGCTGCACTAAAGATGGCTGTGGGAACACACAAGGTCGCATCGAGTTCAACTCTAGCCGAGTTCATACCCACTACATCCACACTATCATGAAGCTGGAGCTGGAAAAACGCTTGGAGGAGCACACGACAGAGACGCCTCCTGAAACTCATCCAGACAGCAGTTCCCTAAACCAACCAGCAGAGATCAGCAGCACGCCAGACATGCCAACATTTCACTTTAACTCAGAGCTACTATCCACAGGAGAGAACAGCTGCAGCAGTGACATGACCGATTCGTCTAGTTCCTCAGGCCAGAGCGAGGATTCTGAATCTGTTGAAAATGTTCCAAGTGAACAGTCGCCGCTGGACGTTGACGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44119
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000056082 Nonsense 331 433 5 6
ENSDART00000109107 Nonsense 331 566 5 5
ENSDART00000135405 None None 201 None 4

The following transcripts of ENSDARG00000038429 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 24 (position 20257795)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 19563949
GRCz11 24 19708368
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCAGAGATCAGCAGCACGCCAGACATGCCAACATTTCACTTTAACTCA[G/T]AGCTACTATCCACAGGAGAGAACAGCTGCAGCAGTGACATGACCGATTCG
Long Flanking Sequence:
GTGTGAAGAAAATCGATAGAGAAGAGAAACGTCAACTTCATGAGCTGCGGACATCGAGAGAAGACTGCGGATGTGACTGTCAAGGCTTCTGTGAGCCAGAGACCTGCAGCTGTAGTTTGGCTGGGATCAAATGTCAGGTAAGCAATTCCCAACAGACTTCTTTGAGAACATCACTTACCAAGTTTGTGGGTAATATTCACAAGTATCATCCATGACAGCAGAAAGTAACGCATTATTCTTTGGCTTCACAGATGGACCACTCATCCTTCCCATGTGGCTGCACTAAAGATGGCTGTGGGAACACACAAGGTCGCATCGAGTTCAACTCTAGCCGAGTTCATACCCACTACATCCACACTATCATGAAGCTGGAGCTGGAAAAACGCTTGGAGGAGCACACGACAGAGACGCCTCCTGAAACTCATCCAGACAGCAGTTCCCTAAACCAACCAGCAGAGATCAGCAGCACGCCAGACATGCCAACATTTCACTTTAACTCA[G/T]AGCTACTATCCACAGGAGAGAACAGCTGCAGCAGTGACATGACCGATTCGTCTAGTTCCTCAGGCCAGAGCGAGGATTCTGAATCTGTTGAAAATGTTCCAAGTGAACAGTCGCCGCTGGACGTTGACGAAAACGGACTTACAAGAATCCTAAGCTTTAGCGACACAGACAATGAAGACTGTTCTATCAGGGAGCGCAATGACAACTGTGACTACCAACAGAAAAAGAGCGAAGGGTCGATGGGTTATGGCATCTTCAGTACAGAGGACGACAAGCTCAACATGTCACAAACAGACAACAGTCGCACAGCCATGTCTGAACTTTTAGACGAGAACGCTAATCAAGGTAACGGACTATTCCACAGCAGCTTCATCCCACATACGCCCTCGCCTTCCATCGATCATTCGGCCAGCTACATGGACCTTAGCCTGTCATCCGAGTCAGACTTAGAATTCTTTGATGGATTTCCTTGTTTGGGACCGAGCTCGCTATACAACTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39443
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
ENSDART00000056082 None None 433 None 6
ENSDART00000109107 Nonsense 495 566 5 5
ENSDART00000135405 None None 201 None 4

The following transcripts of ENSDARG00000038429 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 24 (position 20257301)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 19563455
GRCz11 24 19707874
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTAGAATTCTTTGATGGATTTCCTTGTTTGGGACCGAGCTCGCTATA[C/A]AACTCCCTAAAGGAGTATGAGCACGTGGACAACTTCTTTCAGTTCCAGTT
Long Flanking Sequence:
AACTCAGAGCTACTATCCACAGGAGAGAACAGCTGCAGCAGTGACATGACCGATTCGTCTAGTTCCTCAGGCCAGAGCGAGGATTCTGAATCTGTTGAAAATGTTCCAAGTGAACAGTCGCCGCTGGACGTTGACGAAAACGGACTTACAAGAATCCTAAGCTTTAGCGACACAGACAATGAAGACTGTTCTATCAGGGAGCGCAATGACAACTGTGACTACCAACAGAAAAAGAGCGAAGGGTCGATGGGTTATGGCATCTTCAGTACAGAGGACGACAAGCTCAACATGTCACAAACAGACAACAGTCGCACAGCCATGTCTGAACTTTTAGACGAGAACGCTAATCAAGGTAACGGACTATTCCACAGCAGCTTCATCCCACATACGCCCTCGCCTTCCATCGATCATTCGGCCAGCTACATGGACCTTAGCCTGTCATCCGAGTCAGACTTAGAATTCTTTGATGGATTTCCTTGTTTGGGACCGAGCTCGCTATA[C/A]AACTCCCTAAAGGAGTATGAGCACGTGGACAACTTCTTTCAGTTCCAGTTGCCTACCTACCCCAGCCTTCCTCAAGCTGTCGACCCAGGAACATGTCTCCTGGAGTCTCTGATCGGCTTGTCAGATTCTGTCCCAGAACCTCCGACTACTTTCACGGACAATCAAATGCTAGAAGATGCCATGAAGCTGTCAGTGATGGAGTCTTTAAAGGTCTAATGGGGGACTCTTGTATGATCACTGTATAAATGAACTATGGGATTGTAAATGAATGCCATTTGTTTTCTTTTTGAATGGAGACCCATCGCGGGATATCAATATTTGCATTATCTGCCTTTAAGATGTTAGCAAAGCATTAAGTTATTATAACAATCTTTATTATCATTATTGCCATCGCAGTGGCAGCTAACATTTCAGTTCAAAAACAAGTCTGGCCGACTGATTTTTGAATATTTGTACATATGGCCAGGAAGGTGAAGAAATTTTCACCCACATTGGTGGTA
Associated Phenotype:
Not determined