Busch Lab

ZMP

ctrb1

Ensembl ID:
ENSDARG00000090428
ZFIN ID:
ZDB-GENE-030131-1171
Description:
chymotrypsin B1 [Source:RefSeq peptide;Acc:NP_997783]
Human Orthologues:
CTRB1, CTRB2
Human Descriptions:
chymotrypsinogen B1 [Source:HGNC Symbol;Acc:2521]
chymotrypsinogen B2 [Source:HGNC Symbol;Acc:2522]
Mouse Orthologue:
Ctrb1
Mouse Description:
chymotrypsinogen B1 Gene [Source:MGI Symbol;Acc:MGI:88559]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa11393 Nonsense Available for shipment Available now
sa21002 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11393
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
ENSDART00000037346 None None 263 None 7
ENSDART00000109691 Nonsense 48 459 2 13

The following transcripts of ENSDARG00000090428 do not overlap with this mutation:

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 36522967)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34796810
GRCz11 7 35068287
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCCAGGATTGTRAACGGTGAGGAGGCTGTCCCTCATTCCTGGCCCTGG[C/T]AGGTGTCTCTGCAGRTATGAAYAGACAGATTTTCACTTACAGATGACATT
Long Flanking Sequence:
GTCATTTGTTTGAGATGAAATGCATAATATATATTCCACTTTTATGAAATCATGTCCATGAAATATGACAGACCTTCTTCCGATACAATTAGCTCCTGCAAGTGTTAGCAATAACAAGTGACACGTACAGCTAAAAGTGCTCAAAGTACTCAATGGAAAGTCAGCAAATTCTGAGAATGAGAATGTTGCAAAATATGTAAATAAGCAGGAAGGTCAGATATATAAACCCCTCGAGTTGGTGAGACATTGGTGACTCAGAAATGGCTTTCGTCTGGATTTTGTCGTGCCTTGCCTTGATTGGAACAGCATATGGTAAATTGCTGATTTTTTCCCTCTTATTTAACAATTTGAATGAATGTGTCCCACTTTGATTTATATAAAAATTTTAACAAGTGCTTTTTTATTCTGAAGGCTGTGGCGTTCCTGCCATCCCTCCTGTTATTACCGGTTATGCCAGGATTGTAAACGGTGAGGAGGCTGTCCCTCATTCCTGGCCCTGG[C/T]AGGTGTCTCTGCAGGTATGAACAGACAGATTTTCACTTACAGATGACATTAGGATAGGCAACTGTGAATAAAAAAATTGATCTGATGTTTAATGTAAGGACTCCACCGGCTTCCACTTCTGCGGAGGCTCCCTGATCAACGAGTGGTGGGTTGTGACTGCTGCTCACTGCAACGTCAGGTAAGACAGCATTGACGCTTTGTTTCTCCATCATGCAATGAATTTAAGACGTATGTGCAAATTTGAGAGTAAAATAGTCAAATCTTTTTATTAGGACCTCTCACCGTGTCATCCTGGGTGAGCATGATCGTTCCTCCAATGCTGAGCCCATTCAGACCATGACCGTTGGAAAGGTATGGTGAACTCTAAAAAATGCTAGGTCATTGTTACTCCATGTTGGGTCAAATTTAGATAAATCCAACAGTTGGGTTAAAACGTGTCATTTACATGGTTTAAATGTTGGGTTTGTCCATATTTAACCCAATGCTGGGTTAGGACAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21002
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000037346 Nonsense 187 263 6 7
ENSDART00000109691 Nonsense 383 459 12 13

The following transcripts of ENSDARG00000090428 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 36532891)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34806734
GRCz11 7 35078211
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCCTGCTCCAGCAGGCCGCTCTGCCTCTGCTGACCAATGATGACTGC[A/T]AGCGTTACTGGGGAACCAACATCACTGATCTGATGATCTGCGCTGGAGCT
Long Flanking Sequence:
TTAATAATGTAAAAAGCATGAACATACCCTGAACTATGTGTGGGATTTTGATAGAAAGTGAGAAGAGCATTCTCAAAGATTGATACTTAAAAATCTGAACGCCAATGTGTCTGCACCTTTTTCCCAACAGTCCATCAAGCATCCTAACTACAACAGCTTCACCATCAACAATGACATCCTGCTGATCAAGCTGGCCACTCCTGCTAAGATCAACACTCACGTGTCTCCTGTGTGTCTCGCCGAGACCAACGACAACTTCCCTGGTGGCATGAAGTGTGTGACCTCTGGATGGGGCCTGACCAGATACAATGGCAAGTATTATTGGATATAAAGAAGGCTCGATCTCTATCCTGAAATGTCTTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGGAAAGCTTTTAAAATGCTGCCAATCTGTCCTTCAGCTCCCGATACTCCTGCCCTGCTCCAGCAGGCCGCTCTGCCTCTGCTGACCAATGATGACTGC[A/T]AGCGTTACTGGGGAACCAACATCACTGATCTGATGATCTGCGCTGGAGCTTCTGGTGTCTCTTCTTGCATGGTGAGCTCCCGGATGAACAGATTTGACTATTGTTGTAATGCCTGCTTGATTGTTCGCTCACACACTGTCTTTGTTTTCCAGGGTGACTCTGGTGGTCCTCTGGTGTGTGAGAACAACAGAGTTTGGACTTTGGTTGGTATCGTGTCCTGGGGCAGCAGCACTTGCTCCACCTCCACTCCTGCCGTCTACGCCCGTGTCACCAAACTCCGTGCCTGGGTTGACCAGACCATTGCTTCCAACTAAAGCAGCAATGAATCCTGTCATCAATAAACTTATATGACATGACCTTTGATTTAGTTTCATTGCATTAATTATTATAAAGGTTGCATATTAGAAAATATATTTTATTGATCATATTTCAAATAGACAAACTAAATCTTATTCTTAGTACCCCAATTTTAGGAATTATTGTGCACTGTTCAAATAAGG
Associated Phenotype:
Not determined