Busch Lab

ZMP

LOC571201

Ensembl ID:
ENSDARG00000093893
Human Orthologue:
CCBL2
Human Description:
cysteine conjugate-beta lyase 2 [Source:HGNC Symbol;Acc:33238]
Mouse Orthologue:
Ccbl2
Mouse Description:
cysteine conjugate-beta lyase 2 Gene [Source:MGI Symbol;Acc:MGI:2677849]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa1832 Essential Splice Site Available for shipment Available now
sa38549 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa1832
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000139731 Essential Splice Site 218 448 6 13
Genomic Location (Zv9):
Chromosome 6 (position 21433813)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 25121544
GRCz11 6 25221353
KASP Assay ID:
554-1823.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAAACCAAGGCTATCATCATCAACACTCCTAATAAYCCTATTGGAAAA[G/A]TAAGGTCACATACAGTTAAAGTCAGAATTRWTAGCCCCCCTTTGATTTTT
Long Flanking Sequence:
TGTATGGAAAAGTCTGTGATCGTCAGCTTGACCCTTTTAAGGAAATCTTGGTCACAGTAGGTGCATATGGTTCTTTGTTCAGCACTATGCAGGCTCTGGTTGAGGAAGGAGATGAGGTGAAACATTTGGCACTTATATTTAATGTTTTAATGAATAATTTGCATAAATATAATAAGACATGCATCCTTATCCCATGCTTTCAGGTTGTTATCATAGAACCTTTTTTTGACACTTATGTACCTATGGTGAAAATGGCAGGGGCCAAACCTGTTTTAATACCCTTGCGATTGGTAGGTAAGCCTTTTCTGTTGTAAAAAATTACAGTGTTCAGCATATTTACATGAATCATAACACTTGATTGCCCTGTTCTGTAGAAGTCGACTGCAACAACTGGTATAAGTAGTGCTGACTGGGTTCTGGACCAGGAAGAACTTGCTAGTAAATTCAACTCCAAAACCAAGGCTATCATCATCAACACTCCTAATAACCCTATTGGAAAA[G/A]TAAGGTCACATACAGTTAAAGTCAGAATTGTTAGCCCCCCTTTGATTTTTTTTTATATATTTCCCAAATGATGTTTAACAGAGCAAAGAATTTTTTAAAACATATTTTTAATATATATTTTTGTAGTATTTATTTGTTTTATTTCGACTAGAATAAATGCATTTTTTTATTTTTTAGAACCTATTTTAAGGTCAAAATTATTAGCAACTTTAAGCTATTTTTTTTGATAGTCTACAGAACAAACCATCGTTATATAATAACTTGCCTAATTACCCTAACCTGCCCAGTTTACTTTATTAACCTAGTTAAGCCTTTAAATGTCCCTTTAAGCTGTAAAGAAGTGTCTTGAAAAGTGTCTTGAAAAATATCTAGTCAAATATAATTTACTGTCATAGATTGGGGAAAAAATTAACAGGGAGGCTAATAATTCAGGGGTGCTAATAATTCTGACTTCAACTGTAAATGACATGTCAAGTGGGTATGATTTTCAGGGAAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38549
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000139731 Essential Splice Site 314 448 9 13
Genomic Location (Zv9):
Chromosome 6 (position 21439971)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 25127702
GRCz11 6 25227511
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGACTGTCATGCAGAACAGTCTGTATACATGTCCAACACCATTACAGG[C/T]AAGTTCTGGATGTGGTATTTTATGGTTCTGGTTGTATACAATCCACTTTT
Long Flanking Sequence:
ATACAAGTGTATAGCAAGTAGTGATGTTGGTTCCACAATTATTATTATCAAGTGTTCATGAGATGGATTGCCTGAGGGAAGAAACTGCTTCTGTGTTGGGCTGTTCTGGTGCACAGTGCTCGGTAGCATCGATCAGAAGGTAAAAGTTAAAAGAGGCATAGGGAGAAAAAAAGGTTTTGGAGTACTTGAGGGCGAGTAACTGATGAGTACGTTTTTGTTTGAACTACCCCTTTACTTGATATAAGCCATTGTATTTCTGTTTTTGTGTCTTGACATAATTATGCATACATTTTTATTATTATTTTTTTATTTGCTTTTTTTCCCCTTAGCAACAGAATAGTACGATGCAAATCAATGGCAGTATTTTTAATTTTTACTTCATTTATAATATTTGTTTGTTTGTTTGTAGTTGGGCTGGTCCATTGGGCCTGAACACCTGATCAAACACCTGCAGACTGTCATGCAGAACAGTCTGTATACATGTCCAACACCATTACAGG[C/T]AAGTTCTGGATGTGGTATTTTATGGTTCTGGTTGTATACAATCCACTTTTCTATACAAGGTGTTTCTGCACAACAGGAGGCTGTTGGCCGGGGTCTTCTTCGGGACTTTGAGCTGATGGGTCAGCCAGACTGCTACTTCTCCTCTCTGGCTTTAGAACTGGAGGGTAAAAGAAATCGCATGGCTGCCATATTGGCTCAGACCGGCATGACTCCAGTGGTTCCTGAAGGAGGATATTTCATTATGGCTGATGTCACAGCGCTCAGTAAGTGCCCTAAAGTGATGTTTGTTAAGGTAATTACATTTACTCAGGCACATTGAGATTCATCTGATTAGTGTTGTTCTGTCTTGTCTATTGAATGTAGATCAGGATCTGACACATATGGGAGATGATGAACCATATGATTACAAGTTTGTCAAGTGGATGATAAAAGAGAAGGTAGACTCTTTTCTGATTTTAAGAATAATTACCAAAAAGTAAAATGCTATTATTTATTTATTT
Associated Phenotype:
Not determined