Busch Lab

ZMP

bcl2l13

Ensembl ID:
ENSDARG00000062370
ZFIN ID:
ZDB-GENE-050419-215
Description:
bcl-2-like protein 13 [Source:RefSeq peptide;Acc:NP_001038356]
Human Orthologue:
BCL2L13
Human Description:
BCL2-like 13 (apoptosis facilitator) [Source:HGNC Symbol;Acc:17164]
Mouse Orthologue:
Bcl2l13
Mouse Description:
BCL2-like 13 (apoptosis facilitator) Gene [Source:MGI Symbol;Acc:MGI:2136959]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa10792 Nonsense Available for shipment Available now
sa36637 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10792
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
ENSDART00000090156 Nonsense 130 485 5 7
ENSDART00000129290 Nonsense 130 485 4 6
ENSDART00000140632 Nonsense 130 485 5 7

The following transcripts of ENSDARG00000062370 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 20379221)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20609444
GRCz11 18 20598510
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGAGAAATGTCCTAAGTGGTGATTTTNGTATGTGTCTCATGCAGTGACT[T/A]GAACTTYGAATGCTTCAGAGCAGCAGTGGACGAGGTTTCCTCTCACGCTC
Long Flanking Sequence:
TAAATCTGGAATCTCTAAAGTCATCTGCCTCTCTCTCTTATTTCTCAGCTTTTTCCAGGACTGGTTTTGATCAGCACACATCCCCAGTGTTCAGTCCAGCCAATCCAGAGAGCTCGATAGAGGACAGTCTGGCAGTATTGGGGGACCGCGTCTCTCGGGACCTGGACACACACCTGTTTTCCGCCACTAATACGCTTCTGAGCAGGTCATTAAAAAGTCTAGTGAAAATTTCCTGGCTGTTTTAGTCTTTGGAAAACAAAATCTAGCAAATGATGCTTTATTGGCAGAGGTCTATACCAGAAAAATGCATTGTGTAAACAGCCTGCTCACAGTTGTTATAAGTTATACGACACGTTAAGTGAGTTCAAATGACTATTCTTGACATTTAACTTAAATATTGACTGAAAACTTTCAACATATGTCATCTTGATGTTTTTAGAAGACCCAAATACAGAGAAATGTCCTAAGTGGTGATTTTGTATGTGTCTCATGCAGTGACT[T/A]GAACTTCGAATGCTTCAGAGCAGCAGTGGACGAGGTTTCCTCTCACGCTCAAGGAGGATGGAGCAAGGTAGATCAAAACACATCAGTGTAATCACACATGCACAATACCCCCAGAAGAGATTATGTTTTCATAAGTGCTTAATTTTTGTATTCCGTGACTTTGTTGTTCTGTTTAGGTGTTGGTACCTTTAGTATTGTTACAAGCCCTGCAGGCCAAGGGTCAATCGCTAGAAGCTCTGCTCCAGTGTGGTTTGCGTTACCTTGAAGAATCACAGGCAGACTTCATCATTCAGCAGGGAGGATGGGTAACTGACTAATACAGTTTAGAGACTAAATAATTAGCCCTGTGATATTTGAAGTCAAATATTTCCTTAGTGATGTTTAACAGCCATATTTCCTACTATATTTTTCTTCTGAAGAAAGTTTTATATTTTTTAGTTTGCCTGAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36637
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
ENSDART00000090156 Nonsense 452 485 7 7
ENSDART00000129290 Nonsense 452 485 6 6
ENSDART00000140632 Nonsense 452 485 7 7

The following transcripts of ENSDARG00000062370 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 20365851)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20596074
GRCz11 18 20585140
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACCTCCCAATCCCAAGTCCTGCGGAGGTGCAGACCACGTCAGTGCCA[C/T]AAGCCGAGTCCGCCGAGCTCCCCGTGCTGCTATATGGCGGTGCTGCCCTG
Long Flanking Sequence:
TGGCTGAGGAGCAGAGCGAGAACAACTCCTCGAACTCTGACATAGTGCATGTGGAGCGTGAAGATGCTGAGCTGCTGGAAGAAGCTGGAGAGACGGTGGAGGAAGGAGAGCTGCAGAGTAGCGTACTCAGTGTTCTGGGCAGTGAGAGCGAACTCGCTGCTGTCCGAGAACAAGAGTCTGCTGCACCTGAGCTGCTTGCAGAACCAGTGGTGATGGAGATCCCTCCCCCTCCTTCTCCTCCTCCTCCTCCTCCTTCAGCATTGGCAGAGCAAGAGCTCCCGCCTGTCCATGCTGCTGTTACAGCCTCAATCCCTGTGCCTGAGCCTGAACTTCAGTCTCAGCCTGTTCCAGCTCCTGTGGAGCCACCTCCATCATCCCCACCTGAACCCGAAGCAACCCTGGAGCAAGAGATTCTTTCAGAGGTTGAGCTGAAGACCTCCTCCCGATCTCCAGACCTCCCAATCCCAAGTCCTGCGGAGGTGCAGACCACGTCAGTGCCA[C/T]AAGCCGAGTCCGCCGAGCTCCCCGTGCTGCTATATGGCGGTGCTGCCCTGGTGGCCGTCGCTGCAGTGTTGGCCTTCGGAGCTCTAGCCTACAGGAAGAAGTAGAAAGTCCTTGACTGTCCATGACCTCGCTGTATCTCTTGCCCTGTGGTTAACGTGCTGCCACAAGCTGCACTTTATGGGAAAATAAGTACTCCTCTTATTTGTGTCATACTAGTTTGTTTTCCGTTCTCATTGCTTTTATTCTTAGGCGTAGTTCTGGAAACCAGCTTTATGGCTGGACGGGAACTTGCAGGTGCAGATTCAGGTTTCTTTCATGCTGTATTTGTGAACATTGGAGTGACCCGTTTCATGGGCTGCGACTGAGGTTTTGCCTGGATCCTTAATATTAACTAAAGAAACATCAAGGCTTCTGAATTATAAAAAAACAAAGGGATAGATCACCCAAAACACAAAATGAGCTGTTAGTTTATTCACCTGCAGGACATTCAGGTTATAGCT
Associated Phenotype:
Not determined