Busch Lab

ZMP

si:ch211-191j22.6

Ensembl ID:
ENSDARG00000062293
ZFIN ID:
ZDB-GENE-091118-40
Human Orthologue:
QPCTL
Human Description:
glutaminyl-peptide cyclotransferase-like [Source:HGNC Symbol;Acc:25952]
Mouse Orthologue:
Qpctl
Mouse Description:
glutaminyl-peptide cyclotransferase-like Gene [Source:MGI Symbol;Acc:MGI:1914619]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa32342 Nonsense Available for shipment Available now
sa43628 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa32342
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089898 Nonsense 112 391 2 7
Genomic Location (Zv9):
Chromosome 21 (position 20155948)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 21291437
GRCz11 21 21328073
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGTATTTCCAGCTGCGACCCATTCTCATTCAGCGACAGCCTGGAAGT[C/T]GAGGAAGTCGAGCTGTTCGTAAAGTAAGACATGTCTGATTTACTATCAGA
Long Flanking Sequence:
AATATTGAGAGAAAAAAAACTTTGGTTATTTATAGTGAGTAAGGATTTATTTGATTGGATAATCAATCGTGAGCTGATGTGGGACCAGCTGAGAACAATCATAAGCATGTGATCCTCTCGAAATTAGTTTATAAATAAACTTCACTTAAACAATGTGAGGGTGAGTAAATAGTTAGTAATAGTTTCCTTTAACATTTTTTGGAAAGCAAAACAGTTCTTCTATGCCATCACTGTGAAAACCCATTTTTGGAAATTGTCTGTAAATAGGCACTACTTTTTAAAACTGAAATTTCATGAGTATATTGCAATAATGAGAATATCTTGCTAATTCTTTATGTTTCTGTCACCACATATTCACCATCTTTATTCTCTTGTAGCTGAATCACCAGCCAGGTAAACCCACTGTTGCCCAAGTGAAGCGGCTCATCTCGCAGGTGAATTGGGAAAGACTGTGGTATTTCCAGCTGCGACCCATTCTCATTCAGCGACAGCCTGGAAGT[C/T]GAGGAAGTCGAGCTGTTCGTAAAGTAAGACATGTCTGATTTACTATCAGATTTGAATGAAATCTCAGATCCTATTAAATATGTTAGAATCCATCATAATTCAGTGTCTGCCATTTCTGTGGTTTTAGCACATCTTTTCTCAGCTGGATTCTCTTTCGGCTGGCTGGTCTGTTGAAGTGGACTCTTTCATCTCTGAAACCCCGCGTGGCCCAGTTAGCTTCTCTAATATCCTGGCTGTGTTGGACCCGATGGCTCCCCGAAGACTGCTTTTGGCTTGTCACTATGACTCTAAATTGATACCTTCAGACGCAAGTGAGCCACAGAAGGTGTTTGTGGGTGCCAGTGACTCAGCCGTACCCTGTGCCATGATGCTGGAACTGGTCACAGCTTTGGACGCACACCTGAAAAAGCACAAGCAGCTGGTGAGACAAAGTGTTACAGTTATTCTTTAAAAGAAACTATTTTGAGATATTTATATAAACTTTTGATGTCACTACATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43628
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
ENSDART00000089898 Nonsense 264 391 4 7
Genomic Location (Zv9):
Chromosome 21 (position 20159121)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 21294610
GRCz11 21 21331246
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATCTCGCAGAATACATGTCCAGCATTCCTCATCCACCGGGATCTGAA[C/T]AAACCACACTTCTCAATGCCGTGGTAAGATGACATGAATGTGTATGTGCC
Long Flanking Sequence:
CTTCATTTTTTTTCCAGACTTCTGAATAGCTGCAGTGCTGTTGAATTCAGAGTCAGATCTGTTGTTTAACTTGCACCAGTGCCAGCAGCTACAAAACACTGCAAGACTGGAAAGGGTTTTGATGAGGAGAGAAGATCGTTGCAACCTACATAGCAGCTGTGGAATATCAAGTTTCTCATCCTTGGGGACTTGCTATTGATTTTATTTGCAAAGTTTAGTATAATAATAAAACAACTTCCTCCTCATTCAATGTGGAAGTAAAATGGCCATGATTTTAGTTTGGTAAACAGGGTCCTGCAGCAGTGTCATTTGATTGATTTTTGTGTGTGATTTGATTGTCTGTTCACTTTATTTTTGTGAAGATGTCCAGGGTGACCCTTCAGCTGGTCTTCTTTGATGGAGGAGAGGCGTTCGAGCAGTGGTCTCCGACAGACTCATTATATGGTTCACGGCATCTCGCAGAATACATGTCCAGCATTCCTCATCCACCGGGATCTGAA[C/T]AAACCACACTTCTCAATGCCGTGGTAAGATGACATGAATGTGTATGTGCCTGTGTGTGTGTTTTGTTGTTTTTAAAGGGATAGTACATTTTGAAAAAGAAAAACCCAGCAGTCCATTCAAAAACACTCTAAAATGCAAATAGATTTAATGTAAATCGACTACCTTGATGTCAAAATAACATGAAATTAACATCTAAAATTGATGTCGATCAACACATCAAAAATCACTTACAGGACTGTTCTTTCATTGATTTTATGTGTTTTTGATGCCCATATTAGATGTCAAGTTGATGTTGTCTTGACATCAAGGTTGTTTACGTGCATTGTAGAGATACAAAATCCAGTGTGAATAGTCATGTTACAGTCGTCACTATAACAGGTGAAACATACAGAAAAAATTTACTTTACATTCAACTCATTTTGCTAGTGGCGATACACTCTTTTCCTCTACATATGCCCCATATCTTTTATCATAAACACCATATTTCTGGAAAACATTGT
Associated Phenotype:
Not determined