Busch Lab

ZMP

wu:fj34h01

Ensembl ID:
ENSDARG00000059961
ZFIN ID:
ZDB-GENE-030131-7797
Human Orthologue:
CHPF2
Human Description:
chondroitin polymerizing factor 2 [Source:HGNC Symbol;Acc:29270]
Mouse Orthologue:
Chpf2
Mouse Description:
chondroitin polymerizing factor 2 Gene [Source:MGI Symbol;Acc:MGI:1917522]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa44673 Nonsense Mutation detected in F1 DNA Not yet available
sa14922 Nonsense Available for shipment Available now
sa45290 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44673
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
ENSDART00000083967 Nonsense 136 766 2 4
Genomic Location (Zv9):
Chromosome 7 (position 44157151)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 41147451
GRCz11 7 41427524
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACACACTTGGGGTTGCGGTCAATAAAACAGTAGCTCACCATTTCCAT[C/T]GAACCTTCTTTTTCACTGGCCTTCGAAGTGCAAAGGCGCCACACGGCATG
Long Flanking Sequence:
AGAGAAATGCACGGCAAGTAGCGCAGACAACATTGTGTCGTGTGACCCCAAAAATTTTATAGATTTTATTTTATTTTTATAAACAATTTTATAATTATTTATTAGATTTTATGGAGATGCACTCCCACTGCAAAGTCATACCAATTGATCTAACATTCTAAATTCTTTCCAAATAGTGATATGAAGTCACATAGTGAAATTGTATTCATATCGCAATATATATCGCAAAAAATGTTTCAATGTTAGATTTTTCTAATATTATACAGCTCTATGCACATGCATAGAGAGAGAAATGCCGAAAACTGGATGCCTATGTTTATATCTGCCAACCTTTTTATAGTTAAATATATAATAATATATTTGTTTGCTTTCACAGGACTCGCTACATCCACACAGAGCTGGGCATCCGAGAACGGCTTCTGGTGGGCATCCTGAGCTCACGTGCCACTCTGAACACACTTGGGGTTGCGGTCAATAAAACAGTAGCTCACCATTTCCAT[C/T]GAACCTTCTTTTTCACTGGCCTTCGAAGTGCAAAGGCGCCACACGGCATGGCGGTCATCGCTCATGGTGATGACCGACCCGTCTGGCTGATGTATGAAACCATACGACACCTCCACCAGCATCACGCCAATGAGTATGACTGGTTTTACCTTGCACAGGACGATACGTACACACAAGCTGAAAGGATCATGGAGCTGGTTAATCACCTCAGTGCGGGACAGGACATGTACATGGGGCGGGCAGAGGAATTTATTGGGGGTGAAGAACGTGCCCGATATTGCCATGGCGGATATGGGTACCTGCTGTCACGAAGCCTTCTAGCACGACTGCAGCCACATCTGGACTCTTGTCGAAACGACATCCTTAGCGTCAGGCCAGACGAGTGGCTTGGTCGATGCATCATTGATTACCTGGGTCTTAGCTGTGTGGAGAAGCATCAGGTGAGGAAACATTTATATGAATGCACATGAAGAGCTAAAACCTACTTACCATAGCTGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14922
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
ENSDART00000083967 Nonsense 671 766 4 4
Genomic Location (Zv9):
Chromosome 7 (position 44162353)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 41152653
GRCz11 7 41432726
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTGCGTGATGGCCACTTTGACCGGCAYGTCTTYGAAGAAGCTTGTTTTTA[T/A]AACGCMGATTACATGGCTGCCCGCACAAAGATGGCGGCTGACATCCTGGA
Long Flanking Sequence:
GACCAAGACTTTGTGGGCAACTTCTTGGACATGTACGTCATGAATGCTCTGGATACCCATGACAATGCTCTGCTCACCTTCTTGTTTGTTTATGACCCTTTCGATGCCCAAAGAGTCAGTCAGACGGATGTCTTTGCTGGTGTTAAAGCCATGATTGGTGAGGTAGAGAAACGTTACGGCGACGTCAAGATCCCTTGGATCAGTGTAAAGACTGAAGTTCCCTCACAGGTCAAGCTAATGGACATCATCTCCAAGAAGCACCCAGTAGACACTCTGTTCTTCCTGGCCAGTGTATGGACTGAGGTCAACGCTGACTTTCTCAACCGCTGTCGGATGAATGCTATCAGCAATTGGCAGGTCTTCTTCCCAATCCACTTTCAAGAGTACAGTCCTGCTTTGGTCTACCGCGACCAGCAGCCTTCTGCTGCTTCATCATTTGCATCTGAAACTTTGCGTGATGGCCACTTTGACCGGCACGTCTTTGAAGAAGCTTGTTTTTA[T/A]AACGCAGATTACATGGCTGCCCGCACAAAGATGGCGGCTGACATCCTGGACAACGATGAGTTGCTGGAGAGCATGGATGTCTATGAGATCTTTGTACGTTACTCTGGGTTGCATGTGTTTCGGGCTGTGGAGCCGGCGCTAGTACAGAAGTATGTGCACAGGGAATGTAACCCACGCTTTAGCGAGGACATCTATCACCGCTGTGTGCTCAGTAACCTGGAGGGGCTGGCCTCTCGATCACACCTAGCCATGGCTTTGTTTGAACAGGAGCAGGCCAACAGCACCTGAACCAACTAATGCTGCAATGTTAAGACGAAACAAACTTCTTGATTCTGGTTTAGGTGGCCTTAATTGACCTACTGATATTGCTCCAGTCAATTGCACCCTGATGCTGTGAACGTCTTTGCAAAGATCATCCAGTGAACTCAGTTTAACGAAATACAATGACGATGCCTTGCTGAAAAGACTAGTTCACATTACAATGAACTTTGTCTTCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45290
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083967 Nonsense 722 766 4 4
Genomic Location (Zv9):
Chromosome 7 (position 44162506)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 41152806
GRCz11 7 41432879
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGGTTGCATGTGTTTCGGGCTGTGGAGCCGGCGCTAGTACAGAAGTA[T/A]GTGCACAGGGAATGTAACCCACGCTTTAGCGAGGACATCTATCACCGCTG
Long Flanking Sequence:
ATTGGTGAGGTAGAGAAACGTTACGGCGACGTCAAGATCCCTTGGATCAGTGTAAAGACTGAAGTTCCCTCACAGGTCAAGCTAATGGACATCATCTCCAAGAAGCACCCAGTAGACACTCTGTTCTTCCTGGCCAGTGTATGGACTGAGGTCAACGCTGACTTTCTCAACCGCTGTCGGATGAATGCTATCAGCAATTGGCAGGTCTTCTTCCCAATCCACTTTCAAGAGTACAGTCCTGCTTTGGTCTACCGCGACCAGCAGCCTTCTGCTGCTTCATCATTTGCATCTGAAACTTTGCGTGATGGCCACTTTGACCGGCACGTCTTTGAAGAAGCTTGTTTTTATAACGCAGATTACATGGCTGCCCGCACAAAGATGGCGGCTGACATCCTGGACAACGATGAGTTGCTGGAGAGCATGGATGTCTATGAGATCTTTGTACGTTACTCTGGGTTGCATGTGTTTCGGGCTGTGGAGCCGGCGCTAGTACAGAAGTA[T/A]GTGCACAGGGAATGTAACCCACGCTTTAGCGAGGACATCTATCACCGCTGTGTGCTCAGTAACCTGGAGGGGCTGGCCTCTCGATCACACCTAGCCATGGCTTTGTTTGAACAGGAGCAGGCCAACAGCACCTGAACCAACTAATGCTGCAATGTTAAGACGAAACAAACTTCTTGATTCTGGTTTAGGTGGCCTTAATTGACCTACTGATATTGCTCCAGTCAATTGCACCCTGATGCTGTGAACGTCTTTGCAAAGATCATCCAGTGAACTCAGTTTAACGAAATACAATGACGATGCCTTGCTGAAAAGACTAGTTCACATTACAATGAACTTTGTCTTCATTTACTCATGCTCACATCGCATTCAACGTTCTTTTTGGACAAAACAGTTGAAGAATGTTATTGGTTCATACAATGAATGTCAAAGGTGATCATTTCTTAAACATTTCTTCTTATGTGTACCACATGTGAAAGAAATTCAGGTTTTGAAGTAAGCCG
Associated Phenotype:
Not determined