Busch Lab

ZMP

zgc:162724

Ensembl ID:
ENSDARG00000054827
ZFIN ID:
ZDB-GENE-070424-72
Description:
hypothetical protein LOC100038788 [Source:RefSeq peptide;Acc:NP_001083037]
Human Orthologue:
C3orf32
Human Description:
chromosome 3 open reading frame 32 [Source:HGNC Symbol;Acc:24809]
Mouse Orthologue:
D630042P16Rik
Mouse Description:
RIKEN cDNA D630042P16 gene Gene [Source:MGI Symbol;Acc:MGI:2443733]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa44990 Nonsense Mutation detected in F1 DNA Not yet available
sa37553 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44990
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
ENSDART00000024756 Nonsense 59 417 3 14
ENSDART00000060014 Nonsense 23 381 2 13
ENSDART00000130604 Nonsense 55 413 2 13
Genomic Location (Zv9):
Chromosome 22 (position 33709470)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 31071008
GRCz11 22 31020203
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGTGACCAGGATGGCGCGTCAGGTCCAGGCAGATCTTATGGAACTTG[T/A]ACAGGTAATCAATATTTATTTTTCCTAAAGTTGAACTCAAATATCTCTTT
Long Flanking Sequence:
CTTTGTTTTTGTAGTAAACCACTTCTCATTGGAATGTATCATGAGATCGTCACGTTGCGCTGCTGCTTCCTGACTCTCAAAACGAAAGTTGACAGTTCACTTGCTACAATGGACAAGACGCACTTGTTGAGGTATGATCGAGAAAAAAAACAGCAAAATCACGAAGAAATGTCTGTTAGGACAAACGTAAATTAAACATTATTTAAGGTAGCGAGGAATTACTTATAAGACATATTTTAAAAAAGCAACAAACAAAAAAAATACTGAAAAATACGGTCGTTTGTTTTGGTCAGTGAGGGAAATAAGTGTCTCAGTTCTCGTTTTTTTTTTCTGACGGTTTTGTTGTCAACTTTTATTTATCGCTGTACTTTTGTACATATTGAATAAAAACACGTGTTTGTGGCTTACAGTTCTCTCTCTCATACTCTTTCTCTCTCTCTCTGTGTGTGTGACAGTGACCAGGATGGCGCGTCAGGTCCAGGCAGATCTTATGGAACTTG[T/A]ACAGGTAATCAATATTTATTTTTCCTAAAGTTGAACTCAAATATCTCTTTACACATATTTATTTCTCTAAAATTTAAAAGTGCACATTTACACAAGATACAATCCCAAAAAGGTTTATATTAGATAATATCTAATATATATTCATAAATACTGTCAAAAATAGTTCACCCCTGTGTTTACATCAGCAAAAGTAACATGAGAGAAAAAAAAGTTTCCTGTTTCTGCTGTTTCCTCATTGCAGGAATAGCTTAGTCACAGCTGAAAAAACAAGAGTTCAAAGAGTGACAGATAGTATGATGAAATGTGTTTTTTATTATTTTTTTTGTACATTCACTAGATCCAAACATGGAGGCAAATGATGGGGCGACAGCTCCTCCTGCTGATATGATGCCTGTGGTTCCTGGATATGAGAATTTGGGACCTAATGGTGAGAAAAATTTCAGTAGTTTAAGCTGAATCTATGCATGATGTATTGATGTTGCTAATGAATATGATAGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37553
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024756 Essential Splice Site 91 417 4 14
ENSDART00000060014 Essential Splice Site 55 381 3 13
ENSDART00000130604 Essential Splice Site 87 413 3 13
Genomic Location (Zv9):
Chromosome 22 (position 33709041)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 31070579
GRCz11 22 31019774
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGATATGATGCCTGTGGTTCCTGGATATGAGAATTTGGGACCTAATGG[T/C]GAGAAAAATTTCAGTAGTTTAAGCTGAATCTATGCATGATGTATTGATGT
Long Flanking Sequence:
TCTCTCTCTCTCTGTGTGTGTGACAGTGACCAGGATGGCGCGTCAGGTCCAGGCAGATCTTATGGAACTTGTACAGGTAATCAATATTTATTTTTCCTAAAGTTGAACTCAAATATCTCTTTACACATATTTATTTCTCTAAAATTTAAAAGTGCACATTTACACAAGATACAATCCCAAAAAGGTTTATATTAGATAATATCTAATATATATTCATAAATACTGTCAAAAATAGTTCACCCCTGTGTTTACATCAGCAAAAGTAACATGAGAGAAAAAAAAGTTTCCTGTTTCTGCTGTTTCCTCATTGCAGGAATAGCTTAGTCACAGCTGAAAAAACAAGAGTTCAAAGAGTGACAGATAGTATGATGAAATGTGTTTTTTATTATTTTTTTTGTACATTCACTAGATCCAAACATGGAGGCAAATGATGGGGCGACAGCTCCTCCTGCTGATATGATGCCTGTGGTTCCTGGATATGAGAATTTGGGACCTAATGG[T/C]GAGAAAAATTTCAGTAGTTTAAGCTGAATCTATGCATGATGTATTGATGTTGCTAATGAATATGATAGTGACTTTATGAGTGAATATGAGTGACTTTTTATTTCATCCTCAGTTATTCCGCCTTCACATTTTGGATCATCACAACCACAAGCCCCACCCCGAGCTCCAGAGAGACGCTTTGAGTAAGAAAATGAAATGATTCATGATTTCAGTTTTAATTATTTGAATAGTTCTACATGAAGTCTAAGCACCAAAACGTTTACTCGTTCTTTATTCTGTGTATGCAGTGGTGCAAAGTAACAAGCTACAAATACTCAAATTAAGTTTTTCCGAGAAATTGACATTTGCTAAGTAATTCTAAAAATATGTACTTTTATGTTCTCTAAGTATATTTTTAGTGCTGTATCGGTACTTTTACTCCACTATTTTGTTTTTTGGCAAAGTAATGGAACTTTTGCTTGAGGATGATTTTTTTACAACATCACAATAAAAGCAACCTT
Associated Phenotype:
Not determined