Busch Lab

ZMP

zgc:163107

Ensembl ID:
ENSDARG00000020041
ZFIN ID:
ZDB-GENE-070521-7
Description:
UPF0505 protein C16orf62 homolog [Source:UniProtKB/Swiss-Prot;Acc:A4VCH4]
Human Orthologue:
C16orf62
Human Description:
chromosome 16 open reading frame 62 [Source:HGNC Symbol;Acc:24641]
Mouse Orthologue:
9030624J02Rik
Mouse Description:
RIKEN cDNA 9030624J02 gene Gene [Source:MGI Symbol;Acc:MGI:1918767]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa41974 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa41975 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8607 Nonsense Mutation detected in F1 DNA Not yet available
sa35224 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa13664 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa41974
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:
G > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052537 Splice Site, Nonsense 6 963 2 30
Genomic Location (Zv9):
Chromosome 12 (position 12274434)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11130087
GRCz11 12 11168390
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAAATGTTAAAATGTCAGCTTTTATGTAAATGTGTGTGTTCTGCACAG[G/A]CACTCCAGGAGCCGTAAATATGACAGTGAGTGGCAGGCGAGTCGTTTGGA
Long Flanking Sequence:
CATGGCTTCAGTTCAATGGTAGGAAATGTTGACACTTTTACATATTTAACGCCATCAAACTCGAACGTGATGTTTTTAATAAACATGGTATTGACAATTATGTATATTCTACTAAAACCTCTAGCGGTTAAATATAGCTGTAGAGTAAACTGTGGTGCAGAGCTTTGACAGTAACGTTATGTTTTAGTGCTTTATTTAGAGCCTTTTAAATTATTACTTTGGTAACGTTATCAAACGTCATACTGACTTGGTACATAGTCCGATACTATGACATTTACGTACACTTACTGTATTGACGTAGCGTAAGTATGTATATAATATCTAGTATCTGTAACTTACTATGAAAATATCATGTTTTTGGTCATGACCAACAATTAAACTACAAACATATAAGAATGTGTATATTTTGGTAGTTTTAAATTTGCTTCCAGTCATGTCTAGCATTAGTGTCTAAAATGTTAAAATGTCAGCTTTTATGTAAATGTGTGTGTTCTGCACAG[G/A]CACTCCAGGAGCCGTAAATATGACAGTGAGTGGCAGGCGAGTCGTTTGGAGGTTTCAGCAGTGGAGTTCAGTGACTATCATCCACTCAAAGCCATCACGGTACATCTACAACCTCCATGCATACTCATTGAACTGTGTCATCTAAAATATATTACTCTTTTTCTGTTAACTGAAGTTCTACATGCTGGAGTGGGCTACCCCTGGTAAATTACATTTCTATAATGGTTAACTGGCTGGCAGTTTGTTCAACCACCTGCTGATCTCTACATTTATCAAGTCATATTCAGAAAATGATTTAATAATATAAAAATGATCTAATATGTAATTATGTTGTTGTCTAGTAATCAAGGTTCCACAAGTAGGCTAATGTCATTCCTGGAATATCATGAAATATTAGGAATTATCTGGTCTATTGCAGACACTAAAAGTCATATGTTTTCTCTATATATTTCTCCAAGTCATGCAATATCATGGTTTGTATCATTTCTTTGATCTATACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41975
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052537 Essential Splice Site 424 963 14 30
Genomic Location (Zv9):
Chromosome 12 (position 12285126)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11140779
GRCz11 12 11179082
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTCTGCTAACTGAGATGATGGACAGATGCAAGAAGTTAGGCAACAAG[T/A]AAGATCTCACCACTGAGGCACTTTTCAATGGAAAATTTTGCATTGTTTTT
Long Flanking Sequence:
AATATTTCTACCTGATGAACTCATACTTCGACCTGTTAAGGTATTCCTTTTCAGTCAGTATTTTATTATATCCATGTTGTTTTTATATAACATATTTAAATATAAATAAATAAATATTAACAATTATGTTCAACAACAAACAACTTTACACTGAAAATGTGGAGCAAAGGTGGCATGGCTTTTCCACATTACTTTGGTAAAATTTACATTAGTTACCCTTATGTGATAAGAAATACATTTGTTGCATTGTTTTTTTAATCTTTTGTTAATGTATTCATTATATATGAAATAAAAATTTACCTTTTTATTGAAAGTTTATTGATAGTTCCTATTTTTTCAGGTCTAGTAAATAATGTGAAAAGACTTTTTATTTAATTTAATCTTGTAAGCTTTGTAAGGGCCTTTCAAAGTGTTTATGATCAGATATGTTTGATCTGCTTTGTCCTTTAAAGGTTCTGCTAACTGAGATGATGGACAGATGCAAGAAGTTAGGCAACAAG[T/A]AAGATCTCACCACTGAGGCACTTTTCAATGGAAAATTTTGCATTGTTTTTAGATAAACGCATGATAACAGCATATTTCTTAAATATCTACAAACATATGGTATTTTATGCTATAGAACAATAACAAGTAAAATCTCACCACTGAGGCACACTGTATATGTAATATTTACTGATCAATGAAAATCATGCACTTTTTTATTAATATGTATGGGTGGGCTTTGTGGACTAGTAAACAGCTACCTACCCCCATTTAGCATTGTGCTTACATGGGCAAGCATCTTAATCTACAGTGCATTTAGTCATGTCAAGTTGAGCTTTATTGTCATTCCTTTTCATGTGTCTACGTAAAGTGGCTCGGAATCTTGTGTTCATGGTGATACAAATAAATAAACATAACTATCAACAGAGCAATTTTTAAAACCTAAACAATACATGGCTAACATACTTGAGCTGTAATCTGACCCAAGACAGACTATAGAAGTACTTTACGTAATGCAGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8607
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052537 Nonsense 481 963 16 30
Genomic Location (Zv9):
Chromosome 12 (position 12286156)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11141809
GRCz11 12 11180112
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTGCATCTCTGGGCCGCAGTCTGTCCTGTGCKGACCCTCCAGAGAGC[G/T]AGAGACTCTCCATACTCAATGAAGCCTGGAAGGTCATCACTAAAGTTCGC
Long Flanking Sequence:
AATAGCAGGACGTTCACAATCATTTGTGGTACATTCACGAGTAAATATTTGTTTTATCTATTTGAGTTCTTGTAACATGGAGTTCATAAGAAAGTGTTTGCTGCATATACAGTATAGAGTAATGTGAGTATATACACTTCAGTATACACTGATTGTCTTTTCTTCCCCATAGTGCTCTTCTGCTAAACTCTGTCATGTGGGCGTTTCGGGCTGAATTTGTTGCAACGAGAGCAACAGACTTCATTGGCATGATCAAAGACTGTGATGAAGCTGGATTTCCCAAGGTGACTGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACCCAATAACAAAGCTACAGACAGGGCATAATTACTTTGTTGAATTTCAGTGTCATAATTTCTTCTCATGATCCTCTGTGCTTTTCAGCACTTGTTGTTTGCATCTCTGGGCCGCAGTCTGTCCTGTGCTGACCCTCCAGAGAGC[G/T]AGAGACTCTCCATACTCAATGAAGCCTGGAAGGTCATCACTAAAGTTCGCAGCCCACGGGTAAACACATCAGTTTTTCTCTAAATGTTTGAAAAACACAGAAACAATGACCATATTCAGGGATAGCTTGTCACCCCCATGACATATCAGTTGGTTGCTGAGCATGAATCTGTTTAATGTGTTTAAATGCAATTGTTTAGCCCAGATACAACGCATGGCTTGCATCACAAGTTGTTTCTTTGCTGTATATCTCAATCAGCTCCCTTGTATTAGAGGTTGTGAATCAGTAGGTTCTGTACTCAAATTTGGGCACAGTTACAGGACAGTGATGAACTTTGTTCACTAGTATGTTTGCATGGACACCAGTGCTAATACGATTAAGACAATACTCTGATTAAGAGTCTTTCATTCAAACATGTAAACAGAGATTTTTGATTATCTTAATCCAACTAAAGTCATAATCTAAACACTAATCAAATTAAAACATGCATGGTATTCCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35224
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052537 Essential Splice Site 546 963 19 30
Genomic Location (Zv9):
Chromosome 12 (position 12290193)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11145846
GRCz11 12 11184149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACATTGATGTTGTCAGAGCACTTCATTGCTCTTCTTTTGTTTCTTTCC[A/T]GTTGCAGTCAGTGATTAAGAAGATCCTCACCTACTTCCATGATTTCTCAA
Long Flanking Sequence:
AGCCTCCCACCAGTGCCGATATACAGCCATATCGCACTGCTACTCGTGTGATATTGCTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACTGACAAAGGCACATATGCGAAAATTCATTTTCTTTTGTTTCTCTTGTGATTTTATTTAATAAATAATTTACATCACCATGTCCTTATCATTTGAAGAAATTAGGTCTACTGTATCTTGTAGAGCTCTGTGGTTTACATTTAACACAATAATCTGACTTAGTTTTTTTAGTATGCCATTACATATTTCTTCCTTGTAGAAACGGGAGGTGAACACTGTTCTTGCTGATATCATCAAACACATGACTCCAGACAGAGCTTTTGAAGATGCATATCCACAGGTTAGCCAGAAACATACAGTAGATATTAAAAAGATAATATGACATTGATGTTGTCAGAGCACTTCATTGCTCTTCTTTTGTTTCTTTCC[A/T]GTTGCAGTCAGTGATTAAGAAGATCCTCACCTACTTCCATGATTTCTCAATGCTTTTTTCGATGGTATGAATACAGAACTGTGCATCATTCAGTATTGAATTTAGATAACAGTCTCCATATATATTTAGTGTTGTTAAACAATATCTATATGGCTATATCTAAAGAGATAGCGTATTTAAATAAAGGAAAATTCTGCAACCAACCATTTACTCCTCCTCCACTTGCCTACACCTGTTTGAGTTACTTTCCTTTGTTGAACTTGAAGGAAGATAGTACTCTTTTAATAAAAAAACAACATATTGTTTCTTTTAAGAAAGTAGAATTTAAATTGAATGTAAATTTAAAAATTTAATTACTTACACTTATATGGTCAAACTTTTAGTTGAAATGCCACCTTTTAACATTTCTAATTAGTTTATATTTGTTTTGGTAATTCAGTCAATTAAATAAATGCAACACTTTTTATATACAACATTTCTAATATACTACAAATGAATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13664
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052537 Essential Splice Site 740 963 25 30
Genomic Location (Zv9):
Chromosome 12 (position 12296375)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 11152028
GRCz11 12 11190331
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATCTGCTGTCTGGACAARTAGCGCTGGCCAACCAGTGTCTGTCCCAGG[G/A]TAAGTGGGTGCTGGAGATTTTGCTTTTCAAAGATATTTTTSCWGACYAAG
Long Flanking Sequence:
CTACATACAAGTCTATAGTTACTGGTTTCCAAAAACAATTTTGTGTTCATCTTAAGAAAATAATTTCTAAAGGTTTGAAACAAGTGAAGGGTGAGTTAACAATAACAGAAATTAAATTTTAGGGTGAACTATCCCTTTAAATCTCATGCAAATTTGTTGTCTTGATAATGTTGCAAAAAAAATATATATATATATATATACATTTATATATCTTTAATTTGCAATCTTTTACAAAACTTGTTTTATTTTCGAATGGAGTGAAATGTGGTCTGTTTGGGAGATGTTTTTGACAGACATAATCTAGACCTTCTCAACAATAATGTTGAATTATTGTTTTATGCCATAATAGTCTGAGGTTCTGCTGTTGTGTTTTGTTTATTTCCAGGCATGTGCCGCCTACAGCTTCATCACCATTCCATCCCTCACGAACATCTTCAGCCGCCTCAACCTCTATCTGCTGTCTGGACAAGTAGCGCTGGCCAACCAGTGTCTGTCCCAGG[G/A]TAAGTGGGTGCTGGAGATTTTGCTTTTCAAAGATATTTTTCCAGACCAAGGGTGCATTTATTCAACCGAATATACAGTACAAACAGTAATATTGTTAAGATTAAAAATAATAATAATCCTGAGATATCAAAGCAAACTTTTCAGCATTCATTTTTTTCAGAAAACACAAACATTTAAAAAAAAATTGTAAACTATAAAAGTGTTTGCCATCATTTGATACATTTTCAATATCTTTAATTAATGTGTGCATTAAAAAAATTACTCTTGGTAGCCCATTCCTGCCACTAAATAAAAAATTATAAAAATGTTATTGAGACTTTTTTTTTAATCTCATTGCATAATACAAACTCGCAATTGAGACTTTCTAAAAAATCATGAGATGCAAACTCAAAATTGCAAGAAGTACACTAAAAATTTTGAGAAATAAAGCCAAAATTCTGAGAAATAAAGGTGCTACTGTGTGATATAAAGACAGACTTCAGAGATAAAAGTCTCAATTC
Associated Phenotype:
Not determined