Busch Lab

ZMP

c14orf159

Ensembl ID:
ENSDARG00000005179
ZFIN ID:
ZDB-GENE-070725-6
Description:
C14orf159 protein [Source:UniProtKB/TrEMBL;Acc:A9JRU8]
Human Orthologue:
C14orf159
Human Description:
chromosome 14 open reading frame 159 [Source:HGNC Symbol;Acc:20498]
Mouse Orthologue:
9030617O03Rik
Mouse Description:
RIKEN cDNA 9030617O03 gene Gene [Source:MGI Symbol;Acc:MGI:2444813]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa25046 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa28907 Nonsense Mutation detected in F1 DNA Not yet available
sa14039 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa25046
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062067 Essential Splice Site 200 617 None 12
ENSDART00000124041 Essential Splice Site 201 284 None 7
ENSDART00000136921 None None 164 None 4

The following transcripts of ENSDARG00000005179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 38928132)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 38813029
GRCz11 17 38760614
KASP Assay ID:
554-7449.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCCATCCCACTGGCGCATGGAGGACCTGTTCATATTGGAGATCCTAG[T/G]ATGGACTTTTTTTTTAAAGAAAGTATATGATGGAACTTTATCTTGTTATA
Long Flanking Sequence:
CAGGGAGGACTGTCCAGAGTACTGTGTGTTTGAGAATGGCAGGCTAATGAAGAAGGTTTCTAGTTTGTCCTCCTTTACCTCTGAACTGGAGCACATGGTCACTTTCTACCTCGGCTGTAGTTTTGGCTTTGAATCGGCCTTGACAGCCGCTGGGGTTCCGGTGAGAAATGTGGAGCAGGGCAGAAACGTCAGCATGTACAAGGTCAGTTCAAGCCGCAAGCCTGGATTACATCCACATGCAGTGAGAGCCTACAGCATATTACTTGATGTTGCTTGTGTCTGATATTTTCTTCTTCAAAATCTTAATAAAATAACTAAAAGAAAGTGTTTTTTTTTTTTTTTTTGCAGACCTCAGTGCCTTGTATTAAAGCAGGTCAGATTCATTGTCCAATGGTGGTGACTATGAGACCAGTACCAGAAGACAAGCTGGACGCTACTGCTCAATGCACACATGCCATCCCACTGGCGCATGGAGGACCTGTTCATATTGGAGATCCTAG[T/G]ATGGACTTTTTTTTTAAAGAAAGTATATGATGGAACTTTATCTTGTTATATAAAGTTATCTTATTTTAATGCAATTTAATTAATTTACCAATTTATGTAATCACATTGTCCTAAACATTCAGATCCATTGCTCAGTATTTAGTCGAAGCACCCTTTTGACCTAATACAGCCATGCATCATTTTGGAAAAGATACAATAAGTGTTTCACATCTGGATTTGGGGATCCTCTGCTATTCCTCCTTGCAGATCCTCTTCAGTTCTGTCAGGTTGGTTGGTAAGCGTTGGTGGACAGCCGTTTTTTTATAGTAGGTCTCTCCAGAGATACTCAATTGGGCTTAAGTTGAAGCTCTGGCTAGGCTATTCAAGAACAGTCATGGAGTTGTTGTAAAGTCACTCCTTCGTTATTTTAAACCTTCAACCCAGACTGAAGCCCTGAGCACTCTGGAGAAGGTTTTCATCCAGGATATCCTTGTACTTGACAAGCATTCATCTTTCCCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28907
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
ENSDART00000062067 Nonsense 272 617 6 12
ENSDART00000124041 Nonsense 273 284 7 7
ENSDART00000136921 None None 164 None 4

The following transcripts of ENSDARG00000005179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 38924268)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 38809165
GRCz11 17 38756750
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCGATCAAAAAGCAGAAGCCATTTCTCCCCTCTCTCTGGAGCCAGCA[C/T]AGCGCCCTTTGACATTCCGCATTTCCCAGGATCCTCAGCATTACAGCATG
Long Flanking Sequence:
TTTGGACTGTGAGGGAAAACGAAGCACCCGGAGGAAACCCACGCGAACACGAGGAGAACATGCAAACTACATACAGGAATGCCAACTGACCCAACTGAGACTCAAACCAAAGACCTTCCTGCTGTGAGGTGGCAGTGCTACCCACAGAGCCACCGTGTCGCCCTCTCATTTACTGTAAAATGTAAAAATGTCACCTTGTACAGTTTTGTTTTGCACATTTGCTGCTGTTAGTGAAGCAGAAATGATACACCCCACCTTTAGAATTTAATGTCACTGGGTTTCCGGTACAATTAAGCTTCTGTTTCTTTAATGTCACTTTTTTTGCAGCATGAACAGATTTATATATTTTTACTCAGTGTGTAGGAGAGCAGCTGTTGACCTTTATTTTTATTTTTTTAAATGTTGCAGAGTCCGCTCTAGCGTTCACACACTCTCCTGGCTGCATGTTCATCACCGATCAAAAAGCAGAAGCCATTTCTCCCCTCTCTCTGGAGCCAGCA[C/T]AGCGCCCTTTGACATTCCGCATTTCCCAGGATCCTCAGCATTACAGCATGGCCAGTGAAAGAGCCGTTCAACAAATCCGAGCAATTGAGGAGCTCGCTGTTGAAGACCCAGGTATGAAGCAACTTAGTTTGTTCCCAGGAAAAGTACAGTATAAGAATGATTAAAATCTAAATTTGTAAGATTTAAAAAACTAATACAATAGTGTTATATATTGTGCTGACTTTAGCCTAACTAGTCACTTTAGTAACGTGGATCATGTCTAAATGCTCATGCTAATGGCATAACACACCCTAGATTTCTGATTTGGTTTTATAGAAAACAATGAAGCACCAAAGATTCTTTCAGATCCCCCCGTGTCTGCAATCTGGGTGTCATTCTTGATGAGTCATTGGAACTAGACAAACAGATCAGTTCTGTTATTGGCTTCAGTTTTTATCAACTACGTTTCCTGTCTGAAGTTAAACACTTTTTAAATCCCACCACTCTAGGCTGGGGCTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14039
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062067 Nonsense 491 617 10 12
ENSDART00000124041 None None 284 None 7
ENSDART00000136921 None None 164 None 4

The following transcripts of ENSDARG00000005179 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 38914993)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 38799890
GRCz11 17 38747475
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGCGTGTGCAGGGATTGGAGATGGAGGTAATGAGCTTGGTATGGGT[A/T]AAGTCAAAGCAGCAGTTAAAGCCCACATGCCTAAYGGGAAGCTGATTGCA
Long Flanking Sequence:
TTTAAGGCTAATTATTTATTTTTGATTGAGTCAAGTGAATAAATTTAGATGTGAACCCATTACCCTCATTTTTTTATTGGATGAATAAACACTTTATGGATATTTTTGCTTTGATTAGAGCTATATCTACTTGTTTAGAACAACAAGATCATTTAAATTAATTGACTTTCTTCAACAAGACAAATATGCTTTGTATCAGGTTAGATAAAATTGTTCTTATAGAGATCAAAAAATAATGTTTAAGGCAAATTATTATTTTTTTCATTGGGTCAGGTGATCAAATACTGAATGATGAGCACAATTTTATTTTTGTGTGAACTATCCCTTTAACAATCGCAACGCTTGAATCATCAACTTTGTTCCAAATTAAGGATAAGTTCAGGCTCAAGGGAAGACCTTAATGAGATATGTCACCTCTTTGGAGCAGGATTAATTGTGTGTGTCTGTGTTTGTGTGCGTGTGCAGGGATTGGAGATGGAGGTAATGAGCTTGGTATGGGT[A/T]AAGTCAAAGCAGCAGTTAAAGCCCACATGCCTAACGGGAAGCTGATTGCATGCGATGTGGCTGCGGATTTCGCCATCACAGCAGGTGAACACACCTCACACTGAGAAAACACATAATACATGTCTGTTTCCAGGAGCTCAACACGCAATGCTTATAAGTTTGGCATTCAAACTTTGGAAATTATATTTCTGATATTAAAGGAAGTGCAACAGCGGTCACTGCATCCATCAACATTGCATCTGTGTTGCTAAATGCAGGACTCTCAAGTCTCACACATATTCACTTTCACACCTACATTTTAGGCTATTCAGACACACCACACCTTGTATTTCTCATAGACTGTAAAAGATATGGATGCAGTATCCATGACATCACCCATAGGTTTCTTAAAAACGCAAAAGAAGCTACAAGTAGGCGCCAACCGACGCCATTTTGTTCGCGCATCATCACCTTGAGATACCAAACAAGGGCAAAGCGTGAGCGGAGCTACAGACGCATGC
Associated Phenotype:
Not determined