ZMP
im:7154960
Ensembl ID:
ZFIN ID:
Human Orthologue:
C19orf6
Human Description:
chromosome 19 open reading frame 6 [Source:HGNC Symbol;Acc:17039]
Mouse Orthologue:
ORF61
Mouse Description:
open reading frame 61 Gene [Source:MGI Symbol;Acc:MGI:2177957]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14860 | Nonsense | Available for shipment | Available now |
sa35049 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5840 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14860
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085158 | Nonsense | 253 | 694 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 11 (position 14325930)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14027226 |
GRCz11 | 11 | 14084885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAATATTCTTTGGAATATGGTTTCCTAAGGCTATCCCAGGCCACACGT[C/T]AACGACTCAACATCCCTGTTATGGTGGTGACCCTTGGTAAGTATTGATNNCC
Long Flanking Sequence:
AATAAAATGTTGATTCATTTTGTCAAAAGTCACAAACCTAAATCTTGTAGATATGAATTTCTCAATGTTTTAGAGCACATTAGCCCATATAGTAGTATATTTATAGTAAAACCTAAAAAAACCTTCTTGGGGATTATTGGGATTTATGGGGATATTGTTAAAGCATACTGCCAAAAACTAAACATTGTTTATTTCAGAGGACCTTTATTCCACATTTTCTAAATCTGACATAACACTTTCCAAACCTGACATAATTTCCAGATTCAAAATGTATAAGATGGGCAGCACATAATTAATTGAATGTTTTAGGCTTTTAATAAAGAAAGTAGAAATGTAGTAACGTGACATGATGGCCTTTTAGACAAATTTTATAGTTTCAGTGAAGCTGTCTGCATTTTTCAATCTTTGTGTTTGTTTTGTGTGTAGTGTGGCCGCAAGAAGAGTATATTGTTGAATATTCTTTGGAATATGGTTTCCTAAGGCTATCCCAGGCCACACGT[C/T]AACGACTCAACATCCCTGTTATGGTGGTGACCCTTGGTAAGTATTGATCCTTTAGGATATTAGGGAGTTATTCACCCAAAAAACGGATATGCTGTTATCATTTAGTCACTTGTTTATATCTGTTTAGTTTTCTTTATTCCATGCAGTGAACACAAAAGCATTTTATTTACTTTACTATTACTTAAATTCTATAGTTAGTTATAAAAAACATGGAAACACAGTTCTGGAATCACTGGAAGGTGAGTAAACTATTAGCAATGCATCACAAGTGGACAACTCAAAAAACGTGTTAATAATTCAGCATAGCTTCTCAGATATTCTAAATGCATTGTGATCCTTTCGAATCTATACCGAGTTTAAATTTGACTAATAAATGGCACAGTATGTTTTTTTAAACCGCTGTTGTCTGCTTGCCTCCATTTCTTTACACGAACCACTTAAACATAAAATAATCATTAATAAATGTAAGAAAGGTTTAAGCAAATTAGAAGAGTGTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35049
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000085158 | Nonsense | 254 | 694 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 11 (position 14325927)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14027223 |
GRCz11 | 11 | 14084882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATTCTTTGGAATATGGTTTCCTAAGGCTATCCCAGGCCACACGTCAA[C/T]GACTCAACATCCCTGTTATGGTGGTGACCCTTGGTAAGTATTGATCCTTT
Long Flanking Sequence:
AAAATGTTGATTCATTTTGTCAAAAGTCACAAACCTAAATCTTGTAGATATGAATTTCTCAATGTTTTAGAGCACATTAGCCCATATAGTAGTATATTTATAGTAAAACCTAAAAAAACCTTCTTGGGGATTATTGGGATTTATGGGGATATTGTTAAAGCATACTGCCAAAAACTAAACATTGTTTATTTCAGAGGACCTTTATTCCACATTTTCTAAATCTGACATAACACTTTCCAAACCTGACATAATTTCCAGATTCAAAATGTATAAGATGGGCAGCACATAATTAATTGAATGTTTTAGGCTTTTAATAAAGAAAGTAGAAATGTAGTAACGTGACATGATGGCCTTTTAGACAAATTTTATAGTTTCAGTGAAGCTGTCTGCATTTTTCAATCTTTGTGTTTGTTTTGTGTGTAGTGTGGCCGCAAGAAGAGTATATTGTTGAATATTCTTTGGAATATGGTTTCCTAAGGCTATCCCAGGCCACACGTCAA[C/T]GACTCAACATCCCTGTTATGGTGGTGACCCTTGGTAAGTATTGATCCTTTAGGATATTAGGGAGTTATTCACCCAAAAAACGGATATGCTGTTATCATTTAGTCACTTGTTTATATCTGTTTAGTTTTCTTTATTCCATGCAGTGAACACAAAAGCATTTTATTTACTTTACTATTACTTAAATTCTATAGTTAGTTATAAAAAACATGGAAACACAGTTCTGGAATCACTGGAAGGTGAGTAAACTATTAGCAATGCATCACAAGTGGACAACTCAAAAAACGTGTTAATAATTCAGCATAGCTTCTCAGATATTCTAAATGCATTGTGATCCTTTCGAATCTATACCGAGTTTAAATTTGACTAATAAATGGCACAGTATGTTTTTTTAAACCGCTGTTGTCTGCTTGCCTCCATTTCTTTACACGAACCACTTAAACATAAAATAATCATTAATAAATGTAAGAAAGGTTTAAGCAAATTAGAAGAGTGTTCATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5840
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000085158 | Essential Splice Site | 306 | 694 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 11 (position 14323058)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14024354 |
GRCz11 | 11 | 14082013 |
KASP Assay ID:
554-3951.1 (used for ordering genotyping assays)
KASP Sequence:
ATTCTAATGTCCAGTGTGAAGGCATTAGCAGAGAATGAGGAAAACAAAGG[T/C]AAACAATTACGTGTTCTCCCAAAAGATCAGTGCTTCCTTCTTGAGTGCAT
Long Flanking Sequence:
TTCCTTACAATTGAAGCTGACAGGTTCTAACGTTGTCTTAACTAATGCTCAACACAAACAAATCTGTTAAAATTTCAAAAAAGGTACTCCAGTGTTTCTTGAACCTTTAAATAGAGAGTATCATTGTTTATATTCCAGTTGGCTATGTTAAATCACTCATGTTTATTTTGCAAGATTAGATCAATTGTTCAGATGGAGCCTATACACAGTGGTGGACATAACTTCAGTTGTATGCAGGTGTACATGGTGCACAAATTCAGACCAGATGTGGCACTATATAAGCTTTTTTTATGTAATTTATCAGCCCATTGTATTGATCCAAACATGTAAGGCTTTCATTGTGAATCTCTGTCAATCTCTCTCTGCTTGTCTGTAGATCCAATGAAAGATCAGTGCTTTGGAGATGGTTTCAGTCGCTTCCTCCTGGACGAGTGCCTGGGTTATGATGATATTCTAATGTCCAGTGTGAAGGCATTAGCAGAGAATGAGGAAAACAAAGG[T/C]AAACAATTACGTGTTCTCCCAAAAGATCAGTGCTTCCTTCTTGAGTGCATAATTACAATGTCAGAGATTGATTGTGTGCTTTTAGGCTTCCTCAGGAACGTGGTGTCTGGAGAACACTATCGTTTTGTCAGCATGTGGATGGCTCGTACCTCCTACCTGGCAGCTTTTGTAATAATGGTTATCTTTGTGAGTACTTTTACTACAATGTAGTTATTATTGATGTTAAGATTATGCGTGTGATGTCATCACATCAGTTAGAATAAGGCATTTAGTATAATAAAGCGTTTAGTTACCTTAGGGGTGTCAAACTCTTCCTGGAGGGCTGCAGCCCTGCTCAGTTTAGTTTGAACACTGCTTTAACACACTCAAGCTGCGTTCACACTGTACTTTTCTCCCCTTAGACTTCCAGTCATATTCCTGCTAAGTTTCGCAGTTTGCTGTGTTGCAAAGTTCAAGCTTGGTGACCTCTGGCCTGCGAAATAAGAAAATGTGACTGTGTG
Associated Phenotype:
Not determined