ZMP
LOC559650
Ensembl ID:
Human Orthologue:
C14orf101
Human Description:
chromosome 14 open reading frame 101 [Source:HGNC Symbol;Acc:20185]
Mouse Orthologue:
6720456H20Rik
Mouse Description:
RIKEN cDNA 6720456H20 gene Gene [Source:MGI Symbol;Acc:MGI:2443219]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23165 | Nonsense | Available for shipment | Available now |
sa39177 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16408 | Nonsense | Available for shipment | Available now |
sa23166 | Nonsense | Available for shipment | Available now |
sa23167 | Nonsense | Available for shipment | Available now |
sa14447 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23165
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113427 | Nonsense | 53 | 684 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 44177462)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44017140 |
GRCz11 | 17 | 44130905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGTTTACAGTAGTGTTTTTTCCCCACAGGTGGCTCATCCTCCAGGATA[T/A]CCTCTCTTCACCATGATGTCTTCTCTGATGCTCTCCCTGCTGCCTCTTAG
Long Flanking Sequence:
ACTATGGCTTATCGCAGTTCAGTAAAGCTAACTGACATGGCCTTCAGCCTTATGAAAATTGTTTAGAGGGATCATTTGGCTGGGACCCCCATTCCTGCTTTGATCTTGAACTCATACTAGCTTTTAGACACCCGCTTGTCCACCGAGTTTCCAATCCATCCCTCAAACAACCACTTCTACGAGTGGTTTCTTGCTCTTCGCTCAAGTGCGCAGCATTTTCCAGCCTGCTGTGCCTGTGTGTGCGTTATCAGGCTAGTAGGAGCGAGACAGCCTTTAATAGCTCTAGTCCTTATCGCTCCTTAGGGGACTTAGTGCCTAATTGCTGGGAAGGCAAGGAGACAGGAGATCAGACTTTGAGGGAGGGGGAGGACAGTGTGGCGCTGTAACCCGTAAAACTGAGGTCTGCCTTTGAAAGCTGAACTGTATGATGATGGGTGGTGGTTCTACGTGTAGGTTTACAGTAGTGTTTTTTCCCCACAGGTGGCTCATCCTCCAGGATA[T/A]CCTCTCTTCACCATGATGTCTTCTCTGATGCTCTCCCTGCTGCCTCTTAGCTCTCCGGCACACAGTATCAATGTGCTGTGTGCTGTGTTTGGGGCCGGGGCGAGTGGAGCCCTCTGCTTCACCGTCTGCAGGTACACCACTCTTATACTGTAAAATACTGTAAAGTTCTGCTTTGTTCATCAGTTAAGGGTTAAAAAATTTTGTGATACCTGAGCAGCAAGTTTACTGTTATACACCCATGTGGATTATTGCAATGTCTCGATGAAGGTGTAAATATTAGGGCAGGGTTAAAAAAAGATATGCACTACTGTGCAAAAGTCTTAGGCCACCGCCAGCTTTGGGAGCCTACGACTTCTGCACAAATCTATGTATCTAAAAGGTATGAAGCGTACTTTTGGGTGAACCACACCTTTAATATACAAACAAAAAATATGGGAAATGTGAACAATATTCAGAACTATATTATTGTTCGAATCAAAAGTATTTGTTTAAATTGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39177
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113427 | Essential Splice Site | 156 | 684 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 44208740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44048418 |
GRCz11 | 17 | 44162183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCAGCCTGTTTCCACTGTGCAGATACTGTTCAGCAGAAGAAGAAGG[T/G]ACTATAAACTCGTTGATCCTCAATCATGCAAAACATTAGTATTTTAAATT
Long Flanking Sequence:
CAATTTAAATTGAGAATCAATACTGAATTGAGCGCACACACACACGAACACACACACAGAAAAACTAATATTTTTTTTATTGTTTGCTTATACTTACTCTAAATTGGTCCCTTAAAAATGTAAAGGGACATTTATTTTTATATTTGTAGCCTAAAATGACTTTTTCAAAAAAATTTATGGCATTTTTTTTTAAGTCTCAAGACTTTCAAAAAGCTGAAGAGACTGAAAAATGCTAAATTTTAACTCACAGATCATTGTAAATTCCTACTACTTATAAACAACTGTCTAAAAGTGCATCTCTCTTATCTCCTTTGTGCCCAGGGTGGCAGAGCCTGGTCCAGGGGCCGTCCTGGCTGGTGGAGTGTTTGCAGTGTCCAGGCTGGTGTGGCAGTGGTCAGTCGTGGCTGAAGTCTTTTCACTTAACAACTTGTTTGTGGGTGTCCTCTTCTCCCTTTCAGCCTGTTTCCACTGTGCAGATACTGTTCAGCAGAAGAAGAAGG[T/G]ACTATAAACTCGTTGATCCTCAATCATGCAAAACATTAGTATTTTAAATTTATTTATATCCATGTTTTGGTCTTTCTCAGTTTGCACTATGGGGGGCGCTGTTCTGTGGGCTGAGCCTGTGTAATCAGCACACACTAGTTCTGTATGTTGTCGTCATAATTCCCTGGGCCCTACTGCATCTCTATACACATAATGTAAGTATTGACAATCATGCTGCCAGCATTCCAGTCATGTAAATAAATAAAATATACACTACCAGTCAAAAGTTTGGTGTCAGTTTTTTTTTTTTTTTCAGTTTTCTTTTTAAGAAATATATTCTGTTCATCAAGACGTTTATTAAATGTGAAATAATTGTTAAATATTTATTCAAATAAAAAAGCTGCTTTCTTATTGTATGTAGTTTCAAATTAAATTATTACTAATTTAATAATAATATTAATAATAATAATCATAATAATAATTAATATTAAAGTGATTTCTGAAGGACTGAAGAATGAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16408
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113427 | Nonsense | 178 | 684 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 44208886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44048564 |
GRCz11 | 17 | 44162329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCTGTTCTGTGGGCTGAGCCTGTGTAATCAGCACACACTAGTTCTGTA[T/A]GTTGTCGTYATAATTCCCTGGGCCCTACTGCATCTCTATACACATAATGT
Long Flanking Sequence:
TAGCCTAAAATGACTTTTTCAAAAAAATTTATGGCATTTTTTTTTAAGTCTCAAGACTTTCAAAAAGCTGAAGAGACTGAAAAATGCTAAATTTTAACTCACAGATCATTGTAAATTCCTACTACTTATAAACAACTGTCTAAAAGTGCATCTCTCTTATCTCCTTTGTGCCCAGGGTGGCAGAGCCTGGTCCAGGGGCCGTCCTGGCTGGTGGAGTGTTTGCAGTGTCCAGGCTGGTGTGGCAGTGGTCAGTCGTGGCTGAAGTCTTTTCACTTAACAACTTGTTTGTGGGTGTCCTCTTCTCCCTTTCAGCCTGTTTCCACTGTGCAGATACTGTTCAGCAGAAGAAGAAGGTACTATAAACTCGTTGATCCTCAATCATGCAAAACATTAGTATTTTAAATTTATTTATATCCATGTTTTGGTCTTTCTCAGTTTGCACTATGGGGGGCGCTGTTCTGTGGGCTGAGCCTGTGTAATCAGCACACACTAGTTCTGTA[T/A]GTTGTCGTCATAATTCCCTGGGCCCTACTGCATCTCTATACACATAATGTAAGTATTGACAATCATGCTGCCAGCATTCCAGTCATGTAAATAAATAAAATATACACTACCAGTCAAAAGTTTGGTGTCAGTTTTTTTTTTTTTTTCAGTTTTCTTTTTAAGAAATATATTCTGTTCATCAAGACGTTTATTAAATGTGAAATAATTGTTAAATATTTATTCAAATAAAAAAGCTGCTTTCTTATTGTATGTAGTTTCAAATTAAATTATTACTAATTTAATAATAATATTAATAATAATAATCATAATAATAATTAATATTAAAGTGATTTCTGAAGGACTGAAGAATGAAGCTGAAAATTTATCTTTAAAATCACTAAAATAAATGATTAAATTAAATGATAAACTACTGTACTTTTAAACAGTTATTTTATAGTGCAATAACATTTCACAATTTTACAATTTGTACAGTATTTTTGATTAAATAAATACAGCCTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23166
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113427 | Nonsense | 375 | 684 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 44217744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44057422 |
GRCz11 | 17 | 44171187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTGACTGGTCATCTAGGCAAAGGGACGGTGTGGAACACAGGAGCCT[G/A]GATACTCACTGCAGGCCTCATATCACACATGATCAGCTTAAACCACAGGT
Long Flanking Sequence:
TATTTATATAGTGATTTTACACTGTAGATTGTGTCAAAGCCGCCTAACATAGAAGTTCTAATAAAGTCCAGATTTCAGAGTTAAAGTTCAGTGCAGTGGTTTATTTAAAATATAATATTCATTTTGTGTGAACTGATCGTAATCCCTTTTTTTATACCCTCAGACTGCGCTGTATTTTTGTCTGCTTGATTGTCACCATGGTAAGCATCTACTCTGTGTTCTTTGCCTGGAGAGCAAACCTGAACATCGAGAAGCCTCTTCTACTGGGAGTGGTGAGTTTAAAGATTAGGATATACATCTTACATAAATAACATTTCTTTATATGATATAAGGTACTTCAAATGGCCATAAATAAATGTACTGTATGTGTGTTTAGGTGGAGCGCTTCTGGCTGCAGGCGGATGCAGGCGTGTGTGTTCTGGCTGGTCTGGGACTGAGTTGGCTTGTGTGTTGTTTGACTGGTCATCTAGGCAAAGGGACGGTGTGGAACACAGGAGCCT[G/A]GATACTCACTGCAGGCCTCATATCACACATGATCAGCTTAAACCACAGGTAAACCATTCAATAATAATCATATATTATTCAAGCAATCATTGTTTAAACACCATTAAACATTTTTTTGTAAAGTGTGCAAAATGCCTTTTCAACTTCGGAAAGAAGGCTGATATGTTGGCAATAGAGGTCTTAATTTGTTGGCTGAAAATGTTTCTATTAAGGCAGATGGCATGGTGTTTAACAAAAAGTATATGATTTATTTTTACAAGATTTTTAGTTTTGTATATGTGTAAAGGTAAATTTTTCAGTTTGTTAAAACATTACTGTTCTAAATGTGAAATTAATACTGTTCGGAATCAACAACACAGTAATTTCAACATAGGCATTAATATCTTTACAAAAGAAATATATTATACATTGGATATATATATATTGGTAAAATATATATACAAAAGACTGATTGCACAAAAATATTAGGCACAAAAATATTATAATGTTTTTACATTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23167
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113427 | Nonsense | 506 | 684 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 44229679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44069357 |
GRCz11 | 17 | 44183122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTGGGCTTGTGTACAGCAGGCCAGTGTTTGTATGTATTGGTCTCACT[G/T]AGGGTGACCCCAGCTGGGAGGGGAGTTTCTCTCGTTGGCCCTGGGGCGTC
Long Flanking Sequence:
TTTATTAAATTCACCTTTAGCGAATTTTTAGAACTGTGGGGAAAACTGGAGCACCCAGAGGGAACCCATGCAAACACGTGGAGAACATGCAAACTCCACACAGAAATGCCAACTGGCCCAGCTGGGACTTAAATCAATAACCGTATTGCTGTGAGGCGACAGTGCTAACCACTGAGCCACCATGCTGCCTGTTTTACTCAAATATATAACTATAAATTATATAAAAAAAAATAAATGTGATGTATTTTTTTATTAGATTTTTTGTATTTTCTAACTTTATCTACTGCATTACACTAATTGTGACTTGTCGTAGTGTTTTCATGCTGTTGTTCTTTTGATTTTACTGAGTATTTTGATACTATAAGCTTATTTCACTAGTGAACATGCTTATAAGGAGTTAGCCACTCATTTGCAATGCTAATAAGTGACTCGCACTGATGGTCAGTTTCTGCTCTGGGCTTGTGTACAGCAGGCCAGTGTTTGTATGTATTGGTCTCACT[G/T]AGGGTGACCCCAGCTGGGAGGGGAGTTTCTCTCGTTGGCCCTGGGGCGTCTGTGAGCAGCTGTTACCTGTCAAGACCCCATTTGACCCAAAGAAGTGGGCCCAAAAAACACACAACCTTTACAACTGGAGTGAGCCACACGACAGGTGAGCCGCGTGGATTATGTTTGGAGTTTATTAAGTGAATTAAGTATGTTTGGGCAATGAACTATTGTTTGGTTTGCCAATACATCTTCTGTTATTATGTGGACTATCATGTTTGCAGCTTAAATAAACACTATAGCCTGTACAATTTAATTAATACATTTCTAATTCCAGGTTGTGACCCTAAACAAAATTGCTCATGATTTATACATCCGCATAAATTAGCCATTGTTGTAATTTATATGGCATTATTTGCAATGTGGAAAAAAGTTCTATACAACACAAGTCACAACAATAGCTAAATTATATGGCAATTCAGCAATTGCATTATCTTAAGCTTGCTAGGTTTATGTTTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14447
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 |
---|---|---|---|---|---|
ENSDART00000113427 | Nonsense | 590 | 684 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 44233692)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44073370 |
GRCz11 | 17 | 44187135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGACWGCCTTTTTCCTGTTTGACCTKGCTGAGAATGCGGAGAAAGAA[C/T]AGCAGGGTCGCCTTTACGAGATTTCCTACAAAGTAAGTTAKACATTTCAT
Long Flanking Sequence:
ATGGGGCGTTCAGCACGGAGAGAGCTTCCAAAGACAGGCAAGGTTGAAGATCAGCTGTTGTATGGTTTGAAGATATGCAGAATACGATTCGCCGGATTACCGGCTGCTTTTAAACTTGCATTTTAAGTCTGCACTTGACAACACTGCTTTGATGCCATCTTAATGTATACGAAGAGGAAATAGCGTTTGACATTTTGGGGAATGTTTTTTCTTTTTGGTTATTTTATGAAAGTAACATGTTGAGGAATATTATCAGAGTAGCTTTGCTACACAACAAAATTTCTTTTATTTAACTATTTCAGCTTCCATCCTGGGTCTTGGGAGAGAGTTGCCAACGAGGAGATGTGGCAGGCCAGGTAAAACACATATTACTGCTGCCATGACTTTGTAACGCTTAATATGTAGTTAAGTATTTACATATTGGTTCTTTTATTCCATCACAATTTAGGATGAAGACAGCCTTTTTCCTGTTTGACCTTGCTGAGAATGCGGAGAAAGAA[C/T]AGCAGGGTCGCCTTTACGAGATTTCCTACAAAGTAAGTTAGACATTTCATAATACACTACCTGACAAAAGTGTTGTCGTGGATCACAGTTGTAAGAGCAACAAATAATGACTTCTAGTTGATAATTTGGAAAAGTGGCAGAAGGTAGATTTTTCTGATAATAATCTGTTGAACTGCATCCCAATCTTCTCAAATACTGGAGAAGACCTATTGGAACCTGCATGGACCCAAGATTCTTACCGAATTCAGTCAAGTTTGGTGAAGGAAAAATCATGGTGGTGTGCAGAGTCGATGGTAACATTAACACCCTGAGGGATCAAGACATTTGTGCTGCCCATTACATTACAAACTACAGGACCGGGCAAATCCTTTAGCAGGATAGCGCTGCTTGTCGTACTTCAGCCTTCATATCAAAGTTCATGTGTGCAAAGAAGGTCAAGGTGCTCCAGGATTGGCCAGCCCAGTCACCAGACATGAACATTATTGAGCATGACTGGGGTT
Associated Phenotype:
Not determined