ZMP
LOC559514
Ensembl ID:
Human Orthologue:
TNRC18
Human Description:
trinucleotide repeat containing 18 [Source:HGNC Symbol;Acc:11962]
Mouse Orthologue:
Tnrc18
Mouse Description:
trinucleotide repeat containing 18 Gene [Source:MGI Symbol;Acc:MGI:3648294]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33269 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15126 | Nonsense | Available for shipment | Available now |
sa33270 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1164 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
sa33271 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20097 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33269
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 |
---|---|---|---|---|---|
ENSDART00000103486 | Nonsense | 325 | 2925 | 4 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 40438136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40301496 |
GRCz11 | 3 | 40443354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGGACGATGAAACCATCCGACCAGGGGGCCACCTTTCTAACGACAAA[C/T]AGAAAAGATGCGATTCAGTTGCTACATCAGCTGGCACTCTGCATGTTTCG
Long Flanking Sequence:
ACCTGCCAGGTTCAGTGCACTCCCAGTCTGCAATGGCTAGAAGCCCAGTGGCTCACATGCCTGGCTCCTTCTCCAGGGAAAGGGAGTCCTTACCTCCTCACAAAAGCTCTAAAGAGTCGAGCAGAGATGTGGGAAAAGAAAAGCCCTGTAAGAGTGACCTAGCCCACTCCCTCCCAAGGAAAGAACGAGAAAAACCAAAAGAGGAGTCACGGCCTCACAGTGTGGTGGACCTCACCTTGGATCTCAAGGCGGAAGATGAGCGCAGGGTAGGCAACTTGGAGAGGCCTGCAAAAACTACAGAGCATGCTCGGCCTTTCTTTCACCAGCACTCGCCTGCTCTAAGTAACACGGACACTAAACCCAAACAAACTAACCATAGTTTACTTGGCAACTCCGGGACAAGCAGCGGCACGCCAACCCGACATCAGAGTACAGAACAGGACAGGAGGGACAGGGACGATGAAACCATCCGACCAGGGGGCCACCTTTCTAACGACAAA[C/T]AGAAAAGATGCGATTCAGTTGCTACATCAGCTGGCACTCTGCATGTTTCGTATGCCAGTCCCTCTTCCCTGCAGCCCAGCCCATCCCATCTCCCGCCCAGGCTGGTGTCCTCTGGCACCTACCCTCCCCCTCACCACATGCCGCCCAGCATGTACCCACTCTACTCTACAACGAAAGAGCCAGGCAAAGAACACAGAGTGATAGCTCCTACTTATGTGCCTTCTGTCGAGGTTTACGATGAGCGAAAAGGGCCAATTCAAATTGCCTCCCAAGCTCGAGATAATAAAAATGACAAGAGCAGGGAGAGGGAATCGCACAGATCAGCCCTGCAGTTGGGAAATGAGAGAACACTTATGGACCATGGTCGATCCTCCGTTAGGAGCGAGTCGCCGCCTCACGGGGATGTCAAAAGAGACATTTTACGAGAGGAAGGCTCGATAATTAGGTCAAATGGTTTGGCCATGAAAAAGCCTTTGCATTTGGAAATGTGCACAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15126
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 |
---|---|---|---|---|---|
ENSDART00000103486 | Nonsense | 477 | 2925 | 4 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 40438593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40301953 |
GRCz11 | 3 | 40443811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAAGAGACATTTTACGAGAGGAAGGCTCGATAATTAGGTCAAATGGTT[T/A]GGCCATGAAAAAGCCTTTGCATTTGGAAATGTGCACAAATAAATCTGGAA
Long Flanking Sequence:
CGATGAAACCATCCGACCAGGGGGCCACCTTTCTAACGACAAACAGAAAAGATGCGATTCAGTTGCTACATCAGCTGGCACTCTGCATGTTTCGTATGCCAGTCCCTCTTCCCTGCAGCCCAGCCCATCCCATCTCCCGCCCAGGCTGGTGTCCTCTGGCACCTACCCTCCCCCTCACCACATGCCGCCCAGCATGTACCCACTCTACTCTACAACGAAAGAGCCAGGCAAAGAACACAGAGTGATAGCTCCTACTTATGTGCCTTCTGTCGAGGTTTACGATGAGCGAAAAGGGCCAATTCAAATTGCCTCCCAAGCTCGAGATAATAAAAATGACAAGAGCAGGGAGAGGGAATCGCACAGATCAGCCCTGCAGTTGGGAAATGAGAGAACACTTATGGACCATGGTCGATCCTCCGTTAGGAGCGAGTCGCCGCCTCACGGGGATGTCAAAAGAGACATTTTACGAGAGGAAGGCTCGATAATTAGGTCAAATGGTT[T/A]GGCCATGAAAAAGCCTTTGCATTTGGAAATGTGCACAAATAAATCTGGAAATAGCCCAGATGCCAGGGACTTGACTAACACTACATCAAAACACATGATCAGAACAGGACTCGAGACTGAATCCCGCAGCCAAGAGCGGGATAGGGTTCAAAGATCTACCCATTCCTTCTCTGGAATGGATCCAAGTTCGCTTCACACTGAGCAGCATCCGTTGAAGACCTTGGGTTCTGCTGAGCCCAAATGGAAGCCTTTCGAGATGGGCAATTATGCTACCAGTCACATGGCTGCATTGGCAGCCCAACACAACCACGGAGCCCGAGGTGAGGAAGAGGGCAAGCAAATGTACCTAGACACTACTAGCTTGCACAGACCAGTAGGCAGCAGTGGAAGTCCTGATGGACATGGGGAGGTTTCAGCTATGCAGAGCCTCATCAAATATAGTGGCAACTTCTCCAGTGAGTCTGGCTCTAGGCACGGATCCGATAGTCGTAGTCCATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33270
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103486 | Essential Splice Site | 1459 | 2925 | 12 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 40450661)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40314021 |
GRCz11 | 3 | 40455879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCTGCTGTTTGGAGTCAAGCTACAGACATTAATCTTGCTTTTTCACTT[A/T]GATGTTCTCCAAATCCTCTTTGGAGGGAATGGATGCCGCAGAAGTAGACT
Long Flanking Sequence:
ATACAAGTATTCAGTAGTTTACTTCACAATAAAAATAAATGTATTAAATTAAAGCTGTTAATAAACTTCTTCCACCGAAAAAGCACAATTCTGTTGAACACAAAAGAAGCTATGCTAAAGAATGTTGGAAACTAACAACCATTGACTACCGTTGTTTTTGTTTGTCCTACTATGGATGTCAATGGAAGTCAAGAGTGAGTAAGGGTGTGCATGTCTACCGAAGTAGGGTTTTTTTTCTGATAAAATATATTATGTTAGTCACTTTTTCAAGGTTTTCAATATATATAAACTTTAATAAAAGTGACACTGAGAGGAAAATGGGAATATCATCAGGAAATAATTGCTTGAGCAAGTTTACGACTGGGCCAAAACCCCGTCAAATGCATTGTCTAGCACCACCACTGTTTCCCGGTCATTTGATTTCAGCTGGATGCCCATAACCAGTGTTAATAGCTGCTGTTTGGAGTCAAGCTACAGACATTAATCTTGCTTTTTCACTT[A/T]GATGTTCTCCAAATCCTCTTTGGAGGGAATGGATGCCGCAGAAGTAGACTACCGCGTGAGACTGGCTGAGCTGCAGCAGCGCTACAAAGAAAAGCAACGAGAGCTGGTCAAACTGCAGAGACGGAGAGACAAAGAGTGAGTCTTTACATTACCTCCCATTGCAGCACTTCATTAACGCCGCTAATTGCAAACTACCTCACTTAATCCCACTAACAGCCAGACAAACGGCAATTTATGATCTCTCTGATTCACAGAGAGAAACGGCAGCAGCAACAACAACATATCCAACAGCAGGAGAGGAACAGAAGTTTAGCCCGCAGGGGCCCAGGACGTCCCCGAAAGAGGAAACATGGCCTGTGTGCGCTGTCTCCACCCTCCAGCAAGTTGGATTCGAGATGTGCAAAGTGAGTATGGAGCTCGGGCACCGTTAAGGTCCAGCTGTGCTCCACACAGCCTGCCCTGCAGCTGAACACACTGTTGTTTTGCAGGTTGAGCAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1164
Status:
Confirmed mutation in F2 line
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103486 | Essential Splice Site | 1553 | 2925 | 13 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 40451066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40314426 |
GRCz11 | 3 | 40456284 |
KASP Assay ID:
554-1074.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTGTGCGCTGTCTCCACCCTCCAGCAAGTTGGATTCGAGATGTGCAAA[G/A]TGAGTATGGAGCTCGGGCACCGTTAAGGYCCAGCTGTGCTCCACACAGCC
Long Flanking Sequence:
TTCCCGGTCATTTGATTTCAGCTGGATGCCCATAACCAGTGTTAATAGCTGCTGTTTGGAGTCAAGCTACAGACATTAATCTTGCTTTTTCACTTAGATGTTCTCCAAATCCTCTTTGGAGGGAATGGATGCCGCAGAAGTAGACTACCGCGTGAGACTGGCTGAGCTGCAGCAGCGCTACAAAGAAAAGCAACGAGAGCTGGTCAAACTGCAGAGACGGAGAGACAAAGAGTGAGTCTTTACATTACCTCCCATTGCAGCACTTCATTAACGCCGCTAATTGCAAACTACCTCACTTAATCCCACTAACAGCCAGACAAACGGCAATTTATGATCTCTCTGATTCACAGAGAGAAACGGCAGCAGCAACAACAACATATCCAACAGCAGGAGAGGAACAGAAGTTTAGCCCGCAGGGGCCCAGGACGTCCCCGAAAGAGGAAACATGGCCTGTGTGCGCTGTCTCCACCCTCCAGCAAGTTGGATTCGAGATGTGCAAA[G/A]TGAGTATGGAGCTCGGGCACCGTTAAGGTCCAGCTGTGCTCCACACAGCCTGCCCTGCAGCTGAACACACTGTTGTTTTGCAGGTTGAGCAGAAGTGTGCTTTACTCAGAGGACTCGGAAAGCGGGGAGGTGCTGAGAAAGCGCTTTCGGGCCTCTAACAGAGATGAGGAGGAGGAGGAGGAAGACGGCAGCAGCGCGTTGAAATTGAAGAAGAAGAAAAAGAGCTGGGGCGAGCAGGAGGCATGTTCAAGCTTCTCTCATGAGGTTGGTCTCTTTTATACTGGAGTCATACTAAAGCAATTCTGGCTTCGAAACATTCGAGATTTTGTTGAACCAACATGTTGTTTCTAGTTAGAGCCATGGTGCTCCAAACATGAGCTTTGCTGTTCCTACAAGTGATGCAGGTTCAAGTTTTGCCAAGGCTGAATCATTTTCTTTTAGATAGCCCATTCAATACTCATTTGGTGCAATCTCTATTGACAGGTCCCAAAAATGGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33271
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103486 | Nonsense | 1620 | 2925 | 15 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 40451568)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40314928 |
GRCz11 | 3 | 40456786 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATACTCATTTGGTGCAATCTCTATTGACAGGTCCCAAAAATGGCTGTG[A/T]AGAAGAGCCGAGTAAGCGAGCAGGAGCAGTTGGCATCCAAACTCGACAAG
Long Flanking Sequence:
GAGTATGGAGCTCGGGCACCGTTAAGGTCCAGCTGTGCTCCACACAGCCTGCCCTGCAGCTGAACACACTGTTGTTTTGCAGGTTGAGCAGAAGTGTGCTTTACTCAGAGGACTCGGAAAGCGGGGAGGTGCTGAGAAAGCGCTTTCGGGCCTCTAACAGAGATGAGGAGGAGGAGGAGGAAGACGGCAGCAGCGCGTTGAAATTGAAGAAGAAGAAAAAGAGCTGGGGCGAGCAGGAGGCATGTTCAAGCTTCTCTCATGAGGTTGGTCTCTTTTATACTGGAGTCATACTAAAGCAATTCTGGCTTCGAAACATTCGAGATTTTGTTGAACCAACATGTTGTTTCTAGTTAGAGCCATGGTGCTCCAAACATGAGCTTTGCTGTTCCTACAAGTGATGCAGGTTCAAGTTTTGCCAAGGCTGAATCATTTTCTTTTAGATAGCCCATTCAATACTCATTTGGTGCAATCTCTATTGACAGGTCCCAAAAATGGCTGTG[A/T]AGAAGAGCCGAGTAAGCGAGCAGGAGCAGTTGGCATCCAAACTCGACAAGGCCTTGTCCCTCACTAAGCTCAATAAATTCAGCAAGCCTTCTTGTAAGTTCATAGACGGTTCCTCAGGGAAGTCCAGGCCTAGCTCTGGAAGCAGAGTCCCAATGCTCACCGATTTAGATGTAAGAGTTAAGATGGGGAAATCAAGCCTGTCAAAAGATCTCGGCATCTTTCAGAAGACTTCCAAAGGAGGTAAAAGCAAAACGGCTGCCAAAACGAAGCCTTCTGAAGCGTGCCTTAAGGGAAAAGGCCAGAGGAAAGCACCTTATTCTCCAGTGAGGTCAGAAATCAGCAGCTATTCTAACAGTAAGTCTGTTTTGTTGTTGTCAGTGTTTGATTTCTGATGTAAACATGTTACCACAAATGTTTTTTCTTCCATCTGTGTTTTGCTTTCTTTCATATTTTCCCTTTTATGATAATATCTGTTATTAAAAAGTGCTGTGGCACTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20097
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 |
---|---|---|---|---|---|
ENSDART00000103486 | Nonsense | 1980 | 2925 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 40462467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 40325827 |
GRCz11 | 3 | 40467685 |
KASP Assay ID:
2259-3923.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCCCGGGAGTTCAGTTTTGACCTTACAGCGGATGGGAGTGAAGACGAA[C/T]AGTGGACACGGCGGAGGAGCGAACGCATCTTCCTCCATGATGCTGCTCAG
Long Flanking Sequence:
TGTTTAGATGAAAAAAATATTGACTTTACTAAAATAGCCATGTGTACAGTTATGCCTGAGGTATTTCGTAAACATTTTACTATTTTCTTTTTATTTGCAAGAGATCTAATTGATTTAACCATGCTCGAGACAGTTACACCATAGGACAGTTTTGTAAAAGAATGGAATAACAGTTTTTAAGTTAAGAGGTCCATTGGAGACAAAGAAATGTCACATGAAAGCGTATTGCGTGTTTGCTTTAAGTAATAATTAAATGTTATATCTTCTGGATTGTAGGTACGGAGTTTGAGTTTACCGATTCGGAGAGTGATGTCAAGACAAGAAAGAAGTTTCCGTCGCTGTTGCATGGCAAGAGATCCGCTCCCGAGCTTCCTCTCTTGCCTCCCGCGAGCGTGATGCGTGACGACTCCAGCCCCACCAAGCGTGGACGCAAACCCAAGAAACCCAAGTCTCCCCGGGAGTTCAGTTTTGACCTTACAGCGGATGGGAGTGAAGACGAA[C/T]AGTGGACACGGCGGAGGAGCGAACGCATCTTCCTCCATGATGCTGCTCAGTCCACCCCCATCTCCCCGTCCAGCAAAACTCCTCTTCCGCTCACTCCCAAACCTGCTCGCGGCCCCAAAACCTCCCCGCAGAGCCCCAAGGAACTGGTCAAAGCCAAGGAGGTGAAAGATCCCAGCAAGGTAAGCCATTGTTTTATTGATATATCTCAAATCTTGCTTGCCAGCCACAACCAAACGGTATGGGCGCTTGATACCACCAGCAGGTGTCCTGCTACATTTGTCGGACAAGGAAGCCTCCCGCTGTGAGTGTCATGTTGTTGGACACAAAAGGATGACTGCAGCTTGCCAGGCTACAATTACTAACCATCACCATTCCTCCCTCCGAGTCCTCCCGTGTTTTTCCTTTCTCTTAAGTGTTCAGTACACGGCTGCCTATTAATGTTTACTTGTCTATCCAGTGTTGTTGAATGGCTGTAATGTCTGGGAGAACTGAGCCCGATT
Associated Phenotype:
Not determined