ZMP
LOC792697
Ensembl ID:
Human Orthologue:
TRIP6
Human Description:
thyroid hormone receptor interactor 6 [Source:HGNC Symbol;Acc:12311]
Mouse Orthologue:
Trip6
Mouse Description:
thyroid hormone receptor interactor 6 Gene [Source:MGI Symbol;Acc:MGI:1343458]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20902 | Nonsense | Available for shipment | Available now |
sa20901 | Nonsense | Available for shipment | Available now |
sa40864 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17712 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20902
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 |
---|---|---|---|---|---|
ENSDART00000100798 | Nonsense | 86 | 570 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 21149351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19739787 |
GRCz11 | 7 | 19991755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGCCATGCAACACCAGCATCCAGATGATCGCTCAGGGTCTGCCACATA[T/A]CATCAGTTGACCCCCCAGTTAGGAGACCGATACTATGCCCCAGGGCCCAA
Long Flanking Sequence:
TCATCCCCTTCCATCGAATTGGCTCGATCACTGTCTCTCCACTCCACCAATAGCTGGTGTGTGGTGAGCGCACTGGCGCCGATGTCCTGTGGCAGCCGTCGCATCATCCAAGTGGATGCTGCACACTGGTGGTGGTGTGGAGAGACCCCCCTCATGATTGTAAAGCGCTTTGGGTGTATGGCCATACACAATAAATGCGCTATATAAATACACATTACATTACATAAAAACTCTCATGTTATTTTGACTTGGTAAAAAGCTAGCATAGCTTCAAACATAACATAATTAACAAAACATAAGCATTATGCGGTTTTAATGTATTTATTTTTAAACATGGTTAGAAATTATTGGTTTGAACTGACTGTATGATCTGTTGTGTGTGTTTAAAAATAAGGCATGAATATTGTCAGTCTGTGCTTTGTAACTTTACCAGTGTGTGTATGCTTAGGTGGAGCCATGCAACACCAGCATCCAGATGATCGCTCAGGGTCTGCCACATA[T/A]CATCAGTTGACCCCCCAGTTAGGAGACCGATACTATGCCCCAGGGCCCAAAGAAGACCACCACACCTGGAACCCCCGCATGACCAGCCATGAACTCCATGTCAGTGATACCCACACATTCATTTATAATTAATTCTAGTGCATGAGCAGGACTTGTTGTGTAGTGTAAATATGCTTCAGATTGTCAGTCATTCCCTTAAACAATGGGGTAGGGAAAATATATCAAGAAATTTATAATGCTGTCATAACTCGTGCTCTTTATTACACTTTCTAGAAGACTTAGGGTGTGTTAAAGGTTTGGTTTGATTAAAATGGTCTTCTGGTTTGATTGCTATGTTATCCACTATGCCATTCATTTGAACAAGTATGAGCACTGCCATTTGAACCTTGATGCACACCAAACTATTGGACTGAGACACTTTAAAATAAAATCTAATAAAATATATTTCCTTTAGCTTTGGTTGTTAGTGCAAGTTCTAAGTGAAACAAGTATGAATGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20901
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100798 | Nonsense | 151 | 570 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 21147054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19737490 |
GRCz11 | 7 | 19989458 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTCTCTTACATGCATGCTGGCAGACCTGGACAGCCACCCTCAGAGCT[C/G]AAGCACACAGGTAAAACACATCTATGCTGACATGTCACATGATCCTTCAT
Long Flanking Sequence:
TCGGTCCTAGAGGGCAGGTGTCCTGCTAAGTTTAGCTCCAACTTGCTTCAAAACACCTGTCAGGAAGTTTCTAGTGTATCTAATAGGAGATTAATTAGCTGGTTCAGGTGTGTTTGACTAGTGTTGGAGCTAAACTCTCCAGGACATCGACCCTCCAGGACCGAGTTTGGACACCTTTGGTGTGAACGGGCAGGCAAAACAATCAGATATAGACAACAACTCTAAACTGAACATCAAGACCTGACAGTGTAAACATGACCATAGAGTACTAAAGGATGACTGAATTTTCTTTATTGACCTCTTATTATTTAAAAAAAAAGAAAGAAACACATTCCCCCACCTTTTATCAGTAAGCATCTCAAACGTACAATGAAGTGTGTATTGTTTGTGGCTGTTGTTTACTCAGAATCGGGGATCAGAGAAGCACATCTCTACTATTGATGCAGATATAGACTCTCTTACATGCATGCTGGCAGACCTGGACAGCCACCCTCAGAGCT[C/G]AAGCACACAGGTAAAACACATCTATGCTGACATGTCACATGATCCTTCATGAATCACTCTAATATTCATTATTATTGTTATTATTATTATTAATAATGGTAATAGTAATAAAAGCAATAATGACTGGAGAAATAATTTCATTTGAAACTTATTTCTCCATATTTGAGCATTCTTTAAAACACTTGGCATAATGTAAGTACGCAAAAAAGTTAACAAAATATCTAATTTGTTTTATTTTTTGGGGATATTTTGATGAAAAAAAACATACATTATGTGACATTAAATTTTTATGTATTCATGTTTATGTGTTTATGAAGTGTGTGTTTTTGTGTTTTTTTTTCTGTAAAATATTTCAATTCTGAATCTCAATTTCAAAATCTGCAGACTGACTGATTTTTTTAAATTGCTTATTACCTCCTTTATACTTGAAATCAAGGCAAAAGTTGAGTAGGAAATGCCAATCTACAGGGAATGATTGATATTGTGGCATTTTCACATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40864
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100798 | Nonsense | 416 | 570 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 21143593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19734029 |
GRCz11 | 7 | 19985997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTGTATCACCTGTCATGCCCGACTCAGAGGCCAGCCCTTTTATGCAT[T/G]AGACAGGAAGAGCTACTGTGAGAACTGCTACATAGTATGTTTTTTGGTCC
Long Flanking Sequence:
TGGTGTGTTTATTGTGTGAAAAATTTAATAATTTTTTTCCCATTGTAAGCTGATCATATTCACAGAATGGCTGAGTAGTAGTATAACTTTTTTTGAATACTTAGTATGAGAGGTATAAAAATTTAAATCCATAATAAAAACAGAGAGGTCCTGTATGATTAAAAGTGAACAATCTTTCATGTTCTGCCAGCAGGGGTCAGCCCCGCATCCAGAGGAAGAGTTGGATCGACTCACCAAGAAGTTGGTGTATGACATGAATCACCCCCCTACTGAGGAGTATTTTGGTATGCTCCCATGTTTTACATCTTCAGTAATGCATTTCTGCTTATTTTATTAGGGTCATGGCTCAATCTTTTTTCCCTCAGGTCGATGTGCTCGCTGTGGGGATAATGTTCTGGGAGATGGCAGCGGCTGTATTGCCATGGAGCAGGTGTTTCATGTGGAGTGTTTCACCTGTATCACCTGTCATGCCCGACTCAGAGGCCAGCCCTTTTATGCAT[T/G]AGACAGGAAGAGCTACTGTGAGAACTGCTACATAGTATGTTTTTTGGTCCTTTTTAAGTGCTTTTAGTTCCTTTCTGTAGCACATTTCGCATTCATAAAAAATCACTTTCTTTTTTTTAATTTTATTTGTTCTTTGTGTCTCTCTTCACAGAGCACACTTGAGCGCTGTTCAAAATGCTCTGAGCCCATCCTAGACCGGATCCTGAGGGCCATGGGCAAGGCATACCACCCTCGCTGCTTCACCTGTGTGGTTTGCGGCTGTTGTCTGGATGGAGTGCCTTTTACTGTGGATGCAACATCTCAGATCCACTGCATTGATGACTTTCACAGGTTTTTGCCCTCTTCTCTTCCTAGATATGACTTTGAACCCACAAAACAAGACTTAACTTACATGGGTATGTTTGTGGGAATAACCAAAGTACATTGTATGAGTTGCTGCATGATTCTGGTAAAAATGTGAATCATGATTTTTTTTTTTGCTTAAAATCAAGATTACGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17712
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100798 | Essential Splice Site | 527 | 570 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 21141733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19732169 |
GRCz11 | 7 | 19984137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATCGTTGCACTGGATCGCAGTTTCCATGTTAACTGTTACGTATGTGAG[G/A]TAAGGATTTTTACACWTGAGTTTATTTTATGTGGAAGTACATATAWAGAC
Long Flanking Sequence:
TAAGACCACTTCAGATGTTGTCTACTATATATAGATTTTTTATTAATTTATTGAAATTTCCATTGCTGTTCTCAATATTTAGATTTAGATAGATCATCATATTCCAGATTTCCTGAATTTATAACAAAGTATAGCTCAAAAGACGATGATGATGCATACATCTTCCCCCATGCCCACCCCCCAAAAATATACCCATATGCCTGTTTTTGTGATCCAGGGTAATACATTGTGTAAATGTTTTTTTTTTATTATTATTTATAAATCACCTAAAGCAGGTATTGGAATGGCATGGTGTTTTTCTTTACTAATTATGCTTTGACTCAATCCGATATCCTATATGAACTTACTTGATAAAACATTTTGCTGTCTGTGTGAGCAGGAAGTTTGCTCCTCGCTGCTCAGTATGTGGTCAACCCATAATGCCAGAGCCTGGGCAAGAAGAGACGGTGAGGATCGTTGCACTGGATCGCAGTTTCCATGTTAACTGTTACGTATGTGAG[G/A]TAAGGATTTTTACACATGAGTTTATTTTATGTGGAAGTACATATATAGACCATATTTCTAAAAATCTGAAAGAAGTTTGTGTTTTTACATGTGCAGCATGCATTTAGTGCTTTGACAGAAAATCTTCGTCTTAATAAGCGATATTAATAAATCTGCATTTTGTTTAACTTTATTAAATATATTCCGAAATAGATTAAATTTAGATGCTGCAGCACCCTATTTTCCATACTTTACACTTGATTGTCTTTCACTGTAAATGAGTTTTTAAAATTGTAATGTTTAATTAAATATGCAAATGTAGTGGAATATAAACTGAATTACTAAAATCTAAAGTTTCAATAAAGCCACATTCTATATGTATTATTTTTATTTAGTTTGTTTATTTATGACAGTTAGACATGTTTAGTATGGTGAGTTTAGATGTCTCTCTTTATCTTTCAGTATTTTAGAAAATACCTTCAATAGTCAGGGAAAAAAAATTAATATTCATCATGTTTTAG
Associated Phenotype:
Not determined