ZMP
thoc2
Ensembl ID:
ZFIN ID:
Description:
THO complex subunit 2 [Source:RefSeq peptide;Acc:NP_001003847]
Human Orthologue:
THOC2
Human Description:
THO complex 2 [Source:HGNC Symbol;Acc:19073]
Mouse Orthologues:
BC005561, Thoc2
Mouse Descriptions:
THO complex 2 Gene [Source:MGI Symbol;Acc:MGI:2442413]
cDNA sequence BC005561 Gene [Source:MGI Symbol;Acc:MGI:3040669]
cDNA sequence BC005561 Gene [Source:MGI Symbol;Acc:MGI:3040669]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42361 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13841 | Nonsense | Available for shipment | Available now |
sa17955 | Nonsense | Available for shipment | Available now |
sa6339 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35651 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16669 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42361
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 |
---|---|---|---|---|---|
ENSDART00000054610 | Nonsense | 157 | 1452 | 7 | 34 |
ENSDART00000054611 | Nonsense | 157 | 1504 | 7 | 36 |
ENSDART00000106626 | Nonsense | 157 | 1560 | 7 | 39 |
ENSDART00000115408 | Nonsense | 157 | 1560 | 7 | 38 |
The following transcripts of ENSDARG00000037503 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 12672828)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12108601 |
GRCz11 | 14 | 12414615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTATTTTCTTATTTAACTTTCCATCCTTCTCCCTGCAGTTACAAACAG[C/T]AAAAGTTCAATTTGTTGCGTGAGGAGAATGAAGGTTATGCTAAACTGATC
Long Flanking Sequence:
CTCATACATACAAACAGAAAATAAATAGGAGTTTGTACATATTAAAGTAATTTTTATTTCTGAACTATTTTGTTTATTTATTTATTATAATATTTTTTTTTCTGGAATAACTACTTATTTAAATAACTGCATTGTGAAATCTAAAATCACTGTGAAATAAAATTACATTGTATTTTGTTTACACCACTCACCCCTAATTGTGGTGAATCTATAAAATGACTCTGGCTGTATTTTACTGTAAATGAATTGCATGGCACTAAGCACTCATTTCTCCCTCTCTATTTAATCAGCACTTCTTTTACATGCCACTAATTATTTCATTAACATAAGCATGATAAAATTAATTGTTCATGCTGGCATTATTGTCTCACTGCTGACTGCCCACTAGAACCTTTCACTAATAGGCTTGTTATTTTTGTTAGACTTGAATTATTGTTGATGACTGCATAAAATTATTTTCTTATTTAACTTTCCATCCTTCTCCCTGCAGTTACAAACAG[C/T]AAAAGTTCAATTTGTTGCGTGAGGAGAATGAAGGTTATGCTAAACTGATCACAGAGCTTGGCCAAGATCTGACCGGGAATCTCACCAGTCACATCGTCCTTGAGAACATCAAGTCATTAATAGGTACAGTATGAATGCATCACCTTTCTTCATGGAGTGCTAATCCTCTTCTTTACATGATGCCTTGCGATTCCTGATGTGGTTAAACTAATATTATTAAAATTTACTACTTGGTGGTTTACTCGAAAAATAAAATTGTCATCATTCACTCACCCTCAGGTTGTTTCAATCTTGTACATTTGTTTTTTTTCTGCTGAACACAAAGGAAGATATTTGGAATAATATCAGTAACCAAACAGATGTTGTCAACCATTTACTGCTTATAGTAGATTTATTATTTATTTTATATTAAATTATGATTTTTTTTTTCTCCATGACTTGTTGGACATTTTTTTATTAAATCACACTGAAGGACTAAAAAAATAAAAATTTTATCGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13841
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054610 | Nonsense | 538 | 1452 | 15 | 34 |
ENSDART00000054611 | Nonsense | 590 | 1504 | 16 | 36 |
ENSDART00000106626 | Nonsense | 603 | 1560 | 17 | 39 |
ENSDART00000115408 | Nonsense | 603 | 1560 | 17 | 38 |
The following transcripts of ENSDARG00000037503 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 12695167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12130940 |
GRCz11 | 14 | 12436954 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CYCATAACTCCAGTGGTGGACTCTCTCAAATACYTAACATCTCTCAACTA[T/G]GATGTACTGGCCTGTATCCNTTTYAAAAGGCTTTTATATATAAATATAGGT
Long Flanking Sequence:
ATTATGTGAGTATTTAGTTGATTAAGAAATGAACCTAAATTAGATTTGGCCAATAATCATAGCTAGGTTGGACCATACTTGACAATAACTGATAAATTAATTGATGGTTTTTAAAATTAGTAGTGGATTACAAAAATAGCGTAAACATAAATGTACTAAATGAATGTTAATGTCAATTGTACTTATATAGCACTATTTAACACAACCAGAGGTTGACCAATGTGCTGCACAGTACACATCACAACAGAGAGAGAGGAAAAAAATAATAAAAAATTATATATATATATATATATATATATTATGTGTGTATAAAATGTGTGTATTTAATAAAAAAAAATACAGCACTCCTGTTATCAATGTTTAATGGTGCATGAATAATAACCAGTTACTGAATGTCCTTTTATTCTCTCTCTCTTTAAGATTCTGTCTCAGATCCAGTGGTACGACAACCTCATAACTCCAGTGGTGGACTCTCTCAAATACTTAACATCTCTCAACTA[T/G]GATGTACTGGCCTGTATCCTTTCAAAAGGCTTTTATATATAAATATAGGTAGTAGGTAGCGTCAGAAAGCCGTGTGTGTATAGACTATCCTGTCACAAAATGCGGCGAAAATTCAACACGACAAGAATAGTTTGATAGCAGTGTTTACATGTTTACACTTGGAGAGCAGCATTTATAGTGGATCTTTCAGCCCATAGTATTTTAGTGATATTGCCGTACTGTAAACTTAGTAACTGAATCATTTTGACTTGGGTAGGTCTTTAAAAACTCAAAGAATACTGCTGACGATACAAACTAACTTTGCCCTCTGAATAATCAAATGAAGGACACTGATCACACACACTTACCAAATCTGTAGAGACAGGACAATCAACAGCAACTGGAGCAGTGTCATTTTTAAAAAGAGATGAGCAGCAAATCCGGATTTCACCATTTCCAGATGCAAAAAGCTCTTTAACTTGTCTTGGCAACACAACGTGGCGTCTCTCTGCTGTCTGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17955
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 |
---|---|---|---|---|---|
ENSDART00000054610 | Nonsense | 806 | 1452 | 21 | 34 |
ENSDART00000054611 | Nonsense | 858 | 1504 | 22 | 36 |
ENSDART00000106626 | Nonsense | 871 | 1560 | 23 | 39 |
ENSDART00000115408 | Nonsense | 871 | 1560 | 23 | 38 |
The following transcripts of ENSDARG00000037503 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 12713875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12149648 |
GRCz11 | 14 | 12455662 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCATGAGGCTGTMGTGTCTCTTCATTTGYCAAAGGTGTGGGATGATCTT[C/T]GACCACAATTCTACGCCACATTCTGGTCCCTCACCATGTATGACCTGGCA
Long Flanking Sequence:
CACAGCTCTCAATGAATGAAAACCTCCAGCTTTTAAACTATTGTTTTAAACTATTAATTCTTTTTTTTTTTAAAGTAACTCAATCATTAATATGACTTGTCTTTTTGATTTTTTTAATGATTTAAATCGGTGATGAACTTAATTTTCAGACACTTTGGTCATAATATTAAAGAAGTTTGTACTAAAAATTATAGTACAAAATGATCTTACAATTCTAATATATCGTTGCTCTCACTGTGACGTTACCCCTTTTTTGTTAAGAACTGTTTTTTTGTGCATTTGTACACTCATCAGGACATTGTTGTGCTTGAGTGAATTGTAATGCAAGCCTGCTGTCTTTGTGTTTCCACCAGTCCAAGTATGATGAATTGAAAAAGGCAGAGAAGGGGAACAGGCAGCAGCAGAAAGTCCATAAGTACATCACAGCCTGCGAGCAGGTTATGGCTCCTGTTCATGAGGCTGTCGTGTCTCTTCATTTGCCAAAGGTGTGGGATGATCTT[C/T]GACCACAATTCTACGCCACATTCTGGTCCCTCACCATGTATGACCTGGCAGTACCACACAATGCCTACGACCGAGAAGTCAACAAGCTTAAGATGCAGATCAAATCCATTGATGATAACACTGAGATGGTGAGATTTCTTTCATATATCATAGAACTAACGACATGTGAAGAGTCCTCTTGAATAGCATGAAAAGATTATGTAAACGGTGTGCTACCCACACAGCAATTTTCAGGTTTCTATTCTTTATACACTTTACAGCTATTTAAGACGCTAATCAAAAAGTGACTTCAACAACTCAATCATAAAGACATCACCCATTGAATGAGGAGAGATTTCTTTTGAGTTTAAGACTCTTATAGTTCGATTTAAACCTTTGGGATCTAAAGGGATTTTGTGGTCCTTGGGATGTTTGCAAATGCTCTGACATTTGTGCTTATTTCTTTAATGGAGAATAAACATTAGTTTTATATCTCGTTTCTAATAACAGATTTTTTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6339
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 |
---|---|---|---|---|---|
ENSDART00000054610 | Nonsense | 955 | 1452 | 24 | 34 |
ENSDART00000054611 | Nonsense | 1007 | 1504 | 25 | 36 |
ENSDART00000106626 | Nonsense | 1020 | 1560 | 26 | 39 |
ENSDART00000115408 | Nonsense | 1020 | 1560 | 26 | 38 |
The following transcripts of ENSDARG00000037503 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 12718141)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12153914 |
GRCz11 | 14 | 12459928 |
KASP Assay ID:
554-4457.1 (used for ordering genotyping assays)
KASP Sequence:
CCCTCTAAATCTGTTTCTTTATTCATCTAGGTCTTCTCTGAYATCATCTA[T/G]ACGGTAGCGAGTTGCACAGAGAATGAGTCCCGCCGMTATGGTCGTTTTTT
Long Flanking Sequence:
TCCCACCTTATCCTTCCTCGCTCTTCAGACACGTCGCGTGCACCCTGTCAAACAATACCAAATCACTACCACACCTGACAGCTGAGCAGGACTCTATGTGAGGAAAGTTTACTCACACATGACTTGTTTTAGTTCTTTTGGTCCGTTTATAAACTTTGCAGTGTGAAAGCGAACCGGACCAAGAGCAAAGAGCAACAATGTAACAATTTTAATCCCTGTTTCGGGACAACTGAATCGATTCAAAGGTGTGAAAGCACCCTTAATTCTGCTAAACAACAGCTTGCTTGCCATGTGTTTCTGTGCCAGTGACTGCAGTCAAAGAGAATACAGTATTATCTAGCATTCAAGTTTGATGCTGTCATTTAGTTTTTATCTAAATGTTCAAAGTATTTATAATCATTTTATATTCATTAAAAATCCATGACCCTGTGTGCATTGTCAACCTACTAACCCTCTAAATCTGTTTCTTTATTCATCTAGGTCTTCTCTGATATCATCTA[T/G]ACGGTAGCGAGTTGCACAGAGAATGAGTCCCGCCGATATGGTCGTTTTTTGTGTTGCATGTTAGAGACTGTCACTCGATGGCACAGTGACAGAGCCATTTATGAGAAGGTATGGTGTGCCTTTATGATTGATGATTCGTTTAAACTGTTAATGCTGTCTCTACACTGTCCTAGTAGTAGCTGTGAACTGTGAATTTTTAGATGTTTGCAAACAAAAAAATGACGAAATCAAAAATAATTTGCAGTAATTACTTATTAAATAACAAAATGATTTTGTCTTTTTAAAATGAAACTTGGTAACAATAAATTATTCTGATTTTAAGAAACGTGTAGAAATGAGCCCCTTTCACACATACAGACCTTTCTGGAAAATTACCAGCAATTTTCCGGAAAGGTCTGTATGTGTAAATAGGTCCTTACTGGTAAATTTGTTATAAATAAAAATATATATAAATTCATAAAAAAAATACATACATACATACATACATACTAGGGATGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35651
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054610 | Nonsense | 972 | 1452 | 24 | 34 |
ENSDART00000054611 | Nonsense | 1024 | 1504 | 25 | 36 |
ENSDART00000106626 | Nonsense | 1037 | 1560 | 26 | 39 |
ENSDART00000115408 | Nonsense | 1037 | 1560 | 26 | 38 |
The following transcripts of ENSDARG00000037503 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 12718191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12153964 |
GRCz11 | 14 | 12459978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGGTAGCGAGTTGCACAGAGAATGAGTCCCGCCGATATGGTCGTTTTT[T/A]GTGTTGCATGTTAGAGACTGTCACTCGATGGCACAGTGACAGAGCCATTT
Long Flanking Sequence:
AACAATACCAAATCACTACCACACCTGACAGCTGAGCAGGACTCTATGTGAGGAAAGTTTACTCACACATGACTTGTTTTAGTTCTTTTGGTCCGTTTATAAACTTTGCAGTGTGAAAGCGAACCGGACCAAGAGCAAAGAGCAACAATGTAACAATTTTAATCCCTGTTTCGGGACAACTGAATCGATTCAAAGGTGTGAAAGCACCCTTAATTCTGCTAAACAACAGCTTGCTTGCCATGTGTTTCTGTGCCAGTGACTGCAGTCAAAGAGAATACAGTATTATCTAGCATTCAAGTTTGATGCTGTCATTTAGTTTTTATCTAAATGTTCAAAGTATTTATAATCATTTTATATTCATTAAAAATCCATGACCCTGTGTGCATTGTCAACCTACTAACCCTCTAAATCTGTTTCTTTATTCATCTAGGTCTTCTCTGATATCATCTATACGGTAGCGAGTTGCACAGAGAATGAGTCCCGCCGATATGGTCGTTTTT[T/A]GTGTTGCATGTTAGAGACTGTCACTCGATGGCACAGTGACAGAGCCATTTATGAGAAGGTATGGTGTGCCTTTATGATTGATGATTCGTTTAAACTGTTAATGCTGTCTCTACACTGTCCTAGTAGTAGCTGTGAACTGTGAATTTTTAGATGTTTGCAAACAAAAAAATGACGAAATCAAAAATAATTTGCAGTAATTACTTATTAAATAACAAAATGATTTTGTCTTTTTAAAATGAAACTTGGTAACAATAAATTATTCTGATTTTAAGAAACGTGTAGAAATGAGCCCCTTTCACACATACAGACCTTTCTGGAAAATTACCAGCAATTTTCCGGAAAGGTCTGTATGTGTAAATAGGTCCTTACTGGTAAATTTGTTATAAATAAAAATATATATAAATTCATAAAAAAAATACATACATACATACATACATACTAGGGATGTAACGGTATCAGAATTTCACGGTTCGGTAATACCTCGGTATGAATGTCACGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16669
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054610 | Splice Site, Nonsense | 1382 | 1452 | 31 | 34 |
ENSDART00000054611 | Splice Site, Nonsense | 1434 | 1504 | 32 | 36 |
ENSDART00000106626 | Splice Site, Nonsense | 1459 | 1560 | 34 | 39 |
ENSDART00000115408 | Splice Site, Nonsense | 1459 | 1560 | 34 | 38 |
The following transcripts of ENSDARG00000037503 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 12739949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12175722 |
GRCz11 | 14 | 12481736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGACCGCTCCAAAGAGAGGGAAAAGAAAGAAGACCGGAAGGACCGAAAA[C/T]GAGTAAGTCCTCTKTATTGGAGGAAGCAGTTTTTAAGCATCWCAAATGTT
Long Flanking Sequence:
GAAAGTCACTGATTACTAAAGAATAATAACTTGATGCATTCATAGATGGTAGTAGCAGCGTTGTTGTGTAAAACCAAATGGTTGACAGATTGTTTTTTGATTTTATGCTAGCTAGCACAATTCTTGAACACTTTTCACATGCAGTTTTTTGGCGCATTGTAGCTCTGATGTGAGTCATATGAAATAATTGCATATGTAAGTTCAGCAGGGGCCTTGAGCTTTTAATAGAGTGCTTGGACTTCCTGTCGGTGTGTCAGATTGTCAGGTGCAACTCTAATGGGGCATGCTAATGAAAGGCAGCAGGCCACTGTGAGGGCTAGTGTGCTCCATCTGTAAGACATTAACCTTCTATCATCTTTGCATCTGTCCTTTAGCACCATCCTAACCACACCACAGTCCTGTCCAAGATCAAAGAGAAGGATGATGAGAAGAAAGAGTCTGATAAATCCAGGGACCGCTCCAAAGAGAGGGAAAAGAAAGAAGACCGGAAGGACCGAAAA[C/T]GAGTAAGTCCTCTGTATTGGAGGAAGCAGTTTTTAAGCATCACAAATGTTATTGAGCAGGACATTTTACAAGGCTTAAACCAACAAATTCTCAATAAAGCCTTTTGCTGAATCATGCTTTGTGATTGAAGCAAAACATTGCAAATCCCACTTGTGAAAGCTTAATTCACACTTAAATACATTATTTAAATTACTTGACCTTCATGCTCATGCACCAGCATATTTCTTTCATTGGTCCAGATGCCATATCATTCCCTCATGTTTTAAGAGTTTTACAGCAGTTATTAGTATGCCTAAAAAGCACTATTTTAAGTTGTGCTGTCTTTCTCCCTTCACGCTTATAGGACTACTTGAACAGCGATCGCGAGATGAGCCAGGAAGCCAAACGCCGCAAAGATGAAAATGGAATGAGTAAGCCTATCTTTTAAATTTGTTTTGCCTGCTGCCAAGAGCACGAGAGCTAGCGAACCAGAAAGTGTTTTTCTCAGCAGCAGAGGCAAT
Associated Phenotype:
Not determined