ZMP
LOC559362
Ensembl ID:
Human Orthologues:
RP1-130H16.18, TBC1D10A, TBC1D10B, TBC1D10C
Human Descriptions:
TBC1 domain family, member 10A [Source:HGNC Symbol;Acc:23609]
TBC1 domain family, member 10B [Source:HGNC Symbol;Acc:24510]
TBC1 domain family, member 10C [Source:HGNC Symbol;Acc:24702]
TBC1 domain family, member 10B [Source:HGNC Symbol;Acc:24510]
TBC1 domain family, member 10C [Source:HGNC Symbol;Acc:24702]
Mouse Orthologues:
Tbc1d10a, Tbc1d10b, Tbc1d10c
Mouse Descriptions:
TBC1 domain family, member 10a Gene [Source:MGI Symbol;Acc:MGI:2144164]
TBC1 domain family, member 10b Gene [Source:MGI Symbol;Acc:MGI:1915699]
TBC1 domain family, member 10c Gene [Source:MGI Symbol;Acc:MGI:1922072]
TBC1 domain family, member 10b Gene [Source:MGI Symbol;Acc:MGI:1915699]
TBC1 domain family, member 10c Gene [Source:MGI Symbol;Acc:MGI:1922072]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32523 | Nonsense | Available for shipment | Available now |
sa10061 | Nonsense | Available for shipment | Available now |
sa32522 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32523
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 |
---|---|---|---|---|---|
ENSDART00000125836 | Nonsense | 413 | 617 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 16850919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16397463 |
GRCz11 | 25 | 16493863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCGAATAAAGAAAACACAAAAATCAGTACAGCTTCTTTCAGCGATGGA[C/T]AGCTGCACGATGAAAAACCTTTGCAAGAAACTGCCAAGAAAGGTGAGCCA
Long Flanking Sequence:
ATTAAAATACATACATAAAATGTTTTTATTCATAATTACATATGTTTATATAGTATTATTTATTAGTTTAGTTGTCATTTCAATCACTTCGGTACATCAGATTAAATTTAAAACTAAAAATAAAGAAATATTTATTTGGCATTTATCTATCATTTATTTTATTTCAATTATATTAATCAACAAAATTGTTGTTTTTATTTAGTTTATGTATTTAATATCTAGCCTTATAATTTAGTAATTTAACTATAATAATCATATGTGTTTGTTTGTTTGTTTTCTGCACGTTTATGCATTCAATTAATGTTGTTTTTTTTCGTTTGTTTTAACTTGTATTAATTTATCTATCTTTAAATTTGTTTTTATGTATCTATTTTTGGTATAACAAGTGTCTTGTATAAATGTTGCACATACAAACAATAAACTTCTCTTTCACATCTCTCTTTGCAGAGAAAGCGAATAAAGAAAACACAAAAATCAGTACAGCTTCTTTCAGCGATGGA[C/T]AGCTGCACGATGAAAAACCTTTGCAAGAAACTGCCAAGAAAGGTGAGCCAGTTCATAGAGATCATTTATAGCTAATTCAGCCCTAATAGTGCATCGACTGGAAAGTCGAATAATGCAGCATAACTTAATAATGTAATACAACTGGCACAAAGCCCGTAAAGAGAATAGGGTAAAACCCTTGTTCTTGAGGTCAGCCAATCATACTGTACATTCAATGTTAAGTGAATTACAGAGAGCAGCACTGTCACCTACCCGACTACAAACACCAAAACAGACGCTCTCAAACACAATACAGCCCACATTTCCTTGCTCTGCTGATGAGATTATAGACCAGGAGTGTTCAAACTCTGTCCTGGAGGGCCTGTGTCCTGCATAGTTTAGCTCCAACTTCTATCAATACACCTCCCTGAAGTTCCTAGTATATCTAGAAAGAGCTTGATAAGCTGGTTAAGGTGTGTTTAATTGGGGTTGGAACTAAAATACGCAGGACACTGGCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10061
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 |
---|---|---|---|---|---|
ENSDART00000125836 | Nonsense | 417 | 617 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 16850907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16397451 |
GRCz11 | 25 | 16493851 |
KASP Assay ID:
2261-9509.1 (used for ordering genotyping assays)
KASP Sequence:
AAAACACAAAAATCAGTACAGCTTCTYTCRGCGATGGACAGCTGCACGAT[G/T]AAAAMCCTTTGCAAGAAACTGCCAAGAAAGGTRAGCCAGTTCATAGAGAT
Long Flanking Sequence:
ACATAAAATGTTTTTATTCATAATTACATATGTTTATATAGTATTATTTATTAGTTTAGTTGTCATTTCAATCACTTCGGTACATCAGATTAAATTTAAAACTAAAAATAAAGAAATATTTATTTGGCATTTATCTATCATTTATTTTATTTCAATTATATTAATCAACAAAATTGTTGTTTTTATTTAGTTTATGTATTTAATATCTAGCCTTATAATTTAGTAATTTAACTATAATAATCATATGTGTTTGTTTGTTTGTTTTCTGCACGTTTATGCATTCAATTAATGTTGTTTTTTTTCGTTTGTTTTAACTTGTATTAATTTATCTATCTTTAAATTTGTTTTTATGTATCTATTTTTGGTATAACAAGTGTCTTGTATAAATGTTGCACATACAAACAATAAACTTCTCTTTCACATCTCTCTTTGCAGAGAAAGCGAATAAAGAAAACACAAAAATCAGTACAGCTTCTTTCAGCGATGGACAGCTGCACGAT[G/T]AAAAACCTTTGCAAGAAACTGCCAAGAAAGGTGAGCCAGTTCATAGAGATCATTTATAGCTAATTCAGCCCTAATAGTGCATCGACTGGAAAGTCGAATAATGCAGCATAACTTAATAATGTAATACAACTGGCACAAAGCCCGTAAAGAGAATAGGGTAAAACCCTTGTTCTTGAGGTCAGCCAATCATACTGTACATTCAATGTTAAGTGAATTACAGAGAGCAGCACTGTCACCTACCCGACTACAAACACCAAAACAGACGCTCTCAAACACAATACAGCCCACATTTCCTTGCTCTGCTGATGAGATTATAGACCAGGAGTGTTCAAACTCTGTCCTGGAGGGCCTGTGTCCTGCATAGTTTAGCTCCAACTTCTATCAATACACCTCCCTGAAGTTCCTAGTATATCTAGAAAGAGCTTGATAAGCTGGTTAAGGTGTGTTTAATTGGGGTTGGAACTAAAATACGCAGGACACTGGCCCTAAAGGACCGAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32522
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 |
---|---|---|---|---|---|
ENSDART00000125836 | Nonsense | 546 | 617 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 16838304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 16384848 |
GRCz11 | 25 | 16481248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTGAGGTCAGGGCCTGTCGGTAAAGTGGCCCGAAGAAGGAGCCGAGAT[C/T]AATCCAGAAGAGGAAGTTCCTTCCATTCGAGGAGTCGGCGCTCTAGATCT
Long Flanking Sequence:
AAATAGAATTAGTTTCTTGGAGCATGTAAATAATTTTTTTCTGCAGAGATAAAAAATCCTAAGCATTTAGCCCTATATAAATTTGAAATTTCTTGACTGTTTTTAAAATGTCTTAAAGTCTCAAATATGACTGCAGTAACCCTGTATTAACAGTTGTTATGACCTAGATCAATGTTTCTTAACCACGTTTCTGAAGGACTACAACACTGCATGTTTTGGATGTCTCCTTTGTCTGTCCTATTGCAGGCCTTTCAGTCTCTGCTAATGAGACACTGAAAATGTGCAGAGTTTGTGGTCCTCCAGGAACATGGTTGAGTAGCACTGTTTCAGATGGTCAATTTGCGTCTTTTTTCTTGCAAATATGTGTCAATTTTATGACCCCAAAAAGTGTCTAAATAAATTTTAAGTAATGATTTCTGACCCTTCACAGCTCCGACTCTTCAGCCTGGCGCGTGAGGTCAGGGCCTGTCGGTAAAGTGGCCCGAAGAAGGAGCCGAGAT[C/T]AATCCAGAAGAGGAAGTTCCTTCCATTCGAGGAGTCGGCGCTCTAGATCTCAGCAAACACCAGCTATAAAGACTGTGCAACCCGAGAGCAACAAGACTGATGATTGTAAAGAAACCCCAAACAGGTAGTGAATCATTCATGCATATTAGTTTTATATTGGCACAGCAAAAGCTTTTTTTATTCTCTACCATAAACATTTGGTCTCTAATGACATTAATAATAACGTGTTTTGGGTTAGGATTAAACTGACAGGTGGTCCCGCTGGTTTGGTTTGGCAGGTTCACTTGCTAAAGAGTGGTTAGTTATAATGAGTCTTTAATCTAGACTGAATCCCTCACAGTGAAAGTGATTAATGTAATGGTATGGATTCTCTACAACAGAAGGATTTAAATGAAATCATAAGTAACTGTGAAAGATGATGCTTTAATACGACAAATGAGTTTTATGGGCTTATTTTACTATTTTTGATTGGAATTCATGTGGATTAGTTTGATCTTTAA
Associated Phenotype:
Not determined