ZMP
HMGXB3
Ensembl ID:
Description:
HMG box domain containing 3 [Source:HGNC Symbol;Acc:28982]
Human Orthologue:
HMGXB3
Human Description:
HMG box domain containing 3 [Source:HGNC Symbol;Acc:28982]
Mouse Orthologue:
Hmgxb3
Mouse Description:
HMG box domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2441817]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35625 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9952 | Nonsense | Available for shipment | Available now |
sa10782 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35625
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 |
---|---|---|---|---|---|
ENSDART00000110721 | Nonsense | 731 | 1222 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 3072597)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2842937 |
GRCz11 | 14 | 3094054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCAGCATTTAAGCATTACTGCAGTTTGTGTGTTTGTATTCTCAGGTT[T/A]GTTTAATGTCGGAAATAAACTCCTGGTGACGCTGGATTTGTTCTTTAAGA
Long Flanking Sequence:
TTATTTCGGCTTCAATGAAGGCAGTTATTAATATTTTAAAAACCAATTTTGGGACAAAATTATTAGCGCCTTTAAACTAATTTTTTTCTGATAATCTACATAACAAACCATCGTTATACAATAACCTGCCTAATTATACTAACCTGCCTAGGTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTCGAAAAATATCTATTCAAATATTATTTACTGTCATCATAGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGCTTAGAAATGCGCTGAAACAATCTTCCCTCTGTTAAACAGAAATTGTATTATATAAATGAAAATAAAAGTACAGCAATACCTCAATGTTACTAAAATCACACATTACTATAAGCATTAATTGTAACACTGAGAAGGCAACATGTTCATGTATCTCAGCATTTAAGCATTACTGCAGTTTGTGTGTTTGTATTCTCAGGTT[T/A]GTTTAATGTCGGAAATAAACTCCTGGTGACGCTGGATTTGTTCTTTAAGATGAGGAATCAGATCCGACTGGGGGACGAACCTGCTCAAGCTGCTCTCAGTATCATCACAAACGCACAGACAGGTGCTTCCTCATCTTTATACACTTCTGCCTAAAAGCAGCAGTAAGATTTTTGAATATTGTAATCCATGCCTTTAAAGGGAAACTAATAAATCACTTCTTATAAGGGGTTAAAACACAGTTGTGTGGCAAAAGTGTATGTACATAACCAGCTTCTCATGGTAAAAGTGTATAAATTGTATTATTTATACCCACACGTCTGCAGAAACGCTTTGATTGTGTATTTAGTGTTCCTTGTGTGTTTTTTAGACGGTGTGTTTACATCGGATCAGACATCTCGTATTCAGGAGCTGTTCTGCAGTGGTTTCTGGGCATTTGAGTGTCTGACGCTTCGAGATTATAACGACATGATCTGTGGCATCTGCGGCATCGCTCCAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9952
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 |
---|---|---|---|---|---|
ENSDART00000110721 | Nonsense | 1038 | 1222 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 3065760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2849774 |
GRCz11 | 14 | 3100891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGTGGCAGACTGTGCCCAGAAGGTGGCGCTCTGTGCTGAYGTGTCCTA[T/A]CCTCAACTCGCCAAACAGATGTGGGGGGAAAACCAGGGCTGTTTCTCTGA
Long Flanking Sequence:
CATGTTCTCCCCATGTTGGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGACAAACACATGCTCTGTTGGTGAATAAAAAAAACTAGATTGGTCGTAGTGTGTGAGTGTGTGTAAATGAAAGGGTGTATGGGTTTTTCCCAATACTGGGTTGGGAAAGGGCATCTGCTGTATAAAACATATGCTGGAATAGTTGGCGATTCATTCCACTGTGGTGACCCCTGATAAATAAGGGACTTAGCCTAAGGAAAATAAATAAATGAATGAATGAATGAATTAAAAAAATTACACTAATGAAGAGTCCTCATAAAGCACAAAAACAATTATGTGTGTGTGTGTGTTTGTCATCTGCACAGGTGGTTTGCGGCTCGAAGTATATCGTGCGCAGAGAAAGTGCTCGCGATCACTTGGACCTGCTGCTGTCCTCCAGATTCTGGCCGCCAGTGTATGTGGCAGACTGTGCCCAGAAGGTGGCGCTCTGTGCTGACGTGTCCTA[T/A]CCTCAACTCGCCAAACAGATGTGGGGGGAAAACCAGGGCTGTTTCTCTGATCCCACAGCAGCTCCACAGGTCAGAAAATAATAGTATTATACTCTGTTACATTTTAAAGTGTTAAACACAAATATAAAGGAGTATATTATTAAGTTGTATTGATGTTAGTAATTATTATAATTTTTTACATTAGTATAGTTCATGTGAAATGATTATAATAGTTGTCAGTGTGCTGCAGTTTTCTTTTTTAAGAACTAAAATGTTTTTAAAATAGTGTATATACATTATGCATTAAATAAATCTAATAATAGCAATTATCATATTTATTAATAATAACATCATATAATTTTTTTTTTCTGTCCTCATTCCAGACAGGTCTGCTTTTGTTTCTTTGATTGAAAATCAAAAACAAATATTTTTAAATATTGAATTAACATTACATATTAAAACTATAATAACAATATTATTATTATTATTTAATATCATATTGTAATTTGAAACTGTCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10782
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 |
---|---|---|---|---|---|
ENSDART00000110721 | Nonsense | 1062 | 1222 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 3063881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2851653 |
GRCz11 | 14 | 3102770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RCACAACCATCTCAACAATAATWWTGCACATCTCCTGTTGTGTTTCAGTA[T/G]GTCTCSTGCTCRGAGCTCCAGGATCAGCCATACAGTCTGGACCTCACCGT
Long Flanking Sequence:
GCCTAGGCGCATTTCAAGGTTCGTTTGACAAGTGTGAGTGCTCCGAATCAGGCCCAGGCGTGGCTCAGTTGGCCGGCCCTGGCCCGGTTGGAAGAAGTGTGCCAGAGCAAGGTTCACTTGGGCCCAAAACCGAAGATGCAACATCACTTGTTTCATTAATCATTCTTACTGTTCAATAAACACAAACTGTCGTAGATTATTAAAGATGCACGCTTCTCTTCTGTTAAATTGAGCAGCGCATCAATGATGTTGTAAGTGTGCTCCAGCTCGGTTGCAATGTGAGTGCAGACCGTGGGGGAGATGGGAGGGGGGCATGCGTGCTTCAGCATGATTCAAGTCAACTGTACATAGTGTGAGTACGCCCTAAATGACTTTGAATGTGGCTAGTTGTTGGTGCCAGACGGGCTGCTCTGAGTATTTCAGAAGCTGCTGATCTACTGGGATTTTCACGCACAACCATCTCAACAATAATTATGCACATCTCCTGTTGTGTTTCAGTA[T/G]GTCTCGTGCTCAGAGCTCCAGGATCAGCCATACAGTCTGGACCTCACCGTGACCGACTCCAACCCTCAGCTCCACCCGCTCACCAAATCCACCTCCCGCTGGATGGTACGACCCGACACACCCACCTCCACCCTCAAGGACGCCCACTACAACATCAGCCTATGTAGAGAATTGGAGCCCTACGCCAGCCTGAGCGCCCAGATCTGTGAGCCAAACAACCACAAACCAACGCAAGTGTTCCAGAACGCAGCGTATTATTACCTGTACAACCGTCTGCTGGACTTCCTGAGCAGCAGAGACATCGTGAACCAGCAGATCACAGACGTGCTGAGCTCCTGCCAGCCTGGAGAGGTGCTGATGATCAGAGACGCCCTTTACAGACTGGGCATCGCTCATGTTAACACTGAACAGGAGGACGAGGAGGATGGAGGACACGCACACACTGATGGGGTAGTAGAGCTGGAAGAGCTGATGCTCGTCTGATGCAGGTTTACGTACAC
Associated Phenotype:
Not determined