ZMP
runx2b
Ensembl ID:
ZFIN IDs:
Description:
runt-related transcription factor 2b [Source:RefSeq peptide;Acc:NP_998027]
Human Orthologue:
RUNX2
Human Description:
runt-related transcription factor 2 [Source:HGNC Symbol;Acc:10472]
Mouse Orthologue:
Runx2
Mouse Description:
runt related transcription factor 2 Gene [Source:MGI Symbol;Acc:MGI:99829]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32315 | Nonsense | Available for shipment | Available now |
| sa14504 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32315
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 |
|---|---|---|---|---|---|
| ENSDART00000048978 | None | None | 328 | None | 5 |
| ENSDART00000082265 | Nonsense | 140 | 463 | 3 | 8 |
| ENSDART00000082276 | None | None | 327 | None | 8 |
| ENSDART00000082283 | None | None | 181 | None | 2 |
| ENSDART00000125384 | None | None | 37 | None | 2 |
| ENSDART00000125898 | Nonsense | 126 | 450 | 2 | 8 |
| ENSDART00000130609 | Nonsense | 178 | 502 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 44085019)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 44156178 |
| GRCz11 | 20 | 44053256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGAATTATTCAGCGGAGCTCAGGAATGCCTCAGGGGTTATGAAGAAC[C/T]AGGTGGCCCGCTTCAATGACCTGCGCTTTGTGGGACGAAGCGGAAGAGGT
Long Flanking Sequence:
AAATTAGTCTCACTTCTAGCTTGTTTTTTTTTAATACAAACTGTTTAATAATTAATTAGTCAGTTTAATGTTATTAAAGTTCAAATGGATCATAAGACTAATTTGATTCAGTTTGCAGTAAACATTTAAGAAAAAGTGTCATTTTTAAAGTGCATGCAATACATTTATATGAAATATAAAAGCATTTATATTTTTCACTGAGGTTTGTAAACAGCAGTAATCATTCATCAGAAACTGCATGCATTAAACATTTCATTAATTTTAAAATAACTTTGCATCATATTTGCTATTGTCTGCATAGTCTTGCTATAAAATAACAATCGCTGAACTTTCTGATGAACAGGATATCTTTCTTGCACAGTTTGAAGCATTGTATCTTGTTCTCTCCACAGGTGGTGGCCCTGGGTGAGGTTCCCGATGGGACTGTGGTCACAGTGATGGCCGGAAATGATGAGAATTATTCAGCGGAGCTCAGGAATGCCTCAGGGGTTATGAAGAAC[C/T]AGGTGGCCCGCTTCAATGACCTGCGCTTTGTGGGACGAAGCGGAAGAGGTCAGTACATCTTATGATTTTTTTATTTATTTAGTAATAATCATTGCAGTACTTGCTTTGTCATTTAATTTTATGCAAGTTGCATATAATTGATTCTTGTTCAGAATGGTCTATATCAAAAATTAGCTTAACTGGGTGTTTTAAGCTTGCCTACAGCATTTTGGTTATTACCGCTTTCGTTATAGAATATTAGCTACCATCAAACCATGAAATAGCCTAACATGGAAGGATTGGAGTCATGTATATTAAATAATTCATCACTGAAGATGATTGCATGGATACAGGGCACTTAATTATTATTATATAGTGAAAAAAAAATGGATGATTCTAAAATATTATTGTAAATGGATGCGTTGAAATGGAATTTGAGGTATGGAATATTGTTTTTGAGTGCTGAATGAAATAAATATATATAAAGGTAATTGTCACTTTATATCAAAGTCACAAAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14504
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 |
|---|---|---|---|---|---|
| ENSDART00000048978 | Nonsense | 115 | 328 | 4 | 5 |
| ENSDART00000082265 | Nonsense | 251 | 463 | 6 | 8 |
| ENSDART00000082276 | Nonsense | 114 | 327 | 7 | 8 |
| ENSDART00000082283 | None | None | 181 | None | 2 |
| ENSDART00000125384 | None | None | 37 | None | 2 |
| ENSDART00000125898 | Nonsense | 237 | 450 | 5 | 8 |
| ENSDART00000130609 | Nonsense | 289 | 502 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 44037670)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 44108829 |
| GRCz11 | 20 | 44005907 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTTTTTATTTATTTTTTACCCATCCTCTTGTTTGTTCCTTCAGATCCA[C/T]GACAGGCTCAATCTTCCCCACCATGGTCATACGACCAGACATACCCATCG
Long Flanking Sequence:
AAGAAAAACAAATACCGTGGAAGTCAGTGGTTACAGGTTTTCAGCATTTTTCAAAATATCTTTAATTGTGTTCAACAAAAATCTTGTTTTGAAAAAAGTGTTATCTTAAAAAAATATCTTATATTGAAAAATGTTAGAAACTTGTAACCATTGACTTTCATAGTAGGAAAAAGGAATACTATGGAAGTCAGTGGTTACAGGTTTCCAACATTTTTCAAAATATCTTTATTTGTGTTCAACATAAATAAATGAATAATATTAAATATAAATAATAATAATTTTTTAATAAAAAATACAAATGTTTCACTTCATAAAATCTGTCTGTATCAGTAGGAATGGCAGATAATCATTTTTTCATTTCCACTATTTGTTTTTGTTTTGTTTGTTTTTACACTCAAAGGGCTGTTAGCTGGTGACTATCATTATATTCTGTAATGTTCTACTGAAGACATTTTTTTATTTATTTTTTACCCATCCTCTTGTTTGTTCCTTCAGATCCA[C/T]GACAGGCTCAATCTTCCCCACCATGGTCATACGACCAGACATACCCATCGTACCTAAGTCCCATGGCCTCCCCGTCGGTTCACTCCACCACTCCGCTGTCGTCCAGCCGGGCCACGGGTCTGCCCTCCATCAGCGATGTGCCCAGACGTCTTCCAGGTAACCTCCAGCCTCAGGCCTACAGCAGGTGCGCCTCCGACACTGCAGTGGGCACAAAGTTTATGCACATTTACACACATTTACAAATATGTAAACGTTTTTGAATGATAATTGAAAACTAAGGCGTTTATTTTCTGCTTTTATAACATCTCTTCAAATTGATATCAGTCAAAATTATTAGCCTCCTGTGAAATTGAAAAAAAGAAAGTGATGGGCTAGCACATTAAGTATTTCATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAGTCACTGGTTCTAGTCCTTACCAAGCCAGCCGACGTTTCTGTGCGGAGTTTAC
Associated Phenotype:
Not determined