Busch Lab

ZMP

runx2b

Ensembl ID:
ENSDARG00000059233
ZFIN IDs:
ZDB-GENE-040629-4, ZDB-GENE-040629-4, ZDB-GENE-040629-4, ZDB-GENE-040629-4, ZDB-GENE-040629-4
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
sa25144 Nonsense Mutation detected in F1 DNA Not yet available
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.
Availability:
Order Allele From ZIRC
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:
sa25144
Status:
Mutation detected in F1 DNA
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
ENSDART00000048978 None None 328 None 5
ENSDART00000082265 Nonsense 152 463 3 8
ENSDART00000082276 None None 327 None 8
ENSDART00000082283 None None 181 None 2
ENSDART00000125384 None None 37 None 2
ENSDART00000125898 Nonsense 138 450 2 8
ENSDART00000130609 Nonsense 190 502 4 8
Genomic Location (Zv9):
Chromosome 20 (position 44084983)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 44156142
GRCz11 20 44053220
KASP Assay ID:
554-7459.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTTATGAAGAACCAGGTGGCCCGCTTCAATGACCTGCGCTTTGTGGGA[C/T]GAAGCGGAAGAGGTCAGTACATCTTATGATTTTTTTATTTATTTAGTAAT
Long Flanking Sequence:
CAAACTGTTTAATAATTAATTAGTCAGTTTAATGTTATTAAAGTTCAAATGGATCATAAGACTAATTTGATTCAGTTTGCAGTAAACATTTAAGAAAAAGTGTCATTTTTAAAGTGCATGCAATACATTTATATGAAATATAAAAGCATTTATATTTTTCACTGAGGTTTGTAAACAGCAGTAATCATTCATCAGAAACTGCATGCATTAAACATTTCATTAATTTTAAAATAACTTTGCATCATATTTGCTATTGTCTGCATAGTCTTGCTATAAAATAACAATCGCTGAACTTTCTGATGAACAGGATATCTTTCTTGCACAGTTTGAAGCATTGTATCTTGTTCTCTCCACAGGTGGTGGCCCTGGGTGAGGTTCCCGATGGGACTGTGGTCACAGTGATGGCCGGAAATGATGAGAATTATTCAGCGGAGCTCAGGAATGCCTCAGGGGTTATGAAGAACCAGGTGGCCCGCTTCAATGACCTGCGCTTTGTGGGA[C/T]GAAGCGGAAGAGGTCAGTACATCTTATGATTTTTTTATTTATTTAGTAATAATCATTGCAGTACTTGCTTTGTCATTTAATTTTATGCAAGTTGCATATAATTGATTCTTGTTCAGAATGGTCTATATCAAAAATTAGCTTAACTGGGTGTTTTAAGCTTGCCTACAGCATTTTGGTTATTACCGCTTTCGTTATAGAATATTAGCTACCATCAAACCATGAAATAGCCTAACATGGAAGGATTGGAGTCATGTATATTAAATAATTCATCACTGAAGATGATTGCATGGATACAGGGCACTTAATTATTATTATATAGTGAAAAAAAAATGGATGATTCTAAAATATTATTGTAAATGGATGCGTTGAAATGGAATTTGAGGTATGGAATATTGTTTTTGAGTGCTGAATGAAATAAATATATATAAAGGTAATTGTCACTTTATATCAAAGTCACAAAAGGAGTTTTTCTTGTAATTGGGGGTTACAAACATGTATTT
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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