ZMP
prdm2b
Ensembl ID:
ZFIN ID:
Description:
PR domain containing 2 [Source:UniProtKB/TrEMBL;Acc:A5XCD8]
Human Orthologue:
PRDM2
Human Description:
PR domain containing 2, with ZNF domain [Source:HGNC Symbol;Acc:9347]
Mouse Orthologue:
Prdm2
Mouse Description:
PR domain containing 2, with ZNF domain Gene [Source:MGI Symbol;Acc:MGI:107628]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31835 | Nonsense | Available for shipment | Available now |
sa15771 | Nonsense | Available for shipment | Available now |
sa41846 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9522 | Nonsense | Available for shipment | Available now |
sa21919 | Nonsense | Available for shipment | Available now |
sa8982 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31835
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111907 | None | None | 227 | None | 4 |
ENSDART00000125431 | Nonsense | 33 | 1582 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 27140093)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25968918 |
GRCz11 | 11 | 26206534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTGTTTGCTCCAATAGAATTTTTCTGCATGTGTCTCTACAGGTGTCT[G/A]GGCATCTAGATTAATACCAAAAGGCAAACGATTTGGACCATTTGTAGGAG
Long Flanking Sequence:
CAGTCGCATTGGTGAGGAACGGCAGGCTTGAGAACTGCTAAATGATTTCGTTAATGAGAAAACATGTTTATTATTGCAGCATTTCTTTTACTCTGCTGCTGTCCTACATATTTGGCTTTAAACACAAATGGCCATTTCAAGTATTTACAAAGTTAGCATTAGACTTTTTGACAGTTGACTGGTTTGCCTGGTCAACATTGAGAAGCAGAGAATGCTAAACAAGGAGCTGCAAACAACATAACTGCAGTCTTATTTTGTTTGCTGTTTGAAATAGAGAATGTGCGTTACGCTGTGGCGGTGCCCTAGAAATATTCAGATAAATGTTTAATATCCAATGCTCTAAAAAATGGCTCTGCGAGAGAGTCTCTGGAGATCTTAAAGTGGCTCGTTCTGATTCATGCTCAAAAATCTGATGTACTGAAATGACACGCACAAAAAAAAAGTTTGTTTCCAGTGTTTGCTCCAATAGAATTTTTCTGCATGTGTCTCTACAGGTGTCT[G/A]GGCATCTAGATTAATACCAAAAGGCAAACGATTTGGACCATTTGTAGGAGAGCGAAAGAAGAGGTCTCAAGTGACGAGCAATGTTTACATGTGGGAGGTGTGTATCAGATATTGTGTAGAGAAGGGTTTTAGTTCTGTCAGAGGTATTATAAACTGACGAAAATAAAGCTTAAAGGGATAGCGCCCTCAAAAATTAAAATTCATTAATCATTTTCACATCCTCCACTTCTTTCAAAACTGTTTTAACACAAAAGAAGAAATTTTGAAGAATGTTGTAAACCTGTACATTTTTATTTTTGGGTGAACTGTCCCTTTAACGAGCCCATATTTTGCATCATAAAAGGTCATATTTTGGTTTTGGGGGTTTCCAACAAAAGGTGATGTGCATGCAAGGTCAAAAAACACTTTCATTATTTTATAATATGCATTTATTTTTACCCAATTATCCCACTGACTCCCATATGATTCGTTCAGCGATTGATTTGTTCCCAAACCCCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15771
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 |
---|---|---|---|---|---|
ENSDART00000111907 | None | None | 227 | None | 4 |
ENSDART00000125431 | Nonsense | 828 | 1582 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 27127714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25956539 |
GRCz11 | 11 | 26194155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCACATGTAAAAAGAAAGAAACCCAATACTAGCATTTTAGAGAAAGTGK[T/A]AATGAATGAGTATGCWGGGCTAAACTCACCTGGAGAAGAAGAATCCAACA
Long Flanking Sequence:
TCAGAAACCAGCCATTGGTCTAATTACAGACAGTAGATTGACCACCCCACTTTCAGTAACTTCACTGCCTGCTGTCCAGGGTAAGTTTAAAAGAAGAACTGCCTCCCCTCCCACAACTTCACAGAATAGCCCACCACAAAGAAATGACAACACAAACTCCGCAACTGGGGTTACGTGTTCTCTGAAGGTGCCAAAGATGGAAAGCGTGACAGATTCTTGGACTTCGCCCAGCAAAGATCATGGGGACACAGAGAGTTTGACAGGAAAAGACTGGTCTCCCTCAAGAAGTGGTGGGAATTCTTGCAATCAGCAGCCGCTTGACCTTTCAAATTCCTTTAGTAAACGAGACGATAGCATAAGCAGAGGGTCTGGAGAGGCTGTGCTTGACTTAAGTATGAGCCGTAAAAGTCCTGTTGACCATGAAGTAAAGACAGGCTCAGCAACACTACCGCCACATGTAAAAAGAAAGAAACCCAATACTAGCATTTTAGAGAAAGTGT[T/A]AATGAATGAGTATGCTGGGCTAAACTCACCTGGAGAAGAAGAATCCAACACTGTTGGAAGCCCTGATGCTTTTTCATCATCCGAGAGTGCCACATGTGTTGCCCCTTCTAGTCCTGGGTCAGGATCAGAACGCCTTCCTTGTGAATCAACCTCTCCCCCCTCCCTGACCCTTATGACTATCAATCCGTCCTCGCCCTCTTCATCAAGTATAGCATCATCTACCCCACCTCCTCCAGTCTTACCCACTATCCCATCTCCGCCACCTTTATCATCAAAGCATTTTCCGTTGTCTGACGCCTTAACACCTTCCCCTTTTCCAGTGTTGTCCCCTAAAATGTCCCCTAAAGCTGTTGATAGTTTAGAAGATGTTTCAGATTCATCTGCTTTAACAGAACCATGCCATGATGCATTAAATTCCATTGTTAGTGAATCAAACCAAACTGCTGAGCAGTTAGACTCTGTAAATTCTCCTCTGCCTCAGGATGCAAAAAGACATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41846
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 |
---|---|---|---|---|---|
ENSDART00000111907 | None | None | 227 | None | 4 |
ENSDART00000125431 | Nonsense | 1006 | 1582 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 27126904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25955729 |
GRCz11 | 11 | 26193345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCAGCAAATTGCATTCGCCACAGAGGAGCTCAGAGGCTGATGACAACT[T/G]AATTATAGAGGATGTAAGAAAAAAAGAGGAGATGGTAGACATAACTGCAA
Long Flanking Sequence:
CCCTTTTCCAGTGTTGTCCCCTAAAATGTCCCCTAAAGCTGTTGATAGTTTAGAAGATGTTTCAGATTCATCTGCTTTAACAGAACCATGCCATGATGCATTAAATTCCATTGTTAGTGAATCAAACCAAACTGCTGAGCAGTTAGACTCTGTAAATTCTCCTCTGCCTCAGGATGCAAAAAGACATTGTACAGCAGATTCATCTTCAAAGTCGGAAACACTACTTGAGGGCTCAACCCATGATTCTAAGCCTCAGTTTTTAAAAACTGCAGACCAAGCAGGTTCTTCTCACCTGGAGTGGGATACTTCCTCTGAAAGCAACCAAAGCCATTCCTGTGAAGGAACTCTCCCCCAAGACCTTAATAATAAAACAGAAGTCAGACAAAAATCAAAGTCTCCCCTTTCTACAGTACAATCAACTCCTAAAAAGGAATCCTCATCCCCAAACTTTCTCAGCAAATTGCATTCGCCACAGAGGAGCTCAGAGGCTGATGACAACT[T/G]AATTATAGAGGATGTAAGAAAAAAAGAGGAGATGGTAGACATAACTGCAAATGGGGCTGACGTTTCACCTGGAACTTCAGTTAGAAGTTCTGATGAGGTTGACTCTGCAGAGCGGGAGACTTTTGTCAAAAGTTTTGTGTGCAACGTCTGTAAAGAGCCATTCCGCTCCATCAAAGACCTTAGTGGTCATATAATAGAGCATGCATCAGAGTGGCCTTTTAAGTGTGAGTTTTGCGTGCAGTTATTTGGTAACGCCACTGCTCTTCTCGAACACCGCTCGTCTCTCCACGGGGTGGGAAGAATTTATGTTTGCTCTATTTGCTCAAAGGAGTTTGCCTTCCTCTGCAATCTTCAGCAACATCAAAGTGACCTACATCCAAGTCAGAGTTGCACTCACACTGCCGTTGAAAATGGAAAGCTCAGACCTCAGAACTACACAAATCCAGCTTGTGCAAATATAGAGAAAGATGCTGTTCTTGACTCAACTGCTGGGGCTCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9522
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 |
---|---|---|---|---|---|
ENSDART00000111907 | None | None | 227 | None | 4 |
ENSDART00000125431 | Nonsense | 1262 | 1582 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 27126117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25954942 |
GRCz11 | 11 | 26192558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTTTACCACACACAATATCCCCCAAACATTTAGCACTGCAATCCGCTG[T/A]ACCAAATGTGGAAACAGCTTTGACAACATGCCTGAGCTACACAAACACAT
Long Flanking Sequence:
CACGGGGTGGGAAGAATTTATGTTTGCTCTATTTGCTCAAAGGAGTTTGCCTTCCTCTGCAATCTTCAGCAACATCAAAGTGACCTACATCCAAGTCAGAGTTGCACTCACACTGCCGTTGAAAATGGAAAGCTCAGACCTCAGAACTACACAAATCCAGCTTGTGCAAATATAGAGAAAGATGCTGTTCTTGACTCAACTGCTGGGGCTCCCTCTGAGAATTCTTCTGAGGAGCATAACAATGACACTAACAAGGTGGAAGAAGAGGAAGGTGGACATGAAGACCCTACAGAAGAGCTATACACTACAATAAAGATTATGGCATCTGAGGCTGGCAAGCCAAAAGGTCCAGATGTCCGGCTTGGCATTAATCAGCACTACCCAAGTTTCAAGCCTCCACCTTTTCCTTACCACAACCGATCCCCGGATGGCTCAGTTGCCTCTGCCACTAATTTTACCACACACAATATCCCCCAAACATTTAGCACTGCAATCCGCTG[T/A]ACCAAATGTGGAAACAGCTTTGACAACATGCCTGAGCTACACAAACACATATTAGTTTGTGCTAATGCTAGTGATAAGAGACGTTATACCCCTAAGAAGAATCCCATTCCTCTCAAGCAGGTTGTGAAACAATCTCCTAATGGTATTTCTCCAACAGGACCTTCAACTGGGCAGAATGCCTTCCGCAGAATGGGTCAACCAAAAAGGCTTAACTTTAACCAAGATTTAACATCCAAAGTCAAGTTATCAGCCCTAAATAAGAAGAAAAACCAGCTTGTCCAGAAAGCTATATCACAGAAGAACAAATTTGCAGCTTCTGCAAAGAAACCGACAGCCCGGGTAAAGGAAGAGGAGACTCGTGAGGTCCATGCATGTCCATACTGTAGTCGAGAGTTCACATACCCAGCCAGTCTTACGAAACATATTGCTTGCAGCTGCCCGCAAAGACCTGTTGCCAAGAAGTTGAAAAAAGGTGCTCTGACACCTCAAGACAAAAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21919
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 |
---|---|---|---|---|---|
ENSDART00000111907 | None | None | 227 | None | 4 |
ENSDART00000125431 | Nonsense | 1361 | 1582 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 27125822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25954647 |
GRCz11 | 11 | 26192263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCAGCCCTAAATAAGAAGAAAAACCAGCTTGTCCAGAAAGCTATATCA[C/T]AGAAGAACAAATTTGCAGCTTCTGCAAAGAAACCGACAGCCCGGGTAAAG
Long Flanking Sequence:
AGCTATACACTACAATAAAGATTATGGCATCTGAGGCTGGCAAGCCAAAAGGTCCAGATGTCCGGCTTGGCATTAATCAGCACTACCCAAGTTTCAAGCCTCCACCTTTTCCTTACCACAACCGATCCCCGGATGGCTCAGTTGCCTCTGCCACTAATTTTACCACACACAATATCCCCCAAACATTTAGCACTGCAATCCGCTGTACCAAATGTGGAAACAGCTTTGACAACATGCCTGAGCTACACAAACACATATTAGTTTGTGCTAATGCTAGTGATAAGAGACGTTATACCCCTAAGAAGAATCCCATTCCTCTCAAGCAGGTTGTGAAACAATCTCCTAATGGTATTTCTCCAACAGGACCTTCAACTGGGCAGAATGCCTTCCGCAGAATGGGTCAACCAAAAAGGCTTAACTTTAACCAAGATTTAACATCCAAAGTCAAGTTATCAGCCCTAAATAAGAAGAAAAACCAGCTTGTCCAGAAAGCTATATCA[C/T]AGAAGAACAAATTTGCAGCTTCTGCAAAGAAACCGACAGCCCGGGTAAAGGAAGAGGAGACTCGTGAGGTCCATGCATGTCCATACTGTAGTCGAGAGTTCACATACCCAGCCAGTCTTACGAAACATATTGCTTGCAGCTGCCCGCAAAGACCTGTTGCCAAGAAGTTGAAAAAAGGTGCTCTGACACCTCAAGACAAAAACAGGAGTCTCAGAAGTCGAGCTACTGACTCTGAAGTCAAACAAGAAGCAGTTTCTGGATCAAGCACACCGTCCTTGGGAAAAACCAGAGCTCGAACCTCTGAACCAGTTGAGAATGAAGCTCCAGCAGCAAATAAAGGCAAAGAACCTCAGGTACGTACTAAGAGGCCATCCTCAAATGTAGTCAACGCTGCCCCACAAATTAAGAAAGGCAAAAAAAGCAATGAGCCATTGACTTTTATAACTCCTGCTGTTACTGATGACTCTTCAACACGACCACCATCTAAAATGCAACGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8982
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111907 | None | None | 227 | None | 4 |
ENSDART00000125431 | Essential Splice Site | 1496 | 1582 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 11 (position 27125415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 25954240 |
GRCz11 | 11 | 26191856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTACWAAGAGGCCATCCTCAAATGTAGTCAACGCTGCCCCACAAATTAA[G/A]AAAGGCAAAAAAAGCAATGAGMCATTGACTTTTATAACTCCTGCTGTTAC
Long Flanking Sequence:
AAAAGGCTTAACTTTAACCAAGATTTAACATCCAAAGTCAAGTTATCAGCCCTAAATAAGAAGAAAAACCAGCTTGTCCAGAAAGCTATATCACAGAAGAACAAATTTGCAGCTTCTGCAAAGAAACCGACAGCCCGGGTAAAGGAAGAGGAGACTCGTGAGGTCCATGCATGTCCATACTGTAGTCGAGAGTTCACATACCCAGCCAGTCTTACGAAACATATTGCTTGCAGCTGCCCGCAAAGACCTGTTGCCAAGAAGTTGAAAAAAGGTGCTCTGACACCTCAAGACAAAAACAGGAGTCTCAGAAGTCGAGCTACTGACTCTGAAGTCAAACAAGAAGCAGTTTCTGGATCAAGCACACCGTCCTTGGGAAAAACCAGAGCTCGAACCTCTGAACCAGTTGAGAATGAAGCTCCAGCAGCAAATAAAGGCAAAGAACCTCAGGTACGTACTAAGAGGCCATCCTCAAATGTAGTCAACGCTGCCCCACAAATTAA[G/A]AAAGGCAAAAAAAGCAATGAGCCATTGACTTTTATAACTCCTGCTGTTACTGATGACTCTTCAACACGACCACCATCTAAAATGCAACGTGGATTTAAAGAGGTGGTGGTCAAGAAGGAGGTTGTTGACAAGAAAGAGGTAGTTGTTAAAAAGGAAGTTGTCAACAAGGAGGTTGGTGATAAAAAAGAGGCAGCAGTCAAGAAGGAGGTTGTTGATAAAAAAGAGGCAGCAGTCAAGAAGGAGGTTGTTGACAAAAAAGAGGCAGCTGTCAAGAAGGAGGTTGTTGTGAAAACGGCACAATCTAAGAAGGAGGAACGTTTTTCAGCTAGGATGCGGGAGAGGAAAGGTGGGCCGGTGACACGAAGTGTACAGATGACAAGTGCTCCTTCAGAAGTAAAGAACGAAGACCTCTTAATCAATGAACCAGGGCAGTCTGAGGTATTTCATATTTAGCATTGATATATATATTATGTTTTCAGTTACATTTTTATAGTTTGAGT
Associated Phenotype:
Not determined