ZMP
zfand2a
Ensembl ID:
ZFIN IDs:
Description:
AN1-type zinc finger protein 2B [Source:RefSeq peptide;Acc:NP_956811]
Human Orthologue:
ZFAND2B
Human Description:
zinc finger, AN1-type domain 2B [Source:HGNC Symbol;Acc:25206]
Mouse Orthologue:
Zfand2b
Mouse Description:
zinc finger, AN1 type domain 2B Gene [Source:MGI Symbol;Acc:MGI:1916068]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa683 | Nonsense | Available for shipment | Available now |
sa2100 | Essential Splice Site | Available for shipment | Available now |
sa30840 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40144 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa683
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 |
---|---|---|---|---|---|
ENSDART00000055155 | Nonsense | 123 | 282 | 4 | 9 |
ENSDART00000127680 | Nonsense | 123 | 282 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 43234957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42674523 |
GRCz11 | 3 | 43380538 |
KASP Assay ID:
554-0591.1 (used for ordering genotyping assays)
KASP Sequence:
CAGAAGGAAATGATCCGGGTGACGTGTGACCAGTGCCACYTAAACTACTG[T/A]CTCAAACACAGGCATCCACTCGACCATGACTGTAAGACTGACAACAAGCC
Long Flanking Sequence:
TTTTAAATTTCACTATTTATGATTGAATGTAAATTCCAGAAGTGAAAACAAGGACCCAGAAGGCTTAAAAACATTTATTGAATTAATGTTATCCGCTTTAAATTAAAATTTATATTTATTTTTAAATGAAAATTTTATTTTATCTCTTTCAAGATTGTATGTATCTGGTACAAGTTATTATTGTTTTTTTTTTTTGTTCAGGACGTCCAGGTTCCTGTATGTCCATTGTGCAACATCCCCATTCCCATCCGAAGAGGAGAAATGCCAGATATCAAAGTCGGCGAGCACATAGACAGAGACTGCAAATCTGACCCTGCCCAGAGGAAACGAAAGGTACCAAACGCATAGGATGAGGAGAAAGATAATGACATCACTCCAAAATGAACACCCACATGATTGTTTATCTCCCTGCAGATCTTTACTAATAAATGCTCGAAGGGCGGCTGTAAGCAGAAGGAAATGATCCGGGTGACGTGTGACCAGTGCCACCTAAACTACTG[T/A]CTCAAACACAGGCATCCACTCGACCATGACTGTAAGACTGACAACAAGCCGGTCTCCAAATCAGGGTAAGCCTGGTTTTCATGCGGATCAGTGATGCTCTCAGGAGGAATAGGGATCTACTAATGGTGGGGTTTGTTTTGTTTTGTAGGCATGCAGCTTTAATGAGGGCTCAGGGCTCTTCTTCCAGTAACACAGCAGCTTCATCCACTAGAGGGAGCTCTAGGAACATGTCTAATGGAGTCACTGGAAACGCCAGACCTCAGAGCAGTAGGTAAGTACATTTTGGAAAACACAGTGTCCTCAGAAGTGTCAGTTCAATATACGCCAACCACTTAGAAGCTTGAGGTTGTTGAAATGCTTTTAAAAGGGGTTTCTGGCAAATAAAACACTTTCACCAATTCACTTTTTAGTACTTTGATAGGTAGTTCAGCAAAATATGAAATTCTCATTTATTCACCCTCAAGTGGTTTCAAAACTTATGTAAAAATCCTCTGTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2100
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055155 | Essential Splice Site | 145 | 282 | 4 | 9 |
ENSDART00000127680 | Essential Splice Site | 145 | 282 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 43234890)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42674590 |
GRCz11 | 3 | 43380605 |
KASP Assay ID:
554-2804.1 (used for ordering genotyping assays)
KASP Sequence:
CACTCGACCATGACTGTAAGACTGACAACAAGCCGGTCTCCAAATCAGGG[T/C]AAGCCTGGTTTTCATGCGGAYCAGTGATGCTCTCWGGAGGAMTAGGGRTC
Long Flanking Sequence:
AAAACATTTATTGAATTAATGTTATCCGCTTTAAATTAAAATTTATATTTATTTTTAAATGAAAATTTTATTTTATCTCTTTCAAGATTGTATGTATCTGGTACAAGTTATTATTGTTTTTTTTTTTTGTTCAGGACGTCCAGGTTCCTGTATGTCCATTGTGCAACATCCCCATTCCCATCCGAAGAGGAGAAATGCCAGATATCAAAGTCGGCGAGCACATAGACAGAGACTGCAAATCTGACCCTGCCCAGAGGAAACGAAAGGTACCAAACGCATAGGATGAGGAGAAAGATAATGACATCACTCCAAAATGAACACCCACATGATTGTTTATCTCCCTGCAGATCTTTACTAATAAATGCTCGAAGGGCGGCTGTAAGCAGAAGGAAATGATCCGGGTGACGTGTGACCAGTGCCACCTAAACTACTGTCTCAAACACAGGCATCCACTCGACCATGACTGTAAGACTGACAACAAGCCGGTCTCCAAATCAGGG[T/C]AAGCCTGGTTTTCATGCGGATCAGTGATGCTCTCAGGAGGAATAGGGATCTACTAATGGTGGGGTTTGTTTTGTTTTGTAGGCATGCAGCTTTAATGAGGGCTCAGGGCTCTTCTTCCAGTAACACAGCAGCTTCATCCACTAGAGGGAGCTCTAGGAACATGTCTAATGGAGTCACTGGAAACGCCAGACCTCAGAGCAGTAGGTAAGTACATTTTGGAAAACACAGTGTCCTCAGAAGTGTCAGTTCAATATACGCCAACCACTTAGAAGCTTGAGGTTGTTGAAATGCTTTTAAAAGGGGTTTCTGGCAAATAAAACACTTTCACCAATTCACTTTTTAGTACTTTGATAGGTAGTTCAGCAAAATATGAAATTCTCATTTATTCACCCTCAAGTGGTTTCAAAACTTATGTAAAAATCCTCTGTTGTGTTCAACAGAAAAAAGCAAAGAAAGGTTTGAAAAGGTTTGAGGGTGAGTATATGATGACAGACATCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30840
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055155 | Essential Splice Site | 186 | 282 | 5 | 9 |
ENSDART00000127680 | Essential Splice Site | 186 | 282 | 6 | 10 |
ENSDART00000055155 | Essential Splice Site | 186 | 282 | 5 | 9 |
ENSDART00000127680 | Essential Splice Site | 186 | 282 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 43234684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42674796 |
GRCz11 | 3 | 43380811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAACATGTCTAATGGAGTCACTGGAAACGCCAGACCTCAGAGCAGTAGG[T/G]AAGTACATTTTGGAAAACACAGTGTCCTCAGAAGTGTCAGTTCAATATAC
Long Flanking Sequence:
AAAGTCGGCGAGCACATAGACAGAGACTGCAAATCTGACCCTGCCCAGAGGAAACGAAAGGTACCAAACGCATAGGATGAGGAGAAAGATAATGACATCACTCCAAAATGAACACCCACATGATTGTTTATCTCCCTGCAGATCTTTACTAATAAATGCTCGAAGGGCGGCTGTAAGCAGAAGGAAATGATCCGGGTGACGTGTGACCAGTGCCACCTAAACTACTGTCTCAAACACAGGCATCCACTCGACCATGACTGTAAGACTGACAACAAGCCGGTCTCCAAATCAGGGTAAGCCTGGTTTTCATGCGGATCAGTGATGCTCTCAGGAGGAATAGGGATCTACTAATGGTGGGGTTTGTTTTGTTTTGTAGGCATGCAGCTTTAATGAGGGCTCAGGGCTCTTCTTCCAGTAACACAGCAGCTTCATCCACTAGAGGGAGCTCTAGGAACATGTCTAATGGAGTCACTGGAAACGCCAGACCTCAGAGCAGTAGG[T/G]AAGTACATTTTGGAAAACACAGTGTCCTCAGAAGTGTCAGTTCAATATACGCCAACCACTTAGAAGCTTGAGGTTGTTGAAATGCTTTTAAAAGGGGTTTCTGGCAAATAAAACACTTTCACCAATTCACTTTTTAGTACTTTGATAGGTAGTTCAGCAAAATATGAAATTCTCATTTATTCACCCTCAAGTGGTTTCAAAACTTATGTAAAAATCCTCTGTTGTGTTCAACAGAAAAAAGCAAAGAAAGGTTTGAAAAGGTTTGAGGGTGAGTATATGATGACAGACATCTAATTTTTAGATTAACATTAATTTTTAAATTCACTTCAAATTAATTTATCTAGCTTTTTTTTTACTATAGTTATTCTTTCAAAGTAGATTTACCAAAAGTGTGTGTAGGTGTGTTATTATATTACAATCAAAATTAGAAAGAGTTAAGGCGTGAGTGGGGTGGAAGGTCACGTGTGTGTATATATATATATATTGTTGTTCTGCACGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40144
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055155 | Essential Splice Site | 186 | 282 | 5 | 9 |
ENSDART00000127680 | Essential Splice Site | 186 | 282 | 6 | 10 |
ENSDART00000055155 | Essential Splice Site | 186 | 282 | 5 | 9 |
ENSDART00000127680 | Essential Splice Site | 186 | 282 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 43234684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42674796 |
GRCz11 | 3 | 43380811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAACATGTCTAATGGAGTCACTGGAAACGCCAGACCTCAGAGCAGTAGG[T/G]AAGTACATTTTGGAAAACACAGTGTCCTCAGAAGTGTCAGTTCAATATAC
Long Flanking Sequence:
AAAGTCGGCGAGCACATAGACAGAGACTGCAAATCTGACCCTGCCCAGAGGAAACGAAAGGTACCAAACGCATAGGATGAGGAGAAAGATAATGACATCACTCCAAAATGAACACCCACATGATTGTTTATCTCCCTGCAGATCTTTACTAATAAATGCTCGAAGGGCGGCTGTAAGCAGAAGGAAATGATCCGGGTGACGTGTGACCAGTGCCACCTAAACTACTGTCTCAAACACAGGCATCCACTCGACCATGACTGTAAGACTGACAACAAGCCGGTCTCCAAATCAGGGTAAGCCTGGTTTTCATGCGGATCAGTGATGCTCTCAGGAGGAATAGGGATCTACTAATGGTGGGGTTTGTTTTGTTTTGTAGGCATGCAGCTTTAATGAGGGCTCAGGGCTCTTCTTCCAGTAACACAGCAGCTTCATCCACTAGAGGGAGCTCTAGGAACATGTCTAATGGAGTCACTGGAAACGCCAGACCTCAGAGCAGTAGG[T/G]AAGTACATTTTGGAAAACACAGTGTCCTCAGAAGTGTCAGTTCAATATACGCCAACCACTTAGAAGCTTGAGGTTGTTGAAATGCTTTTAAAAGGGGTTTCTGGCAAATAAAACACTTTCACCAATTCACTTTTTAGTACTTTGATAGGTAGTTCAGCAAAATATGAAATTCTCATTTATTCACCCTCAAGTGGTTTCAAAACTTATGTAAAAATCCTCTGTTGTGTTCAACAGAAAAAAGCAAAGAAAGGTTTGAAAAGGTTTGAGGGTGAGTATATGATGACAGACATCTAATTTTTAGATTAACATTAATTTTTAAATTCACTTCAAATTAATTTATCTAGCTTTTTTTTTACTATAGTTATTCTTTCAAAGTAGATTTACCAAAAGTGTGTGTAGGTGTGTTATTATATTACAATCAAAATTAGAAAGAGTTAAGGCGTGAGTGGGGTGGAAGGTCACGTGTGTGTATATATATATATATTGTTGTTCTGCACGGT
Associated Phenotype:
Not determined