ZMP
hey2
Ensembl ID:
ZFIN ID:
Description:
Hairy/enhancer-of-split related with YRPW motif protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q9I9L0]
Human Orthologue:
HEY2
Human Description:
hairy/enhancer-of-split related with YRPW motif 2 [Source:HGNC Symbol;Acc:4881]
Mouse Orthologue:
Hey2
Mouse Description:
hairy/enhancer-of-split related with YRPW motif 2 Gene [Source:MGI Symbol;Acc:MGI:1341884]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10785 | Essential Splice Site | Available for shipment | Available now |
sa16273 | Nonsense | Available for shipment | Available now |
sa29430 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23783 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10785
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 |
---|---|---|---|---|---|
ENSDART00000023531 | Essential Splice Site | 110 | 324 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 39618881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 39690537 |
GRCz11 | 20 | 39593172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATGACAGTGGATCATCTGAAGATGCTTCAGGCCACAGGAGGAAAAGG[T/C]AGRCCGCATGTTATTGGCTCACCACCTAAWGCTGTAGTGAAATCTGAGCA
Long Flanking Sequence:
AGATATCCCAAGATGCCATTTTAAATTAAAAAGATGTCCATTTTTGAAACTAATGAAGACAGCAGAAGTCAAGGATACATTTGATTTATTTGCCTGACATGTTTACTGCTCCAAAATATTGTAAATGTTTCTCAAAATAAAATATATTGTGTTAGGAGGGGAAACAAGTTTTAGTTTTTTCACTCAGACATTAAAACAGAATATATTTTAGAGCAATAATTACAATACCGTAAAAGTGTGATAAAGTTATCATACCATCAGAATCTTATACCGGAGCATGCCTACTTGCAATATGAAAAGTATTAGTTCTAGTAATTATAATAAATCAAAAGTAAGTGGAAGAGTGTGTTGTCACGTTATTTCATCAAAGCAGTCATATTAAAAACTCCTCGCATGTATCCTGTTTCTTCTCCCAAGGGATCTGCCAAGTTGGAGAAAGCGGAAATATTGCAGATGACAGTGGATCATCTGAAGATGCTTCAGGCCACAGGAGGAAAAGG[T/C]AGACCGCATGTTATTGGCTCACCACCTAATGCTGTAGTGAAATCTGAGCACGGAGTTCCCTTTTGACCAGATTAAAGTGGAAATCAATGTTAATGGTAGGATTGAACTCGTGGGAAAGTGCCGGCAGGACAAAAGAAGCACTTGACCCTGGGATTGTGTTTGCTTTCATAAATCCATGGGAGGGGAGTGGAGCCACATTCACAGGCTGCACTGTTGGGGGTTTGTTAGGGCTTTCAGATGAGTGTTAAAACCGGTGCACAGAGGAGAGAAAACAAACATACAAACAGGTCAGGTCACAATCCCAGTCTGTGTAGCTTTAGCTTCTCCAGCGCGGTGGGGCTGCGTTTCATTCATTCTGACCAGTGGTAACTTTTGGCCTTGTGAAACAGAAGTTGCAAGTACCTTTGCTATTCTGAATAGTCATGTACAGTATGTGTAATAATGTGAAAAGATAAGTTGGGTGGGGCCTGATTGGATTGTTGTTGTTGGCTATTAGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16273
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 |
---|---|---|---|---|---|
ENSDART00000023531 | Nonsense | 136 | 324 | 5 | 5 |
ENSDART00000023531 | Nonsense | 136 | 324 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 39615842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 39687498 |
GRCz11 | 20 | 39590133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTTCTTGAGCATCGGCTTCCGGGAGTGTCTGACTGAAGTGGCCAGGTA[T/G]TTGAGCTCTGTGGAAGGCCTGGACTCCAGCGACCCTCTCCGTGTCCGTCT
Long Flanking Sequence:
CTAGAACCATCACTGCTTCAGATGGCGTCTTTAATAGTTCACATTGTATGATTGTTACACAAGTGAAAGAGCATCGATTTGCCTTTGATTTCTGGCATTTGTCGGGAATTTCTCAAAACCTGTTGTCGAGTCAAAATCTTGACAAAAATCATGCAGTCTGAACTCGGCTTTAGGGGTTAATAATATTGACCTTAAAATGGTTTTCAAAGAATTAAAAACTGCTTTTATTCTAGCTGACATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTTTAGGAATTACAGTAAAAAATGTCTTGCTCTGTTAAACATCATTTGGGAAATATTTGAACAAAGGTATCAAAATTCACAGGCGGTGTGTGTATTTAAAGATTCACTAGTATGCTCATTTGAATAATTCTCAATATTTTTTGTCAGGATATTTCGACGCTCATTCTCTGGCCATGGACTTCTTGAGCATCGGCTTCCGGGAGTGTCTGACTGAAGTGGCCAGGTA[T/G]TTGAGCTCTGTGGAAGGCCTGGACTCCAGCGACCCTCTCCGTGTCCGTCTGGTTTCTCACCTCAGCAGCTGTGCCTCGCAGAGGGAAGCAGCCGCCATGACCACATCCATAGCCCATCACCAGCAGGCCCTTCACCCGCACCACTGGGCTGCCGCTTTGCATCCCATTCCTGCTGCGTTCCTGCAGCAGAGCGGACTTCCCTCCTCAGAGAGCTCCTCCGGCAGGCTGTCTGAGGCTCCTCAAAGAGGTGCAGCCCTTTTCTCCCATAGTGACTCGGCACTCAGAGCGCCCTCTACTGGAAGTGTGGCTCCTTGCGTGCCACCGCTGTCCACTTCTCTGCTTTCGTTATCAGCGACCGTTCACGCAGCAGCTGCTGCAGCTGCAGCTCAAACCTTCCCTCTATCATTTCCCGCTGGATTCCCACTCTTCAGCCCCAGCGTTACAGCATCTTCAGTGGCTTCTTCCACCGTGAGCTCTTCCGTTTCCACATCCACCACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29430
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 |
---|---|---|---|---|---|
ENSDART00000023531 | Nonsense | 136 | 324 | 5 | 5 |
ENSDART00000023531 | Nonsense | 136 | 324 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 39615842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 39687498 |
GRCz11 | 20 | 39590133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCTTGAGCATCGGCTTCCGGGAGTGTCTGACTGAAGTGGCCAGGTA[T/A]TTGAGCTCTGTGGAAGGCCTGGACTCCAGCGACCCTCTCCGTGTCCGTCT
Long Flanking Sequence:
CTAGAACCATCACTGCTTCAGATGGCGTCTTTAATAGTTCACATTGTATGATTGTTACACAAGTGAAAGAGCATCGATTTGCCTTTGATTTCTGGCATTTGTCGGGAATTTCTCAAAACCTGTTGTCGAGTCAAAATCTTGACAAAAATCATGCAGTCTGAACTCGGCTTTAGGGGTTAATAATATTGACCTTAAAATGGTTTTCAAAGAATTAAAAACTGCTTTTATTCTAGCTGACATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTTTAGGAATTACAGTAAAAAATGTCTTGCTCTGTTAAACATCATTTGGGAAATATTTGAACAAAGGTATCAAAATTCACAGGCGGTGTGTGTATTTAAAGATTCACTAGTATGCTCATTTGAATAATTCTCAATATTTTTTGTCAGGATATTTCGACGCTCATTCTCTGGCCATGGACTTCTTGAGCATCGGCTTCCGGGAGTGTCTGACTGAAGTGGCCAGGTA[T/A]TTGAGCTCTGTGGAAGGCCTGGACTCCAGCGACCCTCTCCGTGTCCGTCTGGTTTCTCACCTCAGCAGCTGTGCCTCGCAGAGGGAAGCAGCCGCCATGACCACATCCATAGCCCATCACCAGCAGGCCCTTCACCCGCACCACTGGGCTGCCGCTTTGCATCCCATTCCTGCTGCGTTCCTGCAGCAGAGCGGACTTCCCTCCTCAGAGAGCTCCTCCGGCAGGCTGTCTGAGGCTCCTCAAAGAGGTGCAGCCCTTTTCTCCCATAGTGACTCGGCACTCAGAGCGCCCTCTACTGGAAGTGTGGCTCCTTGCGTGCCACCGCTGTCCACTTCTCTGCTTTCGTTATCAGCGACCGTTCACGCAGCAGCTGCTGCAGCTGCAGCTCAAACCTTCCCTCTATCATTTCCCGCTGGATTCCCACTCTTCAGCCCCAGCGTTACAGCATCTTCAGTGGCTTCTTCCACCGTGAGCTCTTCCGTTTCCACATCCACCACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23783
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023531 | Nonsense | 201 | 324 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 39615649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 39687305 |
GRCz11 | 20 | 39589940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGGCTGCCGCTTTGCATCCCATTCCTGCTGCGTTCCTGCAGCAGAGC[G/T]GACTTCCCTCCTCAGAGAGCTCCTCCGGCAGGCTGTCTGAGGCTCCTCAA
Long Flanking Sequence:
AAAATGGTTTTCAAAGAATTAAAAACTGCTTTTATTCTAGCTGACATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTTTAGGAATTACAGTAAAAAATGTCTTGCTCTGTTAAACATCATTTGGGAAATATTTGAACAAAGGTATCAAAATTCACAGGCGGTGTGTGTATTTAAAGATTCACTAGTATGCTCATTTGAATAATTCTCAATATTTTTTGTCAGGATATTTCGACGCTCATTCTCTGGCCATGGACTTCTTGAGCATCGGCTTCCGGGAGTGTCTGACTGAAGTGGCCAGGTATTTGAGCTCTGTGGAAGGCCTGGACTCCAGCGACCCTCTCCGTGTCCGTCTGGTTTCTCACCTCAGCAGCTGTGCCTCGCAGAGGGAAGCAGCCGCCATGACCACATCCATAGCCCATCACCAGCAGGCCCTTCACCCGCACCACTGGGCTGCCGCTTTGCATCCCATTCCTGCTGCGTTCCTGCAGCAGAGC[G/T]GACTTCCCTCCTCAGAGAGCTCCTCCGGCAGGCTGTCTGAGGCTCCTCAAAGAGGTGCAGCCCTTTTCTCCCATAGTGACTCGGCACTCAGAGCGCCCTCTACTGGAAGTGTGGCTCCTTGCGTGCCACCGCTGTCCACTTCTCTGCTTTCGTTATCAGCGACCGTTCACGCAGCAGCTGCTGCAGCTGCAGCTCAAACCTTCCCTCTATCATTTCCCGCTGGATTCCCACTCTTCAGCCCCAGCGTTACAGCATCTTCAGTGGCTTCTTCCACCGTGAGCTCTTCCGTTTCCACATCCACCACATCCCAACAGAGCAGCGGGAGCAGCAGTAAACCATACCGACCGTGGGGAACTGAAGTGGGAGCGTTTTAAATGTTGGATTTAAATGTTGGACGTCTTCCATGCTTTGTACATAAAGGAAAGCAGCGGCTATTGTGCCTGCTTCGGTCAGCAGCATGGGCTTTTGTCTTCCTCTACACTTGTGCACATATGCAGCGT
Associated Phenotype:
Not determined