ZMP
ERBB4 (3 of 5)
Ensembl ID:
Description:
v-erb-a erythroblastic leukemia viral oncogene homolog 4 (avian) [Source:HGNC Symbol;Acc:3432]
Human Orthologue:
ERBB4
Human Description:
v-erb-a erythroblastic leukemia viral oncogene homolog 4 (avian) [Source:HGNC Symbol;Acc:3432]
Mouse Orthologue:
Erbb4
Mouse Description:
v-erb-a erythroblastic leukemia viral oncogene homolog 4 (avian) Gene [Source:MGI Symbol;Acc:MGI:104
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24834 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25517 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32585 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32584 | Essential Splice Site | Available for shipment | Available now |
| sa6573 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19414 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24834
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 |
|---|---|---|---|---|---|
| ENSDART00000092114 | Nonsense | 150 | 609 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 6247146)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6695735 |
| GRCz11 | 1 | 7379168 |
KASP Assay ID:
554-7622.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAAGACGGTGTGTGCGGAGCAGTGTGACGGTCGATGTTTTGGACCGTA[T/G]GTCAGTAACTGCTGTCACCGTGAATGTGCAGGGGGCTGTTTCGGACCCAA
Long Flanking Sequence:
AGAAAAACAAAATCATACTTAATACTTCTAGTTATACAGCCCTACTTATAGTTACTGAATAAAGAAATGCATATATTTCAGACTAAATGCATTCTGTATGTTATGTTAAAATTCTGTACGGCACCTTGAGTGAGAGCTCTTGTGAACTGGTTGATCTTCATGTGGCACAACCTGTGGTGATGTGCTCTGTGTGGGTGGCAAACACAAAAAAGAGGGACGGCAGGGATGGCAGGTTCAGTTTTCACCACATAATTAGCTATAATTAAAGAGGATCCAGAACCATAGAGTGTCACCACTGATCAGGGGTTGCACAGTTTCTCTGACAAATAATAGATTTAAGGTTTTTGCTCTGTCCTGCTGACTTTTGACATAGTTACAGAGAAGTAAAGTTATAAAGTGAGCGGATAAATATGAGCGGAGGGCTTCACTATTGTGTTTGTTATTACAGTGACGAAGACGGTGTGTGCGGAGCAGTGTGACGGTCGATGTTTTGGACCGTA[T/G]GTCAGTAACTGCTGTCACCGTGAATGTGCAGGGGGCTGTTTCGGACCCAAAGACACAGACTGCTTTGTACGTCATCTTTCTTTCATTTATGATTGTAAAATGTTGGGGTAATTATCTTCCTTTTTTTAACTTGTTCGAAATAAACTCACCGGCCACTTTATTAGGTACACCTGTCCAACTAATTGTTAACGCAAATTTCTACTCAGCCGATCACATGGCAGCAACGCAATGCATTTAGGCATGTAGACATGGTCAACACAATCTGCTGTAGTTCAAACTGAGCATCAGAATGGGAAAGAAAGATTATTTTAGTCACTTTGAACATGGCATGGTTGTTGGTGCCAGATGGGCTGGTCTGAGTATTTCAGAAACTGCTAATCTACTGGGATTTTCACGCACAACCATCTCTCAAAATATCCAGTGAGTGGAAGTTCTGTGGGCACAAATGCCTTGTTGATGCCAGGGGTCCAAGTAGAATTGTTCGAGCTGATAGAAACGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25517
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092114 | Essential Splice Site | 173 | 609 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 6246462)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6696419 |
| GRCz11 | 1 | 7379852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATGTTTTATCCGTCAAACCTGAGCTCATGTGACTGTTTTCTGTTTTC[A/T]GGCTTGCACCAACTTTAATGACAGTGGTGCCTGCGTGACTCAATGTCCTC
Long Flanking Sequence:
TGTTAACGCAAATTTCTACTCAGCCGATCACATGGCAGCAACGCAATGCATTTAGGCATGTAGACATGGTCAACACAATCTGCTGTAGTTCAAACTGAGCATCAGAATGGGAAAGAAAGATTATTTTAGTCACTTTGAACATGGCATGGTTGTTGGTGCCAGATGGGCTGGTCTGAGTATTTCAGAAACTGCTAATCTACTGGGATTTTCACGCACAACCATCTCTCAAAATATCCAGTGAGTGGAAGTTCTGTGGGCACAAATGCCTTGTTGATGCCAGGGGTCCAAGTAGAATTGTTCGAGCTGATAGAAACGCAACAGTAACTCTAATAACCACTCATTACAACTAAGGTATATAGAAGAGCATCTCTGAACGCACAACAAGTCCAACCTTGAGGGGGGTGGGCTACAGCAGCAGAAGACCGCACCGGGCTTATTATAGTGATTATAGTCATGTTTTATCCGTCAAACCTGAGCTCATGTGACTGTTTTCTGTTTTC[A/T]GGCTTGCACCAACTTTAATGACAGTGGTGCCTGCGTGACTCAATGTCCTCAACCATTCGTCTACAATCCAACGACCTTCCAGCTCGAGCACAATCCCAATGCCAAATACACCTATGGAGCTTTCTGTGTCAAGAAATGCCCACGTGAGTTGCACTAAATAAACAAATTAATAAATAACGTTGTAAAATATAGTGGAAGTTTTCTTATGTTGTTGTAATATTTCACAGTATTACTGTTTTGAATACGTAAATGCAGACTTGGTCAACATAAGAGAATTATACAAGAGCAATGGTAAGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGGAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGGAGACGGAAGGAAGGAAGGAAGGAAGGAAGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32585
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 |
|---|---|---|---|---|---|
| ENSDART00000092114 | Nonsense | 187 | 609 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 6246416)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6696465 |
| GRCz11 | 1 | 7379898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGGCTTGCACCAACTTTAATGACAGTGGTGCCTGCGTGACTCAATG[T/A]CCTCAACCATTCGTCTACAATCCAACGACCTTCCAGCTCGAGCACAATCC
Long Flanking Sequence:
TGCATTTAGGCATGTAGACATGGTCAACACAATCTGCTGTAGTTCAAACTGAGCATCAGAATGGGAAAGAAAGATTATTTTAGTCACTTTGAACATGGCATGGTTGTTGGTGCCAGATGGGCTGGTCTGAGTATTTCAGAAACTGCTAATCTACTGGGATTTTCACGCACAACCATCTCTCAAAATATCCAGTGAGTGGAAGTTCTGTGGGCACAAATGCCTTGTTGATGCCAGGGGTCCAAGTAGAATTGTTCGAGCTGATAGAAACGCAACAGTAACTCTAATAACCACTCATTACAACTAAGGTATATAGAAGAGCATCTCTGAACGCACAACAAGTCCAACCTTGAGGGGGGTGGGCTACAGCAGCAGAAGACCGCACCGGGCTTATTATAGTGATTATAGTCATGTTTTATCCGTCAAACCTGAGCTCATGTGACTGTTTTCTGTTTTCAGGCTTGCACCAACTTTAATGACAGTGGTGCCTGCGTGACTCAATG[T/A]CCTCAACCATTCGTCTACAATCCAACGACCTTCCAGCTCGAGCACAATCCCAATGCCAAATACACCTATGGAGCTTTCTGTGTCAAGAAATGCCCACGTGAGTTGCACTAAATAAACAAATTAATAAATAACGTTGTAAAATATAGTGGAAGTTTTCTTATGTTGTTGTAATATTTCACAGTATTACTGTTTTGAATACGTAAATGCAGACTTGGTCAACATAAGAGAATTATACAAGAGCAATGGTAAGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGGAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGGAGACGGAAGGAAGGAAGGAAGGAAGGAAGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGACGGATGGACATACGGACGGATGGATGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32584
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092114 | Essential Splice Site | 258 | 609 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 6242806)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6700459 |
| GRCz11 | 1 | 7383892 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTACAATACGGTATCTCATATGCCTGTGTATGTTTGTTTGTGGTGTTT[A/G]GTGTGTGATGGTATAGGAACCGGCAGCCTTCAATCAGCCCAAACTGTTGA
Long Flanking Sequence:
CCAATTTCAACATCAGTAATTAAAAAAAGAGACTTGTTGTGTTTCTATCACTCTAATCCAGTATGACTGTGGAAACACTACAACAACACACAGTTCTGCCTAAACAGCCTCCAAAAGTTAGATGCCTTTTAAATATGCAAAAAAAAAATAAATAAAATAGACAAAAGTCTCAGCTGTTACAAAAAAAAGGGAAAAAAAAAGATTCGTCAATAATCTGGAGAATTGCAGAGGTTATAGAGGTCAGAAAGTCACCTACAATGCTGTACATCTCCACGAACAGATTAATAGTGCTTTAATAATAAAAATAAAAACTCCCTCTCTCATTCAAAAGCAAACTCAAGCATCTTCAACTGTTGTTAATGTTCTGAGCAAAAGATCAGGAGGTTAAACAACTAAGTCATTTTTTAACATCCCTTTATGCTCATATGATTTAAAGTGTGCCTGTATTACTAGTACAATACGGTATCTCATATGCCTGTGTATGTTTGTTTGTGGTGTTT[A/G]GTGTGTGATGGTATAGGAACCGGCAGCCTTCAATCAGCCCAAACTGTTGATTCCAGCAACATTGAGAAGTTTGTCAACTGCACCAAGATCAACGGCAACCTCATCTTCCTCATCACAGGCATCAAAGGGTGAGGAATCTTTAAGTCTTTGGGCCTGACAGTGTGTGATATTCCCAGATTACATTTGTGTTTCTCTTTGAACTGCTGCGTGCCCTAAAAAGCAGCTATAAGTGGTTGTCAGCTGCTCCTGAAATGCGTTGCGGAGAGTGGGATTTGATGTACATCGACTCAAATGTTGCTCAGAAGAAATATTTCTAAAGACACGTGATTTGTGACCTTGACGCAAAACTCCCACCGAGGTCAACCTTGTTGTTTCCAGGATATCAAGAGACTGTCTTTTGAGTTATTACAGAAATTTTGAGAGATAAATGTACTCTCTCTCCCTCCCCTTTTACATGTTAGAAAATTTAGTATTTATAATTAAGTGTATGAATATGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6573
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092114 | Nonsense | 371 | 609 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 6238826)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6704440 |
| GRCz11 | 1 | 7387873 |
KASP Assay ID:
554-4664.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGTGGTATTTCTCTGCTGATCCTRAAGCAGCGCTGGATCACGTCTCTG[C/T]AGTTTCAGTCTCTGAGAGAGATCAGCGCYGGTAACGTCTACATGACCAAC
Long Flanking Sequence:
TTCATCGTGTATATAAGCAAGATGCAGAAGCCTGTGTGGAACCCGCTAGGTGATGCATTGAGTGTATGCTTTACGAACTAGTTCAAGTGTCTTCTGGGCTAGTTTTTATTTCTGTGTGAAGATTACATGTTCTCCCTATGTTGGCATGGGTTTCCTCCTGGTGCTCAGCCCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTCGACCTGCCTGGTTTTAGAGGGGTTTTGGCCACTTTCAGGCTGGTTTCCAGCCATTTCCAGCCTTGTCTTAACAAATGAAATGAATGATTATAAGGCATGTTTAGAAATATCTAAATGGTGTGTGATCATTATACGGTCTCTGTTTTTGCTGTGTTTTTGGAAATCATTGGTTTGGAAATCCTAAAATTATCCTTCAGTCTCATTTGCTTGTGTATTTTATTTTGCCAGTGGTATTTCTCTGCTGATCCTAAAGCAGCGCTGGATCACGTCTCTG[C/T]AGTTTCAGTCTCTGAGAGAGATCAGCGCTGGTAACGTCTACATGACCAACAACAGCCAGCTTTGCTTCTACAGCACAGTCAACTGGACGTCTCTGTTTCGCACCAGCACACAGAAAGCCAAGATCAAGGACAACAGAGACCCCAGAGAGTGCTGTGAGTCAATGCTATCAGACACGTTCAGTCAAATTATCTTAAAGGATTTTACAGCCTAAAATTCACCATGATTTTAGAAATGAAGTGTGACATAAATCACATAAATGCTATTTAAAGAAATATTCACTTACACACTGTAGTTCAAATTACAATTCATGCTATTAAATACTTAAATAAAAAAGGTAATATTGCAATAATAGGTGAGTAATAAGCCGGTTACCATCCTATTATTGAAGCATTAGCTGTTTTTGGTAGTTATAAAGTATTATTTTATTCTATATCTGTAATCCTACACTGTAAAAAAACACCGTTAAATTACAGACATTTACCATAAAATAACAAACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19414
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092114 | Essential Splice Site | 498 | 609 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 1 (position 6220652)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6722359 |
| GRCz11 | 1 | 7405792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTTCAACAAGTTAAGTGTCATTCTCCTGTATTCTGTTTTCATGTTTT[A/G]GGGACCAGATCACTGTGTGAAGTGTCTGCATCTCAAAGACGGGCCCAACT
Long Flanking Sequence:
AGAATGTAGGAACTCGCCCAACCATGTGACTTTCGCTTCAAAATGCACAATTAGATCAAATATCTATCAATTTGTTTGTGTTGTGAACAGCGCCATGCGGGATAGTTCAACTAAACTTGAAATTTACTCACTATTTACTCAACCTCAAGTGGTTCCAAACCTTAATGAGTGTAAAACACAAAAGAAGTTACTTTGAAAAATGTTAGAAACCTGTAACCATTGACTTCCATAGTAAGAAAAACAAGCACTATGAAAGTCAATGGTTAGAGGTTTTTAACATTTTGCAAAATAACTTATTTTGTGTTCAGACAGGTTTAGAAAAAGGTAAAGGAGGAGTAAATAATGATAGATTTTTTTAGTTTTGGGTGAACTATCCCTATACCTTTTTTTTTTTACTAAATAATCAAGCTCACAGAGGACCAAAAAGGGTCTCTACATATGTTATAGTTTCATTTTCAACAAGTTAAGTGTCATTCTCCTGTATTCTGTTTTCATGTTTT[A/G]GGGACCAGATCACTGTGTGAAGTGTCTGCATCTCAAAGACGGGCCCAACTGTGTGGAGAAATGCCCTGACGGTCTGCAGGGAGCAAACAGCTTTATCTTCAAATATCCCGAGACCAACAACGAGTGCCATCCCTGCCACCCCAACTGCACGCAGGGGTTAGTATCTGCATGCTTGTGTGTTTCCTCCAGGTCAGCTCTATGCCAGTGTGATGTCATCGTTGTCATTGCAGCTGTAATAATTACATTATGAATGTCTTATAGCTGCTTGCCTTGATAAAGTCTTCAATTTATGATTTATTATCCGCTACATTCAATTCAATTCAATTCAGCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAACGCAGCTTCACATAAATGGTCATAGTAACTGGATCAGGGTAGTTCAGTTTTTAGTGTTTAAGTTCAGTTGCATGCATGGACGAATAAACAATCATAAATATAAACACAACACTGGACGTAAGATCAACTTT
Associated Phenotype:
Not determined