ZMP
erbb3b
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100149258 [Source:RefSeq peptide;Acc:NP_001122291]
Human Orthologue:
ERBB3
Human Description:
v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian) [Source:HGNC Symbol;Acc:3431]
Mouse Orthologue:
Erbb3
Mouse Description:
v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian) Gene [Source:MGI Symbol;Acc:MGI:95
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14974 | Nonsense | Available for shipment | Available now |
sa18520 | Nonsense | Available for shipment | Available now |
sa37713 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14974
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049893 | Nonsense | 85 | 1430 | 3 | 28 |
ENSDART00000128510 | Nonsense | 85 | 1429 | 3 | 29 |
ENSDART00000138974 | Nonsense | 85 | 1426 | 3 | 28 |
Genomic Location (Zv9):
Chromosome 23 (position 25538587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25324707 |
GRCz11 | 23 | 25251248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATRACATGCTTGACNTTTCTTCTAGAGTATCCGAGAGGTCACCGGCTA[C/A]ATCCTCWTTGCGATGAACCAGTTTCGCAAGTTACCTTTGAATCAGCTCMG
Long Flanking Sequence:
ACTTTTAGACTAGGGTTTCTCAAGCCACCATAAAGTTGGTCTACGAGCTTTACTTTTCTAGTTTAATCTGAAATATTTGACGAAATATTGTAAGAATTCAGATTTTTTTTGGGAAATGTAGATTGTAAACTGTAAATTTTATTGATGCTGAAATAATATAGTGTGCAGCTGTAGTTGTTAAATAGTTCTGAATGGCCCACATACAGTACGTCATAAACAAATGTAATTGTTCTCTTTTCCTAGTTTGTACTGGCACTAAAAATGCTCTGAGCTCCACGGGCACCCCAGAACAGCACTACAACAACCTTAAAGAGCGCTACACCGGATGTGAGATCGTCATGGGCAATCTTGAGATTACACAGATGGAGAATGACCTCGATTTCTCCTTTCTTGGAGTAAGAAGCTGTTTTACCTACCTGTATGGAGTGCTAAATGGTTGGTTTGGCCTTGAGATAACATGCTTGACTTTTCTTCTAGAGTATCCGAGAGGTCACCGGCTA[C/A]ATCCTCATTGCGATGAACCAGTTTCGCAAGTTACCTTTGAATCAGCTCAGAGTGATTCGTGGCAGCAGCTTGTATGACAAAGAATGGGCTCTTTCTGTCTTTCATAACTTTGACACTCACACTGGCCTGGAAGATCTGGGCCTCACCAACCTCACAGGTGAGATTGAGATCAGAATATAAAAATACACCTTTTCCTATGCTCCATGTTGCTTTGCGCAAATATTGGAACACATGACTTCTGTTAAGCTGTAAGCAATCAGAGAAGCGTAACCCCAAAATGTCATTGTAAGATTGTAAGATTCATTGTAATGTTTCTTATCTAATAACTTGGGATCAGATCACTGAATATGCAACATCTGGTAGTAACCGTAAATCTTTGGAGGAAATTTGGTCAAAATAACCTAAAGGTTTTTTTTCACACATATTTATCCCAATTTTATTGTTTTAAATTCTGCTTTCAGCCAAAGGTAGTGAAAAGTTTCAGACTCATAACACATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18520
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 |
---|---|---|---|---|---|
ENSDART00000049893 | Nonsense | 840 | 1430 | 21 | 28 |
ENSDART00000128510 | Nonsense | 839 | 1429 | 22 | 29 |
ENSDART00000138974 | Nonsense | 836 | 1426 | 21 | 28 |
ENSDART00000049893 | Nonsense | 840 | 1430 | 21 | 28 |
ENSDART00000128510 | Nonsense | 839 | 1429 | 22 | 29 |
ENSDART00000138974 | Nonsense | 836 | 1426 | 21 | 28 |
Genomic Location (Zv9):
Chromosome 23 (position 25565609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25351729 |
GRCz11 | 23 | 25278270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATGTATTATCTGGAGGAGCACTGCATGGCCCATAGGAACCTGGCTGCA[C/T]GAAACATACTGCTCAAGAGTGACTACATAGTACAGATCTCGGACTTTGGG
Long Flanking Sequence:
TCTAGGCACTGGGTGGGGATTTTTAAATGTCTTTGCATGAATCTGTATCACAGTTTTCATAACAATGTGTTCCCGCACAACAGTTTTTAACACTGATAATAATAATATCAAATCTTTCTTGAGCAGCAAGGATCATGTAACAGTGAAATCTGAAATAATCGTAAAAAAGATTTTAAACTACATACAAAAAGAAAACAATTCTTTAAAAATGAAATAATAATTGTAAAGTTCAGCTGCACTTTAGAATATTTCAGAATATATATACAAACTTCAAATAATTTAATTTATTCATTTCACAACATGAAATAATCTTACTGATCTCAAACTTTTGACTTATGTATGTATGTACTGATGTATGCTGTTAAAATTCATTTTTGAAGAAATCCTTTGTGTTTGTCCAGTAGATATTTGTGCACTTTATTTATTCTCAATGCATATGTATATTTTAGGGCATGTATTATCTGGAGGAGCACTGCATGGCCCATAGGAACCTGGCTGCA[C/T]GAAACATACTGCTCAAGAGTGACTACATAGTACAGATCTCGGACTTTGGGGTTGCAGATCTGCTCTATCCAGATGATAAGAAATATGTGTACAGTGAACACAAGGTAAACTCTCTTGAATAAAAAGATAATGTGTTAATGCATTAATAACTACATTATTAAACATTACAGAATTACAATTCTAAATTGATGCTTTGTTTTAATGTGATTTTTTTATTCTTACATGAATTTTCTTTTATAATGCCGATTTAATGCTCTAGGATTTTTTTTATATATATTATCAGTGTTTAAATCTGTAATTATATATTGCTAAGTATTTTTGATTAATTACATTTTTAAAAAGAACAGTATTTATTTGAAATAGACAACTTTTTGTGTTATTATAAATGTATGTACTGTCACTTGATCAATTTAATGCACCCTTACTGAATAAAAGTGTTAATTTTCTACAAAATAAAAATATAATTAACCATTGAAAGGTAATGCGTATACTTTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37713
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 |
---|---|---|---|---|---|
ENSDART00000049893 | Nonsense | 1210 | 1430 | 28 | 28 |
ENSDART00000128510 | Nonsense | 1209 | 1429 | 29 | 29 |
ENSDART00000138974 | Nonsense | 1206 | 1426 | 28 | 28 |
Genomic Location (Zv9):
Chromosome 23 (position 25574286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25360406 |
GRCz11 | 23 | 25286947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACCATTTAAAACCAGCATCCCTTGTTTCTGCACACATATGTAGCAGTT[T/A]ACCTCAGAAAAAAGAAATGGACTCAGCACAAACCCAAGATGAAATTTTAC
Long Flanking Sequence:
TAATAAGGAACATCCAGGATCTGTTTCTCTGCTCTTCTTTATTATTTTTTATGCATTATAGAAGTATCGGATTGGGTTTTGATATCGGTAGATACTTAAAATCAAATGACTCAGACTCGAGGGCAAAAAAATCTGATCAGAACATCCCTAATTACAAGTACAAGTGACAAGTGTGTTGACCAAAGTTGCAGCTAAAGTCTACAGGAAGGTAGATCTTAGAGAACAGGGTTGGGCACCCCTGGCAAAGTGCATAAACACTGACCCAGCCCTAGACCCCCAACTTTGTTTACCTTTCTAACACATATCTTCTTGTTTAGATTTCAGAAGTGCTGTTCCTCATGGTAGGACATCCAGAAACTCCAAAAGCACTCCAAAAACAGATGCCACGCAAGAGTACGAGCTAATGAACAAACAGACAAACAAACTTTCCTCCTCGCCCACAGACAGCACTGACCATTTAAAACCAGCATCCCTTGTTTCTGCACACATATGTAGCAGTT[T/A]ACCTCAGAAAAAAGAAATGGACTCAGCACAAACCCAAGATGAAATTTTACCACAGAAAAGAGAAACAGACTCAATACAAAGCCAAGAGAACAATTTACCACAGAAAAGTGAAACGGACTCAACTCAAACCCAAGAGTCAGAGAAGGATGCTAGTTTTCAACCTGACAACTTGGAGTCTGCTGAAAACTGTCTGATTGGATCGGAAACATTAAACGATGGTGGTCAATCTGAAGATGAAGAACAGCTGCCACGATTGGCGATGGTCGAATATGAATACATGGACATACGTACAGATGAACACCAACAAAATGTAGCTGGCAAACGTACAACAAACGGTCCAAATGAGGTGGAGAGGGAAGCGATTTATCAAAATATAAGTCAGCCTCTAAGATTTCATGAAAATCCAGATTCTGCTGGCAATACGATGCAGAGGCGCGGTGAATATGTGGACATGGAGGCATCTGGGAGAAGTGGCTGTGAGGTTGGAGATTATCAGAATG
Associated Phenotype:
Not determined