ZMP
efnb2a
Ensembl ID:
ZFIN ID:
Description:
Ephrin-B2a [Source:UniProtKB/Swiss-Prot;Acc:O73874]
Human Orthologue:
EFNB2
Human Description:
ephrin-B2 [Source:HGNC Symbol;Acc:3227]
Mouse Orthologue:
Efnb2
Mouse Description:
ephrin B2 Gene [Source:MGI Symbol;Acc:MGI:105097]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| hu3393 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa13177 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3393
Status:
Confirmed mutation in F2 line
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 |
|---|---|---|---|---|---|
| ENSDART00000026011 | Nonsense | 86 | 332 | 2 | 5 |
The following transcripts of ENSDARG00000020164 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 27145028)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 26300814 |
| GRCz11 | 9 | 26111683 |
KASP Assay ID:
1083-0001.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAGTATTATAAACTCTATATGGTTCCTCTGGAACAGCTAAAGTCCTG[T/A]CAGGTCACAAAAGCAGACACGCCTCTACTCAACTGCGTCAAGCCAGACCA
Long Flanking Sequence:
TTTGAGTGCTTGGCATCAGAGAGACTATTTGCTTTTATTCTTAAGTATGAGCTGTGAGTCAACACCTTTGTCTGCTTCTCGCTGCTCCATTTTCTTCCCAAAAAAACCCCTGCAAAAAACACTTGCGCATGCAGTTTTAGATCGTCTCGCTTGCTCTCCTCTGTTTTTATGATCCAGCAAGTTGTTCAGAACCTGTTTTATCCTTTATAATCGCAGCTGAATAATTAATCACCCTCTTTTAATTATTGATCAACACCATGCTTCATGATCCATTTTTGATCTAGAGAGAAATGCGAGTTTGATTTATCATCCGCCATGTGTCTGACTCTCTCTTTCTGATTCTTTTTCTCCTGAAGGTTTGTGCCAGGACAGGGTCTGGTGCTGTATCCGCAGATTGGGGATAAGATGGACATAGTTTGCCCACGTGTGGAAGGTGGTTCAATGGAAGGAGTGGAGTATTATAAACTCTATATGGTTCCTCTGGAACAGCTAAAGTCCTG[T/A]CAGGTCACAAAAGCAGACACGCCTCTACTCAACTGCGTCAAGCCAGACCAGGACGTCAAATTCACCCTCAAATTCCAGGAGTTCAGCCCAAACCTTTGGGGCCTGGAGTTCTTCAGAGGGAAAGACTACTACATTATCTGTGAGTATGCTATCTGTAAACCACCATTTGCCCCTCTGTTCTGGCCAATTACGTTTGTTTATGTGGTTTCGAGTACCGAGAAATGTTGACATTGCGGCGCGAGCTACATTAGTTATGTTTTAGTGGGTCGTGGTGCAAATAATGACACGTTTATACGACCTGTGTTTGTTTACAACAGCTGGAATGGTTGTTAGTTCCAGAGTTAGACAGACGGAAAGTTTCTGTTTGTGAGTGGCATTGGACCAGTGCAGTGCGTATGTACACAAACACACGACTTCTCGTATTTGCCTCGTATCGTTTTGCATGTGGGTTGAATTTTTTACATTTGCGAGAACAATAACTGCTCACCTGGCTCACCAGG
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13177
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 |
|---|---|---|---|---|---|
| ENSDART00000026011 | Nonsense | 210 | 332 | 5 | 5 |
The following transcripts of ENSDARG00000020164 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 27156680)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 26312466 |
| GRCz11 | 9 | 26123335 |
KASP Assay ID:
2260-1900.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTNNCCCTCTCTTAGATGCATCTCCTCATGGGGAAGAYAAGGGAGAT[G/T]GAAATAAATYCTCATCAGTCATTGGCTCAGAGGTGGCCCTGTTTGCCTGC
Long Flanking Sequence:
TGATCCATTCCTTTGCAGTACGTGGGTCCTTCACTGGGCCTTTTTCCTTTCGCAAAGAAACCTTCCAAAGACGTCGATTTCTTACTAATTTTGCTGCTTGTGGGTTAAATTTGGTTGCTCAACTAACCAAGATTCAATTCAATTCAATTCAATTCAGCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATAAATAGTCATAGTAACTGGAACAGTGTGGTTCAGTAACTGAAACAGTGTAGTTCAGTGTAGTTCAAGATGTAACAGAAAGAATGGAGTAAATAAAAGATCGTTCAGACTCAGATAATAAAAAAAAGGAAAAATAATTAATGATTTCTTGTGCAGCCCGGTACCAACTTATCCACAGACTGGTACCGGTTCGCAGCCCGGTGGTTGAGGACCACTACTCTAGTTCTTTTGTTAATTTCTCTTTTTTTTCCCTCTCTTAGATGCATCTCCTCATGGGGAAGATAAGGGAGAT[G/T]GAAATAAATCCTCATCAGTCATTGGCTCAGAGGTGGCCCTGTTTGCCTGCATCGCCTCAGCAAGCGTCATCGTCATCATCATAATCATCATGCTAGTTTTCCTTCTCCTGAAGTATCGACGACGTCATCGCAAACACTCTCCTCAACACGCCACCACGTTGTCACTCAGCACATTAGCCACGCCCAAGAGGGGCGGCAGCGGCGGCAACAACAACGGCTCAGAGCCGAGCGACATCATCATCCCACTGCGGACTGCTGACAGCGTCTTCTGCCCGCATTATGAGAAAGTGAGCGGCGATTACGGACACCCTGTTTACATCGTACAGGAAATGCCGCCACAGAGCCCAGCAAACATCTATTACAAGGTGTGAAAATGGACACGCTATTTTTTCCCGGACATTTTAACTCTAACCCCTCACATGCCCCTCGATGAACCCCCAGTTGGCGGCATCGATGCCTGAGCTCACCCTCGTTCTGCCCCCTCTTATTTTATTTTGTTG
Associated Phenotype:
Not determined