ZMP
NP_571883.1
Ensembl ID:
Description:
ephrin B2b [Source:RefSeq peptide;Acc:NP_571883]
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 |
|---|---|---|---|
| hu2971 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa25519 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu2971
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 |
|---|---|---|---|---|---|
| ENSDART00000023180 | Nonsense | 78 | 334 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 6783557)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6966774 |
| GRCz11 | 1 | 7650207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAGCCAGGCTCCACTGAGCAGACGAACATTGAATACTTCCGGGTCTA[T/A]CTTGTTCCCAAAGAACAACTCGAGACCTGCCATGTTACTAAAAGCGACAT
Long Flanking Sequence:
TAACTAACGTCATCAAAAATAAATACTGTAATAAATATATTATTATTATTATTTTGTTGTCAACTTTGTTTCGGATCCTTTTTTATTTATTTAAAAATAACATTTTTACACGACAACATTTTTTTAAATTGATACAATATTTAAAATATTTTATGTTTCTTAGAAAACGACAACTTGGTTTTCTTATTTAAAATGATCCACCAGACACCAACGCTTTTGCTGTGAGGATAACCGTACTACTCCAAACACACAACTTTGAAGTTCTCACGCCTCATGAATACACTATTGAGAGTTAATTCATTATTATGCATGCTAATCAGTCTGTTTTATTCCATTTCTGTAACTCTATAAGATATTTAACATCACCTTGTTCCCCACAGGTTTGTCCCAGGAAGAGGTGTAGTATTATACCCTCAGATCGGAGACAAAATGGACATTGTGTGTCCAAGAATCAAGCCAGGCTCCACTGAGCAGACGAACATTGAATACTTCCGGGTCTA[T/A]CTTGTTCCCAAAGAACAACTCGAGACCTGCCATGTTACTAAAAGCGACATGTTACTGCTCAACTGTGACAAGCCGGACCAGGACGTCAAATTCACCTTCAAGTTTCAAGAGTTCAGCCCCAACCTGTGGGGCCTGGAGTTCTTAAGAGGGAAGGACTATCACATCATCTGTAAGTTTATTGCCACTCTCATTCAAGAATTTACCTCAGGTGCTGATTCATGATCAGTTTTCACCTCCCTTGCCAGCTGTAACACTATGCAGAAGGAGCCAAATGCTCAACTGATCCCACCCGGGGGAATTTCAGCCTCCGGCATTGTCTCCCAAGATATCTTTTCCTTGTTTTCGTCTGGGAAGGCGACTGAATAATGTAGCCCTCAAAAAATAAAGAACAAATCAAGTTGATGGGAATGGAAATGTGTTAAATGCTTTGGCAAGAGCGTTTACCACACAAGATGTCCTTACTCATTTAACAGACGCGTACGAGCGATAAAATCGATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25519
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 |
|---|---|---|---|---|---|
| ENSDART00000023180 | Nonsense | 131 | 334 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 6783716)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 6966615 |
| GRCz11 | 1 | 7650048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTCAGCCCCAACCTGTGGGGCCTGGAGTTCTTAAGAGGGAAGGACTA[T/G]CACATCATCTGTAAGTTTATTGCCACTCTCATTCAAGAATTTACCTCAGG
Long Flanking Sequence:
TTAGAAAACGACAACTTGGTTTTCTTATTTAAAATGATCCACCAGACACCAACGCTTTTGCTGTGAGGATAACCGTACTACTCCAAACACACAACTTTGAAGTTCTCACGCCTCATGAATACACTATTGAGAGTTAATTCATTATTATGCATGCTAATCAGTCTGTTTTATTCCATTTCTGTAACTCTATAAGATATTTAACATCACCTTGTTCCCCACAGGTTTGTCCCAGGAAGAGGTGTAGTATTATACCCTCAGATCGGAGACAAAATGGACATTGTGTGTCCAAGAATCAAGCCAGGCTCCACTGAGCAGACGAACATTGAATACTTCCGGGTCTATCTTGTTCCCAAAGAACAACTCGAGACCTGCCATGTTACTAAAAGCGACATGTTACTGCTCAACTGTGACAAGCCGGACCAGGACGTCAAATTCACCTTCAAGTTTCAAGAGTTCAGCCCCAACCTGTGGGGCCTGGAGTTCTTAAGAGGGAAGGACTA[T/G]CACATCATCTGTAAGTTTATTGCCACTCTCATTCAAGAATTTACCTCAGGTGCTGATTCATGATCAGTTTTCACCTCCCTTGCCAGCTGTAACACTATGCAGAAGGAGCCAAATGCTCAACTGATCCCACCCGGGGGAATTTCAGCCTCCGGCATTGTCTCCCAAGATATCTTTTCCTTGTTTTCGTCTGGGAAGGCGACTGAATAATGTAGCCCTCAAAAAATAAAGAACAAATCAAGTTGATGGGAATGGAAATGTGTTAAATGCTTTGGCAAGAGCGTTTACCACACAAGATGTCCTTACTCATTTAACAGACGCGTACGAGCGATAAAATCGATTTGTCATGAAGAGGCGAATAAACACAATGTTACAGGGGCCATTTATACTACATTTTCAGCCAAAAACGGGAAACTTTTTATGCGTTTTGCCTATTCGTTTTACTTGACAGCAACATTTTTTATGACTGAAAATGCATAAAGATATTTAAAATGCTGTTGTCA
Associated Phenotype:
Not determined