ZMP
ephb4a
Ensembl ID:
ZFIN ID:
Description:
eph receptor B4a [Source:RefSeq peptide;Acc:NP_571489]
Human Orthologue:
EPHB4
Human Description:
EPH receptor B4 [Source:HGNC Symbol;Acc:3395]
Mouse Orthologue:
Ephb4
Mouse Description:
Eph receptor B4 Gene [Source:MGI Symbol;Acc:MGI:104757]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11431 | Nonsense | Available for shipment | Available now |
hu3445 | Nonsense | Available for shipment | Available now |
sa13275 | Nonsense | Available for shipment | Available now |
sa33770 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30869 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11431
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 |
---|---|---|---|---|---|
ENSDART00000059042 | Nonsense | 67 | 989 | 3 | 18 |
ENSDART00000121947 | Nonsense | 67 | 987 | 3 | 17 |
ENSDART00000133074 | Nonsense | 40 | 960 | 2 | 16 |
The following transcripts of ENSDARG00000040346 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 70810152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 67698590 |
GRCz11 | 5 | 68453888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGAGGAGGTCAGTGGTCTGGRTGAGGAGAACAACAGTGTGCGGACCTA[T/A]CAGATCTGCCAGGCGGACGGCTCCAGCAGTCATTGGCTGCGYAGTAAGCT
Long Flanking Sequence:
ATGAAGTATTTAAAGTACACATGAAATCAAAACTAAGCCTGTTGATTTGATTAGCTCACAGCGCTAGCTTTGTGGTGAACAATTCATCTGTGTAGGGCATTAAGACAAAAAAAATAGTTTGTCCTTGTAATCTTTAATCAAAATCTGTAAATGCACTTCCTGTTTGTTTTTTGTGATCACACCTATCTGAGGTATTGGGCGTGGCTAACATACTTAACCACGCCCCTCCAGCTGTCACTTTTGACAACAAACAGAAATGGTGAAGAGGAGGAGGAGGAGTCTGTTAGGCTATAATAACTCTCTCAAAAAATCCTTTTCCAATCACCTCGCAGTAGAAAAAAACAAGCCCCGCCCACTCATGTATGATTCAGTTTCTCTAGGAATAAGTAAAAAATAAATAAATAAAAGTCGCAGCTTCTGGACTTTAAGTGATTTTTGTGTGTTTTGCAGTGGGAGGAGGTCAGTGGTCTGGATGAGGAGAACAACAGTGTGCGGACCTA[T/A]CAGATCTGCCAGGCGGACGGCTCCAGCAGTCATTGGCTGCGTAGTAAGCTGATCGAGCGGCGGGGGGCGTCACAGGTGTACGTGGAGCTGTTCTTCACTATGGTTGAGTGTTCATCTCGAAACACACACCACCGCTCCTGCAAAGAGACTTTCAACCTTTATTACTACCAAAGCGACACGGATGACGCCACAGCCACCCACCCGGCGTGGATGGAGAACCCCTACACCAAGGTGAACACATACTGATGAATATACACTAGTCTGCATGCACATTTGGAGTACATGTGAAGTTCCCACTTTTGTATTAACCACTACAGTGGGGGAAATAAGTATTGAACACGTCACCGTTTTTTTTTTTGTTCAGAAAACATATTTCTTAAGATGATGTTAACTTGAAATTGTCACAAAAAAGTCCATATATGTAACATAAACTAAACTAATTAGTTCCTAAACAAAGTTGAAATGATGCAGGGAAAAAAAGTATTGAACACATGAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu3445
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 |
---|---|---|---|---|---|
ENSDART00000059042 | Nonsense | 245 | 989 | 4 | 18 |
ENSDART00000121947 | Nonsense | 245 | 987 | 4 | 17 |
ENSDART00000133074 | Nonsense | 218 | 960 | 3 | 16 |
The following transcripts of ENSDARG00000040346 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 70813967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 67694775 |
GRCz11 | 5 | 68450073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACGCAGCACAGCCTGGCCCCAGTCCCAGACCGCCCAAGATGTTCTGC[G/T]GAGAAGATGGACAGTGGGTGGACCAGCCCACCACCACCTGCACTTGCCTG
Long Flanking Sequence:
CACTGCCAACTAGTGTTTCGGAAGTGTTAATGCAGACCAACAGAAACAGCGCGCAGAAGTATAAATGCACAGCTACGCGCGTTGCATGCACCGTGGGTTACGCCGGTCACTTGACGCAGAAGTATAAACCAGGCTTAAGTGTGAACTCTTTTAGCACACCTTTAGGATGATCAATATATAATTGTGTTTTTATTCTCCAGGTGGACACAGTGGCCGCAGACTTCCTACTGCGCAAAGGCGGAGAGAAGAAAGTCAACGTGAAGACGCTGCGTTTGGGCCCGTTGAGCAAGCGTGGATTCTACCTGGCGTTTCAGGCTCAGGGCGCGTGCATGGCTCTGCTCTCCGTGCGTGTTTTCTTCAAGAAGTGTCCGGCGCTCACGCGCTCACTATCCGTCTTCCCGGAGACCGTTCCCCGCTCGCTGGTCCAGGAGGCAGTGGGCCAGTGTGTGGCCAACGCAGCACAGCCTGGCCCCAGTCCCAGACCGCCCAAGATGTTCTGC[G/T]GAGAAGATGGACAGTGGGTGGACCAGCCCACCACCACCTGCACTTGCCTGCCGGGCTTCGAGGCCAGCCATGGAGAGCTGGAGTGTAGAGGTGAGCGAGAGCAAACACAACAGACTGAAGAGCAAGCTAATTTAAGATTGGAAATATAAGCAAATAAAATCAAGCTGAGGTTTTCTGGATTCTGAGGAAAACTGCTAAATAAACCTTTGGCAATGCAGGTAACAAGTGTTGAGGAAGTTACTTTTAAAAAGTAATAGATTGCAAATGACTGATTACTACTGGAAAATTGTAATCGGATTACTTTACTAGTCATTCAAAAAGTAATCAGATTACTAATTGCTTGTTACTTTTAGTTTAACTCTGTTTTTTATTGAAATCTGTTCGTCAGAGAGCCACAGCATCAGATACACAGAATCATTAGACATCAACTGCTCCAGTGTGGTGGTAGAATACAATTTTGCTCACGTTTTCTTTCTCTCTGAATAAAACAATAATTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13275
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 |
---|---|---|---|---|---|
ENSDART00000059042 | Nonsense | 362 | 989 | 6 | 18 |
ENSDART00000121947 | Nonsense | 362 | 987 | 6 | 17 |
ENSDART00000133074 | Nonsense | 335 | 960 | 5 | 16 |
The following transcripts of ENSDARG00000040346 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 70830557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 67678185 |
GRCz11 | 5 | 68433483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAGTGGAGYGAGCCRTTGGACAGCGGCGGCCRYTCGGATCTCAGCTA[C/A]AGSGTGGAGTGTAGGATGTGCTCCACCCCTGGAAGTCCCTGCACACTATG
Long Flanking Sequence:
CAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAAACTAGGTTAATTAGGTTAAGTTAGAGTTATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTAGACAATCGTAAAAACAATAAAGCTTAAGCGGTTAATAATATTGACCTTAAAATGGTTTTAAATAAATTAAAAACTGATTTAATTCCAGACGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTAAAGGAATACTGCGAAAAATTTCTTGCTCTGCTAAACATCATTTGGGAAATATTTAAAAAAGAAAACTCACAGGAGGGTGAATAATTCTGAGGTCAACTATGATGGACAATGGAGTGTTACAGATGCATGAAGTGTTTTTGTTATTGTGTTCAGGTCCTCCGTCGTCTCCGCGCAGCCCCGTCCCGCAAGTAAACGACACATCTCTGACTCTGGAGTGGAGCGAGCCGTTGGACAGCGGCGGCCGCTCGGATCTCAGCTA[C/A]AGCGTGGAGTGTAGGATGTGCTCCACCCCTGGAAGTCCCTGCACACTATGCAGTGACGGTGTGAATTATCGGCCGTCCCAAACAGGGATCCAAGGCCGGCGCGTGAGCATTTGGGGTCTGAGACCTCACACCACCTACAGCTTCACTGTCATGGCCCTCAACGGGGTCTCCGCTCAGAGTCAGCAGGGGCCTGCAGGAGAGACCATCAACATCACCACCAGTCCCAATGGTGAGAATGAGAAACAGCAGGTTTTATACCACAATACTTCTTTAGTATGGTGTAGGGCCTCCTTATTCGGCCAACACAGCATCAGTTGGTCTTGGGAATGACAGATACAGGATGTTGAGCCATTCTTCTTGCAGAGTAGTGGCCAGGTCACTGCGTGATGCTGTTGGAGGAAAACATTTCCTAACTCGCTCCTCCAAAACACCCCAAAGTGCTTAATAATGTTTAGATCTGGTGACTGTGCAGGCCATATGAGATGTTCAACTTCATATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33770
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 |
---|---|---|---|---|---|
ENSDART00000059042 | Nonsense | 515 | 989 | 8 | 18 |
ENSDART00000121947 | Nonsense | 515 | 987 | 8 | 17 |
ENSDART00000133074 | Nonsense | 488 | 960 | 7 | 16 |
The following transcripts of ENSDARG00000040346 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 70832589)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 67676153 |
GRCz11 | 5 | 68431451 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGTTTTGAGCGACTTGCGAAGGGCCACGCAGTATGAGGTTCAAGTC[C/T]GAGCTCGGACATTCGCCGGATATGGAAGCTTTGGTAAAGCCATCCTCTTT
Long Flanking Sequence:
TAATGTAATGCTAATTTATTTCAACTGTACTACATTTGCTCAAATAAACATTCAATCAAGTATCAAAATATGCATTATGTTCACTCATACCTATATTTTTTGAGTATTAAAGTGACTTTTGCTTACATTCAGGACATATCCCATTTGATCAGTGCATAAAACCACCCAGGATTTACTCAGGATAATGTGTTTTCTCCTCAGTGTAGTTCACTGTGTTTTTATACCTCCATTGTTTTTATGAGCTCTCCCTATATCTCTTGCTCCAGTTTTCTCATGCTTGTGTTTTATCGATCTCTCTCTCTCTGTGCACTGTTTACACTGCAAACATGCCAGACTAATTAACAATTAATACATTGAAACGCCTCAGAGAAGTTATTGAAGATGTTTTCTCGTGACAGGAGCGCGGATCTGAAGAAAACTCCTGTCATTATATGGAGAGCAATAACAACGAGGTGGTTTTGAGCGACTTGCGAAGGGCCACGCAGTATGAGGTTCAAGTC[C/T]GAGCTCGGACATTCGCCGGATATGGAAGCTTTGGTAAAGCCATCCTCTTTCGAACTCTACCTGACGGTAAGACATTTATACAAGGTAATGGAATTTCTGGAATATAAAGTGTCTATTTCAGACTAGGCATGGGATGATAACTGGTATCAAGGTTTAGCGCGGTTTGGTAAAAGTCAAGGTTTTAAAATCGCCAAAATGTTCTGTTAGACTATTTCTACCGTGTTTTTACAAGTGTTTTATTAAGTTTTTAGGGCAACAGTAGCTCCAGCTGAAAGGCACCCTCCATATCAAAAGCTACTGGTAATCTCATGATATAGGAAACACCTAGAAAACATATCACTAATACACCGTACAACCATCGTTAGCCAACTAAAATCTCCTACACACCGGGACGCTTTTCGTTTGCGTTAACCGTCAGCGTTTTACGAGACATTTTTCAGTATTCAAACACAATCGCTTTTCACAGGCGTCAAGCTGAAGAGTATGCAAAATCACTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30869
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059042 | Nonsense | 863 | 989 | 15 | 18 |
ENSDART00000121947 | Nonsense | 863 | 987 | 15 | 17 |
ENSDART00000133074 | Nonsense | 836 | 960 | 14 | 16 |
The following transcripts of ENSDARG00000040346 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 70851664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 67657078 |
GRCz11 | 5 | 68412376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCCGCCGGACTGTCCCACATACTTGCACCAGCTGATGCTGGACTGCTG[G/A]CAGAAGGAGAGGACGGCCCGGCCACGCTTCGCCAACATCGTCTCAGCTCT
Long Flanking Sequence:
CTCCCTCCAACTTTGCTTCGTATCTAATTTCTGTGCTATCGTAATAAAGTCAAAATCAGAAAAATTATGTTAAAAATGTTGCAGTAAGTTCATTTCTTTGAAAGAATGAAATAGCTTTTTAAGTAAGGATCCATTAAATTGATCAAAAATAATAAATGTCCAATTTTTAATAAATTTTCTTCATTTAAAACACAAAAGAAATGAGTTCTTAAAACTATTATGTTTAAAAATATGTCGGAAAAAAATCTACACTCCGTTAAACAGCATTTAGGGAATATTTTGAAAAAGAATACAATTGACAGGCGCTCTTCAGCTGTATGTATTTTGGCTAATACATCCTAGGTAATATTGATCTGATGTATTGAGTTTGTTCCTCCTGTCATCAACATAGTGTATTGTGTTTGACCCAATCAGGTGATTAATGCCATTGAGCAGGATTACCGTCTGCCACCGCCGCCGGACTGTCCCACATACTTGCACCAGCTGATGCTGGACTGCTG[G/A]CAGAAGGAGAGGACGGCCCGGCCACGCTTCGCCAACATCGTCTCAGCTCTGGACAAGCTGATCCGCAACCCGGCCTCACTCAAAATCACAGCGCAGGAGGGGGCGGGGTGAGACTCTGATCCACAACACTTCTACATCACTCAATGCCGCAGCGAGCGCAGATTGAGAACAACACTAAGCAAATACATCTAGTTTATTACGTTTTGTCTTCTTCTTTTATCTCATTCAATTTTGATTCCGTTTTATTTAGTTTTTGTCTTGTTTTGTTTTTTGTTCATTTTAATTAGTTTTTGTGTTTTGTTGTTTTATTTTGTTTAGTTTTGTCTTATTTCAGTTGTTTTTGTTTTTTGTTATGTTTTTTGTTAGTTTTCATTTTATTTAATTTTTGTTTTATTTTGGTCTTGTTTCGTTGTTTTATTTTTGTTTTTATTTTGTTTTTGTCTTGTTTTGTTTTGTTTTTGTCTCATTTTGTTTCCGTTTCATTTTGTTTTTGTCTTGTT
Associated Phenotype:
Not determined