ZMP
bhlhe41
Ensembl ID:
ZFIN ID:
Description:
class E basic helix-loop-helix protein 41 [Source:RefSeq peptide;Acc:NP_001034196]
Human Orthologue:
BHLHE41
Human Description:
basic helix-loop-helix family, member e41 [Source:HGNC Symbol;Acc:16617]
Mouse Orthologue:
Bhlhe41
Mouse Description:
basic helix-loop-helix family, member e41 Gene [Source:MGI Symbol;Acc:MGI:1930704]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2955 | Essential Splice Site | F2 line generated | Not yet available |
sa10095 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2955
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061106 | Essential Splice Site | 42 | 421 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 15785352)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16137118 |
GRCz11 | 18 | 16126184 |
KASP Assay ID:
554-2706.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCTACATGTGCAAATCCAAAAGGGGGATGAAGAGAGAGGAAGGAAAGG[T/A]AAGCAAACTGTGGACCCGTGATGAAAACGTGACATTCACGTAACACTCAG
Long Flanking Sequence:
CTCATTTAATTCCCAGACTCTGGAGCTGGTGCAGTTTACACGTGAGTCAGCGCGCGGTTCCTGGAGAAGGCGCGCGTGCGCGGTAGTGGCCACGCGCAGTGTGAGTGCGCGAGAGCGCTGGGCAAAGTGGCAGCTCAGGCGAGCGCGCACACACACATCATCATCATTCAGAGGTGCTGCGCGAGACCGGACACAACGCACTGCCGCTCCGCTCAGATATTGGATTAACCAAACCTCACTGTATAACAAAGTGGAACAAAGTTATGGAAGAAAGAATATCGAGAATGCAGAACAGACAGTTTCTGGATCACGCGGATTTCTTGGGGTAATTTTATATTTGCTTGTTTTGCTTTTAATTAACGCATGCATTAATTTTGCAAGGTATCAAAACGAATTTATTATATTTTTAAAAAAAATAATGTTTTCTTTTATCAGGGTGGAATATTCATCGCTCTACATGTGCAAATCCAAAAGGGGGATGAAGAGAGAGGAAGGAAAGG[T/A]AAGCAAACTGTGGACCCGTGATGAAAACGTGACATTCACGTAACACTCAGTGACACTTGCTGTTAAGTATGCGAGTTATAATAATTACTTTACGAACTTTTGCAGTAGCTCATACTTTTATCATCCGCAGGACGCGTACAAGTTACCACACAGACTGATCGAGAAAAAGAGGAGGGACCGAATAAATGAATGTATTGGGCAGCTGAAGGATTTATTACCCGAACATCTCAAACTCACGGTAAAGTTGTTTAGTTTTGTTAACATGTGTTCTGCAAATGTATCTCCCCACATAAGGAAAGTCGGAAAGTATAGACACGCTTTAAATGTTCGTGTTGTCTTACAGACTCTGGGTCACTTGGAAAAAGCGGTGGTTCTGGAACTGACGCTGAAGCATTTGAACGCTTTGACAGCTGTCACAGAGCAGCAGCACCAGAAGATCATCGCTTTGCAGAACGGTAAATTACATAATGTTCAGCCCACACAATGCAATTAGACTAACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10095
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 |
---|---|---|---|---|---|
ENSDART00000061106 | Nonsense | 328 | 421 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 15787257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16139023 |
GRCz11 | 18 | 16128089 |
KASP Assay ID:
2261-2011.1 (used for ordering genotyping assays)
KASP Sequence:
GCATCATACATGCCTTTATTTGACAAAAGTCATTTGGAGAAGTTGGTGTA[T/A]CCAGCAGCAGCGGCGGCGGCATTGACCACACCATTTCCATGGCTTTACCC
Long Flanking Sequence:
CTCATCAACCACCTACACAAAGTTTCTGCTCAGTTCCAGCCAGGCACAGGGATCCTGCAGCAGCCAGTGGCAGGAGACGACGCTCCAGAGCGGGACACCCAGAGAGATCCTCAAGCCAACTGCGTCCCTGTCATCCAGAGGACTCAAAACCTCGAGCTTAATGAGAACGACACTGACACAGACAGCGGGTATGGAGGAGAGGCTGAGAAAGGCGATGGAAAGAGCGAGAAAGGATGCGACACAGCAAAAGGAGTTAAAATCAAGCAGGAGTTTGGAGATGAACGTGTCACTAAAAAAGCTAAAATGAACTGGTCGGCGAATGGTGGTTCAGATTCCACAAGTACGCGACCAGATGTGGCGCTTATGAACTCTTTAATGGGAATGACCGGGGTTGGTGGACAACAAACTCCCTTTTGCATGCCGTTTTACTTCATAAACCCGTCTGCAGCAGCATCATACATGCCTTTATTTGACAAAAGTCATTTGGAGAAGTTGGTGTA[T/A]CCAGCAGCAGCGGCGGCGGCATTGACCACACCATTTCCATGGCTTTACCCTGGGATCCCCACACACGCCTCTGCTGCAGCCGCAGCAGCCATCGCTTTCCCCAACGCATCCACCGATAAAACCTCTGGATTTGATGCAGCGTCGTCAAAAGATGACGAGCCGGAGTCTCCTGATGATGACCTGTCCAATGAGGCCGACCTGGCCTCTCCTGCATCTGAAGATCACGGCTCAGAAATTGATACAAGTCATCAGCCCCAAAGAAATGACAATGATGGTACATAAAGCTGATGTTTCGACCTTTGAATACACACTAGTTTGCTTGTAAAACCGCTATTTATCTGTTTCTCTTAATTTAATTGTCATTAAGTATTTACTATAGTGTTTCTATGGATTTCCAAACGAAAAGCTGTTCTTTTGTTTGTTTTTTTGCATTATTATTGGTATTATTAAAAACTCAAAACTTCACGTCAAATTGGTTTACCTTTTTTTTTTAGGGGAGA
Associated Phenotype:
Not determined