ZMP
scxa
Ensembl ID:
ZFIN ID:
Description:
scleraxis homolog A [Source:RefSeq peptide;Acc:NP_001076538]
Human Orthologues:
SCXA, SCXB
Human Descriptions:
scleraxis homolog A (mouse) [Source:HGNC Symbol;Acc:24312]
scleraxis homolog B (mouse) [Source:HGNC Symbol;Acc:32322]
scleraxis homolog B (mouse) [Source:HGNC Symbol;Acc:32322]
Mouse Orthologue:
Scx
Mouse Description:
scleraxis Gene [Source:MGI Symbol;Acc:MGI:102934]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36755 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23414 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36755
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105192 | Nonsense | 50 | 204 | 1 | 2 |
ENSDART00000145363 | Nonsense | 45 | 199 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 3564418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3060991 |
GRCz11 | 19 | 3001889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCTCGGATGATCGCTCATTTCACCTGGACACTTCAGGGTATGATCTT[A/T]AAGTTGGAAGAAAGAGGAAATCCAGTGTAGGGGGTGGCGGACGGCTGATT
Long Flanking Sequence:
TCCCACAACCTATAAAGCACAACCATACTGAAACACTCAGTGAAACCACACGTGGGTCTCAGCACGGGGGAGAGCCAGCGCTGCACAGAGACAGAAAGCCGGAGGAGTGTGTGTGTGCATGTGTATGTTTGAGGATACAAAACGTGGATTTCAGAGCTGATGGGATGTGAGTGAGGACAATCTCCAATATCAACCCGTCAGGATCAGTTCCCCAAGAGAAATGTAATACTGGAGCGCAACTGTACCAGAGGACCAAACAAGTGCAGGACTCATTGAGATTCATGCGTTTGGAACTTTAGAGCAATTGCAAGAAGCATTCGAGAGCCTTGTGGAGAGCGTTAGAAATCAAGTTGATGATGTCTTTTGCGATGGTGCGACCGGCTCCGAGCCGATACGTGTATTCTGACATCTCAATGATGTCGGAGGATGATGAAAACGGCAGCGAGAGCTCAGGCTCGGATGATCGCTCATTTCACCTGGACACTTCAGGGTATGATCTT[A/T]AAGTTGGAAGAAAGAGGAAATCCAGTGTAGGGGGTGGCGGACGGCTGATTGGTGTAACACCAACCATTCCCACCGGGACAATCGGCCATGTGCCAGAGATCCGTCAACGCAATGCTGCCAATGCACGAGAGCGGGATCGCACCAACAGCGTCAACACGGCATTCACAGCATTGAGGACTCTCATCCCTACAGAGCCTGCTGACCGGAAGCTGTCCAAGATCGAGACCTTGCGGCTGGCGTCCAGTTACATCTCTCATCTGGGGAACGTGCTGCTGGTGGGTGAAGCTTGCGGAGATGGACAGCCGTGCCACAGCGGAGGACCCTCCACCTCAAACTACTACCACCACCACGGCTCACCCAGCCGGGACTCGGAGAACTCGCAGCCCAAACAGATCTGCACATTCTGCCTCAGCAACCAGAGGAAAATGGTAAGTCAGACACACGCAGGTGTTCTCCGTTAAAGGTTGTGCAATGATCTGGACAACTTCAAGTCCACAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23414
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 |
---|---|---|---|---|---|
ENSDART00000105192 | Nonsense | 155 | 204 | 1 | 2 |
ENSDART00000145363 | Nonsense | 150 | 199 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 19 (position 3564733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 3061306 |
GRCz11 | 19 | 3002204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTGCTGCTGGTGGGTGAAGCTTGCGGAGATGGACAGCCGTGCCACAGC[G/T]GAGGACCCTCCACCTCAAACTACTACCACCACCACGGCTCACCCAGCCGG
Long Flanking Sequence:
ATTCGAGAGCCTTGTGGAGAGCGTTAGAAATCAAGTTGATGATGTCTTTTGCGATGGTGCGACCGGCTCCGAGCCGATACGTGTATTCTGACATCTCAATGATGTCGGAGGATGATGAAAACGGCAGCGAGAGCTCAGGCTCGGATGATCGCTCATTTCACCTGGACACTTCAGGGTATGATCTTAAAGTTGGAAGAAAGAGGAAATCCAGTGTAGGGGGTGGCGGACGGCTGATTGGTGTAACACCAACCATTCCCACCGGGACAATCGGCCATGTGCCAGAGATCCGTCAACGCAATGCTGCCAATGCACGAGAGCGGGATCGCACCAACAGCGTCAACACGGCATTCACAGCATTGAGGACTCTCATCCCTACAGAGCCTGCTGACCGGAAGCTGTCCAAGATCGAGACCTTGCGGCTGGCGTCCAGTTACATCTCTCATCTGGGGAACGTGCTGCTGGTGGGTGAAGCTTGCGGAGATGGACAGCCGTGCCACAGC[G/T]GAGGACCCTCCACCTCAAACTACTACCACCACCACGGCTCACCCAGCCGGGACTCGGAGAACTCGCAGCCCAAACAGATCTGCACATTCTGCCTCAGCAACCAGAGGAAAATGGTAAGTCAGACACACGCAGGTGTTCTCCGTTAAAGGTTGTGCAATGATCTGGACAACTTCAAGTCCACAAACAAGCTGGAGAAATAGTGACAGAGGTGTAAAATACTGCTGAACCTCAGGGAGGGATGAGAGCAGGTCTGATTTATTCCCTGCAAGTAAGGTCACTGAGGGCAATCACTATAGCAAGTCCAAAACTACTGAAGTTAACTTTAGCAGAGTATCTTTCAAACAAGTAGGACTTGACAAACAAGACTAAGCAGCTAACTTCTAAAAAGAGCACTGCAAAAACTTGATGATAATGTTTTGAGGCATGAGCAATCATGGCTGTAGACGGTCTGTCATTGATTTTCCTGAATTGGCCAACTGTCTTTTACTGAATCTGCGTCG
Associated Phenotype:
Not determined