ZMP
SPTBN4 (1 of 3)
Ensembl ID:
Description:
spectrin, beta, non-erythrocytic 4 [Source:HGNC Symbol;Acc:14896]
Human Orthologue:
SPTBN4
Human Description:
spectrin, beta, non-erythrocytic 4 [Source:HGNC Symbol;Acc:14896]
Mouse Orthologue:
Spnb4
Mouse Description:
spectrin beta 4 Gene [Source:MGI Symbol;Acc:MGI:1890574]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39219 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39218 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23377 | Nonsense | Available for shipment | Available now |
sa32220 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39219
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 |
---|---|---|---|---|---|
ENSDART00000078561 | Nonsense | 108 | 1177 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 44477909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46063403 |
GRCz11 | 18 | 46061421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGATGTGGCGTAACTCTGTGCTGTTCATCTGCTCTCAGACTCTTCAG[C/T]GAGAGCTTCATGGCCACCGCTCGCGGGTGGAGGACGTCCTGGAGCGAGCA
Long Flanking Sequence:
TGTCAAAGCATTTCAAACAAGCTGTATCAGCCTGGATTCGAACCCACTATCCCCGCACGGTAGTCAGAAACCTTAATCGCTCCACTAAATCACAGGTTCAAGCCTACAAAGTGGGGTTTAATACCTCAATTAGCTCAACTGTTCTTTGCTGCAGCTGTTCCAGTGCAATACATAAAAAATCACCACTAGGTGTCATTGTAGAGTGGGGTTTCGAAATGTTTCGAAGATTCGACACATTTGCTGCGACTGTTTCAGGGTTTCATGAAGCCTCGCTTTGCCCACCACTACTTTCCTGCAGATTTCTGTTGCACATCATACAATTATCAAGTGCTGTTCAGGTCCTAATTAATTGGCTCAGGTGTGTTTGAACAGGGTTGGAGCTTAACTATGCAGAAAGGTAGAAATCCAGCAACAGGGTTGAGCACCCCTGTTTTAGACAATGTTTGTGAAATGAGATGTGGCGTAACTCTGTGCTGTTCATCTGCTCTCAGACTCTTCAG[C/T]GAGAGCTTCATGGCCACCGCTCGCGGGTGGAGGACGTCCTGGAGCGAGCAGGTCTCATCTCCTCCATCCGCAGTCCAGAGGCCGACAGTATCCGGGCCGGCATGGAGCAGCTCCATCAGCTGTGGGAGGCACTGTGGGCAGAGACGGAGCGCCGGCAGCTCACACTGGACGCCATGTACCAGGCACAGCAGTACTACTTTGATGTGGCAGAGGTGGAGGCCTGGCTGAGCGAACAGGAGCTGCACATGATGAATGAGGAGACCGGGAAGGTAGGATGACTGTGGGGATTAGGGTTGTTCTGCTACTGTTTCTAGTATCGGAAATACCAATAATGCAAACATTCTGGTATTGGGGAGTATTTGAAACCATAAACCAATCCGATGCCATCTTCTTAAATTAGACATGTGCACAGCCTTTTTATAATTCAGTTCATCTTTATATCTATAGTGCTTTTACAATGTAGATAGTGTTAACGCAGCTTAAAGGGCACCTATGGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39218
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 |
---|---|---|---|---|---|
ENSDART00000078561 | Nonsense | 209 | 1177 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 44475990)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46061484 |
GRCz11 | 18 | 46059502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTCTGTCTGTTCAGGATGAGGCCAGTACTCTGCAGCTGCTGAAGAAA[C/T]AGCTGGTGCTCGAGCAGACCATCGAGGACTATGCAGAAACCATCGGCCTG
Long Flanking Sequence:
GTGCGGTCCCCCCACCCACCAATATTGATTGAGCACCCCTAGTATTCAGCTTAAAGTGACATTTAAAAGCTTAACTGGGTTAAATAGGCAAGTCATTGTTTGTTCTGTATACATTAAAAACAAATATTGTTTAAGGGGGCTAATAATATTGACTGTAAAATGGTTTTAAAAAAGTTAAAAACTGCTTTTATTCTAGCCAAAATAAAACAAGACTTTCTCCTAAAGAAAAAAAAATATTTATAGGAAATACTATGAAAAATTCCTGAATCTGTTAAACCTCATTTTTGAAATATTAAAAAAAGAAACTAAATTTGACTTACACTGTATATACAGTAGTGCCACTGGTCCAGCAGACAGAAAAATGGACACTAGTGTAGACGTTATTTTCAGCCGAGGTCACCTGGCAGCATTATTGCAGATGCTATAGCTGATGACACAGAAGGATGAATGTATCTCTGTCTGTTCAGGATGAGGCCAGTACTCTGCAGCTGCTGAAGAAA[C/T]AGCTGGTGCTCGAGCAGACCATCGAGGACTATGCAGAAACCATCGGCCTGCTGTCTCAGCAGTGCAGACAGTTGCTTGAGCTCGGACATCCAGACTGGTGAATGATCAGCAGTCGCCTTACACTCAAACATCCACTGACTGCATCTCTACATACTATCATGAAATAATAATGAACAATACTTGTGCAGCATTCGTTAATCATAGTTGAACATTTACAGGAGTAACCGATGTCAGAGATGTGCTCCTGTGAATGAAATCCAGGTTTATGTTCGTGTTTCAGTGAGCAGATCAGCAAGCGTCAGTCTCAGATCGACAGGCTGTACGTGTCTCTGAAGGACCTGGTGGAGGAGAGGAAGTCTCGTCTGGAGCAGCAGTATTGGCTCTATCAGCTGAACAGAGAAGTGGATGAGCTGGAGCAGTGGATCGCGGAGAGAGAGGTCATCGCCAGCTCCACTGAACTCGGACAGGACTTTGAGCACGTCACGGTCAGTTCATCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23377
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078561 | Nonsense | 448 | 1177 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 44468054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46053548 |
GRCz11 | 18 | 46051566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACATGTTTTCCTCAGGTAAGACAGCTACAGGAGAGCGCAGCACAGCTC[C/T]GAACGGTTTACGCCGGTGAGAAAGCAGAGGCAATTGCCATGCAGGAACAC
Long Flanking Sequence:
CCATATTAATAGCATGTCAGTTTGGCTTGCTCACCGCTGGACAAGCACTAGTGGCTTTTAACACATGAGAGAGGGTTCTTTTGCTGTGCTCGTGTTTAAGGAGGCGTGGCTCTAGACGGCAGGGGAGGGACTGTGATTCAGAGATTTATGCTAAGCTGTTAGCATTGTGGAAGATCACCTACTGCACCTTTAAGCCTTTACATGTCACTTTAAGCTGAATTCTAGTATCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATGGTAAAGATAAAATAGATGAGTTATTAGAAATGAGTTATTAAAACTATTATGATTAGAAATGGGTTGAAAAAATCTCTCCGCTAAACAGAAAGTGGGTAAATAAATAGGTAAAGGGGGCTAATAATTCAAGGGGTTAATAACTCTGACTTCAACTTAATCAGTTTGTGGATAGATCTCTCTCACACATGTTTTCCTCAGGTAAGACAGCTACAGGAGAGCGCAGCACAGCTC[C/T]GAACGGTTTACGCCGGTGAGAAAGCAGAGGCAATTGCCATGCAGGAACACGAGGTGATGCAGGCGTGGAAAGAGCTGCTGATATCTTGTGAGGACTGCCGAATGCAGATAACCACAGCCACAGACAAGCTACGTTTCTTCGGGATGGTGCGTGACCAGCTGATGTGGATGGAAAGCATCATCTGCCAGATAGGAACTGGGGAGAAGCCAAGGTAGGACACACATGCTGGGACACTCGCTCTCCACTTATAGAAACTCATTAAGGTGCTTTAACATTATAATGCATGAAGATTTGCATCAGAGCAGATGGAGATTAGCCACTGTGGCCGCTGGAGTGTATTATAGATATCATACCACGTGCACAGATAAATGATAAGGTGGTAAGTGCATAACCTGCAAGAGTATTTATTCTTCCGATCAAGCATAATAGTTCTGTGTTTATTAAGAGCACTGTGTAGGAAAACAATAGATCTGTTACAAAACTTTTTGAGCTGCTACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32220
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078561 | Essential Splice Site | 943 | 1177 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 44453713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 46039207 |
GRCz11 | 18 | 46037225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACGTTAGCAGAGATTGTGGAGCAGCTTCAGGAAAGAGAAGCAGCACAG[G/A]TGTGTGGACAGTCTGTTTGTTTCTCTTGTTCAAACTACATTAGGTCACAT
Long Flanking Sequence:
TATCATAATTATAATAATAATATTAATAATAATAATATAAGTAAAAATCATAATATAATAAATATAAATATAATAATATAAATATAAAGTATAATTGAGCCTTAACAGAGCTTAACTCCACACACAGTAGAGAAGGTAATTAAAAACATTGACCTGGAAAAATTTGATCGATTATAGGTCCTGAATGTCGATTTCGATTTCTTTTCGATTAATCAGCCAGCCCTGGCGTCGGCCATCAGTATAAGAGAGCACACTGATTGGTCATTCAGCAAGGAATCATTGCGAGAACAAAAACGACAACTCAAGTAAACAATACAAGTCAAGAAGGACAGAAGCCAGCTGTTATTTCTCTGCATTTCTCAAATATTTGCAGACGATATAGATTATTAGATTAAGAGACCTATTGCAAGGTTTCAGACTTCCCCTTTTATGTTGGCAGGGAGAAAAGATCCACGTTAGCAGAGATTGTGGAGCAGCTTCAGGAAAGAGAAGCAGCACAG[G/A]TGTGTGGACAGTCTGTTTGTTTCTCTTGTTCAAACTACATTAGGTCACATGCTCATTATTACCTTATATTTGAAACTCAGGCTAGAGGAGAGATTCCACGACTCCCCAATGGATTGCCGGAAAAGACTTCTCGACCGGACCGGCCTCGGGCTCGGGATAGACCCAAACCGAGAAGACGACCAAGACCCAAGGAACCAACAGCTGGCGAAACACGACGCTCGAGGTCTGCTCCAGCTCAGAGCAGTCCACAAGTACCCCTGCCACCCACCCACACGGCCCAGCACGAAGGGTTCCTCTTCCGAAAAATTGACATCGAGGGCCAAAAGAAGAGTTCAAACAGGTGGGATTTTGTGGTCTAACCATTAAGGGTACATGGCATGGAATTAGCATGGAAATGGCTAAACTAAATATGCCAATCAGTATGATTGGTTATTCAAAGCTATGCTAATTTTGTTATTAGCATTGTGTATTGATGCTAGAGCACTGACATTTTTAATACA
Associated Phenotype:
Not determined