ZMP
LOC100001503
Ensembl ID:
Human Orthologue:
THSD7A
Human Description:
thrombospondin, type I, domain containing 7A [Source:HGNC Symbol;Acc:22207]
Mouse Orthologue:
Thsd7a
Mouse Description:
thrombospondin, type I, domain containing 7A Gene [Source:MGI Symbol;Acc:MGI:2685683]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36254 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28740 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16268 | Nonsense | Available for shipment | Available now |
sa15789 | Nonsense | Available for shipment | Available now |
sa22945 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28741 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36254
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 |
---|---|---|---|---|---|
ENSDART00000110471 | Nonsense | 266 | 1648 | 2 | 29 |
Genomic Location (Zv9):
Chromosome 16 (position 50164773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47030604 |
GRCz11 | 16 | 46997310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCGGTGGTGTTGCCGACCTCCACGGCCGCCCCCGTGCGCGCTGTGCGC[C/T]AAACCCGCCGGCGGAAGGGCAAGGAGCGGAAGGGCAGCAGAGACCCGGAG
Long Flanking Sequence:
ACAAAGAACTGTACGACTGGCGGCGGGGCGCGTGGAATCAGTGCGTGCCCATATCTCTGCGCACCGGCCGCACAGAAGCCTGTCTGCAGGGAGAGGAGGGCATCCAAACACGCGAAGTGTACTGCTCGCTCCGAGCGGACGGCTCGACAGCAGATGATGCCATCTGTGAGTACTTTGAGCCCAAACCCAGACAGGAACAGGCTTGTCTTATTCCGTGCCCTAAGGACTGTGTGGTGACTGAATTCACCCCGTGGACCACCTGCTCTAAGACATGCGGGTTGGGTTTGCAGAACCGTGTTCGATCTGTAGTGGCGCCGCCGCTTTTCGGTGGACTTCCGTGCCCGAATTTGACTGAGTTCCAGACGTGCGCGCCGAGGGCCTGCGAGGGCCGAGAGACGGTTTTTAATCTGAGAGTGGGCGGCTGGAGCGAGTGCCAGAGTTTGCCAGTGCCTCCGGTGGTGTTGCCGACCTCCACGGCCGCCCCCGTGCGCGCTGTGCGC[C/T]AAACCCGCCGGCGGAAGGGCAAGGAGCGGAAGGGCAGCAGAGACCCGGAGATGCGGGAGCTCATCAAGAGCAAGAGAAACCGCAACCGGCTCAGTCGGATGGAGGATGACCTCTGGAATATGGAAATAGGATTTCAGGCCCGACAAGTGGTTTGCGTTCATCGAAATGGAAGTACAGTGCCGCTCAGGTTAGTGACTTTCAGCATTAGAACTAAAGAGCTAATTTGGCATGAATAAACATGAGGTTTTGACGAATGCATGCATGCTGTGCAGTGTTAGTAGCCTACTGTAAGCAGTGTTGGGAAAAAAAAGTAATAAATTAAAATCAAGTCATTTAGTTAGTAGTAATAGGAGTGTGTGATTTTGCATTCTTAAAAGATTACGATCATGTGTTACATTATTTACCTAACAACAAGCCATTCTCACAAACATTGGCTGTGAATTTTGATTTCTTTGTGGACGAGTTGAATAGTGAAAATCCTACAACCTTGAAATAGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28740
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110471 | Nonsense | 822 | 1648 | 11 | 29 |
Genomic Location (Zv9):
Chromosome 16 (position 50306370)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47171946 |
GRCz11 | 16 | 47098026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGCTATCGAGTGATCATTCAGAGGCCAGCCAATGGAGGTCAGGAGTG[T/A]CCAGACACCCTTTATGAAGAGAAAGACTGCGCAGCTCCATCTGTCTGTCC
Long Flanking Sequence:
GAACCACCAACTTATCCAGTATATGTTTTACACAGCGGATGCTCTTCCAGCCGCAACCCATCTCTGGGAAACATCCATACACACTCATTTGCTGTCATTCCATCCCTCCATCCATAATTTTGTGTCTGCCATCCGTCCATCCATCCATCTATCCATTCATCCATCCATTCATTCATCTATTCATCCATCCATCCATCCATCTATCCGTCGTCTTTGTTATTCCATCCATTGCATTCAATGCTCTATCTTTCTGTCTCTATGTCTGATCATCTGTTGCTCCCTCTGTCCGTCATTCCATCCATCCGTCATTCCCTCCTTCCATCCATATTTCTGTCTGTCTTCCATTCCATCATTCCTCCATCTGTTGTTTTACCCCCCGCCAGAATAATTAAGCATGATATGAACTGACTGTTTGAAATGACAGGTGCAAATGGACAGAAGAATAAGCAGTCTCGCTATCGAGTGATCATTCAGAGGCCAGCCAATGGAGGTCAGGAGTG[T/A]CCAGACACCCTTTATGAAGAGAAAGACTGCGCAGCTCCATCTGTCTGTCCTGGTTACAGGTATGTCTTTACCCACAACTGATCTATTTCACATTTATTCACATTCAGTATAAACCTGATGAAACAAAGTTAGGATTTTATCGACCTGCTTAATTCAAATGAGTTTGTTTTCCAAAAGCAGTGGGTTTTTCAATGTGTCTCAAGTTAAGGTGGCTAATTGGGATTTACAATTCACCAACTGATCAACGTCTGCTGAAAATTATACTGAAGTTGCTTTCAACTTGCAGGTGGAAAACACACAAATGGCGTAAATGTCAGCTGGTTCCGTGGAGCATCCGCAGAGACAGTAAAGGAGCTCAGGAGAACTGCGGAGCTGGAATCCAGACTCGAGGTACTGTATGTCAGCTGTCATGCATATTATCAGTAATCCCTTGACCTCTTGAGCCCTTTCACACACTATAGGTGCAATACGGCGCCAAATGTACTCATTGTAAGCTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16268
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110471 | Nonsense | 1051 | 1648 | 15 | 29 |
Genomic Location (Zv9):
Chromosome 16 (position 50340522)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47206098 |
GRCz11 | 16 | 47131980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAATGGTCAAACTGGTCACGCTGCAGTAAATCCTGYGGCAGTGGTGTT[A/T]AAGTTCGCTCAAAATGGCTCAGAGAAAAGCCTTACAAYGGAGGAAGACCC
Long Flanking Sequence:
CCAAAGATGCTCTATTGGATTGAGATCTGGTGACTGTGGAGGCCATTTGAGTACAGTGAACTCAATATTCAAAGTCACTTAAATCACCTTCCCCACTCTGATGCTCAGTTTGAACTGCAACAGATTGTCTTGACCATGTCTAAATGCATTGAGTTGCTGCCATGTGATTGGCTGATTGAGTTGGACAGGTGTACCTAATAAAATGGCCCATGAGTGTATTTGCTGTTCTTGTGCACTTAAAAAAAAAAAAAAAAAACATTTCGGGCAGGCATCCATTAATTTAATCCTTGAAACCTTGTAGACATTTTATATTAACAACCAGCTACATTACACACTGCTAATGTAATATTCAAAAACGAAAAGCTTTTGTGAGTTGACCATTTGGAATTTGTTTTTCAGGGTATATCGAGGAGGCCTGCATTGTTCCCTGTCCTTCTGACTGTAAACTGAGTGAATGGTCAAACTGGTCACGCTGCAGTAAATCCTGTGGCAGTGGTGTT[A/T]AAGTTCGCTCAAAATGGCTCAGAGAAAAGCCTTACAACGGAGGAAGACCCTGCCCAAAACTGGACCACCTGAACCAGGTAAACATTCCCCTTCCATATGCCTAAATGTATTATTAAAGTTTTTGAGTGTTTTGGTTTGGTTTGTTTTTTTGTTTTGGTTTGAATTGGGTTGGTTTGTTTTGTGGTTTTGGATTTGTTTGTTTGTTGTTTTTGCTTGTTTTGGTTTTGTTGTTTTTTTGTTTTGTTTTTTTTTTTTGTTTTTTTGGGGGGGGGGGGGGGGGGCTTGGTTTATTTTTTTGGTTTGGGTTTTTCAGTTTTTGTTTGTTTTTTTGTTTTTTTGTTTTGTTTTGGGTTTGGTTTGGATTTTTTGTATGTTTGTTTTGGTTTGGTTTTTTGTTTTGTTTTGATTTGTTGTTTGGTTTTGTTTGTTTTTGTGTTATTTTGTTTTATCTTATTTTGTTTGAATTTAATTCATTGGAATTTCTTAGAATTTAATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15789
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 |
---|---|---|---|---|---|
ENSDART00000110471 | Nonsense | 1191 | 1648 | 19 | 29 |
Genomic Location (Zv9):
Chromosome 16 (position 50352274)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47217850 |
GRCz11 | 16 | 47143327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCGTGCACTGGAAGAGGAGATCGGGAGAGGAYGGCGTTCGCTCTGCGTT[T/A]GCCTAAAGAGGGAGAGGACTGTCCTGTCAGCATGCAGACYGAGCCCTGCC
Long Flanking Sequence:
TATCATACTAGCAGCTGTAATGCATCCAGTCTTGAGAAGAATAAAGGATTTTTTACCTATATTAGGTATGCTTTTAAAATATTATTATATTTTAGCATTATTTGAATCTTTGTTTCATAATAGTTTTAGTTTTAGTAAATATAAATAACAACCCTGATGCCATTATCTTATTTTTGCCTGTTATAATTGTTTTGTGCATCTAAGATGTGTCTTTTATATCTCAGTAAAACACCTGCTAAGAAACATCAGAGCAGTATCATTTTTAGGTTAGGCCAACAGGGACGTCATTTTACCCTGACATGAAATGACCTCAGCGAGAGCCAGCAGACATAAAAAACCAGAGCAGGTCATTTAAAGGCTCTTGTTAAACAGTAAAAGAGCAGCTTGAGGAGAAACATAAGAGAATTACGGGCTCAGTAAAAGCCTAGTGTGTTTTGTGCTCCTGTTAAAGCCGTGCACTGGAAGAGGAGATCGGGAGAGGACGGCGTTCGCTCTGCGTT[T/A]GCCTAAAGAGGGAGAGGACTGTCCTGTCAGCATGCAGACCGAGCCCTGCCTGCTCAACCGCAACTGCTTCCACTACAGCTACAATATCACTGGTGAGCATCACCACAAAACAATACATCAGTTAGGATCAGTTTTGAATTCTGTGTTTGCTGTGGGACACATTTTTGTGGTTGTGCAATTTTGTAATTACATATAGAGTTGGTAAACTACACCCACTTCTACTATTACTAACATATAATAACAATAATAATAATAGTAATAATAATTATAATCATTTCTAAATAAAAACTAAGAAATGTTAAGATGTCTGTTATCATCAAAATGGCTATATGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAGTAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATTTCTCAATAAAAACTAAGAAATATTAAGATGTCTGTCATCATCAAGATGGCTATATAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22945
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 |
---|---|---|---|---|---|
ENSDART00000110471 | Nonsense | 1583 | 1648 | 27 | 29 |
Genomic Location (Zv9):
Chromosome 16 (position 50381790)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47247366 |
GRCz11 | 16 | 47172453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCCACCCTGCCCACCACTGTACAGCCTGGACGCGTCGGACGCACGTG[G/A]TACTTACAGCCTTTTGGAGCAGGTAAACGTGTTTCACTTCTGTTAGCAAA
Long Flanking Sequence:
TACTACATTAGTGTTTCTGGGTCTTTCCAAAAAAGGAAAAATGTATAACTTAATAACATTAGCCTGAAGAGAGAAAGACAAATGTTCTCCATTAGCTATTGCATAATACATCAGCAGCACTGACACGATTTTCAGTAACTTAATGGCAAGGTAATAAAACTCAGTATAGTGTTATAAATGTGTGAAGTTGATAACAGTGTAAATGTGTCATCACGCTTTATATAAAAAGGCTCCATAAGCTGTGAATTGGGTCAGAAGCGGATGCAGATTGAATGATGTGTGTTTGTGTTCCTCTGCTGCCCTCTGCAGGAGGCCGTGTGTATGTGCGAGGAGGGCTTTACTGAAGTGCTCACCACCGAGGGAGCGCTGGAGCAGTGCGCACCCATTCCTGTGCTGGAAATCCCCACTGCTGGAGACAAGAAGGCTGATGTGAAGACCAGCCGGGCTATCAATCCCACCCTGCCCACCACTGTACAGCCTGGACGCGTCGGACGCACGTG[G/A]TACTTACAGCCTTTTGGAGCAGGTAAACGTGTTTCACTTCTGTTAGCAAATACACGTTTCCCCGATTTCTGTTTAACAGAGAATAGTTTACAAATTGTAACCTCCAGCATAAATATGCTATTAAACTCACTGAAATATTGCTGACAATAGCTAAAAAAAAATGCATTGCTTTAAAATGGAAAACAGACATTGATGTACCAATTGGACTGTGGATCTCAGAAGTTTGCAACTGTATCCCATTGGAGAAGATCACATATTCTTTGAGAGGAAAGGGTGAATTATTTAAAAAGATTTGGAATCAATTTTGGAATAAATTTAAAACAGTACCACTTGATTTAAATTTGACAAGATAGTTCTTTTCCACTGGTTTTATACTCCTATTATTATTACCTATTATCTCCACCCTTTTTTATTTATTTATTTGTATTTTACTTATTTTTTATACTGTGTATGATTTACTTTAGTCTGTTTGCTGCTTTGTTTTGATGTTCTGTATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28741
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110471 | Nonsense | 1584 | 1648 | 27 | 29 |
Genomic Location (Zv9):
Chromosome 16 (position 50381793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47247369 |
GRCz11 | 16 | 47172456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACCCTGCCCACCACTGTACAGCCTGGACGCGTCGGACGCACGTGGTA[C/A]TTACAGCCTTTTGGAGCAGGTAAACGTGTTTCACTTCTGTTAGCAAATAC
Long Flanking Sequence:
TACATTAGTGTTTCTGGGTCTTTCCAAAAAAGGAAAAATGTATAACTTAATAACATTAGCCTGAAGAGAGAAAGACAAATGTTCTCCATTAGCTATTGCATAATACATCAGCAGCACTGACACGATTTTCAGTAACTTAATGGCAAGGTAATAAAACTCAGTATAGTGTTATAAATGTGTGAAGTTGATAACAGTGTAAATGTGTCATCACGCTTTATATAAAAAGGCTCCATAAGCTGTGAATTGGGTCAGAAGCGGATGCAGATTGAATGATGTGTGTTTGTGTTCCTCTGCTGCCCTCTGCAGGAGGCCGTGTGTATGTGCGAGGAGGGCTTTACTGAAGTGCTCACCACCGAGGGAGCGCTGGAGCAGTGCGCACCCATTCCTGTGCTGGAAATCCCCACTGCTGGAGACAAGAAGGCTGATGTGAAGACCAGCCGGGCTATCAATCCCACCCTGCCCACCACTGTACAGCCTGGACGCGTCGGACGCACGTGGTA[C/A]TTACAGCCTTTTGGAGCAGGTAAACGTGTTTCACTTCTGTTAGCAAATACACGTTTCCCCGATTTCTGTTTAACAGAGAATAGTTTACAAATTGTAACCTCCAGCATAAATATGCTATTAAACTCACTGAAATATTGCTGACAATAGCTAAAAAAAAATGCATTGCTTTAAAATGGAAAACAGACATTGATGTACCAATTGGACTGTGGATCTCAGAAGTTTGCAACTGTATCCCATTGGAGAAGATCACATATTCTTTGAGAGGAAAGGGTGAATTATTTAAAAAGATTTGGAATCAATTTTGGAATAAATTTAAAACAGTACCACTTGATTTAAATTTGACAAGATAGTTCTTTTCCACTGGTTTTATACTCCTATTATTATTACCTATTATCTCCACCCTTTTTTATTTATTTATTTGTATTTTACTTATTTTTTATACTGTGTATGATTTACTTTAGTCTGTTTGCTGCTTTGTTTTGATGTTCTGTATTGTTAAC
Associated Phenotype:
Not determined