ZMP
NP_001177687.1
Ensembl ID:
Description:
collagen type V alpha-3b [Source:RefSeq peptide;Acc:NP_001177687]
Human Orthologue:
COL5A3
Human Description:
collagen, type V, alpha 3 [Source:HGNC Symbol;Acc:14864]
Mouse Orthologue:
Col5a3
Mouse Description:
collagen, type V, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:1858212]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32811 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9301 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12865 | Nonsense | Available for shipment | Available now |
sa19639 | Essential Splice Site | Available for shipment | Available now |
sa13950 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32811
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 |
---|---|---|---|---|---|
ENSDART00000014072 | Nonsense | 79 | 1675 | 2 | 64 |
Genomic Location (Zv9):
Chromosome 1 (position 60259597)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 58577294 |
GRCz11 | 1 | 59283739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGGCTTATAAGATTGACAAGAAAATCCAAGTTAGTGTGCCAACCAGC[C/T]AGCTCTTCCCAGGTATGAAGCACACACACACTCACACACACACTCACACA
Long Flanking Sequence:
AGGTTGTTGTGAAAGTCTTTCCAAATGAGTTCAGCTTTTCTTGTCTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTAGCAATGCTGATTACATTTGTGTGTTTGTGTGTGTGTAGCAATGCTGAGTACATTTGTGTGTGTGTGTGTGTGTGTGTGTGTAGCCATGCTGAGAACGTTAATATGTGTGTGTTTCACAAGCTCCAGGGCTGATATGAAGAGACGTATGACCAGTCCGGACCTGCATGCAGATATTTACACACAAACACACACACATACGAGAGCGGATCTGATTTCTGTCCATCAGTCTGTAAAGTAACAGATAGTGTTGTCTCCAGCAGCCAATCCCATCGATGTGCTGAAGGTTTTGGACCTATCAGAGTCCATGGAGGGTGTGTCTTTGGAGGCGGGGCTCTGCAGCAGTAGGCGGGGTTCAGAGGAGGCCGATCTGGCTTATAAGATTGACAAGAAAATCCAAGTTAGTGTGCCAACCAGC[C/T]AGCTCTTCCCAGGTATGAAGCACACACACACTCACACACACACTCACACAAACATACCCAAAGCCTGCAGCTTCACAGATGATCAAATACATGTGTGTCAGGGGTCTGATGCTTGAGAAAATGGGCAGTTTCCGTCTGATTCTGATTGGTTGAGTCACATTCTAAGCTGCAGTAAAGTACTCTACACACACCAGCGGCGGATCACAGTGTGTCTGTGGCTGCTTCTCTGTTGCTCTGCACTCATTTTGTTGTGACTGCCATGTGTTTTGTTCGTGTCATCAGCTGATTTTATATCTGCTGAGTTTATTGAGTGTTATACAGCAGAACTGCTCATGAAGCAGCGCTCTTCAGTCAGCTCATAACAGCTCTGAGAATACCCGAGACCTTCAGCTGCTCTACATTCACCTGTTGGGGGATTTTTGCTTCACTTCACCACAGCGGTCGATAAACTCGCCATCACTTCACTTGAAGGAGACTGTCATGAAGCCTTTATAATCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9301
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014072 | Essential Splice Site | 963 | 1675 | 39 | 64 |
Genomic Location (Zv9):
Chromosome 1 (position 60244663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 58562360 |
GRCz11 | 1 | 59268805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTGGATTAAAGGGAGGGACGGGGCCAATCGGGCCCCCAGGACCTGCYG[T/C]ATGTGTTCAGATCTCAGTATCTTMAGWAATCTCTCAACACTCATGRATAT
Long Flanking Sequence:
ATAGCCGTATGCTGCAGTCTGAGGTGCAGTTTAGGACTCGTTTCTATTCAGCTGATTTTCTATTCTGTATTTTTGCAGGGTAATACAGGAGAAACTGGACCGATGGGGGAACGAGGACACCCGGGATCCCCAGGACCTGCTGGAGAGCAAGGTTTACCTGGAGCCGCAGGGAAGGAGGGTTCAAAGGTGAGAAAATCCTTTTGAGCATTAAGAACTTCCCTTTTTAGCACTCATGACTTCCTTCAGTCATAACTTCGGTGTGTTCGGTCATCAGGGGGATCCTGGAGGTCAAGGCACTTCCGGGAAGAACGGTCCCACAGGTCTGAAGGGCTTCCGTGGCAGTCGTGGAGCACCGGGTGCCATGGTAACCTAAGAACACCTTCTGTCCTCTGTCAGGCTTTCTGATTGGCCAGGTTTGTCATGTGACCTGTGTTCTCTCGTGTAGGGGCCAGTTGGATTAAAGGGAGGGACGGGGCCAATCGGGCCCCCAGGACCTGCTG[T/C]ATGTGTTCAGATCTCAGTATCTTAAGTAATCTCTCAACACTCATGGATATATTCCCTGAAATAATCGGTCTGCTTTTCTTCCCAGGGGCCCACAGGTGAACGAGGACCCCCTGGATTGGCTGGTGCCATTGGTCAGCCCGGTCGACCTGGAACCAGCGGAGGGCCCGGACCAATGGGAGAGAAGGGAGAGCCAGTAAGGCACGCCTCCACACCTGAAGACCTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTAACTGTGTGTGTGTTGTCAGGGAGACAAAGGTCTGATCGGACCTGCAGGACAGGATGGTGAGCAGGGGCCTGTGGGACTACCAGGAGCAGCCGGCCCTCCAGGACCCCCAGGAGAGGATGGAGACAAGGTGATGAAGGCATATTTCAACACCCCCATGTCTTCCACACAGATTCTCCACACGATATCGCAGTTTAAGTTGCCTGAAAGCAAACACAGAAGACAGGATTGAGGAGAACACGGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12865
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 |
---|---|---|---|---|---|
ENSDART00000014072 | Nonsense | 1082 | 1675 | 44 | 64 |
Genomic Location (Zv9):
Chromosome 1 (position 60239400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 58557097 |
GRCz11 | 1 | 59263542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGTGTGTGTGTGTCAGGGTGTGGATGGTGAGGTYGGGCCTACAGGA[C/T]AGCAGGGCAWGTACGGACAGAAAGGAGACGAAGGGGCCCGAGGATTYAAG
Long Flanking Sequence:
ATGTCCTACAACTTTACACAAACAGCTGGAAACAAGTCCTCAAACCATACACAACAACTGAAACAAATCTTAAATGTACTTACAGGCTGCTGGTCTAGATGCTGATAAAGTGCTTCTCTTCTGAAGTCTCTTAATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGGGGGAAACTGGAGCTCCAGGACAGAAAGGCAGCAAAGGAGACAAAGGAGAATCAGTGAGTGACTGAACTAAAACACACACACACACACACACACACACACACACATGTCCAAGTGTCACTGATGATGTAAATCTGCACTCAGGGGCCTCCAGGTCCAGTCGGCTCTCAGGGGCCTGAGGGGCAGCCAGGAGCGCCGGTGAGTGTGTTTAATAAGGGGAAACTGGGGGTCTTCATCTCCTCACCGTGTGTTTGGAGTGTGTGATTAAGTATGTGTGTGTGTGTGTGTGTGTGTGTCAGGGTGTGGATGGTGAGGTTGGGCCTACAGGA[C/T]AGCAGGGCATGTACGGACAGAAAGGAGACGAAGGGGCCCGAGGATTCAAGGGCTCCAGGGGCCCGGGGGGACTGCAGGTACACCAGCACTCAACACTGATCCTCTGTCTGATTAAAGACTCGAACTAAACTCACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGGGAATGCCTGGTCCTCCTGGAGAGAAAGGAGAGAGCGGGAACTCTGGTCTGCTGGTGAGCTCATGATTGATCGGTCTGTGTTGATCAGCTCATGTTGAGGATATCAGCTTCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGCAGGGTCCTCCTGGTCAGTTTGGTCCTAGAGGAGCTCAGGGGCCCTCTGGTGGACAGGTAAACACACACATCTTGTGTTTAAGCTAAAGTTACGCAGATCTGGGAATGAGGAGCTAATAGTCGACTGAATCAGACAAATGTCTAATTTAAATATGCAAATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19639
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 |
---|---|---|---|---|---|
ENSDART00000014072 | Essential Splice Site | 1323 | 1675 | 54 | 64 |
Genomic Location (Zv9):
Chromosome 1 (position 60234249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 58552047 |
GRCz11 | 1 | 59258492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTGGGAAGCCGGGTCCTCAAGGTCTTCCAGGAATCCCAGGACCAGCG[G/A]TGAGATCCTCGACTCCTCAGGGGGTTTCCACACTTCCACACAGCAGGTTC
Long Flanking Sequence:
AATATGCATTATACCTCATCAGGGAGGAGCTGAATGAATGTTTAATCTGTATATCCTGCATTTTGCACACTGACGAGCATGTGACCCGGTGCTGCTGTAGTCATTGCATATACTGAACGTTCATTATTTGACTATGCTGAGGAATTCAGCCAGATTTTCTTTCAAATATAAAACAAGCATTAATAAATGACGTGTGAGAGTAGAGATGGGCTGAGCAGATGATGCATTCCAGAGGTCTGGCCAGCAGCTGAAACACACCATCCTCATTGAGTTTACATCTGCTTCTGTCAATCACCTTAAGGAGCTGATCAGCAGACCTCAGAGAAGAAGATCTGCTCACTGATGCTGCCAGACATGTTTGTGGTCATGTTTTCTGTGTTTTCTACTTTCAGGGCGCTCCGGGATACGAGGGCATTATAGGGAAGCCGGGGCCGGTGGGTGGGCAGGGGACCTCTGGGAAGCCGGGTCCTCAAGGTCTTCCAGGAATCCCAGGACCAGCG[G/A]TGAGATCCTCGACTCCTCAGGGGGTTTCCACACTTCCACACAGCAGGTTCAGGAACATTCGGAAGCACAAGAGCATCGGGCTGTTGACCTGAGACTCTGCAGACCAGAGCTGAGTCTCTAGAATTAATTCTTAGCATAGTTTTTTAAGAGCGCTTAGAGCGCTGTCTGCTGTTAAAAACTAGCATATACCGCCATCTGCTGTTAAAAACTAGCGAATACAGCAATCTGCTGTTAAAAACTAACGTATACCGCCATCTGCTGTTAAAAAACTACCGAATACGGCAATCTGCTATTAAAAACTAGCGAATACAGCAATCTGCTGTAAAAACTAACATATAGCGCCATCTGCTGTTATAAAACTTTGCGAATACGGCAATCTGCTGTTAAAAACTAGAGTATAGCGCCATCTGCTGTTCAAAAACTAGCATCTACCTCTGTATACTGTTTAAAAAGTAGCGTATAGCATGTCTACTATTAAAAACTACAGTATAGCGCCACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13950
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014072 | Essential Splice Site | 1323 | 1675 | 54 | 64 |
Genomic Location (Zv9):
Chromosome 1 (position 60234248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 58552046 |
GRCz11 | 1 | 59258491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTMTGGGAAGCCGGGTCCKCAAGGTCTTCCAGGAAWCCCAGGACCAGCGG[T/C]GAGATCCTCGACTCCTCAGGRGGTTTCCACACTTCCACAMAGCAGGTTCA
Long Flanking Sequence:
ATATGCATTATACCTCATCAGGGAGGAGCTGAATGAATGTTTAATCTGTATATCCTGCATTTTGCACACTGACGAGCATGTGACCCGGTGCTGCTGTAGTCATTGCATATACTGAACGTTCATTATTTGACTATGCTGAGGAATTCAGCCAGATTTTCTTTCAAATATAAAACAAGCATTAATAAATGACGTGTGAGAGTAGAGATGGGCTGAGCAGATGATGCATTCCAGAGGTCTGGCCAGCAGCTGAAACACACCATCCTCATTGAGTTTACATCTGCTTCTGTCAATCACCTTAAGGAGCTGATCAGCAGACCTCAGAGAAGAAGATCTGCTCACTGATGCTGCCAGACATGTTTGTGGTCATGTTTTCTGTGTTTTCTACTTTCAGGGCGCTCCGGGATACGAGGGCATTATAGGGAAGCCGGGGCCGGTGGGTGGGCAGGGGACCTCTGGGAAGCCGGGTCCTCAAGGTCTTCCAGGAATCCCAGGACCAGCGG[T/C]GAGATCCTCGACTCCTCAGGGGGTTTCCACACTTCCACACAGCAGGTTCAGGAACATTCGGAAGCACAAGAGCATCGGGCTGTTGACCTGAGACTCTGCAGACCAGAGCTGAGTCTCTAGAATTAATTCTTAGCATAGTTTTTTAAGAGCGCTTAGAGCGCTGTCTGCTGTTAAAAACTAGCATATACCGCCATCTGCTGTTAAAAACTAGCGAATACAGCAATCTGCTGTTAAAAACTAACGTATACCGCCATCTGCTGTTAAAAAACTACCGAATACGGCAATCTGCTATTAAAAACTAGCGAATACAGCAATCTGCTGTAAAAACTAACATATAGCGCCATCTGCTGTTATAAAACTTTGCGAATACGGCAATCTGCTGTTAAAAACTAGAGTATAGCGCCATCTGCTGTTCAAAAACTAGCATCTACCTCTGTATACTGTTTAAAAAGTAGCGTATAGCATGTCTACTATTAAAAACTACAGTATAGCGCCACCTG
Associated Phenotype:
Not determined