ms4a17a.5

Ensembl ID:

ENSDARG00000092204

ZFIN ID:

ZDB-GENE-040912-55

Description:

membrane-spanning 4-domains, subfamily A, member 17A.5 [Source:RefSeq peptide;Acc:NP_001004629]

Human Orthologues:

MS4A12, MS4A15, MS4A2, MS4A3, MS4A4A, MS4A8B, RP11-312N17.2

Human Descriptions:

Membrane-spanning 4-domains subfamily A member 18 [Source:UniProtKB/Swiss-Prot;Acc:Q3C1V0]
membrane-spanning 4-domains, subfamily A, member 12 [Source:HGNC Symbol;Acc:13370]
membrane-spanning 4-domains, subfamily A, member 15 [Source:HGNC Symbol;Acc:28573]
membrane-spanning 4-domains, subfamily A, member 2 (Fc fragment of IgE, high affinity I, receptor fo
membrane-spanning 4-domains, subfamily A, member 3 (hematopoietic cell-specific) [Source:HGNC Symbol
membrane-spanning 4-domains, subfamily A, member 4 [Source:HGNC Symbol;Acc:13371]
membrane-spanning 4-domains, subfamily A, member 8B [Source:HGNC Symbol;Acc:13380]

Mouse Orthologues:

AC134839.1, Ms4a15, Ms4a2, Ms4a3, Ms4a4b, Ms4a4c, Ms4a4d, Ms4a8a

Mouse Descriptions:

membrane-spanning 4-domains, subfamily A, member 15 Gene [Source:MGI Symbol;Acc:MGI:3617853]
membrane-spanning 4-domains, subfamily A, member 2 Gene [Source:MGI Symbol;Acc:MGI:95495]
membrane-spanning 4-domains, subfamily A, member 3 Gene [Source:MGI Symbol;Acc:MGI:2158468]
membrane-spanning 4-domains, subfamily A, member 4B Gene [Source:MGI Symbol;Acc:MGI:1913083]
membrane-spanning 4-domains, subfamily A, member 4C Gene [Source:MGI Symbol;Acc:MGI:1927656]
membrane-spanning 4-domains, subfamily A, member 4D Gene [Source:MGI Symbol;Acc:MGI:1913857]
membrane-spanning 4-domains, subfamily A, member 8A Gene [Source:MGI Symbol;Acc:MGI:1927657]

Allele Name	Consequence	Status	Availability
sa38444	Nonsense	Mutation detected in F1 DNA	Not yet available
sa26360	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa38444

Status:

Mutation detected in F1 DNA
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
ENSDART00000075598	Nonsense	45	234	2	7
ENSDART00000147574	Nonsense	51	155	2	5
ENSDART00000147908	Nonsense	51	240	2	7

Genomic Location (Zv9):

Chromosome 4 (position 60704330)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	75085455
GRCz11	4	76662193

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACAGCGTGTAGCAGGAGTTTCACCTCGTCAAGGAAATCAGGCCTTTCTT[A/T]AAGGCCAACCGAAAGCCCTCGGGGTGAGAAATCTCCCTTAAACCCAGATA

Long Flanking Sequence:

GAAACCTGACTGAAACACTTCAAAAACATATAGCGGAAACATAAAATGTTATTCCAGTACTTCTGTGACTATTTGATTGTTTGTTCCTCAAACACTAAAGAACGAAGCTCTCAGAGAATAGTGAGATCGAAGCATTAATAAACGAATACAAATCAGACGACTGTCATTCATTATTGTCTTTTTATTGTCACTTGTGATACCTTGTCTGATTGGCAATGTGATGTATATCATAGTTCAGATAATATTTATACAAATGTAGTTATAATATTTATCTATATTTTACTGATAATGGTATCCTCGTTTGCTTTATTTTGATTTTGTACAGGTCCATTTGATACTCTGAAACTGAAATGTCGACTGTCAGAACCATGAATCCTTCAACGATTGTCATCCAGCTTCAGCCACCGACACAAACAGCAACTGTGACCAGTTCTTCTGTGCCTGTGCGCATACAGCGTGTAGCAGGAGTTTCACCTCGTCAAGGAAATCAGGCCTTTCTT[A/T]AAGGCCAACCGAAAGCCCTCGGGGTGAGAAATCTCCCTTAAACCCAGATAACACACATTAACACACAGCATGTTATTCTGCTTTACTTTATAAAATACTCTCATCATTCTCACACTGTTCCCTCTTATTTCTCACAGACTGTCCAGATAATGATCGGTGTGGTGACTCTCCTGTTGGAAATCGTGTGTACAAGTTATGGATATTATCTCTTCCTCTTCACTGGTGCTTCTTACTGGGGATCTCTGATTGTAAGAAACAATTACCATGTTGTCCTAGATAACACAAGCTACAGTGTGTAATCAACCAGAATACATCTTACTGTCACATTTACAGTCACTAAAAGAACATGAAAATGTTTTTGTGTTTCAGTATGTGTGTAACATTGTTTTTGCAGGCGAGGCAGTGGCGCAGTGGGTAGCACGTTCGCCTTACAGCAAGAAGGTCGCTAGTTCGAACCTTGGCTCAGTAGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCC

Associated Phenotype:

Not determined

Allele Name:

sa26360

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075598	Essential Splice Site	90	234	4	7
ENSDART00000147574	Essential Splice Site	96	155	4	5
ENSDART00000147908	Essential Splice Site	96	240	4	7

Genomic Location (Zv9):

Chromosome 4 (position 60706073)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	75087198
GRCz11	4	76663936

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATATATATTTTCCAACATAAGCTGTAAGTTTTGCTCTTCTCTCTGTTCTC[A/G]GTACATTATTGCAGGCTCGCTCTCCATTGCTGCTGAAAACAAAATTAATT

Long Flanking Sequence:

AAGGTTGGGAAAGGACAAGGACTCGAGTGCAGTCAATTATGGGTATTTATTAATTATTAAAAACGGCAACAAGAACAACCCTGAGGAACAAACTAGACTGAAAGGGAACAGGACATGACATGACTCTCAGGAAGAATGACAAAAGTAGGACAACGAACTGGCACAGGACAGCAGACATGAGGAGACTATAAAGAAGAAATAATTAGCAAACAAACAGGTGCAAGTACTAAACTGACAATGGGTTAACTAGTGCTAGACTGAGCTCTGAACACAAACAAAATACACACCAAGATGGCGCTCATATAAAAGACAAACACAGACAACAACAGGAAAAGAGAGCTCGACCTGAAAAAACTTGAGCCGAGCACAACATACAAGACAAGACAGGACTAGTGTCTGGTTCATGCGGCAGTAAAATGCTCATTCTGGTTGAGTATCATGTATATCTGTATATATATTTTCCAACATAAGCTGTAAGTTTTGCTCTTCTCTCTGTTCTC[A/G]GTACATTATTGCAGGCTCGCTCTCCATTGCTGCTGAAAACAAAATTAATTCACCAACCGGTTTATGTTTGGTATGTACACAACACTTGATCTTTTCATGGGTCTACACACTGGATGCTTGTAAAATTTGGTCTGTAAGGATTTATGCATAAATATTCTTTTTTCTGTGCTAATAGAGTATTGAACACAGACTTTCCATGTAATCACTAAAGCCCTGCTCACACTGTGAGATTTCAGCCACGATTTTGTCATCTATCAATCCTAAAAGATTCCTGAAATCCCAGGCTAAAATCTGTGATCTTTGATCGTTGGTTTGACGTGTTCACACACAGCCGATTCGTGCTCGTTGTGATCAGATTTTTCCTCTGATGAAGTAAGAAAAGCCACTACAGATTGTTTATGTTTGCTGTAAGGAATCATTTCAGAATGCGGGATAGTGAAAGTGTCACGGGTGGATGACGTCAAACTCCGGGGGTGTTTTCTTTCGTGTTTGGCGCGTCT

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details